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1 - 25 of 105 results for author:"Hou S."Drop in Literature Citations

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Lack of association of two polymorphisms of IRF5 with Behcet's disease.

Li H., Yang P., Jiang Z., Hou S., Xie L.

Mol. Vis. 15:2018-2021(2009) · Mapped (14)

Haplotype analysis of single nucleotide polymorphisms in the vascular endothelial growth factor (VEGFA) gene and antidepressant treatment response in major depressive disorder.

Tsai S.J., Hong C.J., Liou Y.J., Chen T.J., Chen M.L., Hou S.J., Yen F.C., Yu Y.W.

Psychiatry Res 169:113-117(2009) · Mapped (7)

Monocyte chemoattractant protein (MCP)-1 -2518 A/G SNP in Chinese Han patients with VKH syndrome.

Hou S., Yang P., Xie L., Du L., Zhou H., Jiang Z.

Mol. Vis. 15:1537-1541(2009) · Mapped (2)

Ankrd17, an ubiquitously expressed ankyrin factor, is essential for the vascular integrity during embryogenesis.

Hou S.C., Chan L.W., Chou Y.C., Su C.Y., Chen X., Shih Y.L., Tsai P.C., Shen C.K., Yan Y.T.

FEBS Lett. 583:2765-2771(2009) · Mapped (61)

No association of CTLA-4 polymorphisms with susceptibility to Behcet disease.

Du L., Yang P., Hou S., Zhou H., Kijlstra A.

Br J Ophthalmol 93:1378-1381(2009) · Mapped (8)

Characterization of the role of full-length CRMP3 and its calpain-cleaved product in inhibiting microtubule polymerization and neurite outgrowth.

Aylsworth A., Jiang S.X., Desbois A., Hou S.T.

Exp. Cell Res. 315:2856-2868(2009) · Mapped (2)

Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.

Li K., Yang P., Zhao M., Hou S., Du L., Zhou H., Kijlstra A.

Mol. Vis. 15:955-961(2009) · Mapped (3)

Ultrasound stimulates NF-kappaB activation and iNOS expression via the Ras/Raf/MEK/ERK signaling pathway in cultured preosteoblasts.

Hou C.H., Lin J., Huang S.C., Hou S.M., Tang C.H.

J. Cell. Physiol. 220:196-203(2009) · Mapped (3)

Tryptophan hydroxylase 2 gene is associated with major depression and antidepressant treatment response.

Tsai S.J., Hong C.J., Liou Y.J., Yu Y.W., Chen T.J., Hou S.J., Yen F.C.

Prog. Neuropsychopharmacol. Biol. Psychiatry 33:637-641(2009) · Mapped (4)

PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome.

Meng Q., Liu X., Yang P., Hou S., Du L., Zhou H., Kijlstra A.

Mol. Vis. 15:386-392(2009) · Mapped (5)

Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.

Hou S., Yang P., Du L., Zhou H., Lin X., Liu X., Kijlstra A.

Mol. Vis. 14:2597-2603(2008) · Mapped (2)

Clinical and genetic study of a novel mutation in the REEP1 gene.

Liu S.G., Che F.Y., Heng X.Y., Li F.F., Huang S.Z., Lu d.e. G., Hou S.J., Liu S.E., Wang Q., Wang H.P. et al.

Synapse 63:201-205(2009) · Mapped (8)

Association between polymorphisms of FCRL3, a non-HLA gene, and Behcet's disease in a Chinese population with ophthalmic manifestations.

Li K., Zhao M., Hou S., Du L., Kijlstra A., Yang P.

Mol. Vis. 14:2136-2142(2008) · Mapped (1,387)

Encapsulated in silica: genome, proteome and physiology of the thermophilic bacterium Anoxybacillus flavithermus WK1.

Saw J.H., Mountain B.W., Feng L., Omelchenko M.V., Hou S., Saito J.A., Stott M.B., Li D., Zhao G., Wu J. et al.

Genome Biol. 9:R161.1-R161.16(2008) · UniProtKB (2,819)

Interleukin-1 beta (C-511T) genetic polymorphism is associated with cognitive performance in elderly males without dementia.

Tsai S.J., Hong C.J., Liu M.E., Hou S.J., Yen F.C., Hsieh C.H., Liou Y.J.

Neurobiol. Aging 0:0-0(2008) · Mapped (9)

Control of TANK-binding kinase 1-mediated signaling by the gamma(1)34.5 protein of herpes simplex virus 1.

Verpooten D., Ma Y., Hou S., Yan Z., He B.

J. Biol. Chem. 284:1097-1105(2009) · Mapped (3)

Endothelial nitric oxide synthase genetic variation and essential hypertension risk in Han Chinese: the Fangshan study.

Niu W.Q., Qi Y., Zhang L.T., Qi Y.X., Wang B., Hou S.Q., Zhai X.Y., Qiu C.C.

J Hum Hypertens 23:136-139(2009) · Mapped (9)

Molecular basis of recognition of human osteopontin by 23C3, a potential therapeutic antibody for treatment of rheumatoid arthritis.

Du J., Hou S., Zhong C., Lai Z., Yang H., Dai J., Zhang D., Wang H., Guo Y., Ding J.

J. Mol. Biol. 382:835-842(2008) · Mapped (8)

SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease.

Hou S., Yang P., Du L., Zhou H., Lin X., Liu X., Kijlstra A.

Clin. Immunol. 129:170-175(2008) · Mapped (2)

Influence of DNA repair gene polymorphisms on the initial repair of MMS-induced DNA damage in human lymphocytes as measured by the alkaline comet assay.

Ryk C., Routledge M.N., Allan J.M., Wild C.P., Kumar R., Lambert B., Hou S.

Environ. Mol. Mutagen. 49:669-675(2008) · Mapped (48)

Complete genome sequence of the extremely acidophilic methanotroph isolate V4, Methylacidiphilum infernorum, a representative of the bacterial phylum Verrucomicrobia.

Hou S., Makarova K.S., Saw J.H., Senin P., Ly B.V., Zhou Z., Ren Y., Wang J., Galperin M.Y., Omelchenko M.V. et al.

Biol. Direct 3:26-26(2008) · UniProtKB (2,470)

The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus).

Ming R., Hou S., Feng Y., Yu Q., Dionne-Laporte A., Saw J.H., Senin P., Wang W., Ly B.V., Lewis K.L. et al.

Nature 452:991-996(2008) · UniProtKB (1)

Identification of natural coumarin compounds that rescue defective DeltaF508-CFTR chloride channel gating.

Xu L.N., Na W.L., Liu X., Hou S.G., Lin S., Yang H., Ma T.H.

Clin. Exp. Pharmacol. Physiol. 35:878-883(2008) · Mapped (46)

Crystal structure of chimeric antibody C2H7 Fab in complex with a CD20 peptide.

Du J., Wang H., Zhong C., Peng B., Zhang M., Li B., Hou S., Guo Y., Ding J.

Mol. Immunol. 45:2861-2868(2008) · Mapped (3)

Reciprocal regulation of the Ca2+ and H+ sensitivity in the SLO1 BK channel conferred by the RCK1 domain.

Hou S., Xu R., Heinemann S.H., Hoshi T.

Nat. Struct. Mol. Biol. 15:403-410(2008) · Mapped (15)

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