These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
194 related articles for article (PubMed ID: 18273862)
21. Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms. Bleyl SB; Saijoh Y; Bax NA; Gittenberger-de Groot AC; Wisse LJ; Chapman SC; Hunter J; Shiratori H; Hamada H; Yamada S; Shiota K; Klewer SE; Leppert MF; Schoenwolf GC Hum Mol Genet; 2010 Apr; 19(7):1286-301. PubMed ID: 20071345 [TBL] [Abstract][Full Text] [Related]
22. Alteration of enhancer of polycomb 1 at 10p11.2 is one of the genetic events leading to development of adult T-cell leukemia/lymphoma. Nakahata S; Saito Y; Hamasaki M; Hidaka T; Arai Y; Taki T; Taniwaki M; Morishita K Genes Chromosomes Cancer; 2009 Sep; 48(9):768-76. PubMed ID: 19484761 [TBL] [Abstract][Full Text] [Related]
23. Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries). Muncke N; Jung C; Rüdiger H; Ulmer H; Roeth R; Hubert A; Goldmuntz E; Driscoll D; Goodship J; Schön K; Rappold G Circulation; 2003 Dec; 108(23):2843-50. PubMed ID: 14638541 [TBL] [Abstract][Full Text] [Related]
24. A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. Bleyl S; Nelson L; Odelberg SJ; Ruttenberg HD; Otterud B; Leppert M; Ward K Am J Hum Genet; 1995 Feb; 56(2):408-15. PubMed ID: 7847375 [TBL] [Abstract][Full Text] [Related]
25. Overexpression of ankyrin repeat domain 1 enhances cardiomyocyte apoptosis by promoting p53 activation and mitochondrial dysfunction in rodents. Shen L; Chen C; Wei X; Li X; Luo G; Zhang J; Bin J; Huang X; Cao S; Li G; Liao Y Clin Sci (Lond); 2015 May; 128(10):665-78. PubMed ID: 25511237 [TBL] [Abstract][Full Text] [Related]
26. Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue. Crocini C; Arimura T; Reischmann S; Eder A; Braren I; Hansen A; Eschenhagen T; Kimura A; Carrier L Basic Res Cardiol; 2013 May; 108(3):349. PubMed ID: 23572067 [TBL] [Abstract][Full Text] [Related]
27. The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. Panza E; Gimelli G; Passalacqua M; Cohen A; Gimelli S; Giglio S; Ghezzi C; Sparatore B; Heye B; Zuffardi O; Rugarli E; Meitinger T; Romeo G; Ravazzolo R; Seri M Int J Mol Med; 2007 Mar; 19(3):429-35. PubMed ID: 17273791 [TBL] [Abstract][Full Text] [Related]
28. Shared Segment Analysis and Next-Generation Sequencing Implicates the Retinoic Acid Signaling Pathway in Total Anomalous Pulmonary Venous Return (TAPVR). Nash D; Arrington CB; Kennedy BJ; Yandell M; Wu W; Zhang W; Ware S; Jorde LB; Gruber PJ; Yost HJ; Bowles NE; Bleyl SB PLoS One; 2015; 10(6):e0131514. PubMed ID: 26121141 [TBL] [Abstract][Full Text] [Related]
29. Prenatal diagnosis of a mixed type of total anomalous pulmonary venous return. Cormier CM; Kramer LA; Gupta-Malhotra M Fetal Diagn Ther; 2010; 27(2):118-20. PubMed ID: 20110650 [TBL] [Abstract][Full Text] [Related]
30. Asymptomatic total anomalous pulmonary venous connection with double drainage in a young adult: a case report. Yalta K; Turgut OO; Yilmaz A; Yilmaz MB; Manduz S; Karadas F; Dogan K; Tandogan I Heart Surg Forum; 2007; 10(3):E211-2. PubMed ID: 17599892 [TBL] [Abstract][Full Text] [Related]
31. Targeted inhibition of ANKRD1 disrupts sarcomeric ERK-GATA4 signal transduction and abrogates phenylephrine-induced cardiomyocyte hypertrophy. Zhong L; Chiusa M; Cadar AG; Lin A; Samaras S; Davidson JM; Lim CC Cardiovasc Res; 2015 May; 106(2):261-71. PubMed ID: 25770146 [TBL] [Abstract][Full Text] [Related]
32. Acute pulmonary edema in a newborn with infracardiac type total anomalous pulmonary venous return and surgical repair. Yalçinbaş YK; Erek E; Salihoğlu E; Oztürk N; Mamur G; Soybir N; Sarioğlu A; Sarioğlu T Turk J Pediatr; 2004; 46(2):179-81. PubMed ID: 15214752 [TBL] [Abstract][Full Text] [Related]
33. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation. Jamieson RV; Farrar N; Stewart K; Perveen R; Mihelec M; Carette M; Grigg JR; McAvoy JW; Lovicu FJ; Tam PP; Scambler P; Lloyd IC; Donnai D; Black GC Hum Mutat; 2007 Oct; 28(10):968-77. PubMed ID: 17492639 [TBL] [Abstract][Full Text] [Related]
34. Clinical Presentation and Therapy of Total Anomalous Pulmonary Venous Return. Haas NA; Driscoll DJ; Rickert-Sperling S Adv Exp Med Biol; 2024; 1441():587-591. PubMed ID: 38884734 [TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis and antenatal history of total anomalous pulmonary venous return. Chen YY; Hsu CY Taiwan J Obstet Gynecol; 2006 Sep; 45(3):283-5. PubMed ID: 17175483 [TBL] [Abstract][Full Text] [Related]
36. Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment. Schneider E; Märker T; Daser A; Frey-Mahn G; Beyer V; Farcas R; Schneider-Rätzke B; Kohlschmidt N; Grossmann B; Bauss K; Napiontek U; Keilmann A; Bartsch O; Zechner U; Wolfrum U; Haaf T Hum Mol Genet; 2009 Feb; 18(4):655-66. PubMed ID: 19028668 [TBL] [Abstract][Full Text] [Related]
37. ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene. Moulik M; Vatta M; Witt SH; Arola AM; Murphy RT; McKenna WJ; Boriek AM; Oka K; Labeit S; Bowles NE; Arimura T; Kimura A; Towbin JA J Am Coll Cardiol; 2009 Jul; 54(4):325-33. PubMed ID: 19608030 [TBL] [Abstract][Full Text] [Related]
38. Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation. Bocciardi R; Giorda R; Buttgereit J; Gimelli S; Divizia MT; Beri S; Garofalo S; Tavella S; Lerone M; Zuffardi O; Bader M; Ravazzolo R; Gimelli G Hum Mutat; 2007 Jul; 28(7):724-31. PubMed ID: 17373680 [TBL] [Abstract][Full Text] [Related]
39. Cardiac distribution of alpha-hANP in an infant with total anomalous pulmonary venous return. Sakai T; Tanioka F; Kudoh T; Oyama T; Matsuki A Agressologie; 1989 Feb; 30(2):101-2. PubMed ID: 2525350 [TBL] [Abstract][Full Text] [Related]
40. Common arterial trunk associated with a homeodomain mutation of NKX2.6. Heathcote K; Braybrook C; Abushaban L; Guy M; Khetyar ME; Patton MA; Carter ND; Scambler PJ; Syrris P Hum Mol Genet; 2005 Mar; 14(5):585-93. PubMed ID: 15649947 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]