Takayanagi M - Search Results

1

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia.

Kure S, Shinka T, Sakata Y, Osamu N, Takayanagi M, Tada K, Matsubara Y, Narisawa K. Kure S, et al. Among authors: takayanagi m. J Hum Genet. 1998;43(2):135-7. doi: 10.1007/s100380050055. J Hum Genet. 1998. PMID: 9621520

2

Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia.

Sakamoto O, Ohura T, Matsubara Y, Takayanagi M, Tsuchiya S. Sakamoto O, et al. Among authors: takayanagi m. J Hum Genet. 2007;52(1):48-55. doi: 10.1007/s10038-006-0077-2. Epub 2006 Oct 31. J Hum Genet. 2007. PMID: 17075691

3

Non-ketotic hyperglycinemia: a life-threatening disorder in the neonate.

Tada K, Kure S, Takayanagi M, Kume A, Narisawa K. Tada K, et al. Among authors: takayanagi m. Early Hum Dev. 1992 Jun-Jul;29(1-3):75-81. doi: 10.1016/0378-3782(92)90060-t. Early Hum Dev. 1992. PMID: 1396281 Review.

4

Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.

Kure S, Takayanagi M, Narisawa K, Tada K, Leisti J. Kure S, et al. Among authors: takayanagi m. J Clin Invest. 1992 Jul;90(1):160-4. doi: 10.1172/JCI115831. J Clin Invest. 1992. PMID: 1634607 Free PMC article.

5

Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia.

Takayanagi M, Kure S, Sakata Y, Kurihara Y, Ohya Y, Kajita M, Tada K, Matsubara Y, Narisawa K. Takayanagi M, et al. Hum Genet. 2000 Mar;106(3):298-305. doi: 10.1007/s004390051041. Hum Genet. 2000. PMID: 10798358

6

Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation.

Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Suzuki Y, Sakura N, Takayanagi M, Iinuma K, Ohura T. Yang X, et al. Among authors: takayanagi m. Mol Genet Metab. 2004 Aug;82(4):329-33. doi: 10.1016/j.ymgme.2004.05.002. Mol Genet Metab. 2004. PMID: 15308131

7

Assignment of Gldc encoding glycine decarboxylase to mouse chromosome 19C by in situ hybridization and a CA repeat polymorphism in the Gldc gene.

Shinka T, Kure S, Sakata Y, Takayanagi M, Matsubara Y, Narisawa K. Shinka T, et al. Among authors: takayanagi m. Cytogenet Cell Genet. 1998;83(3-4):260-1. doi: 10.1159/000015200. Cytogenet Cell Genet. 1998. PMID: 10072599 No abstract available.

8

Rapid diagnosis of glycine encephalopathy by 13C-glycine breath test.

Kure S, Korman SH, Kanno J, Narisawa A, Kubota M, Takayanagi T, Takayanagi M, Saito T, Matsui A, Kamada F, Aoki Y, Ohura T, Matsubara Y. Kure S, et al. Among authors: takayanagi m, takayanagi t. Ann Neurol. 2006 May;59(5):862-7. doi: 10.1002/ana.20853. Ann Neurol. 2006. PMID: 16634033

9

Molecular and clinical analyses of Japanese patients with carbamoylphosphate synthetase 1 (CPS1) deficiency.

Kurokawa K, Yorifuji T, Kawai M, Momoi T, Nagasaka H, Takayanagi M, Kobayashi K, Yoshino M, Kosho T, Adachi M, Otsuka H, Yamamoto S, Murata T, Suenaga A, Ishii T, Terada K, Shimura N, Kiwaki K, Shintaku H, Yamakawa M, Nakabayashi H, Wakutani Y, Nakahata T. Kurokawa K, et al. Among authors: takayanagi m. J Hum Genet. 2007;52(4):349-354. doi: 10.1007/s10038-007-0122-9. Epub 2007 Feb 20. J Hum Genet. 2007. PMID: 17310273

10

Pilot study of gas chromatographic-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease.

Kuhara T, Shinka T, Inoue Y, Ohse M, Zhen-wei X, Yoshida I, Inokuchi T, Yamaguchi S, Takayanagi M, Matsumoto I. Kuhara T, et al. Among authors: takayanagi m. J Chromatogr B Biomed Sci Appl. 1999 Aug 6;731(1):141-7. doi: 10.1016/s0378-4347(99)00205-4. J Chromatogr B Biomed Sci Appl. 1999. PMID: 10492000

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