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Virology Journal
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October 20, 2011
Hepatitis C virus infection: molecular pathways to insulin resistance
Fahed 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 cultures
Huma 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 Chemotherapy
Leonard 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 Society
Junaid 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> L
Huma 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 economics
Marin 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 ataxia
Andrea 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 ataxia
Andrea 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 Pakistan
Memoona 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 syndrome
Vincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Virology Journal
|
October 20, 2011
Hepatitis C virus infection: molecular pathways to insulin resistance
Fahed 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 cultures
Huma 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 Chemotherapy
Leonard 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 Society
Junaid 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> L
Huma 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 economics
Marin 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 ataxia
Andrea 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 ataxia
Andrea 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 Pakistan
Memoona 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 syndrome
Vincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Page
of 3