Titlebook: Chromogranins; Functional and Clini Karen B. Helle,Dominique Aunis Book 2002 The Editor(s) (if applicable) and The Author(s), under exclusi

duodenum

书目名称Chromogranins影响因子(影响力)




书目名称Chromogranins影响因子(影响力)学科排名




书目名称Chromogranins网络公开度




书目名称Chromogranins网络公开度学科排名




书目名称Chromogranins被引频次




书目名称Chromogranins被引频次学科排名




书目名称Chromogranins年度引用




书目名称Chromogranins年度引用学科排名




书目名称Chromogranins读者反馈




书目名称Chromogranins读者反馈学科排名

生命

GRUEL

The Condensed Matrix of Mature Chromaffin Granulesration and essentially absent at a granule concentration of 2 mg protein/mL (Fig. 2). The lack of latency at high granule protein concentration most likely reflects the decrease in homospecific DBH activity by increasing matrix protein concentration as shown in Fig. 3. As the matrix- dependent inhib

GRATE

Inositol 1,4,5-Trisphosphate Receptor and Chromogranins A and B in Secretory GranulesIn light of these observations, it is natural to think that the conformational changes of the IP.R that occur as a result of IP. binding (Mignery and Südhof 1990) will be transmitted instantly to the coupled CGA and CGB in the secretory granules, causing their conformational changes. It may then be

Fibrin

领带

领带

LIMIT

Proteolytic Processing of Chromograninsen attributed with functional data. In addition, various fragments were shown to be liberated by the action of prohormone convertases. This is in accordance with the concept that these peptides represent the mediators of at least part of the yet unidentified physiological functions of the chromogran

Intractable

Endothelial Handling of Chromogranin Aerminal peptides activate endothelial cells by affecting the membrane potential. Nevertheless, bovine aorta endothelial cells (BAEC) bind and intemalise intact CGA in a temperature-dependent manner, and the binding occurs by low affinity and high capacity. BAEC do not express specific, high affinity

可互换

Chromogranin A and Its Derived Peptides in the Rat and Procine Gastro-Entero-Pancreatic Systemretion during ontogeny and in the mature neuroendocrine cell population of the GEP system. The dynamic changes probably reflect the differential expression of proteolytic enzymes that take part in the processing of CGA. Understanding the mechanisms that control the expression and processing of CGA-d