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

214 related items for PubMed ID: 22759786

  • 1. Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.
    Coxon TL, Brook AH, Barron MJ, Smith RN.
    Cells Tissues Organs; 2012; 196(5):420-30. PubMed ID: 22759786
    [Abstract] [Full Text] [Related]

  • 2. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).
    Masuya H, Shimizu K, Sezutsu H, Sakuraba Y, Nagano J, Shimizu A, Fujimoto N, Kawai A, Miura I, Kaneda H, Kobayashi K, Ishijima J, Maeda T, Gondo Y, Noda T, Wakana S, Shiroishi T.
    Hum Mol Genet; 2005 Mar 01; 14(5):575-83. PubMed ID: 15649948
    [Abstract] [Full Text] [Related]

  • 3. 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 20; 23(1):893. PubMed ID: 37985977
    [Abstract] [Full Text] [Related]

  • 4. A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.
    Barron MJ, Brookes SJ, Kirkham J, Shore RC, Hunt C, Mironov A, Kingswell NJ, Maycock J, Shuttleworth CA, Dixon MJ.
    Hum Mol Genet; 2010 Apr 01; 19(7):1230-47. PubMed ID: 20067920
    [Abstract] [Full Text] [Related]

  • 5. [Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión].
    Tremillo-Maldonado O, Molina-Frechero N, González-González R, Bologna-Molina R.
    Gac Med Mex; 2019 Apr 01; 155(1):101-107. PubMed ID: 30799455
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
    Hart PS, Aldred MJ, Crawford PJ, Wright NJ, Hart TC, Wright JT.
    Arch Oral Biol; 2002 Apr 01; 47(4):261-5. PubMed ID: 11922869
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta.
    Wang SK, Zhang H, Lin HC, Wang YL, Lin SC, Seymen F, Koruyucu M, Simmer JP, Hu JC.
    Int J Mol Sci; 2024 Jun 01; 25(11):. PubMed ID: 38892321
    [Abstract] [Full Text] [Related]

  • 10. The phosphorylation of serine55 in enamelin is essential for murine amelogenesis.
    Dong C, Lamichhane B, Yamazaki H, Vasquez B, Wang J, Zhang Y, Feng JQ, Margolis HC, Beniash E, Wang X.
    Matrix Biol; 2022 Aug 01; 111():245-263. PubMed ID: 35820561
    [Abstract] [Full Text] [Related]

  • 11. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
    Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT.
    Arch Oral Biol; 2003 Aug 01; 48(8):589-96. PubMed ID: 12828988
    [Abstract] [Full Text] [Related]

  • 12. ENAM Mutations Can Cause Hypomaturation Amelogenesis Imperfecta.
    Wang YL, Lin HC, Liang T, Lin JC, Simmer JP, Hu JC, Wang SK.
    J Dent Res; 2024 Jun 01; 103(6):662-671. PubMed ID: 38716742
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. ENAM mutations and digenic inheritance.
    Zhang H, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Wang SK, Wright JT, Havel MW, Zhang C, Kim JW, Simmer JP, Hu JC.
    Mol Genet Genomic Med; 2019 Oct 01; 7(10):e00928. PubMed ID: 31478359
    [Abstract] [Full Text] [Related]

  • 15. Genes and related proteins involved in amelogenesis imperfecta.
    Stephanopoulos G, Garefalaki ME, Lyroudia K.
    J Dent Res; 2005 Dec 01; 84(12):1117-26. PubMed ID: 16304440
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Alteration of conserved alternative splicing in AMELX causes enamel defects.
    Cho ES, Kim KJ, Lee KE, Lee EJ, Yun CY, Lee MJ, Shin TJ, Hyun HK, Kim YJ, Lee SH, Jung HS, Lee ZH, Kim JW.
    J Dent Res; 2014 Oct 01; 93(10):980-7. PubMed ID: 25117480
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Mouse genetic background influences the dental phenotype.
    Li Y, Konicki WS, Wright JT, Suggs C, Xue H, Kuehl MA, Kulkarni AB, Gibson CW.
    Cells Tissues Organs; 2013 Oct 01; 198(6):448-56. PubMed ID: 24732779
    [Abstract] [Full Text] [Related]

  • 20. Cytomegalovirus induces stage-dependent enamel defects and misexpression of amelogenin, enamelin and dentin sialophosphoprotein in developing mouse molars.
    Jaskoll T, Abichaker G, Htet K, Bringas P, Morita S, Sedghizadeh PP, Melnick M.
    Cells Tissues Organs; 2010 Oct 01; 192(4):221-39. PubMed ID: 20484882
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.