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Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma.

Fujiwara-Okada Y., Matsumoto Y., Fukushi J., Setsu N., Matsuura S., Kamura S., Fujiwara T., Iida K., Hatano M., Nabeshima A. et al.

Br. J. Cancer 108:836-847(2013) · Mapped (6)

Naturally occurring PD-1+ memory phenotype CD8 T cells belong to nonconventional CD8 T cells and are cyclophosphamide-sensitive regulatory T cells.

Sakuraba K., Shibata K., Iwamoto Y., Yoshikai Y., Yamada H.

J. Immunol. 190:1560-1566(2013) · Mapped (2)

A distinct sensitization pattern associated with asthma and the thymic stromal lymphopoietin (TSLP) genotype.

Iijima H., Kaneko Y., Yamada H., Yatagai Y., Masuko H., Sakamoto T., Naito T., Hirota T., Tamari M., Konno S. et al.

Allergol Int 62:123-130(2013) · Mapped (3)

Asthma phenotypes in Japanese adults - their associations with the CCL5 and ADRB2 genotypes.

Kaneko Y., Masuko H., Sakamoto T., Iijima H., Naito T., Yatagai Y., Yamada H., Konno S., Nishimura M., Noguchi E. et al.

Allergol Int 62:113-121(2013) · Mapped (6)

Examination of serum pepsinogen in functional dyspepsia.

Tahara T., Shibata T., Okubo M., Yamashita H., Yoshioka D., Yonemura J., Maruyama N., Kamano T., Kamiya Y., Fujita H. et al.

Hepatogastroenterology 59:2516-2522(2012) · Mapped (3)

8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair.

Sheng Z., Oka S., Tsuchimoto D., Abolhassani N., Nomaru H., Sakumi K., Yamada H., Nakabeppu Y.

J. Clin. Invest. 122:4344-4361(2012) · Mapped (8)

Toxicogenomic biomarkers for renal papillary injury in rats.

Uehara T., Kondo C., Morikawa Y., Hanafusa H., Ueda S., Minowa Y., Nakatsu N., Ono A., Maruyama T., Kato I. et al.

Toxicology 303:1-8(2013) · Mapped (8)

Transmembrane topology and oligomeric structure of the high-affinity choline transporter.

Okuda T., Osawa C., Yamada H., Hayashi K., Nishikawa S., Ushio T., Kubo Y., Satou M., Ogawa H., Haga T.

J. Biol. Chem. 287:42826-42834(2012) · UniProtKB (1)

Association of genetic polymorphisms in IL17A and IL17F with gastro-duodenal diseases.

Hayashi R., Tahara T., Shiroeda H., Matsue Y., Minato T., Nomura T., Yamada H., Saito T., Matsunaga K., Fukuyama T. et al.

J Gastrointestin Liver Dis 21:243-249(2012) · Mapped (3)

ZNF385B is characteristically expressed in germinal center B cells and involved in B-cell apoptosis.

Iijima K., Yamada H., Miharu M., Imadome K., Miyagawa Y., Akimoto S., Kobayashi K., Okita H., Nakazawa A., Fujiwara S. et al.

Eur. J. Immunol. 42:3405-3415(2012) · UniProtKB (2) · Mapped (3)

Mutations in non-structural 5A and rapid viral response to pegylated interferon-alpha-2b plus ribavirin therapy are associated with therapeutic efficacy in patients with genotype 1b chronic hepatitis C.

Yano Y., Seo Y., Miki A., Saito M., Kato H., Hamano K., Oya M., Ouchi S., Fujisawa T., Yamada H. et al.

Int. J. Mol. Med. 30:1048-1052(2012) · Mapped (1)

The human CD10 lacking an N-glycan at Asn(628) is deficient in surface expression and neutral endopeptidase activity.

Sato B., Katagiri Y.U., Iijima K., Yamada H., Ito S., Kawasaki N., Okita H., Fujimoto J., Kiyokawa N.

Biochim. Biophys. Acta 1820:1715-1723(2012) · UniProtKB (1)

Genetic and functional analyses implicate the NUDT11, HNF1B, and SLC22A3 genes in prostate cancer pathogenesis.

Grisanzio C., Werner L., Takeda D., Awoyemi B.C., Pomerantz M.M., Yamada H., Sooriakumaran P., Robinson B.D., Leung R., Schinzel A.C. et al.

Proc. Natl. Acad. Sci. U.S.A. 109:11252-11257(2012) · Mapped (4)

Effects of -1018G>A polymorphism of HRH2 (rs2607474) on the severity of gastric mucosal atrophy.

Yamada H., Tahara T., Shiroeda H., Hayashi R., Saito T., Nakamura M., Tsuchishima M., Tsutsumi M., Shibata T., Arisawa T.

J Gastrointestin Liver Dis 21:139-143(2012) · Mapped (1)

Association between common genetic variant of HRH2 and gastric cancer risk.

Arisawa T., Tahara T., Ozaki K., Matsue Y., Minato T., Yamada H., Nomura T., Hayashi R., Matsunaga K., Fukumura A. et al.

Int. J. Oncol. 41:497-503(2012) · Mapped (1)

NFKB1 polymorphism is associated with age-related gene methylation in Helicobacter pylori-infected subjects.

Arisawa T., Tahara T., Shiroeda H., Yamada H., Nomura T., Hayashi R., Saito T., Fukuyama T., Otsuka T., Nakamura M. et al.

Int. J. Mol. Med. 30:255-262(2012) · Mapped (1)

The CRKL gene encoding an adaptor protein is amplified, overexpressed, and a possible therapeutic target in gastric cancer.

Natsume H., Shinmura K., Tao H., Igarashi H., Suzuki M., Nagura K., Goto M., Yamada H., Maeda M., Konno H. et al.

J Transl Med 10:97-97(2012) · Mapped (1)

Measurement of TFF3 mRNA in aspirates from thyroid nodules using mesh filtration: the first clinical trial in 130 cases.

Yamada H., Takano T., Kihara M., Hirokawa M., Yoshida H., Watanabe M., Iwatani Y., Hidaka Y., Miyauchi A.

Endocr. J. 59:621-630(2012) · Mapped (1)

Molecular characterization of a fully human chimeric T-cell antigen receptor for tumor-associated antigen EpCAM.

Shirasu N., Yamada H., Shibaguchi H., Kuroki M., Kuroki M.

J. Biomed. Biotechnol. 2012:853879-853879(2012) · Mapped (1)

Genetic polymorphisms of IL17A and pri-microRNA-938, targeting IL17A 3'-UTR, influence susceptibility to gastric cancer.

Arisawa T., Tahara T., Shiroeda H., Matsue Y., Minato T., Nomura T., Yamada H., Hayashi R., Saito T., Matsunaga K. et al.

Hum. Immunol. 73:747-752(2012) · Mapped (3)

Association between dopamine beta hydroxylase rs5320 polymorphism and smoking behaviour in elderly Japanese.

Ella E., Sato N., Nishizawa D., Kageyama S., Yamada H., Kurabe N., Ishino K., Tao H., Tanioka F., Nozawa A. et al.

J. Hum. Genet. 57:385-390(2012) · Mapped (1)

Autosomal dominant occult macular dystrophy with an RP1L1 mutation (R45W).

Hayashi T., Gekka T., Kozaki K., Ohkuma Y., Tanaka I., Yamada H., Tsuneoka H.

Optom Vis Sci 89:684-691(2012) · Mapped (2)

Methionine excess in diet induces acute lethal hepatitis in mice lacking cystathionine gamma-lyase, an animal model of cystathioninuria.

Yamada H., Akahoshi N., Kamata S., Hagiya Y., Hishiki T., Nagahata Y., Matsuura T., Takano N., Mori M., Ishizaki Y. et al.

Free Radic. Biol. Med. 52:1716-1726(2012) · Mapped (5)

The high-affinity choline transporter CHT1 is regulated by the ubiquitin ligase Nedd4-2.

Yamada H., Imajoh-Ohmi S., Haga T.

Biomed. Res. 33:1-8(2012) · Mapped (6)

Association between nerve growth factor gene polymorphism and executive dysfunction in Japanese patients with early-stage Alzheimer's disease and amnestic mild cognitive impairment.

Nagata T., Shinagawa S., Nukariya K., Nakayama R., Nakayama K., Yamada H.

Dement Geriatr Cogn Disord 32:379-386(2011) · Mapped (1)

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