204 件中 81 - 100 件目
英語 :Takahashi S, Matsumoto N, Okayama A, Suzuki N, Araki A, Okajima K, Tanaka H, Miyamoto A , FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome , Clin Genet, 82 (569 - 573) , 2012 , (IF:3.128)
英語 :Xiaojuan H, Takahashi S, Suzuki H, Hashikawa T, Kulkarni AB, Mikoshiba K, Ohshima T , Hypomyelination phenotype caused by impaired differentiation of oligodendrocytes in Emx1-cre mediated Cdk5 conditional knockout mice , Neurochem Res, 36 (1293 - 1303) , 2011 , (IF:2.722)
英語 :Tachi N, Takahashi S, Jo M, Shinoda M , A new mutation of GCH1 in triplets family with dopa-responsive dystonia , Eur J Neurol, 18 (1191 - 1193) , 2011 , (IF:3.692)
英語 :Hara M, Nishi Y, Yamashita Y, Yoh J, Takahashi S, Nagamitsu SI, Kakuma T, Hosoda H, Kangawa K, Kojima M, Matsuishi T , Ghrelin levels are reduced Rett syndrome patients with eating difficulties , Int J Dev Neurosci, 29 (899 - 902) , 2011 , (IF:2.418)
英語 :Muto A, Oguni H, Takahashi Y, Shirasaka Y, Sawaishi Y, Yano T, Hoshida T, Osaka H, Nakasu S, Akasaka N, Sugai K, Miyamoto A, Takahashi S, Suzuki M, Ohmori I, Nabatame S, Osawa M , Nationwide survey (incidence, clinical course, prognosis) of Rasmussen’s encephalitis. , Brain Dev , 32 (445 - 453) , 2010 , (IF:2.119)
英語 :Takahashi S, Ohshima T, Hirasawa M, Pareek TK, Bugge TH, Morozov A, Fujieda K, Brady RO, Kulkarni AB , Conditional deletion of neuronal cyclin-dependent kinase 5 in developing forebrain results in microglial activation and neurodegeneration. , Am J Pathol, 176 (320 - 329) , 2010 , (IF:5.697)
英語 :Zheng YL, Li BS, Rudrabhatla P, Shukla V, Amin ND, Maric D, Kesavapany S, Kanungo J, Pareek TK, Takahashi S, Grant P, Kulkarni AB, Pant HC , Phosphorylation of p27Kip1 at Thr187 by Cyclin-dependent Kinase 5 Modulates Neural Stem Cell Differentiation , Mol Biol Cell , 21 (3601 - 3614) , 2010 , (IF:5.979)
英語 :Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K , Increased expression of matrix metalloproteinase-9 and hepatocyte growth factor in the cerebrospinal fluid of infants with posthemorrhagic hydrocephalus , Early Hum Dev, 86 (251 - 254) , 2010 , (IF:2.122)
英語 :Tanaka H, Amamiya S, Takahashi S, Suzuki N, Araki A, Ohinata J, Fujieda K , Effect of neonatal hypoxia on the development of intraspinal serotonergic fibers in relation to spinal motoneurons. , Brain Dev, 32 (4) (268 - 274) , 2010 , (IF:2.119)
英語 :Maimaiti M, Takahashi S, Okajima K, Suzuki N, Ohinata J, Araki A, Tanaka H, Mukai T, Fujieda K , Silent exonic mutation in the acid-alpha-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing, , J Hum Genet , 54 (493 - 496) , 2009 , (IF:2.431)
英語 :Matsumoto N, Takahashi S, Toriumi N, Sarashina T, Makita Y, Tachibana Y, Fujieda K , Acute disseminated encephalomyelitis in an infant with incontinentia pigmenti. , Brain Dev, 31 (625 - 628) , 2009 , (IF:2.119)
英語 :Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K , Transforming growth factor-b1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways , Biochem Biophys Res Comm, 383 (475 - 479) , 2009 , (IF:2.648)
英語 :Ohinata J, Suzuki N, Araki A, Takahashi S, Fujieda K, Tanaka H , Actigraphic assessment of sleep disorders in children with chronic fatigue syndrome , Brain Dev, 30 (329 - 333) , 2008 , (IF:2.119)
英語 : Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M and Fujieda K , Matrix metalloproteinases in infants with posthemorrhagic hydrocephalus. , Early Hum Dev, 84 (137 - 139) , 2008 , (IF:1.738)
英語 :Takahashi S, Ohinata J, Suzuki N, Amamiya S, Kajihama A, Sugai R, Araki A, Fujieda K, Tanaka H , Molecular analysis and anticonvulsant therapy in two patients with glucose transporter 1 deficiency syndrome: A successful use of zonisamide for controlling the seizures. , Epilepsy Res , 80 (18 - 22) , 2008 , (IF:2.405)
英語 :Takahashi S, Ohinata J, Makita Y, Suzuki N, Araki A, Sasaki A, Murono K, Tanaka H, Fujieda K , Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome. , Clin Genet, 73 (257 - 261) , 2008 , (IF:3.206)
英語 :Okamoto T, Shirai M, Kokubo M, Takahashi S, Kajino M, Takase M, Sakata H and Oki J , Human milk reduces the risk of retinal detachment in extremely low birth weight infants. , Pediatr Int, 49 (894 - 897) , 2007 , (IF:0.7)
英語 :Takahashi S, Ohshima T, Cho A, Sreenath T, Iadarola MJ, Pant HC, Kim Y, Nairn AC, Brady RO, Greengard P and Kulkarni AB: , Increased activity of cyclin-dependent kinase 5 leads to attenuation of cocaine-mediated dopamine signaling. , Proc Natl Acad Sci USA , 102 (1737 - 1742) , 2005 , (IF:9.643)
英語 :Takahashi S, Kulkarni AB , Mutant superoxide dismutase 1 causes motor neuron degeneration independent of cyclin-dependent kinase 5 activation by p35 or p25. , J Neurochem , 88 (1295 - 1304) , 2004 , (IF:4.26)
英語 :Griffin SV, Hiromura K, Pippin J, Petermann AT, Blonski MJ, Krofft R, Takahashi S, Kulkarni AB, and Shankland SJ , Cyclin-dependent kinase 5 is a regulator of podocyte differentiation, proliferation, and morphology. , Am J Pathol , 165 (1175 - 1185) , 2004 , (IF:5.697)
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