398 related articles for article (PubMed ID: 11406633)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
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. Enamel ultrastructure and protein content in X-linked amelogenesis imperfecta.
Wright JT; Aldred MJ; Crawford PJ; Kirkham J; Robinson C
Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):192-9. PubMed ID: 8361731
[TBL] [Abstract][Full Text] [Related]
8. A developmental comparison of matrix metalloproteinase-20 and amelogenin null mouse enamel.
Bartlett JD; Skobe Z; Lee DH; Wright JT; Li Y; Kulkarni AB; Gibson CW
Eur J Oral Sci; 2006 May; 114 Suppl 1():18-23; discussion 39-41, 379. PubMed ID: 16674657
[TBL] [Abstract][Full Text] [Related]
9. Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.
Caterina JJ; Skobe Z; Shi J; Ding Y; Simmer JP; Birkedal-Hansen H; Bartlett JD
J Biol Chem; 2002 Dec; 277(51):49598-604. PubMed ID: 12393861
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
Collier PM; Sauk JJ; Rosenbloom SJ; Yuan ZA; Gibson CW
Arch Oral Biol; 1997 Mar; 42(3):235-42. PubMed ID: 9188994
[TBL] [Abstract][Full Text] [Related]
14. A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta.
Greene SR; Yuan ZA; Wright JT; Amjad H; Abrams WR; Buchanan JA; Trachtenberg DI; Gibson CW
Arch Oral Biol; 2002 Mar; 47(3):211-7. PubMed ID: 11839357
[TBL] [Abstract][Full Text] [Related]
15. Enamel matrix proteins and ameloblast biology.
Deutsch D; Catalano-Sherman J; Dafni L; David S; Palmon A
Connect Tissue Res; 1995; 32(1-4):97-107. PubMed ID: 7554940
[TBL] [Abstract][Full Text] [Related]
16. Altered amelogenin self-assembly based on mutations observed in human X-linked amelogenesis imperfecta (AIH1).
Paine ML; Lei YP; Dickerson K; Snead ML
J Biol Chem; 2002 May; 277(19):17112-6. PubMed ID: 11877393
[TBL] [Abstract][Full Text] [Related]
17. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1).
Aldred MJ; Crawford PJ; Roberts E; Thomas NS
Hum Genet; 1992 Dec; 90(4):413-6. PubMed ID: 1483698
[TBL] [Abstract][Full Text] [Related]
18. Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expression.
Guo F; Feng J; Wang F; Li W; Gao Q; Chen Z; Shoff L; Donly KJ; Gluhak-Heinrich J; Chun YH; Harris SE; MacDougall M; Chen S
J Cell Physiol; 2015 Aug; 230(8):1871-82. PubMed ID: 25545831
[TBL] [Abstract][Full Text] [Related]
19. Rescue of the murine amelogenin null phenotype with two amelogenin transgenes.
Gibson CW; Li Y; Suggs C; Kuehl MA; Pugach MK; Kulkarni AB; Wright JT
Eur J Oral Sci; 2011 Dec; 119 Suppl 1(Suppl 1):70-4. PubMed ID: 22243230
[TBL] [Abstract][Full Text] [Related]
20. The leucine-rich amelogenin peptide alters the amelogenin null enamel phenotype.
Gibson CW; Li Y; Daly B; Suggs C; Yuan ZA; Fong H; Simmons D; Aragon M; Kulkarni AB; Wright JT
Cells Tissues Organs; 2009; 189(1-4):169-74. PubMed ID: 18701811
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
