Kuribayashi I - Search Results

1

Cloning and expression of a cDNA for human cytochrome P-450aldo as related to primary aldosteronism.

Kawainoto T, Mitsuuchi Y, Ohnishi T, Ichikawa Y, Yokoyama Y, Sumimoto H, Toda K, Miyahara K, Kuribayashi I, Nakao K, et al. Kawainoto T, et al. Among authors: kuribayashi i. Biochem Biophys Res Commun. 1990 Nov 30;173(1):309-16. doi: 10.1016/s0006-291x(05)81058-7. Biochem Biophys Res Commun. 1990. PMID: 2256920

2

Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients.

Mitsuuchi Y, Kawamoto T, Naiki Y, Miyahara K, Toda K, Kuribayashi I, Orii T, Yasuda K, Miura K, Nakao K, et al. Mitsuuchi Y, et al. Among authors: kuribayashi i. Biochem Biophys Res Commun. 1992 Jan 31;182(2):974-9. doi: 10.1016/0006-291x(92)91827-d. Biochem Biophys Res Commun. 1992. PMID: 1346492

3

Human poly(ADP-ribose) polymerase gene. Cloning of the promoter region.

Yokoyama Y, Kawamoto T, Mitsuuchi Y, Kurosaki T, Toda K, Ushiro H, Terashima M, Sumimoto H, Kuribayashi I, Yamamoto Y, et al. Yokoyama Y, et al. Among authors: kuribayashi i. Eur J Biochem. 1990 Dec 12;194(2):521-6. doi: 10.1111/j.1432-1033.1990.tb15647.x. Eur J Biochem. 1990. PMID: 2125269 Free article.

4

Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients.

Mitsuuchi Y, Kawamoto T, Miyahara K, Ulick S, Morton DH, Naiki Y, Kuribayashi I, Toda K, Hara T, Orii T, et al. Mitsuuchi Y, et al. Among authors: kuribayashi i. Biochem Biophys Res Commun. 1993 Feb 15;190(3):864-9. doi: 10.1006/bbrc.1993.1128. Biochem Biophys Res Commun. 1993. PMID: 8439335

5

Structural and functional characterization of human aromatase P-450 gene.

Toda K, Terashima M, Kawamoto T, Sumimoto H, Yokoyama Y, Kuribayashi I, Mitsuuchi Y, Maeda T, Yamamoto Y, Sagara Y, et al. Toda K, et al. Among authors: kuribayashi i. Eur J Biochem. 1990 Oct 24;193(2):559-65. doi: 10.1111/j.1432-1033.1990.tb19372.x. Eur J Biochem. 1990. PMID: 2171939 Free article.

6

Isolation of a full-length cDNA encoding mouse aromatase P450.

Terashima M, Toda K, Kawamoto T, Kuribayashi I, Ogawa Y, Maeda T, Shizuta Y. Terashima M, et al. Among authors: kuribayashi i. Arch Biochem Biophys. 1991 Mar;285(2):231-7. doi: 10.1016/0003-9861(91)90354-l. Arch Biochem Biophys. 1991. PMID: 1897929

7

Steroid 11-beta-hydroxylase deficiency caused by compound heterozygosity for a novel mutation, p.G314R, in one CYP11B1 allele, and a chimeric CYP11B2/CYP11B1 in the other allele.

Kuribayashi I, Nomoto S, Massa G, Oostdijk W, Wit JM, Wolffenbuttel BH, Shizuta Y, Honke K. Kuribayashi I, et al. Horm Res. 2005;63(6):284-93. doi: 10.1159/000087074. Epub 2005 Jul 15. Horm Res. 2005. PMID: 16024935

8

A missense mutation (GGC[435Gly]-->AGC[Ser]) in exon 8 of the CYP11B2 gene inherited in Japanese patients with congenital hypoaldosteronism.

Kuribayashi I, Kuge H, Santa RJ, Mutlaq AZ, Yamasaki N, Furuno T, Takahashi A, Chida S, Nakamura T, Endo F, Doi Y, Onishi S, Shizuta Y. Kuribayashi I, et al. Horm Res. 2003;60(5):255-60. doi: 10.1159/000074041. Horm Res. 2003. PMID: 14614232

9

[Steroid 11beta-hydroxylase deficiency--focusing on the CYP11B2/CYP11B1 chimera which has been recently discovered as the causing gene--].

Kuribayashi I. Kuribayashi I. Seikagaku. 2006 Aug;78(8):749-55. Seikagaku. 2006. PMID: 16986724 Review. Japanese. No abstract available.

10

A novel nonsense mutation in the Cyp11B1 gene from a subject with the steroid 11beta-hydroxylase form of congenital adrenal hyperplasia.

Kuribayashi I, Massa G, van den Tooren-de Groot HK, Oostdijk W, Wit JM, Shizuta Y. Kuribayashi I, et al. Endocr Res. 2003 Nov;29(4):377-81. doi: 10.1081/erc-120026943. Endocr Res. 2003. PMID: 14682466

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