156 related articles for article (PubMed ID: 10618637)
1. Evidence for regulation of amelogenin gene expression by 1,25-dihydroxyvitamin D(3) in vivo.
Papagerakis P; Hotton D; Lezot F; Brookes S; Bonass W; Robinson C; Forest N; Berdal A
J Cell Biochem; 1999 Dec; 76(2):194-205. PubMed ID: 10618637
[TBL] [Abstract][Full Text] [Related]
2. Differential epithelial and mesenchymal regulation of tooth-specific matrix proteins expression by 1,25-dihydroxyvitamin D3 in vivo.
Papagerakis P; MacDougall M; Berdal A
Connect Tissue Res; 2002; 43(2-3):372-5. PubMed ID: 12489183
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.
Barron MJ; Brookes SJ; Kirkham J; Shore RC; Hunt C; Mironov A; Kingswell NJ; Maycock J; Shuttleworth CA; Dixon MJ
Hum Mol Genet; 2010 Apr; 19(7):1230-47. PubMed ID: 20067920
[TBL] [Abstract][Full Text] [Related]
5. Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation.
Ravassipour DB; Hart PS; Hart TC; Ritter AV; Yamauchi M; Gibson C; Wright JT
J Dent Res; 2000 Jul; 79(7):1476-81. PubMed ID: 11005731
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. 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]
9. X-linked amelogenesis imperfecta may result from decreased formation of tyrosine rich amelogenin peptide (TRAP).
Li W; Gao C; Yan Y; DenBesten P
Arch Oral Biol; 2003 Mar; 48(3):177-83. PubMed ID: 12648554
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Expression of amelogenin in odontoblasts.
Papagerakis P; MacDougall M; Hotton D; Bailleul-Forestier I; Oboeuf M; Berdal A
Bone; 2003 Mar; 32(3):228-40. PubMed ID: 12667550
[TBL] [Abstract][Full Text] [Related]
12. Unraveling the science of tooth enamel.
Bonett JB
Penn Dent J (Phila); 2005; ():6-9. PubMed ID: 16173233
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4.
Shemirani R; Le MH; Nakano Y
J Dent Res; 2023 Oct; 102(11):1210-1219. PubMed ID: 37563801
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
