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4. IRF6 and SPRY4 Signaling Interact in Periderm Development. Kousa YA; Roushangar R; Patel N; Walter A; Marangoni P; Krumlauf R; Klein OD; Schutte BC J Dent Res; 2017 Oct; 96(11):1306-1313. PubMed ID: 28732181 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. Peyrard-Janvid M; Leslie EJ; Kousa YA; Smith TL; Dunnwald M; Magnusson M; Lentz BA; Unneberg P; Fransson I; Koillinen HK; Rautio J; Pegelow M; Karsten A; Basel-Vanagaite L; Gordon W; Andersen B; Svensson T; Murray JC; Cornell RA; Kere J; Schutte BC Am J Hum Genet; 2014 Jan; 94(1):23-32. PubMed ID: 24360809 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Van der Woude Syndrome With a Novel Mutation in the IRF6 Gene. Ural A; Bilgen F; Çakmakli S; Bekerecioğlu M J Craniofac Surg; 2019 Jul; 30(5):e465-e467. PubMed ID: 31299817 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing. Khandelwal KD; Ishorst N; Zhou H; Ludwig KU; Venselaar H; Gilissen C; Thonissen M; van Rooij IA; Dreesen K; Steehouwer M; van de Vorst M; Bloemen M; van Beusekom E; Roosenboom J; Borstlap W; Admiraal R; Dormaar T; Schoenaers J; Vander Poorten V; Hens G; Verdonck A; Bergé S; Roeleveldt N; Vriend G; Devriendt K; Brunner HG; Mangold E; Hoischen A; van Bokhoven H; Carels CE J Dent Res; 2017 Feb; 96(2):179-185. PubMed ID: 27834299 [TBL] [Abstract][Full Text] [Related]
15. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Wang Y; Sun Y; Huang Y; Pan Y; Jia Z; Ma L; Ma L; Lan F; Zhou Y; Shi J; Yang X; Zhang L; Jiang H; Jiang M; Yin A; Cheng J; Wang L; Yang Y; Shi B Gene; 2016 Aug; 588(1):69-73. PubMed ID: 27129939 [TBL] [Abstract][Full Text] [Related]
16. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. Leslie EJ; Koboldt DC; Kang CJ; Ma L; Hecht JT; Wehby GL; Christensen K; Czeizel AE; Deleyiannis FW; Fulton RS; Wilson RK; Beaty TH; Schutte BC; Murray JC; Marazita ML Clin Genet; 2016 Jul; 90(1):28-34. PubMed ID: 26346622 [TBL] [Abstract][Full Text] [Related]
17. Genetic heterogeneity in Van der Woude syndrome: identification of NOL4 and IRF6 haplotype from the noncoding region as candidates in two families. Kumari PK; Ali A; Singh SK; Chaurasia A; Raman R J Genet; 2018 Mar; 97(1):275-285. PubMed ID: 29666346 [TBL] [Abstract][Full Text] [Related]
18. Interferon Regulatory Factor 6 Controls Proliferation of Keratinocytes From Children With Van der Woude Syndrome. Hixon K; Rhea L; Standley J; Canady FJ; Canady JW; Dunnwald M Cleft Palate Craniofac J; 2017 May; 54(3):281-286. PubMed ID: 27115562 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Novel lip pit phenotypes and mutations of IRF6 in Van der Woude syndrome patients from Pakistan. Malik S; Wilcox ER; Naz S Clin Genet; 2014 May; 85(5):487-91. PubMed ID: 23713753 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]