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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  (as in rga-delta17) causes a GA-insensitive dwarf phenotype.
4 ally normal while homozygotes demonstrated a 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 ulted in impaired chloroplast function and a dwarf phenotype.
10 (Arabidopsis thaliana) resulted in a similar dwarf phenotype.
11 p-regulated during cell wall removal exhibit dwarf phenotypes.
12 uble and fer RNAi mutants displayed striking dwarf phenotypes.
13 f null mutants is sufficient to rescue their dwarf phenotypes.
14 is often, but unpredictably, associated with dwarf phenotypes.
15 s of Zea mays, xyl-1, and xyl-2 that display dwarf phenotypes.
16 phatase) of avp1-2 plants resulted in severe dwarf phenotype and abnormal leaf morphology.
17 of-function sly1 mutant has a GA-insensitive dwarf phenotype and accumulates a high level of RGA.
18                 ugt76b1 mutant plants have a dwarf phenotype and constitutive defense response which
19 lines showed reduced leaf number, leaf area, dwarf phenotype and delayed seed germination.
20  Psbrc1 mutant, rms1 exhibiting a relatively dwarf phenotype and more extensive branching at upper no
21      Mutant plants lacking ER-ANT1 exhibit a dwarf phenotype and their seeds contain reduced protein
22                         gonst1 plants have a dwarfed phenotype and a constitutive hypersensitive resp
23 s, reduced stolon formation, together with a dwarfing phenotype and a lack of flowering in the most s
24 ons and glial cells; Br-M3-KO mice) showed a dwarf phenotype associated with a pronounced hypoplasia
25 creen identifies T0 plants with the expected dwarf phenotype associated with knock-out of the target
26 results indicate that the suppression of the dwarf phenotypes associated with bri1-5R1 requires both
27            In addition to the BR-insensitive dwarf phenotype, bin2 mutants exhibited BR insensitivity
28 Ectopic accumulation of IBH1 causes a severe dwarf phenotype, but the cell elongation suppression mec
29                             These mice had a dwarf phenotype characterized by reduced chondrocyte pro
30 with the butterhead cultivar, 'Saffier', the dwarf phenotype conditioned by the dwf2 locus was mapped
31      mekk1 knockout mutants display a severe dwarf phenotype, constitutive callose deposition, and co
32 arf4 (dwf4) mutants of Arabidopsis display a dwarfed phenotype due to a lack of cell elongation.
33  of calmodulin binding resulted in a partial dwarf phenotype in complementation studies.
34 plasma membrane, and the mutants condition a dwarf phenotype in dark-grown shoots and primary roots,
35 trate sterols and is the direct cause of the dwarf phenotype in dwf7.
36 4, is an autosomal recessive trait causing a dwarf phenotype in homozygous mice and has been mapped t
37 of either AtGA2ox7 or AtGA2ox8 also caused a dwarf phenotype in tobacco, indicating that the substrat
38 RGA promoter caused a GA-unresponsive severe dwarf phenotype in transgenic Arabidopsis.
39 mmon genomic region are the basis for stable dwarf phenotypes in P. taeda.
40  biosynthetic genes result in characteristic dwarf phenotypes in plants.
41 aling pathways of gibberellin (GA) can cause dwarfing phenotypes in plants, and the use of such mutat
42           Hemizygous plants displayed a semi-dwarfing phenotype, in which stem length was reduced but
43 e C(3) model system Brachypodium led to mild dwarf phenotypes, increased lignin (~7% to 13%) and S-li
44 activation of HBI1 and its homologs caused a dwarf phenotype, indicating that HBI1 is a positive regu
45                                          The dwarf phenotype is associated with increased plasma leve
46 eatures of light-regulatory mutants, but the dwarfed phenotype is entirely and specifically brassinos
47 owth, we performed a comparative analysis of dwarfing phenotypes manifested in mouse mutants lacking
48 f the beneficial effects associated with the dwarf phenotype may be caused by constitutive activation
49 splay decreased BR responses and enhance the dwarf phenotype of a weak allele of the BR receptor muta
50    The herk1 the1 double mutant enhances the dwarf phenotype of bri1 and partially suppresses bes1-D
51 e have isolated a dominant suppressor of the dwarf phenotype of bri1-5 plants.
52                                          The dwarf phenotype of chico homozygotes was also unnecessar
53                                          The dwarf phenotype of eld1 could not be rescued by treatmen
54 ntial for plant growth as exemplified by the dwarf phenotype of loss-of-function mutants in BRASSINOS
55  atprx71-1 mutation partially suppresses the dwarf phenotype of qua2-1, suggesting that AtPRX71 contr
56                              The pleiotropic dwarf phenotypes of bin5 establish that, unlike all of t
57 impact on auxin homeostasis resulting in the dwarf phenotypes of the xyl mutants.
58 k of stomata in porA-1 may contribute to the dwarfed phenotype of the mutant and thus emphasizes the
59                              In Pinus taeda, dwarf phenotypes originate from abnormal branches, collo
60 gative mutant allele of BAK1 causes a severe dwarf phenotype, resembling the phenotype of null bri1 a
61                          Genetic analyses of dwarfing phenotypes resulting from targeted mutagenesis
62                                          The dwarfed phenotype results because of a failure in normal
63                          These mice showed a dwarf phenotype similar to achondroplasia, the most comm
64 c expression of a hairpin construct led to a dwarf phenotype similar to that of dw/dw peaches.
65          In addition to rescuing the sly1-10 dwarf phenotype, SNE overexpression also restored normal
66 plant Nicotiana sylvestris showed a range of dwarf phenotypes, such as reduced germination, short hyp
67  The homozygous irx1 irx8 exhibited severely dwarfed phenotypes, suggesting that IRX8 is essential fo
68 ation was either lethal or caused an extreme dwarf phenotype, supporting the critical importance of t
69 rom UABs of ACC-treated plants resulted in a dwarfed phenotype that mimicked the growth response in R
70       dwf5 plants display the characteristic dwarf phenotype typical of other BR mutants.
71 duced significantly, and the lines displayed dwarf phenotypes typical of mutants with a GA deficiency
72                        We show that the nana dwarf phenotype was accompanied by altered leaf morpholo
73  2) mutant indicated that the BR-insensitive dwarf phenotype was due to a semidominant mutation in th
74                                         This dwarf phenotype was largely rescued by introduction into
75   This novel mutation confers nondeleterious dwarf phenotypes when transferred to Arabidopsis (Arabid
76 tiolated development in the dark, a severely dwarfed phenotype when grown in the light, and infertili
77 1-3 mutant plants rescued the GA-insensitive dwarf phenotype, which demonstrates that it is a functio
78  plants overexpressing CRY1 also exhibited a dwarf phenotype with reduced size in almost every organ.
79 A double mutant, ga5-2 ga6-2, had an extreme dwarf phenotype with very short siliques.
80 ted down-regulation of tt16 in canola caused dwarf phenotypes with a decrease in the number of inflor
81                 Knockdown of BoiCesA caused "dwarf" phenotype with smaller leaves and a loss of the c