PubMed

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.

Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR.

Head Face Med. 2007 Jan 31;3:8.PMID: 17266769 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.

Hart TC, Hart PS, Gorry MC, Michalec MD, Ryu OH, Uygur C, Ozdemir D, Firatli S, Aren G, Firatli E.

J Med Genet. 2003 Dec;40(12):900-6.PMID: 14684688 [PubMed - indexed for MEDLINE]Related articlesFree article

Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.

Becerik S, Cogulu D, Emingil G, Han T, Hart PS, Hart TC.

Am J Med Genet A. 2009 Jul;149A(7):1392-8.PMID: 19530186 [PubMed - indexed for MEDLINE]Related articles

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 1;14(5):575-83. Epub 2005 Jan 13.PMID: 15649948 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.

Pavlic A, Petelin M, Battelino T.

Arch Oral Biol. 2007 Mar;52(3):209-17. Epub 2006 Nov 27.PMID: 17125728 [PubMed - indexed for MEDLINE]Related articles

Mutational analysis of candidate genes in 24 amelogenesis imperfecta families.

Kim JW, Simmer JP, Lin BP, Seymen F, Bartlett JD, Hu JC.

Eur J Oral Sci. 2006 May;114 Suppl 1:3-12; discussion 39-41, 379.PMID: 16674655 [PubMed - indexed for MEDLINE]Related articles

Enamelin and autosomal-dominant amelogenesis imperfecta.

Hu JC, Yamakoshi Y.

Crit Rev Oral Biol Med. 2003;14(6):387-98. Review.PMID: 14656895 [PubMed - indexed for MEDLINE]Related articlesFree article

Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.

Hart PS, Wright JT, Savage M, Kang G, Bensen JT, Gorry MC, Hart TC.

Eur J Oral Sci. 2003 Aug;111(4):326-31.PMID: 12887398 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 11922869 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2007 Feb 21.PMID: 17316551 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2008 Aug 19.PMID: 18714142 [PubMed - indexed for MEDLINE]Related articlesFree article

Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.

Mårdh CK, Bäckman B, Simmons D, Golovleva I, Gu TT, Holmgren G, MacDougall M, Forsman-Semb K.

Eur J Oral Sci. 2001 Feb;109(1):8-13.PMID: 11330937 [PubMed - indexed for MEDLINE]Related articles

Enamel formation and amelogenesis imperfecta.

Hu JC, Chun YH, Al Hazzazzi T, Simmer JP.

Cells Tissues Organs. 2007;186(1):78-85. Review.PMID: 17627121 [PubMed - indexed for MEDLINE]Related articles

Candidate gene strategy reveals ENAM mutations.

Kang HY, Seymen F, Lee SK, Yildirim M, Tuna EB, Patir A, Lee KE, Kim JW.

J Dent Res. 2009 Mar;88(3):266-9.PMID: 19329462 [PubMed - indexed for MEDLINE]Related articles

Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.

Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y.

J Dent Res. 2002 Nov;81(11):738-42.PMID: 12407086 [PubMed - indexed for MEDLINE]Related articles

Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.

Hyun HK, Lee SK, Lee KE, Kang HY, Kim EJ, Choung PH, Kim JW.

Int Endod J. 2009 Nov;42(11):1039-43.PMID: 19825039 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 11005731 [PubMed - indexed for MEDLINE]Related articlesFree article

MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.

Ozdemir D, Hart PS, Ryu OH, Choi SJ, Ozdemir-Karatas M, Firatli E, Piesco N, Hart TC.

J Dent Res. 2005 Nov;84(11):1031-5.PMID: 16246936 [PubMed - indexed for MEDLINE]Related articlesFree article

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.

Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT.

Arch Oral Biol. 2003 Aug;48(8):589-96.PMID: 12828988 [PubMed - indexed for MEDLINE]Related articles

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).

Lench NJ, Winter GB.

Hum Mutat. 1995;5(3):251-9.PMID: 7599636 [PubMed - indexed for MEDLINE]Related articles