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172 related items for PubMed ID: 24459294
1. Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot. Grunert M, Dorn C, Schueler M, Dunkel I, Schlesinger J, Mebus S, Alexi-Meskishvili V, Perrot A, Wassilew K, Timmermann B, Hetzer R, Berger F, Sperling SR. Hum Mol Genet; 2014 Jun 15; 23(12):3115-28. PubMed ID: 24459294 [Abstract] [Full Text] [Related]
2. Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot. Yuan Y, Gao Y, Wang H, Ma X, Ma D, Huang G. Birth Defects Res A Clin Mol Teratol; 2014 Dec 15; 100(12):973-84. PubMed ID: 25200836 [Abstract] [Full Text] [Related]
5. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. De Luca A, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici ML, Vergara P, De Zorzi A, Versacci P, Digilio MC, Marino B, Dallapiccola B. Clin Genet; 2011 Aug 15; 80(2):184-90. PubMed ID: 20807224 [Abstract] [Full Text] [Related]
6. GATA4 loss-of-function mutations underlie familial tetralogy of fallot. Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM, Qiu XB, Xu YJ, Xu L, Qu XK, Liu X, Fang WY, Huang RT, Xue S, Nemer G. Hum Mutat; 2013 Dec 15; 34(12):1662-71. PubMed ID: 24000169 [Abstract] [Full Text] [Related]
13. Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot. Safari-Arababadi A, Behjati-Ardakani M, Kalantar SM, Jaafarinia M. Cell Mol Biol (Noisy-le-grand); 2018 Mar 31; 64(4):103-107. PubMed ID: 29631691 [Abstract] [Full Text] [Related]
15. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle. Dorn C, Perrot A, Grunert M, Rickert-Sperling S. Adv Exp Med Biol; 2024 Mar 31; 1441():629-644. PubMed ID: 38884738 [Abstract] [Full Text] [Related]
16. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams SG, Keavney BD, Thiruvahindrapuram B, Scherer SW, Bassett AS. Circ Genom Precis Med; 2021 Aug 31; 14(4):e003410. PubMed ID: 34328347 [Abstract] [Full Text] [Related]
17. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. Greenway SC, Pereira AC, Lin JC, DePalma SR, Israel SJ, Mesquita SM, Ergul E, Conta JH, Korn JM, McCarroll SA, Gorham JM, Gabriel S, Altshuler DM, Quintanilla-Dieck Mde L, Artunduaga MA, Eavey RD, Plenge RM, Shadick NA, Weinblatt ME, De Jager PL, Hafler DA, Breitbart RE, Seidman JG, Seidman CE. Nat Genet; 2009 Aug 31; 41(8):931-5. PubMed ID: 19597493 [Abstract] [Full Text] [Related]
18. A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. Nemer G, Fadlalah F, Usta J, Nemer M, Dbaibo G, Obeid M, Bitar F. Hum Mutat; 2006 Mar 31; 27(3):293-4. PubMed ID: 16470721 [Abstract] [Full Text] [Related]
19. Identification of Region-Specific Myocardial Gene Expression Patterns in a Chronic Swine Model of Repaired Tetralogy of Fallot. Charron S, Roubertie F, Benoist D, Dubes V, Gilbert SH, Constantin M, Vieillot D, Elbes D, Quesson B, Bordachar P, Haissaguerre M, Bernus O, Thambo JB, Rooryck C. PLoS One; 2015 Mar 31; 10(8):e0134146. PubMed ID: 26252659 [Abstract] [Full Text] [Related]
20. Hot topics in tetralogy of Fallot. Villafañe J, Feinstein JA, Jenkins KJ, Vincent RN, Walsh EP, Dubin AM, Geva T, Towbin JA, Cohen MS, Fraser C, Dearani J, Rosenthal D, Kaufman B, Graham TP, Adult Congenital and Pediatric Cardiology Section, American College of Cardiology. J Am Coll Cardiol; 2013 Dec 10; 62(23):2155-66. PubMed ID: 24076489 [Abstract] [Full Text] [Related] Page: [Next] [New Search]