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 *

251 related articles for article (PubMed ID: 22295061)

  • 1. Fishing the molecular bases of Treacher Collins syndrome.
    Weiner AM; Scampoli NL; Calcaterra NB
    PLoS One; 2012; 7(1):e29574. PubMed ID: 22295061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Proteasomal inhibition attenuates craniofacial malformations in a zebrafish model of Treacher Collins Syndrome.
    Rosas MG; Lorenzatti A; Porcel de Peralta MS; Calcaterra NB; Coux G
    Biochem Pharmacol; 2019 May; 163():362-370. PubMed ID: 30849304
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathogenesis of POLR1C-dependent Type 3 Treacher Collins Syndrome revealed by a zebrafish model.
    Lau MC; Kwong EM; Lai KP; Li JW; Ho JC; Chan TF; Wong CK; Jiang YJ; Tse WK
    Biochim Biophys Acta; 2016 Jun; 1862(6):1147-58. PubMed ID: 26972049
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome.
    Dixon J; Brakebusch C; Fässler R; Dixon MJ
    Hum Mol Genet; 2000 Jun; 9(10):1473-80. PubMed ID: 10888597
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reduced TCOF1 mRNA level in a rhesus macaque with Treacher Collins-like syndrome: further evidence for haploinsufficiency of treacle as the cause of disease.
    Shows KH; Ward C; Summers L; Li L; Ziegler GR; Hendrickx AG; Shiang R
    Mamm Genome; 2006 Feb; 17(2):168-77. PubMed ID: 16465596
    [TBL] [Abstract][Full Text] [Related]  

  • 7. POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4.
    Sanchez E; Laplace-Builhé B; Mau-Them FT; Richard E; Goldenberg A; Toler TL; Guignard T; Gatinois V; Vincent M; Blanchet C; Boland A; Bihoreau MT; Deleuze JF; Olaso R; Nephi W; Lüdecke HJ; Verheij JBGM; Moreau-Lenoir F; Denoyelle F; Rivière JB; Laplanche JL; Willing M; Captier G; Apparailly F; Wieczorek D; Collet C; Djouad F; Geneviève D
    Genet Med; 2020 Mar; 22(3):547-556. PubMed ID: 31649276
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The transcription of the main gene associated with Treacher-Collins syndrome (TCOF1) is regulated by G-quadruplexes and cellular nucleic acid binding protein (CNBP).
    Gil Rosas M; Centola C; Torres M; Mouguelar VS; David AP; Piga EJ; Gomez D; Calcaterra NB; Armas P; Coux G
    Sci Rep; 2024 Mar; 14(1):7472. PubMed ID: 38553547
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tissue specific roles for the ribosome biogenesis factor Wdr43 in zebrafish development.
    Zhao C; Andreeva V; Gibert Y; LaBonty M; Lattanzi V; Prabhudesai S; Zhou Y; Zon L; McCann KL; Baserga S; Yelick PC
    PLoS Genet; 2014 Jan; 10(1):e1004074. PubMed ID: 24497835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders.
    Calo E; Gu B; Bowen ME; Aryan F; Zalc A; Liang J; Flynn RA; Swigut T; Chang HY; Attardi LD; Wysocka J
    Nature; 2018 Feb; 554(7690):112-117. PubMed ID: 29364875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Treacher Collins syndrome: unmasking the role of Tcof1/treacle.
    Sakai D; Trainor PA
    Int J Biochem Cell Biol; 2009 Jun; 41(6):1229-32. PubMed ID: 19027870
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Treacher Collins syndrome.
    Dixon J; Trainor P; Dixon MJ
    Orthod Craniofac Res; 2007 May; 10(2):88-95. PubMed ID: 17552945
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tcof1-Related Molecular Networks in Treacher Collins Syndrome.
    Dai J; Si J; Wang M; Huang L; Fang B; Shi J; Wang X; Shen G
    J Craniofac Surg; 2016 Sep; 27(6):1420-6. PubMed ID: 27300466
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients.
    Masotti C; Ornelas CC; Splendore-Gordonos A; Moura R; Félix TM; Alonso N; Camargo AA; Passos-Bueno MR
    BMC Med Genet; 2009 Dec; 10():136. PubMed ID: 20003452
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning and functional characterization of the Xenopus orthologue of the Treacher Collins syndrome (TCOF1) gene product.
    Gonzales B; Yang H; Henning D; Valdez BC
    Gene; 2005 Oct; 359():73-80. PubMed ID: 16125876
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis of the TCOF1 gene in 11 Japanese patients with Treacher Collins Syndrome and mechanism of mutagenesis.
    Horiuchi K; Ariga T; Fujioka H; Kawashima K; Yamamoto Y; Igawa H; Sugihara T; Sakiyama Y
    Am J Med Genet A; 2005 May; 134(4):363-7. PubMed ID: 15759264
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel Human Pluripotent Stem Cell-Derived Neural Crest Model of Treacher Collins Syndrome Shows Defects in Cell Death and Migration.
    Serrano F; Bernard WG; Granata A; Iyer D; Steventon B; Kim M; Vallier L; Gambardella L; Sinha S
    Stem Cells Dev; 2019 Jan; 28(2):81-100. PubMed ID: 30375284
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Treacher Collins Syndrome: the genetics of a craniofacial disease.
    Kadakia S; Helman SN; Badhey AK; Saman M; Ducic Y
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):893-8. PubMed ID: 24690222
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
    So RB; Gonzales B; Henning D; Dixon J; Dixon MJ; Valdez BC
    Gene; 2004 Mar; 328():49-57. PubMed ID: 15019983
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.
    Su PH; Chen JY; Chen SJ; Yu JS
    J Formos Med Assoc; 2006 Jun; 105(6):518-21. PubMed ID: 16801042
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.