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{{r|Space Quest V: The Next Mutation}}

{{r|Mutation}}

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...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

Some used "[[mutation]]" to refer to variations with low allele frequency. ...if a different polypeptide sequence is produced they are ''[[nonsynonymous mutation|nonsynonymous]]''.

{{r|Mutation}}

...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers

...s'' is the inability to respond to vaopressin, (for instance if there is a mutation affecting the V2 vasopressin receptor) and cannot be treated in this way. ...hypothalamic diabetes insipidus is most commonly a consequence of a point mutation in the vasopressin gene, usually in the region coding for vasopressin-assoc

...//www.blackwellpublishing.com/ridley/classictexts/wright.asp "The roles of mutation, inbreeding, crossbreeding and selection in evolution"] ''Proc. 6th Int. Co

...ooks at how large scale changes may be caused by evolutionary mechanisms—[[mutation]], [[migration]], [[genetic drift]], and [[natural selection]].<ref>[http:/

Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.

...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.

...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 ...siology involving the [[voltage-gated potassium channel]]. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).."<

...man}}</ref> and the formation of 5-HOU is the largest contributor for this mutation, because the base that was formally a cytosine base paired with guanine, is

...] to promote [[natriuresis]], and hence a deficiency of this peptide, or a mutation of the receptor results in salt-sensitive hypertension in mice.

...e quantitative estimates of viral titers, measurement of recombination and mutation rates, the statistical validation of radioactive decay measurements, and th

{{r|Mutation}} {{r|Mutation}}

...a pore through which ions flow, carrying type A potassium current (IA). A mutation in the Sh gene reduces the conductance of charge across the neuron since th

...test for some lissencephaly variants, but only those with a known genetic mutation. ...ncy. There are also a number of genetic causes of lissencephaly, including mutation of the [[reelin]] gene (on [[chromosome 7]]),<ref>Hong SE, Shugart YY, Huan

Examples include prothrombin gene G-->A20210 mutation.<ref name="pmid9669991">{{cite journal| author=Margaglione M, Brancaccio V, | [[Methylenetetrahydrofolate reductase]] mutation||colspan="2" align="center"|No association

{{r|Mutation}}

...I. A punctual mutation was found in nucleotide 1367 of the rpoBgene. That mutation show strains of rifampin-resistant M.leprae in two of the three patients t

...erimental evolution studies, those with rapid [[generation time]]s, high [[mutation rate]]s, large [[population size]]s, and small sizes increase the feasibili ...epistasis, the effect of each mutation declines with increasing numbers of mutation. Understanding whether the majority of genetic interactions are synergistic

...l to the parent(s), thus allowing evolution to proceed by means other than mutation.

...e = Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients b ...ient had an ELA-2 defect but her parents did not, suggesting a spontaneous mutation.<ref name=Carlsson/>

...ferred heterodimeric partner (4). On the other hand, overexpression and/or mutation of ErbB-2 are thought to lead to spontaneous dimerisation and the stabiliza

...eptin's role in energy balance came from ''db/db'' mice. These mice have a mutation in the gene coding for leptin receptors and therefore, even though their ad Experiment ii) shows that a single mutation in the ''ob'' gene prevents leptin synthesis, this has also been proven to

...etection of DNA can help in "detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relat

Mutation in the UDP-glycuronosyltransferase gene cause [[Gilbert Syndrome]]<ref>{{O

..., Torgerson TR, Russell LJ, Lejtenyi C et al.| title=FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome. | journal=N Engl J Med | year=

...is/her offspring, presuming that his/her partner does not also carry the [[mutation]].

...e of vowel mutation more commonly referred to as ''[[i-umlaut]]'' (UK: ''i-mutation''). The [[French language|French]] term ''mouillure'' (German ''Mouillierun

* Caporale, LH (2003) Natural selection and emergence of mutation phenotype: An Update of the Evolutionary Synthesis Considering Mechanisms t

Caused by mutation, the pathway for Vocal Learning developed out of a pre-existing non-vocal m

=== Mutation === ...nt, and anticipated, by decades, the subsequent work on [[adaptation]] and mutation by bacterial chemists and microbiologists.

=== Mutation === ...nt, and anticipated, by decades, the subsequent work on [[adaptation]] and mutation by bacterial chemists and microbiologists.

...sed. While [[codon]]s for different [[amino acid]]s may change in a random mutation (changing the sequence coding a gene), this doesn't necessarily alter the p

| title = The Mutation of the Russian Secret services | url =http://www.agentura.ru/english/dosie/mutation/}}</ref> A small analysis group, on the order of 10 people, had assisted th

...age virtually all types of macromolecules: carbohydrates, nucleic acids ([[mutation]]s), lipids ([[lipid peroxidation]]) and amino acids (e.g. conversion of [[

...utations in a large population and then screen the progeny for the desired mutation. A similar process can be used in both plants and prokaryotes.

...an Carp]], with little to recommend it as a potential aquarium fish, but a mutation occurred which developed lovely gold patches on the body which eventually t

...] and a liquid.<ref>Ní Chiosáin (1999).</ref> However, under ''[[consonant mutation]]'' (changing consonants according to some rule), other sequences can occur

...he repetitive nature of these sequences causes the rapid accumulation of [[mutation]]s, which allows their use as highly variable [[molecular markers]]. Such m The high mutation rate of microsatellite loci gives them a far greater resolution than more t