1 - 25 of 104 results for author:"Hotta Y." in Literature citations
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| Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population. Hosono K., Ishigami C., Takahashi M., Park D.H., Hirami Y., Nakanishi H., Ueno S., Yokoi T., Hikoya A., Fujita T. et al. PLoS ONE 7:e31036-e31036(2012) · Mapped (4) |
| MALDI-TOF MS analysis of ribosomal proteins coded in S10 and spc operons rapidly classified the Sphingomonadaceae as alkylphenol polyethoxylate-degrading bacteria from the environment. Hotta Y., Sato H., Hosoda A., Tamura H. FEMS Microbiol. Lett. 330:23-29(2012) · UniProtKB (174) |
| Clinical features of a Japanese case with Bothnia dystrophy. Nojima K., Hosono K., Zhao Y., Toshiba T., Hikoya A., Asai T., Kato M., Kondo M., Minoshima S., Hotta Y. Ophthalmic Genet. 33:83-88(2012) · Mapped (1) |
| Multiple translocation of the AVR-Pita effector gene among chromosomes of the rice blast fungus Magnaporthe oryzae and related species. Chuma I., Isobe C., Hotta Y., Ibaragi K., Futamata N., Kusaba M., Yoshida K., Terauchi R., Fujita Y., Nakayashiki H. et al. PLoS Pathog. 7:e1002147-e1002147(2011) · UniProtKB (13) |
| Mammalian Gcm genes induce Hes5 expression by active DNA demethylation and induce neural stem cells. Hitoshi S., Ishino Y., Kumar A., Jasmine S., Tanaka K.F., Kondo T., Kato S., Hosoya T., Hotta Y., Ikenaka K. Nat. Neurosci. 14:957-964(2011) · Mapped (15) |
| MafB interacts with Gcm2 and regulates parathyroid hormone expression and parathyroid development. Kamitani-Kawamoto A., Hamada M., Moriguchi T., Miyai M., Saji F., Hatamura I., Nishikawa K., Takayanagi H., Hitoshi S., Ikenaka K. et al. J. Bone Miner. Res. 26:2463-2472(2011) · Mapped (3) |
| Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations. Nakanishi H., Ohtsubo M., Iwasaki S., Hotta Y., Usami S., Mizuta K., Mineta H., Minoshima S. J. Hum. Genet. 56:484-490(2011) · Mapped (1) |
| A case of aniridia with unilateral Peters anomaly. Sawada M., Sato M., Hikoya A., Wang C., Minoshima S., Azuma N., Hotta Y. J AAPOS 15:104-106(2011) · Mapped (12) |
| Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation. Ohtsubo M., Sato M., Hikoya A., Hosono K., Minoshima S., Hotta Y. Jpn. J. Ophthalmol. 54:624-626(2010) · Mapped (1) |
| No association between glutathione-synthesis-related genes and Japanese schizophrenia. Hanzawa R., Ohnuma T., Nagai Y., Shibata N., Maeshima H., Baba H., Hatano T., Takebayashi Y., Hotta Y., Kitazawa M. et al. Psychiatry Clin. Neurosci. 65:39-46(2011) · Mapped (12) |
| Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1. Nakanishi H., Ohtsubo M., Iwasaki S., Hotta Y., Takizawa Y., Hosono K., Mizuta K., Mineta H., Minoshima S. J. Hum. Genet. 55:796-800(2010) · Mapped (15) |
| Establishment of a peritoneal mesothelial cell line from a transgenic rat harbouring the temperature-sensitive simian virus 40 large T-antigen gene. Hotta Y., Kaneko K., Inuma J., Inami Y., Aruga S., Shimaoka T., Sekiguchi Y., Io H., Hamada C., Obinata M. et al. Nephrol. Dial. Transplant. 25:1825-1832(2010) · Mapped (2) |
| Identification of 11 novel mutations in USH2A among Japanese patients with Usher syndrome type 2. Nakanishi H., Ohtsubo M., Iwasaki S., Hotta Y., Mizuta K., Mineta H., Minoshima S. Clin. Genet. 76:383-391(2009) · Mapped (1) |
| Fibroblast growth factor 21 regulates lipolysis in white adipose tissue but is not required for ketogenesis and triglyceride clearance in liver. Hotta Y., Nakamura H., Konishi M., Murata Y., Takagi H., Matsumura S., Inoue K., Fushiki T., Itoh N. Endocrinology 150:4625-4633(2009) · Mapped (1) |
| Fgf16 is required for cardiomyocyte proliferation in the mouse embryonic heart. Hotta Y., Sasaki S., Konishi M., Kinoshita H., Kuwahara K., Nakao K., Itoh N. Dev. Dyn. 237:2947-2954(2008) · Mapped (30) |
| Low leptin but high insulin resistance of smokers in Japanese men. Hotta Y., Yatsuya H., Toyoshima H., Matsushita K., Mitsuhashi H., Takefuji S., Oiso Y., Tamakoshi K. Diabetes Res. Clin. Pract. 81:358-364(2008) · Mapped (5) |
| Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa. Wang C., Nakanishi N., Ohishi K., Hikoya A., Koide K., Sato M., Nakamura M., Hotta Y., Minoshima S. Ophthalmic Genet. 29:29-32(2008) · Mapped (2) |
| Three novel mutations of the PAX6 gene in Japanese aniridia patients. Kawano T., Wang C., Hotta Y., Sato M., Iwata-Amano E., Hikoya A., Fujita N., Koyama N., Shirai S., Azuma N. et al. J. Hum. Genet. 52:571-574(2007) · Mapped (12) |
| Adiponectin level and left ventricular hypertrophy in Japanese men. Mitsuhashi H., Yatsuya H., Tamakoshi K., Matsushita K., Otsuka R., Wada K., Sugiura K., Takefuji S., Hotta Y., Kondo T. et al. Hypertension 49:1448-1454(2007) · Mapped (3) |
| SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma. Funayama T., Mashima Y., Ohtake Y., Ishikawa K., Fuse N., Yasuda N., Fukuchi T., Murakami A., Hotta Y., Shimada N. Invest. Ophthalmol. Vis. Sci. 47:5368-5375(2006) · Mapped (13) |
| Fission yeast Tor2 links nitrogen signals to cell proliferation and acts downstream of the Rheb GTPase. Uritani M., Hidaka H., Hotta Y., Ueno M., Ushimaru T., Toda T. Genes Cells 11:1367-1379(2006) |
| BMP4 expression in the developing rat retina. Maruyama Y., Mikawa S., Hotta Y., Sato K. Brain Res. 1122:116-121(2006) · Mapped (3) |
| Fgf16 is essential for pectoral fin bud formation in zebrafish. Nomura R., Kamei E., Hotta Y., Konishi M., Miyake A., Itoh N. Biochem. Biophys. Res. Commun. 347:340-346(2006) · UniProtKB (1) |
| Polymorphism of beta-adrenergic receptors and susceptibility to open-angle glaucoma. Inagaki Y., Mashima Y., Fuse N., Funayama T., Ohtake Y., Yasuda N., Murakami A., Hotta Y., Fukuchi T., Tsubota K. Mol. Vis. 12:673-680(2006) · Mapped (6) |
| Fgf21 is essential for haematopoiesis in zebrafish. Yamauchi H., Hotta Y., Konishi M., Miyake A., Kawahara A., Itoh N. |