「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 |
| sition can create phenotypically significant | mutations and alter the cell's genome size. |
| ssumes that genetic differences arise due to | mutations and genetic drift. |
| During each round, random | mutations and perturbations are introduced to the bioc |
| oko Ohta in 1973 (including only deleterious | mutations) and expanded in the early 1990s to include |
| 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 |
| nd human subjects begin to exhibit grotesque | mutations and disfigurement. |
| ting some individuals with fewer deleterious | mutations, and some with more. |
| rveillance that functions to detect nonsense | mutations and prevent the expression of truncated or e |
| Certain | mutations and the activation of certain cell-cycle con |
| ying molecular/genetic changes producing DNA | mutations and genome instability, which contribute to |
| Mutations and variants of the CK1ε phosphorylation sit | |
| f sexual reproduction, the fitness effect of | mutations, and the effect of adaptation to different l |
| is happening depends on the frequency of new | mutations, and on the size of the population, but is i |
| 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 |
| 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 |
| ing all tongues have, and do undergo various | mutations, and corruptions, this alone doth alwaies co |
| 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 |
| Chemicals that induce | mutations are called mutagens. |
| Some | mutations are dominant, some are recessive. |
| Resistance | mutations are known for all approved NRTIs. |
| Other resistance | mutations are L80V/I, V173L and L180M. |
| Furthermore | mutations are directly linked to quantum leaps. |
| 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 |
| FLCN | mutations are detected by sequencing in 88% of proband |
| Patients with such | mutations are congenitally insensitive to pain and lac |
| Specific point | mutations are made and the transcription of the gene i |
| These | mutations are likely not wholly causative and should i |
| Scanning refers to the fact that many | mutations are sometimes indiscriminately performed alo |
| f molecular evolution, while the majority of | mutations are deleterious, the majority of mutations t |
| These | mutations are somatic, which means they are acquired d |
| These | mutations are in exon 8 (atypical form) and exon 8a (c |
| Ironically, these two | mutations are both shared by the Low pain sensitivity |
| The results of these | mutations are highly variable, some producing function |
| reditary nonpolyposis colorectal cancer, the | mutations are biallelic in CMMR-D. |
| NLRP3 | mutations are responsible for the autoinflammatory dis |
| (A) If | mutations are induced by the media, roughly the same n |
| The vowel | mutations are the product of the assimilation of one v |
| region, Grenache noir and its gris and blanc | mutations are used in the production of the fortified |
| These types of | mutations are associated with papillary thyroid carcin |
| RET loss of function | mutations are associated with the development of Hirsc |
| nerally green in color (both lutino and blue | mutations are rare, but do exist in captivity) with a |
| 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 |
| 1253 and 1351c have the same | mutations at position A-911, G-977 in exon 7 of FOXP2 |
| 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. |
| 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 |
| are called teratogens; these may also cause | mutations, but their effect on development is not rela |
| s seeks to saturate with insertions or point | mutations, but instead of for the entire genome, it sa |
| top the spread of Tiberium and its monstrous | mutations by retrieving the extraterrestrial Tacitus d |
| resence of nitrous acid can cause transition | mutations, by converting cytosine to uracil. |
| germline point | mutations) can be passed on. |
| Due to the damaging effects that | mutations can have on genes, organisms have mechanisms |
| Mutations can cause the osteochondrodysplasias pseudoa | |
| Neutral | mutations can accumulate over time due to genetic drif |
| Furthermore, such | mutations can show how the specific structure of that |
| Mutations can be inherited or can arise de novo early | |
| petite | mutations can be induced using a variety of mutagens, |
| Burns has said that the | mutations can be read as a metaphor for adolescence, s |
| ily in human cancer (24, 29), and that point | mutations can activate the oncogenic potential of cell |
| It has been shown that the | mutations cause defective U12 splicing. |
| SOD2 knockout or null | mutations cause growth inhibition on respiratory carbo |
| Mutations cause constitutive action of Flt3 leading to | |
| hairy, odd-skipped, paired and runt - where | mutations caused the deletion of a particular region o |
| Conversely, | mutations causing this enzyme to be overexpressed are |
| Other | mutations causing MH have been identified, although in |
| were able to accurately identify single-gene | mutations causing beta-thalassemia. |
| 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 |
| Benzer also proposed missense and nonsense | mutations from his rII studies. |
| urifying selection which removes deleterious | mutations from a population. |
| 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 |
| At least 11 distinct | mutations have been identified. |
| Although not all | mutations have a noticeable phenotypic effect, the com |
| 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. |
| Currently, | mutations have been identified in six COX assembly fac |
| When enough | mutations have occurred and become stable in a populat |
| Several polymorphisms and | mutations have been described in this gene, some of wh |
| Many | mutations have been identified in affected patients, b |
| Many of the CACNA1H | mutations have a measurable effect on channel kinetics |
| These | mutations have been shown to cause diverse changes in |
| 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 protein cause congenital myotonia. | |
| Mutations in Ran disrupt DNA synthesis. | |
| Mutations in this gene cause vitiligo. | |
| Several | mutations in the Pxr sRNA gene have been observed. |
| Certain | mutations in OCA2 result in type 2 oculocutaneous albi |
| Mutations in the PC gene cause pyruvate carboxylase de | |
| It is caused by | mutations in the SPRED1 gene. |
| The disease is caused by | mutations in the ceruloplasmin gene. |
| HSH is caused by | mutations in the TRPM6 gene. |
| Mutations in Cbfa1/Runx2 are associated with the disea | |
| Familial dysautonomia is caused by | mutations in the IKBKAP gene. |
| Mutations in the NEK8 gene associated with nephronopht | |
| Mutations in this gene also cause a Wernicke's-like en | |
| Mutations in this gene may be associated with autism. | |
| Mutations in the ACAT1 gene cause beta-ketothiolase de | |
| Mutations in this gene cause Rubinstein-Taybi syndrome | |
| Mutations in this gene are associated with meningioma. | |
| Mutations in this gene are associated with familial hy | |
| Mutations in either gene are links to Waardenburg synd | |
| Mutations in the ASS gene cause type I citrullinemia. | |
| Mutations in the XPNPEP3 gene are associated with cili | |
| Mutations in the ACVR1 are associated with fibrodyspla | |
| Mutations in the HMGCL gene cause 3-hydroxy-3-methylgl | |
| Mutations in this protein cause pseudoxanthoma elastic | |
| Mutations in this gene have been linked to cryptogenic | |
| Mutations in class A genes affect sepals and petals. | |
| Mutations in the Shine-Dalgarno sequence can reduce tr | |
| Patients with | mutations in this gene develop Wolcott-Rallison syndro |
| Mutations in this gene may be associated with rheumato | |
| Mutations in either genes result in a lipid disorder, | |
| Mutations in the SALL4 gene cause Duane-radial ray syn | |
| Mutations in this gene cause corticosterone methyl oxi | |
| There are currently 20 | mutations in CACNA1H associated with CAE. |
| e the radical alterations that resulted from | mutations in homeobox genes were termed homeotic mutat |
| Mutations in the SLC26A2 gene cause diastrophic dyspla | |
| In November 2008 | mutations in the glucocerebrosidase gene were the muta |
| This is thought to cause | mutations in the p53 gene, an important gene in preven |
| In 85% of patients, ADPKD is caused by | mutations in the gene PKD1 on chromosome 16 (TRPP1); i |
| Mutations in this gene have been associated with conge | |
| Mutations in the CPS1 gene cause carbamoyl phosphate s | |
| ent of bronchial tree altered due to genetic | mutations in metalloproteinases - ADAM-33 |
| Mutations in the SLC26A2 (DTDST) gene, located at huma | |
| Mutations in the gene encoding this protein cause epid | |
| Mutations in this gene are associated with the autosom | |
| Orofaciodigital syndrome type 1 is caused by | mutations in the OFD1 gene. |
| Mutations in this gene result in autosomal recessive s | |
| Mutations in CNDP1 are responsible for carnosinase def | |
| It is non-progressive and is linked to | mutations in DCN gene encoding decorin protein. |
| Mutations in protocadherin genes and their expression | |
| Mutations in the AAAS gene are responsible for Triple | |
| Mutations in this gene have been associated with X-lin | |
| Mutations in this gene are associated with erythrocyto | |
| CTX is associated with | mutations in the CYP27A1 gene, located on chromosome 2 |
| Mutations in emerin cause X-linked recessive Emery-Dre | |
| Mutations in this gene are associated with achromatops | |
| Mutations in the gene are associated with N-Acetylglut | |
| Mutations in this gene are associated with epidermolys | |
| PathoDB: Pathologically relevant | mutations in transcription factors and their binding s |
| Mutations in this gene are a cause of Kostmann syndrom | |
| Mutations in the intracellular part of this receptor a | |
| The disorder has been associated with | mutations in the L1CAM gene. |
| Mutations in NR5A1 can produce intersex genitals, abse | |
| Mutations in the EP300 gene have been identified in se | |
| Mutations in gene encoding myotubularin-related protei | |
| Mutations in this gene are associated with heparin cof | |
| Mutations in this gene result in both X-linked congeni | |
| Mitochondrial | mutations in this enzyme may be associated with some f |
| It is associated with | mutations in the chloride channel gene CLCN1. |
| Mutations in the KRT3 encoding this protein have been | |
| A number of human diseases arise from | mutations in VWA domains. |
| Mutations in the palmitoyl protein thioesterase gene c | |
| SCADD is caused by | mutations in the ACADS gene, located on chromosome 12q |
| Mutations in this gene are associated with Usher syndr | |
| Mutations in the MTRNR1 gene may be associated with he | |
| Mutations in this gene have been associated with cardi | |
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