BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

298 related articles for article (PubMed ID: 33127760)

  • 1. CHD7 regulates cardiovascular development through ATP-dependent and -independent activities.
    Yan S; Thienthanasit R; Chen D; Engelen E; Brühl J; Crossman DK; Kesterson R; Wang Q; Bouazoune K; Jiao K
    Proc Natl Acad Sci U S A; 2020 Nov; 117(46):28847-28858. PubMed ID: 33127760
    [No Abstract]   [Full Text] [Related]  

  • 2. CHARGEd with neural crest defects.
    Pauli S; Bajpai R; Borchers A
    Am J Med Genet C Semin Med Genet; 2017 Dec; 175(4):478-486. PubMed ID: 29082625
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome.
    Balow SA; Pierce LX; Zentner GE; Conrad PA; Davis S; Sabaawy HE; McDermott BM; Scacheri PC
    Dev Biol; 2013 Oct; 382(1):57-69. PubMed ID: 23920116
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes.
    Meisner JK; Martin DM
    Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):81-89. PubMed ID: 31833191
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome.
    Gage PJ; Hurd EA; Martin DM
    Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):7923-30. PubMed ID: 26670829
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The cardiac phenotype in patients with a CHD7 mutation.
    Corsten-Janssen N; Kerstjens-Frederikse WS; du Marchie Sarvaas GJ; Baardman ME; Bakker MK; Bergman JE; Hove HD; Heimdal KR; Rustad CF; Hennekam RC; Hofstra RM; Hoefsloot LH; Van Ravenswaaij-Arts CM; Kapusta L
    Circ Cardiovasc Genet; 2013 Jun; 6(3):248-54. PubMed ID: 23677905
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inappropriate p53 activation during development induces features of CHARGE syndrome.
    Van Nostrand JL; Brady CA; Jung H; Fuentes DR; Kozak MM; Johnson TM; Lin CY; Lin CJ; Swiderski DL; Vogel H; Bernstein JA; Attié-Bitach T; Chang CP; Wysocka J; Martin DM; Attardi LD
    Nature; 2014 Oct; 514(7521):228-32. PubMed ID: 25119037
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and molecular effects of CHD7 in the heart.
    Corsten-Janssen N; Scambler PJ
    Am J Med Genet C Semin Med Genet; 2017 Dec; 175(4):487-495. PubMed ID: 29088513
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.
    Schnetz MP; Bartels CF; Shastri K; Balasubramanian D; Zentner GE; Balaji R; Zhang X; Song L; Wang Z; Laframboise T; Crawford GE; Scacheri PC
    Genome Res; 2009 Apr; 19(4):590-601. PubMed ID: 19251738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
    Lalani SR; Safiullah AM; Fernbach SD; Harutyunyan KG; Thaller C; Peterson LE; McPherson JD; Gibbs RA; White LD; Hefner M; Davenport SL; Graham JM; Bacino CA; Glass NL; Towbin JA; Craigen WJ; Neish SR; Lin AE; Belmont JW
    Am J Hum Genet; 2006 Feb; 78(2):303-14. PubMed ID: 16400610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chd7 Is Critical for Early T-Cell Development and Thymus Organogenesis in Zebrafish.
    Liu ZZ; Wang ZL; Choi TI; Huang WT; Wang HT; Han YY; Zhu LY; Kim HT; Choi JH; Lee JS; Kim HG; Zhao J; Chen Y; Lu Z; Tian XL; Pan BX; Li BM; Kim CH; Xu HA
    Am J Pathol; 2018 Apr; 188(4):1043-1058. PubMed ID: 29353058
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromatin remodeling by the CHD7 protein is impaired by mutations that cause human developmental disorders.
    Bouazoune K; Kingston RE
    Proc Natl Acad Sci U S A; 2012 Nov; 109(47):19238-43. PubMed ID: 23134727
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellum.
    Reddy NC; Majidi SP; Kong L; Nemera M; Ferguson CJ; Moore M; Goncalves TM; Liu HK; Fitzpatrick JAJ; Zhao G; Yamada T; Bonni A; Gabel HW
    Nat Commun; 2021 Sep; 12(1):5702. PubMed ID: 34588434
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.
    Yao H; Hill SF; Skidmore JM; Sperry ED; Swiderski DL; Sanchez GJ; Bartels CF; Raphael Y; Scacheri PC; Iwase S; Martin DM
    JCI Insight; 2018 Feb; 3(4):. PubMed ID: 29467333
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Role of Chd7 in zebrafish: a model for CHARGE syndrome.
    Patten SA; Jacobs-McDaniels NL; Zaouter C; Drapeau P; Albertson RC; Moldovan F
    PLoS One; 2012; 7(2):e31650. PubMed ID: 22363697
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CHD7 cooperates with PBAF to control multipotent neural crest formation.
    Bajpai R; Chen DA; Rada-Iglesias A; Zhang J; Xiong Y; Helms J; Chang CP; Zhao Y; Swigut T; Wysocka J
    Nature; 2010 Feb; 463(7283):958-62. PubMed ID: 20130577
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The ATP-dependent chromatin remodeling enzymes CHD6, CHD7, and CHD8 exhibit distinct nucleosome binding and remodeling activities.
    Manning BJ; Yusufzai T
    J Biol Chem; 2017 Jul; 292(28):11927-11936. PubMed ID: 28533432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome.
    Basson MA; van Ravenswaaij-Arts C
    Trends Genet; 2015 Oct; 31(10):600-611. PubMed ID: 26411921
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.
    Schulz Y; Wehner P; Opitz L; Salinas-Riester G; Bongers EM; van Ravenswaaij-Arts CM; Wincent J; Schoumans J; Kohlhase J; Borchers A; Pauli S
    Hum Genet; 2014 Aug; 133(8):997-1009. PubMed ID: 24728844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo Splice Site Mutation of the CHD7 Gene in a Chinese Patient with Typical CHARGE Syndrome.
    Wang S; Lin Y; Liang P; Li Q; Li W; Wang Z; Wang J; Chen J; Zha D
    ORL J Otorhinolaryngol Relat Spec; 2022; 84(5):417-424. PubMed ID: 35078197
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.