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 *

168 related articles for article (PubMed ID: 16446857)

  • 1. [Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta].
    Urzúa O B; Ortega P A; Rodríguez M L; Morales B I
    Rev Med Chil; 2005 Nov; 133(11):1331-40. PubMed ID: 16446857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ENAM mutations in autosomal-dominant amelogenesis imperfecta.
    Kim JW; Seymen F; Lin BP; Kiziltan B; Gencay K; Simmer JP; Hu JC
    J Dent Res; 2005 Mar; 84(3):278-82. PubMed ID: 15723871
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.
    Pavlic A; Petelin M; Battelino T
    Arch Oral Biol; 2007 Mar; 52(3):209-17. PubMed ID: 17125728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
    Mårdh CK; Bäckman B; Holmgren G; Hu JC; Simmer JP; Forsman-Semb K
    Hum Mol Genet; 2002 May; 11(9):1069-74. PubMed ID: 11978766
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.
    Hart TC; Hart PS; Gorry MC; Michalec MD; Ryu OH; Uygur C; Ozdemir D; Firatli S; Aren G; Firatli E
    J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
    Shore RC; Bäckman B; Elcock C; Brook AH; Brookes SJ; Kirkham J
    Cells Tissues Organs; 2010; 191(4):301-6. PubMed ID: 19923784
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    Kida M; Ariga T; Shirakawa T; Oguchi H; Sakiyama Y
    J Dent Res; 2002 Nov; 81(11):738-42. PubMed ID: 12407086
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta.
    Rajpar MH; Harley K; Laing C; Davies RM; Dixon MJ
    Hum Mol Genet; 2001 Aug; 10(16):1673-7. PubMed ID: 11487571
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M; Bazrafshani MR; Poulton K; Jaber S; Naeem E; Blinkhorn AS
    J Investig Clin Dent; 2011 Feb; 2(1):16-22. PubMed ID: 25427323
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families.
    Urzúa B; Ortega-Pinto A; Farias DA; Franco E; Morales-Bozo I; Moncada G; Escobar-Pezoa N; Scholz U; Cifuentes V
    Acta Odontol Scand; 2012 Jan; 70(1):7-14. PubMed ID: 21504268
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotype of ENAM mutations is dosage-dependent.
    Ozdemir D; Hart PS; Firatli E; Aren G; Ryu OH; Hart TC
    J Dent Res; 2005 Nov; 84(11):1036-41. PubMed ID: 16246937
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diversity of clinical, radiographic and genealogical findings in 41 families with amelogenesis imperfecta.
    Adorno-Farias D; Ortega-Pinto A; Gajardo P; Salazar A; Morales-Bozo I; Werlinger F; Rojas-Flores S; Molina-Berríos A; Echeverría-López S; Jara-Sandoval J; Jara L; Urzúa B
    J Appl Oral Sci; 2019 Apr; 27():e20180359. PubMed ID: 30970114
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 48(8):589-96. PubMed ID: 12828988
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta.
    Wang X; Zhao Y; Yang Y; Qin M
    PLoS One; 2015; 10(3):e0116514. PubMed ID: 25769099
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 23(1):893. PubMed ID: 37985977
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Wright JT; Savage M; Kang G; Bensen JT; Gorry MC; Hart TC
    Eur J Oral Sci; 2003 Aug; 111(4):326-31. PubMed ID: 12887398
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.
    Lindemeyer RG; Gibson CW; Wright TJ
    Pediatr Dent; 2010; 32(1):56-60. PubMed ID: 20298654
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.