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.
300 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]
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]