BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 36183038)

  • 1. Enamel defects in Acp4
    Liang T; Wang SK; Smith C; Zhang H; Hu Y; Seymen F; Koruyucu M; Kasimoglu Y; Kim JW; Zhang C; Saunders TL; Simmer JP; Hu JC
    Sci Rep; 2022 Oct; 12(1):16477. PubMed ID: 36183038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificity.
    Liang T; Hu Y; Smith CE; Richardson AS; Zhang H; Yang J; Lin B; Wang SK; Kim JW; Chun YH; Simmer JP; Hu JC
    Mol Genet Genomic Med; 2019 Sep; 7(9):e929. PubMed ID: 31402633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recessive Mutations in
    Kim YJ; Lee Y; Kasimoglu Y; Seymen F; Simmer JP; Hu JC; Cho ES; Kim JW
    J Dent Res; 2022 Jan; 101(1):37-45. PubMed ID: 34036831
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants.
    Hytönen MK; Arumilli M; Sarkiala E; Nieminen P; Lohi H
    Hum Genet; 2019 May; 138(5):525-533. PubMed ID: 30877375
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FAM20A is essential for amelogenesis, but is dispensable for dentinogenesis.
    Li L; Saiyin W; Zhang H; Wang S; Xu Q; Qin C; Lu Y
    J Mol Histol; 2019 Dec; 50(6):581-591. PubMed ID: 31667691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.
    Seymen F; Kim YJ; Lee YJ; Kang J; Kim TH; Choi H; Koruyucu M; Kasimoglu Y; Tuna EB; Gencay K; Shin TJ; Hyun HK; Kim YJ; Lee SH; Lee ZH; Zhang H; Hu JC; Simmer JP; Cho ES; Kim JW
    Am J Hum Genet; 2016 Nov; 99(5):1199-1205. PubMed ID: 27843125
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genetic model for the secretory stage of dental enamel formation.
    Simmer JP; Hu JC; Hu Y; Zhang S; Liang T; Wang SK; Kim JW; Yamakoshi Y; Chun YH; Bartlett JD; Smith CE
    J Struct Biol; 2021 Dec; 213(4):107805. PubMed ID: 34715329
    [TBL] [Abstract][Full Text] [Related]  

  • 8.
    Wang YL; Lin HC; Liang T; Lin JC; Simmer JP; Hu JC; Wang SK
    J Dent Res; 2024 Jun; 103(6):662-671. PubMed ID: 38716742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Amelogenin phosphorylation regulates tooth enamel formation by stabilizing a transient amorphous mineral precursor.
    Shin NY; Yamazaki H; Beniash E; Yang X; Margolis SS; Pugach MK; Simmer JP; Margolis HC
    J Biol Chem; 2020 Feb; 295(7):1943-1959. PubMed ID: 31919099
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.
    Brookes SJ; Barron MJ; Smith CEL; Poulter JA; Mighell AJ; Inglehearn CF; Brown CJ; Rodd H; Kirkham J; Dixon MJ
    Hum Mol Genet; 2017 May; 26(10):1863-1876. PubMed ID: 28334996
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Enamel formation and amelogenesis imperfecta.
    Hu JC; Chun YH; Al Hazzazzi T; Simmer JP
    Cells Tissues Organs; 2007; 186(1):78-85. PubMed ID: 17627121
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The protein composition of normal and developmentally defective enamel.
    Wright JT; Hall K; Yamauchi M
    Ciba Found Symp; 1997; 205():85-99; discussion 99-106. PubMed ID: 9189619
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.
    El-Sayed W; Parry DA; Shore RC; Ahmed M; Jafri H; Rashid Y; Al-Bahlani S; Al Harasi S; Kirkham J; Inglehearn CF; Mighell AJ
    Am J Hum Genet; 2009 Nov; 85(5):699-705. PubMed ID: 19853237
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
    Kim JW; Zhang H; Seymen F; Koruyucu M; Hu Y; Kang J; Kim YJ; Ikeda A; Kasimoglu Y; Bayram M; Zhang C; Kawasaki K; Bartlett JD; Saunders TL; Simmer JP; Hu JC
    Clin Genet; 2019 Mar; 95(3):375-383. PubMed ID: 30506946
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of Fam83h truncation mutation on enamel developmental defects in male C57/BL6J mice.
    Zheng X; Huang W; He Z; Li Y; Li S; Song Y
    Bone; 2023 Jan; 166():116595. PubMed ID: 36272714
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Enamel Phenotype in Homozygous Fam83h Truncation Mice.
    Wang SK; Hu Y; Smith CE; Yang J; Zeng C; Kim JW; Hu JC; Simmer JP
    Mol Genet Genomic Med; 2019 Jun; 7(6):e724. PubMed ID: 31060110
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stim1 Regulates Enamel Mineralization and Ameloblast Modulation.
    Furukawa Y; Haruyama N; Nikaido M; Nakanishi M; Ryu N; Oh-Hora M; Kuremoto K; Yoshizaki K; Takano Y; Takahashi I
    J Dent Res; 2017 Nov; 96(12):1422-1429. PubMed ID: 28732182
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reconstructing impairment of secretory ameloblast function in porcine teeth by analysis of morphological alterations in dental enamel.
    Witzel C; Kierdorf U; Dobney K; Ervynck A; Vanpoucke S; Kierdorf H
    J Anat; 2006 Jul; 209(1):93-110. PubMed ID: 16822273
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cellular and chemical events during enamel maturation.
    Smith CE
    Crit Rev Oral Biol Med; 1998; 9(2):128-61. PubMed ID: 9603233
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.