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Muhammad Ayub

Showing results (231-240 of 261) with videos related to

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Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
American Journal of Human Genetics|September 13, 2016
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic FeaturesAnide Johansen, Rasim O Rosti, Damir Musaev, et al.
Human Genetics|September 1, 2019
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimatesQing Ouyang, Brian C Kavanaugh, Lena Joesch-Cohen, et al.
American Journal of Human Genetics|May 1, 2012
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disabilityMuzammil Ahmad Khan, Muhammad Arshad Rafiq, Abdul Noor, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 12, 2013
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disabilityEske M Derks, Muhammad Ayub, Kimberly Chambert, et al.
American Journal of Human Genetics|December 17, 2009
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationAsif Mir, Liana Kaufman, Abdul Noor, et al.
Journal of Medical Internet Research|September 4, 2020
Current Challenges of Digital Health Interventions in Pakistan: Mixed Methods AnalysisAbdul Momin Kazi, Saad Ahmed Qazi, Nazia Ahsan, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Medcomm|March 25, 2024
A novel in-frame deletion in KIF5C gene causes infantile onset epilepsy and psychomotor retardationSantasree Banerjee, Qiang Zhao, Bo Wang, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Pageof 27

Showing results (231-240 of 261) with videos related to

Sort By:
Pageof 27
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
American Journal of Human Genetics|September 13, 2016
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic FeaturesAnide Johansen, Rasim O Rosti, Damir Musaev, et al.
Human Genetics|September 1, 2019
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimatesQing Ouyang, Brian C Kavanaugh, Lena Joesch-Cohen, et al.
American Journal of Human Genetics|May 1, 2012
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disabilityMuzammil Ahmad Khan, Muhammad Arshad Rafiq, Abdul Noor, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 12, 2013
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disabilityEske M Derks, Muhammad Ayub, Kimberly Chambert, et al.
American Journal of Human Genetics|December 17, 2009
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationAsif Mir, Liana Kaufman, Abdul Noor, et al.
Journal of Medical Internet Research|September 4, 2020
Current Challenges of Digital Health Interventions in Pakistan: Mixed Methods AnalysisAbdul Momin Kazi, Saad Ahmed Qazi, Nazia Ahsan, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Medcomm|March 25, 2024
A novel in-frame deletion in KIF5C gene causes infantile onset epilepsy and psychomotor retardationSantasree Banerjee, Qiang Zhao, Bo Wang, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Pageof 27