Mouse Mos protooncogene product is present and functions during oogenesis.
about
Identification of protein tyrosine phosphatase 1B and casein as substrates for 124-v-Mos.How eggs arrest at metaphase II: MPF stabilisation plus APC/C inhibition equals Cytostatic FactorMG-132, an inhibitor of proteasomes and calpains, induced inhibition of oocyte maturation and aneuploidy in mouse oocytesStem-loop binding protein accumulates during oocyte maturation and is not cell-cycle-regulated in the early mouse embryoCyclins and cyclin-dependent kinases: a biochemical viewMicrotubules in the metaphase-arrested mouse oocyte turn over rapidlyCytostatic factor proteins are present in male meiotic cells and beta-nerve growth factor increases mos levels in rat late spermatocytes.Proteasomal activity is required to initiate and to sustain translational activation of messenger RNA encoding the stem-loop-binding protein during meiotic maturation in mice.Neuropathological changes in transgenic mice carrying copies of a transcriptionally activated Mos protooncogene.The 'second-codon rule' and autophosphorylation govern the stability and activity of Mos during the meiotic cell cycle in Xenopus oocytes.Differential occurrence of CSF-like activity and transforming activity of Mos during the cell cycle in fibroblastsMos is not required for the initiation of meiotic maturation in Xenopus oocytes.Mos induces the in vitro activation of mitogen-activated protein kinases in lysates of frog oocytes and mammalian somatic cellsMos overexpression in Swiss 3T3 cells induces meiotic-like alterations of the mitotic spindle.The c-mos gene product is required for cyclin B accumulation during meiosis of mouse eggs.Zinc requirement during meiosis I-meiosis II transition in mouse oocytes is independent of the MOS-MAPK pathway.c-mos expression in mouse oocytes is controlled by initiator-related sequences immediately downstream of the transcription initiation site.Mos in the oocyte: how to use MAPK independently of growth factors and transcription to control meiotic divisions.Involvement of mitogen-activated protein kinase cascade during oocyte maturation and fertilization in mammals.Zinc maintains prophase I arrest in mouse oocytes through regulation of the MOS-MAPK pathway.Effects of the v-mos oncogene on Xenopus development: meiotic induction in oocytes and mitotic arrest in cleaving embryos.A characterization of cytostatic factor activity from Xenopus eggs and c-mos-transformed cells.Ser-3 is important for regulating Mos interaction with and stimulation of mitogen-activated protein kinase kinaseCENP-E is an essential kinetochore motor in maturing oocytes and is masked during mos-dependent, cell cycle arrest at metaphase II.Inhibition of v-Mos kinase activity by protein kinase AThe casein kinase II beta subunit binds to Mos and inhibits Mos activitymos gene transforming efficiencies correlate with oocyte maturation and cytostatic factor activitiesv-mos proteins encoded by myeloproliferative sarcoma virus and its ts159 mutant.pp39mos is associated with p34cdc2 kinase in c-mosxe-transformed NIH 3T3 cells.Genomic RNA profiling and the programme controlling preimplantation mammalian development.Murine homologues of the Drosophila gustavus gene are expressed in ovarian granulosa cells.Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytesTranslational control by cytoplasmic polyadenylation of c-mos mRNA is necessary for oocyte maturation in the mouseInhibition of HIV-LTR gene expression by oligonucleotides targeted to the TAR elementRegulation of Cell Division.Cell cycle regulation of glucocorticoid receptor function.Identification of Dss1 as a 12-O-tetradecanoylphorbol-13-acetate-responsive gene expressed in keratinocyte progenitor cells, with possible involvement in early skin tumorigenesis.12-O-tetradecanoylphorbol-13-acetate and UV radiation-induced nucleoside diphosphate protein kinase B mediates neoplastic transformation of epidermal cells.Transcription of c-mos protooncogene in the pig involves both tissue-specific promoters and alternative polyadenylation sites.Possible role of p38 MAPK-MNK1-EMI2 cascade in metaphase-II arrest of mouse oocytes.
P2860
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P2860
Mouse Mos protooncogene product is present and functions during oogenesis.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
name
Mouse Mos protooncogene product is present and functions during oogenesis.
@ast
Mouse Mos protooncogene product is present and functions during oogenesis.
@en
Mouse Mos protooncogene product is present and functions during oogenesis.
@nl
type
label
Mouse Mos protooncogene product is present and functions during oogenesis.
@ast
Mouse Mos protooncogene product is present and functions during oogenesis.
@en
Mouse Mos protooncogene product is present and functions during oogenesis.
@nl
prefLabel
Mouse Mos protooncogene product is present and functions during oogenesis.
@ast
Mouse Mos protooncogene product is present and functions during oogenesis.
@en
Mouse Mos protooncogene product is present and functions during oogenesis.
@nl
P2093
P2860
P356
P1476
Mouse Mos protooncogene product is present and functions during oogenesis.
@en
P2093
G F Vande Woude
R Buccione
R C Moschel
R S Paules
P2860
P304
P356
10.1073/PNAS.86.14.5395
P407
P577
1989-07-01T00:00:00Z