Published 1994
by New York Academy of Sciences in New York, N.Y .
Written in English
Edition Notes
Statement | edited by Ivan N. Rich and Terence R.J. Lappin. |
Series | Annals of the New York Academy of Sciences ;, v. 718 |
Contributions | Rich, Ivan N., 1950-, Lappin, Terence R. J., New York Academy of Sciences. |
Classifications | |
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LC Classifications | Q11 .N5 vol. 718, QP92 .N5 vol. 718 |
The Physical Object | |
Pagination | xiii, 376 p. : |
Number of Pages | 376 |
ID Numbers | |
Open Library | OL1086735M |
ISBN 10 | 0897668375, 0897668383 |
LC Control Number | 94010689 |
The 22 papers provide a broad coverage of the rapid advances in the study of erythropoiesis. Discusses how heme and its derivatives contribute to the proliferation, differentiation, and maturation of the eurythron, the use of genetic engineering to correct globin gene derangements, various regulators of erythropoiesis as analyzed both in vivo and in vitro, and other topics. Developmental biology of erythropoiesis. Palis J(1), Segel GB. Author information: (1)University of Rochester Medical Center, Department of Pediatrics, NY , USA. A newborn infant represents the culmination of developmental events from conception through organogenesis. Red cells are critically important for survival and growth of the by: Molecular biology of erythropoietin. Jelkmann W(1). Author information: (1)Institute of Physiology, University of Luebeck, Luebeck, Germany. The glycoprotein hormone erythropoietin (EPO) is an essential viability and growth factor for the erythrocytic progenitors. EPO is mainly produced in the by: Erythropoietins, Erythropoietic Factors, and Erythropoiesis: Molecular, Cellular, Preclinical, and Clinical Biology (Milestones in Drug Therapy) 2nd, revised and extended ed. Edition by Steven G. Elliott (Editor), MaryAnn Foote (Editor), Graham Molineux (Editor) & 0 moreFormat: Hardcover.
Its focus on erythropoiesis represents an attempt to cover a rapidly expanding field, which has gone from elegant studies of erythro poietin physiology, to molecular biology, to clinical applications and again to physiology. The rapid development has been made possible by cloning of erythropoietin gene and the availability of recombinant hormone. Its focus on erythropoiesis represents an attempt to cover a rapidly expanding field, which has gone from elegant studies of erythro poietin physiology, to molecular biology, to clinical applications and again to physiology. The rapid development has been made possible by cloning of erythropoietin gene and the availability of recombinant : Springer US. The newest theories in erythropoiesis (receptors, signaling), manufacturing, new formulations, and clinical research are discussed. This book is of interest to researchers and clinical investigators in academia and biotechnology and pharmaceutical companies, to clinical research associates, clinical monitors, and physician investigators. Molecular biology of erythropoietin Article Literature Review (PDF Available) in Internal Medicine 43(8) September with Reads How we measure 'reads'.
Since the meeting on Molecular and Cellular Aspects of Erythropoietin and Erythropoiesis in September [1], we have witnessed several major developments in the study of red blood cell production. Several of these developments were discussed as theoretical considerations at that : Ivan N. Rich, Ivan N. Rich. from book Molecular Basis of Molecular Biology of Erythropoiesis. Erythropoietin is the primary cytokine regulating erythroid cell maturation by signaling through its receptor to activate Author: James Palis. This short life span necessitates the process erythropoiesis, which is the formation of red blood cells. All blood cell s are formed in the bone marrow. This is the erythrocyte factory, which is soft, highly cell ar tissue that fills the internal cavities of bones. Erythropoiesis (from Greek 'erythro' meaning "red" and 'poiesis' meaning "to make") is the process which produces red blood cells (erythrocytes), which is the development from erythropoietic stem cell to mature red blood cell.. It is stimulated by decreased O 2 in circulation, which is detected by the kidneys, which then secrete the hormone erythropoietin.