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Oocyte maturation and

Posada, J., Sanghera, J Pelech, S., Aebersold, R., and Cooper, J. A. (1991). Tyrosine phosphorylation and activation of homologous protein kinases during oocyte maturation and mitogenic activation of fibroblasts. Mol. Cell. Biol. 11 2517-2528,... [Pg.49]

Schwab MS, Kim SH, Terada N et al 1999 The p70(S6K) controls selective mRNA translation during oocyte maturation and early embryogenesis in Xenopus laevis. Mol Cell Biol 19 2485— 2494... [Pg.73]

Replacement of the famesyl group by lipid analogues could be performed for full length Ras proteins in vitro by means of the enzyme famesyltrans-ferase. When such partially modified Ras constructs were applied in Xenopus oocytes the cellular machinery completed modification (endoprotease activity, carboxymethylation and palmitoylation). In these cases the H-Ras famesyl group could be stripped off most of its isoprenoid features that distinguish it from a fatty add without any apparent effect on its ability to induce oocyte maturation and activation of mitogen-activated protdn kinase In contrast, replacement by the less hydrophobic isoprenoid geranyl causes severely delayed oocyte activation. [Pg.379]

There is ever more evidence that the results obtained with low doses can equal those earlier obtained with larger doses, while in principle reducing the risk of over-stimulation. Where human chorionic gonadotropin is concerned, a dose of 3300 IU now appears to be sufficient, at least in high responders, to provide adequate oocyte maturation and fertilization (29), whereas doses of 5000 or 10 000 U have often been used. [Pg.202]

The sexual dimorphism of cuticular hydrocarbons is completed during the first three days after imaginal eclosion. During the same period, important physiological events take place, female oocyte maturation and vitellogenesis. A number of mutations have been described which affect ovarian development or endocrine control. These mutants were used to elucidate a possible hormone control mechanism used to regulate hydrocarbon biosynthesis. [Pg.259]

Tokumoto, T., M. Yamashita and Y. Nagahama. Proteasome during oocyte maturation and egg activation in goldfish, Carassius auratus. Zool. Sci. 9 1162 1992. [Pg.393]

It is now apparent that teleost vitellogenesis involves a suite of distinct Vgs and product yolk proteins with specific functions during oocyte maturation and development of embryos and larvae. Thus vitellogenesis is a far more complicated and interesting process than was previously thought. These complications in the... [Pg.433]

Matsubara, T., N. Ohkubo, T. Andoh, C.V. Sullivan and A. Hara. Two forms of vitellogenin, yielding two distinct lipovitellins, play different roles during oocyte maturation and early development of barfin flounder, Verasper moseri, a marine teleost that spawns pelagic eggs. Dev. Biol. 213 18-32, 1999. [Pg.468]

A LOCAL REGULATOR OF OVULATION, OOCYTE MATURATION, AND LUTEAL FUNCTION... [Pg.109]

While several functions for NO have been identified, the signal transduction pathway(s) that are utilized by NO at critical stages of ovarian development have not yet been definitively elucidated. The ecNOS- and iNOS-deficient mice provide excellent tools for the dissection of the relative functions for each isoform in the ovary. Furthermore, the study of ovarian NOS provides an experimental system in which the roles of ecNOS and iNOS in development (follicular and oocyte maturation) and differentiation (formation of the corpus luteum) can be studied. [Pg.122]

Volume 5 of Advances in Developmental Biochemistry consists of seven chapters that review specific aspects of development in several different organisms including mollusks, flies, and mice. Five of the seven chapters address aspects of fertilization, including capacitation of sperm (Chapter 3), the acrosome reaction (Chapter 7), gamete adhesion (Chapters 2 and 6), and oocyte maturation and ovulation (Chapter 4). [Pg.252]

In Chapter 4, Olson discusses ovarian nitric oxide, a local regulator of ovulation, oocyte maturation, and luteal function in mammals. Although this is a relatively new area of investigation, there is compelling evidence that nitric oxide is a local regulator of all of these key ovarian processes in mammals. The author provides an experimental basis for this conclusion and for future studies. [Pg.253]

Phospho-Signaling at Oocyte Maturation and Fertilization Set Up for Embryogenesis and Beyond Part I. Protein Kinases... [Pg.447]

For conclusion, please refer to the section 3 of the chapter entitled "Rhospho-signaling at Oocyte Maturation and Fertilization Set Up for Embryogenesis and Beyond Rart 11. Kinase Regulators and Substrates" by Mahbub Hasan et al. [Pg.469]

McGinnis LK, Carroll DJ, Kinsey WH. 2011a. Protein tyrosine kinase signaling during oocyte maturation and fertilizatiort Mol Reprod Dev. 78(10-ll) 831-845. [Pg.484]

Muslin AJ, MacNicol AM, Williams LT. 1993. Raf-1 protein kinase is important for progesterone-induced Xenopus oocyte maturation and acts downstream of mos. Mol Cell Biol 13(7) 4197-4202. [Pg.485]

Pelech SL, Tombes RM, Meijer L, Krebs EG. 1988. Activation of myelin basic protein kinases during echinoderm oocyte maturation and egg fertilization. Dev Biol 130(l) 28-36. [Pg.487]

Sakamoto I, Takahara K, Yamashita M, Iwao Y. 1998. Changes in cyclin B during oocyte maturation and early embryonic cell cycle in the newt, Cynops pyrrhogaster requirement of germinal vesicle for MPF activation. Dev Biol 195(l) 60-69. [Pg.490]

Strieker SA. 2009. Interactions between mitogen-activated protein kinase and protein kinase C signaling during oocyte maturation and fertilization in a marine worm. Mol Reprod Dev 76(8) 708-721. [Pg.493]

Sun QY, Rubinstein S, Breitbart H. 1999. MAP kinase activity is downregulated by phorbol ester during mouse oocyte maturation and egg activation in vitro. Mol Reptrod Dev 52(3) 310-318. [Pg.493]

Zhang K, Hansen PJ, Ealy AD. 2010a. Fibroblast growth factor 10 enhances bovine oocyte maturation and developmental competence in vitro. Reproduction 140(6) 815-826. [Pg.497]


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See also in sourсe #XX -- [ Pg.119 ]




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