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Frontiers in Immunology
|
May 11, 2026
Correction: Combinational therapeutic strategies to overcome resistance to immune checkpoint inhibitors
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
Frontiers in Immunology
|
May 9, 2025
Combinational therapeutic strategies to overcome resistance to immune checkpoint inhibitors
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
Molecular Cancer
|
January 15, 2025
Resistance mechanisms to immune checkpoint inhibitors: updated insights
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
The International Journal of Biochemistry & Cell Biology
|
January 7, 2015
Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome
Reham M Milhem, Lihadh Al-Gazali, Bassam R Ali
Journal of Biomedical Science
|
June 27, 2024
The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy
Nesrin Gariballa, Feda Mohamed, Sally Badawi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 9, 2012
A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract
Nadia A Akawi, Bassam R Ali, Lihadh Al-Gazali
American Journal of Medical Genetics. Part A
|
May 3, 2017
Endoplasmic reticulum retention of xylosyltransferase 1 (XYLT1) mutants underlying Desbuquois dysplasia type II
Nesreen K Al-Jezawi, Bassam R Ali, Lihadh Al-Gazali
NPJ Genomic Medicine
|
May 20, 2026
AI-genomics synergy for drug repurposing in breast cancer: an interpretability-driven framework
Rahaf M Ahmad, Salahdein Aburuz, Bassam R Ali, et al.
Molecular Syndromology
|
February 28, 2022
Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New Features
Elif Yilmaz Gulec, Bassam R Ali, Anne John, et al.
Pharmacogenomics
|
May 5, 2017
Pharmacogenomics in pediatric acute lymphoblastic leukemia: promises and limitations
Zeina N Al-Mahayri, George P Patrinos, Bassam R Ali
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of 18
Search research articles
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Showing results (11-20 of 173) with videos related to
Sort By:
Page
of 18
Frontiers in Immunology
|
May 11, 2026
Correction: Combinational therapeutic strategies to overcome resistance to immune checkpoint inhibitors
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
Frontiers in Immunology
|
May 9, 2025
Combinational therapeutic strategies to overcome resistance to immune checkpoint inhibitors
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
Molecular Cancer
|
January 15, 2025
Resistance mechanisms to immune checkpoint inhibitors: updated insights
Besan H Alsaafeen, Bassam R Ali, Eyad Elkord
The International Journal of Biochemistry & Cell Biology
|
January 7, 2015
Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome
Reham M Milhem, Lihadh Al-Gazali, Bassam R Ali
Journal of Biomedical Science
|
June 27, 2024
The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy
Nesrin Gariballa, Feda Mohamed, Sally Badawi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 9, 2012
A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract
Nadia A Akawi, Bassam R Ali, Lihadh Al-Gazali
American Journal of Medical Genetics. Part A
|
May 3, 2017
Endoplasmic reticulum retention of xylosyltransferase 1 (XYLT1) mutants underlying Desbuquois dysplasia type II
Nesreen K Al-Jezawi, Bassam R Ali, Lihadh Al-Gazali
NPJ Genomic Medicine
|
May 20, 2026
AI-genomics synergy for drug repurposing in breast cancer: an interpretability-driven framework
Rahaf M Ahmad, Salahdein Aburuz, Bassam R Ali, et al.
Molecular Syndromology
|
February 28, 2022
Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New Features
Elif Yilmaz Gulec, Bassam R Ali, Anne John, et al.
Pharmacogenomics
|
May 5, 2017
Pharmacogenomics in pediatric acute lymphoblastic leukemia: promises and limitations
Zeina N Al-Mahayri, George P Patrinos, Bassam R Ali
Page
of 18