Naiki Y - Search Results

1

Comparison of physician- and self-assessed pubertal onset in Japanese children.

Saito-Abe M, Nishizato M, Yamamoto-Hanada K, Yang L, Fukami M, Ito Y, Ihara K, Iwabuchi A, Okamoto S, Naiki Y, Ohya Y, Horikawa R. Saito-Abe M, et al. Among authors: naiki y. Front Pediatr. 2023 Mar 21;11:950541. doi: 10.3389/fped.2023.950541. eCollection 2023. Front Pediatr. 2023. PMID: 37025288 Free PMC article.

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: naiki y. 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

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

4

Tuberculous tenosynovitis in the elbow joint.

Asaka T, Takizawa Y, Kariya T, Nitta E, Yasuda T, Fujita M, Sawasaki S, Naiki Y, Nakatani N, Doushita T, Miura T, Ueda F, Takamori M, Matsushima A. Asaka T, et al. Among authors: naiki y. Intern Med. 1996 Feb;35(2):162-5. doi: 10.2169/internalmedicine.35.162. Intern Med. 1996. PMID: 8680108 Free article.

5

An outbreak of enteritis induced by methicillin-resistant Staphylococcus aureus producing enterotoxin types A and C, toxic shock syndrome toxin-1 and coagulase type II.

Kaneko A, Mori T, Fujino T, Nakamura A, Naiki Y, Mutoh M, Nagata A, Kirikae T. Kaneko A, et al. Among authors: naiki y. Jpn J Infect Dis. 2000 Oct;53(5):212-4. Jpn J Infect Dis. 2000. PMID: 11135710 No abstract available.

6

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. J Clin Endocrinol Metab. 1993 Dec;77(6):1677-82. doi: 10.1210/jcem.77.6.7903314. J Clin Endocrinol Metab. 1993. PMID: 7903314

7

A novel single-base substitution (380C>T) that activates a 5-base downstream cryptic splice-acceptor site within exon 5 in almost all transcripts in the human mitochondrial acetoacetyl-CoA thiolase gene.

Nakamura K, Fukao T, Perez-Cerda C, Luque C, Song XQ, Naiki Y, Kohno Y, Ugarte M, Kondo N. Nakamura K, et al. Among authors: naiki y. Mol Genet Metab. 2001 Feb;72(2):115-21. doi: 10.1006/mgme.2000.3125. Mol Genet Metab. 2001. PMID: 11161837

8

Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3beta-hydroxysteroid dehydrogenase (3betaHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3betaHSD deficiency disorder.

Zhang L, Mason JI, Naiki Y, Copeland KC, Castro-Magana M, Gordon-Walker TT, Chang YT, Pang S. Zhang L, et al. Among authors: naiki y. J Clin Endocrinol Metab. 2000 Apr;85(4):1678-85. doi: 10.1210/jcem.85.4.6539. J Clin Endocrinol Metab. 2000. PMID: 10770215

9

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. Fukami M, et al. Among authors: naiki y. J Clin Endocrinol Metab. 2005 Jan;90(1):414-26. doi: 10.1210/jc.2004-0810. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483095

10

Hearing loss in Turner syndrome.

Morimoto N, Tanaka T, Taiji H, Horikawa R, Naiki Y, Morimoto Y, Kawashiro N. Morimoto N, et al. Among authors: naiki y. J Pediatr. 2006 Nov;149(5):697-701. doi: 10.1016/j.jpeds.2006.06.071. J Pediatr. 2006. PMID: 17095347

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