G
Gregory W. Aponte
Researcher at University of California, Berkeley
Publications - 22
Citations - 1627
Gregory W. Aponte is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Cellular differentiation & Receptor. The author has an hindex of 17, co-authored 22 publications receiving 1582 citations.
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Journal ArticleDOI
The pathway of infection of Autographa californica nuclear polyhedrosis virus in an insect host.
TL;DR: An immunohistochemical study was conducted to detect the temporal infection sequence of Autographa californica M nuclear polyhedrosis virus in Trichoplusia ni larvae and stained patterns indicated that the initial infection occurred in the midgut, simultaneously in columnar epithelial and regenerative cells, but that subsequently this tissue recovered.
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Mechanisms of Desensitization and Resensitization of Proteinase-activated Receptor-2
Stephan K. Böhm,Lev M. Khitin,Eileen F. Grady,Gregory W. Aponte,Donald G. Payan,Nigel W. Bunnett +5 more
TL;DR: PAR-2-mediated Ca2+ mobilization desensitizes by irreversible receptor cleavage, protein kinase C-mediated termination of signaling, and PAR-2 targeting to lysosomes and resensitized by mobilization of large Golgi stores and synthesis of new receptors.
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Molecular sorting in the secretory pathway
TL;DR: In this article, peptide hormones were used as affinity ligands to purify a set of 25-kilodalton proteins from canine pancreatic tissue and their ligand specificities and patterns of expression have the characteristics of sorting carriers.
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Cell cycle and hormonal control of nuclear-cytoplasmic localization of the serum- and glucocorticoid-inducible protein kinase, Sgk, in mammary tumor cells. A novel convergence point of anti-proliferative and proliferative cell signaling pathways.
TL;DR: This study implicates the nuclear-cytoplasmic shuttling of sgk as a requirement for cell cycle progression and represents a novel convergence point of anti-proliferative and proliferative signaling in mammary tumor cells.
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GPR93 Activation by Protein Hydrolysate Induces CCK Transcription and Secretion in STC-1 Cells
TL;DR: The data indicate that GPR93 can contribute to the observed induction of CCK expression and secretion by peptone and provide evidence that G protein-coupled receptors can transduce dietary luminal signals.