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1 |
Material Type: Tese de Doutorado
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Psychanalyse et génétique médicale : une rencontre possible à partir du syndrome du chromosome X fragileVarela, Andrea SousaBiblioteca Digital de Teses e Dissertações da USP; Universidade de São Paulo; Instituto de Psicologia 2017-10-05Acesso online. A biblioteca também possui exemplares impressos. |
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Material Type: Livro
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The Fragile X syndromeK. E Davies (Kay E.)Oxford New York Oxford University Press 1989Localização: FOB - Fac. Odontologia de Bauru (616.043 F842 ) e outros locais(Acessar) |
3 |
Material Type: Artigo
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FMRP regulates postnatal neuronal migration via MAP1BMessaoudi, Salima ; Allam, Ada ; Stoufflet, Julie ; Paillard, Theo ; Le Ven, Anaïs ; Fouquet, Coralie ; Doulazmi, Mohamed ; Trembleau, Alain ; Caille, IsabelleeLife, 2024-05, Vol.12 [Periódico revisado por pares]England: eLife Science Publications, LtdTexto completo disponível |
4 |
Material Type: Artigo
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Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping diseaseIshiura, Hiroyuki ; Shibata, Shota ; Yoshimura, Jun ; Suzuki, Yuta ; Qu, Wei ; Doi, Koichiro ; Almansour, M Asem ; Kikuchi, Junko Kanda ; Taira, Makiko ; Mitsui, Jun ; Takahashi, Yuji ; Ichikawa, Yaeko ; Mano, Tatsuo ; Iwata, Atsushi ; Harigaya, Yasuo ; Matsukawa, Miho Kawabe ; Matsukawa, Takashi ; Tanaka, Masaki ; Shirota, Yuichiro ; Ohtomo, Ryo ; Kowa, Hisatomo ; Date, Hidetoshi ; Mitsue, Aki ; Hatsuta, Hiroyuki ; Morimoto, Satoru ; Murayama, Shigeo ; Shiio, Yasushi ; Saito, Yuko ; Mitsutake, Akihiko ; Kawai, Mizuho ; Sasaki, Takuya ; Sugiyama, Yusuke ; Hamada, Masashi ; Ohtomo, Gaku ; Terao, Yasuo ; Nakazato, Yoshihiko ; Takeda, Akitoshi ; Sakiyama, Yoshio ; Umeda-Kameyama, Yumi ; Shinmi, Jun ; Ogata, Katsuhisa ; Kohno, Yutaka ; Lim, Shen-Yang ; Tan, Ai Huey ; Shimizu, Jun ; Goto, Jun ; Nishino, Ichizo ; Toda, Tatsushi ; Morishita, Shinichi ; Tsuji, ShojiNature genetics, 2019-08, Vol.51 (8), p.1222-1232 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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The translation of translational control by FMRP: therapeutic targets for FXSDarnell, Jennifer C ; Klann, EricNature neuroscience, 2013-11, Vol.16 (11), p.1530-1536 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Fragile X syndrome and associated disorders: Clinical aspects and pathologySalcedo-Arellano, Maria Jimena ; Dufour, Brett ; McLennan, Yingratana ; Martinez-Cerdeno, Veronica ; Hagerman, RandiNeurobiology of disease, 2020-03, Vol.136, p.104740-104740, Article 104740 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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The molecular biology of FMRP: new insights into fragile X syndromeRichter, Joel D ; Zhao, XinyuNature reviews. Neuroscience, 2021-04, Vol.22 (4), p.209-222 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 GeneLiu, X. Shawn ; Wu, Hao ; Krzisch, Marine ; Wu, Xuebing ; Graef, John ; Muffat, Julien ; Hnisz, Denes ; Li, Charles H. ; Yuan, Bingbing ; Xu, Chuanyun ; Li, Yun ; Vershkov, Dan ; Cacace, Angela ; Young, Richard A. ; Jaenisch, RudolfCell, 2018-02, Vol.172 (5), p.979-992.e6 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
9 |
Material Type: Artigo
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Altered Neuronal and Circuit Excitability in Fragile X SyndromeContractor, Anis ; Klyachko, Vitaly A. ; Portera-Cailliau, CarlosNeuron (Cambridge, Mass.), 2015-08, Vol.87 (4), p.699-715 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
10 |
Material Type: Artigo
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Genetic Removal of p70 S6 Kinase 1 Corrects Molecular, Synaptic, and Behavioral Phenotypes in Fragile X Syndrome MiceBhattacharya, Aditi ; Kaphzan, Hanoch ; Alvarez-Dieppa, Amanda C. ; Murphy, Jaclyn P. ; Pierre, Philippe ; Klann, EricNeuron (Cambridge, Mass.), 2012-10, Vol.76 (2), p.325-337 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |