Arahata K - Search Results

1

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM. Beggs AH, et al. Among authors: arahata k. Am J Hum Genet. 1991 Jul;49(1):54-67. Am J Hum Genet. 1991. PMID: 2063877 Free PMC article.

2

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

Beggs AH, Neumann PE, Arahata K, Arikawa E, Nonaka I, Anderson MS, Kunkel LM. Beggs AH, et al. Among authors: arahata k. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):623-7. doi: 10.1073/pnas.89.2.623. Proc Natl Acad Sci U S A. 1992. PMID: 1731332 Free PMC article.

3

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.

Arahata K, Beggs AH, Honda H, Ito S, Ishiura S, Tsukahara T, Ishiguro T, Eguchi C, Orimo S, Arikawa E, et al. Arahata K, et al. J Neurol Sci. 1991 Feb;101(2):148-56. doi: 10.1016/0022-510x(91)90039-a. J Neurol Sci. 1991. PMID: 2033400

4

[Muscular dystrophy].

Tsukahara T, Ishiura S, Arahata K, Sugita H. Tsukahara T, et al. Among authors: arahata k. Tanpakushitsu Kakusan Koso. 1990 May;35(7 Suppl):1246-53. Tanpakushitsu Kakusan Koso. 1990. PMID: 2192396 Japanese. No abstract available.

5

Quadriceps myopathy: forme fruste of Becker muscular dystrophy.

Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H. Sunohara N, et al. Among authors: arahata k. Ann Neurol. 1990 Nov;28(5):634-9. doi: 10.1002/ana.410280506. Ann Neurol. 1990. PMID: 2260849

6

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.

Arahata K, Hoffman EP, Kunkel LM, Ishiura S, Tsukahara T, Ishihara T, Sunohara N, Nonaka I, Ozawa E, Sugita H. Arahata K, et al. Proc Natl Acad Sci U S A. 1989 Sep;86(18):7154-8. doi: 10.1073/pnas.86.18.7154. Proc Natl Acad Sci U S A. 1989. PMID: 2674948 Free PMC article.

7

[The pathogenesis of Duchenne muscular dystrophy--defects of the membrane cytoskeleton "dystrophin"].

Arahata K, Sugita H. Arahata K, et al. Nihon Rinsho. 1989 Aug;47(8):1857-64. Nihon Rinsho. 1989. PMID: 2685400 Review. Japanese. No abstract available.

8

Dystrophin and the membrane hypothesis of muscular dystrophy.

Arahata K, Sugita H. Arahata K, et al. Trends Pharmacol Sci. 1989 Nov;10(11):437-9. doi: 10.1016/S0165-6147(89)80005-7. Trends Pharmacol Sci. 1989. PMID: 2692255 Review. No abstract available.

9

Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing.

Khurana TS, Prendergast RA, Alameddine HS, Tomé FM, Fardeau M, Arahata K, Sugita H, Kunkel LM. Khurana TS, et al. Among authors: arahata k. J Exp Med. 1995 Aug 1;182(2):467-75. doi: 10.1084/jem.182.2.467. J Exp Med. 1995. PMID: 7629506 Free PMC article.

10

Elevated basic fibroblast growth factor in the serum of patients with Duchenne muscular dystrophy.

D'Amore PA, Brown RH Jr, Ku PT, Hoffman EP, Watanabe H, Arahata K, Ishihara T, Folkman J. D'Amore PA, et al. Among authors: arahata k. Ann Neurol. 1994 Mar;35(3):362-5. doi: 10.1002/ana.410350320. Ann Neurol. 1994. PMID: 8122890

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

193 results

Search Page

Filters