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METTL23, a transcriptional partner of GABPA, is essential for human cognition.
Reiff, Rachel E; Ali, Bassam R; Baron, Byron; Yu, Timothy W; Ben-Salem, Salma; Coulter, Michael E; Schubert, Christian R; Hill, R Sean; Akawi, Nadia A; Al-Younes, Banan; Kaya, Namik; Evrony, Gilad D; Al-Saffar, Muna; Felie, Jillian M; Partlow, Jennifer N; Sunu, Christine M; Schembri-Wismayer, Pierre; Alkuraya, Fowzan S; Meyer, Brian F; Walsh, Christopher A; Al-Gazali, Lihadh; Mochida, Ganeshwaran H.
Afiliação
  • Reiff RE; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Harvard-Massachusetts Institute of Technology (MIT) Division of Health Sciences and Technology, Cambridge, MA 021
  • Ali BR; Department of Pathology, College of Medicine and Health Sciences.
  • Baron B; Department of Anatomy, Faculty of Medicine and Surgery, University of Malta, Msida MSD2080, Malta.
  • Yu TW; Division of Genetics and Genomics, Department of Medicine Department of Pediatrics Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA Program in Medical and Population Genetics, Broad Institute of MIT and Harvard University, Cambridge, MA 02142,
  • Ben-Salem S; Department of Pathology, College of Medicine and Health Sciences.
  • Coulter ME; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Harvard-Massachusetts Institute of Technology (MIT) Division of Health Sciences and Technology, Cambridge, MA 021
  • Schubert CR; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Department of Pediatrics Research Laboratory of Electronics and Department of Electrical Engineering and Computer
  • Hill RS; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
  • Akawi NA; Department of Pathology, College of Medicine and Health Sciences.
  • Al-Younes B; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.
  • Kaya N; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.
  • Evrony GD; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Program in Biological and Biomedical Sciences and.
  • Al-Saffar M; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Department of Paediatrics, College of Medicine and Health Sciences, United Arab Emirates University, PO Box 17666
  • Felie JM; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
  • Partlow JN; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
  • Sunu CM; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
  • Schembri-Wismayer P; Department of Anatomy, Faculty of Medicine and Surgery, University of Malta, Msida MSD2080, Malta.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
  • Meyer BF; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.
  • Walsh CA; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA Department of Pediatrics Department of Neurology, Harvard Medical School, Boston, MA 02115, USA Program in Medica
  • Al-Gazali L; Department of Paediatrics, College of Medicine and Health Sciences, United Arab Emirates University, PO Box 17666, Al-Ain, United Arab Emirates.
  • Mochida GH; Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Department of Pediatrics Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA ganesh.mochida@childrens.harvard.edu.
Hum Mol Genet ; 23(13): 3456-66, 2014 Jul 01.
Article em En | MEDLINE | ID: mdl-24501276
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metilases de Modificação do DNA / Fator de Transcrição de Proteínas de Ligação GA Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metilases de Modificação do DNA / Fator de Transcrição de Proteínas de Ligação GA Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article