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1 cient to obtain gene conversion in initially heterozygous mutants.
2 alues of both positive and negative dP/dt in heterozygous mutants.
3 bosis response was severely reduced for both heterozygous mutants.
4 e dental epithelium and mesenchyme of double heterozygous mutants.
5 ignificantly reduced in Clock homozygous and heterozygous mutants.
6 that was no more severe than that of single heterozygous mutants.
7 of wild-type alpha1beta2gamma2 receptors or heterozygous mutant alpha1(A322D)beta2gamma2 receptors,
8 rafficking and/or accelerated endocytosis of heterozygous mutant alpha1beta2gamma2 receptors containi
10 cartilage from the knee joints of the double-heterozygous mutant and surgically treated mice were exa
11 copy numbers in ovulated oocytes from EndoG heterozygous mutant and wild-type mice are similar, sugg
12 e strain but decreasing catalase activity in heterozygous mutants and no detectable catalase in a hom
14 t quail exhibited gray plumage, whereas MLPH heterozygous mutants and wild-type quail exhibited dark
15 between those persons who were homozygous or heterozygous mutants and wildtype/pseudo-wildtype (p = 0
16 e 73.3% for p53 wild-type fetuses, 52.5% for heterozygous mutants, and 2.2% for p53-null mutants.
17 our onset, incidence and progression in Pten-heterozygous mutants, and leads to female sterility with
19 um stress, and fecundity enhancement in E(z) heterozygous mutants are accompanied by changes in the e
22 enes expressed during wing development in 27 heterozygous mutants, as well as their co-isogenic wild
25 res from E12.5 homozygous mutant (bcl-x-/-), heterozygous mutant (bcl-x+/-), and wild-type (bcl-x+/+)
26 one morphogenetic protein receptor-2 (BMPR2)-heterozygous, mutant (BMPR2(+/-)) mice have a genetic tr
31 selectively targeting the WT U2AF1 allele in heterozygous mutant cells could induce cancer cell death
34 nctionally independent domains, we undertook heterozygous mutant crossing between Phr1(Delta8,9) and
35 ar, both male and female homozygous and male heterozygous mutants develop impaired glucose tolerance
39 Myocardial hypoplasia in GATA4/GATA6 double heterozygous mutant embryos is associated with reduced p
40 finding of exencephaly in about 15% of rybp heterozygous mutant embryos, and by Rybp's distinct neur
41 misexpressed in engrailed cells in hedgehog heterozygous mutant embryos, larvae show a dominant phen
46 hat deletion of the WT allele in U2AF1(S34F) heterozygous mutant-expressing hematopoietic cells (i.e.
47 g ENL tumor (ENL(T)) mutations and show that heterozygous mutant expression in Six2(+) nephrogenic or
48 increase in foxc1a levels in homozygous and heterozygous mutant eyes, suggesting a mechanism for fox
53 coding PMCA1 caused embryolethality, whereas heterozygous mutants had no overt disease phenotype.
57 hus, heterozygous and homozygous or compound heterozygous mutants have very different clinical phenot
59 CA2 mRNA was reduced by approximately 45% in heterozygous mutant hearts and that SERCA2 protein and m
63 mal gene can be disrupted, and the resulting heterozygous mutant is unlikely to display a phenotype.
64 s, the phenotype of the lymph gland of Zfpr8 heterozygous mutants is dominantly enhanced by the l(1)d
76 in the mammalian heart, we examined compound heterozygous mutant mice and found conduction system and
80 oints was dramatically reduced in the double-heterozygous mutant mice compared with that in the type
81 nally, we propose that soluble KITL in Sld/+ heterozygous mutant mice complements a dosage effect of
88 nterestingly, we found that cells from EndoG heterozygous mutant mice exhibit increased resistance to
90 ectrophysiological studies demonstrated that heterozygous mutant mice have a specific defect in hippo
91 opment, we generated, through breeding, IRF4 heterozygous mutant mice in the NZB background (NZB IRF4
92 taneous cell death of spermatogonia in EndoG heterozygous mutant mice is significantly reduced compar
93 ed an F2 intercross between insulin receptor heterozygous mutant mice on B6 and 129/Sv backgrounds (B
98 scular endothelial cells isolated from Foxc2 heterozygous mutant mice showed a marked reduction in It
108 f osteoclasts were not altered in the double heterozygous mutant mice, indicating that the defect lie
109 chanism of MHE, both Ext1(+/-) and Ext2(+/-) heterozygous mutant mice, which mimic the genetic status
116 phenotypes, our lab recently created a Myt1l heterozygous mutant mouse inspired by a clinically relev
118 rs for Parkinson's disease (PD) are a set of heterozygous mutant (MT) alleles of the GBA1 gene that e
119 , a finding relevant to our understanding of heterozygous mutant myosins found in disease states like
126 ary phase survival was prolonged in a double heterozygous mutant of the metabolic enzyme non-quiescen
127 ductive tracts of Hoxa-10 and Hoxa-11 single heterozygous mutants of both sexes were primarily unaffe
129 urbations of the cell cycle oscillator using heterozygous mutants of mitotic kinases and phosphatases
132 us mutants spontaneously form cysts, whereas heterozygous mutants (original or base corrected) expres
133 ic mice bearing both the v-Ha-ras gene and a heterozygous mutant p53 allele tend to retain the Ink4a
134 cted with an apparent dominant ZSD in whom a heterozygous mutant PEX6 allele (c.2578C>T [p.Arg860Trp]
136 d whether phenotypes are also present in the heterozygous-mutant populations that comprise the vast m
139 ors and a maximum lifespan of 22 days, while heterozygous mutants (RL/+) exhibit autistic-like behavi
140 ient for the Bloom's syndrome helicase, such heterozygous mutants segregate homozygous daughter cells
146 ice had no detectable CuZn-SOD activity, and heterozygous mutants (Sod1 +/-) showed a 50% decrease co
150 00(DeltaKASH), or in klar and msp-300 double heterozygous mutants, the MSP-300 nuclear ring and the a
152 nctionally complemented lpat2 in transformed heterozygous mutants to produce the lpat2/lpat2 genotype