Fukushima H - Search Results

1

Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes.

Hayashi J, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y, et al. Hayashi J, et al. Among authors: fukushima h. J Biol Chem. 1994 Jul 22;269(29):19060-6. J Biol Chem. 1994. PMID: 7518448 Free article.

2

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: fukushima h. J Pediatr. 1992 Jan;120(1):62-6. doi: 10.1016/s0022-3476(05)80599-2. J Pediatr. 1992. PMID: 1370535

3

Detection of the A to G(3243) mutation of mitochondrial DNA in Japanese families with mitochondrial encephalomyopathies.

Inui K, Tsukamoto H, Fukushima H, Taniike M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: fukushima h. J Inherit Metab Dis. 1992;15(3):311-4. doi: 10.1007/BF02435964. J Inherit Metab Dis. 1992. PMID: 1405464 No abstract available.

4

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy.

Taniike M, Fukushima H, Yanagihara I, Tsukamoto H, Tanaka J, Fujimura H, Nagai T, Sano T, Yamaoka K, Inui K, et al. Taniike M, et al. Among authors: fukushima h. Biochem Biophys Res Commun. 1992 Jul 15;186(1):47-53. doi: 10.1016/s0006-291x(05)80773-9. Biochem Biophys Res Commun. 1992. PMID: 1632786

5

Molecular study of Duchenne and Becker muscular dystrophies in Japanese.

Tsukamoto H, Inui K, Fukushima H, Nishigaki T, Taniike M, Tanaka J, Okada S. Tsukamoto H, et al. Among authors: fukushima h. J Inherit Metab Dis. 1991;14(5):819-24. doi: 10.1007/BF01799956. J Inherit Metab Dis. 1991. PMID: 1779629 No abstract available.

6

Sequencing and expression of a full-length cDNA for human alpha-L-fucosidase.

Fukushima H, Nishimoto J, Okada S. Fukushima H, et al. J Inherit Metab Dis. 1990;13(5):761-5. doi: 10.1007/BF01799583. J Inherit Metab Dis. 1990. PMID: 2174090 No abstract available.

7

One base deletion in the cysteine-rich domain of the dystrophin gene in Duchenne muscular dystrophy patients.

Tsukamoto H, Inui K, Matsuoka T, Yanagihara I, Fukushima H, Okada S. Tsukamoto H, et al. Among authors: fukushima h. Hum Mol Genet. 1994 Jun;3(6):995-6. doi: 10.1093/hmg/3.6.995. Hum Mol Genet. 1994. PMID: 7951251 No abstract available.

8

Krabbe disease: isolation and characterization of a full-length cDNA for human galactocerebrosidase.

Sakai N, Inui K, Fujii N, Fukushima H, Nishimoto J, Yanagihara I, Isegawa Y, Iwamatsu A, Okada S. Sakai N, et al. Among authors: fukushima h. Biochem Biophys Res Commun. 1994 Jan 28;198(2):485-91. doi: 10.1006/bbrc.1994.1071. Biochem Biophys Res Commun. 1994. PMID: 8297359

9

Molecular defects in Krabbe disease.

Tatsumi N, Inui K, Sakai N, Fukushima H, Nishimoto J, Yanagihara I, Nishigaki T, Tsukamoto H, Fu L, Taniike M, et al. Tatsumi N, et al. Among authors: fukushima h. Hum Mol Genet. 1995 Oct;4(10):1865-8. doi: 10.1093/hmg/4.10.1865. Hum Mol Genet. 1995. PMID: 8595408

10

Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease.

Sakai N, Inui K, Tatsumi N, Fukushima H, Nishigaki T, Taniike M, Nishimoto J, Tsukamoto H, Yanagihara I, Ozono K, Okada S. Sakai N, et al. Among authors: fukushima h. J Neurochem. 1996 Mar;66(3):1118-24. doi: 10.1046/j.1471-4159.1996.66031118.x. J Neurochem. 1996. PMID: 8769874

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