「Mutation」の共起表現(1語右で並び替え)

「Mutation」の共起表現一覧(1語右で並び替え)

Mutation

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ore all ten men who carry the chromosome with mutation A are the direct male line descendants of the
If through a mutation a character appears that has a beneficial inf
"If through a mutation a character appears that is neither advantage
In this mutation, a mismatch in the DNA replication causes iso
If through a mutation a character appears that has an injurious eff
In those who are heterozygous for the mutation, about 28-44% of total hemoglobin (Hb) is HbC
imatinib and who had the drug resistant T315I mutation achieved cytogenetic response in 28% of patie
of a hermit (Crazy Wanda) who gave birth to a mutation after being raped by the monster, and finally
suggested that "Tafarch" (which takes a soft mutation after porth to become "Dafarch") was a person
apse strength, independent of the Genderblind mutation, allowed researchers to "turn fly homosexuali
d hyperbilirubinemia, so it appears that this mutation alone may be a necessary but not sufficient f
This mutation also results in muscle cell death by apoptosi
Unless the mutation also has a regulatory effect, synonymous subs
This mutation also interferes with fat deposition, resultin
The Ino mutation also induces changes in the nestling.
When a mutation alters a protein that plays a critical role i
e, laying down the ground work for decades of mutation analysis and genetic engineering, and setting
that discontinuous variations could arise by mutation and be transmitted to offspring via stable no
relationship in whippets between a myostatin mutation and racing performance.
oalescence time), assumes that the effects of mutation and selection are constant across sequence li
an hand, the chant, the voice, the clefs, the mutation and the keys; in 13 chapters with mensural mu
rsing a Darwinian evolution based upon random mutation and a struggle for survival, fractal geometry
level being driven by the random processes of mutation and genetic drift, largely independent from n
more polar epoxy-diols, which can then cause mutation and induce cancer development.
proliferation-associated genes, and its gene mutation and increased expression may be associated wi
esignated as G2a3b1a based on having the L140 mutation and a further subgroup based on having the va
rregular conjugations are the result of vowel mutation and elision.
isic acid 1,2-dioxygenase (typically due to a mutation) and is associated with alkaptonuria.
beta decay, iodine-131 is notable for causing mutation and death in cells which it penetrates, and o
n-based innovation (contributing new content, mutation, and recombination), in order to implement co
specifically those capable of causing genetic mutation and of contributing to the development of tum
ve diagnosis rest with LCAT gene analysis for mutation and functional activity.
clear that the populace has been afflicted by mutation and madness.
sed before nasals (which may be the result of mutation) and, occasionally, vowels; these forms are b
Fantails with this mutation are known as Silky or Lace Fantails.
elf - people are being born in whom the P.A.S mutation are not present.
DNA damages and mutation are fundamentally different.
sn't the only symptom, as insanity and bodily mutation are evident in many cases.
ence one should expect the time between the A mutation arising and the population becoming fixed for
among the nucleotides in neighboring DNA of a mutation as the result of recent and strong positive n
This is apparently a spontaneous mutation, as tests including crosses were performed th
ects of radiation and other agents on genetic mutation, as well as the process of mutation itself an
The first common appearances with Think About Mutation as took place in November and December, 1995
EA5 patients have a cysteine to phenylalanine mutation at position 104.
, and craniofacial dysmorphism due to genetic mutation at locus 8q22-23.
those with Creutzfeldt-Jakob disease carry a mutation at codon 178 of the prion protein gene.
syndrome is caused by a maternally-inherited mutation at position 8344 in the mitochondrial genome
on is said to be a non-degenerate site if any mutation at this position results in amino acid substi
f many closely-related genotypes are only one mutation away from each other, then genotypes in the g
The first man to carry mutation B was also a direct male line descendant of t
heterozygosity reflects the diversity of the mutation base for many autosomal recessive genetic dis
Mutation based fuzzers mutate existing data samples to
Their mutation began with their relative Eva Van Dam, who ha
ge (or absence thereof) of DNA for a specific mutation by a selected restriction enzyme that will no
Beck: The Art of Mutation, by Nevin Martell; published Simon and Shuste
There is a feather mutation called Silky that gives an interesting lace e
Mutation can result in several different types of chan
This suggests that the second mutation can occur in different types of cells and at
It may begin as a sporadic mutation, can be associated with non-genetic congenita
This mutation causes a small, nonfunctional form of the pro
actosidase A (a-GAL A, encoded by GLA) due to mutation causes a glycolipid known as globotriaosylcer
One silent mutation causes the dopamine receptor D2 gene to be le
rders, the polyglutamine diseases, occur if a mutation causes a polyglutamine tract in a specific ge
The first mutation causes an obligate cheat (OC) phenotype to em
The mutation causes sialic acid to build up in the cells.
inked recessive manner, which means a genetic mutation causing the disorder is located on the X chro
s in the ALAS2 resulted in a loss-of-function mutation causing X-linked sideroblastic anemia.
subjects including recombination, DNA repair, mutation, cell cycle control, tubulin, chromatin, nucl
fly Drosophila melanogaster suggest that if a mutation changes a protein produced by a gene, this wi
leaf, shoot or flower, which due to a genetic mutation clearly differs from the rest of the plant, a
80 persons are carriers of a cystic fibrosis mutation, compared with an average of 1 in 25 elsewher
isting 93 common mutations, after its initial mutation compilation in 2007 of 80 mutations.
mination then, that persons with the L140 SNP mutation comprise a separate subgroup of G2a3b1.
In a study using a mixture of wildtype and mutation containing DNA amplified by regular PCR or CO
ticized Behe's claim that no amount of random mutation could bring about the diversity of life in ex
was the first to establish that a single DNA mutation could lead to a human disease, and the first
repair proteins, this conclusion was based on mutation data that was later shown to affect a differe
Galactosemia (GALT) Mutation Database
Furthermore each mutation defines a set of specific Y chromosomes calle
ion end up carrying at least one (additional) mutation depends heavily on the genomic mutation rate
the Arcandam books is the Livre de l'estat et mutation des temps of 1550.
La mutation des signes (1972)
A genetic mutation disrupting the function of one gene in a path
This point mutation disrupts the mitochondrial gene for tRNA-Lys
er it is important to note that likelihood of mutation does not indicate the likelihood for the evol
vent, a new phenotype emerged via spontaneous mutation dubbed phoenix (PX).
If left unrepaired, AP sites can lead to mutation during semiconservative replication.
ted in the PAM250 matrix have experienced 250 mutation events for every 100 amino acids, yet only 80
cular evidence supported the theory that most mutation events at the molecular level are slightly de
essential to galactokinase function in point mutation experiments.
Tour 1999 Foreteller's Mutation Final: The Genome Control (March 15, 2000)
M168 is simply the mutation first discovered that distinguishes his male
rozygote carriers of a common disease causing mutation for CESD are more common than previously thou
for sequences that have experienced one point mutation for every hundred amino acids.
Ear tuft is a mutation found in the Araucana chicken breed.
are predicted to be inactive based on a point mutation found in the active site sequence.
This was the first mutation found in the Kozak sequence.
nation frequency even exceeds the frame shift mutation frequency (slipped strand mispairing) of (ave
The mutation frequency is the number of individuals in a p
Currently, no specific genetic mutation has been established as the cause of fibrocho
The mutation has proven not to be achondroplasia, but is m
the removal of 12 nucleotides where a genetic mutation has occurred followed by a DNA polymerase, re
One such mutation has been developed into the American Ringtail
An advantageous mutation has a positive effect on the phenotype, and t
While the G2a1 mutation has not been dated in a scholarly publication
This mutation has also been identified in other European co
A rare mutation has occurred within the vampire community.
DJ-1 damage and mutation have been conclusively linked to the onset of
wi, affects certain species or is an invidual mutation) have their sphincteral orifice in their face
O2b*, i.e. those that do not exhibit the 47z mutation, have been detected among the indigenous popu
y graduate Xavier is publishing his thesis on mutation; his foster sister Raven, a waitress, lives w
This mutation, however, behaves inconsistently.
Even among patients homozygous for this mutation, however, there is a wide spectrum of disease
He is best known for the deterministic mutation hypothesis explaining the maintenance of sexu
A mutation in this gene results in one form of Zellweger
ACHP has been associated with a mutation in the LMBR1 gene.
CGD2 is caused by a mutation in the TGFBI gene, located on chromosome 5q31
Mutation in this gene, which is located in a tail-to-t
NBS is caused by a mutation in the NBS1 gene, located at human chromosome
Mutation in the gene in humans leads to a lupus phenot
A missense mutation in the GCGR gene is associated with diabetes
f chemistry by the understanding that it is a mutation in the order of genetic base pairs in the DNA
Mutation in any one of four genes can lead to BLS II.
Sarcosinemia is thought to be caused by a mutation in the sarcosine dehydrogenase gene.
For example, a mutation in a caretaker gene coding for a DNA repair p
Another mutation in the OCA2 is found common to nearly all peo
ns laboratory strain; a similar strain with a mutation in the yA marker gene involved in green pigme
Ellis-van Creveld syndrome is caused by a mutation in the EVC gene, as well as by a mutation in
XLH is associated with a mutation in the PHEX gene sequence, located on the hum
is an abnormal hemoglobin with a single point mutation in the β chain.
ely high probability of developing the second mutation in at least one other cell in their bodies.
CSCD is associated with a mutation in the gene that encodes the protein decorin,
nherited degenerative myopathy resulting from mutation in the emerin gene.
coustic syndrome is thought to be caused by a mutation in a gene on the X chromosome.
In horses, a mutation in the middle of the EDNRB gene, Ile118Lys, w
he body does not produce enough CPSI due to a mutation in the genetic code, resulting in poor metabo
order, Hirschsprung disease type 2, is due to mutation in endothelin receptor type B gene.
A genetic mutation in the PFKM gene results in Tarui's disease,
he mRNA strands themselves undergo a missense mutation in which a protein coding sequence is mutated
s a skin condition resulting from a recurrent mutation in KRT14.:557
er (discovered in 2003 and 2004) is caused by mutation in the transporter of thyroid hormone, MCT8,
xplains Lionel was conducting tests regarding mutation in sea life when he was attacked and apparent
) is an X-linked dominant disease caused by a mutation in the IKBKG gene.
y in N-Acetyl Glutamate Synthase or a genetic mutation in the gene coding for the enzyme, will lead
anelle unique to yeast cells with a secretory mutation in the genes sec7 and sec14.
of function of the sodium channel occurs is a mutation in the gene that disrupts the sodium channel'
ICF syndrome can be caused by a mutation in the DNA-methyltransferase-3b (Dnmt3b) gene
re congenital disease of the skin caused by a mutation in the KIND1 gene.
s cannot synthesize adenine due to a nonsense mutation in one of the enzymes involved in biosyntheti
Hyperprolinemia type I is caused by a mutation in the PRODH gene, which codes for the enzyme
s Spider-Man out of the room and triggers the mutation in Gambit, Storm, Emma Frost and Wolverine, a
autosomal dominant manner, and results from a mutation in the EYA1 gene.
A silent mutation in the multidrug resistance 1 gene, which cod
visible genetic markers such as an eye color mutation in an economically important species like the
A mutation in this gene has been correlated with T-cell
ines, where one harbours a disease-associated mutation in an endogenous gene, just as it occurs in r
llar myopathy diseases and is the result of a mutation in the gene that codes for desmin which preve
testinal stromal tumors (GIST) with the D842V mutation in the PDGFRA gene
son), and the identification of a key genetic mutation in lymphoma development (Lieber).
In people with congenital myotonia due to a mutation in CLCN1, the ion channel admits too few chlo
-Loken syndrome type 5 has been identified to mutation in the NPHP1 gene which adversely affects the
syndrome") is a cutaneous condition caused by mutation in the SNAP29 gene.
A mutation in CHEK2 gene results in decreased DNA-repair
If a mutation in the IVD gene reduces or eliminates the act
be effective in patients that have the G551D mutation in the defective protein that causes the dise
27 November: A mutation in the genes of the H1N1 virus has been detec
lial dysautonomia have two copies of the same mutation in each cell, which causes part of the IKBKAP
invulnerable to most weaponry because of the mutation in their cell structure.
Mutation in the INPP5E associated with Joubert syndrom
If a mutation in the ACAT1 gene reduces or eliminates the a
ring Drosophila research, it was found that a mutation in the gene, MAD, in the mother, repressed th
It can be caused by mutation in the OXCT1 gene.
Very recently a mutation in a second gene, Glycerol-3-phosphate dehydr
ensity lipoprotein (HDL) cholesterol due to a mutation in the hepatic lipase gene.
The disorder is caused by a mutation in the ACADSB gene, located on the long arm o
If a mutation in the ACAD8 gene reduces or eliminates the a
ecessive metabolic disorder associated with a mutation in the enzyme adenine phosphoribosyltransfera
In humans the most common naturally occurring mutation in the medium-chain acyl-CoA dehydrogenase is
air-rule genes are defined by the effect of a mutation in that gene, which causes the loss of the no
The discovery of amylomaize occurred as a mutation in a normal inbred line and from that one mut
A mutation in the Sh gene reduces the conductance of cha
ndrome is a rare genetic disorder caused by a mutation in the MAOA gene.
In addition, a mutation in Dock5 has been associated with the rupture
t least some case, the gene lesion involves a mutation in the CSB gene.
Virtually all cases are due to a mutation in the MEFV gene on the sixteenth chromosome,
significant finding, suggesting that a point mutation in a single virus gene has a major impact upo
In 2000, a rare mutation in codon 23 was reported causing autosomal do
One documented autosomal recessive mutation in a family that carries DKC has been found i
Mutation in one of the family members (bestrophin 1) i
A mutation in this gene, which alters the normal splice
been implicated in the polled intersex (PIS) mutation in goats.
ring Drosophila research, it was found that a mutation in the gene, MAD, in the mother, repressed th
ntly focuses on measuring rate of spontaneous mutation in Drosophila.
SD is caused by a mutation in the SLC17A5 gene, located at human chromos
Only one mutation in one patient has so far been found.
s of antibiotics usually results from genetic mutation in the gyrB subunit.
A mutation in KCNJ8 has been associated with cardiac arr
In other cases, a mutation in the GLI3 gene itself is responsible for th
to develop rapidly, which is attributed to a mutation in a protein chip caused by Batou's natural o

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