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Muhammad Ansar

Showing results (31-40 of 191) with videos related to

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Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 12, 2026
Proceedings of the 12<sup>th</sup> International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related DisordersFabrizio Vacca, Binnaz Yalcin, Lars Kaestner, et al.
Environmental Pollution (Barking, Essex : 1987)|July 21, 2023
Impact and mitigation of lead, cadmium and micro/nano plastics in fragrant riceMuhammad Imran, Muhammad Ansar Farooq, Ayesha Batool, et al.
Plos One|June 27, 2015
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31Rabia Habib, Muhammad Ansar, Manuel Mattheisen, et al.
Plants (Basel, Switzerland)|February 15, 2022
Potassium and Humic Acid Synergistically Increase Salt Tolerance and Nutrient Uptake in Contrasting Wheat Genotypes through Ionic Homeostasis and Activation of Antioxidant EnzymesGhulam Abbas, Sadia Rehman, Manzer H Siddiqui, et al.
Acta Dermato-Venereologica|January 29, 2010
Mutations in lipase H gene underlie autosomal recessive hypotrichosis in five Pakistani familiesUmm-e Kalsoom, Rabia Habib, Bushra Khan, et al.
European Journal of Dermatology : EJD|November 15, 2012
Mutations in the gene phospholipase C, delta-1 (PLCD1) underlying hereditary leukonychiaHina Mir, Saadullah Khan, Muhammad Shoaib Arif, et al.
Journal of Genetics|September 6, 2014
Genetic analysis of a consanguineous Pakistani family with Leber congenital amaurosis identifies a novel mutation in GUCY2D geneMuzammil Ahmad Khan, Verena Rupp, Muhammad Ayaz Khan, et al.
Japanese Journal of Ophthalmology|September 14, 2011
Genetic analysis of four Pakistani families with achromatopsia and a novel S4 motif mutation of CNGA3Muhammad Arif Nadeem Saqib, Bilal Malik Awan, Mehwish Sarfraz, et al.
Cureus|November 3, 2025
Acute Thrombocytopaenia Induced by Teicoplanin in a Patient With Right Leg CellulitisMuhammad Ansar, Daneer S Rahanu, Nyein Su Wai, et al.
Genes|March 29, 2023
A Biallelic Truncating Variant in the TPR Domain of GEMIN5 Associated with Intellectual Disability and Cerebral AtrophyNazia Ibrahim, Shagufta Naz, Francesca Mattioli, et al.
Pageof 20

Showing results (31-40 of 191) with videos related to

Sort By:
Pageof 20
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 12, 2026
Proceedings of the 12<sup>th</sup> International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related DisordersFabrizio Vacca, Binnaz Yalcin, Lars Kaestner, et al.
Environmental Pollution (Barking, Essex : 1987)|July 21, 2023
Impact and mitigation of lead, cadmium and micro/nano plastics in fragrant riceMuhammad Imran, Muhammad Ansar Farooq, Ayesha Batool, et al.
Plos One|June 27, 2015
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31Rabia Habib, Muhammad Ansar, Manuel Mattheisen, et al.
Plants (Basel, Switzerland)|February 15, 2022
Potassium and Humic Acid Synergistically Increase Salt Tolerance and Nutrient Uptake in Contrasting Wheat Genotypes through Ionic Homeostasis and Activation of Antioxidant EnzymesGhulam Abbas, Sadia Rehman, Manzer H Siddiqui, et al.
Acta Dermato-Venereologica|January 29, 2010
Mutations in lipase H gene underlie autosomal recessive hypotrichosis in five Pakistani familiesUmm-e Kalsoom, Rabia Habib, Bushra Khan, et al.
European Journal of Dermatology : EJD|November 15, 2012
Mutations in the gene phospholipase C, delta-1 (PLCD1) underlying hereditary leukonychiaHina Mir, Saadullah Khan, Muhammad Shoaib Arif, et al.
Journal of Genetics|September 6, 2014
Genetic analysis of a consanguineous Pakistani family with Leber congenital amaurosis identifies a novel mutation in GUCY2D geneMuzammil Ahmad Khan, Verena Rupp, Muhammad Ayaz Khan, et al.
Japanese Journal of Ophthalmology|September 14, 2011
Genetic analysis of four Pakistani families with achromatopsia and a novel S4 motif mutation of CNGA3Muhammad Arif Nadeem Saqib, Bilal Malik Awan, Mehwish Sarfraz, et al.
Cureus|November 3, 2025
Acute Thrombocytopaenia Induced by Teicoplanin in a Patient With Right Leg CellulitisMuhammad Ansar, Daneer S Rahanu, Nyein Su Wai, et al.
Genes|March 29, 2023
A Biallelic Truncating Variant in the TPR Domain of GEMIN5 Associated with Intellectual Disability and Cerebral AtrophyNazia Ibrahim, Shagufta Naz, Francesca Mattioli, et al.
Pageof 20