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Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability.
Sheikh, Taimoor I; Vasli, Nasim; Pastore, Stephen; Kharizi, Kimia; Harripaul, Ricardo; Fattahi, Zohreh; Pande, Shruti; Naeem, Farooq; Hussain, Abrar; Mir, Asif; Islam, Omar; Girisha, Katta Mohan; Irfan, Muhammad; Ayub, Muhammad; Schwarzer, Christoph; Najmabadi, Hossein; Shukla, Anju; Sladky, Valentina C; Braun, Vincent Zoran; Garcia-Carpio, Irmina; Villunger, Andreas; Vincent, John B.
Afiliação
  • Sheikh TI; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, M5T 1R8, Canada.
  • Vasli N; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Pastore S; Molecular Genetics Laboratory, North York General Hosptial Genetics Program, Toronto, ON, M2K 1E1, Canada.
  • Kharizi K; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, M5T 1R8, Canada.
  • Harripaul R; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, M5T 1R8, Canada.
  • Fattahi Z; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Pande S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, 19834, Iran.
  • Naeem F; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, M5T 1R8, Canada.
  • Hussain A; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Mir A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, 19834, Iran.
  • Islam O; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
  • Girisha KM; General and Health Systems Psychiatry, Centre for Addiction and Mental Health, Toronto, ON, M5T 1R8, Canada.
  • Irfan M; Department of Psychiatry, University of Toronto, Toronto, ON, M5T 1R8, Canada.
  • Ayub M; Human Molecular Genetics Lab, Department of Biological Sciences, FBAS, International Islamic University, Islamabad, Pakistan.
  • Schwarzer C; Human Molecular Genetics Lab, Department of Biological Sciences, FBAS, International Islamic University, Islamabad, Pakistan.
  • Najmabadi H; Department of Diagnostic Radiology, Queens University, Kingston, ON, K7L 2V7, Canada.
  • Shukla A; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
  • Sladky VC; Department of Mental Health, Psychiatry and Behavioural Sciences, Peshawar Medical College, Riphah International University, Islamabad, Pakistan.
  • Braun VZ; Lahore Institute of Research & Development, Lahore, 51000, Pakistan.
  • Garcia-Carpio I; Department of Psychiatry, Queen's University, Kingston, ON, K7L 3N6, Canada.
  • Villunger A; Department of Pharmacology, Medical University of Innsbruck, Innsbruck, Austria.
  • Vincent JB; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, 19834, Iran.
Transl Psychiatry ; 11(1): 1, 2021 01 05.
Article em En | MEDLINE | ID: mdl-33414379

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína Adaptadora de Sinalização CRADD / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína Adaptadora de Sinalização CRADD / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article