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 *

407 related articles for article (PubMed ID: 32784565)

  • 1. A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate.
    Sylvester B; Brindopke F; Suzuki A; Giron M; Auslander A; Maas RL; Tsai B; Gao H; Magee W; Cox TC; Sanchez-Lara PA
    Genes (Basel); 2020 Aug; 11(8):. PubMed ID: 32784565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.
    Brosch S; Baur M; Blin N; Reinert S; Pfister M
    Int J Mol Med; 2007 Jul; 20(1):85-9. PubMed ID: 17549393
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
    Tan EC; Lim EC; Yap SH; Lee ST; Cheng J; Por YC; Yeow V
    Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Mutations in Van Der Woude Families From Ethiopia.
    Eshete M; Alade A; Abate F; Mossey PA; Awotoye WA; Busch T; Hailu A; Demissie Y; Butali A
    J Craniofac Surg; 2022 Mar-Apr 01; 33(2):e138-e140. PubMed ID: 34643600
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing.
    Pengelly RJ; Upstill-Goddard R; Arias L; Martinez J; Gibson J; Knut M; Collins AL; Ennis S; Collins A; Briceno I
    Clin Genet; 2015 Nov; 88(5):441-9. PubMed ID: 25441681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6.
    Little HJ; Rorick NK; Su LI; Baldock C; Malhotra S; Jowitt T; Gakhar L; Subramanian R; Schutte BC; Dixon MJ; Shore P
    Hum Mol Genet; 2009 Feb; 18(3):535-45. PubMed ID: 19036739
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: review of the literature.
    Salahshourifar I; Wan Sulaiman WA; Halim AS; Zilfalil BA
    Eur J Med Genet; 2012 Jun; 55(6-7):389-93. PubMed ID: 22440537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 21.