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Items: 13

1.

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.

2.

Enamelin and autosomal-dominant amelogenesis imperfecta.

Hu JC, Yamakoshi Y.

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

PMID:
14656895
3.

Amelogenesis imperfecta: an introduction.

Gadhia K, McDonald S, Arkutu N, Malik K.

Br Dent J. 2012 Apr 27;212(8):377-9. doi: 10.1038/sj.bdj.2012.314. Review.

PMID:
22538897
4.

Amelogenesis imperfecta.

Crawford PJ, Aldred M, Bloch-Zupan A.

Orphanet J Rare Dis. 2007 Apr 4;2:17. Review.

5.

The molecular etiologies and associated phenotypes of amelogenesis imperfecta.

Wright JT.

Am J Med Genet A. 2006 Dec 1;140(23):2547-55. Review.

6.

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
7.

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
8.

[Phenotype analysis and the molecular mechanism of enamel hypoplasia].

Lv P, Gao XJ.

Beijing Da Xue Xue Bao Yi Xue Ban. 2009 Feb 18;41(1):121-3. Review. Chinese.

9.

Molecular biology of hereditary enamel defects.

Aldred MJ, Crawford PJ.

Ciba Found Symp. 1997;205:200-5; discussion 205-9. Review.

PMID:
9189626
10.

Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.

UrzĂșa B, Ortega-Pinto A, Morales-Bozo I, Rojas-Alcayaga G, Cifuentes V.

Biochem Genet. 2011 Feb;49(1-2):104-21. doi: 10.1007/s10528-010-9392-6. Epub 2010 Dec 3. Review.

PMID:
21127961
11.

Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.

de la Dure-Molla M, Quentric M, Yamaguti PM, Acevedo AC, Mighell AJ, Vikkula M, Huckert M, Berdal A, Bloch-Zupan A.

Orphanet J Rare Dis. 2014 Jun 14;9:84. doi: 10.1186/1750-1172-9-84. Review.

12.

The molecular basis of hereditary enamel defects in humans.

Wright JT, Carrion IA, Morris C.

J Dent Res. 2015 Jan;94(1):52-61. doi: 10.1177/0022034514556708. Epub 2014 Nov 11. Review.

13.

Amelogenesis Imperfecta; Genes, Proteins, and Pathways.

Smith CEL, Poulter JA, Antanaviciute A, Kirkham J, Brookes SJ, Inglehearn CF, Mighell AJ.

Front Physiol. 2017 Jun 26;8:435. doi: 10.3389/fphys.2017.00435. eCollection 2017. Review.

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