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 *

256 related articles for article (PubMed ID: 27321946)

  • 21. Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
    Qin H; Xu HZ; Xuan K
    Arch Oral Biol; 2013 Sep; 58(9):1180-6. PubMed ID: 23731659
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 8(11):e80393. PubMed ID: 24312213
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population.
    Inagaki Y; Ogawa T; Tabata MJ; Nagata Y; Watanabe R; Kawamoto T; Moriyama K; Tanaka T
    J Hum Genet; 2021 Aug; 66(8):769-775. PubMed ID: 33611338
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families.
    Zhao Y; Ren J; Meng L; Hou Y; Liu C; Zhang G; Shen W
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2334. PubMed ID: 38069551
    [TBL] [Abstract][Full Text] [Related]  

  • 25.
    Yu M; Liu H; Liu Y; Zheng J; Wu J; Sun K; Feng H; Liu H; Han D
    Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293320
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.
    Zhang L; Yu M; Wong SW; Qu H; Cai T; Liu Y; Liu H; Fan Z; Zheng J; Zhou Y; Feng H; Han D
    Hum Mutat; 2020 Nov; 41(11):1957-1966. PubMed ID: 32906216
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deleterious Variants in
    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; 20(21):. PubMed ID: 31652981
    [TBL] [Abstract][Full Text] [Related]  

  • 28.
    Yu M; Fan Z; Wong SW; Sun K; Zhang L; Liu H; Feng H; Liu Y; Han D
    J Dent Res; 2021 Apr; 100(4):415-422. PubMed ID: 33164649
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
    Nikopensius T; Annilo T; Jagomägi T; Gilissen C; Kals M; Krjutškov K; Mägi R; Eelmets M; Gerst-Talas U; Remm M; Saag M; Hoischen A; Metspalu A
    J Dent Res; 2013 Jun; 92(6):507-11. PubMed ID: 23603338
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel PAX9 compound heterozygous variants in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9 variants.
    Ren J; Zhao Y; Yuan Y; Zhang J; Ding Y; Li M; An Y; Chen W; Zhang L; Liu B; Zheng S; Shen W
    J Appl Oral Sci; 2023; 31():e20220403. PubMed ID: 36995881
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel missense mutation of LRP6 identified by whole-exome sequencing in a Chinese family with non-syndromic tooth agenesis.
    Wang H; Liu Y; Zheng Y; Zhao X; Lin S; Zhang Q; Zhang X
    Orthod Craniofac Res; 2021 May; 24(2):233-240. PubMed ID: 32844563
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Sequence Variants in the
    Bilal M; Hayat A; Umair M; Ullah A; Khawaja S; Malik E; Burmeister M; Bibi N; Umm-E-Kalsoom ; Memon MI; Basit S; Ahmad W; Khan B
    Genet Test Mol Biomarkers; 2020 Sep; 24(9):600-607. PubMed ID: 32762550
    [No Abstract]   [Full Text] [Related]  

  • 33. Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family.
    Zhao Y; Hou Y; Ren J; Gao X; Meng L; Liu Y; Xing C; Shen W
    Arch Oral Biol; 2023 Oct; 154():105759. PubMed ID: 37422997
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Oligodontia and curly hair occur with ectodysplasin-a mutations.
    Lee KE; Ko J; Shin TJ; Hyun HK; Lee SH; Kim JW
    J Dent Res; 2014 Apr; 93(4):371-5. PubMed ID: 24487376
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
    Zhang H; Kong X; Ren J; Yuan S; Liu C; Hou Y; Liu Y; Meng L; Zhang G; Du Q; Shen W
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1684. PubMed ID: 33943035
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
    Yue H; Liang J; Yang K; Hua B; Bian Z
    Eur J Oral Sci; 2016 Jun; 124(3):228-33. PubMed ID: 27090353
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.
    Lammi L; Arte S; Somer M; Jarvinen H; Lahermo P; Thesleff I; Pirinen S; Nieminen P
    Am J Hum Genet; 2004 May; 74(5):1043-50. PubMed ID: 15042511
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel PAX9 mutations cause non-syndromic tooth agenesis.
    Mitsui SN; Yasue A; Masuda K; Watanabe K; Horiuchi S; Imoto I; Tanaka E
    J Dent Res; 2014 Mar; 93(3):245-9. PubMed ID: 24436340
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Functional study of novel PAX9 variants: The paired domain and non-syndromic oligodontia.
    Sun K; Yu M; Yeh I; Zhang L; Liu H; Cai T; Feng H; Liu Y; Han D
    Oral Dis; 2021 Sep; 27(6):1468-1477. PubMed ID: 33078491
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.