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Bassam R Ali

Showing results (111-120 of 173) with videos related to

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Plos One|June 12, 2026
Cardiologists' perspectives on pharmacogenomics implementation in a hybrid health system: A qualitative study from the United Arab EmiratesMaram O Abbas, Azhar T Rahma, Iffat Elbarazi, et al.
Molecular and Cellular Biochemistry|November 6, 2012
Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutationsAlistair N Hume, Anne John, Nadia A Akawi, et al.
Biomolecules|May 24, 2024
Reelin Regulates Developmental Desynchronization Transition of Neocortical Network ActivityMohammad I K Hamad, Obada Rabaya, Abdalrahim Jbara, et al.
Meta Gene|March 1, 2016
Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patientsHamdy Moselhy, Valsamma Eapen, Nadia A Akawi, et al.
The Pharmacogenomics Journal|January 6, 2026
Combined Role of CYP3A4 and CYP3A5 genetic variants in tacrolimus dose-adjusted trough levels: a clinical retrospective study in kidney transplant patientsAnna Tsironi, Effrosyni Mendrinou, Stavroula Siamoglou, et al.
Biochemical Pharmacology|September 22, 2025
Evaluation of the functional impact of rare CYP2C19 missense variants identified in understudied Populations: An Integrated in silico and in vitro analysisReema Saleous, Eiji Hishinuma, Zeina N Al-Mahayri, et al.
Toxics|August 25, 2023
Genotoxicity of Occupational Pesticide Exposures among Agricultural Workers in Arab Countries: A Systematic Review and Meta-AnalysisMoustafa Sherif, Khadija Ramadhan Makame, Linda Östlundh, et al.
Saudi Medical Journal|April 13, 2011
New and known mutations associated with inborn errors of metabolism in a heterogeneous Middle Eastern populationBassam R Ali, Jozef L Hertecant, Fatima A Al-Jasmi, et al.
Genetic Testing and Molecular Biomarkers|November 24, 2011
Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates populationImen Ben-Rebeh, Jozef L Hertecant, Fatma A Al-Jasmi, et al.
BMC Medical Genetics|March 4, 2018
Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalusNesreen K Al-Jezawi, Aisha M Al-Shamsi, Jehan Suleiman, et al.
Pageof 18

Showing results (111-120 of 173) with videos related to

Sort By:
Pageof 18
Plos One|June 12, 2026
Cardiologists' perspectives on pharmacogenomics implementation in a hybrid health system: A qualitative study from the United Arab EmiratesMaram O Abbas, Azhar T Rahma, Iffat Elbarazi, et al.
Molecular and Cellular Biochemistry|November 6, 2012
Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutationsAlistair N Hume, Anne John, Nadia A Akawi, et al.
Biomolecules|May 24, 2024
Reelin Regulates Developmental Desynchronization Transition of Neocortical Network ActivityMohammad I K Hamad, Obada Rabaya, Abdalrahim Jbara, et al.
Meta Gene|March 1, 2016
Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patientsHamdy Moselhy, Valsamma Eapen, Nadia A Akawi, et al.
The Pharmacogenomics Journal|January 6, 2026
Combined Role of CYP3A4 and CYP3A5 genetic variants in tacrolimus dose-adjusted trough levels: a clinical retrospective study in kidney transplant patientsAnna Tsironi, Effrosyni Mendrinou, Stavroula Siamoglou, et al.
Biochemical Pharmacology|September 22, 2025
Evaluation of the functional impact of rare CYP2C19 missense variants identified in understudied Populations: An Integrated in silico and in vitro analysisReema Saleous, Eiji Hishinuma, Zeina N Al-Mahayri, et al.
Toxics|August 25, 2023
Genotoxicity of Occupational Pesticide Exposures among Agricultural Workers in Arab Countries: A Systematic Review and Meta-AnalysisMoustafa Sherif, Khadija Ramadhan Makame, Linda Östlundh, et al.
Saudi Medical Journal|April 13, 2011
New and known mutations associated with inborn errors of metabolism in a heterogeneous Middle Eastern populationBassam R Ali, Jozef L Hertecant, Fatima A Al-Jasmi, et al.
Genetic Testing and Molecular Biomarkers|November 24, 2011
Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates populationImen Ben-Rebeh, Jozef L Hertecant, Fatma A Al-Jasmi, et al.
BMC Medical Genetics|March 4, 2018
Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalusNesreen K Al-Jezawi, Aisha M Al-Shamsi, Jehan Suleiman, et al.
Pageof 18