Yamamoto M - Search Results

1

Repair by Src kinase of function-impaired RET with multiple endocrine neoplasia type 2A mutation with substitutions of tyrosines in the COOH-terminal kinase domain for phenylalanine.

Kato M, Takeda K, Kawamoto Y, Iwashita T, Akhand AA, Senga T, Yamamoto M, Sobue G, Hamaguchi M, Takahashi M, Nakashima I. Kato M, et al. Among authors: yamamoto m. Cancer Res. 2002 Apr 15;62(8):2414-22. Cancer Res. 2002. PMID: 11956105

2

Differential expression of inflammation- and apoptosis-related genes in spinal cords of a mutant SOD1 transgenic mouse model of familial amyotrophic lateral sclerosis.

Yoshihara T, Ishigaki S, Yamamoto M, Liang Y, Niwa J, Takeuchi H, Doyu M, Sobue G. Yoshihara T, et al. Among authors: yamamoto m. J Neurochem. 2002 Jan;80(1):158-67. doi: 10.1046/j.0022-3042.2001.00683.x. J Neurochem. 2002. PMID: 11796754 Free article.

3

Parallel expression of neurotrophic factors and their receptors in chronic inflammatory demyelinating polyneuropathy.

Yamamoto M, Ito Y, Mitsuma N, Li M, Hattori N, Sobue G. Yamamoto M, et al. Muscle Nerve. 2002 Apr;25(4):601-4. doi: 10.1002/mus.10074. Muscle Nerve. 2002. PMID: 11932979

4

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity.

Niwa J, Ishigaki S, Hishikawa N, Yamamoto M, Doyu M, Murata S, Tanaka K, Taniguchi N, Sobue G. Niwa J, et al. Among authors: yamamoto m. J Biol Chem. 2002 Sep 27;277(39):36793-8. doi: 10.1074/jbc.M206559200. Epub 2002 Jul 26. J Biol Chem. 2002. PMID: 12145308 Free article.

5

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: yamamoto m. J Neurochem. 2002 Aug;82(3):576-84. doi: 10.1046/j.1471-4159.2002.00998.x. J Neurochem. 2002. PMID: 12153481 Free article.

6

Differential age-dependent trophic responses of nodose, sensory, and sympathetic neurons to neurotrophins and GDNF: potencies for neurite extension in explant culture.

Niwa H, Hayakawa K, Yamamoto M, Itoh T, Mitsuma T, Sobue G. Niwa H, et al. Among authors: yamamoto m. Neurochem Res. 2002 Jun;27(6):485-96. doi: 10.1023/a:1019896502774. Neurochem Res. 2002. PMID: 12199153

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: yamamoto m. 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: yamamoto m. Arch Neurol. 2002 Nov;59(11):1771-6. doi: 10.1001/archneur.59.11.1771. Arch Neurol. 2002. PMID: 12433265

9

Identification of novel sequence variants in the neurofilament-light gene in a Japanese population: analysis of Charcot-Marie-Tooth disease patients and normal individuals.

Yoshihara T, Yamamoto M, Hattori N, Misu K, Mori K, Koike H, Sobue G. Yoshihara T, et al. Among authors: yamamoto m. J Peripher Nerv Syst. 2002 Dec;7(4):221-4. doi: 10.1046/j.1529-8027.2002.02028.x. J Peripher Nerv Syst. 2002. PMID: 12477167

10

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Hattori N, et al. Among authors: yamamoto m. Brain. 2003 Jan;126(Pt 1):134-51. doi: 10.1093/brain/awg012. Brain. 2003. PMID: 12477701 Review.

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