BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 38069551)

  • 1. 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]  

  • 2. Novel MSX1 variants identified in families with nonsyndromic oligodontia.
    Zheng J; Yu M; Liu H; Cai T; Feng H; Liu Y; Han D
    Int J Oral Sci; 2021 Jan; 13(1):2. PubMed ID: 33419968
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.
    Xuan K; Jin F; Liu YL; Yuan LT; Wen LY; Yang FS; Wang XJ; Wang GH; Jin Y
    Arch Oral Biol; 2008 Aug; 53(8):773-9. PubMed ID: 18374898
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype pattern analysis of pathogenic
    Ren J; Gan S; Zheng S; Li M; An Y; Yuan S; Gu X; Zhang L; Hou Y; Du Q; Zhang G; Shen W
    Front Genet; 2023; 14():1142776. PubMed ID: 37056289
    [No Abstract]   [Full Text] [Related]  

  • 5. A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.
    Xue J; Gao Q; Huang Y; Zhang X; Yang P; Cram DS; Liang D; Wu L
    Clin Chim Acta; 2016 Oct; 461():135-40. PubMed ID: 27485761
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.
    Zhang XX; Wong SW; Han D; Feng HL
    Chin J Dent Res; 2015; 18(4):229-34. PubMed ID: 26629556
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia.
    Ma T; Liu Y; Zhao X; Wu J; Wang H; Chen J; Liu P; Zhang X; Zhang X
    Ann Hum Genet; 2020 Jan; 84(1):97-101. PubMed ID: 31469409
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel mutations in MSX1 causing oligodontia.
    Yang L; Liang J; Yue H; Bian Z
    PLoS One; 2020; 15(1):e0227287. PubMed ID: 31914153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.
    Wong SW; Liu HC; Han D; Chang HG; Zhao HS; Wang YX; Feng HL
    Mutagenesis; 2014 Sep; 29(5):319-23. PubMed ID: 24914010
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene.
    Abid MF; Simpson MA; Petridis C; Cobourne MT; Sharpe PT
    Arch Oral Biol; 2017 Mar; 75():8-13. PubMed ID: 27951410
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathway.
    Xin T; Zhang T; Li Q; Yu T; Zhu Y; Yang R; Zhou Y
    Stem Cell Res Ther; 2018 Aug; 9(1):221. PubMed ID: 30134957
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
    Salvi A; Giacopuzzi E; Bardellini E; Amadori F; Ferrari L; De Petro G; Borsani G; Majorana A
    Int J Mol Med; 2016 Nov; 38(5):1338-1348. PubMed ID: 27665865
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
    Mu YD; Xu Z; Contreras CI; McDaniel JS; Donly KJ; Chen S
    Genet Mol Res; 2013 Oct; 12(4):4446-58. PubMed ID: 24222224
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
    Shahid M; Balto HA; Al-Hammad N; Joshi S; Khalil HS; Somily AM; Sinjilawi NA; Al-Ghamdi S; Faiyaz-Ul-Haque M; Dhillon VS
    Eur J Med Genet; 2016 Aug; 59(8):377-85. PubMed ID: 27365112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
    Wong SW; Han D; Zhang H; Liu Y; Zhang X; Miao MZ; Wang Y; Zhao N; Zeng L; Bai B; Wang YX; Liu H; Frazier-Bowers SA; Feng H
    J Dent Res; 2018 Feb; 97(2):155-162. PubMed ID: 28910570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.
    Haddaji Mastouri M; De Coster P; Zaghabani A; Jammali F; Raouahi N; Ben Salem A; Saad A; Coucke P; H'mida Ben Brahim D
    Eur J Oral Sci; 2018 Feb; 126(1):24-32. PubMed ID: 29114927
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.