K
Kavita Shah
Researcher at Purdue University
Publications - 111
Citations - 7332
Kavita Shah is an academic researcher from Purdue University. The author has contributed to research in topics: Kinase & Neurodegeneration. The author has an hindex of 46, co-authored 107 publications receiving 6741 citations. Previous affiliations of Kavita Shah include University of California, San Francisco & Novartis Foundation.
Papers
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Journal ArticleDOI
Targets of the cyclin-dependent kinase Cdk1
Jeffrey A. Ubersax,Erika L. Woodbury,Erika L. Woodbury,Phuong N. Quang,Phuong N. Quang,Maria Paraz,Maria Paraz,Justin D. Blethrow,Justin D. Blethrow,Kavita Shah,Kevan M. Shokat,David O. Morgan,David O. Morgan +12 more
TL;DR: The identities of these substrates reveal that Cdk1 employs a global regulatory strategy involving phosphorylation of other regulatory molecules as well as phosphorylated of the molecular machines that drive cell-cycle events.
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Engineering unnatural nucleotide specificity for Rous sarcoma virus tyrosine kinase to uniquely label its direct substrates
TL;DR: The development of a protein engineering-based method to identify the direct substrates of the prototypical protein tyrosine kinase v-Src, which controls fibroblast transformation by the Rous sarcoma virus, is described.
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A Chemical-Genetic Strategy Implicates Myosin-1c in Adaptation by Hair Cells
Jeffrey R. Holt,Susan K.H. Gillespie,D. William Provance,Kavita Shah,Kevan M. Shokat,David P. Corey,John A. Mercer,Peter G. Gillespie +7 more
TL;DR: The speed and specificity of inhibition suggests that myosin-1c participates in adaptation in hair cells, the sensory cells of the inner ear.
Journal ArticleDOI
ERK phosphorylation drives cytoplasmic accumulation of hnRNP-K and inhibition of mRNA translation
Hasem Habelhah,Kavita Shah,Lan Huang,Antje Ostareck-Lederer,Alma L. Burlingame,Kevan M. Shokat,Matthias W. Hentze,Ze'ev Ronai +7 more
TL;DR: The role of MAPK/ERK is established in phosphorylation-dependent cellular localization of hnRNP-K, which is required for its ability to silence mRNA translation.
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Wnt-5A augments repopulating capacity and primitive hematopoietic development of human blood stem cells in vivo.
Barbara Murdoch,Kristin Chadwick,Matthew Martin,Farbod Shojaei,Kavita Shah,Lisa Gallacher,Randall T. Moon,Mickie Bhatia +7 more
TL;DR: In vivo treatment of human repopulating cells with Wnt-5A CM produced a greater proportion of phenotypically primitive hematopoietic progeny that could be isolated and shown to possess enhanced progenitor function independent of continued Wnt -5A treatment, suggesting a potential role for activation of Wnt signaling in managing patients exhibiting poor hematoplastic recovery shortly after stem cell transplantation.