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1 ntify the transcription factor, Usf1, as the responsible gene.
2 oth muscle myosin heavy chain (myh11) as the responsible gene.
3 starting point for the identification of the responsible gene.
4 etic form of polymicrogyria and localize the responsible gene.
5 ies (Junonia coenia) and characterized three responsible genes.
6  serves as a basis for the identification of responsible genes.
7 CTG.CAG, CGG.CCG, or AAG.CTT) in or near the responsible genes.
8 o the discovery of two of the four (or more) responsible genes.
9 R/J and DBA/2J macrophages, and identify the responsible genes.
10                             Discovery of the responsible gene 30 years ago heralded a new age of pion
11                                          The responsible gene acts as a tumor suppressor, and tumors
12 RMD locus set the stage for isolation of the responsible gene and elucidation of a novel patho-mechan
13 ess robust in identifying and validating the responsible gene and/or genetic variants.
14 an arise through several mechanisms, but the responsible genes and pathways are poorly understood.
15                  The discovery of additional responsible genes and the elucidation of the molecular m
16 w are researchers beginning to tease out the responsible genes and the underlying molecular mechanism
17  disease loci may help identification of the responsible genes, and is thus a topic of considerable p
18                 We provide evidence that the responsible gene at LGS1 codes for an enzyme annotated a
19            In none of these entities has the responsible gene been isolated; hence, the possibility t
20 d function, yet in only a few cases have the responsible genes been cloned.
21 ptian patients suspected of PH for the three responsible genes by Sanger sequencing.
22 es between these strains and to map a single responsible gene (called Ltx1) to chromosome 11.
23                      We hypothesize that the responsible gene causes cortical hyperexcitability that
24       A study was undertaken to identify the responsible gene defect underlying late onset spinal mot
25 uch deficits is largely unknown, many of the responsible gene defects have been identified.
26 ton and collaborators, we show that socially responsible gene drives require 0.5 < s < 0.697, a rathe
27 sion levels of circRNAs derived from drought-responsible genes encoding calcium-dependent protein kin
28                                          The responsible gene, encoding methyl-CpG binding protein 2
29 nts defective in IT formation and cloned the responsible gene, ERN1, encoding an AP2/ERF transcriptio
30                        Identification of the responsible gene for SCA26 ataxia will provide further i
31 n sequencing method, we excluded CASK as the responsible gene for the remaining family.
32       Myosin VIIa has been identified as the responsible gene for USH type 1B, and a number of missen
33              Expression analysis of the main responsible genes for Na(+) compartmentalization (i.e. N
34 1, has been mapped to chromosome 13, but the responsible gene has not been identified.
35 1, has been mapped to chromosome 11, but the responsible gene has not been identified.
36 tiple endocrine neoplasia type I because the responsible gene has not yet been isolated.
37 ent cause of ADPHSP in UK families, that the responsible gene has not yet been mapped in a significan
38 e is well established; identification of the responsible genes has proved challenging.
39  is absent from humans and disruption of the responsible genes has shown a lethal phenotype for Esche
40                          However, few of the responsible genes have been identified, and little is kn
41  from primary cilia of kidney cells, but the responsible genes have not been identified.
42                                 None of the 'responsible' genes have previously been identified.
43  risk and genetic mapping has identified the responsible gene in a few mendelian cases.
44 ncoding an RD wall-associated kinase, is the responsible gene in qRglsSB resistant against GLS.
45  markers D16S419 and D16S400, localizing the responsible gene in this family to a 15 centimorgan regi
46 d to three loci: 2p21 (GLC3A), for which the responsible gene is CYP1B1, and 1p36 (GLC3B) and 14q24 (
47 was not identified, implying either that the responsible gene is essential for cell viability, or tha
48                                          The responsible gene is the human minibrain gene, and the ho
49                    The identification of the responsible genes is providing scientists a window into
50 esterolemia were ruled out by sequencing the responsible genes (LDLRAP, LDLR, PCSK9, APOE and APOB),
51                    The identification of the responsible genes may lead to insights into the pathogen
52 -generation sequencing (NGS) to identify the responsible gene mutation in the family.
53  cardiomyopathy, the likelihood of finding a responsible gene mutation varies.
54 ve a relatively high likelihood of finding a responsible gene mutation when testing is properly appli
55                          Genetic analysis of responsible gene of familial Mediterranean fever, MEFV s
56 genetic loci, within which we identified the responsible genes: one locus contains a known xylose-pat
57 rsons with schizophrenia and then mapped the responsible genes onto transcriptome profiles of normal
58 ted with trisomy 21 (Down syndrome), but the responsible gene or genes on chromosome 21 have not been
59 e and concludes with the identification of a responsible gene or genes; the other that begins with a
60 types followed by genotyping to discover the responsible gene or mutation.
61 endent retinal diseases, suggesting that the responsible gene regulates retinal aging, and its impair
62 of heritable factors, but the whereabouts of responsible gene(s) has remained elusive.
63                                          The responsible gene(s) therefore resides in an interval spa
64 c and physical mapping efforts localized the responsible gene(s) to a well-defined region on human ch
65                   To evaluate the mechanisms responsible, gene targeting was used to study long-dista
66 o our family and the new localization of the responsible gene to chromosome 2cen, together with the d
67                                We cloned the responsible gene, trafficking protein, kinesin binding 1
68 p to take prior to further searching for the responsible genes via segregation and linkage studies.
69 ocus for SSNS, as a first step to detect the responsible gene, was thus identified.
70                                          The responsible gene, WASP, has multiple domains, each with
71                              To identify the responsible gene, we sequenced the exomes of five indivi
72                              To identify the responsible genes, we mapped virulence in F(1) progeny d
73                    The identification of the responsible gene will provide new insights into the mole
74          However, identifying the particular responsible genes within these QTL remains a major chall