ライフサイエンスコーパス: male gametophyte

1 e exhibited reduced transmission through the male gametophyte.

2 ontribute to the total RPL10 activity in the male gametophyte.

3 s that show reduced transmission through the male gametophyte.

4 ance in vivo of a specific Rop, rop2, in the male gametophyte.

5 mutated NPG1 is not transmitted through the male gametophyte.

6 nd fem4 mutations affect both the female and male gametophyte.

7 ctivity in peroxisomes primarily affects the male gametophyte.

8 s that SIDECAR POLLEN is indeed expressed in male gametophytes.

9 The fate of male gametophytes after pollen reaches stigmas links pol

10 is essential for the proper function of the male gametophyte, although the synthesis of histidine, l

11 mately 10% of the genes are expressed in the male gametophyte and approximately 9% in the female game

12 alTase) that is expressed exclusively in the male gametophyte and controls the formation of a pollen-

13 hat AtPME48 is specifically expressed in the male gametophyte and is the second most expressed PME in

14 iency results in aberrant development of the male gametophyte and sporophyte.

15 alleles were poorly transmitted through the male gametophyte and were lethal in homozygous plants.

16 DUO1 is required for cell division in male gametophytes and is a target of microRNA 159 (miR15

17 ctivity is required for guided growth of the male gametophytes and pollen tube-ovule interaction.

18 cifically or preferentially expressed in the male gametophyte, and six genes are highly expressed in

19 patterns, provides a protective barrier for male gametophytes, and serves as a mediator of strong an

20 ts demonstrate that ssSPTs are essential for male gametophytes, are important for FB1 sensitivity, an

21 alysis of transporter genes expressed in the male gametophyte at four developmental stages was conduc

22 ransmission, suggesting a requirement in the male gametophyte, but has no paternal effect on seed dev

23 Transmission frequency through the male gametophyte, but not the female, was lower than exp

24 oid embryo production from in vitro-cultured male gametophytes, but this technique remains poorly und

25 The intensification of pollen tube (male gametophyte) competition and enhanced maternal sele

26 An Arabidopsis pollen grain (male gametophyte) consists of three cells: the vegetativ

27 data demonstrate that AtSPP is required for male gametophyte development and pollen maturation in Ar

28 that (1) the delta-subunit is essential for male gametophyte development in Arabidopsis, (2) a distu

29 dition, BAM1, BAM2 and BAM3 are required for male gametophyte development, as well as ovule specifica

30 level of regulation for this transporter in male gametophyte development.

31 of transporters and potential receptors with male gametophyte development.

32 reoisomer of OPDA to produce JA required for male gametophyte development.

33 tic tissues, the young transcriptomes of the male gametophyte displayed greater complexity and divers

34 ull mutant cannot be transmitted through the male gametophyte due to a defect in pollen tube growth.

35 Thus, the details of male gametophyte ecology should shape sporophyte reprodu

36 The haploid pollen grain (male gametophyte) extends a pollen tube that carries two

37 al analyses of insertional mutants affecting male gametophyte function, and should allow detailed gen

38 ese data strongly support a role for rop2 in male gametophyte function, perhaps surprisingly, given t

39 ignaling in vegetative tissue and for normal male gametophyte function.

40 nt T-DNA mutations reveal a role for SEC8 in male gametophyte function.

41 mone that is required for the development of male gametophytes in the homosporous fern Ceratopteris r

42 protuberance formed by the pollen grain, or male gametophyte, in flowering plants.

43 strated reduced transmission of vcl1 through male gametophytes, indicating that vcl1 was expressive a

44 We propose that the totipotency of the male gametophyte is kept in check by an HDAC-dependent m

45 s microspore embryogenesis system, where the male gametophyte is reprogrammed in vitro to form haploi

46 TSA treatment of male gametophytes is associated with the hyperacetylatio

47 The male gametophyte of Arabidopsis thaliana, which is recal

48 ntaxins from these families is lethal in the male gametophyte of Arabidopsis.

49 precocious translation of transcripts in the male gametophyte of M. vestita.

50 lular mechanism of B chromosome drive in the male gametophyte of rye (Secale cereale).

51 es during the development of both female and male gametophytes of Arabidopsis.

52 tivity with trichostatin A (TSA) in cultured male gametophytes of Brassica napus leads to a large inc

53 ion in cell fate determination in developing male gametophytes of M. vestita.

54 ie cell fate determination in the endosporic male gametophytes of the fern, Marsilea vestita.

55 In flowering plants, the haploid male gametophyte or pollen tube (PT) [5] carries two non

56 Although male gametophyte performance primarily involves cellular

57 ends on compatible communication between the male gametophyte (pollen tube) and the maternal tissues

58 In flowering plants, the haploid male gametophytes (pollen grains) are generated in the a

59 oint for sporophytic development controlling male gametophyte production.

60 tion within individual ovules in addition to male gametophyte (sperm) competition and maternal mate c

61 insights into the nature and implications of male gametophyte success.

62 ity depends on the proper development of the male gametophyte, successful pollen germination, tube gr

63 Pollen grains are the male gametophytes that deliver sperm cells to female gam

64 The haploid male gametophyte, the pollen grain, is a terminally diff

65 ical dominance, transition to flowering, and male gametophyte viability.

66 oth kinesins, postmeiotic development of the male gametophyte was severely inhibited.

67 hality in the female gametophyte but not the male gametophyte, which had the redundant LPAT3.