437 related articles for article (PubMed ID: 16938878)
21. Genomewide analysis of gene expression associated with Tcof1 in mouse neuroblastoma.
Mogass M; York TP; Li L; Rujirabanjerd S; Shiang R
Biochem Biophys Res Commun; 2004 Dec; 325(1):124-32. PubMed ID: 15522210
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. 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]
26. A quantitative method for defining high-arched palate using the Tcof1(+/-) mutant mouse as a model.
Conley ZR; Hague M; Kurosaka H; Dixon J; Dixon MJ; Trainor PA
Dev Biol; 2016 Jul; 415(2):296-305. PubMed ID: 26772999
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. 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]
29. Genetic mutations in ribosomal biogenesis gene TCOF1 identified in human neural tube defects.
Wang F; Cheng H; Zhang Q; Guo J
Mol Genet Genomic Med; 2023 May; 11(5):e2150. PubMed ID: 36808708
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Clinical features, treatment and genetic background of Treacher Collins syndrome.
Marszałek B; Wójcicki P; Kobus K; Trzeciak WH
J Appl Genet; 2002; 43(2):223-33. PubMed ID: 12080178
[TBL] [Abstract][Full Text] [Related]
33. First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome.
Beygo J; Buiting K; Seland S; Lüdecke HJ; Hehr U; Lich C; Prager B; Lohmann DR; Wieczorek D
Mol Syndromol; 2012 Jan; 2(2):53-59. PubMed ID: 22712005
[TBL] [Abstract][Full Text] [Related]
34. Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse.
Richter CA; Amin S; Linden J; Dixon J; Dixon MJ; Tucker AS
Hum Mol Genet; 2010 Apr; 19(8):1551-60. PubMed ID: 20106873
[TBL] [Abstract][Full Text] [Related]
35. Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development.
Falcon KT; Watt KEN; Dash S; Zhao R; Sakai D; Moore EL; Fitriasari S; Childers M; Sardiu ME; Swanson S; Tsuchiya D; Unruh J; Bugarinovic G; Li L; Shiang R; Achilleos A; Dixon J; Dixon MJ; Trainor PA
Proc Natl Acad Sci U S A; 2022 Aug; 119(31):e2116974119. PubMed ID: 35881792
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Balancing neural crest cell intrinsic processes with those of the microenvironment in Tcof1 haploinsufficient mice enables complete enteric nervous system formation.
Barlow AJ; Dixon J; Dixon MJ; Trainor PA
Hum Mol Genet; 2012 Apr; 21(8):1782-93. PubMed ID: 22228097
[TBL] [Abstract][Full Text] [Related]
39. Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome.
Isaac C; Marsh KL; Paznekas WA; Dixon J; Dixon MJ; Jabs EW; Meier UT
Mol Biol Cell; 2000 Sep; 11(9):3061-71. PubMed ID: 10982400
[TBL] [Abstract][Full Text] [Related]
40. Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome.
Yan Z; Lu Y; Wang Y; Zhang X; Duan H; Cheng J; Yuan H; Han D
Exp Ther Med; 2018 Sep; 16(3):2645-2650. PubMed ID: 30186496
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
