Your browser doesn't support javascript.
loading
Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.
Jacquemont, Sébastien; Pacini, Laura; Jønch, Aia E; Cencelli, Giulia; Rozenberg, Izabela; He, Yunsheng; D'Andrea, Laura; Pedini, Giorgia; Eldeeb, Marwa; Willemsen, Rob; Gasparini, Fabrizio; Tassone, Flora; Hagerman, Randi; Gomez-Mancilla, Baltazar; Bagni, Claudia.
Afiliação
  • Jacquemont S; Sainte-Justine University Hospital Research Centre, Montreal, QC H3T 1C5.
  • Pacini L; University of Montreal, Montreal, QC H3T 1J4, Canada.
  • Jønch AE; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • Cencelli G; Department of Clinical Genetics, Odense University Hospital.
  • Rozenberg I; Human Genetics, Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
  • He Y; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • D'Andrea L; Neuroscience Translational Medicine, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Pedini G; Biomarker Development, Novartis Institutes for Biomedical Research, Cambridge, MA, USA.
  • Eldeeb M; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • Willemsen R; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • Gasparini F; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California, Davis Medical Center, Sacramento, CA, USA.
  • Tassone F; Department of Clinical Genetics, Erasmus Medical Center, DRRotterdam, Netherlands.
  • Hagerman R; Neuroscience Discovery, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Gomez-Mancilla B; Department of Biochemistry and Molecular Medicine and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute.
  • Bagni C; Department of Pediatric and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis, School of Medicine, Sacramento, CA, USA.
Hum Mol Genet ; 27(21): 3825, 2018 11 01.
Article em En | MEDLINE | ID: mdl-30107584
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article