196 related articles for article (PubMed ID: 31943082)
21. Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/Palate.
Parada-Sanchez MT; Chu EY; Cox LL; Undurty SS; Standley JM; Murray JC; Cox TC
J Dent Res; 2017 Oct; 96(11):1330-1338. PubMed ID: 28767310
[TBL] [Abstract][Full Text] [Related]
22. ARHGAP29 Mutation Is Associated with Abnormal Oral Epithelial Adhesions.
Paul BJ; Palmer K; Sharp JC; Pratt CH; Murray SA; Dunnwald M
J Dent Res; 2017 Oct; 96(11):1298-1305. PubMed ID: 28817352
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
Pegelow M; Peyrard-Janvid M; Zucchelli M; Fransson I; Larson O; Kere J; Larsson C; Karsten A
Eur J Orthod; 2008 Apr; 30(2):169-75. PubMed ID: 18209213
[TBL] [Abstract][Full Text] [Related]
25. IRF6 rs2235371 as a risk factor for non-syndromic cleft palate only among the Deutero-Malay race in Indonesia and its effect on the IRF6 mRNA expression level.
Nasroen SL; Maskoen AM; Soedjana H; Hilmanto D; Gani BA
Dent Med Probl; 2022; 59(1):59-65. PubMed ID: 35226971
[TBL] [Abstract][Full Text] [Related]
26. A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis.
Ferretti E; Li B; Zewdu R; Wells V; Hebert JM; Karner C; Anderson MJ; Williams T; Dixon J; Dixon MJ; Depew MJ; Selleri L
Dev Cell; 2011 Oct; 21(4):627-41. PubMed ID: 21982646
[TBL] [Abstract][Full Text] [Related]
27. A novel RIPK4-IRF6 connection is required to prevent epithelial fusions characteristic for popliteal pterygium syndromes.
De Groote P; Tran HT; Fransen M; Tanghe G; Urwyler C; De Craene B; Leurs K; Gilbert B; Van Imschoot G; De Rycke R; Guérin CJ; Holland P; Berx G; Vandenabeele P; Lippens S; Vleminckx K; Declercq W
Cell Death Differ; 2015 Jun; 22(6):1012-24. PubMed ID: 25430793
[TBL] [Abstract][Full Text] [Related]
28. Shared molecular networks in orofacial and neural tube development.
Kousa YA; Mansour TA; Seada H; Matoo S; Schutte BC
Birth Defects Res; 2017 Jan; 109(2):169-179. PubMed ID: 27933721
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting.
Saadi I; Alkuraya FS; Gisselbrecht SS; Goessling W; Cavallesco R; Turbe-Doan A; Petrin AL; Harris J; Siddiqui U; Grix AW; Hove HD; Leboulch P; Glover TW; Morton CC; Richieri-Costa A; Murray JC; Erickson RP; Maas RL
Am J Hum Genet; 2011 Jul; 89(1):44-55. PubMed ID: 21703590
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. IRF6 mutations in mixed isolated familial clefting.
Rutledge KD; Barger C; Grant JH; Robin NH
Am J Med Genet A; 2010 Dec; 152A(12):3107-9. PubMed ID: 21082654
[TBL] [Abstract][Full Text] [Related]
33. Ablation of the Sox11 Gene Results in Clefting of the Secondary Palate Resembling the Pierre Robin Sequence.
Huang H; Yang X; Bao M; Cao H; Miao X; Zhang X; Gan L; Qiu M; Zhang Z
J Biol Chem; 2016 Mar; 291(13):7107-18. PubMed ID: 26826126
[TBL] [Abstract][Full Text] [Related]
34. A novel IRF6 mutation causing non-syndromic cleft lip with or without cleft palate in a pedigree.
Zhao H; Zhang M; Zhong W; Zhang J; Huang W; Zhang Y; Li W; Jia P; Zhang T; Liu Z; Lin J; Chen F
Mutagenesis; 2018 Sep; 33(3):195-202. PubMed ID: 30053123
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.
Knight AS; Schutte BC; Jiang R; Dixon MJ
Dev Dyn; 2006 May; 235(5):1441-7. PubMed ID: 16245336
[TBL] [Abstract][Full Text] [Related]
38. SPECC1L: a cytoskeletal protein that regulates embryonic tissue dynamics.
Saadi I; Goering JP; Hufft-Martinez BM; Tran PV
Biochem Soc Trans; 2023 Jun; 51(3):949-958. PubMed ID: 37345651
[TBL] [Abstract][Full Text] [Related]
39. Association Studies Between Regulatory Regions of
Wu-Chou YH; Lu YC; Chen KP; Chang HF; Lin YT; Lo LJ
Cleft Palate Craniofac J; 2019 Jul; 56(6):778-785. PubMed ID: 30419764
[TBL] [Abstract][Full Text] [Related]
40. IRF6 is the mediator of TGFβ3 during regulation of the epithelial mesenchymal transition and palatal fusion.
Ke CY; Xiao WL; Chen CM; Lo LJ; Wong FH
Sci Rep; 2015 Aug; 5():12791. PubMed ID: 26240017
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
