Osaka H - Search Results

1

Effect of curcumin in a mouse model of Pelizaeus-Merzbacher disease.

Yu LH, Morimura T, Numata Y, Yamamoto R, Inoue N, Antalfy B, Goto Y, Deguchi K, Osaka H, Inoue K. Yu LH, et al. Among authors: osaka h. Mol Genet Metab. 2012 May;106(1):108-14. doi: 10.1016/j.ymgme.2012.02.016. Epub 2012 Mar 3. Mol Genet Metab. 2012. PMID: 22436581

2

Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.

Osaka H, Kawanishi C, Inoue K, Uesugi H, Hiroshi K, Nishiyama K, Yamada Y, Suzuki K, Kimura S, Kosaka K. Osaka H, et al. Biochem Biophys Res Commun. 1995 Oct 24;215(3):835-41. doi: 10.1006/bbrc.1995.2539. Biochem Biophys Res Commun. 1995. PMID: 7488049

3

MvaI polymorphism in the proteolipid protein (PLP) gene.

Osaka H, Inoue K, Kawanishi C, Yamada Y, Onishi H, Sugiyama N, Suzuki K, Nezu A, Kimura S, Kosaka K. Osaka H, et al. Hum Genet. 1995 Apr;95(4):461. doi: 10.1007/BF00208978. Hum Genet. 1995. PMID: 7705847

4

A duplicated PLP gene causing Pelizaeus-Merzbacher disease detected by comparative multiplex PCR.

Inoue K, Osaka H, Sugiyama N, Kawanishi C, Onishi H, Nezu A, Kimura K, Yamada Y, Kosaka K. Inoue K, et al. Among authors: osaka h. Am J Hum Genet. 1996 Jul;59(1):32-9. Am J Hum Genet. 1996. PMID: 8659540 Free PMC article.

5

Pelizaeus-Merzbacher disease: a novel mutation in the 5'-untranslated region of the proteolipid protein gene.

Kawanishi C, Sugiyama N, Osaka H, Inoue K, Suzuki K, Onishi H, Yamada Y, Nezu A, Kimura S, Kosaka K. Kawanishi C, et al. Among authors: osaka h. Hum Mutat. 1996;7(4):355-7. doi: 10.1002/(SICI)1098-1004(1996)7:4<355::AID-HUMU10>3.0.CO;2-1. Hum Mutat. 1996. PMID: 8723686 No abstract available.

6

Pelizaeus-Merzbacher-like disease: female case report.

Nezu A, Kimura S, Uehara S, Osaka H, Kobayashi T, Haraguchi M, Inoue K, Kawanishi C. Nezu A, et al. Among authors: osaka h. Brain Dev. 1996 Mar-Apr;18(2):114-8. doi: 10.1016/0387-7604(95)00078-x. Brain Dev. 1996. PMID: 8733901

7

Mutations in the proteolipid protein gene in Japanese families with Pelizaeus-Merzbacher disease.

Inoue K, Osaka H, Kawanishi C, Sugiyama N, Ishii M, Sugita K, Yamada Y, Kosaka K. Inoue K, et al. Among authors: osaka h. Neurology. 1997 Jan;48(1):283-5. doi: 10.1212/wnl.48.1.283. Neurology. 1997. PMID: 9008538

8

A new restriction-site polymorphism in the human proteolipid protein gene.

Kawanishi C, Osaka H, Inoue K, Onishi H, Yamada Y, Kosaka K. Kawanishi C, et al. Among authors: osaka h. Clin Genet. 1997 Jan;51(1):75. Clin Genet. 1997. PMID: 9084942 No abstract available.

9

A new missense mutation in exon 6 of the proteolipid protein gene in a patient with Pelizaeus-Merzbacher disease.

Kawanishi C, Osaka H, Owa K, Inoue K, Miyakawa T, Onishi H, Yamada Y, Suzuki K, Kimura S, Kosaka K. Kawanishi C, et al. Among authors: osaka h. Hum Mutat. 1997;9(5):475-6. doi: 10.1002/(SICI)1098-1004(1997)9:5<475::AID-HUMU19>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9143933 No abstract available.

10

An MRI and MRS study of Pelizaeus-Merzbacher disease.

Nezu A, Kimura S, Takeshita S, Osaka H, Kimura K, Inoue K. Nezu A, et al. Among authors: osaka h. Pediatr Neurol. 1998 Apr;18(4):334-7. doi: 10.1016/s0887-8994(97)00212-9. Pediatr Neurol. 1998. PMID: 9588530

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