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1 s, and male Pgam5(-/-) mice were born at sub-Mendelian ratio.
2 type, heterozygous, and homozygous mice in a Mendelian ratio.
3 fl);Nr5a1-Cre(/+) mice were born at a normal Mendelian ratio.
4 bearing progeny rather than the expected 1:1 Mendelian ratio.
5 ding of the mutant mice yielded the expected mendelian ratio.
6 ly normal homozygous mutant mice at a normal Mendelian ratio.
7 ll mice were viable and born at the expected Mendelian ratio.
8 c loci, with inheritance conforming to a 3:1 Mendelian ratio.
9 disease phenotype deviated from the expected Mendelian ratio.
10 -/-) mice that were not born at the expected Mendelian ratio.
11 kout (mVps34(pdKO)) mice, which were born at Mendelian ratios.
12 expressing Y265C pol beta are born at normal Mendelian ratios.
13 ull for Eset were recovered but in less than Mendelian ratios.
14 mice are viable but not born in the expected Mendelian ratios.
15 s a semidominant transgene and segregated in Mendelian ratios.
16 (-) mouse crosses, were born at the expected Mendelian ratio (26.5%; n = 1,080 pups), indicating no e
17 ty and abnormal embryonic growth with skewed Mendelian ratios after day E18.5.
18 ing of heterozygous mutants yielded a normal Mendelian ratio among embryos on gestation day 9.5; howe
19 IKfyve(WT/KO) mice were born at the expected Mendelian ratio and developed into adulthood.
20 onal knockout mice were born at the expected Mendelian ratio and developed normally to adulthood, ind
21 ozygous knock-in animals were born in normal Mendelian ratio and developed normally to adulthood.
22  bKO animals were born close to the expected Mendelian ratio and developed without overt histological
23 -/- mice are live-born at below the expected Mendelian ratio and die at a weaning age with cystic kid
24  mafF null mutant mice were born in a normal Mendelian ratio and displayed no obvious functional defi
25 -) mice were born at a significantly reduced Mendelian ratio and exhibited high mortality between 3 t
26 zygous for DeltaPR were born at the expected Mendelian ratio and exhibited obesity plus insulin resis
27 omozygous Adam17 cyto animals were born at a Mendelian ratio and survived into adulthood with slightl
28       CCR2-/- mice were born at the expected Mendelian ratios and developed normally.
29 Parc knockout mice were born at the expected Mendelian ratios and exhibited no apparent phenotype.
30    Gpr27 knockout mice were born at expected Mendelian ratios and exhibited no gross abnormalities.
31 sphatase-negative mice were born in expected Mendelian ratios and exhibited normal growth and develop
32     Global tbeta4-knockout mice were born at mendelian ratios and exhibited normal heart and blood ve
33 Nlrp2-deficient mice were born with expected Mendelian ratios and that Nlrp2 was dispensable for inna
34 e is well under that predicted by the normal Mendelian ratio, and TR4(-/-) mice demonstrate high rate
35             The Mcoln1(-/-) mice are born in Mendelian ratios, and both male and female Mcoln1(-/-) m
36       ADAM33-null mice were born at expected Mendelian ratios, and both male and females developed no
37         ZO-1cKO mice were viable, had normal Mendelian ratios, and had a normal lifespan.
38 nd colonic enterocytes were born in expected Mendelian ratios, and RelA-null epithelia differentiated
39 amin A/C and emerin are born at the expected Mendelian ratio, are grossly normal at birth but have sh
40               The lal-/lal- mice are born in Mendelian ratios, are normal appearing at birth, and fol
41 s Nrp1(Y297A/Y297A) mice were born at normal Mendelian ratios, arguing against NRP1 functioning exclu
42 pups were represented at the expected normal Mendelian ratios at 1 to 3 days of age but at only 10% o
43     Pure F2 Parp1(+/A) embryos were found at Mendelian ratios at the E3.5 blastocyst stage but died b
44 amin A/C and emerin are born at the expected Mendelian ratio but had a shorter lifespan than those on
45       Klf5 mutant mice were born at a normal Mendelian ratio but had high mortality compared with con
46 rdial Dicer mutant mice are born in expected Mendelian ratios but die immediately after birth with pr
47          These mice are born at the expected Mendelian ratio, but die prematurely from spontaneous ca
48 zygous mutant mice were born at the expected Mendelian ratio, but their growth was impaired.
49 f4(loxP/loxP) mice were born at the expected Mendelian ratio, but they gradually died after birth.
50                These mice are born at normal Mendelian ratios, but display a progressive, systemic hy
51 ed knockouts develop normally, being born in Mendelian ratios, but fail to thrive within 2 weeks, dis
52 ound, knockout animals were also born at sub-Mendelian ratios, but many Adgrl1 null mice survived ges
53 c25a28 (encoding Mfrn2) are born at expected Mendelian ratios, but show decreased male fertility due
54 xpress KrasG12D in utero, are born at normal Mendelian ratios, develop hepatosplenomegaly, anemia, an
55 f the mutated gene were born in the expected Mendelian ratio, developed normally, and showed no appar
56            FLKO mice, while born at a normal Mendelian ratio, developed severe anemia and exhibited p
57 unable to interpret his own data that showed Mendelian ratios, even though he shared with Mendel a mo
58       VENIRKO mice were born at the expected Mendelian ratio, grew normally, were fertile, and exhibi
59 omozygous cardiac betaStop mice were born at Mendelian ratio, had a normal life expectancy, and norma
60     Btbd12-deficient animals are born at sub-Mendelian ratios, have greatly reduced fertility, are de
61 eficient mice are grossly normal and born in Mendelian ratios; however, deficiency of Mmp1a results i
62 onditional mutants were born at the expected Mendelian ratios; however, these died shortly after birt
63 gene was found to be transmitted at a normal Mendelian ratio in mice, in striking contrast to the pro
64        PAK4 knock-out (KO) mice were born at Mendelian ratios in both genders.
65 uble mutant embryos is lower than that for a Mendelian ratio, indicating deletion of Thm1 and Thm2 ca
66 TAFI mice produced offspring in the expected Mendelian ratio, indicating that transmission of the mut
67 c25B and Cdc25C are obtained at the expected Mendelian ratios, indicating that Cdc25B and Cdc25C are
68 minant involved in the generation of the non-Mendelian ratio is epigenetic.
69               In mice lacking Msy2, a normal Mendelian ratio is observed after matings between hetero
70                    Although born in a normal mendelian ratio, no PGT(-/-) mice survived past postnata
71 (a/a) to A(vy)/a offspring from the expected Mendelian ratio of 1:1.
72 a KO:Het:WT ratio approximating the expected Mendelian ratio of 1:2:1.
73 d progeny of R1 plants, Tnt1 segregated in a Mendelian ratio of 3:1 and no new Tnt1 transposition was
74 duced normal-sized and shrunken seeds in the Mendelian ratio of 3:1, and the shrunken seeds could not
75                               The unexpected Mendelian ratio of 4.4% cKO mice was confirmed by genoty
76 his background, we also obtained less than a Mendelian ratio of null offspring suggesting development
77 ned as a significant departure from expected Mendelian ratios of inheritance of an allele or chromoso
78 lta4A/tmDelta4A) offspring with the expected Mendelian ratios of inheritance, and these mice expresse
79         In contrast, we observed appropriate Mendelian ratios of RA+ mAgt+/+, RA+ mAgt+/-, and RA+ mA
80                          Despite appropriate Mendelian ratios of RA- mice that were wildtype (+/+), h
81 heterozygous matings produced mutant mice at Mendelian ratios that had normal viability and fertility
82  (-/-) embryos were detected at the expected Mendelian ratios up to late preimplantation stage (E4.5)
83           Arl3 (-/-) mice were born at a sub-Mendelian ratio, were small and sickly, and had markedly
84 ulations made with odc2 mutants segregate in Mendelian ratios, while ht-a mutants have little effect,
85 breviated Sca(+/AE)) mutant mice are born in Mendelian ratios with no apparent abnormalities in growt
86 homozygous mutants were born at the expected Mendelian ratio without apparent developmental abnormali
87 us mutant mice (Brca1(FL/FL)) were born at a Mendelian ratio without obvious developmental defects.
88        Appl1-null mice were born at expected Mendelian ratios, without obvious phenotypic abnormaliti