Sobue G - Search Results

1

Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.

Ohmori H, Ando Y, Makita Y, Onouchi Y, Nakajima T, Saraiva MJ, Terazaki H, Suhr O, Sobue G, Nakamura M, Yamaizumi M, Munar-Ques M, Inoue I, Uchino M, Hata A. Ohmori H, et al. Among authors: sobue g. J Med Genet. 2004 Apr;41(4):e51. doi: 10.1136/jmg.2003.014803. J Med Genet. 2004. PMID: 15060127 Free PMC article. No abstract available.

2

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.

Misu Ki, Hattori N, Nagamatsu M, Ikeda Si, Ando Y, Nakazato M, Takei Yi, Hanyu N, Usui Y, Tanaka F, Harada T, Inukai A, Hashizume Y, Sobue G. Misu Ki, et al. Among authors: sobue g. Brain. 1999 Oct;122 ( Pt 10):1951-62. doi: 10.1093/brain/122.10.1951. Brain. 1999. PMID: 10506096

3

Anticipation in early- but not late-onset familial amyloid polyneuropathy (TTR met 30) in Japan.

Misu K, Hattori N, Ando Y, Ikeda S, Sobue G. Misu K, et al. Among authors: sobue g. Neurology. 2000 Aug 8;55(3):451-2. doi: 10.1212/wnl.55.3.451-a. Neurology. 2000. PMID: 10932290 No abstract available.

4

ABO-incompatible auxiliary partial orthotopic liver transplant for late-onset familial amyloid polyneuropathy.

Watanabe H, Misu K, Kobayashi T, Hattori N, Doyu M, Yokoyama I, Ando Y, Nakao A, Sobue G. Watanabe H, et al. Among authors: sobue g. J Neurol Sci. 2002 Mar 15;195(1):63-6. doi: 10.1016/s0022-510x(01)00678-5. J Neurol Sci. 2002. PMID: 11867075

5

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

Ikeda S, Nakazato M, Ando Y, Sobue G. Ikeda S, et al. Among authors: sobue g. Neurology. 2002 Apr 9;58(7):1001-7. doi: 10.1212/wnl.58.7.1001. Neurology. 2002. PMID: 11940682 Review.

6

X-Linked inhibitor of apoptosis protein is involved in mutant SOD1-mediated neuronal degeneration.

Ishigaki S, Liang Y, Yamamoto M, Niwa J, Ando Y, Yoshihara T, Takeuchi H, Doyu M, Sobue G. Ishigaki S, et al. Among authors: sobue g. J Neurochem. 2002 Aug;82(3):576-84. doi: 10.1046/j.1471-4159.2002.00998.x. J Neurochem. 2002. PMID: 12153481 Free article.

7

Differentially expressed genes in sporadic amyotrophic lateral sclerosis spinal cords--screening by molecular indexing and subsequent cDNA microarray analysis.

Ishigaki S, Niwa Ji, Ando Y, Yoshihara T, Sawada Ki, Doyu M, Yamamoto M, Kato K, Yotsumoto Y, Sobue G. Ishigaki S, et al. Among authors: sobue g. FEBS Lett. 2002 Nov 6;531(2):354-8. doi: 10.1016/s0014-5793(02)03546-9. FEBS Lett. 2002. PMID: 12417341 Free article.

8

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form.

Koike H, Misu K, Ikeda S, Ando Y, Nakazato M, Ando E, Yamamoto M, Hattori N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Koike H, et al. Among authors: sobue g. Arch Neurol. 2002 Nov;59(11):1771-6. doi: 10.1001/archneur.59.11.1771. Arch Neurol. 2002. PMID: 12433265

9

Caspase-1 and -3 mRNAs are differentially upregulated in motor neurons and glial cells in mutant SOD1 transgenic mouse spinal cord: a study using laser microdissection and real-time RT-PCR.

Ando Y, Liang Y, Ishigaki S, Niwa J, Jiang Y, Kobayashi Y, Yamamoto M, Doyu M, Sobue G. Ando Y, et al. Among authors: sobue g. Neurochem Res. 2003 Jun;28(6):839-46. doi: 10.1023/a:1023258923002. Neurochem Res. 2003. PMID: 12718436

10

Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan.

Sobue G, Koike H, Misu K, Hattori N, Yamamoto M, Ikeda S, Ando Y, Nakazato M, Inukai A. Sobue G, et al. Amyloid. 2003 Aug;10 Suppl 1:32-8. Amyloid. 2003. PMID: 14640040

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