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Journal Abstract Search

464 related items for PubMed ID: 28087736

  • 1. Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
    Ludwig KU, Böhmer AC, Bowes J, Nikolic M, Ishorst N, Wyatt N, Hammond NL, Gölz L, Thieme F, Barth S, Schuenke H, Klamt J, Spielmann M, Aldhorae K, Rojas-Martinez A, Nöthen MM, Rada-Iglesias A, Dixon MJ, Knapp M, Mangold E.
    Hum Mol Genet; 2017 Feb 15; 26(4):829-842. PubMed ID: 28087736
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  • 2. Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen.
    Aldhorae KA, Böhmer AC, Ludwig KU, Esmail AH, Al-Hebshi NN, Lippke B, Gölz L, Nöthen MM, Daratsianos N, Knapp M, Jäger A, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2014 Apr 15; 100(4):307-13. PubMed ID: 24634360
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  • 3. Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
    Ludwig KU, Wahle P, Reutter H, Paredes-Zenteno M, Muñoz-Jimenez SG, Ortiz-Lopez R, Böhmer AC, Tessmann P, Nowak S, Nöthen MM, Knapp M, Rojas-Martinez A, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2014 Jan 15; 100(1):43-7. PubMed ID: 24382704
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  • 4. Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample.
    Böhmer AC, Mangold E, Tessmann P, Mossey PA, Steegers-Theunissen RP, Lindemans J, Bouwman-Both M, Rubini M, Franceschelli P, Aiello V, Peterlin B, Molloy AM, Nöthen MM, Knapp M, Ludwig KU.
    Am J Med Genet A; 2013 Oct 15; 161A(10):2545-9. PubMed ID: 24038802
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  • 6. Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations.
    Gowans LJ, Adeyemo WL, Eshete M, Mossey PA, Busch T, Aregbesola B, Donkor P, Arthur FK, Bello SA, Martinez A, Li M, Augustine-Akpan EA, Deressa W, Twumasi P, Olutayo J, Deribew M, Agbenorku P, Oti AA, Braimah R, Plange-Rhule G, Gesses M, Obiri-Yeboah S, Oseni GO, Olaitan PB, Abdur-Rahman L, Abate F, Hailu T, Gravem P, Ogunlewe MO, Buxó CJ, Marazita ML, Adeyemo AA, Murray JC, Butali A.
    J Dent Res; 2016 Oct 15; 95(11):1245-56. PubMed ID: 27369588
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  • 7. MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.
    Stüssel LG, Hollstein R, Laugsch M, Hochfeld LM, Welzenbach J, Schröder J, Thieme F, Ishorst N, Romero RO, Weinhold L, Hess T, Gehlen J, Mostowska A, Heilmann-Heimbach S, Mangold E, Rada-Iglesias A, Knapp M, Schaaf CP, Ludwig KU.
    J Dent Res; 2022 Mar 15; 101(3):323-330. PubMed ID: 34528480
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  • 12. Polymorphisms at 1q32, 8q24, and 17q22 loci are associated with nonsyndromic cleft lip with or without cleft palate risk in the Slovak population.
    Salagovic J, Klimcakova L, Zabavnikova M, Behunova J, Hudakova T, Fedeles J, Molnarova A, Podracka L.
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2017 Jun 15; 161(2):152-157. PubMed ID: 28422192
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  • 13. Allele-specific transcription factor binding in a cellular model of orofacial clefting.
    Ruff KLM, Hollstein R, Fazaal J, Thieme F, Gehlen J, Mangold E, Knapp M, Welzenbach J, Ludwig KU.
    Sci Rep; 2022 Feb 02; 12(1):1807. PubMed ID: 35110662
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  • 15. Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population.
    Cura F, Böhmer AC, Klamt J, Schünke H, Scapoli L, Martinelli M, Carinci F, Nöthen MM, Knapp M, Ludwig KU, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2016 Feb 02; 106(2):81-7. PubMed ID: 26648166
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  • 16. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
    Mangold E, Böhmer AC, Ishorst N, Hoebel AK, Gültepe P, Schuenke H, Klamt J, Hofmann A, Gölz L, Raff R, Tessmann P, Nowak S, Reutter H, Hemprich A, Kreusch T, Kramer FJ, Braumann B, Reich R, Schmidt G, Jäger A, Reiter R, Brosch S, Stavusis J, Ishida M, Seselgyte R, Moore GE, Nöthen MM, Borck G, Aldhorae KA, Lace B, Stanier P, Knapp M, Ludwig KU.
    Am J Hum Genet; 2016 Apr 07; 98(4):755-62. PubMed ID: 27018475
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  • 17. Association of single nucleotide polymorphisms at 20q12 with nonsyndromic cleft lip with or without cleft palate in a Southern Chinese Han cohort.
    He Y, Huang L, Zheng Y, Chen JH, Tang S.
    Mol Genet Genomic Med; 2020 Jan 07; 8(1):e1028. PubMed ID: 31713353
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  • 18. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
    Leslie EJ, Mansilla MA, Biggs LC, Schuette K, Bullard S, Cooper M, Dunnwald M, Lidral AC, Marazita ML, Beaty TH, Murray JC.
    Birth Defects Res A Clin Mol Teratol; 2012 Nov 07; 94(11):934-42. PubMed ID: 23008150
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  • 19. Genome-wide Analyses Identify a Novel Risk Locus for Nonsyndromic Cleft Palate.
    He M, Zuo X, Liu H, Wang W, Zhang Y, Fu Y, Zhen Q, Yu Y, Pan Y, Qin C, Li B, Yang R, Wu J, Huang Z, Ge H, Wu H, Xu Q, Zuo Y, Chen W, Qin Y, Liu Z, Chen S, Zhang H, Zhou F, Yan H, Yu Y, Yong L, Chen G, Liang B, Cornell RA, Zong L, Wang L, Zou D, Sun L, Bian Z.
    J Dent Res; 2020 Dec 07; 99(13):1461-1468. PubMed ID: 32758111
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