1 - 25 of 38 results for author:"Kishino T." in Literature citations
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| Caspase-4 directly activates caspase-9 in endoplasmic reticulum stress-induced apoptosis in SH-SY5Y cells. Yamamuro A., Kishino T., Ohshima Y., Yoshioka Y., Kimura T., Kasai A., Maeda S. J. Pharmacol. Sci. 115:239-243(2011) · Mapped (5) |
| Downregulated ABCG2 enhances sensitivity to topoisomerase I inhibitor in epidermal growth factor receptor tyrosine kinase inhibitor-resistant non-small cell lung cancer. Ohtsuka K., Ohnishi H., Morii T., Fujiwara M., Kishino T., Ogura W., Chiba M., Matsushima S., Goya T., Watanabe T. J Thorac Oncol 5:1726-1733(2010) · Mapped (5) |
| Identification of annexin A1 as a novel substrate for E6AP-mediated ubiquitylation. Shimoji T., Murakami K., Sugiyama Y., Matsuda M., Inubushi S., Nasu J., Shirakura M., Suzuki T., Wakita T., Kishino T. et al. J. Cell. Biochem. 106:1123-1135(2009) · UniProtKB (1) · Mapped (11) |
| Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene. Miyazaki K., Mapendano C.K., Fuchigami T., Kondo S., Ohta T., Kinoshita A., Tsukamoto K., Yoshiura K., Niikawa N., Kishino T. Gene 432:97-101(2009) · Mapped (4) |
| Abnormalities of epidermal growth factor receptor in lung squamous-cell carcinomas, adenosquamous carcinomas, and large-cell carcinomas: tyrosine kinase domain mutations are not rare in tumors with an adenocarcinoma component. Ohtsuka K., Ohnishi H., Fujiwara M., Kishino T., Matsushima S., Furuyashiki G., Takei H., Koshiishi Y., Goya T., Watanabe T. Cancer 109:741-750(2007) · Mapped (19) |
| Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10. Yamasaki-Ishizaki Y., Kayashima T., Mapendano C.K., Soejima H., Ohta T., Masuzaki H., Kinoshita A., Urano T., Yoshiura K., Matsumoto N. et al. Mol. Cell. Biol. 27:732-742(2007) · Mapped (3) |
| Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain. Mapendano C.K., Kishino T., Miyazaki K., Kondo S., Yoshiura K., Hishikawa Y., Koji T., Niikawa N., Ohta T. J. Hum. Genet. 51:236-243(2006) · UniProtKB (1) |
| PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses. Ichikawa E., Watanabe A., Nakano Y., Akita S., Hirano A., Kinoshita A., Kondo S., Kishino T., Uchiyama T., Niikawa N. et al. J. Hum. Genet. 51:38-46(2006) · Mapped (17) |
| Neuron-specific relaxation of Igf2r imprinting is associated with neuron-specific histone modifications and lack of its antisense transcript Air. Yamasaki Y., Kayashima T., Soejima H., Kinoshita A., Yoshiura K., Matsumoto N., Ohta T., Urano T., Masuzaki H., Ishimaru T. et al. Hum. Mol. Genet. 14:2511-2520(2005) · Mapped (32) |
| Heterozygous TGFBR2 mutations in Marfan syndrome. Mizuguchi T., Collod-Beroud G., Akiyama T., Abifadel M., Harada N., Morisaki T., Allard D., Varret M., Claustres M., Morisaki H. et al. |
| A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family. Okubo A., Miyoshi O., Baba K., Takagi M., Tsukamoto K., Kinoshita A., Yoshiura K., Kishino T., Ohta T., Niikawa N. et al. J. Med. Genet. 41:e97-e97(2004) · Mapped (6) |
| The IHPK1 gene is disrupted at the 3p21.31 breakpoint of t(3;9) in a family with type 2 diabetes mellitus. Kamimura J., Wakui K., Kadowaki H., Watanabe Y., Miyake K., Harada N., Sakamoto M., Kinoshita A., Yoshiura K., Ohta T. et al. J. Hum. Genet. 49:360-365(2004) · Mapped (1) |
| Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32. Yamada T., Mitsuya K., Kayashima T., Yamasaki K., Ohta T., Yoshiura K., Matsumoto N., Yamada H., Minakami H., Oshimura M. et al. Genomics 83:402-412(2004) · UniProtKB (1) |
| LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density. Mizuguchi T., Furuta I., Watanabe Y., Tsukamoto K., Tomita H., Tsujihata M., Ohta T., Kishino T., Matsumoto N., Minakami H. et al. |
| Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting. Kayashima T., Yamasaki K., Joh K., Yamada T., Ohta T., Yoshiura K., Matsumoto N., Nakane Y., Mukai T., Niikawa N. et al. Genomics 81:644-647(2003) · Mapped (4) |
| Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome. Miyake N., Kurotaki N., Sugawara H., Shimokawa O., Harada N., Kondoh T., Tsukahara M., Ishikiriyama S., Sonoda T., Miyoshi Y. et al. Am. J. Hum. Genet. 72:1331-1337(2003) · Mapped (10) |
| Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a. Yamasaki K., Joh K., Ohta T., Masuzaki H., Ishimaru T., Mukai T., Niikawa N., Ogawa M., Wagstaff J., Kishino T. Hum. Mol. Genet. 12:837-847(2003) · Mapped (26) |
| NECC1, a candidate choriocarcinoma suppressor gene that encodes a homeodomain consensus motif. Asanoma K., Matsuda T., Kondo H., Kato K., Kishino T., Niikawa N., Wake N., Kato H. |
| The novel imprinted carboxypeptidase A4 gene (CPA4) in the 7q32 imprinting domain. Kayashima T., Yamasaki K., Yamada T., Sakai H., Miwa N., Ohta T., Yoshiura K., Matsumoto N., Nakane Y., Kanetake H. et al. |
| A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-beta1 (TGF-beta1) and its signaling pathway. Watanabe Y., Kinoshita A., Yamada T., Ohta T., Kishino T., Matsumoto N., Ishikawa M., Niikawa N., Yoshiura K. J. Hum. Genet. 47:478-483(2002) · UniProtKB (2) · Mapped (31) |
| Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family. Komatsu K., Nakamura N., Ghadami M., Matsumoto N., Kishino T., Ohta T., Niikawa N., Yoshiura K. J. Hum. Genet. 47:395-399(2002) · UniProtKB (1) |
| The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting. Yamada T., Kayashima T., Yamasaki K., Ohta T., Yoshiura K., Matsumoto N., Fujimoto S., Niikawa N., Kishino T. Gene 288:57-63(2002) · UniProtKB (1) |
| A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet. Kondoh S., Sugawara H., Harada N., Matsumoto N., Ohashi H., Sato M., Kantaputra P.N., Ogino T., Tomita H., Ohta T. et al. J. Hum. Genet. 47:136-139(2002) · UniProtKB (2) · Mapped (4) |
| Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE). Kayashima T., Matsuo H., Satoh A., Ohta T., Yoshiura K., Matsumoto N., Nakane Y., Niikawa N., Kishino T. |
| Haploinsufficiency of NSD1 causes Sotos syndrome. Kurotaki N., Imaizumi K., Harada N., Masuno M., Kondoh T., Nagai T., Ohashi H., Naritomi K., Tsukahara M., Makita Y. et al. |