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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 21457232)

  • 1. Identification of de novo mutations and rare variants in hypoplastic left heart syndrome.
    Iascone M; Ciccone R; Galletti L; Marchetti D; Seddio F; Lincesso AR; Pezzoli L; Vetro A; Barachetti D; Boni L; Federici D; Soto AM; Comas JV; Ferrazzi P; Zuffardi O
    Clin Genet; 2012 Jun; 81(6):542-54. PubMed ID: 21457232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Directed differentiation of patient-specific induced pluripotent stem cells identifies the transcriptional repression and epigenetic modification of NKX2-5, HAND1, and NOTCH1 in hypoplastic left heart syndrome.
    Kobayashi J; Yoshida M; Tarui S; Hirata M; Nagai Y; Kasahara S; Naruse K; Ito H; Sano S; Oh H
    PLoS One; 2014; 9(7):e102796. PubMed ID: 25050861
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart.
    Esposito G; Butler TL; Blue GM; Cole AD; Sholler GF; Kirk EP; Grossfeld P; Perryman BM; Harvey RP; Winlaw DS
    Am J Med Genet A; 2011 Oct; 155A(10):2416-21. PubMed ID: 22043484
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypoplastic Left Heart Syndrome Sequencing Reveals a Novel NOTCH1 Mutation in a Family with Single Ventricle Defects.
    Durbin MD; Cadar AG; Williams CH; Guo Y; Bichell DP; Su YR; Hong CC
    Pediatr Cardiol; 2017 Aug; 38(6):1232-1240. PubMed ID: 28608148
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.
    Theis JL; Hrstka SC; Evans JM; O'Byrne MM; de Andrade M; O'Leary PW; Nelson TJ; Olson TM
    Hum Genet; 2015 Sep; 134(9):1003-11. PubMed ID: 26164125
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
    Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP
    J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
    Warburton D; Ronemus M; Kline J; Jobanputra V; Williams I; Anyane-Yeboa K; Chung W; Yu L; Wong N; Awad D; Yu CY; Leotta A; Kendall J; Yamrom B; Lee YH; Wigler M; Levy D
    Hum Genet; 2014 Jan; 133(1):11-27. PubMed ID: 23979609
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NOTCH1-Dependent Nitric Oxide Signaling Deficiency in Hypoplastic Left Heart Syndrome Revealed Through Patient-Specific Phenotypes Detected in Bioengineered Cardiogenesis.
    Hrstka SC; Li X; Nelson TJ;
    Stem Cells; 2017 Apr; 35(4):1106-1119. PubMed ID: 28142228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts.
    Reamon-Buettner SM; Ciribilli Y; Inga A; Borlak J
    Hum Mol Genet; 2008 May; 17(10):1397-405. PubMed ID: 18276607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation.
    Adhicary S; Ye S; Lin H; Texter K; Garg V; Zhao MT
    Stem Cell Res; 2023 Feb; 66():103013. PubMed ID: 36599283
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-Wide Association and Inheritance-Based Analyses Implicate Unconventional Myosin Genes in Hypoplastic Left Heart Syndrome.
    Theis JL; Shatila SH; Fogarty ZC; Bamlet WR; Olson TM
    Circ Genom Precis Med; 2023 Feb; 16(1):e003761. PubMed ID: 36580305
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Theis JL; Niaz T; Sundsbak RS; Fogarty ZC; Bamlet WR; Hagler DJ; Olson TM
    Circ Genom Precis Med; 2022 Apr; 15(2):e003523. PubMed ID: 35133174
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of MYH6 variants in hypoplastic left heart syndrome.
    Tomita-Mitchell A; Stamm KD; Mahnke DK; Kim MS; Hidestrand PM; Liang HL; Goetsch MA; Hidestrand M; Simpson P; Pelech AN; Tweddell JS; Benson DW; Lough JW; Mitchell ME
    Physiol Genomics; 2016 Dec; 48(12):912-921. PubMed ID: 27789736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel Insights into the Etiology, Genetics, and Embryology of Hypoplastic Left Heart Syndrome.
    Gabriel GC; Yagi H; Xu X; Lo CW
    World J Pediatr Congenit Heart Surg; 2022 Sep; 13(5):565-570. PubMed ID: 36053093
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.
    Payne AR; Chang SW; Koenig SN; Zinn AR; Garg V
    Pediatr Cardiol; 2012 Jun; 33(5):757-63. PubMed ID: 22349727
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transcriptional Impact of Rare and Private Copy Number Variants in Hypoplastic Left Heart Syndrome.
    Glidewell SC; Miyamoto SD; Grossfeld PD; Clouthier DE; Coldren CD; Stearman RS; Geraci MW
    Clin Transl Sci; 2015 Dec; 8(6):682-9. PubMed ID: 26534787
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The complex genetics of hypoplastic left heart syndrome.
    Liu X; Yagi H; Saeed S; Bais AS; Gabriel GC; Chen Z; Peterson KA; Li Y; Schwartz MC; Reynolds WT; Saydmohammed M; Gibbs B; Wu Y; Devine W; Chatterjee B; Klena NT; Kostka D; de Mesy Bentley KL; Ganapathiraju MK; Dexheimer P; Leatherbury L; Khalifa O; Bhagat A; Zahid M; Pu W; Watkins S; Grossfeld P; Murray SA; Porter GA; Tsang M; Martin LJ; Benson DW; Aronow BJ; Lo CW
    Nat Genet; 2017 Jul; 49(7):1152-1159. PubMed ID: 28530678
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
    Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E
    Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.