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Sally Kornbluth

Researcher at Duke University

Publications -  127
Citations -  12776

Sally Kornbluth is an academic researcher from Duke University. The author has contributed to research in topics: Apoptosis & Xenopus. The author has an hindex of 57, co-authored 127 publications receiving 12234 citations. Previous affiliations of Sally Kornbluth include University of California, San Diego & Rockefeller University.

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Journal ArticleDOI

Membrane localization of the kinase which phosphorylates p34cdc2 on threonine 14.

TL;DR: It is shown that a purified membrane fraction, in the absence of cytoplasm, can promote phosphorylation of cdc2 on both Thr 14 and Tyr 15, suggesting the existence of at least two distinctly localized subpopulations of cDC2 Tyr 15-directed kinases.
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Characterization of the murine BEK fibroblast growth factor (FGF) receptor: activation by three members of the FGF family and requirement for heparin.

TL;DR: It is shown that the addition of heparin greatly enhances the binding of radio-labeled basic FGF to the receptor, so the BEK receptor, like FLG, also requires an interaction with heparan sulfate proteoglycans to facilitate binding to its ligands.
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All aboard the cyclin train: subcellular trafficking of cyclins and their CDK partners

TL;DR: This work has identified the identification of nuclear transport factors responsible for ferrying some of the CDK-cyclins in and out of the nucleus and the demonstration that phosphorylation can regulate these transport processes and the establishment of potential links between cell-cycle checkpoints and the control of CDk-cyclin subcellular localization.
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Scythe: a novel reaper-binding apoptotic regulator.

TL;DR: Immunodepletion of Scythe from extracts completely prevented reaper‐induced apoptosis without affecting apoptosis triggered by activated caspases, and a truncated variant of Scythe lacking the N‐terminal domain induced apoptosis even in the absence of reaper.
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HLA-B-associated transcript 3 (Bat3)/Scythe is essential for p300-mediated acetylation of p53

TL;DR: An essential role is described for HLA-B-associated transcript 3 (Bat3)/Scythe in controlling the acetylation of p53 required for DNA damage responses and thymocytes from Bat3-deficient mice exhibit reduced induction of puma and p21, and are resistant to DNA damage-induced apoptosis in vivo.