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Vickram Srinivas

Researcher at Thomas Jefferson University

Publications -  29
Citations -  4752

Vickram Srinivas is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Chondrocyte & Autophagy. The author has an hindex of 22, co-authored 29 publications receiving 4549 citations.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes

Daniel J. Klionsky, +235 more
- 16 Feb 2008 - 
TL;DR: A set of guidelines for the selection and interpretation of the methods that can be used by investigators who are attempting to examine macroautophagy and related processes, as well as by reviewers who need to provide realistic and reasonable critiques of papers that investigate these processes are presented.
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Hypoxia-inducible Factor-1-mediated Expression of the 6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase-3 (PFKFB3) Gene ITS POSSIBLE ROLE IN THE WARBURG EFFECT

TL;DR: It is shown that one isozyme, PFKFB3, is highly induced by hypoxia and thehypoxia mimics cobalt and desferrioxamine, and could be replicated by the use of an inhibitor of the prolyl hydroxylase enzymes responsible for the von Hippel Lindau (VHL)-dependent destabilization and tagging of HIF-1α.
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MAPK Signaling Up-regulates the Activity of Hypoxia-inducible Factors by Its Effects on p300

TL;DR: The data suggest that MAPK signaling facilitates HIF activation through p300/CBP, and that the C-terminal transactivation domain of HIF-1α is not a direct substrate of MAPK, and Hif-1 α phosphorylation is not required for HIF/CAD/p300 interaction.
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Fate of the hypertrophic chondrocyte: Microenvironmental perspectives on apoptosis and survival in the epiphyseal growth plate

TL;DR: A new concept is presented: hypertrophic cells die through the induction of autophagy, which emphasizes the importance of the local microenvironment, in particular pO(2), in directing chondrocyte survival and apoptosis.
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Characterization of an oxygen/redox-dependent degradation domain of hypoxia-inducible factor alpha (HIF-alpha) proteins.

TL;DR: Analysis of the available cloned sequences of human and mouse members of the HIF-alpha family of proteins revealed an area of about 15 amino acids with strong sequence conservation between all the members, suggesting that the sequences and mechanisms involved in the regulated degradation of the alpha protein subunits are poorly understood.