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1 ically wild-type, in contrast with the mekk1 dwarf phenotype.
2 m, whereas EBS2 over-expression enhances its dwarf phenotype.
3 ally normal while homozygotes demonstrated a dwarf phenotype.
4 (as in rga-delta17) causes a GA-insensitive dwarf phenotype.
5 overexpression of SNE in sly1-10 rescues the dwarf phenotype.
6 LL homeobox gene VAAMANA (VAN) that causes a dwarf phenotype.
7 size, defective cytokinesis, and an overall dwarf phenotype.
8 etinoblastoma gene (Rb) in mice leads to the dwarf phenotype.
9 p-regulated during cell wall removal exhibit dwarf phenotypes.
10 uble and fer RNAi mutants displayed striking dwarf phenotypes.
11 f null mutants is sufficient to rescue their dwarf phenotypes.
13 of-function sly1 mutant has a GA-insensitive dwarf phenotype and accumulates a high level of RGA.
15 Psbrc1 mutant, rms1 exhibiting a relatively dwarf phenotype and more extensive branching at upper no
18 s, reduced stolon formation, together with a dwarfing phenotype and a lack of flowering in the most s
19 ons and glial cells; Br-M3-KO mice) showed a dwarf phenotype associated with a pronounced hypoplasia
20 creen identifies T0 plants with the expected dwarf phenotype associated with knock-out of the target
21 results indicate that the suppression of the dwarf phenotypes associated with bri1-5R1 requires both
23 Ectopic accumulation of IBH1 causes a severe dwarf phenotype, but the cell elongation suppression mec
25 with the butterhead cultivar, 'Saffier', the dwarf phenotype conditioned by the dwf2 locus was mapped
30 4, is an autosomal recessive trait causing a dwarf phenotype in homozygous mice and has been mapped t
31 of either AtGA2ox7 or AtGA2ox8 also caused a dwarf phenotype in tobacco, indicating that the substrat
34 aling pathways of gibberellin (GA) can cause dwarfing phenotypes in plants, and the use of such mutat
36 activation of HBI1 and its homologs caused a dwarf phenotype, indicating that HBI1 is a positive regu
38 eatures of light-regulatory mutants, but the dwarfed phenotype is entirely and specifically brassinos
39 owth, we performed a comparative analysis of dwarfing phenotypes manifested in mouse mutants lacking
40 f the beneficial effects associated with the dwarf phenotype may be caused by constitutive activation
41 splay decreased BR responses and enhance the dwarf phenotype of a weak allele of the BR receptor muta
42 The herk1 the1 double mutant enhances the dwarf phenotype of bri1 and partially suppresses bes1-D
46 atprx71-1 mutation partially suppresses the dwarf phenotype of qua2-1, suggesting that AtPRX71 contr
48 k of stomata in porA-1 may contribute to the dwarfed phenotype of the mutant and thus emphasizes the
49 gative mutant allele of BAK1 causes a severe dwarf phenotype, resembling the phenotype of null bri1 a
55 plant Nicotiana sylvestris showed a range of dwarf phenotypes, such as reduced germination, short hyp
56 The homozygous irx1 irx8 exhibited severely dwarfed phenotypes, suggesting that IRX8 is essential fo
57 ation was either lethal or caused an extreme dwarf phenotype, supporting the critical importance of t
58 rom UABs of ACC-treated plants resulted in a dwarfed phenotype that mimicked the growth response in R
60 duced significantly, and the lines displayed dwarf phenotypes typical of mutants with a GA deficiency
62 2) mutant indicated that the BR-insensitive dwarf phenotype was due to a semidominant mutation in th
64 This novel mutation confers nondeleterious dwarf phenotypes when transferred to Arabidopsis (Arabid
65 tiolated development in the dark, a severely dwarfed phenotype when grown in the light, and infertili
66 1-3 mutant plants rescued the GA-insensitive dwarf phenotype, which demonstrates that it is a functio
67 plants overexpressing CRY1 also exhibited a dwarf phenotype with reduced size in almost every organ.
69 ted down-regulation of tt16 in canola caused dwarf phenotypes with a decrease in the number of inflor
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