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• Mutation
  ...h [[natural selection]] and other [[evolution]]ary processes acts. Without mutation, there are no new [[gene]]s, no new [[allele]]s and, eventually, no evoluti ...], where mutations occur up to 100 times more frequently than the normal [[mutation rate]]. A hotspot can be at an unusual base, e.g., 5-methylcytosine.
  13 KB (2,019 words) - 00:14, 11 November 2007
• Genetic Mutation
  #REDIRECT[[mutation]]
  21 bytes (2 words) - 20:01, 21 June 2007
• Mutation/Definition
  97 bytes (13 words) - 06:26, 23 May 2008
• Mutation/Approval
  12 bytes (1 word) - 00:14, 11 November 2007
• Mutation/Related Articles
  Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.
  1 KB (167 words) - 18:44, 11 January 2010

Page text matches

• Mutations
  #REDIRECT [[Mutation]]
  22 bytes (2 words) - 19:42, 21 June 2007
• Genetic mutations
  #REDIRECT[[mutation]]
  21 bytes (2 words) - 20:02, 21 June 2007
• Genetic Mutation
  #REDIRECT[[mutation]]
  21 bytes (2 words) - 20:01, 21 June 2007
• Genetic Mutations
  #REDIRECT[[mutation]]
  21 bytes (2 words) - 20:05, 21 June 2007
• Kostmann syndrome/Definition
  ...ts; originally thought to be inheritable but possibly due to a spontaneous mutation
  163 bytes (21 words) - 17:29, 30 July 2010
• Kennedy syndrome/Definition
  An [[X-linked]] [[recessive]] form of [[spinal muscular atrophy]] due to a mutation of the gene encoding the [[androgen receptor]].
  167 bytes (22 words) - 15:32, 23 February 2010
• Janus kinase
  ...F, Buser AS, Teo SS, Tiedt R, Passweg JR et al.| title=A gain-of-function mutation of JAK2 in myeloproliferative disorders. | journal=N Engl J Med | year= 200
  1 KB (190 words) - 20:53, 22 August 2010
• Androgen insensitivity syndrome/Definition
  (AIS) Due to a mutation in the androgen receptor such that genetically male individuals (XY) do not
  321 bytes (52 words) - 13:18, 14 January 2009
• Phenotype/Related Articles
  {{r|Mutation}}
  324 bytes (41 words) - 14:51, 17 March 2010
• Genetics/Related Articles
  {{r|gene mutation}}
  251 bytes (35 words) - 14:39, 13 December 2008
• Natural selection/Related Articles
  {{r|Mutation}}
  175 bytes (21 words) - 20:29, 11 November 2007
• Microsatellite/Related Articles
  {{r|Mutation}}
  237 bytes (27 words) - 01:00, 9 February 2010
• Hyperkalemic periodic paralysis
  ...of high potassium levels, sodium channels fail to activate properly. The mutation causes single [[amino acid]] changes in parts of the channel which importan
  2 KB (233 words) - 15:46, 14 February 2009
• Targeted gene replacement
  ...s with [[DNA]]-damaging mutagens. Neither method is useful for producing a mutation in a specific [[genome|genomic]] location, nor are the techniques applicabl ...ntroduced in the 1980s to surmount these difficulties and allow specific [[mutation]]s to be induced in [[mammal]]ian cells. Even a mammalian [[somatic]] [[cel
  2 KB (346 words) - 00:44, 8 May 2008
• Wolff-Parkison-White Syndrome/Definition
  ...ntricles, known as the bundle of Kent. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated prote
  482 bytes (77 words) - 11:57, 2 July 2009
• Germ cell/Related Articles
  {{r|Mutation}}
  493 bytes (63 words) - 16:51, 11 January 2010
• Hyperkalemic periodic paralysis/Related Articles
  {{r|Mutation}}
  478 bytes (61 words) - 17:20, 11 January 2010
• Hereditary spherocytosis/Related Articles
  {{r|Mutation}}
  545 bytes (72 words) - 17:10, 11 January 2010
• Targeted gene replacement/Related Articles
  {{r|Mutation}}
  522 bytes (69 words) - 20:49, 11 January 2010
• Long QT syndrome
  ...indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Rom
  702 bytes (91 words) - 01:33, 11 June 2010