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Results: 1 to 20 of 243

Similar articles for PubMed (Select 15235027)

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.

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
4.

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
5.

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
6.

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 .

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.

X-linked recessive hypomaturation amelogenesis imperfecta: report of case.

Haug RH, Ferguson FS.

J Am Dent Assoc. 1981 Jun;102(6):865-7. No abstract available.

PMID:
6946128
12.

Unraveling the science of tooth enamel.

Bonett JB.

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

PMID:
16173233
13.

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
15.

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta.

Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC.

J Med Genet. 2005 Mar;42(3):271-5. No abstract available.

16.

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
17.

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
18.

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
19.

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
20.

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
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