ライフサイエンスコーパス: sterile mutant

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1 ross a variety of conditions, including male-sterile mutants.

2 tant, ste24, in addition to previously known sterile mutants.

3 be suitable for analysis of defects in male sterile mutants and for investigating other steps of spe

4 The female-sterile mutants are at a selective disadvantage every ti

5 dentified several lethal alleles of the male sterile mutant, bobble (bob).

6 iming of DAF-16-dependent gene activation in sterile mutants coincides with the onset of embryonic de

7 In Arabidopsis, two previously isolated male-sterile mutants display dramatically altered anther cell

8 Although many male-sterile mutants disrupt these key steps, few have been i

9 eport the analysis of a new Arabidopsis male sterile mutant, dysfunctional tapetum1 (dyt1).

10 ization of a novel Arabidopsis thaliana male sterile mutant, excess microsporocytes1 (ems1), that pro

11 e examined a collection of Drosophila female-sterile mutants for defects in translation of maternal m

12 We have isolated a new female sterile mutant from Drosophila melanogaster, which arres

13 phenotype in flowering plants, and many male sterile mutants have defects in somatic and reproductive

14 We identified a female sterile mutant in which each bivalent chromosome often f

15 The microarray datasets from nine rice male sterile mutants, including msp1-4, ostdl1a, gamyb-2, tip

16 NPG1 knockout mutant and a cross with a male sterile mutant indicate that the mutated NPG1 is not tra

17 Subsequently, male sterile mutants invade and increase because they are una

18 rrelated and that resistance in both epr and sterile mutants is dependent on DAF-16 activity.

19 Three male-sterile mutants lacking a range of normal cell types res

20 pment, we characterized a T-DNA-tagged, male-sterile mutant of Arabidopsis, opr3.

21 enotypic and molecular characterization of a sterile mutant of tomato (jasmonic acid-insensitive1 [ja

22 We cloned silky1 (si1), a male sterile mutant of Zea mays that has homeotic conversions

23 nthers of wild-type Arabidopsis and the male-sterile mutant, opr3.

24 g the fluorescence assay, a sampling of male-sterile mutant phenotypes in which spermatogenesis proce

25 A large group of male and female sterile mutants shows defects restricted to early or lat

26 the only Drosophila Adducin, and is a female-sterile mutant that affects both the fusome and ring can

27 d characterization of a new Arabidopsis male-sterile mutant that exhibits meiotic defects.

28 cellent opportunity to identify and maintain sterile mutants that affect sperm and no other cells.

29 ent progresses normally, in contrast to male-sterile mutants that disrupt anther cell fate or functio

30 Synthetic sterile mutants that exacerbate the phenotype of ste4-ts

31 We also examined several well-characterized sterile mutants that exhibit an Epr phenotype.

32 By screening for sterile mutants that show increased ploidy, we have iden

33 From a collection of male sterile mutants, we identified P-element-induced hypomor

34 We have isolated a novel type of sterile mutant, which undergoes one additional S phase u

35 ale-sterile/hermaphrodite status, and female-sterile mutants, which function only as males during sex

36 A seed-sterile mutant with a disrupted TRAF-like gene (At5g2629

37 cale genetic screen and isolated a number of sterile mutants with aberrant ovule development, We prov

38 Male-sterile mutants with subepidermal defects--mac1 (excess

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