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 *

208 related articles for article (PubMed ID: 29660852)

  • 1. Etiology and functional validation of gastrointestinal motility dysfunction in a zebrafish model of CHARGE syndrome.
    Cloney K; Steele SL; Stoyek MR; Croll RP; Smith FM; Prykhozhij SV; Brown MM; Midgen C; Blake K; Berman JN
    FEBS J; 2018 Jun; 285(11):2125-2140. PubMed ID: 29660852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. Chemical screens in a zebrafish model of CHARGE syndrome identifies small molecules that ameliorate disease-like phenotypes in embryo.
    Asad Z; Sachidanandan C
    Eur J Med Genet; 2020 Feb; 63(2):103661. PubMed ID: 31051269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
    Balasubramanian R; Choi JH; Francescatto L; Willer J; Horton ER; Asimacopoulos EP; Stankovic KM; Plummer L; Buck CL; Quinton R; Nebesio TD; Mericq V; Merino PM; Meyer BF; Monies D; Gusella JF; Al Tassan N; Katsanis N; Crowley WF
    Proc Natl Acad Sci U S A; 2014 Dec; 111(50):17953-8. PubMed ID: 25472840
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Aggressive-like behavior and increased glycine transporters in a zebrafish model of CHARGE syndrome.
    Liu H; Liu ZZ
    Behav Brain Res; 2020 Jan; 378():112293. PubMed ID: 31610215
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CHD7 regulates craniofacial cartilage development via controlling HTR2B expression.
    Breuer M; Rummler M; Singh J; Maher S; Zaouter C; Jamadagni P; Pilon N; Willie BM; Patten SA
    J Bone Miner Res; 2024 May; 39(4):498-512. PubMed ID: 38477756
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Mutation update on the CHD7 gene involved in CHARGE syndrome.
    Janssen N; Bergman JE; Swertz MA; Tranebjaerg L; Lodahl M; Schoots J; Hofstra RM; van Ravenswaaij-Arts CM; Hoefsloot LH
    Hum Mutat; 2012 Aug; 33(8):1149-60. PubMed ID: 22461308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14.
    MacLean JE; Wertman JN; Prykhozhij SV; Chedrawe E; Langley S; Steele SL; Ban K; Blake K; Berman JN
    Genes (Basel); 2023 May; 14(5):. PubMed ID: 37239446
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chd7 plays a critical role in controlling left-right symmetry during zebrafish somitogenesis.
    Jacobs-McDaniels NL; Albertson RC
    Dev Dyn; 2011 Oct; 240(10):2272-80. PubMed ID: 21901784
    [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. 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]  

  • 18. Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structures.
    Choo DI; Tawfik KO; Martin DM; Raphael Y
    Am J Med Genet C Semin Med Genet; 2017 Dec; 175(4):439-449. PubMed ID: 29082607
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Identification of one novel CHD7 mutation in a patient from China with atypical CHARGE syndrome.
    Cheng J; Ma D; Wu Y; Luo C; Huang C; Hu P; Zhang J; Jiang T; Xu Z
    Gene; 2015 Oct; 571(2):298-302. PubMed ID: 26187070
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.