Showing results (131-140 of 140) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 140 results.
Nature|September 18, 1999
Endophilin I mediates synaptic vesicle formation by transfer of arachidonate to lysophosphatidic acidA Schmidt, M Wolde, C Thiele, et al.
The EMBO Journal|June 17, 1998
Chromogranin B (secretogranin I), a neuroendocrine-regulated secretory protein, is sorted to exocrine secretory granules in transgenic miceS Natori, A King, A Hellwig, et al.
Genomics|April 1, 1996
Dispersion of chromogranin/secretogranin secretory protein family loci in mammalian genomesS K Mahata, C A Kozak, J Szpirer, et al.
The American Journal of Surgical Pathology|November 1, 1991
Argyrophilic carcinoma of the male breast. A neuroendocrine tumor containing predominantly chromogranin B (secretogranin I)L Scopsi, S Andreola, R Saccozzi, et al.
Brain Research. Molecular Brain Research|January 1, 1992
Differential regulation of chromogranin B/secretogranin I and secretogranin II by forskolin in PC12 cellsM E Thompson, W E Zimmer, L B Wear, et al.
Pflugers Archiv : European Journal of Physiology|November 5, 1997
Molecular basis for different pore properties of potassium channels from the rat brain Kv1 gene familyJ M Gòmez-Hernandez, C Lorra, L A Pardo, et al.
The EMBO Journal|May 1, 1987
The primary structure of human secretogranin I (chromogranin B): comparison with chromogranin A reveals homologous terminal domains and a large intervening variable regionU M Benedum, A Lamouroux, D S Konecki, et al.
The Journal of Biological Chemistry|February 22, 2000
The human AC133 hematopoietic stem cell antigen is also expressed in epithelial cells and targeted to plasma membrane protrusionsD Corbeil, K Röper, A Hellwig, et al.
Cell Death and Differentiation|November 21, 2015
Tissue-specific control of midbody microtubule stability by Citron kinase through modulation of TUBB3 phosphorylationF Sgrò, F T Bianchi, M Falcone, et al.
Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.
Pageof 14