Titlebook: Glycoprotein Hormones; Structure, Function, Joyce W. Lustbader,David Puett,Raymond W. Ruddon Conference proceedings 1994 Springer-Verlag Ne

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Glycosylation and Glycoprotein Hormone Functionhese transferases is hormonally regulated, and the sulfated oligosaccharides produced play a key role in the expression of LH bioactivity in vivo by controlling its circulatory half-life following release into the blood.

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Conference proceedings 1994Pamela Mellon, James Hoeffler, John Nilson, Bruce Weintraub, and Joel Habener. These presentations reflected major advances from the in the understanding concepts offered at the last meeting. Other advances of hormone structure/function included the continuing work by Joyce Lustbader on the determin

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sented by Pamela Mellon, James Hoeffler, John Nilson, Bruce Weintraub, and Joel Habener. These presentations reflected major advances from the in the understanding concepts offered at the last meeting. Other advances of hormone structure/function included the continuing work by Joyce Lustbader on the determin978-1-4613-8388-8978-1-4613-8386-4

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Lehrbuch der Mikrobiologie und Immunbiologie, particularly those responsible for conferring specificity. The absence of a crystallographic structure for any member of the glycoprotein hormone family has, however, prevented a detailed understanding of these contact regions.

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Receptor Binding Regions of hLH and hCGβ-Subunit: Structural and Functional Propertiescule remain largely uncharted. They must, however, be considered an important factor in the alignment and relative contributions of the multiple receptor binding sites revealed in all four glycoprotein hormones by assays of individual synthetic peptides (2–8).

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gerrymander

Cyclic AMP-Mediated Hormonal Regulation of Gene Transcriptiontor serves as the communicative link between the outside and the inside of the cell. In response to the binding of hormone, receptors activate one or more signal transduction pathways, resulting in the generation of the important second messengers, such as cAMP and . (DAG), that in turn activate the protein kinases A and C, respectively (1–5).