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

Journal Abstract Search


196 related items for PubMed ID: 33864320

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Enamelin and autosomal-dominant amelogenesis imperfecta.
    Hu JC, Yamakoshi Y.
    Crit Rev Oral Biol Med; 2003; 14(6):387-98. PubMed ID: 14656895
    [Abstract] [Full Text] [Related]

  • 24. 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; 111():245-263. PubMed ID: 35820561
    [Abstract] [Full Text] [Related]

  • 25. Ultrastructural analyses of deciduous teeth affected by hypocalcified amelogenesis imperfecta from a family with a novel Y458X FAM83H nonsense mutation.
    El-Sayed W, Shore RC, Parry DA, Inglehearn CF, Mighell AJ.
    Cells Tissues Organs; 2010 Aug; 191(3):235-9. PubMed ID: 20160442
    [Abstract] [Full Text] [Related]

  • 26. 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 Aug; 196(5):420-30. PubMed ID: 22759786
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Enamelin Directs Crystallite Organization at the Enamel-Dentine Junction.
    Siddiqui S, Al-Jawad M.
    J Dent Res; 2016 May; 95(5):580-7. PubMed ID: 26912218
    [Abstract] [Full Text] [Related]

  • 29. Simple recessive mutation in ENAM is associated with amelogenesis imperfecta in Italian Greyhounds.
    Gandolfi B, Liu H, Griffioen L, Pedersen NC.
    Anim Genet; 2013 Aug; 44(5):569-78. PubMed ID: 23638899
    [Abstract] [Full Text] [Related]

  • 30. Translational Attenuation by an Intron Retention in the 5' UTR of ENAM Causes Amelogenesis Imperfecta.
    Kim YJ, Lee Y, Zhang H, Wright JT, Simmer JP, Hu JC, Kim JW.
    Biomedicines; 2021 Apr 22; 9(5):. PubMed ID: 33922212
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. 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 31; 3():8. PubMed ID: 17266769
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.
    Volodarsky M, Zilberman U, Birk OS.
    Arch Oral Biol; 2015 Jun 31; 60(6):919-22. PubMed ID: 25827751
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 10.