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Said El Shamieh

Showing results (51-60 of 77) with videos related to

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Frontiers in Genetics|June 2, 2022
Novel Missense and Splice Site Mutations in <i>USH2A</i>, <i>CDH23</i>, <i>PCDH15</i>, and <i>ADGRV1</i> Are Associated With Usher Syndrome in LebanonLama Jaffal, Hanane Akhdar, Hawraa Joumaa, et al.
Genes|February 21, 2019
Novel Missense Mutations in <i>BEST1</i> Are Associated with Bestrophinopathies in Lebanese PatientsLama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Plos One|August 17, 2019
Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy populationVesna Gorenjak, Dwaine R Vance, Alexandros M Petrelis, et al.
Plos One|October 25, 2019
Correction: Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy populationVesna Gorenjak, Dwaine R Vance, Alexandros M Petrelis, et al.
Plos One|March 7, 2014
Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)Marion Neuillé, Said El Shamieh, Elise Orhan, et al.
Journal of Lipid Research|December 4, 2012
A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-CMaria G Stathopoulou, Amélie Bonnefond, Ndeye Coumba Ndiaye, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Investigative Ophthalmology & Visual Science|November 14, 2013
Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindnessElise Orhan, Laurent Prézeau, Said El Shamieh, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
Clinical Chemistry and Laboratory Medicine|April 3, 2020
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French childrenSaid El Shamieh, Maria G Stathopoulou, Amélie Bonnefond, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Frontiers in Genetics|June 2, 2022
Novel Missense and Splice Site Mutations in <i>USH2A</i>, <i>CDH23</i>, <i>PCDH15</i>, and <i>ADGRV1</i> Are Associated With Usher Syndrome in LebanonLama Jaffal, Hanane Akhdar, Hawraa Joumaa, et al.
Genes|February 21, 2019
Novel Missense Mutations in <i>BEST1</i> Are Associated with Bestrophinopathies in Lebanese PatientsLama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Plos One|August 17, 2019
Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy populationVesna Gorenjak, Dwaine R Vance, Alexandros M Petrelis, et al.
Plos One|October 25, 2019
Correction: Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy populationVesna Gorenjak, Dwaine R Vance, Alexandros M Petrelis, et al.
Plos One|March 7, 2014
Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)Marion Neuillé, Said El Shamieh, Elise Orhan, et al.
Journal of Lipid Research|December 4, 2012
A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-CMaria G Stathopoulou, Amélie Bonnefond, Ndeye Coumba Ndiaye, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Investigative Ophthalmology & Visual Science|November 14, 2013
Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindnessElise Orhan, Laurent Prézeau, Said El Shamieh, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
Clinical Chemistry and Laboratory Medicine|April 3, 2020
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French childrenSaid El Shamieh, Maria G Stathopoulou, Amélie Bonnefond, et al.
Pageof 8