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Maria Asif

Showing results (1-10 of 20) with videos related to

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Cureus|April 29, 2024
Valproic Acid-Induced Thrombocytopenia in Treatment-Resistant GABRB3 Genetic Epilepsy: A Case ReportMatthew Schuler, Ali Shammout, Maria Asif, et al.
Cells|February 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic MicrocephalyMaria Asif, Uzma Abdullah, Peter Nürnberg, et al.
Molecular Biology Reports|November 20, 2019
Nesprin-1 impact on tumorigenic cell phenotypesIlknur Sur-Erdem, Muhammed Sajid Hussain, Maria Asif, et al.
Genes|May 4, 2026
Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with <i>SGSH</i> and <i>GALNS</i> DeficienciesFarheen Nasir Awan, Shumaila Zulfiqar, Liza Eiman, et al.
Genes|December 24, 2021
Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani FamiliesAmbrin Fatima, Uzma Abdullah, Muhammad Farooq, et al.
American Journal of Medical Genetics. Part A|December 16, 2021
A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish familyMaria Asif, Ionut Dragos Mocanu, Uzma Abdullah, et al.
Molecular Biology Reports|January 15, 2024
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani familyKomal Aslam, Aysha Saeed, Iffat Jamil, et al.
Plos Genetics|July 8, 2017
Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damageJoakim Klar, Jörg Piontek, Susanne Milatz, et al.
Molecular Biology Reports|June 26, 2024
Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephalyKomal Aslam, Aysha Saeed, Hafiza Iqra Saeed, et al.
Frontiers in Genetics|January 20, 2026
Expanding the mutational spectrum of congenital microcephaly in Pakistani familiesSundas Farooq, Maria Asif, Ansar A Abbasi, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Cureus|April 29, 2024
Valproic Acid-Induced Thrombocytopenia in Treatment-Resistant GABRB3 Genetic Epilepsy: A Case ReportMatthew Schuler, Ali Shammout, Maria Asif, et al.
Cells|February 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic MicrocephalyMaria Asif, Uzma Abdullah, Peter Nürnberg, et al.
Molecular Biology Reports|November 20, 2019
Nesprin-1 impact on tumorigenic cell phenotypesIlknur Sur-Erdem, Muhammed Sajid Hussain, Maria Asif, et al.
Genes|May 4, 2026
Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with <i>SGSH</i> and <i>GALNS</i> DeficienciesFarheen Nasir Awan, Shumaila Zulfiqar, Liza Eiman, et al.
Genes|December 24, 2021
Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani FamiliesAmbrin Fatima, Uzma Abdullah, Muhammad Farooq, et al.
American Journal of Medical Genetics. Part A|December 16, 2021
A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish familyMaria Asif, Ionut Dragos Mocanu, Uzma Abdullah, et al.
Molecular Biology Reports|January 15, 2024
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani familyKomal Aslam, Aysha Saeed, Iffat Jamil, et al.
Plos Genetics|July 8, 2017
Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damageJoakim Klar, Jörg Piontek, Susanne Milatz, et al.
Molecular Biology Reports|June 26, 2024
Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephalyKomal Aslam, Aysha Saeed, Hafiza Iqra Saeed, et al.
Frontiers in Genetics|January 20, 2026
Expanding the mutational spectrum of congenital microcephaly in Pakistani familiesSundas Farooq, Maria Asif, Ansar A Abbasi, et al.
Pageof 2