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CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasis.
Manzini, M Chiara; Xiong, Lan; Shaheen, Ranad; Tambunan, Dimira E; Di Costanzo, Stefania; Mitisalis, Vanessa; Tischfield, David J; Cinquino, Antonella; Ghaziuddin, Mohammed; Christian, Mehtab; Jiang, Qin; Laurent, Sandra; Nanjiani, Zohair A; Rasheed, Saima; Hill, R Sean; Lizarraga, Sofia B; Gleason, Danielle; Sabbagh, Diya; Salih, Mustafa A; Alkuraya, Fowzan S; Walsh, Christopher A.
Afiliação
  • Manzini MC; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Xiong L; Department of Psychiatry, Research Centre of Montreal Mental Health University Institute, University of Montreal, Montreal, QC H1N 3V2, Canada; University of Montreal Hospital Research Centre, Montreal, QC H2L 2W5, Canada.
  • Shaheen R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Tambunan DE; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Di Costanzo S; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Mitisalis V; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Tischfield DJ; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Cinquino A; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Ghaziuddin M; Department of Child and Adolescent Psychiatry, University of Michigan Health System, Ann Arbor, MI 48109, USA.
  • Christian M; University of Montreal Hospital Research Centre, Montreal, QC H2L 2W5, Canada.
  • Jiang Q; Department of Psychiatry, Research Centre of Montreal Mental Health University Institute, University of Montreal, Montreal, QC H1N 3V2, Canada.
  • Laurent S; University of Montreal Hospital Research Centre, Montreal, QC H2L 2W5, Canada.
  • Nanjiani ZA; Ma Ayesha Memorial Centre, University of Karachi, Karachi 75350, Pakistan.
  • Rasheed S; Autism Institute, Karachi 74000, Pakistan.
  • Hill RS; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Lizarraga SB; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Gleason D; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
  • Sabbagh D; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA; Department of
  • Salih MA; Division of Pediatric Neurology, Department of Pediatrics, King Saud University College of Medicine, Riyadh 11461, Saudi Arabia. Electronic address: mustafa_salih05@yahoo.com.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia. Electronic address: falkuraya@kfshrc.edu.sa.
  • Walsh CA; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815-6789, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA; Program in Me
Cell Rep ; 8(3): 647-55, 2014 Aug 07.
Article em En | MEDLINE | ID: mdl-25066123
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtornos Globais do Desenvolvimento Infantil / NF-kappa B / Proteínas de Ligação a DNA / Deficiência Intelectual / Neurônios Limite: Animals / Humans Idioma: En Revista: Cell Rep Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtornos Globais do Desenvolvimento Infantil / NF-kappa B / Proteínas de Ligação a DNA / Deficiência Intelectual / Neurônios Limite: Animals / Humans Idioma: En Revista: Cell Rep Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos