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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 19536562)

  • 1. A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis.
    Ferrero GB; Baldassarre G; Panza E; Valenzise M; Pippucci T; Mussa A; Pepe E; Seri M; Silengo MC
    Eur J Pediatr; 2010 Feb; 169(2):223-8. PubMed ID: 19536562
    [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. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 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. [Van-der-Woude Syndrome].
    Del Frari B; Amort M; Janecke AR; Schutte BC; Piza-Katzer H
    Klin Padiatr; 2008; 220(1):26-8. PubMed ID: 18095255
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
    Ghassibé M; Bayet B; Revencu N; Verellen-Dumoulin C; Gillerot Y; Vanwijck R; Vikkula M
    Eur J Hum Genet; 2005 Nov; 13(11):1239-42. PubMed ID: 16132054
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder.
    Schierz IAM; Amoroso S; Antona V; Giuffrè M; Piro E; Serra G; Corsello G
    Ital J Pediatr; 2022 Jul; 48(1):132. PubMed ID: 35906647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. [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]  

  • 19. Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.
    Du X; Tang W; Tian W; Li S; Li X; Liu L; Zheng X; Chen X; Lin Y; Tang Y
    J Dent Res; 2006 Oct; 85(10):937-40. PubMed ID: 16998136
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.