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Autocrine and Paracrine Mechanisms in Reproductive by Harry T. Haigler (auth.), Lewis C. Krey, Bela J. Gulyas,

By Harry T. Haigler (auth.), Lewis C. Krey, Bela J. Gulyas, John A. McCracken (eds.)

There is a prov1s10n within the constitution of every learn element of the department of analysis provides on the nationwide Institutes of healthiness that stipulates that "workshops" are to be held periodically to assist research part participants of their value determinations of modern advancements of their fields and to spot destiny demanding situations invaluable of research. The Reproductive Endocrinology examine part used to be demonstrated on December thirteen, 1985 to check learn promises and examine education actions on the subject of reproductive endocrinology, together with features of administration of reproductive endocrine problems and hormonal imbalances as regarding infertility and through being pregnant and puberty, breast melanoma and prostate melanoma. It held its first workshop, entitled, "Autocrine and Paracrine Mechanisms in Reproductive Endocrinology," in October, 1988 in Shrewsbury, MA on the Worcester starting place for Experimental Biology. The complaints of this workshop, that are particular herein, mirror the truth that autocrine and paracrine interactions are swiftly being authorized as a thrilling sector of analysis by way of scientists investigating the physiological and biochemical mechanisms of hormone motion within the female and male reproductive platforms. the cloth coated is novel and wide-ranging, extending from theoretical issues of mechanisms of development issue motion and the function of mobile cycle degree in making a choice on hormone motion to investigations of autocrine and paracrine interactions in the course of improvement to discussions of the capability medical ramifications of the elemental study findings. Such an intensive stock is critical for 2 reasons.

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A working model for the role of bFGF in BPH 10 mg of BPH tissue. The sequence of bFGF recognized by Dr. Baird's antiserum is amino acid residues 11-15 (Baird and Ling, 1987). A limitation of the antiserum is the inability of the antibody to recognize amino-terminal truncated forms of bFGF. , 1987). , 1985b). This form of the growth factor has full biologic activity (Gospodarowicz, 1985) but since it is lacking amino acid residues 11-15, it is not recognized by Dr. Baird's antiserum. Thus, the level of bFGF in tissue may be underestimated when this antiserum is used for quantitation, particularly when tissue is extracted at acid pH.

1989. Neutralizing antibodies inhibit binding of bFGF to its receptor but not to heparin. J. BioI. , In press. R. J. 1985. Expression of a hemopoietic growth factor cDNA in a factor-dependent cell line results in an autonomous growth and tumorigenicity. C. A. 1985. Evidence that the v-sis gene product transforms by interaction with the receptor for platelet-derived growth factor. , Imanishi-Kari, T. and Baltimore, D. 1983. Molecular basis of a mouse strain-specific anti-hapten response. Cell, 33:85 Neufeld, G.

1987. Fibroblast growth factors are present in the extracellular matrix produced by endothelial cells in vitro: Implications for a role of heparinase-like enzymes in the neovascular response. Biochem. Biophys. Res. Commun. 142:429. , Mormed P. and Bohlen P. 1986. Immunoreactive fibroblast 43 growth factor (FGF) in a transplantable chondrosarcoma: Inhibition of tumor growth by antibodies to FGF. J. Cell. Biochem. 30:79. D. 1983. Natural history of benign prostatic hypertrophy. In: "Benign Prostatic Hypertrophy", (F.

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