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

125 related items for PubMed ID: 38287639

  • 1. Eight EDA mutations in Chinese patients with tooth agenesis and genotype-phenotype analysis.
    Yu K, Sheng Y, Wang F, Yang S, Wan F, Lei M, Wu Y.
    Oral Dis; 2024 Oct; 30(7):4598-4607. PubMed ID: 38287639
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis.
    Andreoni F, Sgattoni C, Bencardino D, Simonetti O, Forabosco A, Magnani M.
    Mol Genet Genomic Med; 2021 Jan; 9(1):e1555. PubMed ID: 33205897
    [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. 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 Jan; 8(11):e80393. PubMed ID: 24312213
    [Abstract] [Full Text] [Related]

  • 9. De novo EDA mutations: Variable expression in two Egyptian families.
    Gaczkowska A, Abdalla EM, Dowidar KM, Elhady GM, Jagodzinski PP, Mostowska A.
    Arch Oral Biol; 2016 Aug; 68():21-8. PubMed ID: 27054699
    [Abstract] [Full Text] [Related]

  • 10. Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.
    Parveen A, Khan SA, Mirza MU, Bashir H, Arshad F, Iqbal M, Ahmad W, Wahab A, Fiaz A, Naz S, Ashraf F, Mobeen T, Aziz S, Ahmed SS, Muhammad N, Hassib NF, Mostafa MI, Gaboon NE, Gul R, Khan S, Froeyen M, Shoaib M, Wasif N.
    Int J Mol Sci; 2019 Oct 24; 20(21):. PubMed ID: 31652981
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. EDA Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis.
    Su L, Lin B, Yu M, Liu Y, Sun S, Feng H, Liu H, Han D.
    Int J Mol Sci; 2024 Sep 27; 25(19):. PubMed ID: 39408781
    [Abstract] [Full Text] [Related]

  • 13. Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.
    Zhang J, Han D, Song S, Wang Y, Zhao H, Pan S, Bai B, Feng H.
    Eur J Med Genet; 2011 Sep 27; 54(4):e377-82. PubMed ID: 21457804
    [Abstract] [Full Text] [Related]

  • 14. Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families.
    Güven Y, Bal E, Altunoglu U, Yücel E, Hadj-Rabia S, Koruyucu M, Bahar Tuna E, Çıldır Ş, Aktören O, Bodemer C, Uyguner ZO, Smahi A, Kayserili H.
    Cytogenet Genome Res; 2019 Sep 27; 157(4):189-196. PubMed ID: 30974434
    [Abstract] [Full Text] [Related]

  • 15. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.
    Zeng B, Zhao Q, Li S, Lu H, Lu J, Ma L, Zhao W, Yu D.
    Genes (Basel); 2017 Oct 05; 8(10):. PubMed ID: 28981473
    [Abstract] [Full Text] [Related]

  • 16. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation.
    Zeng B, Lu H, Xiao X, Zhou L, Lu J, Zhu L, Yu D, Zhao W.
    Oral Dis; 2015 Nov 05; 21(8):994-1000. PubMed ID: 26411740
    [Abstract] [Full Text] [Related]

  • 17. A novel EDAR variant identified in non-syndromic tooth agenesis: Insights from molecular dynamics.
    Zhao Z, Zhang T, Li T, Ye Y, Feng C, Wang H, Zhang X.
    Arch Oral Biol; 2023 Feb 05; 146():105600. PubMed ID: 36470092
    [Abstract] [Full Text] [Related]

  • 18. Two novel ectodysplasin A gene mutations and prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia.
    Yu K, Shen Y, Jiang CL, Huang W, Wang F, Wu YQ.
    Mol Genet Genomic Med; 2021 Nov 05; 9(11):e1824. PubMed ID: 34582123
    [Abstract] [Full Text] [Related]

  • 19. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr 05; 25(3):646-651. PubMed ID: 29969831
    [Abstract] [Full Text] [Related]

  • 20. Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.
    Ahmed HA, El-Kamah GY, Rabie E, Mostafa MI, Abouzaid MR, Hassib NF, Mehrez MI, Abdel-Kader MA, Mohsen YH, Zada SK, Amr KS, Sayed ISM.
    Genes (Basel); 2021 Sep 08; 12(9):. PubMed ID: 34573371
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.