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Georges Nemer

Showing results (81-90 of 111) with videos related to

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Molecular Genetics & Genomic Medicine|April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patientKameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Plos One|February 7, 2015
Identification of several mutations in ATP2C1 in Lebanese families: insight into the pathogenesis of Hailey-Hailey diseaseWaed Btadini, Ossama K Abou Hassan, Dana Saadeh, et al.
Molecular Genetics and Metabolism|December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlationAkl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Journal of Infection in Developing Countries|May 14, 2014
Passaging impact of H9N2 avian influenza virus in hamsters on its pathogenicity and genetic variabilityHoussam A Shaib, Nelly Cochet, Thierry Ribeiro, et al.
Journal of Gastrointestinal Oncology|October 12, 2019
Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19Rémi Safi, Tala Mohsen-Kanson, Georges Nemer, et al.
Journal of Fungi (Basel, Switzerland)|November 27, 2021
Bioexploration and Phylogenetic Placement of Entomopathogenic Fungi of the Genus <i>Beauveria</i> in Soils of Lebanon Cedar ForestsCharbel Al Khoury, Georges Nemer, Richard Humber, et al.
Plos One|November 25, 2020
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese populationFadi S Saadeh, Rami Z Morsi, Abdallah El-Kurdi, et al.
Cardiac Electrophysiology Clinics|February 28, 2016
The Muscle-Bound HeartMarwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Child Psychiatry and Human Development|February 26, 2026
Sex-Based Differences in Clinical and Social Outcomes in Qatari Youth with ADHDSheema Hashem, Saba F Elhag, Zainab Awada, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomyAkl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Pageof 12

Showing results (81-90 of 111) with videos related to

Sort By:
Pageof 12
Molecular Genetics & Genomic Medicine|April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patientKameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Plos One|February 7, 2015
Identification of several mutations in ATP2C1 in Lebanese families: insight into the pathogenesis of Hailey-Hailey diseaseWaed Btadini, Ossama K Abou Hassan, Dana Saadeh, et al.
Molecular Genetics and Metabolism|December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlationAkl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Journal of Infection in Developing Countries|May 14, 2014
Passaging impact of H9N2 avian influenza virus in hamsters on its pathogenicity and genetic variabilityHoussam A Shaib, Nelly Cochet, Thierry Ribeiro, et al.
Journal of Gastrointestinal Oncology|October 12, 2019
Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19Rémi Safi, Tala Mohsen-Kanson, Georges Nemer, et al.
Journal of Fungi (Basel, Switzerland)|November 27, 2021
Bioexploration and Phylogenetic Placement of Entomopathogenic Fungi of the Genus <i>Beauveria</i> in Soils of Lebanon Cedar ForestsCharbel Al Khoury, Georges Nemer, Richard Humber, et al.
Plos One|November 25, 2020
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese populationFadi S Saadeh, Rami Z Morsi, Abdallah El-Kurdi, et al.
Cardiac Electrophysiology Clinics|February 28, 2016
The Muscle-Bound HeartMarwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Child Psychiatry and Human Development|February 26, 2026
Sex-Based Differences in Clinical and Social Outcomes in Qatari Youth with ADHDSheema Hashem, Saba F Elhag, Zainab Awada, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomyAkl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Pageof 12