BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 20196077)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
    Peyrard-Janvid M; Pegelow M; Koillinen H; Larsson C; Fransson I; Rautio J; Hukki J; Larson O; Karsten AL; Kere J
    Eur J Hum Genet; 2005 Dec; 13(12):1261-7. PubMed ID: 16160700
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [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]  

  • 31. A Complex Intrachromosomal Rearrangement Disrupting
    Al-Kurbi AA; Aliyev E; AlSa'afin S; Aamer W; Palaniswamy S; Al-Maraghi A; Kilani H; Akil AA; Stotland MA; Fakhro KA
    Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107607
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. A novel mutation in IRF6 resulting in VWS-PPS spectrum disorder with renal aplasia.
    de Medeiros F; Hansen L; Mawlad E; Eiberg H; Asklund C; Tommerup N; Jakobsen LP
    Am J Med Genet A; 2008 Jun; 146A(12):1605-8. PubMed ID: 18478600
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
    Scioletti AP; Brancati F; Gatta V; Antonucci I; Peissel B; Pizzuti A; Mortellaro C; Tetè S; Gherlone E; Palka G; Stuppia L
    J Craniofac Surg; 2010 Sep; 21(5):1654-6. PubMed ID: 20856073
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome.
    Yeetong P; Mahatumarat C; Siriwan P; Rojvachiranonda N; Suphapeetiporn K; Shotelersuk V
    Am J Med Genet A; 2009 Nov; 149A(11):2489-92. PubMed ID: 19842205
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.