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Georges Nemer

Showing results (101-110 of 111) with videos related to

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Cholesterol|August 2, 2017
Premature Valvular Heart Disease in Homozygous Familial HypercholesterolemiaAkl C Fahed, Kamel Shibbani, Rabih R Andary, et al.
Iscience|October 26, 2020
Integrative Transcriptome Analyses Empower the Anti-COVID-19 Drug ArsenalNehme El-Hachem, Edward Eid, Georges Nemer, et al.
Frontiers in Genetics|January 13, 2018
A Novel Role for <i>CSRP1</i> in a Lebanese Family with Congenital Cardiac DefectsAmina Kamar, Akl C Fahed, Kamel Shibbani, et al.
Plos One|January 6, 2026
Targeting ceramide metabolism to restore hypoxia-induced apoptosis in p53-deficient colon cancer cellsKaren Mechleb, Nancy Hourani, Maya Fakhry, et al.
BMC Medical Genomics|February 16, 2019
Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic casesMarwan M Refaat, Sylvana Hassanieh, Jad A Ballout, et al.
American Journal of Human Genetics|August 13, 2011
Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysmsLeen Abu-Safieh, Emad B Abboud, Hisham Alkuraya, et al.
Parasite (Paris, France)|July 4, 2025
Repositioning of moxidectin: a promising approach in cutaneous leishmaniasis therapyLynn Al Samra, Mohamad El Nahas, Ilham Mneimneh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|February 1, 2018
Genome-Wide Gene Expression Changes in the Normal-Appearing Airway during the Evolution of Smoking-Associated Lung AdenocarcinomaJacob Kantrowitz, Ansam Sinjab, Li Xu, et al.
Circulation. Genomic and Precision Medicine|September 5, 2020
Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic CardiomyopathyAkl C Fahed, Georges Nemer, Fadi F Bitar, et al.
Human Mutation|September 4, 2013
GATA4 loss-of-function mutations underlie familial tetralogy of fallotYi-Qing Yang, Lara Gharibeh, Ruo-Gu Li, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Cholesterol|August 2, 2017
Premature Valvular Heart Disease in Homozygous Familial HypercholesterolemiaAkl C Fahed, Kamel Shibbani, Rabih R Andary, et al.
Iscience|October 26, 2020
Integrative Transcriptome Analyses Empower the Anti-COVID-19 Drug ArsenalNehme El-Hachem, Edward Eid, Georges Nemer, et al.
Frontiers in Genetics|January 13, 2018
A Novel Role for <i>CSRP1</i> in a Lebanese Family with Congenital Cardiac DefectsAmina Kamar, Akl C Fahed, Kamel Shibbani, et al.
Plos One|January 6, 2026
Targeting ceramide metabolism to restore hypoxia-induced apoptosis in p53-deficient colon cancer cellsKaren Mechleb, Nancy Hourani, Maya Fakhry, et al.
BMC Medical Genomics|February 16, 2019
Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic casesMarwan M Refaat, Sylvana Hassanieh, Jad A Ballout, et al.
American Journal of Human Genetics|August 13, 2011
Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysmsLeen Abu-Safieh, Emad B Abboud, Hisham Alkuraya, et al.
Parasite (Paris, France)|July 4, 2025
Repositioning of moxidectin: a promising approach in cutaneous leishmaniasis therapyLynn Al Samra, Mohamad El Nahas, Ilham Mneimneh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|February 1, 2018
Genome-Wide Gene Expression Changes in the Normal-Appearing Airway during the Evolution of Smoking-Associated Lung AdenocarcinomaJacob Kantrowitz, Ansam Sinjab, Li Xu, et al.
Circulation. Genomic and Precision Medicine|September 5, 2020
Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic CardiomyopathyAkl C Fahed, Georges Nemer, Fadi F Bitar, et al.
Human Mutation|September 4, 2013
GATA4 loss-of-function mutations underlie familial tetralogy of fallotYi-Qing Yang, Lara Gharibeh, Ruo-Gu Li, et al.
Pageof 12