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Bassam R Ali

Showing results (121-130 of 173) with videos related to

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Pharmacogenomics|October 22, 2016
Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacyAikaterini Gravia, Vasiliki Chondrou, Alexandra Kolliopoulou, et al.
Clinical Genetics|January 6, 2022
Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thriveHanadi A Abdelrahman, Nadia Akawi, Aisha M Al-Shamsi, et al.
Molecules (Basel, Switzerland)|October 14, 2022
The Discovery of Small Allosteric and Active Site Inhibitors of the SARS-CoV-2 Main Protease via Structure-Based Virtual Screening and Biological EvaluationRadwa E Mahgoub, Feda E Mohamed, Lara Alzyoud, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblingsSalma Ben-Salem, Nara Sobreira, Nadia A Akawi, et al.
Journal of Personalized Medicine|October 29, 2020
Knowledge and Attitudes of Medical and Health Science Students in the United Arab Emirates toward Genomic Medicine and Pharmacogenomics: A Cross-Sectional StudyAzhar T Rahma, Mahanna Elsheik, Iffat Elbarazi, et al.
Frontiers in Cell and Developmental Biology|August 8, 2024
Cellular and functional evaluation of LDLR missense variants reported in hypercholesterolemic patients demonstrates their hypomorphic impacts on trafficking and LDL internalizationAseel A Jawabri, Anne John, Mohammad A Ghattas, et al.
Human Mutation|April 29, 2026
Identification of a Novel VLDLR Variant in the First Report of CAMRQ1 From Africa: Expanding the Spectrum of Cerebellar Ataxia SyndromesAseel A Jawabri, Ainara Salazar-Villacorta, Henriette Senghor, et al.
Human Genomics|October 25, 2017
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsVasiliki Chondrou, Petros Kolovos, Argyro Sgourou, et al.
Neuroscience and Biobehavioral Reviews|December 4, 2022
Effectiveness of pharmacogenomic tests including CYP2D6 and CYP2C19 genomic variants for guiding the treatment of depressive disorders: Systematic review and meta-analysis of randomised controlled trialsDanilo Arnone, Omar Omar, Teresa Arora, et al.
Human Molecular Genetics|October 24, 2008
Defective cellular trafficking of missense NPR-B mutants is the major mechanism underlying acromesomelic dysplasia-type MaroteauxAlistair N Hume, Jens Buttgereit, Aydah M Al-Awadhi, et al.
Pageof 18

Showing results (121-130 of 173) with videos related to

Sort By:
Pageof 18
Pharmacogenomics|October 22, 2016
Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacyAikaterini Gravia, Vasiliki Chondrou, Alexandra Kolliopoulou, et al.
Clinical Genetics|January 6, 2022
Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thriveHanadi A Abdelrahman, Nadia Akawi, Aisha M Al-Shamsi, et al.
Molecules (Basel, Switzerland)|October 14, 2022
The Discovery of Small Allosteric and Active Site Inhibitors of the SARS-CoV-2 Main Protease via Structure-Based Virtual Screening and Biological EvaluationRadwa E Mahgoub, Feda E Mohamed, Lara Alzyoud, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblingsSalma Ben-Salem, Nara Sobreira, Nadia A Akawi, et al.
Journal of Personalized Medicine|October 29, 2020
Knowledge and Attitudes of Medical and Health Science Students in the United Arab Emirates toward Genomic Medicine and Pharmacogenomics: A Cross-Sectional StudyAzhar T Rahma, Mahanna Elsheik, Iffat Elbarazi, et al.
Frontiers in Cell and Developmental Biology|August 8, 2024
Cellular and functional evaluation of LDLR missense variants reported in hypercholesterolemic patients demonstrates their hypomorphic impacts on trafficking and LDL internalizationAseel A Jawabri, Anne John, Mohammad A Ghattas, et al.
Human Mutation|April 29, 2026
Identification of a Novel VLDLR Variant in the First Report of CAMRQ1 From Africa: Expanding the Spectrum of Cerebellar Ataxia SyndromesAseel A Jawabri, Ainara Salazar-Villacorta, Henriette Senghor, et al.
Human Genomics|October 25, 2017
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsVasiliki Chondrou, Petros Kolovos, Argyro Sgourou, et al.
Neuroscience and Biobehavioral Reviews|December 4, 2022
Effectiveness of pharmacogenomic tests including CYP2D6 and CYP2C19 genomic variants for guiding the treatment of depressive disorders: Systematic review and meta-analysis of randomised controlled trialsDanilo Arnone, Omar Omar, Teresa Arora, et al.
Human Molecular Genetics|October 24, 2008
Defective cellular trafficking of missense NPR-B mutants is the major mechanism underlying acromesomelic dysplasia-type MaroteauxAlistair N Hume, Jens Buttgereit, Aydah M Al-Awadhi, et al.
Pageof 18