戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 n these two strains is conferred by a single dominant gene.
2 g the one patient who had inherited also the dominant gene.
3 were homozygous, 9% of which were found in 4 dominant genes.
4  cortical cataract and involve the action of dominant genes.
5 in sunflower is commonly regulated by single dominant genes.
6  mechanisms account for 48% of phenotypes in dominant genes.
7      These results demonstrate that a single dominant gene accounts for the low VWF phenotype of RIII
8                                          The dominant genes across such multiple regression models in
9 cell polarity, which likely accounts for the dominant gene action and diverse pleiotropic effects ass
10  initially was suggested to be controlled by dominant gene action from two homoeologous genes (ahFAD2
11 tribute to approximately 1% of IGE both as a dominant gene and as a susceptibility allele in complex
12 ing retromer complex, is the third autosomal-dominant gene associated with PD.
13  detailed phenotypes vary, but generally the dominant genes cause a Lewy body disease spectrum wherea
14 6061 revealed the transfer of a single major dominant gene conditioning all stage resistance, herein
15                                     A single dominant gene Ctv present in the trifoliate relative of
16                                            A dominant gene (Ctv) controlled CTV resistance in P. trif
17 ssing, 5' to the gene, conferred by a single dominant gene designated Mmt1.
18 sitivity to SnTox2 was conferred by a single dominant gene designated Snn2, which mapped to the short
19 ovided the most parsimonious fit, although a dominant gene effect could also explain our data.
20                   It represents an autosomal dominant gene for cerebellar ataxia with different varia
21 we report the identification of an autosomal-dominant gene for hereditary spastic paraplegia (HSP) in
22 e substantial progress on locating the major dominant gene for simple resistance hypersensitive respo
23 arter will be double-mutants who inherit the dominant gene from each parent, the offspring from which
24 soybean is sensitive to soil salinity, and a dominant gene, Glyma03g32900 is primarily responsible fo
25 persensitive response (HR) controlled by the dominant gene HRT.
26                                     Rj4 is a dominant gene in soybeans (Glycine max) that restricts n
27 t and WL dominant), over-dominant, and under-dominant genes in all three tissues in hybrids.
28 rtical cataract is explained by additive and dominant genes, individual environment, and age.
29                           At least 40 floral-dominant genes lacked functional annotations and thus ma
30                                In wheat, two dominant genes lead to non-glaucous phenotypes: Inhibito
31 Arabidopsis thaliana and is conferred by the dominant gene LOCUS ORCHESTRATING VICTORIN EFFECTS1 (LOV
32 n in horses is caused by a single incomplete dominant gene (LP).
33 s design is powerful under both additive and dominant-gene models and across a wide range of allele f
34 line mosaicism for a characterized autosomal dominant gene mutation apparently not associated with so
35                                        Known dominant genes need to be considered for recessive inher
36 spring must be single mutants inheriting the dominant gene of one parent and the wild-type allele of
37 n analysis suggested the presence of a major dominant gene on a polygenic background.
38 phology and endocytosis to identify possible dominant gene or genes.
39                                          The dominant gene produces 10 000 times more transcript than
40  moschata) is conferred by three independent dominant genes (R1R2R3).
41 s CSS-associated SMARCB1 mutations result in dominant gene regulatory and morphologic changes during
42 antitative disease resistance in addition to dominant gene resistance that has been well characterize
43    Although Hrl is inherited as an autosomal dominant gene, resistance to HSV-1 is strongly sex biase
44                                 At least two dominant genes, RTM1 and RTM2, are necessary for this re
45 led that the NS phenotype was regulated by a dominant gene(s) that mapped to the A region of H-2b.
46 adic Parkinson's disease, especially for the dominant genes, suggesting that common facets of pathoge
47                        Complement C3 was the dominant gene targeted by TLR9-induced NF-kappaB signali
48 d that resistance was conferred by a single, dominant gene temporarily designated as Lr(kots).
49                         Rfv3 is an autosomal dominant gene that influences the recovery of resistant
50 s a consequence, it is difficult to identify dominant genes that play a role in this process using ge
51 one of the last major unidentified autosomal-dominant genes underlying these common neurodegenerative
52 to mature because of a heritable defect in a dominant gene used by the thymic stroma to 'educate' the
53      Furthermore, the ratio within autosomal dominant gene variants was not significantly different f
54  people with disease attributed to autosomal dominant gene variants was similar to the all-cause grou
55     A resistance locus, behaving as a single dominant gene, was mapped by association with genetic ma
56    Some (but not all) lineage I-specific or -dominant genes were also more frequently associated with
57                                              Dominant genes were estimated to contribute to 38% (95%
58 est mathematical model obtained was a single dominant gene with autosomal transmission, incomplete pe
59 pected of containing one or two heterozygous dominant genes with a significant effect on chiasma freq
60 estimated by pedigree analysis for autosomal dominant genes with incomplete penetrance.