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Muhammad Ansar

Showing results (101-110 of 191) with videos related to

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NPJ Genomic Medicine|November 12, 2021
Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, et al.
Archives of Dermatological Research|June 25, 2009
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasiaZahid Azeem, Syed Kamran-Ul-Hassan Naqvi, Muhammad Ansar, et al.
Genes|August 26, 2023
Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia PatientsRabia Basharat, Kim Rodenburg, María Rodríguez-Hidalgo, et al.
Plants (Basel, Switzerland)|November 18, 2020
Effect of Cadmium Toxicity on Growth, Oxidative Damage, Antioxidant Defense System and Cadmium Accumulation in Two Sorghum CultivarsMuhammad Jawad Hassan, Muhammad Ali Raza, Sana Ur Rehman, et al.
Journal of Child Neurology|October 8, 2009
Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephalyRizwana Kousar, Hira Nawaz, Maryam Khurshid, et al.
Human Genetics|December 25, 2010
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2Sulman Basit, Kwanghyuk Lee, Rabia Habib, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Scientific Reports|May 7, 2015
Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophiesMuhammad Arif Nadeem Saqib, Konstantinos Nikopoulos, Ehsan Ullah, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Plants (Basel, Switzerland)|April 11, 2020
Selenium and Salt Interactions in Black Gram (<i>Vigna mungo</i> L): Ion Uptake, Antioxidant Defense System, and Photochemistry EfficiencyMuhammad Jawad Hassan, Muhammad Ali Raza, Imran Khan, et al.
Pageof 20

Showing results (101-110 of 191) with videos related to

Sort By:
Pageof 20
NPJ Genomic Medicine|November 12, 2021
Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, et al.
Archives of Dermatological Research|June 25, 2009
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasiaZahid Azeem, Syed Kamran-Ul-Hassan Naqvi, Muhammad Ansar, et al.
Genes|August 26, 2023
Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia PatientsRabia Basharat, Kim Rodenburg, María Rodríguez-Hidalgo, et al.
Plants (Basel, Switzerland)|November 18, 2020
Effect of Cadmium Toxicity on Growth, Oxidative Damage, Antioxidant Defense System and Cadmium Accumulation in Two Sorghum CultivarsMuhammad Jawad Hassan, Muhammad Ali Raza, Sana Ur Rehman, et al.
Journal of Child Neurology|October 8, 2009
Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephalyRizwana Kousar, Hira Nawaz, Maryam Khurshid, et al.
Human Genetics|December 25, 2010
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2Sulman Basit, Kwanghyuk Lee, Rabia Habib, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Scientific Reports|May 7, 2015
Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophiesMuhammad Arif Nadeem Saqib, Konstantinos Nikopoulos, Ehsan Ullah, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Plants (Basel, Switzerland)|April 11, 2020
Selenium and Salt Interactions in Black Gram (<i>Vigna mungo</i> L): Ion Uptake, Antioxidant Defense System, and Photochemistry EfficiencyMuhammad Jawad Hassan, Muhammad Ali Raza, Imran Khan, et al.
Pageof 20