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 complex phenotype reflecting the effects of maternal genes and environments.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 Maternal gene products deposited in an animal egg determ

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

41 Maternal gene products drive early development when the

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

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

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

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

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

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

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

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

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

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

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

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

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

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