313 related articles for article (PubMed ID: 12952177)
1. 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]
2. 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]
3. 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]
4. Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations.
Ng FK; Messer LB
Pediatr Dent; 2009; 31(1):20-30. PubMed ID: 19320256
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Amelogenin protein exhibits a modular design: implications for form and function.
Snead ML
Connect Tissue Res; 2003; 44 Suppl 1():47-51. PubMed ID: 12952173
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión].
Tremillo-Maldonado O; Molina-Frechero N; González-González R; Bologna-Molina R
Gac Med Mex; 2019; 155(1):101-107. PubMed ID: 30799455
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A novel AMELX mutation causes hypoplastic amelogenesis imperfecta.
Kim YJ; Kim YJ; Kang J; Shin TJ; Hyun HK; Lee SH; Lee ZH; Kim JW
Arch Oral Biol; 2017 Apr; 76():61-65. PubMed ID: 28130977
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. A novel mutation in the AMELX gene and multiple crown resorptions.
Lee KE; Lee SK; Jung SE; Song SJ; Cho SH; Lee ZH; Kim JW
Eur J Oral Sci; 2011 Dec; 119 Suppl 1():324-8. PubMed ID: 22243263
[TBL] [Abstract][Full Text] [Related]
15. Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta.
Nakamura H; Sawamura D; Goto M; Nakamura H; Kida M; Ariga T; Sakiyama Y; Tomizawa K; Mitsui H; Tamaki K; Shimizu H
Int J Mol Med; 2006 Aug; 18(2):333-7. PubMed ID: 16820943
[TBL] [Abstract][Full Text] [Related]
16. Enamel protein in smooth hypoplastic amelogenesis imperfecta.
Wright JT; Robinson C; Kirkham J
Pediatr Dent; 1992; 14(5):331-7. PubMed ID: 1303537
[TBL] [Abstract][Full Text] [Related]
17. A nomenclature for X-linked amelogenesis imperfecta.
Hart PS; Hart TC; Simmer JP; Wright JT
Arch Oral Biol; 2002 Apr; 47(4):255-60. PubMed ID: 11922868
[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. 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]
20. Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.
Coxon TL; Brook AH; Barron MJ; Smith RN
Cells Tissues Organs; 2012; 196(5):420-30. PubMed ID: 22759786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
