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 *

183 related articles for article (PubMed ID: 31999931)

  • 1. Alteration of Exon Definition Causes Amelogenesis Imperfecta.
    Kim YJ; Kang J; Seymen F; Koruyucu M; Zhang H; Kasimoglu Y; Bayram M; Tuna-Ince EB; Bayrak S; Tuloglu N; Hu JC; Simmer JP; Kim JW
    J Dent Res; 2020 Apr; 99(4):410-418. PubMed ID: 31999931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta.
    Zhang Z; Zou X; Feng L; Huang Y; Chen F; Sun K; Song Y; Lv P; Gao X; Dong Y; Tian H
    BMC Oral Health; 2023 Nov; 23(1):893. PubMed ID: 37985977
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analyses of
    Kim YJ; Kang J; Seymen F; Koruyucu M; Gencay K; Shin TJ; Hyun HK; Lee ZH; Hu JC; Simmer JP; Kim JW
    Front Physiol; 2017; 8():229. PubMed ID: 28473773
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel AMELX mutation causes hypoplastic amelogenesis imperfecta.
    Kim YJ; Kim YJ; Kang J; Shin TJ; Hyun HK; Lee SH; Lee ZH; Kim JW
    Arch Oral Biol; 2017 Apr; 76():61-65. PubMed ID: 28130977
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.
    Santos MC; Hart PS; Ramaswami M; Kanno CM; Hart TC; Line SR
    Head Face Med; 2007 Jan; 3():8. PubMed ID: 17266769
    [TBL] [Abstract][Full Text] [Related]  

  • 6.
    Wang SK; Zhang H; Lin HC; Wang YL; Lin SC; Seymen F; Koruyucu M; Simmer JP; Hu JC
    Int J Mol Sci; 2024 Jun; 25(11):. PubMed ID: 38892321
    [No Abstract]   [Full Text] [Related]  

  • 7. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
    Hu JC; Chan HC; Simmer SG; Seymen F; Richardson AS; Hu Y; Milkovich RN; Estrella NM; Yildirim M; Bayram M; Chen CF; Simmer JP
    PLoS One; 2012; 7(12):e52052. PubMed ID: 23251683
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation in GPR68 causes hypomaturation amelogenesis imperfecta.
    Yu S; Liu D; Yan C; Yuan C; Zhang C; Zheng S
    Arch Oral Biol; 2024 Aug; 164():105991. PubMed ID: 38761453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20.
    Nikolopoulos G; Smith CEL; Poulter JA; Murillo G; Silva S; Lamb T; Berry IR; Brown CJ; Day PF; Soldani F; Al-Bahlani S; Harris SA; O'Connell MJ; Inglehearn CF; Mighell AJ
    Hum Mutat; 2021 May; 42(5):567-576. PubMed ID: 33600052
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
    Ozdemir D; Hart PS; Ryu OH; Choi SJ; Ozdemir-Karatas M; Firatli E; Piesco N; Hart TC
    J Dent Res; 2005 Nov; 84(11):1031-5. PubMed ID: 16246936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel
    Lee Y; Zhang H; Seymen F; Kim YJ; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW
    J Pers Med; 2022 Jan; 12(2):. PubMed ID: 35207639
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Amelogenesis imperfecta: genotype-phenotype studies in 71 families.
    Wright JT; Torain M; Long K; Seow K; Crawford P; Aldred MJ; Hart PS; Hart TC
    Cells Tissues Organs; 2011; 194(2-4):279-83. PubMed ID: 21597265
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Novel
    Duan X; Yang S; Zhang H; Wu J; Zhang Y; Ji D; Tie L; Boerkoel CF
    J Dent Res; 2019 Jul; 98(8):870-878. PubMed ID: 31185186
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
    Khan SA; Khan MA; Muhammad N; Bashir H; Khan N; Muhammad N; Yilmaz R; Khan S; Wasif N
    BMC Med Genet; 2020 May; 21(1):97. PubMed ID: 32380970
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
    Wang SK; Choi M; Richardson AS; Reid BM; Lin BP; Wang SJ; Kim JW; Simmer JP; Hu JC
    Hum Mol Genet; 2014 Apr; 23(8):2157-63. PubMed ID: 24305999
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MMP20 hemopexin domain mutation in amelogenesis imperfecta.
    Lee SK; Seymen F; Kang HY; Lee KE; Gencay K; Tuna B; Kim JW
    J Dent Res; 2010 Jan; 89(1):46-50. PubMed ID: 19966041
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations.
    Koruyucu M; Kang J; Kim YJ; Seymen F; Kasimoglu Y; Lee ZH; Shin TJ; Hyun HK; Kim YJ; Lee SH; Hu JCC; Simmer JP; Kim JW
    J Dent Res; 2018 Aug; 97(9):1064-1069. PubMed ID: 29554435
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Premature stop codon in MMP20 causing amelogenesis imperfecta.
    Papagerakis P; Lin HK; Lee KY; Hu Y; Simmer JP; Bartlett JD; Hu JC
    J Dent Res; 2008 Jan; 87(1):56-9. PubMed ID: 18096894
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic variability in LAMA3-associated amelogenesis imperfecta.
    Wang SK; Zhang H; Wang YL; Seymen F; Koruyucu M; Simmer JP; Hu JC
    Oral Dis; 2023 Nov; 29(8):3514-3524. PubMed ID: 36326426
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing.
    Wang SK; Hu Y; Simmer JP; Seymen F; Estrella NM; Pal S; Reid BM; Yildirim M; Bayram M; Bartlett JD; Hu JC
    J Dent Res; 2013 Mar; 92(3):266-71. PubMed ID: 23355523
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.