1 - 25 of 50 results for author:"Nishimura C." in Literature citations
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| Role of hepatocyte-derived IL-7 in maintenance of intrahepatic NKT cells and T cells and development of B cells in fetal liver. Liang B., Hara T., Wagatsuma K., Zhang J., Maki K., Miyachi H., Kitano S., Yabe-Nishimura C., Tani-Ichi S., Ikuta K. J. Immunol. 189:4444-4450(2012) · Mapped (12) |
| NOX1/NADPH oxidase is involved in endotoxin-induced cardiomyocyte apoptosis. Matsuno K., Iwata K., Matsumoto M., Katsuyama M., Cui W., Murata A., Nakamura H., Ibi M., Ikami K., Zhang J. et al. Free Radic. Biol. Med. 53:1718-1728(2012) · Mapped (2) |
| Potential role of the NADPH oxidase NOX1 in the pathogenesis of 5-fluorouracil-induced intestinal mucositis in mice. Yasuda M., Kato S., Yamanaka N., Iimori M., Utsumi D., Kitahara Y., Iwata K., Matsuno K., Amagase K., Yabe-Nishimura C. et al. Am. J. Physiol. Gastrointest. Liver Physiol. 302:G1133-42(2012) · Mapped (2) |
| Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss. Davarnia B., Babanejad M., Fattahi Z., Nikzat N., Bazazzadegan N., Pirzade A., Farajollahi R., Nishimura C., Jalalvand K., Arzhangi S. et al. Int. J. Pediatr. Otorhinolaryngol. 76:268-271(2012) · Mapped (3) |
| PPARdelta coordinates angiotensin II-induced senescence in vascular smooth muscle cells through PTEN-mediated inhibition of superoxide generation. Kim H.J., Ham S.A., Kim M.Y., Hwang J.S., Lee H., Kang E.S., Yoo T., Woo I.S., Yabe-Nishimura C., Paek K.S. et al. J. Biol. Chem. 286:44585-44593(2011) · Mapped (27) |
| Serum adipokine profiles in Kawasaki disease. Kemmotsu Y., Saji T., Kusunoki N., Tanaka N., Nishimura C., Ishiguro A., Kawai S. Mod Rheumatol 22:66-72(2012) · Mapped (2) |
| DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hildebrand M.S., Morin M., Meyer N.C., Mayo F., Modamio-Hoybjor S., Mencia A., Olavarrieta L., Morales-Angulo C., Nishimura C.J., Workman H. et al. Hum. Mutat. 32:825-834(2011) · UniProtKB (1) |
| Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss. Bazazzadegan N., Sheffield A.M., Sobhani M., Kahrizi K., Meyer N.C., Van Camp G., Hilgert N., Abedini S.S., Habibi F., Daneshi A. et al. Am. J. Med. Genet. A 155A:1202-1211(2011) · Mapped (3) |
| Sp3 transcription factor is crucial for transcriptional activation of the human NOX4 gene. Katsuyama M., Hirai H., Iwata K., Ibi M., Matsuno K., Matsumoto M., Yabe-Nishimura C. FEBS J. 278:964-972(2011) · Mapped (7) |
| Aldose reductase in keratinocytes attenuates cellular apoptosis and senescence induced by UV radiation. Kang E.S., Iwata K., Ikami K., Ham S.A., Kim H.J., Chang K.C., Lee J.H., Kim J.H., Park S.B., Kim J.H. et al. Free Radic. Biol. Med. 50:680-688(2011) · Mapped (3) |
| Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Maga T.K., Nishimura C.J., Weaver A.E., Frees K.L., Smith R.J.H. Hum. Mutat. 31:E1445-E1460(2010) · UniProtKB (7) · Mapped (25) |
| Identification of KCNJ15 as a susceptibility gene in Asian patients with type 2 diabetes mellitus. Okamoto K., Iwasaki N., Nishimura C., Doi K., Noiri E., Nakamura S., Takizawa M., Ogata M., Fujimaki R., Grarup N. et al. Am. J. Hum. Genet. 86:54-64(2010) · Mapped (2) |
| Peroxisome proliferator-activated receptor {delta} regulates extracellular matrix and apoptosis of vascular smooth muscle cells through the activation of transforming growth factor-{beta}1/Smad3. Kim H.J., Kim M.Y., Jin H., Kim H.J., Kang S.S., Kim H.J., Lee J.H., Chang K.C., Hwang J.Y., Yabe-Nishimura C. et al. Circ. Res. 105:16-24(2009) · Mapped (20) |
| Receptor activator of nuclear factor-kappaB ligand-induced mouse osteoclast differentiation is associated with switching between NADPH oxidase homologues. Sasaki H., Yamamoto H., Tominaga K., Masuda K., Kawai T., Teshima-Kondo S., Matsuno K., Yabe-Nishimura C., Rokutan K. Free Radic. Biol. Med. 47:189-199(2009) · Mapped (12) |
| Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene. Hilgert N., Huentelman M.J., Thorburn A.Q., Fransen E., Dieltjens N., Mueller-Malesinska M., Pollak A., Skorka A., Waligora J., Ploski R. et al. Eur. J. Hum. Genet. 17:517-524(2009) · Mapped (3) |
| Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus. Hildebrand M.S., Tack D., McMordie S.J., DeLuca A., Hur I.A., Nishimura C., Huygen P., Casavant T.L., Smith R.J. Genet. Med. 10:797-804(2008) · Mapped (2) |
| Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient. Chan M.R., Thomas C.P., Torrealba J.R., Djamali A., Fernandez L.A., Nishimura C.J., Smith R.J., Samaniego M.D. Am. J. Kidney Dis. 53:321-326(2009) · Mapped (7) |
| Reactive oxygen species derived from NOX1/NADPH oxidase enhance inflammatory pain. Ibi M., Matsuno K., Shiba D., Katsuyama M., Iwata K., Kakehi T., Nakagawa T., Sango K., Shirai Y., Yokoyama T. et al. J. Neurosci. 28:9486-9494(2008) · Mapped (4) |
| GJB2 mutations in Baluchi population. Naghavi A., Nishimura C., Kahrizi K., Riazalhosseini Y., Bazazzadegan N., Mohseni M., Smith R.J., Najmabadi H. J. Genet. 87:195-197(2008) · Mapped (3) |
| Localization of increased insulin-like growth factor binding protein-3 in diabetic rat penis: implications for erectile dysfunction. Soh J., Katsuyama M., Ushijima S., Mizutani Y., Kawauchi A., Yabe-Nishimura C., Miki T. Urology 70:1019-1023(2007) · Mapped (4) |
| Transforming growth factor-beta1 is a molecular target for the peroxisome proliferator-activated receptor delta. Kim H.J., Ham S.A., Kim S.U., Hwang J.Y., Kim J.H., Chang K.C., Yabe-Nishimura C., Kim J.H., Seo H.G. Circ. Res. 102:193-200(2008) · Mapped (3) |
| Myocyte enhancer factor 2B is involved in the inducible expression of NOX1/NADPH oxidase, a vascular superoxide-producing enzyme. Katsuyama M., Ozgur Cevik M., Arakawa N., Kakehi T., Nishinaka T., Iwata K., Ibi M., Matsuno K., Yabe-Nishimura C. FEBS J. 274:5128-5136(2007) · Mapped (2) |
| Genotype-phenotype correlations for SLC26A4-related deafness. Azaiez H., Yang T., Prasad S., Sorensen J.L., Nishimura C.J., Kimberling W.J., Smith R.J. Hum. Genet. 122:451-457(2007) · Mapped (5) |
| Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree. Meyer N.C., Nishimura C.J., McMordie S., Smith R.J. |
| Expression of a peroxisome proliferator-activated receptor gamma 1 splice variant that was identified in human lung cancers suppresses cell death induced by cisplatin and oxidative stress. Kim H.J., Hwang J.Y., Kim H.J., Choi W.S., Lee J.H., Kim H.J., Chang K.C., Nishinaka T., Yabe-Nishimura C., Seo H.G. Clin. Cancer Res. 13:2577-2583(2007) · Mapped (9) |