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 *

421 related articles for article (PubMed ID: 19320256)

  • 1. Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations.
    Ng FK; Messer LB
    Pediatr Dent; 2009; 31(1):20-30. PubMed ID: 19320256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
    Wright JT; Hart PS; Aldred MJ; Seow K; Crawford PJ; Hong SP; Gibson CW; Hart TC
    Connect Tissue Res; 2003; 44 Suppl 1():72-8. PubMed ID: 12952177
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 14(5):575-83. PubMed ID: 15649948
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
    Gutierrez SJ; Chaves M; Torres DM; Briceño I
    Arch Oral Biol; 2007 May; 52(5):503-6. PubMed ID: 17316551
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dental enamel formation and its impact on clinical dentistry.
    Simmer JP; Hu JC
    J Dent Educ; 2001 Sep; 65(9):896-905. PubMed ID: 11569606
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta.
    Nakamura H; Sawamura D; Goto M; Nakamura H; Kida M; Ariga T; Sakiyama Y; Tomizawa K; Mitsui H; Tamaki K; Shimizu H
    Int J Mol Med; 2006 Aug; 18(2):333-7. PubMed ID: 16820943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).
    Lench NJ; Winter GB
    Hum Mutat; 1995; 5(3):251-9. PubMed ID: 7599636
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta.
    Sekiguchi H; Minaguchi K; Machida Y; Yakushiji M
    Bull Tokyo Dent Coll; 1998 Nov; 39(4):275-85. PubMed ID: 10218009
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.
    Urzúa B; Ortega-Pinto A; Morales-Bozo I; Rojas-Alcayaga G; Cifuentes V
    Biochem Genet; 2011 Feb; 49(1-2):104-21. PubMed ID: 21127961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Amelogenesis imperfecta: an introduction.
    Gadhia K; McDonald S; Arkutu N; Malik K
    Br Dent J; 2012 Apr; 212(8):377-9. PubMed ID: 22538897
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfecta.
    Ravassipour DB; Powell CM; Phillips CL; Hart PS; Hart TC; Boyd C; Wright JT
    Arch Oral Biol; 2005 Jul; 50(7):611-23. PubMed ID: 15892947
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular etiologies and associated phenotypes of amelogenesis imperfecta.
    Wright JT
    Am J Med Genet A; 2006 Dec; 140(23):2547-55. PubMed ID: 16838342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Amelogenesis imperfecta--multidisciplinary management from eruption to adulthood. Review and case report.
    Ayers KM; Drummond BK; Harding WJ; Salis SG; Liston PN
    N Z Dent J; 2004 Dec; 100(4):101-4. PubMed ID: 15656432
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
    Kim JW; Simmer JP; Hu YY; Lin BP; Boyd C; Wright JT; Yamada CJ; Rayes SK; Feigal RJ; Hu JC
    J Dent Res; 2004 May; 83(5):378-83. PubMed ID: 15111628
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.
    Hyun HK; Lee SK; Lee KE; Kang HY; Kim EJ; Choung PH; Kim JW
    Int Endod J; 2009 Nov; 42(11):1039-43. PubMed ID: 19825039
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.
    Gu X; Bäckman B; Coates PJ; Cullman I; Hellman U; Lind L; Nylander K
    Acta Odontol Scand; 2006 Apr; 64(2):111-4. PubMed ID: 16546853
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern.
    Bundzman ER; Modesto A
    Braz Dent J; 1999; 10(2):111-6. PubMed ID: 10863398
    [TBL] [Abstract][Full Text] [Related]  

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

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

    [Next]    [New Search]
    of 22.