1 - 25 of
191
results
for author:"Khan S."
in Literature Citations
| Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. Riazuddin S., Anwar S., Fischer M., Ahmed Z.M., Khan S.Y., Janssen A.G., Zafar A.U., Scholl U., Husnain T., Belyantseva I.A. et al. Am. J. Hum. Genet. 85:273-280(2009) · Mapped (2) |
| The ephrinB2/EphB4 axis is dysregulated in osteoprogenitors from myeloma patients and its activation affects myeloma bone disease and tumor growth. Pennisi A., Ling W., Li X., Khan S., Shaughnessy J.D. Jr., Barlogie B., Yaccoby S. Blood 114:1803-1812(2009) · Mapped (15) |
| Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39. Schultz J.M., Khan S.N., Ahmed Z.M., Riazuddin S., Waryah A.M., Chhatre D., Starost M.F., Ploplis B., Buckley S., Velasquez D. et al. Am. J. Hum. Genet. 85:25-39(2009) · UniProtKB (2) · Mapped (3) |
| Dicer-regulated microRNAs 222 and 339 promote resistance of cancer cells to cytotoxic T-lymphocytes by down-regulation of ICAM-1. Ueda R., Kohanbash G., Sasaki K., Fujita M., Zhu X., Kastenhuber E.R., McDonald H.A., Potter D.M., Hamilton R.L., Lotze M.T. et al. Proc. Natl. Acad. Sci. U.S.A. 106:10746-10751(2009) · Mapped (15) |
| Hypermethylated genes as biomarkers of cancer in women with pathologic nipple discharge. Fackler M.J., Rivers A., Teo W.W., Mangat A., Taylor E., Zhang Z., Goodman S., Argani P., Nayar R., Susnik B. et al. Clin. Cancer Res. 15:3802-3811(2009) · Mapped (10) |
| Identification of novel immunodominant epididymal sperm proteins using combinatorial approach. Khan S.A., Suryawanshi A.R., Ranpura S.A., Jadhav S.V., Khole V.V. Reproduction 138:81-93(2009) · UniProtKB (22) |
| Molecular characterization of tetracycline-resistant genes and integrons from avirulent strains of Escherichia coli isolated from catfish. Nawaz M., Khan A.A., Khan S., Sung K., Kerdahi K., Steele R. Foodborne Pathog. Dis. 6:553-559(2009) · UniProtKB (5) |
| Null mutations in LTBP2 cause primary congenital glaucoma. Ali M., McKibbin M., Booth A., Parry D.A., Jain P., Riazuddin S.A., Hejtmancik J.F., Khan S.N., Firasat S., Shires M. et al. Am. J. Hum. Genet. 84:664-671(2009) · Mapped (6) |
| Her-2/neu, p-53, and their coexpression in osteosarcoma. Bakhshi S., Gupta A., Sharma M.C., Khan S.A., Rastogi S. J. Pediatr. Hematol. Oncol. 31:245-251(2009) · Mapped (39) |
| Extracellular, cell-permeable survivin inhibits apoptosis while promoting proliferative and metastatic potential. Khan S., Aspe J.R., Asumen M.G., Almaguel F., Odumosu O., Acevedo-Martinez S., De Leon M., Langridge W.H., Wall N.R. Br. J. Cancer 100:1073-1086(2009) · Mapped (10) |
| Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families. Tariq M., Ayub M., Jelani M., Basit S., Naz G., Wasif N., Raza S.I., Naveed A.K., ullah Khan S., Azeem Z. et al. Br. J. Dermatol. 160:1006-1010(2009) · Mapped (2) |
| Cytoprotective function of heme oxygenase 1 induced by a nitrated cyclic nucleotide formed during murine salmonellosis. Zaki M.H., Fujii S., Okamoto T., Islam S., Khan S., Ahmed K.A., Sawa T., Akaike T. J. Immunol. 182:3746-3756(2009) · Mapped (5) |
| A history of recurrent positive selection at the toll-like receptor 5 in primates. Wlasiuk G., Khan S., Switzer W.M., Nachman M.W. Mol. Biol. Evol. 26:937-949(2009) · UniProtKB (38) · Mapped (2) |
| Growth differentiation factor-15 as a prognostic marker in patients with acute myocardial infarction. Khan S.Q., Ng K., Dhillon O., Kelly D., Quinn P., Squire I.B., Davies J.E., Ng L.L. Eur. Heart J. 30:1057-1065(2009) · Mapped (1) |
| Intermittent hypoxia degrades HIF-2alpha via calpains resulting in oxidative stress: implications for recurrent apnea-induced morbidities. Nanduri J., Wang N., Yuan G., Khan S.A., Souvannakitti D., Peng Y.J., Kumar G.K., Garcia J.A., Prabhakar N.R. Proc. Natl. Acad. Sci. U.S.A. 106:1199-1204(2009) · Mapped (1) |
| PknB-mediated phosphorylation of a novel substrate, N-acetylglucosamine-1-phosphate uridyltransferase, modulates its acetyltransferase activity. Parikh A., Verma S.K., Khan S., Prakash B., Nandicoori V.K. J. Mol. Biol. 386:451-464(2009) · Mapped (2) |
| Human cellular microRNA hsa-miR-29a interferes with viral nef protein expression and HIV-1 replication. Ahluwalia J.K., Khan S.Z., Soni K., Rawat P., Gupta A., Hariharan M., Scaria V., Lalwani M., Pillai B., Mitra D. et al. Retrovirology 5:117-117(2008) · Mapped (1) |
| Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma. Firasat S., Riazuddin S.A., Khan S.N., Riazuddin S. Mol. Vis. 14:2002-2009(2008) · Mapped (6) |
| XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms. Khan S.G., Oh K.S., Emmert S., Imoto K., Tamura D., Digiovanna J.J., Shahlavi T., Armstrong N., Baker C.C., Neuburg M. et al. DNA Repair (Amst.) 8:114-125(2009) · Mapped (3) |
| Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Ahmed Z.M., Masmoudi S., Kalay E., Belyantseva I.A., Mosrati M.A., Collin R.W.J., Riazuddin S., Hmani-Aifa M., Venselaar H., Kawar M.N. et al. Nat. Genet. 40:1335-1340(2008) · UniProtKB (17) · Mapped (3) |
| Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome. Wickremaratchi M.M., Majounie E., Morris H.R., Williams N.M., Lewis H., Gill S.S., Khan S., Heywood P., Hardy J., Wiles C.M. et al. Mov. Disord. 24:138-140(2009) · Mapped (14) |
| The F-domain of estrogen receptor-alpha inhibits ligand induced receptor dimerization. Yang J., Singleton D.W., Shaughnessy E.A., Khan S.A. Mol. Cell. Endocrinol. 295:94-100(2008) · Mapped (53) |
| Expression of forkhead transcription factors in human granulosa cells. Pisarska M.D., Kuo F.T., Tang D., Zarrini P., Khan S., Ketefian A. Fertil. Steril. 91:1392-1394(2009) · Mapped (6) |
| An insecticidal GroEL protein with chitin binding activity from Xenorhabdus nematophila. Joshi M.C., Sharma A., Kant S., Birah A., Gupta G.P., Khan S.R., Bhatnagar R., Banerjee N. J. Biol. Chem. 283:28287-28296(2008) · UniProtKB (4) |
| Induction of HIF-1alpha expression by intermittent hypoxia: involvement of NADPH oxidase, Ca2+ signaling, prolyl hydroxylases, and mTOR. Yuan G., Nanduri J., Khan S., Semenza G.L., Prabhakar N.R. J. Cell. Physiol. 217:674-685(2008) · Mapped (4) |
