172 related articles for article (PubMed ID: 29115498)
1. Association between genotype and phenotype of virulence gene in Van der Woude syndrome families.
Li S; Zhang X; Chen D; Zhao W; Zhang X; Jiao J; Guo L; Yin L; Song X; Liang C; Sun C
Mol Med Rep; 2018 Jan; 17(1):1241-1246. PubMed ID: 29115498
[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. 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]
4. 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]
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. 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]
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. 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]
9. [IRF6 gene mutation analysis in a van Der Woude syndrome family in Henan province].
Wang XF; Xiao MZ; Shi JN; Zhang HB; Hu LD; Kong XY
Shanghai Kou Qiang Yi Xue; 2005 Jun; 14(3):234-7. PubMed ID: 15995766
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome.
Miñones-Suárez L; Mas-Vidal A; Fernandez-Toral J; Llano-Rivas I; González-García M
Pediatr Dermatol; 2012; 29(6):768-70. PubMed ID: 21995291
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A clinical and multi‑omics study of Van der Woude syndrome in three generations of a Chinese family.
Yang K; Dong XY; Wu J; Zhu JJ; Tan Y; Yan YS; Lin L; Zhang DL
Mol Med Rep; 2020 Oct; 22(4):2925-2931. PubMed ID: 32945398
[TBL] [Abstract][Full Text] [Related]
14. A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.
Wu-Chou YH; Lo LJ; Chen KT; Chang CS; Chen YR
BMC Med Genet; 2013 Mar; 14():37. PubMed ID: 23510002
[TBL] [Abstract][Full Text] [Related]
15. [Clinical and genetic features of Chinese kindreds with Van der Woude syndrome caused by interferon regulatory factor 6 mutation].
Du XY; Li XY; Wu B; Xie C; Tian WD
Hua Xi Kou Qiang Yi Xue Za Zhi; 2018 Dec; 36(6):623-627. PubMed ID: 30593107
[TBL] [Abstract][Full Text] [Related]
16. Causal Variations at
Yang CW; Yin B; Shi JY; Shi B; Jia ZL
Cleft Palate Craniofac J; 2024 Jul; 61(7):1134-1142. PubMed ID: 36866619
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Van der Woude Syndrome: IRF6 Mutations.
Sunny AP; Arunachal G; Danda S
Indian J Pediatr; 2019 Nov; 86(11):1070-1071. PubMed ID: 31468312
[No Abstract] [Full Text] [Related]
19. An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects.
Fakhouri WD; Rahimov F; Attanasio C; Kouwenhoven EN; Ferreira De Lima RL; Felix TM; Nitschke L; Huver D; Barrons J; Kousa YA; Leslie E; Pennacchio LA; Van Bokhoven H; Visel A; Zhou H; Murray JC; Schutte BC
Hum Mol Genet; 2014 May; 23(10):2711-20. PubMed ID: 24442519
[TBL] [Abstract][Full Text] [Related]
20. Monozygotic twins with variable expression of Van der Woude syndrome.
Jobling R; Ferrier RA; McLeod R; Petrin AL; Murray JC; Thomas MA
Am J Med Genet A; 2011 Aug; 155A(8):2008-10. PubMed ID: 21739575
[No Abstract] [Full Text] [Related]
[Next] [New Search]
