Tada K - Search Results

1

One of the two genomic copies of the glycine decarboxylase cDNA has been deleted at a 5' region in a patient with nonketotic hyperglycinemia.

Sakakibara T, Koyata H, Ishiguro Y, Kure S, Kume A, Tada K, Hiraga K. Sakakibara T, et al. Among authors: tada k. Biochem Biophys Res Commun. 1990 Dec 31;173(3):801-6. doi: 10.1016/s0006-291x(05)80858-7. Biochem Biophys Res Commun. 1990. PMID: 2268343

2

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemia.

Kure S, Narisawa K, Tada K. Kure S, et al. Among authors: tada k. Biochem Biophys Res Commun. 1991 Feb 14;174(3):1176-82. doi: 10.1016/0006-291x(91)91545-n. Biochem Biophys Res Commun. 1991. PMID: 1996985

3

The impaired expression of glycine decarboxylase in patients with hyperglycinemias.

Kume A, Kure S, Tada K, Hiraga K. Kume A, et al. Among authors: tada k. Biochem Biophys Res Commun. 1988 Jul 15;154(1):292-7. doi: 10.1016/0006-291x(88)90683-3. Biochem Biophys Res Commun. 1988. PMID: 3395333

4

Non-ketotic hyperglycinaemia: molecular lesion, diagnosis and pathophysiology.

Tada K, Kure S. Tada K, et al. J Inherit Metab Dis. 1993;16(4):691-703. doi: 10.1007/BF00711901. J Inherit Metab Dis. 1993. PMID: 8412015 Review.

5

Depletion of cerebral D-serine in non-ketotic hyperglycinemia: possible involvement of glycine cleavage system in control of endogenous D-serine.

Iwama H, Takahashi K, Kure S, Hayashi F, Narisawa K, Tada K, Mizoguchi M, Takashima S, Tomita U, Nishikawa T. Iwama H, et al. Among authors: tada k. Biochem Biophys Res Commun. 1997 Feb 24;231(3):793-6. doi: 10.1006/bbrc.1997.6184. Biochem Biophys Res Commun. 1997. PMID: 9070895

6

Nonketotic hyperglycinemia: biochemical, molecular, and neurological aspects.

Kure S, Tada K, Narisawa K. Kure S, et al. Among authors: tada k. Jpn J Hum Genet. 1997 Mar;42(1):13-22. doi: 10.1007/BF02766917. Jpn J Hum Genet. 1997. PMID: 9183995 Review.

7

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. Among authors: tada k. Hum Genet. 2000 Mar;106(3):298-305. doi: 10.1007/s004390051041. Hum Genet. 2000. PMID: 10798358

8

Genomic analysis of non-ketotic hyperglycinaemia: a partial deletion of P-protein gene.

Tada K, Kure S, Kume A, Hiraga K. Tada K, et al. J Inherit Metab Dis. 1990;13(5):766-70. doi: 10.1007/BF01799584. J Inherit Metab Dis. 1990. PMID: 2246863 No abstract available.

9

Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblasts.

Kure S, Narisawa K, Tada K. Kure S, et al. Among authors: tada k. J Pediatr. 1992 Jan;120(1):95-8. doi: 10.1016/s0022-3476(05)80610-9. J Pediatr. 1992. PMID: 1309867

10

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

Tada K, Kure S, Takayanagi M, Kume A, Narisawa K. Tada K, et al. 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.

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