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Material Type: Artigo
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ALS-associated VRK1 R321C mutation causes proteostatic imbalance and mitochondrial defects in iPSC-derived motor neuronsOliveira, D. ; Assoni, A.F. ; Alves, L.M. ; Sakugawa, A. ; Melo, U.S. ; Teles e Silva, A.L. ; Sertie, A.L. ; Caires, L.C. ; Goulart, E. ; Ghirotto, B. ; Carvalho, V.M. ; Ferrari, M.R. ; Zatz, M.Neurobiology of disease, 2024-08, Vol.198, p.106540, Article 106540 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disabilityFigueiredo, T ; Melo, U S ; Pessoa, A L S ; Nobrega, P R ; Kitajima, J P ; Rusch, H ; Vaz, F ; Lucato, L T ; Zatz, M ; Kok, F ; Santos, SMolecular psychiatry, 2016-08, Vol.21 (8), p.1125-1129 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell typesChaurasia, S. S. ; Rollag, M. D. ; Jiang, G. ; Hayes, W. P. ; Haque, R. ; Natesan, A. ; Zatz, M. ; Tosini, G. ; Liu, C. ; Korf, H. W. ; Iuvone, P. M. ; Provencio, I.Journal of neurochemistry, 2005-01, Vol.92 (1), p.158-170 [Periódico revisado por pares]Oxford, UK: Blackwell Science LtdTexto completo disponível |
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Material Type: Artigo
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Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinZatz, M ; Pavanello, R.C.M ; Lazar, M ; Yamamoto, G.L ; Lourenço, N.C.V ; Cerqueira, A ; Nogueira, L ; Vainzof, MNeuromuscular disorders : NMD, 2014-11, Vol.24 (11), p.986-989 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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African ancestry protects against Alzheimer's disease-related neuropathologySCHLESINGER, D ; GRINBERG, L. T ; DOS SANTOS, Acf ; BRENTANI, H ; PASQUALUCCI, C. A ; NITRINI, R ; JACOB-FILHO, W ; ZATZ, M ; ALBA, J. G ; NASLAVSKY, M. S ; LICINIO, L ; FARFEL, J. M ; SUEMOTO, C. K ; DE LUCENA FERRETTI, R. E ; LEITE, Rep ; DE ANDRADE, M. PMolecular psychiatry, 2013-01, Vol.18 (1), p.79-85 [Periódico revisado por pares]Basingstoke: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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A normal life without muscle dystrophinZatz, M ; Vieira, N.M ; Zucconi, E ; Pelatti, M ; Gomes, J ; Vainzof, M ; Martins-Bach, A.B ; Garcia Otaduy, M.C ; Bento dos Santos, G ; Amaro, E ; Landini, V ; Andrade, TNeuromuscular disorders : NMD, 2015-05, Vol.25 (5), p.371-374 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)Tonini, M.M.O ; Passos-Bueno, M.R ; Cerqueira, A ; Matioli, S.R ; Pavanello, R ; Zatz, MNeuromuscular disorders : NMD, 2004, Vol.14 (1), p.33-38 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strengthAmbrósio, C.E ; Valadares, M.C ; Zucconi, E ; Cabral, R ; Pearson, P.L ; Gaiad, T.P ; Canovas, M ; Vainzof, M ; Miglino, M.A ; Zatz, MNeuromuscular disorders : NMD, 2008-11, Vol.18 (11), p.892-893 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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The human serotonin transporter gene explains why some populations are more optimistic?Nishimura, A L ; Oliveira, J R M ; Zatz, MMolecular psychiatry, 2009-09, Vol.14 (9), p.828-828 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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The Genetics of Alzheimer’s Disease in Brazil: 10 Years of Analysis in a Unique PopulationOliveira, J. R. M. ; Nishimura, A. L. ; Lemos, R. R. ; Zatz, M.Journal of molecular neuroscience, 2009, Vol.37 (1), p.74-79 [Periódico revisado por pares]New York: Humana Press IncTexto completo disponível |