「Mutation」の共起表現一覧(1語右で並び替え)
該当件数 : 442件
| 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 |
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|