Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 227

1.

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
2.

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
3.

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
4.

Enamelin and autosomal-dominant amelogenesis imperfecta.

Hu JC, Yamakoshi Y.

Crit Rev Oral Biol Med. 2003;14(6):387-98. Review.

PMID:
14656895
5.

A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).

Mårdh CK, Bäckman B, Holmgren G, Hu JC, Simmer JP, Forsman-Semb K.

Hum Mol Genet. 2002 May 1;11(9):1069-74.

PMID:
11978766
6.

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
7.

The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.

Shore RC, Bäckman B, Elcock C, Brook AH, Brookes SJ, Kirkham J.

Cells Tissues Organs. 2010;191(4):301-6. doi: 10.1159/000258703. Epub 2009 Nov 14.

8.

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
9.

Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta.

Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ.

Hum Mol Genet. 2001 Aug 1;10(16):1673-7.

PMID:
11487571
10.

A nomenclature for X-linked amelogenesis imperfecta.

Hart PS, Hart TC, Simmer JP, Wright JT.

Arch Oral Biol. 2002 Apr;47(4):255-60. Review.

PMID:
11922868
11.

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. doi: 10.1177/0022034509333180.

PMID:
19329462
12.

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
13.

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.

14.

ENAM mutations in autosomal-dominant amelogenesis imperfecta.

Kim JW, Seymen F, Lin BP, Kiziltan B, Gencay K, Simmer JP, Hu JC.

J Dent Res. 2005 Mar;84(3):278-82.

PMID:
15723871
15.

Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.

Pavlic A, Battelino T, Trebusak Podkrajsek K, Ovsenik M.

Eur J Orthod. 2011 Jun;33(3):325-31. doi: 10.1093/ejo/cjq089. Epub 2010 Nov 10.

PMID:
21068190
16.

Identifying polymorphism in enamelin gene in amelogenesis imperfecta (AI).

Gopinath VK, Yoong TP, Yean CY, Ravichandran M.

Arch Oral Biol. 2008 Oct;53(10):937-40. doi: 10.1016/j.archoralbio.2008.03.007. Epub 2008 May 8.

PMID:
18466877
17.

Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfecta.

Nusier M, Yassin O, Hart TC, Samimi A, Wright JT.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004 Feb;97(2):220-30.

PMID:
14970781
18.

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. Review.

PMID:
12952177
19.

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.

20.

Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation.

Wright JT, Daly B, Simmons D, Hong S, Hart SP, Hart TC, Atsawasuwan P, Yamauchi M.

Eur J Oral Sci. 2006 May;114 Suppl 1:13-7; discussion 39-41, 379.

PMID:
16674656

Supplemental Content

Support Center