Mitsuuchi Y - Search Results

1

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. 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

2

The chimeric gene linked to glucocorticoid-suppressible hyperaldosteronism encodes a fused P-450 protein possessing aldosterone synthase activity.

Miyahara K, Kawamoto T, Mitsuuchi Y, Toda K, Imura H, Gordon RD, Shizuta Y. Miyahara K, et al. Among authors: mitsuuchi y. Biochem Biophys Res Commun. 1992 Dec 15;189(2):885-91. doi: 10.1016/0006-291x(92)92286-7. Biochem Biophys Res Commun. 1992. PMID: 1472060

3

Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans.

Kawamoto T, Mitsuuchi Y, Toda K, Yokoyama Y, Miyahara K, Miura S, Ohnishi T, Ichikawa Y, Nakao K, Imura H, et al. Kawamoto T, et al. Among authors: mitsuuchi y. Proc Natl Acad Sci U S A. 1992 Feb 15;89(4):1458-62. doi: 10.1073/pnas.89.4.1458. Proc Natl Acad Sci U S A. 1992. PMID: 1741400 Free PMC article.

4

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: mitsuuchi y. 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

5

Inborn errors of aldosterone biosynthesis in humans.

Shizuta Y, Kawamoto T, Mitsuuchi Y, Miyahara K, Rösler A, Ulick S, Imura H. Shizuta Y, et al. Among authors: mitsuuchi y. Steroids. 1995 Jan;60(1):15-21. doi: 10.1016/0039-128x(94)00023-6. Steroids. 1995. PMID: 7792802

6

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. Biochem Biophys Res Commun. 1993 Feb 15;190(3):864-9. doi: 10.1006/bbrc.1993.1128. Biochem Biophys Res Commun. 1993. PMID: 8439335

7

Molecular genetic studies on the biosynthesis of aldosterone in humans.

Shizuta Y, Kawamoto T, Mitsuuchi Y, Toda K, Miyahara K, Ichikawa Y, Imura H, Ulick S. Shizuta Y, et al. Among authors: mitsuuchi y. J Steroid Biochem Mol Biol. 1992 Dec;43(8):981-7. doi: 10.1016/0960-0760(92)90326-E. J Steroid Biochem Mol Biol. 1992. PMID: 22217843

8

Cloning of cDNA and genomic DNA for human cytochrome P-45011 beta.

Kawamoto T, Mitsuuchi Y, Toda K, Miyahara K, Yokoyama Y, Nakao K, Hosoda K, Yamamoto Y, Imura H, Shizuta Y. Kawamoto T, et al. Among authors: mitsuuchi y. FEBS Lett. 1990 Sep 3;269(2):345-9. doi: 10.1016/0014-5793(90)81190-y. FEBS Lett. 1990. PMID: 2401360 Free article.

9

A nonsense mutation (TGG [Trp116]-->TAG [Stop]) in CYP11B1 causes steroid 11 beta-hydroxylase deficiency.

Naiki Y, Kawamoto T, Mitsuuchi Y, Miyahara K, Toda K, Orii T, Imura H, Shizuta Y. Naiki Y, et al. Among authors: mitsuuchi y. J Clin Endocrinol Metab. 1993 Dec;77(6):1677-82. doi: 10.1210/jcem.77.6.7903314. J Clin Endocrinol Metab. 1993. PMID: 7903314

10

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: mitsuuchi y. 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.

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