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Items: 1 to 20 of 241

1.

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta.

Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT.

J Med Genet. 2004 Jul;41(7):545-9. No abstract available.

2.

Genes and related proteins involved in amelogenesis imperfecta.

Stephanopoulos G, Garefalaki ME, Lyroudia K.

J Dent Res. 2005 Dec;84(12):1117-26. Review.

PMID:
16304440
3.

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
4.

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
5.

MMP20 hemopexin domain mutation in amelogenesis imperfecta.

Lee SK, Seymen F, Kang HY, Lee KE, Gencay K, Tuna B, Kim JW.

J Dent Res. 2010 Jan;89(1):46-50. doi: 10.1177/0022034509352844. Epub .

6.

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.

7.

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
8.

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.

9.

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
10.

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.

11.

Unraveling the science of tooth enamel.

Bonett JB.

Penn Dent J (Phila). 2005 Spring:6-9. No abstract available.

PMID:
16173233
12.

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. doi: 10.1111/j.1365-2591.2009.01617.x.

PMID:
19825039
14.

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
15.

Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfecta.

Wright JT, Lord V, Robinson C, Shore R.

J Oral Pathol Med. 1992 Oct;21(9):390-4.

PMID:
1432732
16.

Understanding enamel formation from mutations causing X-linked amelogenesis imperfecta.

Lagerström-Fermér M, Landegren U.

Connect Tissue Res. 1995;32(1-4):241-6. Review. No abstract available.

PMID:
7554922
17.

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
18.

Analysis of a kindred with amelogenesis imperfecta.

Wright JT.

J Oral Pathol. 1985 May;14(5):366-74.

PMID:
3925102
19.

An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta.

Michaelides M, Bloch-Zupan A, Holder GE, Hunt DM, Moore AT.

J Med Genet. 2004 Jun;41(6):468-73. No abstract available.

20.

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
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