827 related articles for article (PubMed ID: 15939375)
1. Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.
Ben J; Jabs EW; Chong SS
Gene Expr Patterns; 2005 Jun; 5(5):629-38. PubMed ID: 15939375
[TBL] [Abstract][Full Text] [Related]
2. Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome.
Kim Y; Park JY; Lee TJ; Yoo HW
Int J Mol Med; 2003 Oct; 12(4):465-8. PubMed ID: 12964020
[TBL] [Abstract][Full Text] [Related]
3. A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome.
Gatta V; Scarciolla O; Cupaioli M; Palka C; Chiesa PL; Stuppia L
Mutat Res; 2004 Mar; 547(1-2):49-53. PubMed ID: 15013698
[TBL] [Abstract][Full Text] [Related]
4. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
Item CB; Turhani D; Thurnher D; Yerit K; Sinko K; Wittwer G; Adeyemo WL; Frei K; Erginel-Unaltuna N; Watzinger F; Ewers R
Int J Mol Med; 2005 Feb; 15(2):247-51. PubMed ID: 15647839
[TBL] [Abstract][Full Text] [Related]
5. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Kondo S; Schutte BC; Richardson RJ; Bjork BC; Knight AS; Watanabe Y; Howard E; de Lima RL; Daack-Hirsch S; Sander A; McDonald-McGinn DM; Zackai EH; Lammer EJ; Aylsworth AS; Ardinger HH; Lidral AC; Pober BR; Moreno L; Arcos-Burgos M; Valencia C; Houdayer C; Bahuau M; Moretti-Ferreira D; Richieri-Costa A; Dixon MJ; Murray JC
Nat Genet; 2002 Oct; 32(2):285-9. PubMed ID: 12219090
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome.
Shotelersuk V; Srichomthong C; Yoshiura K; Niikawa N
Int J Mol Med; 2003 Apr; 11(4):505-7. PubMed ID: 12632105
[TBL] [Abstract][Full Text] [Related]
7. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.
Brosch S; Baur M; Blin N; Reinert S; Pfister M
Int J Mol Med; 2007 Jul; 20(1):85-9. PubMed ID: 17549393
[TBL] [Abstract][Full Text] [Related]
8. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
Tan EC; Lim EC; Yap SH; Lee ST; Cheng J; Por YC; Yeow V
Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368
[TBL] [Abstract][Full Text] [Related]
9. Orofacial clefting: update on the role of genetics.
Ghassibe M; Bayet B; Revencu N; Desmyter L; Verellen-Dumoulin C; Gillerot Y; Deggouj N; Vanwijck R; Vikkula M;
B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
[TBL] [Abstract][Full Text] [Related]
10. Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
Peyrard-Janvid M; Pegelow M; Koillinen H; Larsson C; Fransson I; Rautio J; Hukki J; Larson O; Karsten AL; Kere J
Eur J Hum Genet; 2005 Dec; 13(12):1261-7. PubMed ID: 16160700
[TBL] [Abstract][Full Text] [Related]
11. Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfbeta3).
Cheah FS; Jabs EW; Chong SS
Dev Dyn; 2005 Apr; 232(4):1021-30. PubMed ID: 15739231
[TBL] [Abstract][Full Text] [Related]
12. Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6.
Little HJ; Rorick NK; Su LI; Baldock C; Malhotra S; Jowitt T; Gakhar L; Subramanian R; Schutte BC; Dixon MJ; Shore P
Hum Mol Genet; 2009 Feb; 18(3):535-45. PubMed ID: 19036739
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations in the IRF6 gene for Van der Woude syndrome.
Wang X; Liu J; Zhang H; Xiao M; Li J; Yang C; Lin X; Wu Z; Hu L; Kong X
Hum Genet; 2003 Oct; 113(5):382-6. PubMed ID: 12920575
[TBL] [Abstract][Full Text] [Related]
14. Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
Scioletti AP; Brancati F; Gatta V; Antonucci I; Peissel B; Pizzuti A; Mortellaro C; Tetè S; Gherlone E; Palka G; Stuppia L
J Craniofac Surg; 2010 Sep; 21(5):1654-6. PubMed ID: 20856073
[TBL] [Abstract][Full Text] [Related]
15. Two distinct teleost hepatocyte nuclear factor 1 genes, hnf1alpha/tcf1 and hnf1beta/tcf2, abundantly expressed in liver, pancreas, gut and kidney of zebrafish.
Gong HY; Lin CJ; Chen MH; Hu MC; Lin GH; Zhou Y; Zon LI; Wu JL
Gene; 2004 Aug; 338(1):35-46. PubMed ID: 15302404
[TBL] [Abstract][Full Text] [Related]
16. Gene symbol: IRF6. Disease: Van der Woude syndrome.
Item CB; Turhani D; Thurnher D; Sinko K; Yerit K; Galev K; Wittwer G; Lanre Adeyemo W; Klemens F; Ewers R; Watzinger F
Hum Genet; 2004 Jul; 115(2):175. PubMed ID: 15300989
[No Abstract] [Full Text] [Related]
17. Cloning, expression pattern and essentiality of the high-affinity copper transporter 1 (ctr1) gene in zebrafish.
Mackenzie NC; Brito M; Reyes AE; Allende ML
Gene; 2004 Mar; 328():113-20. PubMed ID: 15019990
[TBL] [Abstract][Full Text] [Related]
18. Gene symbol: IRF6. Disease: Van der Woude syndrome.
Mostowska A; Wójcicki P; Kobus K; Trzeciak WH
Hum Genet; 2005 May; 116(6):534. PubMed ID: 15988826
[No Abstract] [Full Text] [Related]
19. Novel IRF6 mutations in Honduran Van der Woude syndrome patients.
Birkeland AC; Larrabee Y; Kent DT; Flores C; Su GH; Lee JH; Haddad J
Mol Med Rep; 2011; 4(2):237-41. PubMed ID: 21468557
[TBL] [Abstract][Full Text] [Related]
20. Molecular cloning and developmental expression of zinc finger transcription factor MTF-1 gene in zebrafish, Danio rerio.
Chen WY; John JA; Lin CH; Chang CY
Biochem Biophys Res Commun; 2002 Mar; 291(4):798-805. PubMed ID: 11866436
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]