1 - 25 of 47 results for author:"Okuyama T." in Literature citations
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| Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis. Sasaki T., Niizeki H., Shimizu A., Shiohama A., Hirakiyama A., Okuyama T., Seki A., Kabashima K., Otsuka A., Ishiko A. et al. J. Dermatol. Sci. 68:36-44(2012) · Mapped (4) |
| Quantitative detection of EGFR mutations in circulating tumor DNA derived from lung adenocarcinomas. Taniguchi K., Uchida J., Nishino K., Kumagai T., Okuyama T., Okami J., Higashiyama M., Kodama K., Imamura F., Kato K. Clin. Cancer Res. 17:7808-7815(2011) · Mapped (19) |
| Cervical pachymeningeal hypertrophy as the initial and cardinal manifestation of mucopolysaccharidosis type I in monozygotic twins with a novel mutation in the alpha-L-iduronidase gene. Furukawa Y., Hamaguchi A., Nozaki I., Iizuka T., Sasagawa T., Shima Y., Demura S., Murakami H., Kawahara N., Okuyama T. et al. J. Neurol. Sci. 302:121-125(2011) · Mapped (7) |
| Induction of c-fos transcription in the medaka brain (Oryzias latipes) in response to mating stimuli. Okuyama T., Suehiro Y., Imada H., Shimada A., Naruse K., Takeda H., Kubo T., Takeuchi H. Biochem. Biophys. Res. Commun. 404:453-457(2011) · UniProtKB (1) |
| The ERK-MAPK pathway regulates longevity through SKN-1 and insulin-like signaling in Caenorhabditis elegans. Okuyama T., Inoue H., Ookuma S., Satoh T., Kano K., Honjoh S., Hisamoto N., Matsumoto K., Nishida E. J. Biol. Chem. 285:30274-30281(2010) · Mapped (3) |
| The effect of CAG repeat polymorphism in the glucocorticoid receptor on stress responses of mice exposed to water-immersion restraint stress. Tomita M., Katsuyama H., Okuyama T., Watanabe Y., Hidaka K., Otsuki T., Nata M. Int. J. Mol. Med. 25:415-420(2010) · Mapped (8) |
| Association between estrogen receptor alpha polymorphisms and equol production, and its relation to bone mass. Katsuyama H., Arii M., Tomita M., Hidaka K., Watanabe Y., Tamechika Y., Okuyama T., Fushimi S., Maeda N., Higashimura T. et al. Int. J. Mol. Med. 23:793-798(2009) · Mapped (58) |
| High frequency of acid alpha-glucosidase pseudodeficiency complicates newborn screening for glycogen storage disease type II in the Japanese population. Kumamoto S., Katafuchi T., Nakamura K., Endo F., Oda E., Okuyama T., Kroos M.A., Reuser A.J., Okumiya T. Mol. Genet. Metab. 97:190-195(2009) · Mapped (2) |
| 5HTT polymorphisms are associated with job stress in Japanese workers. Katsuyama H., Tomita M., Okuyama T., Hidaka K., Watanabe Y., Tamechika Y., Fushimi S., Saijoh K. Leg Med (Tokyo) 11 Suppl 1:S473-6(2009) · Mapped (9) |
| Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype-phenotype correlation. Otomo T., Muramatsu T., Yorifuji T., Okuyama T., Nakabayashi H., Fukao T., Ohura T., Yoshino M., Tanaka A., Okamoto N. et al. J. Hum. Genet. 54:145-151(2009) · UniProtKB (1) · Mapped (4) |
| The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation. Hayashi S., Mizuno S., Migita O., Okuyama T., Makita Y., Hata A., Imoto I., Inazawa J. Am. J. Med. Genet. A 146A:2145-2151(2008) · Mapped (2) |
| Association between serotonin transporter gene polymorphisms and depressed mood caused by job stress in Japanese workers. Katsuyama H., Tomita M., Hidaka K., Fushimi S., Okuyama T., Watanabe Y., Tamechika Y., Otsuki T., Saijoh K., Sunami S. Int. J. Mol. Med. 21:499-505(2008) · Mapped (3) |
| Structural study on mutant alpha-L-iduronidases: insight into mucopolysaccharidosis type I. Sugawara K., Saito S., Ohno K., Okuyama T., Sakuraba H. J. Hum. Genet. 53:467-474(2008) · Mapped (7) |
| p63(TP63) elicits strong trans-activation of the MFG-E8/lactadherin/BA46 gene through interactions between the TA and DeltaN isoforms. Okuyama T., Kurata S., Tomimori Y., Fukunishi N., Sato S., Osada M., Tsukinoki K., Jin H.F., Yamashita A., Ito M. et al. Oncogene 27:308-317(2008) · Mapped (7) |
| Mouse model of paraquat-poisoned lungs and its gene expression profile. Tomita M., Okuyama T., Katsuyama H., Miura Y., Nishimura Y., Hidaka K., Otsuki T., Ishikawa T. Toxicology 231:200-209(2007) · Mapped (1) |
| Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients. Fukami M., Horikawa R., Nagai T., Tanaka T., Naiki Y., Sato N., Okuyama T., Nakai H., Soneda S., Tachibana K. et al. J. Clin. Endocrinol. Metab. 90:414-426(2005) · UniProtKB (1) |
| p51/p63 Controls subunit alpha3 of the major epidermis integrin anchoring the stem cells to the niche. Kurata S., Okuyama T., Osada M., Watanabe T., Tomimori Y., Sato S., Iwai A., Tsuji T., Ikawa Y., Katoh I. J. Biol. Chem. 279:50069-50077(2004) · Mapped (8) |
| Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. Yoshida R., Hasegawa T., Hasegawa Y., Nagai T., Kinoshita E., Tanaka Y., Kanegane H., Ohyama K., Onishi T., Hanew K. et al. J. Clin. Endocrinol. Metab. 89:3359-3364(2004) · Mapped (6) |
| Evolutionarily conserved expression pattern and trans-regulating activity of Xenopus p51/p63. Tomimori Y., Katoh I., Kurata S., Okuyama T., Kamiyama R., Ikawa Y. Biochem. Biophys. Res. Commun. 313:230-236(2004) · UniProtKB (1) |
| Paraquat-induced gene expression in rat lung tissues using a differential display reverse transcription-polymerase chain reaction. Tomita M., Nohno T., Okuyama T., Nishimatsu S., Adachi J. Arch. Toxicol. 76:530-537(2002) · Mapped (3) |
| Activation of prostaglandin E2-receptor EP2 and EP4 pathways induces growth inhibition in human gastric carcinoma cell lines. Okuyama T., Ishihara S., Sato H., Rumi M.A., Kawashima K., Miyaoka Y., Suetsugu H., Kazumori H., Cava C.F., Kadowaki Y. et al. J. Lab. Clin. Med. 140:92-102(2002) · Mapped (3) |
| Crystal structure of the secretory form of membrane-associated human carbonic anhydrase IV at 2.8-A resolution. Stams T., Nair S.K., Okuyama T., Waheed A., Sly W.S., Christianson D.W. Proc. Natl. Acad. Sci. U.S.A. 93:13589-13594(1996) · UniProtKB (1) |
| A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Yanagisawa H., Fujii K., Nagafuchi S., Nakahori Y., Nakagome Y., Akane A., Nakamura M., Sano A., Komure O., Kondo I. et al. Hum. Mol. Genet. 5:373-379(1996) · UniProtKB (1) |
| Carbonic anhydrase IV: purification of a secretory form of the recombinant human enzyme and identification of the positions and importance of its disulfide bonds. Waheed A., Okuyama T., Heyduk T., Sly W.S. Arch. Biochem. Biophys. 333:432-438(1996) · UniProtKB (1) |
| PAX6 missense mutation in isolated foveal hypoplasia. Azuma N., Nishina S., Yanagisawa H., Okuyama T., Yamada M. Nat. Genet. 13:141-142(1996) · UniProtKB (1) |