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Muhammad Ansar

Showing results (81-90 of 191) with videos related to

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American Journal of Medical Genetics. Part A|January 8, 2005
Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31Asif Mir, Muhammad Ansar, Maria H Chahrour, et al.
Pakistan Journal of Pharmaceutical Sciences|April 19, 2021
In-silico pharmacophoric and molecular docking-based drug discovery against the Main Protease (Mpro) of SARS-CoV-2, a causative agent COVID-19Zeshan Haider, Muhammad Muneeb Subhani, Muhammad Ansar Farooq, et al.
Journal of Virological Methods|January 29, 2013
Stable Huh-7 cell lines expressing non-structural proteins of genotype 1a of hepatitis C virusImran Shahid, Sana Gull, Bushra Ijaz, et al.
Plants (Basel, Switzerland)|August 28, 2025
Protective Role of GABA in Aromatic Rice Under Lead and Cadmium Toxicity: Physiological and Biochemical InsightsUmair Ashraf, Shakeel Ahmad Anjum, Fahd Rasul, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Clinical Genetics|April 5, 2019
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limbMuhammad Umair, Muhammad Bilal, Raja H Ali, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulationsAsia Parveen, Muhammad U Mirza, Michiel Vanmeert, et al.
International Journal of Environmental Research and Public Health|October 27, 2022
Evolution Mechanism of Arsenic Enrichment in Groundwater and Associated Health Risks in Southern Punjab, PakistanMuhammad Yousuf Jat Baloch, Wenjing Zhang, Dayi Zhang, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1Muhammad Arshad Rafique, Muhammad Ansar, Syed Muhammad Jamal, et al.
The Journal of Gene Medicine|May 13, 2023
Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genesShazia Khan, Muhammad Umair, Safdar Abbas, et al.
Pageof 20

Showing results (81-90 of 191) with videos related to

Sort By:
Pageof 20
American Journal of Medical Genetics. Part A|January 8, 2005
Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31Asif Mir, Muhammad Ansar, Maria H Chahrour, et al.
Pakistan Journal of Pharmaceutical Sciences|April 19, 2021
In-silico pharmacophoric and molecular docking-based drug discovery against the Main Protease (Mpro) of SARS-CoV-2, a causative agent COVID-19Zeshan Haider, Muhammad Muneeb Subhani, Muhammad Ansar Farooq, et al.
Journal of Virological Methods|January 29, 2013
Stable Huh-7 cell lines expressing non-structural proteins of genotype 1a of hepatitis C virusImran Shahid, Sana Gull, Bushra Ijaz, et al.
Plants (Basel, Switzerland)|August 28, 2025
Protective Role of GABA in Aromatic Rice Under Lead and Cadmium Toxicity: Physiological and Biochemical InsightsUmair Ashraf, Shakeel Ahmad Anjum, Fahd Rasul, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Clinical Genetics|April 5, 2019
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limbMuhammad Umair, Muhammad Bilal, Raja H Ali, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulationsAsia Parveen, Muhammad U Mirza, Michiel Vanmeert, et al.
International Journal of Environmental Research and Public Health|October 27, 2022
Evolution Mechanism of Arsenic Enrichment in Groundwater and Associated Health Risks in Southern Punjab, PakistanMuhammad Yousuf Jat Baloch, Wenjing Zhang, Dayi Zhang, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1Muhammad Arshad Rafique, Muhammad Ansar, Syed Muhammad Jamal, et al.
The Journal of Gene Medicine|May 13, 2023
Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genesShazia Khan, Muhammad Umair, Safdar Abbas, et al.
Pageof 20