By J. S. Parks, M. Kassels, M. C. McKean, J. T. Parks, C. Johnson, L. Meacham (auth.), Eugenio E. MÜller, Daniela Cocchi, Vittorio Locatelli (eds.)
Readers of this publication can replace their wisdom within the fast-moving box of endocrinology and neurobiology. themes pertaining to progress and improvement are greatly reviewed from either uncomplicated technology and scientific viewpoints. facets relating to progress improvement and to the regulate of mobile differentiation and multiplication are mentioned. extra new info is equipped on: man made recombinant human development hormone (rHGH); power diagnostic and healing purposes of the neuropeptide, progress hormone freeing hormone (GHRH); the body structure and physiopathology of the neural keep watch over of progress hormone secretion; the prognosis and remedy of development hormone deficiency or extra states; and the biology, functionality and attainable usage of development components. those very important new findings are suitable to development in pediatrics, pediatric and medical endocrinology, neuroendocrinology and physiology.
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Additional info for Advances in Growth Hormone and Growth Factor Research
E. Muller, D. Cocchi and V. Locatelli Pythagora Press, Roma-Milano and Springer Verlag, Berlin-Heidelberg © 1989 Evolution and structure of the growth hormone gene cluster* J. S. PARKS, M. KAssELS, M. C. McKEAN, J. T. PARKS, C. JoHNSON and L. A. INTRODUCTION Within the past 10 years, molecular genetic techniques have yielded a wealth of new information about growth hormones (GHs), prolactins, and placental lactogens (Pls). Cloned eDNA copies of messenger RNAs permit sequence comparisons of related peptide hormones within and between species.
The large relative increase in CAT expression directed by. the shortest rGH fragments in the LTK- cells suggest that the additional upstream sequences present on the larger fragments act to drastically repress expression from an otherwise functional rGH promoter. Since the 237 -bp fragment in pRGH237 generates the highest levels of CAT in both pituitary and nonpituitary cells, such repressive sequences must lie upstream of the 237. Initial localization of such sequences was provided by analysis of two plasmids containing large deletions, one extending from -1236 to -554, which had virtually no effect on expression in LTK - or CV-1 cells, and another extending from -1236 to -210, which significantly increased CAT expression in the nonpituitary cells.
Cell 345: 601-610 Ivarie RD, Schachter BS, O'Farrel P (1983) The level of expression of the rat growth 28 NATIVE AND BIOSYNTHETIC GROWTH HORMONES hormone gene in liver tumor cells is at least eight orders of magnitude less than that in anterior pituitary cells. Mol Cell Bioi 3: 1460-1467 Killary AM, Fornier REK (1984) A genetic analysis of extinction: transdominant loci regulate expression of liver- specific traits in hepatoma hybrid cells. Cell38: 523-534 Larsen PR, Harney JW, Moore DD (1986) Sequences required for cell-type specific thyroid hormone regulation of rat growth hormone promoter activity.
Advances in Growth Hormone and Growth Factor Research by J. S. Parks, M. Kassels, M. C. McKean, J. T. Parks, C. Johnson, L. Meacham (auth.), Eugenio E. MÜller, Daniela Cocchi, Vittorio Locatelli (eds.)