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Georges Nemer

Showing results (91-100 of 111) with videos related to

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Archives of Dermatological Research|July 19, 2017
Understanding the phenotypic similarities between IFAP and Olmsted syndrome from a molecular perspective: the interaction of MBTPS2 and TRPV3Georges Nemer, Rémi Safi, Firas Kreidieh, et al.
Human Mutation|January 15, 2013
A homozygous frameshift mutation in the HOXC13 gene underlies pure hair and nail ectodermal dysplasia in a Syrian familyMuhammad Farooq, Mazen Kurban, Atsushi Fujimoto, et al.
Clinical Genetics|May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvansGeorges Nemer, Nehme El-Hachem, Edward Eid, et al.
European Journal of Dermatology : EJD|July 26, 2017
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous formTara Bardawil, Abdallah Rebeiz, Myriam Chaabouni, et al.
Oncotarget|October 6, 2017
<i>TBX2</i> subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detectionAthar A Khalil, Smruthy Sivakumar, Frances Anthony San Lucas, et al.
International Journal of Dermatology|December 13, 2017
SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor geneChristina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Journal of Biosocial Science|May 14, 2020
Consanguinity rates among Syrian refugees in Lebanon: a study on genetic awarenessMalak El Sabeh, Mohamed Faisal Kassir, Paola Ghanem, et al.
Journal of the American Heart Association|February 26, 2025
Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk ScoresNahin Khan, Abdullah Shaar, Khalid Kunji, et al.
Human Molecular Genetics|February 8, 2017
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosisYohya Shigehara, Shujiro Okuda, Georges Nemer, et al.
Genes|December 30, 2025
Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature ReviewSheema Hashem, Saba F Elhag, Ajaz A Bhat, et al.
Pageof 12

Showing results (91-100 of 111) with videos related to

Sort By:
Pageof 12
Archives of Dermatological Research|July 19, 2017
Understanding the phenotypic similarities between IFAP and Olmsted syndrome from a molecular perspective: the interaction of MBTPS2 and TRPV3Georges Nemer, Rémi Safi, Firas Kreidieh, et al.
Human Mutation|January 15, 2013
A homozygous frameshift mutation in the HOXC13 gene underlies pure hair and nail ectodermal dysplasia in a Syrian familyMuhammad Farooq, Mazen Kurban, Atsushi Fujimoto, et al.
Clinical Genetics|May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvansGeorges Nemer, Nehme El-Hachem, Edward Eid, et al.
European Journal of Dermatology : EJD|July 26, 2017
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous formTara Bardawil, Abdallah Rebeiz, Myriam Chaabouni, et al.
Oncotarget|October 6, 2017
<i>TBX2</i> subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detectionAthar A Khalil, Smruthy Sivakumar, Frances Anthony San Lucas, et al.
International Journal of Dermatology|December 13, 2017
SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor geneChristina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Journal of Biosocial Science|May 14, 2020
Consanguinity rates among Syrian refugees in Lebanon: a study on genetic awarenessMalak El Sabeh, Mohamed Faisal Kassir, Paola Ghanem, et al.
Journal of the American Heart Association|February 26, 2025
Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk ScoresNahin Khan, Abdullah Shaar, Khalid Kunji, et al.
Human Molecular Genetics|February 8, 2017
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosisYohya Shigehara, Shujiro Okuda, Georges Nemer, et al.
Genes|December 30, 2025
Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature ReviewSheema Hashem, Saba F Elhag, Ajaz A Bhat, et al.
Pageof 12