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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 29631691

  • 21. Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot.
    Kheirollahi M, Khosravi F, Ashouri S, Ahmadi A.
    J Res Med Sci; 2016; 21():24. PubMed ID: 27904570
    [Abstract] [Full Text] [Related]

  • 22. Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot.
    Huang RT, Xue S, Xu YJ, Yang YQ.
    Int J Mol Med; 2013 Jan; 31(1):51-8. PubMed ID: 23175051
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
    Zhao Y, Kang X, Gao F, Guzman A, Lau RP, Biniwale R, Wadehra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Van Arsdell G, Coppola G, Nelson SF, Touma M, UCLA Congenital Heart Defects BioCore Faculty.
    J Mol Med (Berl); 2019 Dec 15; 97(12):1711-1722. PubMed ID: 31834445
    [Abstract] [Full Text] [Related]

  • 25. 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 15; 38(3):547-557. PubMed ID: 27942761
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Genetic Origins of Tetralogy of Fallot.
    Morgenthau A, Frishman WH.
    Cardiol Rev; 2018 Mar 15; 26(2):86-92. PubMed ID: 29045289
    [Abstract] [Full Text] [Related]

  • 29. BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis.
    Shi Y, Li Y, Wang Y, Zhu P, Chen Y, Wang H, Yue S, Xia X, Chen J, Jiang Z, Zhou C, Cai W, Yuan H, Wu Y, Wan Y, Li X, Zhu X, Zhou Z, Dai G, Li F, Mo X, Ye X, Fan X, Zhuang J, Wu X, Yuan W.
    Sci Rep; 2020 Aug 25; 10(1):14167. PubMed ID: 32843646
    [Abstract] [Full Text] [Related]

  • 30. Role of fibrillin-1 genetic mutations and polymorphism in aortic dilatation in patients undergoing intracardiac repair of tetralogy of Fallot.
    Chowdhury UK, Mishra AK, Balakrishnan P, Sharma S, Kabra M, Ray R, Kalaivani M, Gupta R, Govindappa RM, Subramaniam GK.
    J Thorac Cardiovasc Surg; 2008 Sep 25; 136(3):757-66, 766.e1-10. PubMed ID: 18805282
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair.
    Jeewa A, Manickaraj AK, Mertens L, Manlhiot C, Kinnear C, Mondal T, Smythe J, Rosenberg H, Lougheed J, McCrindle BW, van Arsdell G, Redington AN, Mital S.
    Pediatr Res; 2012 Oct 25; 72(4):407-13. PubMed ID: 22797143
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. The tetralogy of Fallot-associated G274D mutation impairs folding of the second epidermal growth factor repeat in Jagged-1.
    Guarnaccia C, Dhir S, Pintar A, Pongor S.
    FEBS J; 2009 Nov 25; 276(21):6247-57. PubMed ID: 19780835
    [Abstract] [Full Text] [Related]

  • 38. DNA microarray and quantitative analysis reveal enhanced myocardial VEGF expression with stunted angiogenesis in human tetralogy of Fallot.
    Peters TH, Sharma V, Yilmaz E, Mooi WJ, Bogers AJ, Sharma HS.
    Cell Biochem Biophys; 2013 Nov 25; 67(2):305-16. PubMed ID: 23897578
    [Abstract] [Full Text] [Related]

  • 39. Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
    Qian Y, Xiao D, Guo X, Chen H, Hao L, Ma X, Huang G, Ma D, Wang H.
    J Transl Med; 2017 Apr 03; 15(1):69. PubMed ID: 28372585
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.