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22 results for author:"Shah G.N." in Literature citations

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Topiramate treatment protects blood-brain barrier pericytes from hyperglycemia-induced oxidative damage in diabetic mice.

Price T.O., Eranki V., Banks W.A., Ercal N., Shah G.N.

Endocrinology 153:362-372(2012) · Mapped (2)

Progressive renal injury from transgenic expression of human carbonic anhydrase IV folding mutants is enhanced by deficiency of p58IPK.

Datta R., Shah G.N., Rubbelke T.S., Waheed A., Rauchman M., Goodman A.G., Katze M.G., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 107:6448-6452(2010) · Mapped (6)

Bicarbonate homeostasis in excitable tissues: role of AE3 Cl-/HCO3-exchanger and carbonic anhydrase XIV interaction.

Casey J.R., Sly W.S., Shah G.N., Alvarez B.V.

Am. J. Physiol., Cell Physiol. 297:C1091-102(2009) · Mapped (14)

Pathogenesis of retinitis pigmentosa associated with apoptosis-inducing mutations in carbonic anhydrase IV.

Datta R., Waheed A., Bonapace G., Shah G.N., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 106:3437-3442(2009) · Mapped (3)

Signal sequence mutation in autosomal dominant form of hypoparathyroidism induces apoptosis that is corrected by a chemical chaperone.

Datta R., Waheed A., Shah G.N., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 104:19989-19994(2007) · UniProtKB (1)

Carbonic anhydrases IV and IX: subcellular localization and functional role in mouse skeletal muscle.

Scheibe R.J., Mundhenk K., Becker T., Hallerdei J., Waheed A., Shah G.N., Sly W.S., Gros G., Wetzel P.

Am. J. Physiol., Cell Physiol. 294:C402-12(2008) · Mapped (12)

Carbonic anhydrase XIV deficiency produces a functional defect in the retinal light response.

Ogilvie J.M., Ohlemiller K.K., Shah G.N., Ulmasov B., Becker T.A., Waheed A., Hennig A.K., Lukasiewicz P.D., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 104:8514-8519(2007) · Mapped (7)

Carbonic anhydrase XIV in skeletal muscle: subcellular localization and function from wild-type and knockout mice.

Wetzel P., Scheibe R.J., Hellmann B., Hallerdei J., Shah G.N., Waheed A., Gros G., Sly W.S.

Am. J. Physiol., Cell Physiol. 293:C358-66(2007) · Mapped (3)

Expression of membrane-bound carbonic anhydrases IV, IX, and XIV in the mouse heart.

Scheibe R.J., Gros G., Parkkila S., Waheed A., Grubb J.H., Shah G.N., Sly W.S., Wetzel P.

J. Histochem. Cytochem. 54:1379-1391(2006) · Mapped (12)

Carbonic anhydrase type II deficiency.

Bolt R.J., Wennink J.M., Verbeke J.I., Shah G.N., Sly W.S., Bokenkamp A.

Am. J. Kidney Dis. 46:A50, 2005:e71-3(2005) · Mapped (2)

Carbonic anhydrase IV and XIV knockout mice: roles of the respective carbonic anhydrases in buffering the extracellular space in brain.

Shah G.N., Ulmasov B., Waheed A., Becker T., Makani S., Svichar N., Chesler M., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 102:16771-16776(2005) · Mapped (7)

Characterization of CA XV, a new GPI-anchored form of carbonic anhydrase.

Hilvo M., Tolvanen M., Clark A., Shen B., Shah G.N., Waheed A., Halmi P., Hanninen M., Hamalainen J.M., Vihinen M. et al.

Biochem. J. 392:83-92(2005) · Mapped (6)

Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation.

Shah G.N., Bonapace G., Hu P.Y., Strisciuglio P., Sly W.S.

Hum. Mutat. 24:272-272(2004) · UniProtKB (1) · Mapped (1)

Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa.

Rebello G., Ramesar R., Vorster A., Roberts L., Ehrenreich L., Oppon E., Gama D., Bardien S., Greenberg J., Bonapace G. et al.

Proc. Natl. Acad. Sci. U.S.A. 101:6617-6622(2004) · Mapped (4)

Expression, assay, and structure of the extracellular domain of murine carbonic anhydrase XIV: implications for selective inhibition of membrane-associated isozymes.

Whittington D.A., Grubb J.H., Waheed A., Shah G.N., Sly W.S., Christianson D.W.

J. Biol. Chem. 279:7223-7228(2004) · UniProtKB (1) · Mapped (2)

Mucopolysaccharidosis VII: clinical, biochemical and molecular investigation of a Brazilian family.

Schwartz I., Silva L.R., Leistner S., Todeschini L.A., Burin M.G., Pina-Neto J.M., Islam R.M., Shah G.N., Sly W.S., Giugliani R.

Clin. Genet. 64:172-175(2003) · UniProtKB (1)

Crystal structure of the dimeric extracellular domain of human carbonic anhydrase XII, a bitopic membrane protein overexpressed in certain cancer tumor cells.

Whittington D.A., Waheed A., Ulmasov B., Shah G.N., Grubb J.H., Sly W.S., Christianson D.W.

Proc. Natl. Acad. Sci. U.S.A. 98:9545-9550(2001) · UniProtKB (1) · Mapped (5)

Mitochondrial carbonic anhydrase CA VB: differences in tissue distribution and pattern of evolution from those of CA VA suggest distinct physiological roles.

Shah G.N., Hewett-Emmett D., Grubb J.H., Migas M.C., Fleming R.E., Waheed A., Sly W.S.

Proc. Natl. Acad. Sci. U.S.A. 97:1677-1682(2000) · UniProtKB (1) · Mapped (1)

Human egasyn binds beta-glucuronidase but neither the esterase active site of egasyn nor the C-terminus of beta-glucuronidase is involved in their interaction.

Islam M.R., Waheed A., Shah G.N., Tomatsu S., Sly W.S.

Arch. Biochem. Biophys. 372:53-61(1999) · UniProtKB (1)

Novel translational repressor (NAT-1) expression is modified by thyroid state and age in brain and liver.

Shah G.N., Li J., Mooradian A.D.

Eur. J. Endocrinol. 139:649-653(1998) · Mapped (2)

Human carbonic anhydrase XII: cDNA cloning, expression, and chromosomal localization of a carbonic anhydrase gene that is overexpressed in some renal cell cancers.

Tuereci O., Sahin U., Vollmar E., Siemer S., Goettert E., Seitz G., Parkkila A.-K., Shah G.N., Grubb J.H., Pfreundschuh M. et al.

Proc. Natl. Acad. Sci. U.S.A. 95:7608-7613(1998) · UniProtKB (1)

Cloning and characterization of a complementary DNA for a thyroid hormone-responsive protein in mature rat cerebral tissue.

Shah G.N., Li J., Schneiderjohn P., Mooradian A.D.

Biochem. J. 327:617-623(1997) · UniProtKB (1) · Mapped (3)

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