BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 27589475)

  • 1. Chromosome 5q33 deletions associated with congenital heart defects.
    Starkovich M; Lalani SR; Mercer CL; Scott DA
    Am J Med Genet A; 2016 Dec; 170(12):3338-3342. PubMed ID: 27589475
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
    Wang J; Hu XQ; Guo YH; Gu JY; Xu JH; Li YJ; Li N; Yang XX; Yang YQ
    Pediatr Cardiol; 2017 Mar; 38(3):547-557. PubMed ID: 27942761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. HAND transcription factors cooperatively specify the aorta and pulmonary trunk.
    Vincentz JW; Firulli BA; Toolan KP; Osterwalder M; Pennacchio LA; Firulli AB
    Dev Biol; 2021 Aug; 476():1-10. PubMed ID: 33757801
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.
    Cohen ASA; Simotas C; Webb BD; Shi H; Khan WA; Edelmann L; Scott SA; Singh R
    Am J Med Genet A; 2020 May; 182(5):1263-1267. PubMed ID: 32134193
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duplication of HEY2 in cardiac and neurologic development.
    Jordan VK; Rosenfeld JA; Lalani SR; Scott DA
    Am J Med Genet A; 2015 Sep; 167A(9):2145-9. PubMed ID: 25832314
    [TBL] [Abstract][Full Text] [Related]  

  • 6. HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure.
    Firulli BA; George RM; Harkin J; Toolan KP; Gao H; Liu Y; Zhang W; Field LJ; Liu Y; Shou W; Payne RM; Rubart-von der Lohe M; Firulli AB
    Cardiovasc Res; 2020 Mar; 116(3):605-618. PubMed ID: 31286141
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.
    Li L; Wang J; Liu XY; Liu H; Shi HY; Yang XX; Li N; Li YJ; Huang RT; Xue S; Qiu XB; Yang YQ
    Int J Mol Med; 2017 Mar; 39(3):711-718. PubMed ID: 28112363
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A functional genetic study identifies HAND1 mutations in septation defects of the human heart.
    Reamon-Buettner SM; Ciribilli Y; Traverso I; Kuhls B; Inga A; Borlak J
    Hum Mol Genet; 2009 Oct; 18(19):3567-78. PubMed ID: 19586923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two novel HAND1 mutations in Chinese patients with ventricular septal defect.
    Cheng Z; Lib L; Li Z; Liu M; Yan J; Wang B; Ma X
    Clin Chim Acta; 2012 Apr; 413(7-8):675-7. PubMed ID: 22032825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.
    Hatemi AC; Güleç C; Cine N; Vural B; Hatırnaz O; Sayitoğlu M; Oztunç F; Saltık L; Kansız E; Erginel Ünaltuna N
    Anadolu Kardiyol Derg; 2011 Jun; 11(4):319-28. PubMed ID: 21561848
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot.
    Weiss K; Applegate C; Wang T; Batista DA
    Am J Med Genet A; 2015 Nov; 167A(11):2702-6. PubMed ID: 26139517
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
    Sun YM; Wang J; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Shi HY; Hou XM; Huang RT; Xue S; Yang YQ
    G3 (Bethesda); 2016 Apr; 6(4):987-92. PubMed ID: 26865696
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
    Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q
    Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SAP30L (Sin3A-associated protein 30-like) is involved in regulation of cardiac development and hematopoiesis in zebrafish embryos.
    Teittinen KJ; Grönroos T; Parikka M; Junttila S; Uusimäki A; Laiho A; Korkeamäki H; Kurppa K; Turpeinen H; Pesu M; Gyenesei A; Rämet M; Lohi O
    J Cell Biochem; 2012 Dec; 113(12):3843-52. PubMed ID: 22821512
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice.
    Firulli BA; Toolan KP; Harkin J; Millar H; Pineda S; Firulli AB
    Cardiovasc Res; 2017 Dec; 113(14):1732-1742. PubMed ID: 29016838
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.
    Giglio S; Graw SL; Gimelli G; Pirola B; Varone P; Voullaire L; Lerzo F; Rossi E; Dellavecchia C; Bonaglia MC; Digilio MC; Giannotti A; Marino B; Carrozzo R; Korenberg JR; Danesino C; Sujansky E; Dallapiccola B; Zuffardi O
    Circulation; 2000 Jul; 102(4):432-7. PubMed ID: 10908216
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene replacement strategies to test the functional redundancy of basic helix-loop-helix transcription factor.
    Firulli AB; Firulli BA; Wang J; Rogers RH; Conway SJ
    Pediatr Cardiol; 2010 Apr; 31(3):438-48. PubMed ID: 20155416
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
    Keitges EA; Pasion R; Burnside RD; Mason C; Gonzalez-Ruiz A; Dunn T; Masiello M; Gebbia JA; Fernandez CO; Risheg H
    Am J Med Genet A; 2013 Jul; 161A(7):1755-8. PubMed ID: 23696316
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
    Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.