「Mutations」の共起表現(1語右で並び替え)

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「Mutations」の共起表現一覧(1語右で並び替え)

Mutations

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"Sublime Mutations, a photographic retrospective of Del LaGrace
indlimbs that are lacking altogether…The p63 mutations act in a dominant fashion in humans, giving
These mutations affect fast inactivation of the encoded sodi
Monilethrix is caused by mutations affecting the genes KRTHB1 (KRT81), KRTHB3 (
as been recompiled in 2008 listing 93 common mutations, after its initial mutation compilation in 2
These mutations allow the creatures to move quickly and even
These mutations, along with mutations that cause cardiofacio
Some mutations alter a gene's DNA base sequence but do not
All NOG mutations altered evolutionarily conserved amino acid
bvious correlation between most of the known mutations and clinical variability seen in BFNC.
Mutations and deficiency in this enzyme are known to c
itions in Florida, owing chiefly to repeated mutations and instability in both civil and ecclesiast
f sexual reproduction, the fitness effect of mutations, and the effect of adaptation to different l
nd human subjects begin to exhibit grotesque mutations and disfigurement.
ting some individuals with fewer deleterious mutations, and some with more.
is happening depends on the frequency of new mutations, and on the size of the population, but is i
sition can create phenotypically significant mutations and alter the cell's genome size.
rveillance that functions to detect nonsense mutations and prevent the expression of truncated or e
riety of applications including detection of mutations and single nucleotide polymorphisms, analysi
s such as repairing genetic damage caused by mutations and functioning as a com-link between Plumbe
Certain mutations and the activation of certain cell-cycle con
hat most protein evolution is due to neutral mutations and genetic drift.
g., racial, familial and spontaneous genetic mutations) and phenotypic data (e.g., age, race, cogni
ssumes that genetic differences arise due to mutations and genetic drift.
ing all tongues have, and do undergo various mutations, and corruptions, this alone doth alwaies co
During each round, random mutations and perturbations are introduced to the bioc
ying molecular/genetic changes producing DNA mutations and genome instability, which contribute to
oko Ohta in 1973 (including only deleterious mutations) and expanded in the early 1990s to include
Mutations and variants of the CK1ε phosphorylation sit
both its ancient roots and its contemporary mutations; and, global modernities and their impact on
theory of natural selection acting on random mutations applies to bacteria as well as to more compl
Some mutations are dominant, some are recessive.
Resistance mutations are known for all approved NRTIs.
These mutations are somatic, which means they are acquired d
Other resistance mutations are L80V/I, V173L and L180M.
RET loss of function mutations are associated with the development of Hirsc
Furthermore mutations are directly linked to quantum leaps.
These mutations are in exon 8 (atypical form) and exon 8a (c
Ironically, these two mutations are both shared by the Low pain sensitivity
Multiple mutations are known: the current (2007) total is 79.
Flt3 mutations are among the most common mutations in acute
TACI mutations are associated with immunodeficiency in huma
The effects of the mutations are generally not severe but a spectrum of c
The results of these mutations are highly variable, some producing function
FLCN mutations are detected by sequencing in 88% of proband
reditary nonpolyposis colorectal cancer, the mutations are biallelic in CMMR-D.
nerally green in color (both lutino and blue mutations are rare, but do exist in captivity) with a
NLRP3 mutations are responsible for the autoinflammatory dis
(A) If mutations are induced by the media, roughly the same n
Patients with such mutations are congenitally insensitive to pain and lac
The vowel mutations are the product of the assimilation of one v
Specific point mutations are made and the transcription of the gene i
region, Grenache noir and its gris and blanc mutations are used in the production of the fortified
These mutations are likely not wholly causative and should i
Scanning refers to the fact that many mutations are sometimes indiscriminately performed alo
These types of mutations are associated with papillary thyroid carcin
f molecular evolution, while the majority of mutations are deleterious, the majority of mutations t
Chemicals that induce mutations are called mutagens.
ns is more likely to be adaptive than random mutations are.
(B) If mutations arise spontaneously during cell divisions pr
Other mutations, as discussed at the beginning of the articl
avoided and relatives are screened for RYR1 mutations as these may make them susceptible to MH.
There are two distinct genetic mutations associated with the Antley-Bixler syndrome p
Genetic studies suggest that the oldest mutations associated with lactase persistence only rea
te all possible (or as close to as possible) mutations at a specific site, or narrow region of a ge
celerates the rate of joining of independent mutations at multiple sites and of grafting new domain
nts for slightly advantageous or deleterious mutations at the molecular level.
1253 and 1351c have the same mutations at position A-911, G-977 in exon 7 of FOXP2
anded DNA undergoing replication can lead to mutations, because in the absence of information from
s like aromatic amines are believed to cause mutations because they are nucleophilic and form stron
tase expression in infants, showing that the mutations become increasingly relevant during developm
s seeks to saturate with insertions or point mutations, but instead of for the entire genome, it sa
are called teratogens; these may also cause mutations, but their effect on development is not rela
resence of nitrous acid can cause transition mutations, by converting cytosine to uracil.
top the spread of Tiberium and its monstrous mutations by retrieving the extraterrestrial Tacitus d
ily in human cancer (24, 29), and that point mutations can activate the oncogenic potential of cell
Furthermore, such mutations can show how the specific structure of that
Mutations can be inherited or can arise de novo early
Due to the damaging effects that mutations can have on genes, organisms have mechanisms
Mutations can cause the osteochondrodysplasias pseudoa
petite mutations can be induced using a variety of mutagens,
Neutral mutations can accumulate over time due to genetic drif
Burns has said that the mutations can be read as a metaphor for adolescence, s
germline point mutations) can be passed on.
SOD2 knockout or null mutations cause growth inhibition on respiratory carbo
Mutations cause constitutive action of Flt3 leading to
It has been shown that the mutations cause defective U12 splicing.
hairy, odd-skipped, paired and runt - where mutations caused the deletion of a particular region o
Other mutations causing MH have been identified, although in
were able to accurately identify single-gene mutations causing beta-thalassemia.
Conversely, mutations causing this enzyme to be overexpressed are
of viruses related by a similar mutation or mutations, competing within a highly mutagenic environ
hanging generation times (If the rate of new mutations depends at least partly on the number of gen
All known mutations disrupt StAR function by altering its START
ntil the early 1970s, the concept of neutral mutations driven to fixation by genetic drift was know
ong is about a boy named Burli, who suffered mutations due to a nuclear power plant disaster.
Darwinian view, a large number of successive mutations, each selected for its usefulness to the sur
slugs, oversized bats, children with genetic mutations enhancing their physical or mental abilities
hanisms of DNA repair, including why certain mutations escape repair and result in cancer.
Three kinds of these mutations exist (although only the first example is co
en functional mitochondrial genes accumulate mutations faster and more freely.
n between both albums, Fight released an EP, Mutations, featuring War of Words studio versions, liv
Mutations for violin and piano, Op.160 (1999)
Somatic mutations found in human cancers of the MH1 domain of
urifying selection which removes deleterious mutations from a population.
Benzer also proposed missense and nonsense mutations from his rII studies.
und-trip tour of his horn, from buzzing mute mutations, grizzly blurts and purring multiphonics to
Combining the different mutations has produced new colors, including blue, blu
Several polymorphisms and mutations have been described in this gene, some of wh
Currently, mutations have been identified in six COX assembly fac
At least 11 distinct mutations have been identified.
Although not all mutations have a noticeable phenotypic effect, the com
Many mutations have been identified in affected patients, b
When enough mutations have occurred and become stable in a populat
Many of the CACNA1H mutations have a measurable effect on channel kinetics
These mutations have been shown to cause diverse changes in
Mutations have been identified in patients with Parkin
Several mutations have been implicated as a cause of Oguchi di
Most of the mutations have been found in exons 8,10 and 16.
forms of myotonia congenita caused by CLCN1 mutations have different patterns of inheritance.
y be harmful, with about 70 percent of these mutations having damaging effects, and the remainder b
Certain mutations, however, have been found to have CNS involv
Some non-synonymous mutations, i.e. mutations that do change the amino aci
GAMT gene mutations impair the ability of the guanidinoacetate m
Mutations in this gene cause the classical phenotype o
Mutations in Ran disrupt DNA synthesis.
Mutations in this gene are involved in the pathogenesi
Mutations in the CDKL5 gene also cause a disorder call
Mutations in this gene cause vitiligo.
Mutations in this gene are associated with 17 alpha-hy
The PC2 form is due to mutations in the genes encoding keratin 6B (protein na
Mutations in the pseudoknot structure have been found
Few of these people will likely have mutations in CACNA1H or GABRG2 as the prevalence of th
s rapid and specific, and it is abrogated by mutations in the pleckstrin homology domain of AKT1.
Mutations in GP1BA, GP1BB, and GP9 have been shown to
These genes regulate the cell cycle and mutations in the genes are involved in some types of c
Several mutations in the Pxr sRNA gene have been observed.
Mutations in EDA give rise to a clinical syndrome char
THB deficiency can be caused by mutations in one of several genes, including GCH1, PCB
Certain mutations in OCA2 result in type 2 oculocutaneous albi
Different mutations in the mouse homologs, En1 and En2, produced
Mutations in the PC gene cause pyruvate carboxylase de
When tested some polyphenols induced DNA mutations in MLL gene, which are common findings in ne
It is caused by mutations in the SPRED1 gene.
Certain mutations in this gene have been associated with idiop
The disease is caused by mutations in the ceruloplasmin gene.
Mutations in this gene have been shown to cause incomp
Mutations in this gene are associated with 2 neurologi
HSH is caused by mutations in the TRPM6 gene.
Mutations in the genes encoding this protein have been
Mutations in Cbfa1/Runx2 are associated with the disea
The genetic basis is the result of mutations in genes that code for proteins (transcripti
Familial dysautonomia is caused by mutations in the IKBKAP gene.
Mutations in the EP300 gene are responsible for a smal
Mutations in the FOXC2 gene are associated with lymphe
syndrome, aHUS), has been strongly linked to mutations in genes of the complement system (including
Mutations in the NEK8 gene associated with nephronopht
Mutations in this gene have been found in Dent's Disea
Mutations in this gene also cause a Wernicke's-like en
Mutations in this gene may be associated with autism.
Mutations in the GPIb beta subunit have been associate
l cycle progression is related to cell size, mutations in Cyclin D and its homologues show a delay
Mutations in the ACAT1 gene cause beta-ketothiolase de
PFIC2 caused by mutations in the ABCB11 gene increases the risk of hep
n a spectrum of skeletal disorders caused by mutations in the gene, which encodes a protein that is
first such model targets the accumulation of mutations in asexual populations and is implemented in
ive disorder caused by a number of different mutations in the OTC gene.
Mutations in this gene cause Rubinstein-Taybi syndrome
Three different recessive, loss of function mutations in the encoded protein have been shown to ca
one method of repair and results in deletion mutations in the genetic code which may initiate the c
Mutations in this gene are associated with meningioma.
Mutations in this gene have been associated with the a
Mutations in the HADHA gene lead to inadequate levels
Mutations in this gene are associated with familial hy
Mutations in the glucocerebrosidase gene cause Gaucher
Mutations in either gene are links to Waardenburg synd
al recessive neurological disorder caused by mutations in the PHYH gene, have impaired α-oxidation
Recessively-inherited mutations in NTE that substantially reduce its catalyt
Mutations in the ASS gene cause type I citrullinemia.
It is caused by mutations in the gene for glial fibrillary acidic prot
disorder due to haploinsufficiency caused by mutations in the CBFA1 gene also called Runx2, located
Mutations in the XPNPEP3 gene are associated with cili
Mutations in the ACVR1 are associated with fibrodyspla
Mutations in the NAGA gene, resulting in alpha-N-acety
Mutations in the HMGCL gene cause 3-hydroxy-3-methylgl
axonal dystrophy have not been found to have mutations in the PLA2G6 gene.
Mutations in this protein cause pseudoxanthoma elastic
Mutations in the NR0B1 gene located on the X chromosom
Mutations in this gene have been linked to cryptogenic
In cells with mutations in DNA repair genes, however, some of these
Mutations in class A genes affect sepals and petals.
Mutations in the Shine-Dalgarno sequence can reduce tr
Some mutations in the globin chain are associated with the
Patients with mutations in this gene develop Wolcott-Rallison syndro
Mutations in the gene encoding GPD1 have been proven t
Mutations in this gene may be associated with rheumato
Mutations in the ACADS gene lead to inadequate levels
Mutations in KCa2.3 are suspected to be a possible und
Mutations in either genes result in a lipid disorder,

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