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.
278 related articles for article (PubMed ID: 19282774)
1. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. de Lima RL; Hoper SA; Ghassibe M; Cooper ME; Rorick NK; Kondo S; Katz L; Marazita ML; Compton J; Bale S; Hehr U; Dixon MJ; Daack-Hirsch S; Boute O; Bayet B; Revencu N; Verellen-Dumoulin C; Vikkula M; Richieri-Costa A; Moretti-Ferreira D; Murray JC; Schutte BC Genet Med; 2009 Apr; 11(4):241-7. PubMed ID: 19282774 [TBL] [Abstract][Full Text] [Related]
2. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6. Busche A; Hehr U; Sieg P; Gillessen-Kaesbach G Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731 [TBL] [Abstract][Full Text] [Related]
3. Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases. Leslie EJ; Standley J; Compton J; Bale S; Schutte BC; Murray JC Genet Med; 2013 May; 15(5):338-44. PubMed ID: 23154523 [TBL] [Abstract][Full Text] [Related]
4. Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. Leslie EJ; Mancuso JL; Schutte BC; Cooper ME; Durda KM; L'Heureux J; Zucchero TM; Marazita ML; Murray JC Am J Med Genet A; 2013 Oct; 161A(10):2535-2544. PubMed ID: 23949966 [TBL] [Abstract][Full Text] [Related]
5. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting. Charzewska A; Obersztyn E; Hoffman-Zacharska D; Lenart J; Poznański J; Bal J Cleft Palate Craniofac J; 2015 Sep; 52(5):e161-7. PubMed ID: 25489771 [TBL] [Abstract][Full Text] [Related]
6. Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome. Alade AA; Buxo-Martinez CJ; Mossey PA; Gowans LJJ; Eshete MA; Adeyemo WL; Naicker T; Awotoye WA; Adeleke C; Busch T; Toraño AM; Bello CA; Soto M; Soto M; Ledesma R; Marquez M; Cordero JF; Lopez-Del Valle LM; Salcedo MI; Debs N; Li M; Petrin A; Olotu J; Aldous C; Olutayo J; Ogunlewe MO; Abate F; Hailu T; Muhammed I; Gravem P; Deribew M; Gesses M; Hassan M; Pape J; Adeniyan OA; Obiri-Yeboah S; Arthur FKN; Oti AA; Olatosi O; Miller SE; Donkor P; Dunnwald MM; Marazita ML; Adeyemo AA; Murray JC; Butali A Mol Genet Genomic Med; 2020 Aug; 8(8):e1355. PubMed ID: 32558391 [TBL] [Abstract][Full Text] [Related]
7. Altered regulation of cell migration in IRF6-mutated orofacial cleft patients-derived primary cells reveals a novel role of Rho GTPases in cleft/lip palate development. Ghassibe-Sabbagh M; El Hajj J; Al Saneh M; El Baba N; Abou Issa J; Al Haddad M; El Atat O; Sabbagh J; Abou Chebel N; El-Sibai M Cells Dev; 2021 Jun; 166():203674. PubMed ID: 33994351 [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. Van der Woude and Popliteal Pterygium Syndromes. Bennun RD; Stefano E; Moggi LE J Craniofac Surg; 2018 Sep; 29(6):1434-1436. PubMed ID: 29916977 [TBL] [Abstract][Full Text] [Related]
10. Two missense mutations of the IRF6 gene in two Japanese families with popliteal pterygium syndrome. Matsuzawa N; Kondo S; Shimozato K; Nagao T; Nakano M; Tsuda M; Hirano A; Niikawa N; Yoshiura K Am J Med Genet A; 2010 Sep; 152A(9):2262-7. PubMed ID: 20803643 [TBL] [Abstract][Full Text] [Related]
11. 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. 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]
14. Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome. Yu Y; Wan Y; Qin C; Yue H; Bian Z; He M Mol Genet Genomic Med; 2020 May; 8(5):e1196. PubMed ID: 32108996 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Toward an orofacial gene regulatory network. Kousa YA; Schutte BC Dev Dyn; 2016 Mar; 245(3):220-32. PubMed ID: 26332872 [TBL] [Abstract][Full Text] [Related]
17. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate. Pegelow M; Koillinen H; Magnusson M; Fransson I; Unneberg P; Kere J; Karsten A; Peyrard-Janvid M Cleft Palate Craniofac J; 2014 Jan; 51(1):49-55. PubMed ID: 23394314 [TBL] [Abstract][Full Text] [Related]
18. A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family With Van der Woude Syndrome. Tan EC; Lim HW; Lim ECP; Lee ST Cleft Palate Craniofac J; 2017 Jul; 54(4):442-445. PubMed ID: 27243668 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan. Malik S; Kakar N; Hasnain S; Ahmad J; Wilcox ER; Naz S Clin Genet; 2010 Sep; 78(3):247-56. PubMed ID: 20184620 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]