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    Results: 1 to 20 of 136

    1.

    We need a detailed phenome in the phenomenon of genetics and congenital heart disease.

    Posch MG, Berger F, Perrot A, Ozcelik C.

    J Med Genet. 2008 May;45(5):320. No abstract available. PMID: 18443152 [PubMed - indexed for MEDLINE]Related articles

    2.

    GATA4 mutation and congenital cardiovascular diseases: importance of phenotype and genetic background clarification.

    Matsuoka R.

    J Mol Cell Cardiol. 2007 Dec;43(6):667-9. Epub 2007 Sep 5. No abstract available. PMID: 17961590 [PubMed - indexed for MEDLINE]Related articles

    3.

    GATA4 mutations in 486 Chinese patients with congenital heart disease.

    Zhang W, Li X, Shen A, Jiao W, Guan X, Li Z.

    Eur J Med Genet. 2008 Nov-Dec;51(6):527-35. Epub 2008 Jul 11.PMID: 18672102 [PubMed - indexed for MEDLINE]Related articles

    4.

    Screening of 99 Danish patients with congenital heart disease for GATA4 mutations.

    Zhang L, Tümer Z, Jacobsen JR, Andersen PS, Tommerup N, Larsen LA.

    Genet Test. 2006 Winter;10(4):277-80.PMID: 17253934 [PubMed - indexed for MEDLINE]Related articles

    5.

    Transcription factor cascades in congenital heart malformation.

    Hatcher CJ, Diman NY, McDermott DA, Basson CT.

    Trends Mol Med. 2003 Dec;9(12):512-5. Review. No abstract available. PMID: 14659463 [PubMed - indexed for MEDLINE]Related articles

    6.

    Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).

    Reamon-Buettner SM, Cho SH, Borlak J.

    BMC Med Genet. 2007 Jun 25;8:38.PMID: 17592645 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    A duplication including GATA4 does not co-segregate with congenital heart defects.

    Joziasse IC, van der Smagt JJ, Poot M, Hochstenbach R, Nelen MR, van Gijn M, Dooijes D, Mulder BJ, Doevendans PA.

    Am J Med Genet A. 2009 May;149A(5):1062-6. No abstract available. PMID: 19353638 [PubMed - indexed for MEDLINE]Related articles

    8.

    Mutations of transcription factors in human with heart disease for understanding the development and mechanisms of congenital cardiovascular heart disease.

    Matsuoka R.

    Adv Exp Med Biol. 2005;565:349-57; discussion 405-15. No abstract available. PMID: 16106988 [PubMed - indexed for MEDLINE]Related articles

    9.

    Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.

    Sarkozy A, Conti E, Neri C, D'Agostino R, Digilio MC, Esposito G, Toscano A, Marino B, Pizzuti A, Dallapiccola B.

    J Med Genet. 2005 Feb;42(2):e16. No abstract available. PMID: 15689439 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits.

    Páez MT, Yamamoto T, Hayashi K, Yasuda T, Harada N, Matsumoto N, Kurosawa K, Furutani Y, Asakawa S, Shimizu N, Matsuoka R.

    Am J Med Genet A. 2008 May 1;146A(9):1158-65.PMID: 18393291 [PubMed - indexed for MEDLINE]Related articles

    11.

    Recent advances in cardiac development with therapeutic implications for adult cardiovascular disease.

    Epstein JA, Parmacek MS.

    Circulation. 2005 Jul 26;112(4):592-7. Review. No abstract available. PMID: 16043659 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart.

    Reamon-Buettner SM, Borlak J.

    J Med Genet. 2005 May;42(5):e32. No abstract available. PMID: 15863664 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.

    Posch MG, Perrot A, Schmitt K, Mittelhaus S, Esenwein EM, Stiller B, Geier C, Dietz R, Gessner R, Ozcelik C, Berger F.

    Am J Med Genet A. 2008 Jan 15;146A(2):251-3. No abstract available. PMID: 18076106 [PubMed - indexed for MEDLINE]Related articles

    14.

    GATA4 as candidate gene for pericardial defects.

    Saffirio C, Marino B, Digilio MC.

    Ann Thorac Surg. 2007 Dec;84(6):2137; author reply 2137. No abstract available. PMID: 18036970 [PubMed - indexed for MEDLINE]Related articles

    15.

    Cardiac development: new concepts.

    Gruber PJ.

    Clin Perinatol. 2005 Dec;32(4):845-55, vii. Review.PMID: 16325665 [PubMed - indexed for MEDLINE]Related articles

    16.

    Bibliography. Current world literature. Molecular genetics.

    [No authors listed]

    Curr Opin Cardiol. 2004 May;19(3):278-87. No abstract available. PMID: 15096962 [PubMed - indexed for MEDLINE]Related articles

    17.

    CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects.

    Sarkozy A, Esposito G, Conti E, Digilio MC, Marino B, Calabrò R, Pizzuti A, Dallapiccola B.

    Am J Med Genet A. 2005 Dec 15;139(3):236-8. No abstract available. PMID: 16278904 [PubMed - indexed for MEDLINE]Related articles

    18.

    The genetics of congenital heart disease.

    Grossfeld PD.

    J Nucl Cardiol. 2003 Jan-Feb;10(1):71-6. Review. No abstract available. PMID: 12569334 [PubMed - indexed for MEDLINE]Related articles

    19.

    Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5: identification of a novel mutation.

    König K, Will JC, Berger F, Müller D, Benson DW.

    Clin Res Cardiol. 2006 Sep;95(9):499-503. Epub 2006 Jul 20. No abstract available. PMID: 16845574 [PubMed - indexed for MEDLINE]Related articles

    20.

    Progress and challenges in the genetics of congenital heart disease.

    Winlaw DS, Sholler GF, Harvey RP.

    Med J Aust. 2005 Feb 7;182(3):100-1. No abstract available. PMID: 15698349 [PubMed - indexed for MEDLINE]Related articlesFree article

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