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Muhammad Tariq

Showing results (931-940 of 945) with videos related to

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Human Molecular Genetics|August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyMuhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Inflammopharmacology|April 16, 2022
Novel acetamide derivatives of 2-aminobenzimidazole prevent inflammatory arthritis in rats via suppression of pro-inflammatory mediatorsAymun Madni Zubair, Muhammad Nasir Hayat Malik, Waqas Younis, et al.
Molecular Genetics and Genomics : MGG|August 24, 2022
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genesAyaz Khan, Shixiong Tian, Muhammad Tariq, et al.
Journal of Viral Hepatitis|January 18, 2023
Hepatitis C prevalence and elimination planning in Pakistan, a bottom-up approach accounting for provincial variationEllen Mooneyhan, Huma Qureshi, Hassan Mahmood, et al.
Stroke|January 26, 2024
Dynamic Imaging of Blood Coagulation Within the Hematoma of Patients With Acute Hemorrhagic StrokeMuhammad E Haque, Seth B Boren, James Mills, et al.
Spine|May 18, 2023
Factors Influencing Maintenance of Alignment and Functional Improvement Following Adult Spinal Deformity Surgery: A 3-Year Outcome AnalysisPeter G Passias, Lara Passfall, Kevin Moattari, et al.
Genes|June 2, 2021
Modifier Genes in Microcephaly: A Report on <i>WDR62</i>, <i>CEP63</i>, <i>RAD50</i> and <i>PCNT</i> Variants Exacerbating Disease Caused by Biallelic Mutations of <i>ASPM</i> and <i>CENPJ</i>Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, et al.
Plos One|December 24, 2011
Large-scale screening of a targeted Enterococcus faecalis mutant library identifies envelope fitness factorsLionel Rigottier-Gois, Adriana Alberti, Armel Houel, et al.
Molecular Genetics & Genomic Medicine|July 18, 2020
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from PakistanSajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, et al.
Research Square|April 16, 2025
CAR T cell-driven induction of iNOS in tumor-associated macrophages promotes CAR T cell resistance in B cell lymphomaMarco Davila, Sae Bom Lee, Yun Pyo Kang, et al.
Pageof 95

Showing results (931-940 of 945) with videos related to

Sort By:
Pageof 95
Human Molecular Genetics|August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyMuhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Inflammopharmacology|April 16, 2022
Novel acetamide derivatives of 2-aminobenzimidazole prevent inflammatory arthritis in rats via suppression of pro-inflammatory mediatorsAymun Madni Zubair, Muhammad Nasir Hayat Malik, Waqas Younis, et al.
Molecular Genetics and Genomics : MGG|August 24, 2022
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genesAyaz Khan, Shixiong Tian, Muhammad Tariq, et al.
Journal of Viral Hepatitis|January 18, 2023
Hepatitis C prevalence and elimination planning in Pakistan, a bottom-up approach accounting for provincial variationEllen Mooneyhan, Huma Qureshi, Hassan Mahmood, et al.
Stroke|January 26, 2024
Dynamic Imaging of Blood Coagulation Within the Hematoma of Patients With Acute Hemorrhagic StrokeMuhammad E Haque, Seth B Boren, James Mills, et al.
Spine|May 18, 2023
Factors Influencing Maintenance of Alignment and Functional Improvement Following Adult Spinal Deformity Surgery: A 3-Year Outcome AnalysisPeter G Passias, Lara Passfall, Kevin Moattari, et al.
Genes|June 2, 2021
Modifier Genes in Microcephaly: A Report on <i>WDR62</i>, <i>CEP63</i>, <i>RAD50</i> and <i>PCNT</i> Variants Exacerbating Disease Caused by Biallelic Mutations of <i>ASPM</i> and <i>CENPJ</i>Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, et al.
Plos One|December 24, 2011
Large-scale screening of a targeted Enterococcus faecalis mutant library identifies envelope fitness factorsLionel Rigottier-Gois, Adriana Alberti, Armel Houel, et al.
Molecular Genetics & Genomic Medicine|July 18, 2020
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from PakistanSajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, et al.
Research Square|April 16, 2025
CAR T cell-driven induction of iNOS in tumor-associated macrophages promotes CAR T cell resistance in B cell lymphomaMarco Davila, Sae Bom Lee, Yun Pyo Kang, et al.
Pageof 95