294 related articles for article (PubMed ID: 16007484)
1. Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus.
Prakash SK; Gibson CW; Wright JT; Boyd C; Cormier T; Sierra R; Li Y; Abrams WR; Aragon MA; Yuan ZA; van den Veyver IB
Calcif Tissue Int; 2005 Jul; 77(1):23-9. PubMed ID: 16007484
[TBL] [Abstract][Full Text] [Related]
2. The small bovine amelogenin LRAP fails to rescue the amelogenin null phenotype.
Chen E; Yuan ZA; Wright JT; Hong SP; Li Y; Collier PM; Hall B; D'Angelo M; Decker S; Piddington R; Abrams WR; Kulkarni AB; Gibson CW
Calcif Tissue Int; 2003 Nov; 73(5):487-95. PubMed ID: 12958690
[TBL] [Abstract][Full Text] [Related]
3. Ultrastructure of forming enamel in mouse bearing a transgene that disrupts the amelogenin self-assembly domains.
Dunglas C; Septier D; Paine ML; Zhu DH; Snead ML; Goldberg M
Calcif Tissue Int; 2002 Aug; 71(2):155-66. PubMed ID: 12073155
[TBL] [Abstract][Full Text] [Related]
4. Of mice and men: anatomy of the amelogenin gene.
Snead ML; Lau EC; Fincham AG; Zeichner-David M; Davis C; Slavkin HC
Connect Tissue Res; 1989; 22(1-4):101-9. PubMed ID: 2689082
[TBL] [Abstract][Full Text] [Related]
5. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
Hu JC; Chan HC; Simmer SG; Seymen F; Richardson AS; Hu Y; Milkovich RN; Estrella NM; Yildirim M; Bayram M; Chen CF; Simmer JP
PLoS One; 2012; 7(12):e52052. PubMed ID: 23251683
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype.
Gibson CW; Yuan ZA; Hall B; Longenecker G; Chen E; Thyagarajan T; Sreenath T; Wright JT; Decker S; Piddington R; Harrison G; Kulkarni AB
J Biol Chem; 2001 Aug; 276(34):31871-5. PubMed ID: 11406633
[TBL] [Abstract][Full Text] [Related]
8. Enamel biomineralization defects result from alterations to amelogenin self-assembly.
Paine ML; Zhu DH; Luo W; Bringas P; Goldberg M; White SN; Lei YP; Sarikaya M; Fong HK; Snead ML
J Struct Biol; 2000 Dec; 132(3):191-200. PubMed ID: 11243888
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Imaging RNA polymerase-amelogenin gene complexes with single molecule resolution using atomic force microscopy.
Crampton N; Thomson NH; Kirkham J; Gibson CW; Bonass WA
Eur J Oral Sci; 2006 May; 114 Suppl 1():133-8; discussion 164-5, 380-1. PubMed ID: 16674675
[TBL] [Abstract][Full Text] [Related]
11. The use of animal models to explore amelogenin variants in amelogenesis imperfecta.
Gibson CW; Kulkarni AB; Wright JT
Cells Tissues Organs; 2005; 181(3-4):196-201. PubMed ID: 16612085
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Enamel structure properties controlled by engineered proteins in transgenic mice.
Fong H; White SN; Paine ML; Luo W; Snead ML; Sarikaya M
J Bone Miner Res; 2003 Nov; 18(11):2052-9. PubMed ID: 14606519
[TBL] [Abstract][Full Text] [Related]
14. Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4.
Wright JT; Hart TC; Hart PS; Simmons D; Suggs C; Daley B; Simmer J; Hu J; Bartlett JD; Li Y; Yuan ZA; Seow WK; Gibson CW
Cells Tissues Organs; 2009; 189(1-4):224-9. PubMed ID: 18714142
[TBL] [Abstract][Full Text] [Related]
15. Cytomegalovirus induces stage-dependent enamel defects and misexpression of amelogenin, enamelin and dentin sialophosphoprotein in developing mouse molars.
Jaskoll T; Abichaker G; Htet K; Bringas P; Morita S; Sedghizadeh PP; Melnick M
Cells Tissues Organs; 2010; 192(4):221-39. PubMed ID: 20484882
[TBL] [Abstract][Full Text] [Related]
16. Analysis of human enamel genes: insights into genetic disorders of enamel.
Lau EC; Slavkin HC; Snead ML
Cleft Palate J; 1990 Apr; 27(2):121-30. PubMed ID: 2187631
[TBL] [Abstract][Full Text] [Related]
17. Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis.
Gruenbaum-Cohen Y; Tucker AS; Haze A; Shilo D; Taylor AL; Shay B; Sharpe PT; Mitsiadis TA; Ornoy A; Blumenfeld A; Deutsch D
J Exp Zool B Mol Dev Evol; 2009 Jul; 312B(5):445-57. PubMed ID: 19097165
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
