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Loubna El Zein

Showing results (1-10 of 14) with videos related to

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Gene Reports|January 25, 2021
Mutational analysis of SARS-CoV-2 <i>ORF8</i> during six months of COVID-19 pandemicAhmad Alkhansa, Ghayas Lakkis, Loubna El Zein
Trends in Genetics : TIG|March 5, 2003
Lateralization defects and ciliary dyskinesia: lessons from algaeLoubna El Zein, Heymut Omran, Patrice Bouvagnet
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|April 3, 2004
Genetics of congenital heart defectsLoubna el Zein, Patrice Schön, Brigitte Chhin, et al.
Journal of Cell Science|August 13, 2009
RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathiesLoubna El Zein, Aouatef Ait-Lounis, Laurette Morlé, et al.
Plos One|June 11, 2015
A Novel Alpha Cardiac Actin (ACTC1) Mutation Mapping to a Domain in Close Contact with Myosin Heavy Chain Leads to a Variety of Congenital Heart Defects, Arrhythmia and Possibly Midline DefectsCéline Augière, Simon Mégy, Rajae El Malti, et al.
Circulation. Cardiovascular Genetics|June 22, 2010
Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction diseaseHui Liu, Loubna El Zein, Martin Kruse, et al.
International Journal of Molecular Sciences|December 11, 2022
Wild Wheat Rhizosphere-Associated Plant Growth-Promoting Bacteria Exudates: Effect on Root Development in Modern Wheat and CompositionHoussein Zhour, Fabrice Bray, Israa Dandache, et al.
The Journal of Experimental Medicine|December 16, 2024
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunityFahd Al Qureshah, Jérémie Le Pen, Nicole A de Weerd, et al.
Human Mutation|November 1, 2020
Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxyHui Liu, Anna-Gaëlle Giguet-Valard, Thomas Simonet, et al.
The Journal of Experimental Medicine|July 9, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosisDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Gene Reports|January 25, 2021
Mutational analysis of SARS-CoV-2 <i>ORF8</i> during six months of COVID-19 pandemicAhmad Alkhansa, Ghayas Lakkis, Loubna El Zein
Trends in Genetics : TIG|March 5, 2003
Lateralization defects and ciliary dyskinesia: lessons from algaeLoubna El Zein, Heymut Omran, Patrice Bouvagnet
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|April 3, 2004
Genetics of congenital heart defectsLoubna el Zein, Patrice Schön, Brigitte Chhin, et al.
Journal of Cell Science|August 13, 2009
RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathiesLoubna El Zein, Aouatef Ait-Lounis, Laurette Morlé, et al.
Plos One|June 11, 2015
A Novel Alpha Cardiac Actin (ACTC1) Mutation Mapping to a Domain in Close Contact with Myosin Heavy Chain Leads to a Variety of Congenital Heart Defects, Arrhythmia and Possibly Midline DefectsCéline Augière, Simon Mégy, Rajae El Malti, et al.
Circulation. Cardiovascular Genetics|June 22, 2010
Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction diseaseHui Liu, Loubna El Zein, Martin Kruse, et al.
International Journal of Molecular Sciences|December 11, 2022
Wild Wheat Rhizosphere-Associated Plant Growth-Promoting Bacteria Exudates: Effect on Root Development in Modern Wheat and CompositionHoussein Zhour, Fabrice Bray, Israa Dandache, et al.
The Journal of Experimental Medicine|December 16, 2024
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunityFahd Al Qureshah, Jérémie Le Pen, Nicole A de Weerd, et al.
Human Mutation|November 1, 2020
Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxyHui Liu, Anna-Gaëlle Giguet-Valard, Thomas Simonet, et al.
The Journal of Experimental Medicine|July 9, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosisDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Pageof 2