Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Isao Kuribayashi"'
Autor:
Jan M. Wit, Bruce H. R. Wolffenbuttel, Yutaka Shizuta, Wilma Oostdijk, Guy Massa, Isao Kuribayashi, Koichi Honke, Satoshi Nomoto
Publikováno v:
Hormone Research in Paediatrics. 63:284-293
Aims: Steroid 11β-hydroxylase deficiency (11β-OHD) is the second most common (5–8%) cause of congenital adrenal hyperplasia (CAH), and results from homozygous or compound heterozygous mutations or deletions of the responsible gene CYP11B1. In ord
Autor:
Fumio Endo, Naohito Yamasaki, Yutaka Shizuta, Yoshinori Doi, Takashi Furuno, Romero Jovel Santa, Saburo Onishi, Isao Kuribayashi, Aldahoodi Ziyad Mutlaq, Toshiro Nakamura, Hideaki Kuge, Akio Takahashi, Shoichi Chida
Publikováno v:
Hormone Research in Paediatrics. 60:255-260
Objectives: To clarify the underlying molecular mechanism of corticosterone methyl oxidase type II (CMO II) deficiency, Japanese patients newly diagnosed with CMO II deficiency were investigated. Methods: We analyzed the patients’ genomic DNA seque
Autor:
Isao Kuribayashi
Publikováno v:
Journal of Power Sources. 63:87-91
Thin composite cellulosic separators (39–85 lem thickness), composed of fine fibrilliform cellulosic fibres (diameter 0.5 to 5.0 μm) embedded in microporous (pore diameter: 10–200 nm) cellulosic film and soaked in ethylene carbonate or other apr
Publikováno v:
Journal of Power Sources. 54:1-5
Various carbonaceous particles having a core-shell structure, produced from graphite and pseudo-graphite coated with pitchblended phenol resin and green mesophase-pitch coated with phenol resin and ground graphite powder, were investigated as active
Autor:
Keigo Yasuda, Yasutake Yamamoto, Kaoru Miyahara, Yasuhiro Naiki, T. Hara, Kiyoshi Miura, Isao Kuribayashi, Tadao Orii, Katsumi Toda, Hiroo Imura, Yasuhiro Mitsuuchi, Yutaka Shizuta, Stanley Ulick, D.H. Morton, Takeshi Kawamoto
Publikováno v:
Biochemical and Biophysical Research Communications. 190:864-869
CYP11B2, the gene coding for steroid 18-hydroxylase (P-450C18), has been recently shown to be the same gene as that for corticosterone methyl oxidase type I and type II (CMO I & II) which were previously postulated to catalyze the final two steps in
Autor:
Katsumi Toda, Yasuhiro Ogawa, Isao Kuribayashi, Takeshi Kawamoto, Masako Terashima, Tomoho Maeda, Yutaka Shizuta
Publikováno v:
Archives of Biochemistry and Biophysics. 285:231-237
A full-length cDNA clone for aromatase P450 has been isolated from a pregnant mouse ovarian cDNA library. The insert of this clone (2394 bp) contains a 1509-bp open reading frame encoding 503 amino acid residues together with a 46-bp 5′-untranslate
Autor:
Hidetoshi Sumimoto, Yasutake Yamamoto, Yutaka Shizuta, Masako Terashima, Yuichi Yokoyama, Isao Kuribayashi, Tomoho Maeda, Katsumi Toda, Yusuke Sagara, Hisao Ikeda, Takeshi Kawamoto, Yasuhiro Mitsuuchi
Publikováno v:
European Journal of Biochemistry. 193:559-565
The gene encoding aromatase P-450 (CYP XIX) has been isolated from two types of human genomic DNA libraries. It spans at least 70 kb and consists of 10 exons. The translational initiation site and the termination site are located in exon 2 and exon 1
Autor:
Isao, Kuribayashi
Publikováno v:
Seikagaku. The Journal of Japanese Biochemical Society. 78(8)
Autor:
Isao, Kuribayashi, Satoshi, Nomoto, Guy, Massa, Wilma, Oostdijk, Jan M, Wit, Bruce H R, Wolffenbuttel, Yutaka, Shizuta, Koichi, Honke
Publikováno v:
Hormone research. 63(6)
Steroid 11beta-hydroxylase deficiency (11beta-OHD) is the second most common (5-8%) cause of congenital adrenal hyperplasia (CAH), and results from homozygous or compound heterozygous mutations or deletions of the responsible gene CYP11B1. In order t
Autor:
Isao, Kuribayashi, Hideaki, Kuge, Romero Jovel, Santa, Aldahoodi Ziyad, Mutlaq, Naohito, Yamasaki, Takashi, Furuno, Akio, Takahashi, Shoichi, Chida, Toshiro, Nakamura, Fumio, Endo, Yoshinori, Doi, Saburo, Onishi, Yutaka, Shizuta
Publikováno v:
Hormone research. 60(5)
To clarify the underlying molecular mechanism of corticosterone methyl oxidase type II (CMO II) deficiency, Japanese patients newly diagnosed with CMO II deficiency were investigated.We analyzed the patients' genomic DNA sequence on all 9 exons of th