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1  theories of Haldane's rule depended on this hemizygosity.
2  quantitative Southern blotting demonstrated hemizygosity.
3 ion of the W chromosome and therefore female hemizygosity.
4 ts in human telencephalic tissue with SHANK3 hemizygosity.
5 es in transmission without increases in male hemizygosity, a high degree of X linkage in these system
6                                However, Atg7 hemizygosity also enhanced tumor initiation and progress
7                                          Il4-hemizygosity also resulted in a modest but detectable dr
8 and a new genetic technique named reciprocal-hemizygosity analysis to achieve the complete dissection
9 sing 7 cases with a somatic deletion causing hemizygosity and 94 with homozygosity (isodisomy).
10 ent study was to evaluate the effect of COMT hemizygosity and molecular haplotypes on gene expression
11               Remarkably, only 52% had 22q11 hemizygosity and only 57% had congenital heart disease r
12                                 We show that hemizygosity and thrum-specific expression of S-linked g
13 aplotype-specific structural variation, gene hemizygosity, and allele-specific gene expression contri
14   We investigated candidate gene expression, hemizygosity, and used mutants, to explore gene function
15          More than one hundred distinct gene hemizygosities are specifically linked to epilepsy, ment
16         We found that the fitness effects of hemizygosity are dependent on the species context, the s
17         We have also implicated LIM-kinase 1 hemizygosity as a contributing factor to impaired visual
18 ne responsible for the phenotypes of 22q11.2 hemizygosity-associated ASD possibly through its role in
19                                              Hemizygosity at the ELN locus was established by typing
20 otential functions of ARVCF, we suggest that hemizygosity at this locus may play a role in the etiolo
21 n and expression pattern of CLTD, we suggest hemizygosity at this locus may play a role in the etiolo
22 ouse models to test the hypothesis that HIC2 hemizygosity causes congenital heart disease.
23 ee exact algorithms for inferring regions of hemizygosity containing genomic deletions of all sizes a
24       Our results suggest that neither LIMK1 hemizygosity (contrary to a previous report) nor STX1A h
25                                    TNFRSF13B hemizygosity does not recapitulate autoimmune features o
26                                              Hemizygosity dosage characterization of the genes on chr
27                                              Hemizygosity for a 1.5-3 Mb region of chromosome 22q11 h
28                                              Hemizygosity for a portion of chromosome 22q11 has been
29 ons or mutations confined to ELN showed that hemizygosity for elastin is responsible for the cardiolo
30  whether any of these defects are because of hemizygosity for ETS1 and FLI1, we characterized the phe
31 t in Jacobsen syndrome are likely because of hemizygosity for ETS1 and FLI1.
32 ession during development could suggest that hemizygosity for GSCL, in combination with hemizygosity
33                                              Hemizygosity for high copy-number alleles of R2d2 is ass
34 t hemizygosity for GSCL, in combination with hemizygosity for other genes in 22q11, contributes to so
35 ults in ovarian development and involves (1) hemizygosity for Tas, a gene located in the region of Ch
36                  Typical deletions result in hemizygosity for TBX1 associated with congenital cardiov
37                            Further, in mice, hemizygosity for Tek led to the formation of severely hy
38 ecessary for normal cardiac development, and hemizygosity for the normal allele can result in altered
39 oss of an entire chromosome 17, resulting in hemizygosity for the p53 locus on 17p and a missense p53
40  of a specific segment of the short arm PAR; hemizygosity for this putative locus probably also contr
41                                  Due to male hemizygosity, GCA for X-linked phenotypes must be due to
42                                           As hemizygosity has major consequences for supergene evolut
43 The sex-biased transmission of the Z and its hemizygosity in females can impact patterns of molecular
44               Here we compare the regions of hemizygosity in four patients with terminal deletions of
45  and morphological deficits caused by SHANK3 hemizygosity in human cortical neurons at different deve
46 ve abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cogni
47 portant target for sexual selection, because hemizygosity in males permits accumulation of alleles, c
48 ich molecular technologies can be applied to hemizygosity in males.
49                                    Thus, ELN hemizygosity in mice and humans induces a compensatory i
50 nomic clone containing ALX4 to 11p11.2, with hemizygosity in patients with deletion of 11p11.2 who ha
51 respect to chromosomal context may be due to hemizygosity in the male.
52                                              Hemizygosity in this region occurs in many malignancies,
53 le amyloid-beta (Abeta) also show that Abca1 hemizygosity increases Abeta deposition only in APP/E4/A
54                                              Hemizygosity is common to all distylous species investig
55 ty (contrary to a previous report) nor STX1A hemizygosity is likely to contribute to any part of the
56 -specific manner, which in addition to Nurr1 hemizygosity is necessary to instigate PD pathogenesis.
57 gy, the distinction between homozygosity and hemizygosity is often ambiguous.
58 us in thrums, but it remains unknown whether hemizygosity is pervasive among distyly S-loci.
59 ur after reduction of chromosome 17p13.13 to hemizygosity, may result in cell cycle deregulation and
60 tolerate monoallelism and whether functional hemizygosity might provide an unappreciated advantage.
61                                   Finally, a hemizygosity modifier screen in the interspecies hybrids
62                         In this study, Porcn hemizygosity occasionally caused ocular defects reminisc
63 t abnormalities, so that it is unlikely that hemizygosity of CDC45 alone is responsible for the cardi
64 n karyotypically normal cells by engineering hemizygosity of defined chr7q segments in a 20-Mb region
65 deleted individuals might be due to combined hemizygosity of DMRT1 and DMRT2.
66                           We have shown that hemizygosity of elastin is responsible for one feature o
67  this model, embryos are null for Tbx1, with hemizygosity of genes in cis with Tbx1 on one chromosome
68  the functional defect of glucose transport: hemizygosity of GLUT1 and nonsense mutations resulting i
69 stablish TEI, providing a mechanism by which hemizygosity of one locus can establish epigenetic memor
70  of HCC driven by loss of macroautophagy and hemizygosity of phosphatase and tensin homolog, which de
71 using approximately 28% and approximately 8% hemizygosity of the ancestral and derived X chromosomes,
72      Individuals with 3 Mb and nested 1.5 Mb hemizygosity of the chromosome 22q11.2 represent genetic
73                               In Drosophila, hemizygosity of the Fab-7 regulatory element triggers in
74 hophysiology in deletion AS and suggest that hemizygosity of the GABRB3-GABRA5-GABRG3 gene cluster ca
75                    Heterozygous mutations or hemizygosity of the GLUT-1 gene cause Glut-1 DS.
76                                              Hemizygosity of the Lgdel region does not eliminate card
77 n the two chromosome sets and in part to the hemizygosity of the X chromosome in Drosophila males.
78                               To accommodate hemizygosity of the X chromosome in male fruit flies, ex
79 e genetic screen that takes advantage of the hemizygosity of the X chromosome in males together with
80                                              Hemizygosity of the X could cause fundamentally differen
81                                        Thus, hemizygosity of the X may underlie much of the faster ma
82 bilities exposed in the phenotype due to the hemizygosity of X-linked genes in the heterogametic sex.
83 Our findings confirm a robust effect of COMT hemizygosity on COMT activity and show complex interacti
84                 However, the impact of DGCR8 hemizygosity on human development is still unclear.
85 ion locus triggers female development, while hemizygosity or homozygosity permits male development.
86 nation, rather than asymmetrical sheltering, hemizygosity, or dosage compensation, is sufficient to a
87 ed by autozygosity, uniparental isodisomy or hemizygosity play a major role in defining HL risk in pr
88     FISH results support our hypotheses that hemizygosity, proximity to centromeric sequences, and ch
89 viations from HWE can be explained by female hemizygosity rather than low heterozygosity.
90                           Consequently, Pten hemizygosity reduces apoptosis by 50%, accelerating prog
91               Examination of humans with ELN hemizygosity revealed a 2.5-fold increase in elastic lam
92 ct was less severe than that caused by mdf-1 hemizygosity, suggesting that MDF-1 causes the PGC arres
93 sis will allow application of the reciprocal hemizygosity test in many organisms.
94                               The reciprocal hemizygosity test is a straightforward genetic test that
95 ous X and Y chromosome assemblies shows that hemizygosity underlies the loss of recombination between
96                                        Shmt1 hemizygosity was associated with a decreased capacity fo
97                                        Shmt1 hemizygosity was associated with increased risk for inte