Tada K - Search Results

1

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.

2

A novel splicing mutation in propionic acidemia associated with a tetranucleotide direct repeat in the PCCB gene.

Ohura T, Narisawa K, Tada K, Iinuma K. Ohura T, et al. Among authors: tada k. Hum Genet. 1995 Jun;95(6):707-8. doi: 10.1007/BF00209492. Hum Genet. 1995. PMID: 7789958

3

The molecular defect in propionic acidemia: exon skipping caused by an 8-bp deletion from an intron in the PCCB allele.

Ohura T, Ogasawara M, Ikeda H, Narisawa K, Tada K. Ohura T, et al. Among authors: tada k. Hum Genet. 1993 Oct;92(4):397-402. doi: 10.1007/BF01247343. Hum Genet. 1993. PMID: 8225321

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

[Nonketotic hyperglycinemia].

Tada K, Kure S. Tada K, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):227-30. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590032 Review. Japanese. No abstract available.

6

A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia.

Kure S, Mandel H, Rolland MO, Sakata Y, Shinka T, Drugan A, Boneh A, Tada K, Matsubara Y, Narisawa K. Kure S, et al. Among authors: tada k. Hum Genet. 1998 Apr;102(4):430-4. doi: 10.1007/s004390050716. Hum Genet. 1998. PMID: 9600239

7

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: tada k. J Hum Genet. 1998;43(2):135-7. doi: 10.1007/s100380050055. J Hum Genet. 1998. PMID: 9621520

8

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

9

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

10

Genetic heterogeneity of propionic acidemia: analysis of 15 Japanese patients.

Ohura T, Miyabayashi S, Narisawa K, Tada K. Ohura T, et al. Among authors: tada k. Hum Genet. 1991 May;87(1):41-4. doi: 10.1007/BF01213089. Hum Genet. 1991. PMID: 2037281

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,241 results

Search Page

Filters