Showing results (891-900 of 7,419) with videos related to
Sort By:
Pageof 742
Nature Genetics|April 22, 2003
Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosisGaël Nicolas, Lydie Viatte, Dan-Qing Lou, et al.Nature Genetics|March 11, 2003
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndromeCatherine Dodé, Jacqueline Levilliers, Jean-Michel Dupont, et al.Nature Genetics|May 6, 2003
Deficiency of Mbd2 suppresses intestinal tumorigenesisOwen J Sansom, Jennifer Berger, Stefan M Bishop, et al.Nature Genetics|November 5, 2002
A mouse model of human L1 retrotranspositionEric M Ostertag, Ralph J DeBerardinis, John L Goodier, et al.Nature Genetics|November 12, 2002
Restoration of type VII collagen expression and function in dystrophic epidermolysis bullosaMei Chen, Noriyuki Kasahara, Douglas R Keene, et al.Nature Genetics|October 22, 2002
Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndromeRuti Parvari, Eli Hershkovitz, Nili Grossman, et al.Nature Genetics|November 16, 2002
The core-binding factor beta subunit is required for bone formation and hematopoietic maturationJanelle Miller, Alan Horner, Terryl Stacy, et al.Nature Genetics|October 29, 2002
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humansLudmila Prokunina, Casimiro Castillejo-López, Fredrik Oberg, et al.Nature Genetics|November 1, 2002
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1Galina V Fitzpatrick, Paul D Soloway, Michael J HigginsNature Genetics|November 1, 2002
Detection of regulatory variation in mouse genesChristopher R Cowles, Joel N Hirschhorn, David Altshuler, et al.Pageof 742