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1 bearing progeny rather than the expected 1:1 Mendelian ratio.
2 s, and male Pgam5(-/-) mice were born at sub-Mendelian ratio.
3 ding of the mutant mice yielded the expected mendelian ratio.
4 type, heterozygous, and homozygous mice in a Mendelian ratio.
5 ly normal homozygous mutant mice at a normal Mendelian ratio.
6 ll mice were viable and born at the expected Mendelian ratio.
7 fl);Nr5a1-Cre(/+) mice were born at a normal Mendelian ratio.
8 c loci, with inheritance conforming to a 3:1 Mendelian ratio.
9 disease phenotype deviated from the expected Mendelian ratio.
10 kout (mVps34(pdKO)) mice, which were born at Mendelian ratios.
11 expressing Y265C pol beta are born at normal Mendelian ratios.
12 ull for Eset were recovered but in less than Mendelian ratios.
13 mice are viable but not born in the expected Mendelian ratios.
14 s a semidominant transgene and segregated in Mendelian ratios.
15 (-) mouse crosses, were born at the expected Mendelian ratio (26.5%; n = 1,080 pups), indicating no e
16 ing of heterozygous mutants yielded a normal Mendelian ratio among embryos on gestation day 9.5; howe
18 onal knockout mice were born at the expected Mendelian ratio and developed normally to adulthood, ind
19 ozygous knock-in animals were born in normal Mendelian ratio and developed normally to adulthood.
20 mafF null mutant mice were born in a normal Mendelian ratio and displayed no obvious functional defi
22 Parc knockout mice were born at the expected Mendelian ratios and exhibited no apparent phenotype.
23 sphatase-negative mice were born in expected Mendelian ratios and exhibited normal growth and develop
24 Global tbeta4-knockout mice were born at mendelian ratios and exhibited normal heart and blood ve
25 Nlrp2-deficient mice were born with expected Mendelian ratios and that Nlrp2 was dispensable for inna
26 e is well under that predicted by the normal Mendelian ratio, and TR4(-/-) mice demonstrate high rate
29 nd colonic enterocytes were born in expected Mendelian ratios, and RelA-null epithelia differentiated
31 s Nrp1(Y297A/Y297A) mice were born at normal Mendelian ratios, arguing against NRP1 functioning exclu
32 pups were represented at the expected normal Mendelian ratios at 1 to 3 days of age but at only 10% o
34 rdial Dicer mutant mice are born in expected Mendelian ratios but die immediately after birth with pr
37 f4(loxP/loxP) mice were born at the expected Mendelian ratio, but they gradually died after birth.
39 ed knockouts develop normally, being born in Mendelian ratios, but fail to thrive within 2 weeks, dis
40 xpress KrasG12D in utero, are born at normal Mendelian ratios, develop hepatosplenomegaly, anemia, an
41 f the mutated gene were born in the expected Mendelian ratio, developed normally, and showed no appar
43 unable to interpret his own data that showed Mendelian ratios, even though he shared with Mendel a mo
45 omozygous cardiac betaStop mice were born at Mendelian ratio, had a normal life expectancy, and norma
46 Btbd12-deficient animals are born at sub-Mendelian ratios, have greatly reduced fertility, are de
47 eficient mice are grossly normal and born in Mendelian ratios; however, deficiency of Mmp1a results i
48 onditional mutants were born at the expected Mendelian ratios; however, these died shortly after birt
49 gene was found to be transmitted at a normal Mendelian ratio in mice, in striking contrast to the pro
51 TAFI mice produced offspring in the expected Mendelian ratio, indicating that transmission of the mut
52 c25B and Cdc25C are obtained at the expected Mendelian ratios, indicating that Cdc25B and Cdc25C are
57 duced normal-sized and shrunken seeds in the Mendelian ratio of 3:1, and the shrunken seeds could not
59 his background, we also obtained less than a Mendelian ratio of null offspring suggesting development
60 ned as a significant departure from expected Mendelian ratios of inheritance of an allele or chromoso
61 lta4A/tmDelta4A) offspring with the expected Mendelian ratios of inheritance, and these mice expresse
64 heterozygous matings produced mutant mice at Mendelian ratios that had normal viability and fertility
66 breviated Sca(+/AE)) mutant mice are born in Mendelian ratios with no apparent abnormalities in growt
67 homozygous mutants were born at the expected Mendelian ratio without apparent developmental abnormali
68 us mutant mice (Brca1(FL/FL)) were born at a Mendelian ratio without obvious developmental defects.
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