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351 related items for PubMed ID: 30134932

  • 1. Dentinogenesis imperfecta type II in Swedish children and adolescents.
    Andersson K, Malmgren B, Åström E, Dahllöf G.
    Orphanet J Rare Dis; 2018 Aug 22; 13(1):145. PubMed ID: 30134932
    [Abstract] [Full Text] [Related]

  • 2. Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.
    Andersson K, Dahllöf G, Lindahl K, Kindmark A, Grigelioniene G, Åström E, Malmgren B.
    PLoS One; 2017 Aug 22; 12(5):e0176466. PubMed ID: 28498836
    [Abstract] [Full Text] [Related]

  • 3. Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.
    Li F, Liu Y, Liu H, Yang J, Zhang F, Feng H.
    Oral Dis; 2017 Apr 22; 23(3):360-366. PubMed ID: 27973701
    [Abstract] [Full Text] [Related]

  • 4. Immunocytochemical detection of dentin matrix proteins in primary teeth from patients with dentinogenesis imperfecta associated with osteogenesis imperfecta.
    Orsini G, Majorana A, Mazzoni A, Putignano A, Falconi M, Polimeni A, Breschi L.
    Eur J Histochem; 2014 Dec 01; 58(4):2405. PubMed ID: 25578972
    [Abstract] [Full Text] [Related]

  • 5. The non-collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II (DGI-II).
    Thotakura SR, Mah T, Srinivasan R, Takagi Y, Veis A, George A.
    J Dent Res; 2000 Mar 01; 79(3):835-9. PubMed ID: 10765957
    [Abstract] [Full Text] [Related]

  • 6. Hereditary dentin defects.
    Kim JW, Simmer JP.
    J Dent Res; 2007 May 01; 86(5):392-9. PubMed ID: 17452557
    [Abstract] [Full Text] [Related]

  • 7. Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
    Kim JW, Hu JC, Lee JI, Moon SK, Kim YJ, Jang KT, Lee SH, Kim CC, Hahn SH, Simmer JP.
    Hum Genet; 2005 Feb 01; 116(3):186-91. PubMed ID: 15592686
    [Abstract] [Full Text] [Related]

  • 8. Molecular basis of human dentin diseases.
    MacDougall M, Dong J, Acevedo AC.
    Am J Med Genet A; 2006 Dec 01; 140(23):2536-46. PubMed ID: 16955410
    [Abstract] [Full Text] [Related]

  • 9. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.
    Wang SK, Chan HC, Makovey I, Simmer JP, Hu JC.
    PLoS One; 2012 Dec 01; 7(12):e51533. PubMed ID: 23227268
    [Abstract] [Full Text] [Related]

  • 10. Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.
    von Marschall Z, Mok S, Phillips MD, McKnight DA, Fisher LW.
    J Bone Miner Res; 2012 Jun 01; 27(6):1309-21. PubMed ID: 22392858
    [Abstract] [Full Text] [Related]

  • 11. Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta.
    Malmgren B, Lindskog S.
    Acta Odontol Scand; 2003 Apr 01; 61(2):72-80. PubMed ID: 12790503
    [Abstract] [Full Text] [Related]

  • 12. Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta.
    Pallos D, Hart PS, Cortelli JR, Vian S, Wright JT, Korkko J, Brunoni D, Hart TC.
    Arch Oral Biol; 2001 May 01; 46(5):459-70. PubMed ID: 11286811
    [Abstract] [Full Text] [Related]

  • 13. Osteogenesis imperfecta and the teeth, eyes, and ears-a study of non-skeletal phenotypes in adults.
    Hald JD, Folkestad L, Swan CZ, Wanscher J, Schmidt M, Gjørup H, Haubek D, Leonhard CH, Larsen DA, Hjortdal JØ, Harsløf T, Duno M, Lund AM, Jensen JB, Brixen K, Langdahl B.
    Osteoporos Int; 2018 Dec 01; 29(12):2781-2789. PubMed ID: 30143849
    [Abstract] [Full Text] [Related]

  • 14. ED-A region-containing isoform of cellular fibronectin is present in dentin matrix in dentinogenesis imperfecta associated with osteogenesis imperfecta.
    Lukinmaa PL, Vaheri A.
    J Dent Res; 1994 Jun 01; 73(6):1187-96. PubMed ID: 8046108
    [Abstract] [Full Text] [Related]

  • 15. A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.
    Zhang X, Chen L, Liu J, Zhao Z, Qu E, Wang X, Chang W, Xu C, Wang QK, Liu M.
    BMC Med Genet; 2007 Aug 08; 8():52. PubMed ID: 17686168
    [Abstract] [Full Text] [Related]

  • 16. Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.
    Malmgren B, Andersson K, Lindahl K, Kindmark A, Grigelioniene G, Zachariadis V, Dahllöf G, Åström E.
    Oral Dis; 2017 Jan 08; 23(1):42-49. PubMed ID: 27510842
    [Abstract] [Full Text] [Related]

  • 17. Dental manifestations of osteogenesis imperfecta and abnormalities of collagen I metabolism.
    Lund AM, Jensen BL, Nielsen LA, Skovby F.
    J Craniofac Genet Dev Biol; 1998 Jan 08; 18(1):30-7. PubMed ID: 9594376
    [Abstract] [Full Text] [Related]

  • 18. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
    Barron MJ, McDonnell ST, Mackie I, Dixon MJ.
    Orphanet J Rare Dis; 2008 Nov 20; 3():31. PubMed ID: 19021896
    [Abstract] [Full Text] [Related]

  • 19. [Oral cavity features in patients suffering from osteogenesis imperfecta].
    Alania KN, Iverieli MB, Abashidze NO, Gogishvili KhB, Chigladze TT.
    Georgian Med News; 2011 Apr 20; (193):34-41. PubMed ID: 21617272
    [Abstract] [Full Text] [Related]

  • 20. Dental findings in osteogenesis imperfecta: I. Occurrence and expression of type I dentinogenesis imperfecta.
    Lukinmaa PL, Ranta H, Ranta K, Kaitila I.
    J Craniofac Genet Dev Biol; 1987 Apr 20; 7(2):115-25. PubMed ID: 3624417
    [Abstract] [Full Text] [Related]

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