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Journal Abstract Search

268 related items for PubMed ID: 36901693

  • 1. A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22.
    Slavec L, Geršak K, Eberlinc A, Hovnik T, Lovrečić L, Mlinarič-Raščan I, Karas Kuželički N.
    Int J Mol Sci; 2023 Feb 21; 24(5):. PubMed ID: 36901693
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  • 6. Toward an orofacial gene regulatory network.
    Kousa YA, Schutte BC.
    Dev Dyn; 2016 Mar 21; 245(3):220-32. PubMed ID: 26332872
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  • 7. Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population.
    He M, Bian Z.
    PLoS One; 2016 Mar 21; 11(7):e0159940. PubMed ID: 27459192
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  • 8. 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 20; 14():37. PubMed ID: 23510002
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  • 9. 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 20; 8(8):e1355. PubMed ID: 32558391
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  • 10. 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 20; 15(5):338-44. PubMed ID: 23154523
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  • 11. 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 20; 52(5):e161-7. PubMed ID: 25489771
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  • 12. 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; 2015 Sep 20; 33(2):e138-e140. PubMed ID: 34643600
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  • 13. 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, CL/P Study Group.
    B-ENT; 2006 Sep 20; 2 Suppl 4():20-4. PubMed ID: 17366841
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  • 14. 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 20; 113(5):382-6. PubMed ID: 12920575
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  • 15. 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 20; 161A(10):2535-2544. PubMed ID: 23949966
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  • 16. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort.
    Wang Y, Sun Y, Huang Y, Pan Y, Jia Z, Ma L, Ma L, Lan F, Zhou Y, Shi J, Yang X, Zhang L, Jiang H, Jiang M, Yin A, Cheng J, Wang L, Yang Y, Shi B.
    Gene; 2016 Aug 15; 588(1):69-73. PubMed ID: 27129939
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  • 17. 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 07; 11(8):. PubMed ID: 32784565
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  • 18. Novel IRF6 variant in orofacial cleft patients from Durban, South Africa.
    Naicker T, Alade A, Adeleke C, Mossey PA, Awotoye WA, Busch T, Li M, Olotu J, Aldous C, Butali A.
    Mol Genet Genomic Med; 2023 May 07; 11(5):e2138. PubMed ID: 36811272
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  • 19. 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 07; 170(9):2404-7. PubMed ID: 27286731
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  • 20. 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 07; 51(1):49-55. PubMed ID: 23394314
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