Hagit Eldar-Finkelman

Affiliations: 
Tel Aviv University, Tel Aviv-Yafo, Tel Aviv District, Israel 
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"Hagit Eldar-Finkelman"
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Publications

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Grieco SF, Cheng Y, Eldar-Finkelman H, et al. (2016) Up-regulation of insulin-like growth factor 2 by ketamine requires glycogen synthase kinase-3 inhibition. Progress in Neuro-Psychopharmacology & Biological Psychiatry
Aloni E, Shapira M, Eldar-Finkelman H, et al. (2015) GSK-3β Inhibition Affects Singing Behavior and Neurogenesis in Adult Songbirds. Brain, Behavior and Evolution. 85: 233-44
Azoulay-Alfaguter I, Elya R, Avrahami L, et al. (2014) Combined regulation of mTORC1 and lysosomal acidification by GSK-3 suppresses autophagy and contributes to cancer cell growth. Oncogene
La Pietra V, La Regina G, Coluccia A, et al. (2013) Design, synthesis, and biological evaluation of 1-phenylpyrazolo[3,4-e]pyrrolo[3,4-g]indolizine-4,6(1H,5H)-diones as new glycogen synthase kinase-3β inhibitors. Journal of Medicinal Chemistry. 56: 10066-78
Avrahami L, Eldar-Finkelman H. (2013) GSK-3 and lysosomes meet in Alzheimer's disease. Communicative & Integrative Biology. 6: e25179
Beurel E, Kaidanovich-Beilin O, Yeh WI, et al. (2013) Regulation of Th1 cells and experimental autoimmune encephalomyelitis by glycogen synthase kinase-3. Journal of Immunology (Baltimore, Md. : 1950). 190: 5000-11
Avrahami L, Licht-Murava A, Eisenstein M, et al. (2013) GSK-3 inhibition: achieving moderate efficacy with high selectivity. Biochimica Et Biophysica Acta. 1834: 1410-4
Avrahami L, Farfara D, Shaham-Kol M, et al. (2013) Inhibition of glycogen synthase kinase-3 ameliorates β-amyloid pathology and restores lysosomal acidification and mammalian target of rapamycin activity in the Alzheimer disease mouse model: in vivo and in vitro studies. The Journal of Biological Chemistry. 288: 1295-306
Lo Monte F, Kramer T, Gu J, et al. (2013) Structure-based optimization of oxadiazole-based GSK-3 inhibitors. European Journal of Medicinal Chemistry. 61: 26-40
Licht-Murava A, Eldar-Finkelman H. (2012) Exploiting substrate recognition for selective inhibition of protein kinases. Current Pharmaceutical Design. 18: 2914-20
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