BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 24728844)

  • 1. 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]  

  • 2. Sema3a plays a role in the pathogenesis of CHARGE syndrome.
    Ufartes R; Schwenty-Lara J; Freese L; Neuhofer C; Möller J; Wehner P; van Ravenswaaij-Arts CMA; Wong MTY; Schanze I; Tzschach A; Bartsch O; Borchers A; Pauli S
    Hum Mol Genet; 2018 Apr; 27(8):1343-1352. PubMed ID: 29432577
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sema3E is required for migration of cranial neural crest cells in zebrafish: Implications for the pathogenesis of CHARGE syndrome.
    Liu ZZ; Guo J; Lu Y; Liu W; Fu X; Yao T; Zhou Y; Xu HA
    Int J Exp Pathol; 2019 Aug; 100(4):234-243. PubMed ID: 31464029
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Rescue of neural crest-derived phenotypes in a zebrafish CHARGE model by Sox10 downregulation.
    Asad Z; Pandey A; Babu A; Sun Y; Shevade K; Kapoor S; Ullah I; Ranjan S; Scaria V; Bajpai R; Sachidanandan C
    Hum Mol Genet; 2016 Aug; 25(16):3539-3554. PubMed ID: 27418670
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.
    Sperry ED; Hurd EA; Durham MA; Reamer EN; Stein AB; Martin DM
    Dev Dyn; 2014 Sep; 243(9):1055-66. PubMed ID: 24975120
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations.
    Okuno H; Renault Mihara F; Ohta S; Fukuda K; Kurosawa K; Akamatsu W; Sanosaka T; Kohyama J; Hayashi K; Nakajima K; Takahashi T; Wysocka J; Kosaki K; Okano H
    Elife; 2017 Nov; 6():. PubMed ID: 29179815
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Study of smell and reproductive organs in a mouse model for CHARGE syndrome.
    Bergman JE; Bosman EA; van Ravenswaaij-Arts CM; Steel KP
    Eur J Hum Genet; 2010 Feb; 18(2):171-7. PubMed ID: 19809474
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.
    Sanlaville D; Etchevers HC; Gonzales M; Martinovic J; Clément-Ziza M; Delezoide AL; Aubry MC; Pelet A; Chemouny S; Cruaud C; Audollent S; Esculpavit C; Goudefroye G; Ozilou C; Fredouille C; Joye N; Morichon-Delvallez N; Dumez Y; Weissenbach J; Munnich A; Amiel J; Encha-Razavi F; Lyonnet S; Vekemans M; Attié-Bitach T
    J Med Genet; 2006 Mar; 43(3):211-217. PubMed ID: 16169932
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Chromatin remodeler CHD7 targets active enhancer region to regulate cell type-specific gene expression in human neural crest cells.
    Sanosaka T; Okuno H; Mizota N; Andoh-Noda T; Sato M; Tomooka R; Banno S; Kohyama J; Okano H
    Sci Rep; 2022 Dec; 12(1):22648. PubMed ID: 36587182
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The chromatin remodeler CHD7 regulates adult neurogenesis via activation of SoxC transcription factors.
    Feng W; Khan MA; Bellvis P; Zhu Z; Bernhardt O; Herold-Mende C; Liu HK
    Cell Stem Cell; 2013 Jul; 13(1):62-72. PubMed ID: 23827709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Morphological and sensorimotor phenotypes in a zebrafish CHARGE syndrome model are domain-dependent.
    Hodorovich DR; Lindsley PM; Berry AA; Burton DF; Marsden KC
    Genes Brain Behav; 2023 Jun; 22(3):e12839. PubMed ID: 36717082
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.