Books, Original Papers & Review Papers- AOKI Masashi -
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[B]:Books [O]:Original Papers [R]:Review Papers
total:479
[2003]
341.[O] Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype..[Neurology,60(11),(2003),1799-1804]Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown R H Jr, Saito H, Itoyama Y
342.[O] Mutant SOD1 linked to familial amyotrophic lateral sclerosis, but not wild-type SOD1, induces ER stress in COS7 cells and transgenic mice..[Biochem Biophys Res Commun,303(2),(2003),496-503]Tobisawa Shinsuke, Hozumi Yasukazu, Arawaka Shigeki, Koyama Shingo, Wada Manabu, Nagai Makiko, Aoki Masashi, Itoyama Yasuto, Goto Kaoru, Kato Takeo
[2002]
343.[O] Miyoshi myopathy patients with novel 5' splicing donor site mutations showed different dysferlin immunostaining at the sarcolemma..[Acta Neuropathol (Berl),104(6),(2002),615-620]Saito Akiko, Higuchi Itsuro, Nakagawa Masanori, Saito Mineki, Hirata Keiko, Suehara Masahito, Yoshida Yoshihiro, Takahashi Toshiaki, Aoki Masashi, Osame Mitsuhiro
344.[O] Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy..[Neurology,59(11),(2002),1689-1693]Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I
345.[R] 最新創薬 薬の分子メカニズム 筋萎縮性側索硬化症に対する治療薬の開発 グルタミン酸仮説からトランスジェニックラットモデルを用いた新規治療法の開発.[Molecular Medicine,39(9), (2002), 1074-1078]青木 正志
346.[R] 臨床に必要な神経化学 トランスジェニックラットによる新しいALSモデル.[Clinical Neuroscience,20(8), (2002), 858-859]青木 正志
347.[R] 【神経疾患と再生医療】 新しい筋萎縮性側索硬化症(ALS)モデル動物.[最新医学,57(7), (2002), 1622-1627]青木 正志, 永井 真貴子, 加藤 昌昭, 糸山 泰人
348.[O] Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy..[Neurology,58(2),(2002),323-325]Tateyama M, Aoki M, Nishino I, Hayashi Y K, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y
[2001]
349.[O] Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease..[J Neurosci,21(23),(2001),9246-9254]Nagai M, Aoki M, Miyoshi I, Kato M, Pasinelli P, Kasai N, Brown R H Jr, Itoyama Y
350.[O] An autopsy case of atypical friedreich's ataxia with chronic idiopathic intestinal pseudo-obstruction.[Clinical Neurology,41,(2001),412-417]Tetsuya Nagata, Masashi Aoki, Takafumi Hasegawa, Yusei Shiga, Takeshi Hayashi, Jun Higuchi, Koji Abe, Takashi Tanno, Hidehiko Konno, Yasuto Itoyama
http://www.ncbi.nlm.nih.gov/pubmed/11808352 http://www.scopus.com/inward/record.url?eid=0035726356&partnerID=40
351.[O] ABCD1 translation-initiator mutation demonstrates genotype-phenotype correlation for AMN..[Neurology,57(11),(2001),1956-1962]O'Neill G N, Aoki M, Brown R H Jr
352.[O] The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin..[Nat Genet,29(2),(2001),189-193]Moreira M C, Barbot C, Tachi N, Kozuka N, Uchida E, Gibson T, Mendonca P, Costa M, Barros J, Yanagisawa T, Watanabe M, Ikeda Y, Aoki M, Nagata T, Coutinho P, Sequeiros J, Koenig M
353.[O] Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation..[Neurosci Lett,312(3),(2001),165-168]Kato M, Aoki M, Ohta M, Nagai M, Ishizaki F, Nakamura S, Itoyama Y
354.[R] ALS models by transgenic animals.[Brain and Nerve,53, (2001), 799-807]M. Aoki, M. Nagai, M. Kato, Y. Itoyama
http://www.ncbi.nlm.nih.gov/pubmed/11596474 http://www.scopus.com/inward/record.url?eid=0034806120&partnerID=40
355.[R] [ALS models by transgenic animals] (No To Shinkei).[No To Shinkei,53(9), (2001), 799-807]Aoki M, Nagai M, Kato M, Itoyama Y
356.[R] 【遺伝子改変動物から神経変性疾患へのアプローチ】 トランスジェニック動物によるALSモデル.[脳と神経,53(9), (2001), 799-807]青木 正志, 永井 真貴子, 加藤 昌昭, 糸山 泰人
357.[O] Establishment of a local cooling model against spinal cord ischemia representing prolonged induction of heat shock protein..[J Thorac Cardiovasc Surg,122(2),(2001),351-357]Motoyoshi N, Sakurai M, Hayashi T, Aoki M, Abe K, Itoyama Y, Tabayashi K
358.[O] The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle..[Hum Mol Genet,10(17),(2001),1761-1766]Matsuda C, Hayashi Y K, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown R H Jr
359.[O] [An autopsy case of atypical Friedreich's ataxia with chronic idiopathic intestinal pseudo-obstruction].[Rinsho Shinkeigaku,41(7),(2001),412-417]Nagata T, Aoki M, Hasegawa T, Shiga Y, Hayashi T, Higuchi J, Abe K, Tanno T, Konno H, Itoyama Y
360.[O] Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy..[Neurology,57(2),(2001),271-278]Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers S M, Oeltjen J, Brown H E, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn R J, Urtizberea J A, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann J S, Brown R H Jr
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