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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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發(fā)表于 2025-3-21 19:11:44 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Glucagon III
編輯Pierre J. Lefèbvre
視頻videohttp://file.papertrans.cn/388/387042/387042.mp4
叢書名稱Handbook of Experimental Pharmacology
圖書封面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
關(guān)鍵詞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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沙發(fā)
發(fā)表于 2025-3-21 23:02:57 | 只看該作者
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
板凳
發(fā)表于 2025-3-22 03:31:42 | 只看該作者
地板
發(fā)表于 2025-3-22 08:12:32 | 只看該作者
5#
發(fā)表于 2025-3-22 11:37:41 | 只看該作者
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
6#
發(fā)表于 2025-3-22 15:08:01 | 只看該作者
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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發(fā)表于 2025-3-22 18:32:29 | 只看該作者
8#
發(fā)表于 2025-3-22 22:31:55 | 只看該作者
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
9#
發(fā)表于 2025-3-23 01:34:48 | 只看該作者
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
10#
發(fā)表于 2025-3-23 07:33:01 | 只看該作者
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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