BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 33393730)

  • 1. The power of zebrafish models for understanding the co-occurrence of craniofacial and limb disorders.
    Truong BT; Artinger KB
    Genesis; 2021 Feb; 59(1-2):e23407. PubMed ID: 33393730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The conserved and divergent roles of Prdm3 and Prdm16 in zebrafish and mouse craniofacial development.
    Shull LC; Sen R; Menzel J; Goyama S; Kurokawa M; Artinger KB
    Dev Biol; 2020 May; 461(2):132-144. PubMed ID: 32044379
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application of zebrafish in the study of craniomaxillofacial developmental anomalies.
    Li K; Fan L; Tian Y; Lou S; Li D; Ma L; Wang L; Pan Y
    Birth Defects Res; 2022 Jul; 114(12):583-595. PubMed ID: 35437950
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Using Zebrafish to Test the Genetic Basis of Human Craniofacial Diseases.
    Machado RG; Eames BF
    J Dent Res; 2017 Oct; 96(11):1192-1199. PubMed ID: 28767277
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD.
    McCarthy N; Wetherill L; Lovely CB; Swartz ME; Foroud TM; Eberhart JK
    Development; 2013 Aug; 140(15):3254-65. PubMed ID: 23861062
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes.
    de Peralta MS; Mouguelar VS; Sdrigotti MA; Ishiy FA; Fanganiello RD; Passos-Bueno MR; Coux G; Calcaterra NB
    Cell Death Dis; 2016 Oct; 7(10):e2397. PubMed ID: 27711076
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
    Debeer P; Van Esch H; Huysmans C; Pijkels E; De Smet L; Van de Ven W; Devriendt K; Fryns JP
    Eur J Med Genet; 2005; 48(4):377-87. PubMed ID: 16378922
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chemical-induced craniofacial anomalies caused by disruption of neural crest cell development in a zebrafish model.
    Liu S; Narumi R; Ikeda N; Morita O; Tasaki J
    Dev Dyn; 2020 Jul; 249(7):794-815. PubMed ID: 32314458
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data.
    Van Otterloo E; Williams T; Artinger KB
    Dev Biol; 2016 Jul; 415(2):171-187. PubMed ID: 26808208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6).
    Ingraham CR; Kinoshita A; Kondo S; Yang B; Sajan S; Trout KJ; Malik MI; Dunnwald M; Goudy SL; Lovett M; Murray JC; Schutte BC
    Nat Genet; 2006 Nov; 38(11):1335-40. PubMed ID: 17041601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ahr2, But Not ahr1a or ahr1b, Is Required for Craniofacial and Fin Development and TCDD-dependent Cardiotoxicity in Zebrafish.
    Souder JP; Gorelick DA
    Toxicol Sci; 2019 Jul; 170(1):25-44. PubMed ID: 30907958
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Grainyhead-like Transcription Factors in Craniofacial Development.
    Carpinelli MR; de Vries ME; Jane SM; Dworkin S
    J Dent Res; 2017 Oct; 96(11):1200-1209. PubMed ID: 28697314
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular dissection of craniofacial development using zebrafish.
    Yelick PC; Schilling TF
    Crit Rev Oral Biol Med; 2002; 13(4):308-22. PubMed ID: 12191958
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression.
    Quintana AM; Geiger EA; Achilly N; Rosenblatt DS; Maclean KN; Stabler SP; Artinger KB; Appel B; Shaikh TH
    Dev Biol; 2014 Dec; 396(1):94-106. PubMed ID: 25281006
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hand abnormalities associated with craniofacial syndromes.
    Panthaki ZJ; Armstrong MB
    J Craniofac Surg; 2003 Sep; 14(5):709-12. PubMed ID: 14501334
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome.
    Schwabe GC; Trepczik B; Süring K; Brieske N; Tucker AS; Sharpe PT; Minami Y; Mundlos S
    Dev Dyn; 2004 Feb; 229(2):400-10. PubMed ID: 14745966
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of adult mineralized tissue zebrafish mutants.
    Andreeva V; Connolly MH; Stewart-Swift C; Fraher D; Burt J; Cardarelli J; Yelick PC
    Genesis; 2011 Apr; 49(4):360-6. PubMed ID: 21225658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle.
    Mönnich M; Kuriger Z; Print CG; Horsfield JA
    PLoS One; 2011; 6(5):e20051. PubMed ID: 21637801
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism.
    Castro VL; Reyes-Nava NG; Sanchez BB; Gonzalez CG; Paz D; Quintana AM
    Genesis; 2020 Dec; 58(12):e23397. PubMed ID: 33197123
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A zebrafish screen for craniofacial mutants identifies wdr68 as a highly conserved gene required for endothelin-1 expression.
    Nissen RM; Amsterdam A; Hopkins N
    BMC Dev Biol; 2006 Jun; 6():28. PubMed ID: 16759393
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.