roebe 0.5.187

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Files changed (2901) hide show
  1. checksums.yaml +7 -0
  2. data/README.md +5852 -0
  3. data/bin/blinking_cursor +7 -0
  4. data/bin/browser +7 -0
  5. data/bin/colourized_tokenitor1 +7 -0
  6. data/bin/colourized_tokenitor2 +7 -0
  7. data/bin/colourized_tokenitor3 +7 -0
  8. data/bin/colourized_tokenitor4 +7 -0
  9. data/bin/colourized_tokenitor5 +7 -0
  10. data/bin/compare_these_two_directories +7 -0
  11. data/bin/create_file_skeleton +7 -0
  12. data/bin/create_my_directories +7 -0
  13. data/bin/create_wpa_supplicant_build_file +7 -0
  14. data/bin/create_zip +7 -0
  15. data/bin/custom_invoke +28 -0
  16. data/bin/delete_empty_files +7 -0
  17. data/bin/display_gcc_version +7 -0
  18. data/bin/do_a_google_search +7 -0
  19. data/bin/extract_gem_file +7 -0
  20. data/bin/fragment_maker +7 -0
  21. data/bin/generate_fstab_file +7 -0
  22. data/bin/handle_xorg_related_boot_phase +7 -0
  23. data/bin/hello_world +7 -0
  24. data/bin/in +7 -0
  25. data/bin/increment_application_version +7 -0
  26. data/bin/increment_application_version_then_push_the_gem +13 -0
  27. data/bin/install_all_registered_fonts +7 -0
  28. data/bin/install_jruby_addons +7 -0
  29. data/bin/install_my_addons +97 -0
  30. data/bin/install_my_addons.rb +97 -0
  31. data/bin/interactive_file_creator +7 -0
  32. data/bin/java_compile_statically +11 -0
  33. data/bin/kill_firefox +7 -0
  34. data/bin/kill_palemoon +7 -0
  35. data/bin/konsole_title +7 -0
  36. data/bin/larrow +7 -0
  37. data/bin/log10 +7 -0
  38. data/bin/menugenerator +7 -0
  39. data/bin/modify_shebang_header +7 -0
  40. data/bin/openpdf1 +7 -0
  41. data/bin/openpdf2 +7 -0
  42. data/bin/openpdf3 +7 -0
  43. data/bin/openpdf4 +7 -0
  44. data/bin/openpdf5 +7 -0
  45. data/bin/openpdf6 +7 -0
  46. data/bin/openpdf7 +7 -0
  47. data/bin/openpdf8 +7 -0
  48. data/bin/openpdf9 +7 -0
  49. data/bin/passwords +7 -0
  50. data/bin/path_generator +7 -0
  51. data/bin/print_this_unicode_symbol +7 -0
  52. data/bin/quick_colour_test +13 -0
  53. data/bin/rarrow +7 -0
  54. data/bin/rdate +7 -0
  55. data/bin/remove_this_substring_from_all_files +7 -0
  56. data/bin/replace_space_with_underscore +7 -0
  57. data/bin/rfirefox +7 -0
  58. data/bin/rinstall2 +7 -0
  59. data/bin/roebe +7 -0
  60. data/bin/roebe_documentation +7 -0
  61. data/bin/roebeshell +11 -0
  62. data/bin/ruby_cat +7 -0
  63. data/bin/ruby_dhcpcd +7 -0
  64. data/bin/run +7 -0
  65. data/bin/rxinitrc +7 -0
  66. data/bin/set_alias_1 +7 -0
  67. data/bin/set_alias_10 +7 -0
  68. data/bin/set_alias_11 +7 -0
  69. data/bin/set_alias_12 +7 -0
  70. data/bin/set_alias_13 +7 -0
  71. data/bin/set_alias_14 +7 -0
  72. data/bin/set_alias_15 +7 -0
  73. data/bin/set_alias_2 +7 -0
  74. data/bin/set_alias_3 +7 -0
  75. data/bin/set_alias_4 +7 -0
  76. data/bin/set_alias_5 +7 -0
  77. data/bin/set_alias_6 +7 -0
  78. data/bin/set_alias_7 +7 -0
  79. data/bin/set_alias_8 +7 -0
  80. data/bin/set_alias_9 +7 -0
  81. data/bin/set_browser +7 -0
  82. data/bin/setpdf1 +7 -0
  83. data/bin/setpdf2 +7 -0
  84. data/bin/setpdf3 +7 -0
  85. data/bin/setpdf4 +7 -0
  86. data/bin/setpdf5 +7 -0
  87. data/bin/setpdf6 +7 -0
  88. data/bin/setpdf7 +7 -0
  89. data/bin/setpdf8 +7 -0
  90. data/bin/setpdf9 +7 -0
  91. data/bin/show_available_users +7 -0
  92. data/bin/show_ten_aliases +7 -0
  93. data/bin/simple_extractor +9 -0
  94. data/bin/start_lighty +7 -0
  95. data/bin/symlink_directories_from_that_directory_to_the_current_directory +7 -0
  96. data/bin/symlink_everything_from_that_directory_to_this_directory +7 -0
  97. data/bin/symlink_files_from_that_directory_to_the_current_directory +7 -0
  98. data/bin/take_screenshot +7 -0
  99. data/bin/to_binary +7 -0
  100. data/bin/tokenitor +7 -0
  101. data/bin/vim_paradise +7 -0
  102. data/bin/wlan +7 -0
  103. data/bin/word_count +7 -0
  104. data/bin/write_what_into +7 -0
  105. data/bin/yaml_check +7 -0
  106. data/doc/README.gen +5790 -0
  107. data/doc/add_ons_for_ruby/README.md +3 -0
  108. data/doc/add_ons_for_ruby/activerecord.md +99 -0
  109. data/doc/add_ons_for_ruby/ansicolor.md +62 -0
  110. data/doc/add_ons_for_ruby/axlsx.md +60 -0
  111. data/doc/add_ons_for_ruby/bundler.md +20 -0
  112. data/doc/add_ons_for_ruby/byebug.md +14 -0
  113. data/doc/add_ons_for_ruby/camping.md +9 -0
  114. data/doc/add_ons_for_ruby/caxlsx.md +72 -0
  115. data/doc/add_ons_for_ruby/cgi.md +124 -0
  116. data/doc/add_ons_for_ruby/chunkypng.md +19 -0
  117. data/doc/add_ons_for_ruby/classifier.md +7 -0
  118. data/doc/add_ons_for_ruby/coderay.md +82 -0
  119. data/doc/add_ons_for_ruby/daemons.md +92 -0
  120. data/doc/add_ons_for_ruby/dl.md +114 -0
  121. data/doc/add_ons_for_ruby/erb.md +25 -0
  122. data/doc/add_ons_for_ruby/erubis.md +124 -0
  123. data/doc/add_ons_for_ruby/ferret.md +16 -0
  124. data/doc/add_ons_for_ruby/ffi.md +28 -0
  125. data/doc/add_ons_for_ruby/fox_and_fxruby.md +492 -0
  126. data/doc/add_ons_for_ruby/fpdf.md +389 -0
  127. data/doc/add_ons_for_ruby/fpm.md +46 -0
  128. data/doc/add_ons_for_ruby/ftp.md +70 -0
  129. data/doc/add_ons_for_ruby/fxruby.md +14 -0
  130. data/doc/add_ons_for_ruby/gist.md +30 -0
  131. data/doc/add_ons_for_ruby/glimmer-libui.md +43 -0
  132. data/doc/add_ons_for_ruby/gmail.md +22 -0
  133. data/doc/add_ons_for_ruby/gosu.md +12 -0
  134. data/doc/add_ons_for_ruby/graphviz.md +246 -0
  135. data/doc/add_ons_for_ruby/gruff.md +95 -0
  136. data/doc/add_ons_for_ruby/hexapdf.md +66 -0
  137. data/doc/add_ons_for_ruby/highline.md +16 -0
  138. data/doc/add_ons_for_ruby/iconv.md +20 -0
  139. data/doc/add_ons_for_ruby/id3lib.md +173 -0
  140. data/doc/add_ons_for_ruby/inline.md +30 -0
  141. data/doc/add_ons_for_ruby/inotify.md +130 -0
  142. data/doc/add_ons_for_ruby/instiki.md +38 -0
  143. data/doc/add_ons_for_ruby/jruby.md +253 -0
  144. data/doc/add_ons_for_ruby/json.md +64 -0
  145. data/doc/add_ons_for_ruby/kramdown.md +34 -0
  146. data/doc/add_ons_for_ruby/lexer.md +19 -0
  147. data/doc/add_ons_for_ruby/libarchive.md +91 -0
  148. data/doc/add_ons_for_ruby/libburn.md +29 -0
  149. data/doc/add_ons_for_ruby/mail.md +51 -0
  150. data/doc/add_ons_for_ruby/md5reverse.md +10 -0
  151. data/doc/add_ons_for_ruby/mechanize.md +195 -0
  152. data/doc/add_ons_for_ruby/memcache.md +22 -0
  153. data/doc/add_ons_for_ruby/midilib.md +35 -0
  154. data/doc/add_ons_for_ruby/mime.md +15 -0
  155. data/doc/add_ons_for_ruby/minitest.md +39 -0
  156. data/doc/add_ons_for_ruby/misc.md +3 -0
  157. data/doc/add_ons_for_ruby/mongrel.md +68 -0
  158. data/doc/add_ons_for_ruby/mp3info.md +121 -0
  159. data/doc/add_ons_for_ruby/mpd.md +16 -0
  160. data/doc/add_ons_for_ruby/mruby.md +13 -0
  161. data/doc/add_ons_for_ruby/nokogiri.md +32 -0
  162. data/doc/add_ons_for_ruby/opal.md +53 -0
  163. data/doc/add_ons_for_ruby/openid.md +10 -0
  164. data/doc/add_ons_for_ruby/padrino.md +4 -0
  165. data/doc/add_ons_for_ruby/passenger.md +4 -0
  166. data/doc/add_ons_for_ruby/prawn.md +269 -0
  167. data/doc/add_ons_for_ruby/pry.md +85 -0
  168. data/doc/add_ons_for_ruby/puma.md +29 -0
  169. data/doc/add_ons_for_ruby/qt_and_kde.md +793 -0
  170. data/doc/add_ons_for_ruby/rack.md +212 -0
  171. data/doc/add_ons_for_ruby/ragel.md +19 -0
  172. data/doc/add_ons_for_ruby/rails.md +97 -0
  173. data/doc/add_ons_for_ruby/ramaze.md +72 -0
  174. data/doc/add_ons_for_ruby/rbenv.md +13 -0
  175. data/doc/add_ons_for_ruby/redcarpet.md +6 -0
  176. data/doc/add_ons_for_ruby/redcloth.md +11 -0
  177. data/doc/add_ons_for_ruby/redmine.md +8 -0
  178. data/doc/add_ons_for_ruby/rmagick.md +555 -0
  179. data/doc/add_ons_for_ruby/roda.md +6 -0
  180. data/doc/add_ons_for_ruby/rspec.md +12 -0
  181. data/doc/add_ons_for_ruby/rtf.md +74 -0
  182. data/doc/add_ons_for_ruby/rubocop.md +84 -0
  183. data/doc/add_ons_for_ruby/ruby_users.md +23 -0
  184. data/doc/add_ons_for_ruby/rubygame.md +403 -0
  185. data/doc/add_ons_for_ruby/ruport.md +23 -0
  186. data/doc/add_ons_for_ruby/rvm.md +17 -0
  187. data/doc/add_ons_for_ruby/sdl.md +200 -0
  188. data/doc/add_ons_for_ruby/sequel.md +55 -0
  189. data/doc/add_ons_for_ruby/setup.md +92 -0
  190. data/doc/add_ons_for_ruby/shoes.md +7 -0
  191. data/doc/add_ons_for_ruby/sinatra_tutorial/sinatra_tutorial.cgi +7 -0
  192. data/doc/add_ons_for_ruby/sinatra_tutorial/sinatra_tutorial.rb +960 -0
  193. data/doc/add_ons_for_ruby/sinatra_tutorial/sinatra_tutorial.sinatra +56 -0
  194. data/doc/add_ons_for_ruby/slop.md +27 -0
  195. data/doc/add_ons_for_ruby/spreadsheet.md +153 -0
  196. data/doc/add_ons_for_ruby/sqlite.md +115 -0
  197. data/doc/add_ons_for_ruby/systemu.md +21 -0
  198. data/doc/add_ons_for_ruby/thor.md +16 -0
  199. data/doc/add_ons_for_ruby/tk.md +468 -0
  200. data/doc/add_ons_for_ruby/tty.md +9 -0
  201. data/doc/add_ons_for_ruby/tty_box.md +28 -0
  202. data/doc/add_ons_for_ruby/tty_prompt.md +25 -0
  203. data/doc/add_ons_for_ruby/vorbistagger.md +33 -0
  204. data/doc/add_ons_for_ruby/watir.md +30 -0
  205. data/doc/add_ons_for_ruby/webrick.md +399 -0
  206. data/doc/add_ons_for_ruby/whois.md +52 -0
  207. data/doc/add_ons_for_ruby/windows.md +346 -0
  208. data/doc/add_ons_for_ruby/writeexcel.md +67 -0
  209. data/doc/add_ons_for_ruby/wxwidgets.md +3 -0
  210. data/doc/add_ons_for_ruby/xml.md +198 -0
  211. data/doc/add_ons_for_ruby/xosd.md +21 -0
  212. data/doc/add_ons_for_ruby/yard.md +39 -0
  213. data/doc/add_ons_for_ruby/zip.md +67 -0
  214. data/doc/core/abbrev.md +31 -0
  215. data/doc/core/argf.md +26 -0
  216. data/doc/core/argv.md +102 -0
  217. data/doc/core/array.md +1142 -0
  218. data/doc/core/base64.md +7 -0
  219. data/doc/core/basic_object.md +24 -0
  220. data/doc/core/benchmarks_and_profiling.md +87 -0
  221. data/doc/core/bigdecimal.md +13 -0
  222. data/doc/core/binding.md +33 -0
  223. data/doc/core/blocks.md +45 -0
  224. data/doc/core/class.md +43 -0
  225. data/doc/core/closure.md +207 -0
  226. data/doc/core/commandline.md +9 -0
  227. data/doc/core/comparable.md +9 -0
  228. data/doc/core/compiling_ruby_c_code.md +1969 -0
  229. data/doc/core/conditional_requires.md +13 -0
  230. data/doc/core/constants.md +87 -0
  231. data/doc/core/csv.md +55 -0
  232. data/doc/core/dir.md +102 -0
  233. data/doc/core/drb.md +121 -0
  234. data/doc/core/encoding.md +158 -0
  235. data/doc/core/enumerable.md +160 -0
  236. data/doc/core/enumerator.md +38 -0
  237. data/doc/core/env.md +12 -0
  238. data/doc/core/errno.md +24 -0
  239. data/doc/core/error_codes_in_ruby.md +19 -0
  240. data/doc/core/etc.md +95 -0
  241. data/doc/core/eval.md +20 -0
  242. data/doc/core/exceptions_and_errors.md +247 -0
  243. data/doc/core/fiber.md +23 -0
  244. data/doc/core/fiddle.md +20 -0
  245. data/doc/core/file.md +388 -0
  246. data/doc/core/fileutils.md +74 -0
  247. data/doc/core/float.md +33 -0
  248. data/doc/core/garbage_collection_in_ruby.md +75 -0
  249. data/doc/core/gem_and_gemspec.md +447 -0
  250. data/doc/core/getoptlang.md +19 -0
  251. data/doc/core/handling_networks.md +63 -0
  252. data/doc/core/hash.md +485 -0
  253. data/doc/core/hooks.md +47 -0
  254. data/doc/core/imap.md +7 -0
  255. data/doc/core/integer.md +106 -0
  256. data/doc/core/io.md +126 -0
  257. data/doc/core/io_console.md +31 -0
  258. data/doc/core/irb.md +180 -0
  259. data/doc/core/iterators.md +194 -0
  260. data/doc/core/kernel.md +227 -0
  261. data/doc/core/keyword_arguments.md +10 -0
  262. data/doc/core/loops.md +24 -0
  263. data/doc/core/marshal.md +123 -0
  264. data/doc/core/math.md +452 -0
  265. data/doc/core/matrix.md +16 -0
  266. data/doc/core/mechanize.md +3 -0
  267. data/doc/core/methods.md +221 -0
  268. data/doc/core/misc.md +1779 -0
  269. data/doc/core/mkmf.md +164 -0
  270. data/doc/core/module.md +76 -0
  271. data/doc/core/mutex.md +63 -0
  272. data/doc/core/nil.md +14 -0
  273. data/doc/core/object.md +238 -0
  274. data/doc/core/objectspace.md +28 -0
  275. data/doc/core/open3.md +24 -0
  276. data/doc/core/open_uri.md +29 -0
  277. data/doc/core/openssl.md +45 -0
  278. data/doc/core/openstruct.md +67 -0
  279. data/doc/core/optparser.md +234 -0
  280. data/doc/core/pathname.md +49 -0
  281. data/doc/core/performance_considerations_in_ruby.md +31 -0
  282. data/doc/core/pp.md +39 -0
  283. data/doc/core/precedence.md +27 -0
  284. data/doc/core/prime.md +13 -0
  285. data/doc/core/proc.md +131 -0
  286. data/doc/core/process.md +303 -0
  287. data/doc/core/pstore.md +23 -0
  288. data/doc/core/psych.md +7 -0
  289. data/doc/core/pty.md +11 -0
  290. data/doc/core/ractor.md +12 -0
  291. data/doc/core/rake.md +130 -0
  292. data/doc/core/random.md +17 -0
  293. data/doc/core/range.md +25 -0
  294. data/doc/core/rational.md +7 -0
  295. data/doc/core/rbconfig.md +39 -0
  296. data/doc/core/rdoc.md +67 -0
  297. data/doc/core/readline.md +306 -0
  298. data/doc/core/refinements.md +23 -0
  299. data/doc/core/regex.md +663 -0
  300. data/doc/core/reline.md +76 -0
  301. data/doc/core/ripper.md +57 -0
  302. data/doc/core/ruby_and_c.md +8 -0
  303. data/doc/core/rubyvm.md +28 -0
  304. data/doc/core/set.md +26 -0
  305. data/doc/core/shellwords.md +34 -0
  306. data/doc/core/signals.md +32 -0
  307. data/doc/core/singleton.md +47 -0
  308. data/doc/core/sockets.md +137 -0
  309. data/doc/core/splat.md +10 -0
  310. data/doc/core/stderr.md +3 -0
  311. data/doc/core/stdin.md +27 -0
  312. data/doc/core/stdout.md +14 -0
  313. data/doc/core/string.md +854 -0
  314. data/doc/core/stringio.md +54 -0
  315. data/doc/core/stringscanner.md +43 -0
  316. data/doc/core/struct.md +52 -0
  317. data/doc/core/subclassing.md +41 -0
  318. data/doc/core/symbols.md +47 -0
  319. data/doc/core/system.md +3 -0
  320. data/doc/core/tcpsocket.md +14 -0
  321. data/doc/core/telnet.md +35 -0
  322. data/doc/core/tempfile.md +34 -0
  323. data/doc/core/threads.md +127 -0
  324. data/doc/core/time.md +335 -0
  325. data/doc/core/tracepoint.md +7 -0
  326. data/doc/core/unicode.md +5 -0
  327. data/doc/core/unittest.md +8 -0
  328. data/doc/core/unprintable_characters.md +17 -0
  329. data/doc/core/uri.md +14 -0
  330. data/doc/core/xml.md +13 -0
  331. data/doc/core/yaml.md +376 -0
  332. data/doc/core/zlib.md +111 -0
  333. data/doc/deprecations/deprecations.md +60 -0
  334. data/doc/documentation_viewer.cgi +87 -0
  335. data/doc/linux_may_have_issues/linux_may_have_issues.md +92 -0
  336. data/doc/misc/how_to_publish.md +49 -0
  337. data/doc/misc/links.md +19 -0
  338. data/doc/misc/the_initialize_method.md +2 -0
  339. data/doc/misc/the_perfect_book.md +14 -0
  340. data/doc/roebeshell/CONFIGURATION_FOR_THE_ROEBE_SHELL.md +381 -0
  341. data/doc/roebeshell/MANIFESTO_FOR_THE_ROEBE_SHELL_COMPONENT.md +391 -0
  342. data/doc/roebeshell/PHILOSOPHY_OF_THE_ROEBE_SHELL.md +64 -0
  343. data/doc/ruby_on_rails_tutorial/data_types_for_rails_migrations.md +11 -0
  344. data/doc/ruby_on_rails_tutorial/ruby_on_rails_tutorial.cgi +404 -0
  345. data/doc/statistics/statistics.md +94 -0
  346. data/doc/the_ruby_philosophy/the_ruby_philosophy.md +209 -0
  347. data/doc/todo/todo_for_the_roebe_project_on_windows.md +4 -0
  348. data/doc/todo/todo_for_the_roebe_shell.md +741 -0
  349. data/examples/README.md +4 -0
  350. data/examples/date_and_time/is_this_day_part_of_that_range.rb +45 -0
  351. data/examples/gui/fxruby/hello_world.rb +11 -0
  352. data/examples/gui/fxruby/text_editor.rb +51 -0
  353. data/examples/misc/argv_encoding_test.rb +38 -0
  354. data/examples/misc/arrays/center_two_arrays.rb +24 -0
  355. data/examples/misc/forking_example/forking_example.rb +28 -0
  356. data/examples/misc/loops/display_coloured_vertical_bars.rb +10 -0
  357. data/examples/rack/README.md +2 -0
  358. data/examples/rack/all_in_one_rack_example.rb +241 -0
  359. data/examples/rack/hello_world_in_rack.rb +44 -0
  360. data/examples/recursion/README.md +2 -0
  361. data/examples/recursion/quadratic_sum_of_a_number.rb +23 -0
  362. data/examples/recursion/reverse_the_string.rb +31 -0
  363. data/examples/recursion/shift_highest_value.rb +30 -0
  364. data/examples/recursion/shuffle_sort_string.rb +35 -0
  365. data/examples/reline/multiline_editing.rb +21 -0
  366. data/examples/reline/simple_example.rb +39 -0
  367. data/examples/rmagick/001_axes.rb +68 -0
  368. data/examples/rmagick/002_basic_2D_canvas.rb +29 -0
  369. data/examples/rmagick/003_a_walking_duck.rb +42 -0
  370. data/examples/rmagick/004_black_rectangle_with_red_border.rb +37 -0
  371. data/examples/rmagick/A_WALKING_DUCK.gif +0 -0
  372. data/examples/rmagick/foobar.png +0 -0
  373. data/examples/tty_box/all_in_one.rb +33 -0
  374. data/lib/roebe/autoinclude.rb +4 -0
  375. data/lib/roebe/autoinclude_encoding.rb +11 -0
  376. data/lib/roebe/autoinclude_open.rb +3 -0
  377. data/lib/roebe/base/base.rb +29 -0
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@@ -0,0 +1,1110 @@
1
+ german('Cellbiology') {
2
+ ruby_favicon
3
+ default_template '
4
+
5
+ div.default {
6
+ margin: 4px;
7
+ margin-top: 12px;
8
+ padding: 0.55em;
9
+ }
10
+
11
+ p.default {
12
+ font-weight: normal;
13
+ padding: 12px;
14
+ }
15
+
16
+ th {
17
+ font-size: larger;
18
+ }
19
+
20
+
21
+ '
22
+ body_css_class 'mar0px s2px padt1px mart0px VERDANAs'
23
+ body_css_style 'background-color: #d3d2d1;'
24
+ default_hyperlinks
25
+ font_size '1.3em'
26
+
27
+ # =========================================================================== #
28
+ # === COMMON_CSS_BORDER
29
+ # =========================================================================== #
30
+ COMMON_CSS_BORDER = 'border: 3px solid mediumslateblue;'
31
+
32
+ smaller_width('pad6px s0_5em mar1px mart0px') {
33
+ h1 'Cell Biology',
34
+ 'mar0px',
35
+ '',
36
+ 'font-size: 3.0em;'
37
+ # ========================================================================= #
38
+ # === Membrane Structure
39
+ # ========================================================================= #
40
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#membrane_structure
41
+ # ========================================================================= #
42
+ fancy2 'Membrane Structure'
43
+ p_default_le {
44
+ e 'Cell membranes are essential: they ultimately <b class="darkblue">help
45
+ maintain life</b>. The cell is enclosed via a <b>plasma membrane</b>. The
46
+ plasma membrane also <b>determines the boundaries of the cell</b>.'
47
+ br
48
+ e 'Gradients - such as ion gradients - established across membranes
49
+ aid in activities such as <b>synthesizing ATP</b>.'
50
+ br
51
+ e 'The plasma membrane contains proteins that act as
52
+ <b>sensors of external signals</b>: the so-called <b>protein sensors</b>,
53
+ also known as <b>receptors</b>. This allows a cell to change its behavior
54
+ in response to environmental cues, including signals from other
55
+ cells. These protein sensors transfer information rather
56
+ than molecules across the membrane. They are thus a way for a cell
57
+ to interact with its environment.'
58
+ br
59
+ e 'The image shown below displays the membrane of a human red blood cell
60
+ seen in a cross section. The bilayer structure of the membrane is
61
+ visible:'
62
+ br
63
+ dimg 'science/cellbiology/electron_micrograph_showing_the_plasma_membrane_of_a_human_red_blood_cell.png',
64
+ 'marl3em round_black1'
65
+ brbr
66
+ e '<b>Membranes</b> are <b>lipid bilayers</b> and such a lipid bilayer
67
+ typically has a <b>diameter</b> of <b>5 nm</b>.'
68
+ br
69
+ e "Typically about 30% of the proteins encoded in an animal’s
70
+ genome are membrane proteins."
71
+ br
72
+ e 'The <b>lipid bilayer</b> provides the basic structure for all cell
73
+ membranes.'
74
+ br
75
+ e 'The main phospholipids in most animal cell membranes are
76
+ the <b>glycerophospholipids</b> - or, more generally, the phospholipids.
77
+ Their tails are usually fatty acids differening in length, containing
78
+ about 14 to 24 carbon atoms. One tail typically has one or more
79
+ than one cis-double bond, and is thus unsatarted. Interestingly
80
+ the other tail does not have any cis-double bond - that is,
81
+ it is a saturated fatty acid.'
82
+ br
83
+ e 'All of the lipid molecules in cell membranes are amphiphilic: that
84
+ is, they have a hydrophilic (“water-loving”) or polar end, and a
85
+ hydrophobic (“water-fearing”) or nonpolar end.'
86
+ br
87
+ e 'By combining different fatty acids and head groups, cells make many
88
+ <b>different glycerophospholipids</b>. <b>Phosphatidylethanolamine</b>,
89
+ <b>phosphatidylserine</b>, and <b>phosphatidylcholine</b> are
90
+ the most abundant ones in <b>mammalian cell membranes</b>.'
91
+ br
92
+ e '<b>Cholesterol</b> is <b>the major sterol found in animal
93
+ cells</b>. The following image shows this as a schematic:'
94
+ br
95
+ dimg 'science/cellbiology/cholesterol_embedded_next_to_phospholipids.png',
96
+ 'mar0_5em marl3em round_black2'
97
+ br
98
+ e 'Curiously enough, <b>cholesterol</b> can flip-flop rapidly in a
99
+ membrane. Nonetheless their primary role in the cellular membrane
100
+ is to stiffen the membrane and thereby decreases the permeability
101
+ of the bilayer to small water-soluble molecules.'
102
+ br
103
+ e 'Synthetic lipid bilayers, called liposomes, can be generated.'
104
+ br
105
+ e 'The lipid bilayer is <b>a two-dimensional fluid</b> - a
106
+ two-dimensional liquid in which the constituent molecules
107
+ are free to move laterally. An average lipid molecule
108
+ diffuses the length of a large bacterial cell (∼2 μm)
109
+ in about 1 second.'
110
+ br
111
+ e 'Interestingly a special class of membrane proteins - called
112
+ <b>flippases</b> - catalyze the rapid flip-flop of phospholipids
113
+ from one monolayer to the other.'
114
+ br
115
+ e 'Certain membrane transport processes and enzyme activities
116
+ cease if the bilayer viscosity is experimentally increased
117
+ beyond a threshold level.'
118
+ br
119
+ e 'The <b>fluidity of a lipid bilayer depends on</b>:'
120
+ br
121
+ cmd 'its composition'
122
+ cmd 'its temperature'
123
+ br
124
+ e 'Fluidity of the membrane is favoured by cis-double bonds in
125
+ the lipid chains, because these bonds produce kinks in the chains
126
+ that make the phosphoglycerids more difficult to pack together.'
127
+ br
128
+ e 'The plasma membranes of most eukaryotic cells are more varied
129
+ than those of prokaryotes and archaea. For instance, eukaryotic
130
+ plasma membranes contain a mixture of different phospholipids.'
131
+ br
132
+ e 'Some phospholipids may have specific roles. For instance,
133
+ the inositol phospholipids are present only in small quantities
134
+ in animal cell membranes, but have crucial functions in
135
+ guiding membrane traffic, as well as a role in cell signaling.'
136
+ br
137
+ e 'Most eukaryotic cells store an excess of lipids in
138
+ <b>lipid droplets</b>. This instantly reveals two
139
+ functions: from lipid droplets the cell may retrieve the
140
+ basic building blocks for membrane synthesis; and the
141
+ cell can also use these dropleds as a food source,
142
+ <b>fueling metabolic energy generation</b>. Adipocytes
143
+ (fat cells) are especially adept at lipid storage.'
144
+ br
145
+ e 'Other cells have smaller lipid droplets; the number and
146
+ size of which vary with the cell’s metabolic state.'
147
+ br
148
+ e 'Lipid droplets form rapidly when cells are exposed
149
+ to high concentrations of fatty acids.'
150
+ br
151
+ e 'Of the total membrane-bound compartments in a given
152
+ eukaryotic cell, Mitochondria (39%) and the Endoplasmic
153
+ reticulum (51%) have the largest share. 50% of the
154
+ proteins in such a cell are somehow associated with a
155
+ membrane.'
156
+ br
157
+ e 'Mature human adipocytes store triglycerides in a single
158
+ fat droplet that almost entirely fills out the cell
159
+ volume.'
160
+ br
161
+ e 'It should be kept in mind that breaking down fatty
162
+ acids yields more energy per mass unit than glucose.'
163
+ br
164
+ e '<b><a href="https://en.wikipedia.org/wiki/Seipin">Seipin</a></b> -
165
+ a transmembrane protein - helps build lipid droplets inside of a
166
+ given cell. It will remain bound to the ER-membrane, being confined
167
+ inside of the <b>ER lumen</b>.'
168
+ br
169
+ e 'In <b>adipocytes</b>, droplets fuse and can reach a gigantic
170
+ size.'
171
+ br
172
+ e 'Membrane proteins typically span the lipid bilayer.'
173
+ br
174
+ e 'Lipid bilayers are virtually impermeable to most polar molecules.'
175
+ }
176
+ # ========================================================================= #
177
+ # === Transmembrane transport
178
+ # ========================================================================= #
179
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#transmembrane_transport
180
+ # ========================================================================= #
181
+ div_default('rounded','hela',COMMON_CSS_BORDER) {
182
+ fancy2 'Transmembrane transport',
183
+ 'mart10px marb1em pad4px'
184
+ p_default_le {
185
+ lee 'The importance of small-molecule transport is reflected in the
186
+ large number of genes in all organisms that code for the
187
+ transmembrane transport proteins involved, which make up 30%
188
+ of the membrane proteins in all cells.'
189
+ br
190
+ lee 'Mammalian cells, such as nerve and kidney cells, devote up to
191
+ two-thirds of their total metabolic energy consumption to
192
+ <b>transport processes</b>.'
193
+ br
194
+ lee 'To perform its function, each transport vesicle that buds
195
+ from a compartment must be selective.'
196
+ br
197
+ lee 'Transport through channels in a cell membrane operate
198
+ much faster than transport mediated by transporters.'
199
+ br
200
+ lee 'Solute flow through channel proteins is <b>always
201
+ passive</b>.'
202
+ br
203
+ lee 'The process by which a transporter transfers a solute
204
+ molecule across the lipid bilayer resembles an
205
+ enzyme–substrate reaction.'
206
+ br
207
+ lee 'By forming a protein-lined pathway across the membrane,
208
+ channels enable specific hydrophilic solutes to cross the
209
+ membrane without coming into direct contact with the
210
+ hydrophobic interior of the lipid bilayer.'
211
+ }
212
+ }
213
+ # ========================================================================= #
214
+ # === HELA TAG
215
+ # ========================================================================= #
216
+ div_default('rounded','hela',COMMON_CSS_BORDER) {
217
+ fancy2 'HeLa Zellen',
218
+ 'mart10px marb1em pad4px'
219
+ p_default_le {
220
+ lee 'HeLa Zellen besitzen <b>wenig RNAsen</b> im Nucleus.'
221
+ br
222
+ lee 'Die entfernten Zellen waren vom humanen Papillomvirus 18 (HPV 18)
223
+ befallen.'
224
+ br
225
+ lee 'Die Zellen von Henrietta waren sowohl durch ein virales Protein,
226
+ welches den p53 Tumorsuppressor inaktiviert, als auch eine Mutation
227
+ in Frau Lacks HLA (Humanes Leukozyten-Antigen) Supergenfamilie auf
228
+ Chromosom 6 zu Tumorzellen entartet.'
229
+ br
230
+ }
231
+ }
232
+ # ========================================================================= #
233
+ # === Mitochondria TAG
234
+ # ========================================================================= #
235
+ div_default('rounded','mitochondria',COMMON_CSS_BORDER) {
236
+ fancy2 'Mitochondria','mart10px marb1em pad4px'
237
+ p_default_le {
238
+ lee 'Mitochondria are like the power plants of the cell because they
239
+ transfer energy from food to ATP. They constitute <b>the power
240
+ sources of eukaryotic cells</b>.'
241
+ br
242
+ lee 'Mitochondria have limited DNA repair capability.'
243
+ br
244
+ lee 'The following image shows some schematic about
245
+ mitochondria.'
246
+ br
247
+ dimg 'science/biology/organelles/MITOCHONDRIUM_OVERVIEW.png',
248
+ 'mar0_5em marl3em round_black4'
249
+ brbr
250
+ }
251
+ }
252
+ # ========================================================================= #
253
+ # === Signal Transduction tag, Signal Amplification
254
+ #
255
+ # rf stdknowledge signal_transduction
256
+ # ========================================================================= #
257
+ div_default('rounded','signal_transduction',COMMON_CSS_BORDER) {
258
+ fancy2 'Signal Transduction und Signal Amplification'
259
+ p_default_le {
260
+ e 'Die grundlegenden Eigenschaft von der Übertragung von Information
261
+ auf/in/zwischen Zellen ("cell signaling") sind sehr stark innerhalb
262
+ der Eukaryoten <b>konserviert</b>.'
263
+ br
264
+ e '1972 wurde zum ersten Mal die Bezeichnung
265
+ "signal transduction" verwendet - Rensing, L. (1972).'
266
+ br
267
+ equote 'Periodic geophysical and biological signals as Zeitgeber and
268
+ exogenous inducers in animal organisms','mars1em'
269
+ br
270
+ abr 'https://www.ncbi.nlm.nih.gov/pubmed/4621276',
271
+ content: 'Pubmed 4621276',
272
+ css_class: 'mars1em BOLD'
273
+ br
274
+ e 'Eine Proteinkinase transferiert das terminale Phosphat
275
+ von ATP auf eine Hydroxyl Gruppe in einem Protein.'
276
+ br
277
+ e 'Eine bedeutende Rolle bei der Signaltransduktion spielt
278
+ auch die <b>Signalamplifikation</b>.'
279
+ br
280
+ abr 'https://highered.mcgraw-hill.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/sites/dl/free/0072437316/120069/bio07.swf::Signal%20Amplification',
281
+ content: 'Signal Amplifikation 7',
282
+ css_class: 'mars1em BOLD'
283
+ abr 'https://highered.mcgraw-hill.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/sites/dl/free/0072437316/120069/bio08.swf::Signal%20Amplification',
284
+ content: 'Signal Amplifikation 8',
285
+ css_class: 'mars1em BOLD'
286
+ }
287
+ }
288
+ # ========================================================================= #
289
+ # === Telomere Tag
290
+ # ========================================================================= #
291
+ div_default('rounded','telomere',COMMON_CSS_BORDER) {
292
+ fancy2 'Telomere',
293
+ 'mart10px marb1em pad4px'
294
+ p_default_le {
295
+ e 'Telomere sind spezielle, kurze Strukturen an den Enden der
296
+ Chromosome in Eukaryoten.'
297
+ br
298
+ lem '<b>telos</b> bedeutet im Griechischen "Ende".'
299
+ lem '<b>meros</b> bedeutet im Griechischen "Teil".'
300
+ br
301
+ e 'Die Länge der Telomere ist ein Indikator für die Teilungskapazität
302
+ einer Zelle.'
303
+ }
304
+ }
305
+ # ========================================================================= #
306
+ # === NPC (The Nuclear Pore Complex)
307
+ # ========================================================================= #
308
+ div_default('rounded','telomere',COMMON_CSS_BORDER) {
309
+ dimg 'science/chemistry/NPC_DETAILS.jpg',
310
+ 'marl2em round_black2'
311
+ }
312
+ # ========================================================================= #
313
+ # === Desmosomes
314
+ # ========================================================================= #
315
+ div_default('rounded','desmosomes',COMMON_CSS_BORDER) {
316
+ fancy2 'Desmosome'
317
+ p_default_le {
318
+ e 'The primary function of the desmosomes is to <b>provide
319
+ mechanical strength</b> to a cell.'
320
+ }
321
+ }
322
+ # ========================================================================= #
323
+ # === Nucleosomes
324
+ # ========================================================================= #
325
+ div_default('rounded','nucleosomes',COMMON_CSS_BORDER) {
326
+ fancy2 'Nucleosomes'
327
+ p_default_le {
328
+ e 'There are approximately 30 million nucleosomes in a
329
+ human cell.'
330
+ }
331
+ }
332
+ # ========================================================================= #
333
+ # === Aerobe Zellatmung
334
+ # ========================================================================= #
335
+ div_default('rounded','Aerobe Zellatmung',COMMON_CSS_BORDER) {
336
+ fancy2 'Aerobe Zellatmung'
337
+ p_default_le {
338
+ e 'Die <b>aerobe Zellatmung</b> ist ein Stoffwechselvorgang, der der
339
+ Energiegewinnung dient. Durch Oxidation organischer Stoffe
340
+ wird hierbei Energie gewonnen. Hierzu wird ein Oxidationsmittel
341
+ benötigt - meistens ist dies molekulare Sauerstoff (O₂).'
342
+ br
343
+ e 'Hierbei wird Glucose aufgespalten, um das vom Körper verwertbare
344
+ Adenosintriphosphat (ATP) zu erhalten.'
345
+ br
346
+ e 'Eine Voraussetzung für diesen Stoffwechselweg ist das Sauerstoff
347
+ vorhanden sein muss. Ist Sauerstoff nicht vorhanden, laufen stattdessen
348
+ <b>anaerobe Stoffwechselwege</b> ab, um Glucose aufzuspalten. Diese sind
349
+ aber weniger effektiv, das heißt es kann weniger Energie in ATP
350
+ gespeichert werden als bei der aeroben Zellatmung.'
351
+ br
352
+ e 'Als Endprodukte werden Kohlendioxid (CO₂) und Wasser (H2₂) frei.'
353
+ }
354
+ }
355
+ # ========================================================================= #
356
+ # === Epithelial cells
357
+ # ========================================================================= #
358
+ div_default('rounded','epithelia_cells',COMMON_CSS_BORDER) {
359
+ fancy2 'Epithelial cells'
360
+ p_default_le {
361
+ e 'Within the epithelium, cells are attached to each other
362
+ <b>directly</b> by <b>cell-cell junctions</b>.'
363
+ br
364
+ e 'The basal lamina can be found between the epithelial tissue
365
+ and the connective tissue.'
366
+ br
367
+ e '<b>Adherens junctions</b> are connected to <b>actin filaments</b>.'
368
+ }
369
+ }
370
+ # ========================================================================= #
371
+ # === Elastin (elastin tag)
372
+ # ========================================================================= #
373
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#elastin
374
+ # ========================================================================= #
375
+ div_default('rounded','elastin',COMMON_CSS_BORDER) {
376
+ fancy2 'Elastin'
377
+ p_default_le {
378
+ e '<b>Elastin</b> (the <i class="BOLD">elastic macromolecule</i>) is
379
+ a very important protein for vertebrates. In humans it is encoded
380
+ by the <b>ELN gene</b>. The human genome has only one ELN gene.
381
+ The DNA segment coding for this gene has a size of about
382
+ 45kb, and can be found on chromosome number 7. It codes for 34
383
+ exons and almost 700 introns. The <b>first exon</b> here is a
384
+ signal peptide that will cause the protein product to
385
+ target to its particular extracellular location.'
386
+ br
387
+ e 'Via <b>alternative splicing</b> several different <b>tissue-specific
388
+ tropoelastin-variants</b> are produced. In humans there are at
389
+ the least eleven different isoforms of Elastin are
390
+ known (respectively have been determined).'
391
+ br
392
+ e '<b>Elastin</b> is a key component of the extracellular matrix.
393
+ It is highly elastic and present in connective tissue - in
394
+ particular in the lungs, the skin as well as in blood
395
+ vessels. In fact, Elastin is approximately 1000 times
396
+ stretchier than collagen.'
397
+ br
398
+ e 'Elastin helps here for these tissues to resume their normal
399
+ shape, after stretching or contracting.'
400
+ br
401
+ e 'Elastin also helps skin to return to its original position
402
+ when it is poked or pinched.'
403
+ br
404
+ e 'Furthermore Elastin is an important load-bearing tissue in
405
+ the bodies of vertebrates and used in places where mechanical
406
+ energy is required to be stored.'
407
+ br
408
+ e 'Elastin is <b>rich in hydrophobic amino acids</b>, such
409
+ as glycine and proline.'
410
+ br
411
+ e 'The soluble precusors of Elastin is called <b>tropoelastin</b>.
412
+ These can be interconnected to form a network/mesh.'
413
+ br
414
+ e 'Conformational disorder is a constitutive feature of elastin
415
+ structure and function.'
416
+ br
417
+ e 'A famous disease caused by a defect in elastin is the
418
+ <b>Marfan syndrome</b>.'
419
+ br
420
+ e '<b>Elastosis</b> is the buildup of elastin in tissues
421
+ (thus, a degenerative disease).'
422
+ br
423
+ e 'In the body, elastin is usually associated with other
424
+ proteins in connective tissues.'
425
+ br
426
+ e 'Elastin is a very long-lived protein, with a half-life
427
+ of over 78 years in humans.'
428
+ br
429
+ boldbr 'Links:'
430
+ br
431
+ selfy 'https://pubmed.ncbi.nlm.nih.gov/10216959/', # From 1999.
432
+ css_class: 'mars1em BOLD'
433
+ }
434
+ }
435
+ # ========================================================================= #
436
+ # === Fluorescence
437
+ # ========================================================================= #
438
+ fancy2 'Fluorescence'
439
+ div_default('rounded','fluorescence',COMMON_CSS_BORDER) {
440
+ dimg 'science/biology/FLUOROPHORE_TABLE.png',
441
+ 'bblack2 mars2em'
442
+ }
443
+ # ========================================================================= #
444
+ # === Der Zellzyklus
445
+ # ========================================================================= #
446
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#der_zellzyklus
447
+ # ========================================================================= #
448
+ fancy2 'Der Zellzyklus'
449
+ div_default('rounded','',COMMON_CSS_BORDER) {
450
+ p_default_le {
451
+ e 'Der Zellzyklus umfasst zwei Phasen:'
452
+ br
453
+ e 'die Interphase'
454
+ e 'die M-Phase (Mitose und Cytokinese)'
455
+ br
456
+ e 'Aus einer Zelle entstehen durch die Mitose zwei neue, genetisch
457
+ identische Zellen.'
458
+ br
459
+ e 'Die Interphase wird unterteilt in: G1-, die S- und die G2-Phase.'
460
+ br
461
+ br
462
+ e 'Bei Nervenzellen dauert die G0-Phase für immer an; sie teilen
463
+ sich nicht mehr.'
464
+ br
465
+ e 'The accuracy of the cell cycle is extremely important for a
466
+ cell.'
467
+ br
468
+ e 'Cycline sind Proteine, deren Konzentration sich im Zellzyklus ändert.'
469
+ br
470
+ e 'The effect of caffeine on the cell cycle is that caffeine overrides
471
+ the cell cycle checkpoint control and creates <b>MUGs</b> ("Mitosis with
472
+ unreplicated genomes").'
473
+ }
474
+ }
475
+ # ========================================================================= #
476
+ # === FRET (FRET tag)
477
+ # ========================================================================= #
478
+ fancy2 'FRET: Förster resonance energy transfer'
479
+ div_default('rounded','FRET',COMMON_CSS_BORDER) {
480
+ p_default_le {
481
+ e 'In FRET the two molecules of interest are each labeled with
482
+ a different fluorochrome, chosen so that the emission spectrum
483
+ of one fluorochrome (the donor) overlaps with the absorption
484
+ spectrum of the other (acceptor).'
485
+ br
486
+ e 'The distance between the two fluorochromes should not exceed
487
+ <b>5 nm</b>.'
488
+ }
489
+ }
490
+ # ========================================================================= #
491
+ # === Das endoplasmatische Retikulum
492
+ # ========================================================================= #
493
+ fancy2 'Das endoplasmatische Retikulum (ER)'
494
+ div_default('rounded','das_endoplasmatische_retikulum',COMMON_CSS_BORDER) {
495
+ p_default_le {
496
+ e 'Alle Proteine mit einer ER-spezifischen Signalsequenz werden während
497
+ der Translation über einen Rezeptor zum ER gebracht.'
498
+ }
499
+ }
500
+ # ========================================================================= #
501
+ # === Rudolf Virchow
502
+ # ========================================================================= #
503
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#rudolf_virchow
504
+ # ========================================================================= #
505
+ fancy2 'Rudolf Virchow'
506
+ div_default('rounded','',COMMON_CSS_BORDER) {
507
+ p_default_le {
508
+ e squote('Jede Zelle entsteht aus einer Zelle')+
509
+ ' hat Rudolf Virchow im Jahre <b>1855</b> erkannt.'
510
+ br
511
+ e 'Original quote from <i>Rudolf Virchow</o>: '+
512
+ squote('omnis cellula e cellula</i>')+
513
+ '; which means <i class="BOLD">all cells arise from cells</i>.'
514
+ }
515
+ }
516
+ # ========================================================================= #
517
+ # === Lysosomes
518
+ # ========================================================================= #
519
+ fancy2 'Lysosomes'
520
+ div_default('rounded','lysosomes',COMMON_CSS_BORDER) {
521
+ p_default_le {
522
+ e 'Durch <b>Endocytose</b> aufgenommenes Material wird in den
523
+ Lysosomen durch <b>saure Hydrolasen</b> abgebaut.'
524
+ br
525
+ e 'Der pH-Wert der Lysosome beträgt etwa 5-6 - daher ist dies
526
+ niedriger als im Cytosol einer Zelle (mit einem pH-Wert von
527
+ etwa <b>7.2</b>).'
528
+ br
529
+ e 'Lysosomes are the principal sites of intracellular digestion.'
530
+ br
531
+ e 'The lysosomal membrane contains <b>a single phospholipid
532
+ layer</b>.'
533
+ }
534
+ }
535
+ # ========================================================================= #
536
+ # === Cell-to-Cell interactions: cellular adhesion
537
+ # ========================================================================= #
538
+ fancy2 'Cell-to-Cell interactions: cellular adhesion'
539
+ div_default('rounded','cellular_adhesion',COMMON_CSS_BORDER) {
540
+ p_default_le {
541
+ e 'Cells use a relatively small repertoire of adhesion mechanisms to
542
+ interact with matrix molecules and each other.'
543
+ br
544
+ e 'Cells modulate adhesion by controlling the surface densitty,
545
+ state of aggregation, and state of activation of their adhesion
546
+ receptors.'
547
+ br
548
+ e 'Most adhesion proteins fall into <b>five large families</b>.'
549
+ br
550
+ e 'These families - at the least four of them - include:'
551
+ numbered_table '
552
+ (1) Ig-CAMs
553
+ (2) cadherins
554
+ (3) integrins
555
+ (4) selectins'
556
+ br
557
+ # ===================================================================== #
558
+ # === E-selectins
559
+ # ===================================================================== #
560
+ e 'The <b>E-selectins</b> are produced by <b>endothelial cells,
561
+ but only when they were stimulated by inflammatory hormones or
562
+ by endoxotins.'
563
+ }
564
+ # ======================================================================= #
565
+ # === Integrins (integrins tag)
566
+ # ======================================================================= #
567
+ h5 'Integrins'
568
+ p_default_le {
569
+ e 'Integrins are unusuall cell-to-cell adhesion molecules in that
570
+ they bind to a variety of different ligands, including
571
+ <b>fibronectin</b> and <b>laminin</b>.'
572
+ }
573
+ }
574
+ # ========================================================================= #
575
+ # === P-Bodies Tag
576
+ # ========================================================================= #
577
+ div_default {
578
+ header_id 'P-Bodies','marb1em'
579
+ lembre 'mRNA decapping ist ein kritischer Schritt in eukaryotischer,
580
+ cytoplasmatischer mRNA Turnover.'
581
+ br
582
+ lembre '<b>Decapping</b> wird durch <b>Dcp2</b> katalysiert (mit Hilfe
583
+ des <b>Coactivators Dcp1</b>) und wird durch decapping enhancer
584
+ proteins unterstützt.'
585
+ br
586
+ lembre 'mRNAs die mit der decapping Maschinerie assoziiert sind können
587
+ in cytoplasmatische mRNP Granules assoziieren - die <b>PBs</b>, also
588
+ die <b>Processing Bodies</b>.'
589
+ }
590
+ # ========================================================================= #
591
+ # === Salmonella versus Listeria
592
+ # ========================================================================= #
593
+ fancy2 'Salmonella versus Listeria'
594
+ p_default_le {
595
+ e '- <b>Salmonella</b> enters by <b>trigger mechanism</b>'
596
+ e '- <b>Listeria</b> enters via <b>zipper mechanism</b>
597
+ (is simpler!)'
598
+ }
599
+ # ========================================================================= #
600
+ # === Ubiquitin
601
+ # ========================================================================= #
602
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#ubiquitin
603
+ # ========================================================================= #
604
+ fancy2 'Ubiquitin'
605
+ p_default_le {
606
+ e '<b>SUMO-1</b> kann Ubiquitinierungen unterdrücken.'
607
+ br
608
+ e 'Es gibt <b>Varianten der Ubiquitinierung</b>, die <b>nicht</b>
609
+ zum Abbau im 26S-Proteasom führt.'
610
+ br
611
+ e 'Attaching an ubiquitine can also be '\
612
+ 'called '+squote('the kiss of death')+'.'
613
+ }
614
+ # ========================================================================= #
615
+ # === The cell theory
616
+ # ========================================================================= #
617
+ fancy2 'The cell theory'
618
+ p_default_le {
619
+ e 'The <b>cell theory</b> states that cells arise only from preexisting
620
+ cells. The cell theory was developed by Schleiden and Schwann.'
621
+ br
622
+ selfy :the_cell_theory,
623
+ css_class: 'mars2em BOLD'
624
+ }
625
+ # ========================================================================= #
626
+ # === Fibroblasten
627
+ # ========================================================================= #
628
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#fibroblasten
629
+ # ========================================================================= #
630
+ fancy2 'Fibroblasten'
631
+ p_default_le {
632
+ e 'Im menschlichen Körper synthetisieren Fibroblasten das <b>Bindegewebe</b>.'
633
+ }
634
+ # ========================================================================= #
635
+ # === Cellular filaments
636
+ # ========================================================================= #
637
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#cellular_filaments
638
+ # ========================================================================= #
639
+ fancy2 'Cellular filaments'
640
+ div_default('rounded','cellular_filaments',COMMON_CSS_BORDER) {
641
+ table2_with_heading('s1em','',
642
+ 'border-collapse: separate; border-spacing: 15px;',
643
+ '<b>Name of the cellular filament</b>','<b>diameter (in n nm)</b>',
644
+ 'microfilaments','<b>7 nm</b>',
645
+ 'intermediate filaments','<b>10 nm</b> '+
646
+ sg('science/biology/ACTIN_FILAMENTS.png',
647
+ 'bblack2 marl5px',
648
+ 'drag_actin_filaments'
649
+ ),
650
+ 'microtubules','<b>20 nm</b>'
651
+ )
652
+ }
653
+ # ========================================================================= #
654
+ # === Protein filaments in a cell
655
+ # ========================================================================= #
656
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#protein_filaments_in_a_cell
657
+ # ========================================================================= #
658
+ fancy2 'Protein filaments in a cell'
659
+ p_default_le {
660
+ reset_the_counter
661
+ counter 'Actin filaments: ø: 5–9 nm','marl3em BOLD'
662
+ counter 'Intermediate filaments: ø: 10 nm','marl3em BOLD'
663
+ counter 'Microtubules: ø: 25 nm','marl3em BOLD'
664
+ }
665
+ # ========================================================================= #
666
+ # === Microtubules
667
+ # ========================================================================= #
668
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#microtubules
669
+ # ========================================================================= #
670
+ fancy2 'Microtubules'
671
+ p_default_le('rounded','',COMMON_CSS_BORDER) {
672
+ e 'Microtubules act as tracks for intracellular transportation.'
673
+ br
674
+ e 'Microtubules have a <b>diameter</b> of about 25 nm and consists of
675
+ α-tubulin and β-tubulin subunits, forming <b>heterodimers</b>.'
676
+ br
677
+ e 'These pairs exhibit a polarity: β-tubulin will <b>always</b>
678
+ point to the plus end, whereas α-tubulin will <b>always</b>
679
+ indicate the minus end (which is in the opposite direction,
680
+ naturally).'
681
+ br
682
+ e 'Taxol will massively reduce microtubule dynamics.'
683
+ br
684
+ e 'Microtubules form tracks from the cell’s centre to the
685
+ periphery for intracellular transport.'
686
+ br
687
+ e 'γ-tubulin can be found in the centrosome.'
688
+ }
689
+ # ========================================================================= #
690
+ # === LDL (low density lipoprotein) transport in the cell
691
+ # ========================================================================= #
692
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#microtubules
693
+ # ========================================================================= #
694
+ fancy2 'LDL (low density lipoprotein) transport in the cell'
695
+ p_default_le {
696
+ e 'The cell has to transport LDL (low density lipoprotein)
697
+ to a lysosome.'
698
+ br
699
+ e 'Cholesterol moves to the endoplasmic reticulum (ER), where it
700
+ inhibits production of LDL receptors - this constitutes a feedback
701
+ loop. One gene that is involved in this regard is<b>PTDSS1</b>,
702
+ an enzyme that synthesizes phosphatidylserine (PS).
703
+ This phospholipid can be found in the inner layer of the plasma
704
+ membrane (PM).'
705
+ br
706
+ e 'In PTDSS1-deficient cells where PS is low, LDL cholesterol
707
+ leaves lysosomes but fails to reach the ER, instead accumulating
708
+ in the PM. The addition of PS restores cholesterol transport
709
+ to the ER. We conclude that LDL cholesterol normally moves
710
+ from lysosomes to the PM. When the PM cholesterol exceeds
711
+ a threshold, excess cholesterol moves to the ER in a
712
+ process requiring PS. In the ER, excess cholesterol acts
713
+ to reduce cholesterol uptake, preventing toxic cholesterol
714
+ accumulation. These studies reveal that one lipid-PS-controls
715
+ the movement of another lipid-cholesterol-between cell
716
+ membranes. We relate these findings to recent evidence
717
+ indicating that PM-to-ER cholesterol transport is mediated
718
+ by GRAMD1/Aster proteins that bind PS and cholesterol.'
719
+ br
720
+ boldbr 'Links:'
721
+ br
722
+ selfy 'https://www.pnas.org/doi/abs/10.1073/pnas.2010682117?url_ver=Z39.88-2003' # 2020
723
+ }
724
+ # ========================================================================= #
725
+ # === Actin filaments
726
+ # ========================================================================= #
727
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#actin_filaments
728
+ # ========================================================================= #
729
+ fancy2 'Actin filaments'
730
+ p_default_le {
731
+ e 'Actin filaments have a diameter of about 7 nm. They are chains of
732
+ actin monomers.'
733
+ br
734
+ e 'Actin monomers can exist in an ATP-bound state, and an ADP-bound
735
+ state.'
736
+ br
737
+ e 'If ATP is bound to actin, actin-ATP molecules begin to
738
+ <b>form filaments</b>.'
739
+ br
740
+ e 'The exchange of ADP with ATP can <b>only</b> occur on free,
741
+ unbound <b>actin-ADP monomers</b>.'
742
+ br
743
+ e '50% of all actin molecules in a cell exist as monomers. A way
744
+ for the cell to control disassembly of actin filaments is
745
+ is to cross-linking proteins towards actin filaments, which
746
+ may stabilize these filaments.'
747
+ br
748
+ e 'Actin filaments connect different spots of the plasma membrane,
749
+ thereby giving the cell its characteristic shape.'
750
+ }
751
+ # ========================================================================= #
752
+ # === Intermediate filaments
753
+ # ========================================================================= #
754
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#intermediate_filaments
755
+ # ========================================================================= #
756
+ fancy2 'Intermediate filaments'
757
+ p_default_le {
758
+ e 'The main purpose of intermediate filaments is to make the cells
759
+ more robust against mechanical stress such as squeezing or
760
+ tearing.'
761
+ br
762
+ e '<b>Intermediate filaments</b> form cell-cell contacts called
763
+ <b>desmosomes</b>.'
764
+ }
765
+ # ========================================================================= #
766
+ # === Cellular Vesicles
767
+ # ========================================================================= #
768
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#cellular_vesicles
769
+ # ========================================================================= #
770
+ fancy2 'Cellular Vesicles'
771
+ p_default_le {
772
+ e 'The <b>Golgi Apparatus</b> makes use of <b>small
773
+ transport vesicles</b>. The diameter of these small transport
774
+ vesicles is about <b>60-80 nm</b>.'
775
+ br
776
+ e 'Individual proteins can contain "zip codes", to determine
777
+ where inside of the cell they may eventually end up.
778
+ <b>Targeting signals</b> are sufficient to guide proteins
779
+ to their final cellular destinations.'
780
+ br
781
+ e 'Proteins destined for the mitochondria typically have
782
+ a N-terminal extension.'
783
+ br
784
+ e '<b>Soluble escort factors</b> can be used as intermediaries
785
+ for transport within the cell.'
786
+ br
787
+ e '<b>Cytochrome c</b> contains an internal signal for import
788
+ into mitochondria.'
789
+ br
790
+ e 'Within a living cell, vesicles are constantly forming - in particular
791
+ at the plasma membrane, the ER, and the Golgi.'
792
+ br
793
+ e 'Once formed, these cellular vesicles deliver their contents
794
+ to destinations within or outside of the cell.'
795
+ br
796
+ e 'These <b>cellular vesicles</b> then travel on cellular
797
+ highways.'
798
+ br
799
+ dimg 'https://i.imgur.com/Thw5yPZ.jpg',
800
+ 'marl3em round_black3'
801
+ }
802
+ # ========================================================================= #
803
+ # === Cellular building blocks
804
+ # ========================================================================= #
805
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#autophagy
806
+ # ========================================================================= #
807
+ fancy2 'Cellular building blocks'
808
+ p_default_le {
809
+ e 'The components of living cells belong primarily to the following
810
+ <b>four main categories</b>:'
811
+ br
812
+ cmd 'carbohydrates: building block are monosaccharides'
813
+ cmd 'lipids: building blocks are fatty acids'
814
+ cmd 'proteins: building blocks are amino acids'
815
+ cmd 'nucleic acids: building blocks are nucleotides'
816
+ }
817
+ # ========================================================================= #
818
+ # === Autophagy
819
+ # ========================================================================= #
820
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#autophagy
821
+ # ========================================================================= #
822
+ fancy2 'Autophagy'
823
+ p_default_le {
824
+ e 'Autophages serve to degrade intracellular material.'
825
+ br
826
+ e 'Cancer cells need autophages.'
827
+ br
828
+ e 'A potent inhibitor of autophagy on the cellular level are aminoacids.'
829
+ }
830
+ # ========================================================================= #
831
+ # === Glossar (glossar tag)
832
+ # ========================================================================= #
833
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/cellbiology/cellbiology.cgi#glossar
834
+ # ========================================================================= #
835
+ fancy2 'Glossar','marb1px'
836
+ glossar(
837
+ 'luminescence:','emitting light spontaneously',
838
+ 'fluorescence:','emitting light on exposure to light'
839
+ )
840
+ # ========================================================================= #
841
+ # === Slogans tag
842
+ # ========================================================================= #
843
+ fancy1 'Slogans'
844
+ p_default_le('s1em') {
845
+ earrow 'The inside of a membrane-enclosed compartment is called a <b>lumen</b>.'
846
+ earrow 'The isolation membrane is selectively coated with the protein
847
+ Atg8.'
848
+ earrow 'The complexity of the trafficking problem is illustrated by
849
+ the fact that this process simultaneously moves thousands of
850
+ different proteins efficiently and accurately between different
851
+ compartments without a mix-up.'
852
+ earrow 'KDEL is both necessary and sufficient.'
853
+ earrow 'The vesicle coat acts as the filter to determine which
854
+ proteins are admitted into the vesicle.'
855
+ earrow 'Delivering virulence factors into a host cell occurs
856
+ through the type III secretion apparatus.'
857
+ earrow 'The ESCRT complex mediates the sorting of cargo into inward
858
+ budding vesicles and the scission of these vesicles.'
859
+ earrow 'In yeast, autophages are found at a site called
860
+ the PAS (pre-autophagosomal structure)'
861
+ earrow 'Defective autophagy promotes pathology.'
862
+ earrow 'Enzymes in the lysosome need an acidic environment.
863
+ They thus require a H+ pump.'
864
+ earrow 'Mycobacterium tuberculosis prevents the fusion of phagosomes
865
+ with lysosomes.'
866
+ earrow 'Die NLS Sequenz besteht aus Lysinen und Argininen, auch
867
+ die Histone werden durch diese basischen Proteine
868
+ <b>festgehalten</b>'
869
+ earrow 'Understanding the complexity of cellular responses to
870
+ environmental insults is a major challenge in cellular biology.'
871
+ earrow 'Epsin and Ep15 are adaptor proteins in the plasma membrane
872
+ that recognize ubiquitination receptors.'
873
+ earrow 'The fact that cargo can be packaged into vesicles supports
874
+ the vesicular transport model.'
875
+ earrow 'The molecular machinery that generates vesicles must
876
+ recognize recruitment signals on transported cargo protein.'
877
+ earrow 'The Plasma Membrane contains proteins that
878
+ act as sensors of external signals.'
879
+ earrow 'Autophagy and Diabetes are connected.'
880
+ earrow 'The ER is full of protein.'
881
+ earrow 'The counteracting activities of kinases and phosphatases
882
+ provide cells with a "switch" that can turn on or turn off
883
+ the function of various proteins.'
884
+ earrow 'Plasma membrane repair in muscle cells depends on
885
+ extracellular Ca2+ and Dysferlin (DYSF).'
886
+ earrow 'Transcytosis mediates the delivery of substances across
887
+ the cell.'
888
+ earrow 'Cells can be considered as a membrane-enclosed piece
889
+ of DNA in an aqueous solution.'
890
+ earrow 'The multivesicle budding machine is like a virus generator.'
891
+ earrow 'The Golgi membrance is covered with tethering factors that
892
+ keep Golgi-derived vesicles close to it.'
893
+ earrow 'Golgi inheritance during mammalian cell division occurs
894
+ through the disassembly, partitioning, and reassembly of
895
+ Golgi membranes.'
896
+ earrow 'The Golgi apparatus is the main site of glycan biosynthesis
897
+ in eukaryotes.'
898
+ earrow 'Phagocytosis is a triggered process.'
899
+ earrow 'The membrane traffic flow along highly organized directional
900
+ routes allows the cell to secrete, eat and remodel its plasma
901
+ membrane.'
902
+ earrow 'A cell culture is "abnormal" because it is not in a
903
+ normal body environment.'
904
+ earrow 'Cells respond to their environment by switching genes
905
+ on or off.'
906
+ earrow 'Sulfation is catalyzed by tyrosylprotein sulfotransferase
907
+ (TPST) in the Golgi apparatus. The Sulfate-Group stems from PAPS.'
908
+ earrow 'The orientation of the unbound head determines kinesin
909
+ movement.'
910
+ earrow 'Individual chromosomes occupy distinct territories in the
911
+ interphase nucleus ("<i>non-random positioning</i>")'
912
+ earrow 'Endocytosis and Phagocytosis mediate the delivery of
913
+ extracellular material to lysososomes while autophagy delivers
914
+ intracellular material to lysosomes.'
915
+ earrow 'Only 1% of the ER comprise of newly-synthesized proteins.'
916
+ earrow 'Oligosaccharide modification occurs in the Golgi.'
917
+ earrow 'COPII Vesicles must be flexible so that the very
918
+ large collagen filaments can be transported.'
919
+ earrow 'The COPII coat can be carried along microtubules.'
920
+ earrow 'Rab conversion regulates the maturation of early
921
+ endosomes to late endosomes.'
922
+ earrow 'Chromosome condensation also silences transcription.'
923
+ earrow 'Stem cells can divide asymmetrically.'
924
+ earrow 'The cell cycle phases are transitions.'
925
+ earrow 'Proteolysis is required for irreversibility of
926
+ mitotic exit.'
927
+ earrow 'Until the very last kinetochore is attached, the cell
928
+ can not enter Anaphase.'
929
+ earrow 'ARF-GAP stimulates GTP hydrolysis.'
930
+ earrow 'Cyclinabhängige Proteinkinasen sind wichtig für die
931
+ Regulation des Zellzyklus.'
932
+ earrow 'Dying cells lose their "dont eat me" signal.'
933
+ earrow 'Aberrante Chromosomen sind sowohl Auslöser als
934
+ auch Folge von Tumorwachstum.'
935
+ e 'Brefeldin A (BFA) rapidly blocks secretion, induces
936
+ disassembly of the Golgi complex and causes a redistribution
937
+ of Golgi components into the endoplasmic reticulum (ER).'
938
+ earrow 'Brefeldin A fuses Golgie to the ER.'
939
+ earrow 'COPI vesicles carry retrograde cargo.'
940
+ earrow 'The retromer is the coat for the tubular carriers
941
+ that deliver mannose-6-phosphate receptors to the
942
+ trans-Golgi Apparatus.'
943
+ earrow 'T-cells undergo inducible functional polarization upon
944
+ contact with their target cell.'
945
+ earrow 'The Golgi Apparatus serves as a sorting station for
946
+ proteins and lipids.'
947
+ earrow '<b>Intermediärfilamente</b> bilden eine strukturelle Stütze.'
948
+ earrow 'Cohesin keeps sister chromatids together.'
949
+ earrow 'Rab GTPases are important for organelle identity.'
950
+ earrow "Transport Proteins in the cell membrane act as the cell's
951
+ smugglers."
952
+ earrow 'Transport Proteins in the cell membrane may accumulate
953
+ solutes against the concentration gradient.'
954
+ earrow 'KDEL serves as a retention signal for some resident ER
955
+ proteins.'
956
+ earrow 'Bei der Nekrose kommt es zu einem ungeregelten,
957
+ zufallsunterworfenen DNA-Abbau.'
958
+ earrow 'Vesicles have the duty to transport proteins from the Golgi
959
+ apparatus to the cell surface area. They will use motor proteins
960
+ and a cytoskeletal track to get closer to their target.'
961
+ earrow 'Attachment of a KK-motif prevents mating.'
962
+ earrow 'The ESCRT complex mediates the sorting of cargo into inward
963
+ budding vesicles and the scission of these vesicles.'
964
+ earrow 'Active DNA is looped out inside of the nucleus.'
965
+ earrow '<b>H2AX</b> can indicate DNA-repair.'
966
+ earrow 'The ARF-GAP1 can sense membrane curvature.'
967
+ earrow 'In the Tay-Sachs disease, the lysosomes are enlarged.'
968
+ earrow '<b>Neutrophils</b> can expel their chromatin (and thus,
969
+ possibly part of their DNA) in order to trap extracellular
970
+ bacteria.'
971
+ earrow 'Xenopus egg extracts are a very useful biochemical system
972
+ used to study the cell cycle.'
973
+ earrow 'By fusing with a lysosome, a cell is able to degrade
974
+ different substances.'
975
+ earrow 'Cisternal maturation is the right model.'
976
+ earrow 'Transcriptionally silent heterochromatin typically
977
+ lies against the nuclear envelope.'
978
+ earrow 'Actin treadmilling drives cell migration.'
979
+ earrow 'The lysosome gives clues on to the metabolism of a cell,
980
+ which may be important for cancer biology.'
981
+ earrow 'Cells can use covalent modification to regulate the
982
+ intrinsic activity of a protein.'
983
+ earrow 'At the CENP-A, Kinetochore assembly occurs.'
984
+ earrow 'Molecular Chaperones are used for folding and unfolding.'
985
+ earrow 'Research in cell biology aims to discover how cells
986
+ work at the molecular level.'
987
+ earrow 'Cells are like tiny black boxes.'
988
+ earrow 'Centromere specification is an epigenetic process.'
989
+ earrow 'The defining characteristic of a eukaryotic cell is
990
+ the nucleus.'
991
+ earrow 'Most organelles are composed of the same lipid membrane
992
+ that creates the plasma membrane of the cell.'
993
+ earrow 'Most of the organelles within the cell use a phospholipid
994
+ bilayer to wall off their contents from the cytosol of the
995
+ cell. The cytosol is the organelle-free part of the
996
+ cytoplasm.'
997
+ earrow 'The plasma membrane is an active interface between the
998
+ cell interior and the surrounding medium.'
999
+ earrow 'The Golgi complex was discovered in 1898 by Italian
1000
+ physician Camillo Golgi and named after him.'
1001
+ earrow 'Die Länge der Telomere ist ein Indikator für die
1002
+ Teilungskapazität einer Zelle.'
1003
+ earrow 'The cytoskeleton functions to provide support and structure
1004
+ to the cell.'
1005
+ earrow 'There are three types of cytoskeletal elements:
1006
+ <b>microtubules</b>, <b>intermediate filaments</b>, and
1007
+ <b>microfilaments</b> (from largest to smallest).'
1008
+ earrow 'Cholesterol is a lipid that is found in the phospholipid
1009
+ bilayer that helps to maintain the fluidity and movement
1010
+ in the membrane.'
1011
+ earrow 'The fluid mosaic model, proposes that integral proteins
1012
+ can move freely within the phospholipid bilayer.'
1013
+ earrow 'Phospholipids have a hydrophobic tail.'
1014
+ earrow 'Eukaryotic cells export and import larger biological
1015
+ molecules through exocytosis and endocytosis.'
1016
+ earrow '<b>Aquaporines</b> can import or export water.'
1017
+ earrow 'Nicht jede tRNA kommt in gleichen Konzentration
1018
+ innerhalb einer Zelle vor; es existiert somit ein
1019
+ <b>tRNA-Gradient</b>.'
1020
+ earrow 'Je länger ein Chromosom ist, umso wahrscheinlicher sind
1021
+ mehrere Crossover Ereignisse im Zuge der Meiose.'
1022
+ earrow 'Transport proteins accumulate solutes in a cell
1023
+ against a given concentration gradient.'
1024
+ earrow 'The eukaryotic cell is a genetic chimera containing
1025
+ genes from two domains of life: the host cell (Eukarya)
1026
+ and the endosymbiont (Bacteria).'
1027
+ earrow "The lysosome allows the cell's lytic activities to
1028
+ be partitioned away from the cytoplasm proper."
1029
+ earrow 'Cells may respond to their environment by switching
1030
+ genes on or off.'
1031
+ earrow 'Chaperones in a given cell will be overexpressed
1032
+ in situations of stress.'
1033
+ earrow 'Die gängige Bezeichnung für Mitochondrien ist Kraftwerke
1034
+ der Zelle.'
1035
+ earrow 'Higher eukaryotic cells typically need about 16 hours
1036
+ for completing their cell cycle.'
1037
+ earrow 'Cells regulate their gene expression in response
1038
+ to their immediate environment.'
1039
+ earrow 'DNA, from the point of view of a cell, can be assumed
1040
+ to be <b>its genomic repository</b>.'
1041
+ earrow "- Water accounts for about 75 percent of a cell's volume.
1042
+ Thus, <b>cells are mostly water</b>."
1043
+ earrow "- DNA is a cell's <b>master molecule</b>."
1044
+ earrow 'A typical human fibroblast, a connective tissue cell,
1045
+ is about 15 μm across.'
1046
+ earrow "- Sugars are the material sources of a cell's energy."
1047
+ earrow 'The cytoplasm is a dense, three-dimensional throbbing blob.'
1048
+ earrow 'A typical cell contains billions of protein molecules.'
1049
+ earrow 'Mitochondria are the power generators, ribosomes are
1050
+ protein factories, lysosomes act as waste-disposal units,
1051
+ and the endoplasmic reticulum labels, sorts and
1052
+ transports molecules.'
1053
+ earrow 'Membranes are designed to separate what is outside the cell
1054
+ from what is inside.'
1055
+ earrow 'All cells interact with molecules in their environment.'
1056
+ earrow 'The cells of a multicellular organism are committed
1057
+ to collaboration.'
1058
+ earrow 'All of the somatic cell lineages in animals are committed
1059
+ to die.'
1060
+ earrow 'All cells use the same molecular building blocks.'
1061
+ earrow 'In <b>multicellular organisms</b> the well-being of the
1062
+ individual cell is often set aside for the benefit of the
1063
+ organism as a whole.'
1064
+ earrow 'Mechanisms of cell cohesion govern the architecture of
1065
+ tissues and organs.'
1066
+ earrow 'Many cells require a specific combination of <b>extracellular
1067
+ survival factors</b> to allow the cell to continue living; when
1068
+ deprived of these signals, the cell activates a suicide program
1069
+ and kills itself - usually by <i>apoptosis</i>.'
1070
+ earrow 'Light travels <b>1.33 times slower</b> in water than in a
1071
+ vacuum.'
1072
+ earrow '<b>Tubulin</b> labeled with caged fluorescein can be injected
1073
+ into a dividing cell, where it is incorporated into microtubles
1074
+ of the mitotic spindle.'
1075
+ earrow '<b>Centromeres</b> act as organizing centers of cell
1076
+ division.'
1077
+ earrow 'The nucleolus is where <b>ribosome biogenesis</b> occurs.'
1078
+ earrow 'Cell differentiation is readily accomplished by turning
1079
+ on stage-specific (stem cell, mesoderm, muscle and so forth)
1080
+ transcription factors to express the repertoire of proteins
1081
+ required for the function of that cell type - myosins in
1082
+ muscle, keratins in skin, or synaptic receptors in neurons.'
1083
+ earrow 'Jede Zellvermehrung läuft als geordnete Kette von
1084
+ Ereignissen ab.'
1085
+ earrow 'Multicellular organisms can be viewed as communities
1086
+ of cells.'
1087
+ earrow 'Cells are nothing more than self-maintaining, replicating
1088
+ droplets.'
1089
+ earrow 'Cells vary enormously in appearance and function.'
1090
+ earrow 'Humans begin life as a single cell.'
1091
+ earrow 'Cells are biochemical factories containing their
1092
+ own genetic blueprints.'
1093
+ earrow 'A growth factor is a cellular signal that tells
1094
+ a cell to divide.'
1095
+ earrow 'Multicellular life cycles are remarkably diverse.'
1096
+ earrow 'The main purpose of mitosis is to make sure that
1097
+ the chromosomes are divided up correctly.'
1098
+ earrow 'Cellular checkpoints are quality control
1099
+ measures for the cell.'
1100
+ }
1101
+ p('mart10px') {
1102
+ roebe_sitemap
1103
+ selfy :local_genetics
1104
+ selfy :local_evolution
1105
+ selfy :local_microbiology
1106
+ selfy :local_apoptose
1107
+ fancy_spacer
1108
+ science_links
1109
+ }
1110
+ }}