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Huma Tariq

Showing results (11-20 of 21) with videos related to

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Virology Journal|October 20, 2011
Hepatitis C virus infection: molecular pathways to insulin resistanceFahed Parvaiz, Sobia Manzoor, Huma Tariq, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|November 9, 2011
An overview: in vitro models of HCV replication in different cell culturesHuma Tariq, Sobia Manzoor, Fahed Parvaiz, et al.
Journal of Oncology Practice|November 19, 2016
Using Data From Ontario's Episode-Based Funding Model to Assess Quality of ChemotherapyLeonard Kaizer, Vicky Simanovski, Carlin Lalonde, et al.
Environmental Science and Pollution Research International|August 9, 2019
Metagenomic analysis of drinking water samples collected from treatment plants of Hyderabad City and Mehran University Employees Cooperative Housing SocietyJunaid Ahmed Kori, Rasool Bux Mahar, Muhammad Raffae Vistro, et al.
Biomed Research International|August 31, 2019
Antioxidant, Antimicrobial, Cytotoxic, and Protein Kinase Inhibition Potential in <i>Aloe vera</i> LHuma Tariq, Muhammad Zia, Ihsan-Ul-Haq, et al.
Journal of Hazardous Materials|May 13, 2025
Oil and gas produced water for cattle, crops, and surface water discharge: Evaluation of chemistry, toxicity and economicsMarin E Wiltse, Brooke Ballenger, Connor B Stewart, et al.
Nature Genetics|March 31, 2019
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.
Nature Genetics|April 28, 2019
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
American Journal of Human Genetics|December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndromeVincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Virology Journal|October 20, 2011
Hepatitis C virus infection: molecular pathways to insulin resistanceFahed Parvaiz, Sobia Manzoor, Huma Tariq, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|November 9, 2011
An overview: in vitro models of HCV replication in different cell culturesHuma Tariq, Sobia Manzoor, Fahed Parvaiz, et al.
Journal of Oncology Practice|November 19, 2016
Using Data From Ontario's Episode-Based Funding Model to Assess Quality of ChemotherapyLeonard Kaizer, Vicky Simanovski, Carlin Lalonde, et al.
Environmental Science and Pollution Research International|August 9, 2019
Metagenomic analysis of drinking water samples collected from treatment plants of Hyderabad City and Mehran University Employees Cooperative Housing SocietyJunaid Ahmed Kori, Rasool Bux Mahar, Muhammad Raffae Vistro, et al.
Biomed Research International|August 31, 2019
Antioxidant, Antimicrobial, Cytotoxic, and Protein Kinase Inhibition Potential in <i>Aloe vera</i> LHuma Tariq, Muhammad Zia, Ihsan-Ul-Haq, et al.
Journal of Hazardous Materials|May 13, 2025
Oil and gas produced water for cattle, crops, and surface water discharge: Evaluation of chemistry, toxicity and economicsMarin E Wiltse, Brooke Ballenger, Connor B Stewart, et al.
Nature Genetics|March 31, 2019
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.
Nature Genetics|April 28, 2019
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
American Journal of Human Genetics|December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndromeVincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Pageof 3