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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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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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Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutationsMelo, U.S. ; Freua, F. ; Lynch, D.S. ; Ripa, B.D. ; Tenorio, R.B. ; Saute, J.A.M. ; de Souza Leite, F. ; Kitajima, J. ; Houlden, H. ; Zatz, M. ; Kok, F.Clinical genetics, 2018-11, Vol.94 (5), p.482-483 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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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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Human Endometrial-Derived Mesenchymal Stem Cells Suppress Inflammation in the Central Nervous System of EAE MicePeron, J. P. S. ; Jazedje, T. ; Brandão, W. N. ; Perin, P. M. ; Maluf, M. ; Evangelista, L. P. ; Halpern, S. ; Nisenbaum, M. G. ; Czeresnia, C. E. ; Zatz, M. ; Câmara, N. O. S. ; Rizzo, L. V.Stem cell reviews, 2012-09, Vol.8 (3), p.940-952 [Periódico revisado por pares]New York: Humana Press IncTexto completo disponível |
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The p.P56S mutation in the VAPB gene is not due to a single founder: the first European caseFunke, AD ; Esser, M ; Krüttgen, A ; Weis, J ; Mitne-Neto, M ; Lazar, M ; Nishimura, AL ; Sperfeld, AD ; Trillenberg, P ; Senderek, J ; Krasnianski, M ; Zatz, M ; Zierz, S ; Deschauer, MClinical genetics, 2010-03, Vol.77 (3), p.302-303 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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Tracking inorganic elements in GRMD blood dogs submitted to hASCs investigated by NAA techniqueMetairon, S. ; Zamboni, C. B. ; Suzuki, M. F. ; Bueno, C. R. ; Andrade, T. O. ; Landini, V. ; Cangussu, E. B. ; Zatz, M.Journal of radioanalytical and nuclear chemistry, 2016-03, Vol.307 (3), p.1645-1649 [Periódico revisado por pares]Dordrecht: Springer NetherlandsTexto completo disponível |
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Material Type: Artigo
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MECHANISMS OF DISEASE: Calpains and DiseaseZatz, Mayana ; Starling, AlessandraThe New England journal of medicine, 2005-06, Vol.352 (23), p.2413 [Periódico revisado por pares]Boston: Massachusetts Medical SocietyTexto completo disponível |
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Material Type: Artigo
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Human Multipotent Mesenchymal Stromal Cells from Distinct Sources Show Different In Vivo Potential to Differentiate into Muscle Cells When Injected in Dystrophic MiceVieira, N. M. ; Zucconi, E. ; Bueno, C. R. ; Secco, M. ; Suzuki, M. F. ; Bartolini, P. ; Vainzof, M. ; Zatz, M.Stem cell reviews, 2010-12, Vol.6 (4), p.560-566 [Periódico revisado por pares]New York: Humana Press IncTexto completo disponível |
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A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13Nishimura, A L ; Mitne-Neto, M ; Silva, H C A ; Oliveira, J R M ; Vainzof, M ; Zatz, MJournal of medical genetics, 2004-04, Vol.41 (4), p.315-320 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |