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[PDF] Top 20 Dicer is required for haploid male germ cell differentiation in mice.

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Dicer is required for haploid male germ cell differentiation in mice.

Dicer is required for haploid male germ cell differentiation in mice.

... revision, Dicer-dependent but Drosha-independent endo-siRNAs were reported in male germ line that can function in post- transcriptional control of a wide variety of protein encoding ... See full document

12

STK31/TDRD8, a germ cell-specific factor, is dispensable for reproduction in mice.

STK31/TDRD8, a germ cell-specific factor, is dispensable for reproduction in mice.

... expressed in germ cells are divided into two ...function in piRNA biogenesis and retrotransposon silencing, while the other group including RNF17/TDRD4 and TDRD5-7 are required for ...during ... See full document

7

Three-step method for proliferation and differentiation of human embryonic stem cell (hESC)-derived male germ cells.

Three-step method for proliferation and differentiation of human embryonic stem cell (hESC)-derived male germ cells.

... 5). In particular, approximately 3% of the GSC-like cells could be differentiated into haploid male germ cells, exhibiting specific markers after only two weeks of short-term culture, although ... See full document

13

The differentiation potential of adipose tissue-derived mesenchymal stem cells into cell lineage related to male germ cells

The differentiation potential of adipose tissue-derived mesenchymal stem cells into cell lineage related to male germ cells

... tissue is a reliable source of Mesenchymal stem cells (MSCs) showing a higher plasticity and transdifferentiation potential into multilineage ...cells. In the present study, adipose tissue-derived ... See full document

9

In vitro germ cell differentiation from cynomolgus monkey embryonic stem cells.

In vitro germ cell differentiation from cynomolgus monkey embryonic stem cells.

... primordial germ cells, and then, the expression during male and female gametogenesis exhibits sex-specific down- regulation similar to SSEA1 ...expression is first identified in migrating ... See full document

10

The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.

The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.

... sex differentiation of the somatic gonads, PGCs themselves differentiate into male or female germ cells at around ...identified in mice, and Nanos2 and Nanos3 have been implicated ... See full document

10

Autophagy and apoptosis act as partners to induce germ cell death after heat stress in mice.

Autophagy and apoptosis act as partners to induce germ cell death after heat stress in mice.

... - In the experiments of heat treatment on the mice testes, TUNEL assay was used for detecting cell ...observed in the spermato- cytes, and occasionally in the spermatogonia and round ... See full document

11

Endogenous Mouse Dicer Is an Exclusively Cytoplasmic Protein.

Endogenous Mouse Dicer Is an Exclusively Cytoplasmic Protein.

... observed in the cytoplasmic fraction. Should the amount of potential nuclear Dicer be below our detection limit, it would amount for less than ...factors in the preparation of the nuclear ...of ... See full document

14

Male germ cell apoptosis and epigenetic histone modification induced by Tripterygium wilfordii Hook F.

Male germ cell apoptosis and epigenetic histone modification induced by Tripterygium wilfordii Hook F.

... represented in Figure 6B and 6C, ...atom in H3K9 and the nitrogen atom in residue Arg414(O…NH1), with a distance of ...atom in H3K9 and the nitrogen atom in residue Arg414 (O…NH2) with ... See full document

9

Differentiation of haploid and diploid fertilities in Gracilaria chilensis affect ploidy ratio

Differentiation of haploid and diploid fertilities in Gracilaria chilensis affect ploidy ratio

... of male gametes or their lack of mobility. The production of tetraspores is considered to require only the growth of diploid tetrasporophytes, tetrasporangia de- velopment and tetraspore production by ... See full document

11

Mind bomb-1 in dendritic cells is specifically required for Notch-mediated T helper type 2 differentiation.

Mind bomb-1 in dendritic cells is specifically required for Notch-mediated T helper type 2 differentiation.

... T cell-mediated immune responses is crucial for protection against different types of pathogenic microorganisms as well as peripheral immune ...result in non- physiological levels of signaling and ... See full document

8

Intact p53-dependent responses in miR-34-deficient mice.

Intact p53-dependent responses in miR-34-deficient mice.

... which in turn results in stabilization and activation of p53, and consequently apoptosis or cell cycle arrest ...) in wild-type MEFs leads to oncogene-induced senescence, but the concomitant ... See full document

12

SCRATCH2 na diferenciação neural em embriões e em células-tronco

SCRATCH2 na diferenciação neural em embriões e em células-tronco

... SCRATCH2 in chicken, human, rat and ...mutants in HEK293T and chicken embryos remain in the nucleus demonstrating that the lack of transcriptional repression is not due a subcellular ... See full document

25

Congenic mice confirm that collagen X is required for proper hematopoietic development.

Congenic mice confirm that collagen X is required for proper hematopoietic development.

... lymphocytes in the thymus ...profile in both the marrow and spleen ...lymphocytes in Tg and perinatal lethal collagen X mice at week-3 and transiently increased levels in KO mice ... See full document

13

Inversin/Nephrocystin-2 is required for fibroblast polarity and directional cell migration.

Inversin/Nephrocystin-2 is required for fibroblast polarity and directional cell migration.

... role in regulating Wnt signaling at the primary cilium to control PCP (discussed in ...[33,34]). In inv 2/2 mice, the hair patterning phenotype is reminiscent to that of PCP defects, ... See full document

15

Cell-extrinsic defective lymphocyte development in Lmna(-/-) mice.

Cell-extrinsic defective lymphocyte development in Lmna(-/-) mice.

... decline in health and premature death at around 6–8 weeks of age ...of cell types, it is difficult to distinguish between cell-autonomous defects in specific tissues of Lmna deficiency ... See full document

11

LRGUK-1 is required for basal body and manchette function during spermatogenesis and male fertility.

LRGUK-1 is required for basal body and manchette function during spermatogenesis and male fertility.

... are required for basal body-to-membrane docking [31], and SAPs are believed to be where axo- neme microtubules are anchored and are thus required for axoneme extension [32 – ...7E). In contrast, the ... See full document

20

Fibroblast growth factor 10-fibroblast growth factor receptor 2b mediated signaling is not required for adult glandular stomach homeostasis.

Fibroblast growth factor 10-fibroblast growth factor receptor 2b mediated signaling is not required for adult glandular stomach homeostasis.

... phenotype in association with FGF10 ...signaling in promoting antralization ...resulted in a SPEM-like phenotype with a shift in localization of TFF2 mRNA in the mouse and cSP mRNA ... See full document

12

Chromosomal gene movements reflect the recent origin and biology of therian sex chromosomes.

Chromosomal gene movements reflect the recent origin and biology of therian sex chromosomes.

... chromosome in the meiotic phase of spermatogenesis (termed male meiotic sex chromosome inactivation [MSCI] [6]), and were therefore selectively fixed during evolution ...[1,7]. In support of this ... See full document

8

Haploid identification using tropicalized haploid inducer progenies in maize

Haploid identification using tropicalized haploid inducer progenies in maize

... out in the 3 TP identified by flow cytometry in ...successful in all three haploids (Figure ...observed in maize DH lines in ...even in comparison to haploid ...pronounced ... See full document

8

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