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Danielle N. Gross
Researcher at University of Pennsylvania
Publications - 8
Citations - 1355
Danielle N. Gross is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Insulin resistance & Insulin. The author has an hindex of 7, co-authored 8 publications receiving 1222 citations. Previous affiliations of Danielle N. Gross include Boston University.
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Journal ArticleDOI
The Role of FoxO in the Regulation of Metabolism
TL;DR: In obese or diabetic states, FoxO1-dependent gene expression promotes some of the deleterious characteristics associated with these conditions, including hyperglycemia and glucose intolerance, but under these same pathophysiological conditions,FoxO1 expression may help drive the expression of genes involved in combating oxidative stress, thereby preserving cellular function.
Journal ArticleDOI
Sustained down-regulation of the epidermal growth factor receptor by decorin. A mechanism for controlling tumor growth in vivo.
György Csordás,Manoranjan Santra,Charles C. Reed,Inge Eichstetter,David J. McQuillan,Danielle N. Gross,Matthew A. Nugent,György Hajnóczky,Renato V. Iozzo +8 more
TL;DR: It is demonstrated that decorin causes a sustained down-regulation of the EGFR and acts as an autocrine and paracrine regulator of tumor growth and could be utilized as an effective anti-cancer agent.
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Insulin regulates adipocyte lipolysis via an Akt-independent signaling pathway
Sarah M. Choi,David F. Tucker,Danielle N. Gross,Rachael M. Easton,Lisa M. DiPilato,Abigail S. Dean,Bob R. Monks,Morris J. Birnbaum +7 more
TL;DR: A noncanonical Akt-independent, phosphoinositide-3 kinase (PI3K)-dependent pathway that regulates adipocyte lipolysis using restricted subcellular signaling is described that selectively alters the PKA phosphorylation of its major lipid droplet-associated substrate, perilipin.
Journal ArticleDOI
The role of FOXO in the regulation of metabolism.
TL;DR: Further clarification of the role of Foxo1 in insulinresponsive tissues will strengthen the understanding and allow us to better combat insulin resistance and diabetes mellitus.
Journal ArticleDOI
p115 Interacts with the GLUT4 Vesicle Protein, IRAP, and Plays a Critical Role in Insulin-stimulated GLUT4 Translocation
Toshio Hosaka,Cydney C. Brooks,Eleonora Presman,Suk-Kyeong Kim,Zidong Zhang,Michael R. Breen,Danielle N. Gross,Elizabeth Sztul,Paul F. Pilch +8 more
TL;DR: The data suggest that p115 has an important and specific role in insulin-stimulated GlUT4 translocation, probably by way of tethering insulin-sensitive Glut4 vesicles at an as yet unknown intracellular site.