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Titlebook: Glucagon III; Pierre J. Lefèbvre Book 1996 Springer-Verlag Berlin Heidelberg 1996 Diabetes.GLP-1.Glukagon.glucagon.molecular biology.patho

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发表于 2025-3-21 19:11:44 | 显示全部楼层 |阅读模式
书目名称Glucagon III
编辑Pierre J. Lefèbvre
视频video
丛书名称Handbook of Experimental Pharmacology
图书封面Titlebook: Glucagon III;  Pierre J. Lefèbvre Book 1996 Springer-Verlag Berlin Heidelberg 1996 Diabetes.GLP-1.Glukagon.glucagon.molecular biology.patho
描述.Glucagon III. complements .Glucagon I. and .II. published in 1983 in this series as .Vols. 66/I. and .II.. These three volumes truly represent a "glucagon encyclopedia" and as such have no competitors in the scientific literature worldwide. In this volume, the most recent data on glucagon molecular biology are reviewed together with clinically relevant information on the role of glucagon in the pathophysiology of diabetes, the place of glucagon in medical imaging or in emergency medicine. Chapters are devoted to newly identified members of the glucagon family such as glucagon-like peptide-1 (GLP-1) and oxyntomodulin. .Glucagon III. is a comprehensive review of all information published on this important hormone since 1983 and is .the. reference book on the subject.
出版日期Book 1996
关键词Diabetes; GLP-1; Glukagon; glucagon; molecular biology; pathophysiology; physiology; metabolic disease
版次1
doihttps://doi.org/10.1007/978-3-642-61150-6
isbn_softcover978-3-642-64718-5
isbn_ebook978-3-642-61150-6Series ISSN 0171-2004 Series E-ISSN 1865-0325
issn_series 0171-2004
copyrightSpringer-Verlag Berlin Heidelberg 1996
The information of publication is updating

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Learn Blockchain by Building Oneignificant progress in the structural characterization of the glucagon receptor has been made due to the application of affinity-labeling approaches (. et al. 1981; .-. and . 1982; . and . 1984; . and . 1985). This technique represents a useful tool in the gathering of information about minor compon
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Learn Data Mining Through Excelctivity (. et al. 1985), but most investigators found the peptide inactive (. 1992). Physiological and pathophysiological studies had clearly shown that the distal intestinal mucosa, in which the glucagon gene is being expressed in the so-called L cells (. et al. 1986; . et al. 1987), contained an i
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https://doi.org/10.1007/978-1-4842-5982-5led “central” epitope) present in all glucagon-containing peptides (including proglucagon itself) and the absence of the C-terminal glucagon epitope, which is masked by the octapeptide in oxyntomodulin and glicentin (Fig. 2). As developed in Sect. B.VII, the “gut GLI” or “enteroglucagon” terminologi
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The Glucagon Receptor Gene: Organization and Tissue Distribution,ignificant progress in the structural characterization of the glucagon receptor has been made due to the application of affinity-labeling approaches (. et al. 1981; .-. and . 1982; . and . 1984; . and . 1985). This technique represents a useful tool in the gathering of information about minor compon
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Glucagon and Glucose Counterregulation,ow the physiological range blood-to-brain glucose transport becomes rate limiting to brain glucose metabolism. Given the survival value of maintenance of the plasma glucose concentration, it is not surprising that physiological mechanisms that very effectively prevent or correct hypoglycemia evolved
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Structure and Function of the Glucagon-Like Peptide-1 Receptor,ved in the stimulation of glucose-induced insulin secretion have now been identified. These are GIP (glucose-dependent insulinotropic polypeptide or gastric inhibitory polypeptide) and GLP-1 (glucagon-like peptide-1).
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