山田憲一郎 (Kenichiro Yamada) - マイポータル - researchmap

基本情報

所属: 愛知県心身障害者コロニー発達障害研究所遺伝学部門研究員

学位: 薬学博士(名古屋市立大学)

J-GLOBAL ID: 200901046257970343
researchmap会員ID: 5000000512

研究キーワード

4

研究分野

2

経歴

5

学歴

4

MISC

20

(Mutoh N., Nakagawa C. W. and Yamada K.) Characterization of Cu, Zn-superoxide dismutase-deficient mutant of fission yeast Schizosaccharomyces pombe.

Curr Genet. 41, 82-88 2002年
(Lescure A., Allmang C., Yamada K., Carbon P, and Krol A.) cDNA cloning, expression pattern and RNA binding analysis of human selenocysteine insertion sequence (SECIS) binding protein 2.

Gene 291(1-2), 279-85 2002年
(Yoneda M., Fujita T., Yamada Y, Yamada K., Fujii A., Inagaki T., Nakagawa H., Kishikawa M., Shimada A., Nagaya M., Azuma T., Kuriyama M. and Wakamatsu N.) Late infantile Hirschsprung disease-mental retardation syndrome with a 3-bp deletion in ZFHXIB.

Neurology in press 2002年
(Mutoh N., Nakagawa C. W. and Yamada K.) Characterization of Cu, Zn-superoxide dismutase-deficient mutant of fission yeast Schizosaccharomyces pombe.

Curr Genet. 41, 82-88 2002年
(Lescure A., Allmang C., Yamada K., Carbon P, and Krol A.) cDNA cloning, expression pattern and RNA binding analysis of human selenocysteine insertion sequence (SECIS) binding protein 2.

Gene 291(1-2), 279-85 2002年
(Yoneda M., Fujita T., Yamada Y, Yamada K., Fujii A., Inagaki T., Nakagawa H., Kishikawa M., Shimada A., Nagaya M., Azuma T., Kuriyama M. and Wakamatsu N.) Late infantile Hirschsprung disease-mental retardation syndrome with a 3-bp deletion in ZFHXIB.

Neurology in press 2002年
(Yamada K., Yamada Y., Nomura N., Miura K., Wakako R., Hayakawa C., Matsumoto A., Kumagai T., Yoshimura I., Miyazaki S., Kato K., Sonta S., Ono H., Yamanaka T., Nagaya M. and Wakamatsu N.) Nonsense and Frameshift Mutations in ZFHXIB, Encoding Smad-Inte・・・

Am J Hum Genet. 69 (6), 1178-1185 2001年
(Yamada K., Yamada Y., Nomura N., Miura K., Wakako R., Hayakawa C., Matsumoto A., Kumagai T., Yoshimura I., Miyazaki S., Kato K., Sonta S., Ono H., Yamanaka T., Nagaya M. and Wakamatsu N.) Nonsense and Frameshift Mutations in ZFHXIB, Encoding Smad-Inte・・・

Am J Hum Genet. 69 (6), 1178-1185 2001年
Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Nobuaki Wakamatsu, Yasukazu Yamada, Kenichiro Yamada, Takao Ono, Noriko Nomura, Hiroko Taniguchi, Hiroshi Kitoh, Norihiro Mutoh, Tsutomu Yamanaka, Kyosuke Mushiake …

Nature Genetics 27(4) 369-370 2001年
Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features

Kenichiro Yamada, Yasukazu Yamada, Noriko Nomura, Kiyokuni Miura, Rie Wakako, Chiemi Hayakawa, Akiko Matsumoto, Toshiyuki Kumagai, Ikuko Yoshimura, Shuji Miyazaki …

American Journal of Human Genetics 69(6) 1178-1185 2001年
A new translational elongation factor for selenocysteyl-tRNA in eucaryotes

Kenichiro Yamada

FEBS Letters 377(3) 313-317 1995年12月27日
A factor protecting [⁷⁵Se]SeCys-tRNA is different from EF-1α

FEBS Lett.347(2-3)137-142(1994) 347(2-3) 137-142 1994年6月27日
A factor protecting mammalian [75Se]SeCys-tRNA is different from EF-1α

Kenichiro Yamada, Takaharu Mizutani, Shin-ichiro Ejiri, Tsuyoshi Totsuka

FEBS Letters 347(2-3) 137-142 1994年6月27日
第21番目のアミノ酸セレノシステインのゆくえ。

生化学（みにれびゅう）66巻,No.6,525-530(1994)
Schizosaccharomyces pombe homologue of glutathione peroxidase,which does not contain selenocysteine,is induced by several stresses and works as an antioxidant.

Yeast 15(11)1125-1132(1999)
Characterization of mSelB, a novel mammalian elongation factor for selenocysteine translation

EMBO J.19(17)4796-4805(2000)
Mutations in SIP1,encoding Smad interacting protein-1,cause a form of Hirschsprung disease

Nat Genet.27(4)369-370(2001)
A new translational elongation factor for Selenocysteyl-tRNA in eucaryotes

FEBS Lett.377(3)313-317(1995)
Schizosaccharomyces pombe homologue of glutathione peroxidase,which does not contain selenocysteine,is induced by several stresses and works as an antioxidant.

Yeast 15(11)1125-1132(1999)
Characterization of mSelB, a novel mammalian elongation factor for selenocysteine translation

EMBO J.19(17)4796-4805(2000)

所属学協会

3

Works(作品等)

1

ZFHXIB欠損症の病態解明

2001年

共同研究・競争的資金等の研究課題

4

先天性精神運動発達遅滞の病因遺伝子の解明

遺伝子科学研究 2000年 - 2005年
Analysis of disease couasing gene of developmental disorder

Gene Science Research 2000年 - 2005年
先天性疾患の病因遺伝子の解明
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