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Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.
Chowdhury R, Ashraf H, Melanson M, Tanada Y, Nguyen M, Silberbach M, Wakimoto H, Benson DW, Anderson RH, Kasahara H. Chowdhury R, et al. Among authors: silberbach m. Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1255-64. doi: 10.1161/CIRCEP.115.002720. Epub 2015 Jul 30. Circ Arrhythm Electrophysiol. 2015. PMID: 26226998 Free PMC article.
Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block.
Pashmforoush M, Lu JT, Chen H, Amand TS, Kondo R, Pradervand S, Evans SM, Clark B, Feramisco JR, Giles W, Ho SY, Benson DW, Silberbach M, Shou W, Chien KR. Pashmforoush M, et al. Among authors: silberbach m. Cell. 2004 Apr 30;117(3):373-86. doi: 10.1016/s0092-8674(04)00405-2. Cell. 2004. PMID: 15109497 Free article.
Heart failure in infants and children.
Madriago E, Silberbach M. Madriago E, et al. Among authors: silberbach m. Pediatr Rev. 2010 Jan;31(1):4-12. doi: 10.1542/pir.31-1-4. Pediatr Rev. 2010. PMID: 20048034 Review. No abstract available.
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.
Prakash SK, Bondy CA, Maslen CL, Silberbach M, Lin AE, Perrone L, Limongelli G, Michelena HI, Bossone E, Citro R; BAVCon Investigators, GenTAC Registry Investigators; Lemaire SA, Body SC, Milewicz DM. Prakash SK, et al. Among authors: silberbach m. Am J Med Genet A. 2016 Dec;170(12):3157-3164. doi: 10.1002/ajmg.a.37953. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27604636 Free PMC article.
80 results