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Georges Nemer

Showing results (61-70 of 111) with videos related to

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The Journal of Dermatological Treatment|March 21, 2017
Retinoids: a journey from the molecular structures and mechanisms of action to clinical uses in dermatology and adverse effectsSamar Khalil, Tara Bardawil, Carla Stephan, et al.
European Journal of Dermatology : EJD|November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasiaMazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Metabolites|April 26, 2024
Computational Applications: Beauvericin from a Mycotoxin into a Humanized DrugCharbel Al Khoury, Sima Tokajian, Nabil Nemer, et al.
Genes|March 28, 2026
Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome SequencingYosra Bejaoui, Yasser Al-Sarraj, Jana Al-Hage, et al.
BMC Medical Genetics|January 4, 2020
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITFAthar Khalil, Samer Bou Karroum, Rana Barake, et al.
Frontiers in Medicine|April 23, 2026
Global trajectories of polygenic risk score research: a systematic bibliometric review of precision medicine, equity, and clinical translationFouad Bitar, Rana Zareef, Roukoz Abou-Karam, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 24, 2007
Modulation of COX-2 expression by statins in human monocytic cellsAïda Habib, Ishraq Shamseddeen, Mona S Nasrallah, et al.
Frontiers in Oncology|November 15, 2018
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the <i>TBX2</i> Subfamily of Tumor Suppressor GenesAthar Khalil, Batoul Dekmak, Fouad Boulos, et al.
Clinical Genetics|August 31, 2023
A X-linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria-like phenotypesLeon Peifer-Weiß, Mazen Kurban, Céline David, et al.
Nutrients|July 29, 2023
The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association StudyNagham Nafiz Hendi, Marlene Chakhtoura, Yasser Al-Sarraj, et al.
Pageof 12

Showing results (61-70 of 111) with videos related to

Sort By:
Pageof 12
The Journal of Dermatological Treatment|March 21, 2017
Retinoids: a journey from the molecular structures and mechanisms of action to clinical uses in dermatology and adverse effectsSamar Khalil, Tara Bardawil, Carla Stephan, et al.
European Journal of Dermatology : EJD|November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasiaMazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Metabolites|April 26, 2024
Computational Applications: Beauvericin from a Mycotoxin into a Humanized DrugCharbel Al Khoury, Sima Tokajian, Nabil Nemer, et al.
Genes|March 28, 2026
Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome SequencingYosra Bejaoui, Yasser Al-Sarraj, Jana Al-Hage, et al.
BMC Medical Genetics|January 4, 2020
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITFAthar Khalil, Samer Bou Karroum, Rana Barake, et al.
Frontiers in Medicine|April 23, 2026
Global trajectories of polygenic risk score research: a systematic bibliometric review of precision medicine, equity, and clinical translationFouad Bitar, Rana Zareef, Roukoz Abou-Karam, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 24, 2007
Modulation of COX-2 expression by statins in human monocytic cellsAïda Habib, Ishraq Shamseddeen, Mona S Nasrallah, et al.
Frontiers in Oncology|November 15, 2018
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the <i>TBX2</i> Subfamily of Tumor Suppressor GenesAthar Khalil, Batoul Dekmak, Fouad Boulos, et al.
Clinical Genetics|August 31, 2023
A X-linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria-like phenotypesLeon Peifer-Weiß, Mazen Kurban, Céline David, et al.
Nutrients|July 29, 2023
The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association StudyNagham Nafiz Hendi, Marlene Chakhtoura, Yasser Al-Sarraj, et al.
Pageof 12