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Asima Zia

Showing results (1-10 of 10) with videos related to

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Acta Diabetologica|January 15, 2015
Data interpretation: deciphering the biological function of Type 2 diabetes associated risk lociAsima Zia, Attya Bhatti, Peter John, et al.
Plos One|December 6, 2018
Exploiting antigen receptor information to quantify index switching in single-cell transcriptome sequencing experimentsYing Yao, Asima Zia, Łukasz Wyrożemski, et al.
Journal of Biomolecular Structure & Dynamics|September 23, 2021
Clinically significant findings of high-risk mutations in human SLC29A4 gene associated with diabetes mellitus type 2 in Pakistani populationSadaf Moeez, Sumbul Khalid, Sania Shaeen, et al.
Immunogenetics|April 24, 2015
Genetic link of type 1 diabetes susceptibility loci with rheumatoid arthritis in Pakistani patientsAysha Karim Kiani, Sidrah Jahangir, Sidrah Jahngir, et al.
Diabetes Research and Clinical Practice|February 10, 2015
Association of 32 type 1 diabetes risk loci in Pakistani patientsAysha Karim Kiani, Peter John, Attya Bhatti, et al.
Clinical Immunology (Orlando, Fla.)|November 16, 2020
T cell receptor repertoire as a potential diagnostic marker for celiac diseaseYing Yao, Asima Zia, Ralf Stefan Neumann, et al.
Human Cell|December 19, 2023
Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9AMaryam Alowaysi, Mohammad Al-Shehri, Amani Badkok, et al.
Stem Cell Research & Therapy|December 19, 2023
HLA-based banking of induced pluripotent stem cells in Saudi ArabiaMaryam Alowaysi, Robert Lehmann, Mohammad Al-Shehri, et al.
Stem Cell Research|July 5, 2023
Generation of myoglobin (MB)-knockout human embryonic stem cell (hESC) line (KAIMRCe002-A-1S) using CRISPR/Cas9 technologyMaryam Alowaysi, Mohammad Al-Shehri, Moayad Baadhaim, et al.
Human Cell|July 9, 2024
Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 geneMaryam Alowaysi, Moayad Baadhaim, Mohammad Al-Shehri, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Acta Diabetologica|January 15, 2015
Data interpretation: deciphering the biological function of Type 2 diabetes associated risk lociAsima Zia, Attya Bhatti, Peter John, et al.
Plos One|December 6, 2018
Exploiting antigen receptor information to quantify index switching in single-cell transcriptome sequencing experimentsYing Yao, Asima Zia, Łukasz Wyrożemski, et al.
Journal of Biomolecular Structure & Dynamics|September 23, 2021
Clinically significant findings of high-risk mutations in human SLC29A4 gene associated with diabetes mellitus type 2 in Pakistani populationSadaf Moeez, Sumbul Khalid, Sania Shaeen, et al.
Immunogenetics|April 24, 2015
Genetic link of type 1 diabetes susceptibility loci with rheumatoid arthritis in Pakistani patientsAysha Karim Kiani, Sidrah Jahangir, Sidrah Jahngir, et al.
Diabetes Research and Clinical Practice|February 10, 2015
Association of 32 type 1 diabetes risk loci in Pakistani patientsAysha Karim Kiani, Peter John, Attya Bhatti, et al.
Clinical Immunology (Orlando, Fla.)|November 16, 2020
T cell receptor repertoire as a potential diagnostic marker for celiac diseaseYing Yao, Asima Zia, Ralf Stefan Neumann, et al.
Human Cell|December 19, 2023
Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9AMaryam Alowaysi, Mohammad Al-Shehri, Amani Badkok, et al.
Stem Cell Research & Therapy|December 19, 2023
HLA-based banking of induced pluripotent stem cells in Saudi ArabiaMaryam Alowaysi, Robert Lehmann, Mohammad Al-Shehri, et al.
Stem Cell Research|July 5, 2023
Generation of myoglobin (MB)-knockout human embryonic stem cell (hESC) line (KAIMRCe002-A-1S) using CRISPR/Cas9 technologyMaryam Alowaysi, Mohammad Al-Shehri, Moayad Baadhaim, et al.
Human Cell|July 9, 2024
Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 geneMaryam Alowaysi, Moayad Baadhaim, Mohammad Al-Shehri, et al.
Pageof 1