Showing results (21-30 of 112) with videos related to
Sort By:
Pageof 12
Human Genetics|December 12, 2003
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyriasLaurent Gouya, Hervé Puy, Anne-Marie Robreau, et al.Nature Genetics|December 26, 2001
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECHLaurent Gouya, Herve Puy, Anne-Marie Robreau, et al.Haematologica|June 5, 2013
Iron refractory iron deficiency anemiaLuigia De Falco, Mayka Sanchez, Laura Silvestri, et al.Journal of Vascular Research|March 31, 2020
Persistence of Intraluminal Thrombus Makes Saccular Aneurysm More Biologically Active than Fusiform in an Experimental Rat ModelHarry Etienne, Clément Journé, Aymeric Rouchaud, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2021
Unsuspected somatic mosaicism for FBN1 gene contributes to Marfan syndromePauline Arnaud, Hélène Morel, Olivier Milleron, et al.Kidney International|April 26, 2013
Hepcidin regulates intrarenal iron handling at the distal nephronBoualem Moulouel, Dounia Houamel, Constance Delaby, et al.Molecular Genetics and Metabolism|January 21, 2019
GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemiaRaêd Daher, Abdellah Mansouri, Alain Martelli, et al.Kidney International Reports|July 26, 2021
Renal Function Decline With Small Interfering RNA Silencing Aminolevulinic Acid Synthase 1 (ALAS1)Hélène Lazareth, Antoine Poli, Yohan Bignon, et al.Human Molecular Genetics|February 6, 2015
The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 alleleMélodie Aubart, Marie-Sylvie Gross, Nadine Hanna, et al.Pediatric Research|May 26, 2018
Characterization and origin of heme precursors in amniotic fluid: lessons from normal and pathological pregnanciesHana Manceau, Vincent Puy, Caroline M Schmitt, et al.Pageof 12