1 - 25 of 339 results for author:"Bhattacharya S." in Literature citations
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| Ciliary neurotrophic factor receptor regulation of adult forebrain neurogenesis. Lee N., Batt M.K., Cronier B.A., Jackson M.C., Bruno Garza J.L., Trinh D.S., Mason C.O., Spearry R.P., Bhattacharya S., Robitz R. et al. J. Neurosci. 33:1241-1258(2013) · Mapped (5) |
| Activation of G protein-coupled bile acid receptor, TGR5, induces smooth muscle relaxation via both Epac- and PKA-mediated inhibition of RhoA/Rho kinase pathway. Rajagopal S., Kumar D.P., Mahavadi S., Bhattacharya S., Zhou R., Corvera C.U., Bunnett N.W., Grider J.R., Murthy K.S. Am. J. Physiol. Gastrointest. Liver Physiol. 304:G527-35(2013) · Mapped (5) |
| Identification of novel series of pyrazole and indole-urea based DFG-out PYK2 inhibitors. Bhattacharya S.K., Aspnes G.E., Bagley S.W., Boehm M., Brosius A.D., Buckbinder L., Chang J.S., Dibrino J., Eng H., Frederick K.S. et al. Bioorg. Med. Chem. Lett. 22:7523-7529(2012) · Mapped (1) |
| Age-related susceptibility to apoptosis in human retinal pigment epithelial cells is triggered by disruption of p53-Mdm2 association. Bhattacharya S., Chaum E., Johnson D.A., Johnson L.R. Invest. Ophthalmol. Vis. Sci. 53:8350-8366(2012) · Mapped (33) |
| Protein tyrosine phosphatase 1B is a key regulator of IFNAR1 endocytosis and a target for antiviral therapies. Carbone C.J., Zheng H., Bhattacharya S., Lewis J.R., Reiter A.M., Henthorn P., Zhang Z.Y., Baker D.P., Ukkiramapandian R., Bence K.K. et al. Proc. Natl. Acad. Sci. U.S.A. 109:19226-19231(2012) · Mapped (19) |
| Endemic transmission of visceral leishmaniasis in Bhutan. Yangzom T., Cruz I., Bern C., Argaw D., den Boer M., Velez I.D., Bhattacharya S.K., Molina R., Alvar J. Am. J. Trop. Med. Hyg. 87:1028-1037(2012) · UniProtKB (1) |
| Functional significance of SRJ domain mutations in CITED2. Chen C.M., Bentham J., Cosgrove C., Braganca J., Cuenda A., Bamforth S.D., Schneider J.E., Watkins H., Keavney B., Davies B. et al. PLoS ONE 7:e46256-e46256(2012) · Mapped (3) |
| Cross species analysis of Prominin reveals a conserved cellular role in invertebrate and vertebrate photoreceptor cells. Nie J., Mahato S., Mustill W., Tipping C., Bhattacharya S.S., Zelhof A.C. Dev. Biol. 371:312-320(2012) · Mapped (13) |
| NMNAT1 mutations cause Leber congenital amaurosis. Falk M.J., Zhang Q., Nakamaru-Ogiso E., Kannabiran C., Fonseca-Kelly Z., Chakarova C., Audo I., Mackay D.S., Zeitz C., Borman A.D. et al. |
| Loss of endothelial furin leads to cardiac malformation and early postnatal death. Kim W., Essalmani R., Szumska D., Creemers J.W., Roebroek A.J., D'Orleans-Juste P., Bhattacharya S., Seidah N.G., Prat A. Mol. Cell. Biol. 32:3382-3391(2012) · Mapped (2) |
| Expression of PRPF31 and TFPT: regulation in health and retinal disease. Rose A.M., Shah A.Z., Waseem N.H., Chakarova C.F., Alfano G., Coussa R.G., Ajlan R., Koenekoop R.K., Bhattacharya S.S. Hum. Mol. Genet. 21:4126-4137(2012) · Mapped (7) |
| Revealing the role of phospholipase Cbeta3 in the regulation of VEGF-induced vascular permeability. Hoeppner L.H., Phoenix K.N., Clark K.J., Bhattacharya R., Gong X., Sciuto T.E., Vohra P., Suresh S., Bhattacharya S., Dvorak A.M. et al. Blood 120:2167-2173(2012) · Mapped (13) |
| Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling. Simrick S., Szumska D., Gardiner J.R., Jones K., Sagar K., Morrow B., Bhattacharya S., Basson M.A. Dev. Dyn. 241:1310-1324(2012) · Mapped (32) |
| Control of neuronal differentiation by sumoylation of BRAF35, a subunit of the LSD1-CoREST histone demethylase complex. Ceballos-Chavez M., Rivero S., Garcia-Gutierrez P., Rodriguez-Paredes M., Garcia-Dominguez M., Bhattacharya S., Reyes J.C. Proc. Natl. Acad. Sci. U.S.A. 109:8085-8090(2012) · Mapped (13) |
| Nprl3 is required for normal development of the cardiovascular system. Kowalczyk M.S., Hughes J.R., Babbs C., Sanchez-Pulido L., Szumska D., Sharpe J.A., Sloane-Stanley J.A., Morriss-Kay G.M., Smoot L.B., Roberts A.E. et al. Mamm. Genome 23:404-415(2012) · Mapped (9) |
| Human heat shock protein 105/110 kDa (Hsp105/110) regulates biogenesis and quality control of misfolded cystic fibrosis transmembrane conductance regulator at multiple levels. Saxena A., Banasavadi-Siddegowda Y.K., Fan Y., Bhattacharya S., Roy G., Giovannucci D.R., Frizzell R.A., Wang X. J. Biol. Chem. 287:19158-19170(2012) · Mapped (51) |
| A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot. Goodship J.A., Hall D., Topf A., Mamasoula C., Griffin H., Rahman T.J., Glen E., Tan H., Palomino Doza J., Relton C.L. et al. Circ Cardiovasc Genet 5:287-292(2012) · Mapped (6) |
| Cochlin, intraocular pressure regulation and mechanosensing. Goel M., Sienkiewicz A.E., Picciani R., Wang J., Lee R.K., Bhattacharya S.K. PLoS ONE 7:e34309-e34309(2012) · Mapped (2) |
| Mechanism of beta-catenin-mediated transcriptional regulation of epidermal growth factor receptor expression in glycogen synthase kinase 3 beta-inactivated prostate cancer cells. Guturi K.K., Mandal T., Chatterjee A., Sarkar M., Bhattacharya S., Chatterjee U., Ghosh M.K. J. Biol. Chem. 287:18287-18296(2012) · Mapped (19) |
| Distinct contributions by ionotropic purinoceptor subtypes to ATP-evoked calcium signals in mouse parotid acinar cells. Bhattacharya S., Verrill D.S., Carbone K.M., Brown S., Yule D.I., Giovannucci D.R. J. Physiol. (Lond.) 590:2721-2737(2012) · Mapped (18) |
| Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa. Maubaret C., Kosmaoglou M., Low S., Chakarova C.F., Bidot S., Thauvin-Robinet C., Robson A.G., Waseem N., Cheetham M.E., Bhattacharya S.S. Mol. Vis. 18:581-587(2012) · Mapped (1) |
| Receptor conformations involved in dopamine D(2L) receptor functional selectivity induced by selected transmembrane-5 serine mutations. Fowler J.C., Bhattacharya S., Urban J.D., Vaidehi N., Mailman R.B. Mol. Pharmacol. 81:820-831(2012) · Mapped (4) |
| Delayed cutaneous wound healing and aberrant expression of hair follicle stem cell markers in mice selectively lacking Ctip2 in epidermis. Liang X., Bhattacharya S., Bajaj G., Guha G., Wang Z., Jang H.S., Leid M., Indra A.K., Ganguli-Indra G. PLoS ONE 7:e29999-e29999(2012) · Mapped (2) |
| Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. Audo I., Bujakowska K., Orhan E., Poloschek C.M., Defoort-Dhellemmes S., Drumare I., Kohl S., Luu T.D., Lecompte O., Zrenner E. et al. Am. J. Hum. Genet. 90:321-330(2012) · UniProtKB (1) |
| Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. Sofat R., Casas J.P., Webster A.R., Bird A.C., Mann S.S., Yates J.R., Moore A.T., Sepp T., Cipriani V., Bunce C. et al. Int J Epidemiol 41:250-262(2012) · Mapped (4) |