420 related articles for article (PubMed ID: 18246078)
1. Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Jones NC; Lynn ML; Gaudenz K; Sakai D; Aoto K; Rey JP; Glynn EF; Ellington L; Du C; Dixon J; Dixon MJ; Trainor PA
Nat Med; 2008 Feb; 14(2):125-33. PubMed ID: 18246078
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.
Dixon J; Jones NC; Sandell LL; Jayasinghe SM; Crane J; Rey JP; Dixon MJ; Trainor PA
Proc Natl Acad Sci U S A; 2006 Sep; 103(36):13403-8. PubMed ID: 16938878
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Prevention of Treacher Collins syndrome craniofacial anomalies in mouse models via maternal antioxidant supplementation.
Sakai D; Dixon J; Achilleos A; Dixon M; Trainor PA
Nat Commun; 2016 Jan; 7():10328. PubMed ID: 26792133
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Face off against ROS: Tcof1/Treacle safeguards neuroepithelial cells and progenitor neural crest cells from oxidative stress during craniofacial development.
Sakai D; Trainor PA
Dev Growth Differ; 2016 Sep; 58(7):577-85. PubMed ID: 27481486
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.
Noack Watt KE; Achilleos A; Neben CL; Merrill AE; Trainor PA
PLoS Genet; 2016 Jul; 12(7):e1006187. PubMed ID: 27448281
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Craniofacial development: current concepts in the molecular basis of Treacher Collins syndrome.
van Gijn DR; Tucker AS; Cobourne MT
Br J Oral Maxillofac Surg; 2013 Jul; 51(5):384-8. PubMed ID: 23036831
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Pathogenic genes and clinical therapeutic strategies for Treacher Collins syndrome].
Yin B; Shi B; Jia ZL
Hua Xi Kou Qiang Yi Xue Za Zhi; 2019 Jun; 37(3):330-335. PubMed ID: 31218872
[TBL] [Abstract][Full Text] [Related]
14. Saving face: rescuing a craniofacial birth defect.
McKeown SJ; Bronner-Fraser M
Nat Med; 2008 Feb; 14(2):115-6. PubMed ID: 18256609
[No Abstract] [Full Text] [Related]
15. 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]
16. The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.
Valdez BC; Henning D; So RB; Dixon J; Dixon MJ
Proc Natl Acad Sci U S A; 2004 Jul; 101(29):10709-14. PubMed ID: 15249688
[TBL] [Abstract][Full Text] [Related]
17. Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein Treacle.
Dixon J; Dixon MJ
Dev Dyn; 2004 Apr; 229(4):907-14. PubMed ID: 15042714
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Treacher Collins syndrome: etiology, pathogenesis and prevention.
Trainor PA; Dixon J; Dixon MJ
Eur J Hum Genet; 2009 Mar; 17(3):275-83. PubMed ID: 19107148
[TBL] [Abstract][Full Text] [Related]
20. The Role of
Grzanka M; Piekiełko-Witkowska A
Int J Mol Sci; 2021 Mar; 22(5):. PubMed ID: 33804586
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]