「mutations」の共起表現一覧(1語右で並び替え)
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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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