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 *

400 related articles for article (PubMed ID: 10218009)

  • 1. 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]  

  • 2. 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]  

  • 3. Molecular basis and consequences of a deletion in the amelogenin gene, analyzed by capture PCR.
    Lagerström-Fermér M; Pettersson U; Landegren U
    Genomics; 1993 Jul; 17(1):89-92. PubMed ID: 8406474
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identifying polymorphism in enamelin gene in amelogenesis imperfecta (AI).
    Gopinath VK; Yoong TP; Yean CY; Ravichandran M
    Arch Oral Biol; 2008 Oct; 53(10):937-40. PubMed ID: 18466877
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1).
    Lench NJ; Brook AH; Winter GB
    Hum Mol Genet; 1994 May; 3(5):827-8. PubMed ID: 8081371
    [No Abstract]   [Full Text] [Related]  

  • 6. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.
    Lagerström-Fermér M; Nilsson M; Bäckman B; Salido E; Shapiro L; Pettersson U; Landegren U
    Genomics; 1995 Mar; 26(1):159-62. PubMed ID: 7782077
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Detection of a novel mutation in X-linked amelogenesis imperfecta.
    Kindelan SA; Brook AH; Gangemi L; Lench N; Wong FS; Fearne J; Jackson Z; Foster G; Stringer BM
    J Dent Res; 2000 Dec; 79(12):1978-82. PubMed ID: 11201048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphism (g2035C>T) in the amelogenin gene.
    Hart PS; Vlaservich AC; Hart TC; Wright JT
    Hum Mutat; 2000 Mar; 15(3):298. PubMed ID: 10679955
    [No Abstract]   [Full Text] [Related]  

  • 10. Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.
    Pavlic A; Battelino T; Trebusak Podkrajsek K; Ovsenik M
    Eur J Orthod; 2011 Jun; 33(3):325-31. PubMed ID: 21068190
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. DNA diagnosis of X-linked amelogenesis imperfecta (AIH1).
    Lench NJ; Brook AH
    J Oral Pathol Med; 1997 Mar; 26(3):135-7. PubMed ID: 9083938
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of amelogenesis imperfecta of deciduous and all permanent teeth.
    Sekiguchi H; Tanakamaru H; Minaguchi K; Machida Y; Yakushiji M
    Bull Tokyo Dent Coll; 2001 Feb; 42(1):45-50. PubMed ID: 11484794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes.
    Salido EC; Yen PH; Koprivnikar K; Yu LC; Shapiro LJ
    Am J Hum Genet; 1992 Feb; 50(2):303-16. PubMed ID: 1734713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1).
    Lagerström M; Dahl N; Nakahori Y; Nakagome Y; Bäckman B; Landegren U; Pettersson U
    Genomics; 1991 Aug; 10(4):971-5. PubMed ID: 1916828
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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; 47(4):261-5. PubMed ID: 11922869
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.