ライフサイエンスコーパス: maternal gene

1 e and 132 were negative for the noninherited maternal gene.

2 ng positive or negative for the noninherited maternal gene.

3 r to what extent this is due to fetal and/or maternal genes.

4 eflecting in part the influence of fetal and maternal genes.

5 resulting embryo and endosperm, but also on maternal genes acting at two stages.

6 Both maternal gene activity and zygotic gene activity are req

7 This provides a link between maternal gene activity and zygotic patterning gene expre

8 In higher plants, seed development requires maternal gene activity in the haploid (gametophytic) as

9 r future research aimed at understanding how maternal genes and environments interact to control the

10 complex phenotype reflecting the effects of maternal genes and environments.

11 on, diet and body composition of the mother, maternal genes, and possibly infant factors such as sex.

12 th the notion that a large proportion of the maternal genes are directly or indirectly under the cont

13 morphogenetic protein Bicoid, encoded by the maternal gene bicoid, is required for the development of

14 Only deletion of the maternal gene can unambiguously resolve its requirement

15 This work demonstrates that a maternal gene controlling localization of (beta)-catenin

16 We changed maternal gene doses of cyclins A and B to test their fun

17 tigated for the presence of the noninherited maternal gene DRB4, exclusive to the DR53 haplotypes.

18 We conditionally eliminated the maternal gene encoding the cell adhesion molecule E-cadh

19 development in mouse embryos exposed to this maternal gene-environment phenomenon.

20 atal antibody levels were mainly affected by maternal genes, environmental variation and costs of pri

21 A study of maternal gene expression changes between different deliv

22 rader-Willi syndrome (PWS), while absence of maternal gene expression leads to Angelman syndrome.

23 exposure to hypoxia during pregnancy alters maternal gene expression patterns in general and, in par

24 transcriptome reconstruction') and show that maternal gene expression profiles are correlated with de

25 pression and AS is caused by a deficiency of maternal gene expression.

26 h fly and worm embryos, respectively, due to maternal gene expression.

27 ce in minor lineages for more recent two-way maternal gene flow between Island Southeast Asia and Nea

28 es, and a negative relationship for strictly maternal genes for Drosophila, using temporal gene expre

29 417) develop a new technology for inhibiting maternal gene function to identify the H3K9 methyltransf

30 n establishing early developmental programs, maternal gene functions have remained elusive due to a p

31 We then examined the association of SNPs in maternal genes FUT2 (rs492602) and TCN2 (rs1801198, rs96

32 derstanding the specific effect of fetal and maternal genes in the context of these yet-unidentified

33 ntly repaired using the homologous wild-type maternal gene instead of a synthetic DNA template.

34 ional assumption that the effective size for maternal genes is approximately equal to the number of f

35 ncreased maternal provision and silencing of maternal genes limiting demands on the mother.

36 genes, it is shown that effective sizes for maternal genes may be considerably higher when female di

37 ng, is determined by the delayed effect of a maternal gene on the chiral twist that takes place durin

38 sms could be operating: mitochondrial genes, maternal genes, or fetal genes expressing only the mater

39 Mutations in the maternal gene pie-1 result in the germline blastomeres a

40 e that activation of Gtl2 and its downstream maternal genes play an essential role in regulating Dlk1

41 eases, we found marked substructuring of the maternal gene pool into four phylogeographic groups.

42 ngly favor a genetic continuity model in the maternal gene pool.

43 Tumorhead (TH) is a novel maternal gene product from Xenopus laevis containing sev

44 Xenopus nuclear factor 7 (xnf7) is a maternal gene product that functi ons in dorsal/ventral

45 e kinase, Xenopus Wee1, is expressed only as maternal gene product.

46 Maternal gene products deposited in an animal egg determ

47 In animals, maternal gene products deposited into eggs regulate embr

48 bryonic development is driven exclusively by maternal gene products deposited into the oocyte.

49 Maternal gene products drive early development when the

50 GLD-1 and POS-1, suggesting that subsets of maternal gene products may be regulated by distinct path

51 al events of embryogenesis are controlled by maternal gene products that are deposited into the devel

52 ol of development is passed from exclusively maternal gene products to those encoded by the embryonic

53 embryonic life reliant on oocyte-transmitted maternal gene products.

54 rning of zygotic determinants is directed by maternal gene products.

55 ibians typically begins with a prepattern of maternal gene products.

56 ly silent cell cycles regulated by inherited maternal gene products: zygotic genome activation commen

57 ible for its spatial precision, but that the maternal gene staufen may be crucial.

58 These patterns are controlled by maternal genes that determine the identities of early em

59 ounder cell identity in C. elegans, may link maternal genes that regulate the establishment of the en

60 the AP axis is generally conserved, but the maternal genes that regulate their expression are not.

61 o-opted through heterochronous expression of maternal genes to result in sib-care, the hallmark of hi

62 achieved by the localized expression of the maternal gene Torso-like (Tsl).

63 Here we show that the Xenopus maternal gene Vg1, a member of the TGF-beta family of ce

64 egulate a class of developmentally important maternal genes whose mRNA has a temporal profile similar

65 Smc3 is a maternal gene with essential functions in the repair of