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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

408 related items for PubMed ID: 27881089

  • 1. Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.
    Bergendal B, Norderyd J, Zhou X, Klar J, Dahl N.
    BMC Med Genet; 2016 Nov 24; 17(1):88. PubMed ID: 27881089
    [Abstract] [Full Text] [Related]

  • 2. Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.
    Yu M, Liu Y, Liu H, Wong SW, He H, Zhang X, Wang Y, Han D, Feng H.
    Am J Med Genet A; 2019 Jan 24; 179(1):57-64. PubMed ID: 30569517
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
    Liu Y, Sun J, Zhang C, Wu Y, Ma S, Li X, Wu X, Gao Q.
    BMC Oral Health; 2024 Jan 27; 24(1):136. PubMed ID: 38280992
    [Abstract] [Full Text] [Related]

  • 11. Role of WNT10A in failure of tooth development in humans and zebrafish.
    Yuan Q, Zhao M, Tandon B, Maili L, Liu X, Zhang A, Baugh EH, Tran T, Silva RM, Hecht JT, Swindell EC, Wagner DS, Letra A.
    Mol Genet Genomic Med; 2017 Nov 27; 5(6):730-741. PubMed ID: 29178643
    [Abstract] [Full Text] [Related]

  • 12. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
    Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P.
    PLoS One; 2013 Nov 27; 8(8):e73705. PubMed ID: 23991204
    [Abstract] [Full Text] [Related]

  • 13. WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
    Song S, Zhao R, He H, Zhang J, Feng H, Lin L.
    Hum Genet; 2014 Jan 27; 133(1):117-24. PubMed ID: 24043634
    [Abstract] [Full Text] [Related]

  • 14. WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.
    Kantaputra P, Kaewgahya M, Kantaputra W.
    Am J Med Genet A; 2014 Feb 27; 164A(2):360-3. PubMed ID: 24311251
    [Abstract] [Full Text] [Related]

  • 15. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.
    He H, Han D, Feng H, Qu H, Song S, Bai B, Zhang Z.
    PLoS One; 2013 Feb 27; 8(11):e80393. PubMed ID: 24312213
    [Abstract] [Full Text] [Related]

  • 16. Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
    Issa YA, Kamal L, Rayyan AA, Dweik D, Pierce S, Lee MK, King MC, Walsh T, Kanaan M.
    Eur J Hum Genet; 2016 Oct 27; 24(10):1430-5. PubMed ID: 27049303
    [Abstract] [Full Text] [Related]

  • 17. Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.
    Tardieu C, Jung S, Niederreither K, Prasad M, Hadj-Rabia S, Philip N, Mallet A, Consolino E, Sfeir E, Noueiri B, Chassaing N, Dollfus H, Manière MC, Bloch-Zupan A, Clauss F.
    Clin Genet; 2017 Nov 27; 92(5):477-486. PubMed ID: 28105635
    [Abstract] [Full Text] [Related]

  • 18. Taurodontism in Brazilian patients with tooth agenesis and first and second-degree relatives: a case-control study.
    Gomes RR, Habckost CD, Junqueira LG, Leite AF, Figueiredo PT, Paula LM, Acevedo AC.
    Arch Oral Biol; 2012 Aug 27; 57(8):1062-9. PubMed ID: 22647425
    [Abstract] [Full Text] [Related]

  • 19. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K, Lian M, Zou D, Huang W, Zhou W, Shen Y, Wang F, Wu Y.
    Oral Dis; 2019 Mar 27; 25(2):523-534. PubMed ID: 30417976
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.