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Items: 1 to 20 of 23

1.

Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.

Bonifas JM, Bare JW, Chen MA, Lee MK, Slater CA, Goldsmith LA, Epstein EH Jr.

J Invest Dermatol. 1992 Nov;99(5):524-7.

2.

Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis.

Fuchs E, Coulombe P, Cheng J, Chan YM, Hutton E, Syder A, Degenstein L, Yu QC, Letai A, Vassar R.

J Invest Dermatol. 1994 Nov;103(5 Suppl):25S-30S. Review.

PMID:
7525738
3.

The molecular genetics of keratin disorders.

Smith F.

Am J Clin Dermatol. 2003;4(5):347-64. Review.

PMID:
12688839
4.

Genetic approaches to understanding the keratinopathies.

Bale SJ, DiGiovanna JJ.

Adv Dermatol. 1997;12:99-113; discussion 114. Review.

PMID:
8973737
5.

Genetic skin disorders of keratin.

Fuchs E.

J Invest Dermatol. 1992 Dec;99(6):671-4. Review. No abstract available.

6.

Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis.

Leigh IM, Lane EB.

Arch Dermatol. 1993 Dec;129(12):1571-7. Review.

PMID:
7504434
7.

New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.

Whittock NV, Ashton GH, Griffiths WA, Eady RA, McGrath JA.

Br J Dermatol. 2001 Aug;145(2):330-5. Review.

PMID:
11531804
8.

Keratins and skin disorders.

Lane EB, McLean WH.

J Pathol. 2004 Nov;204(4):355-66. Review.

PMID:
15495218
9.

Human keratin diseases: hereditary fragility of specific epithelial tissues.

Corden LD, McLean WH.

Exp Dermatol. 1996 Dec;5(6):297-307. Review.

PMID:
9028791
10.

Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis.

Yang JM, Nam K, Kim SW, Jung SY, Min HG, Yeo UC, Park KB, Lee JH, Suhr KB, Park JK, Lee ES.

J Dermatol Sci. 1999 Feb;19(2):126-33. Review.

PMID:
10098704
11.

[Keratin diseases].

Jensen PK, Sørensen CB, Andresen BS, Brandrup F, Veien NK, Buus SK, Gregersen N, Bolund L.

Ugeskr Laeger. 2000 Mar 27;162(13):1867-72. Review. Danish.

PMID:
10765692
12.

Lessons from keratin transgenic and knockout mice.

Magin TM.

Subcell Biochem. 1998;31:141-72. Review. No abstract available.

PMID:
9932492
13.

Epidermolytic hyperkeratosis: applied molecular genetics.

DiGiovanna JJ, Bale SJ.

J Invest Dermatol. 1994 Mar;102(3):390-4. Review.

14.

Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.

Lacz NL, Schwartz RA, Kihiczak G.

Int J Dermatol. 2005 Jan;44(1):1-6. Review.

PMID:
15663649
15.

Keratins and the skin.

Fuchs E.

Annu Rev Cell Dev Biol. 1995;11:123-53. Review.

PMID:
8689554
16.

Keratin gene mutations in human skin disease.

Stevens HP, Rustin MH.

Postgrad Med J. 1994 Nov;70(829):775-9. Review. No abstract available.

17.

Epidermolytic hyperkeratosis.

Bale SJ, Compton JG, DiGiovanna JJ.

Semin Dermatol. 1993 Sep;12(3):202-9. Review.

PMID:
7692917
18.

Ichthyosis bullosa of Siemens: its correct diagnosis facilitated by molecular genetic testing.

Akiyama M, Tsuji-Abe Y, Yanagihara M, Nakajima K, Kodama H, Yaosaka M, Abe M, Sawamura D, Shimizu H.

Br J Dermatol. 2005 Jun;152(6):1353-6. Review.

PMID:
15949009
19.

How do keratinizing disorders and blistering disorders overlap?

Hamada T, Tsuruta D, Fukuda S, Ishii N, Teye K, Numata S, Dainichi T, Karashima T, Ohata C, Furumura M, Hashimoto T.

Exp Dermatol. 2013 Feb;22(2):83-7. doi: 10.1111/exd.12021. Epub 2012 Oct 8. Review.

20.

Histopathologic characterization of epidermolytic hyperkeratosis: a systematic review of histology from the National Registry for Ichthyosis and Related Skin Disorders.

Ross R, DiGiovanna JJ, Capaldi L, Argenyi Z, Fleckman P, Robinson-Bostom L.

J Am Acad Dermatol. 2008 Jul;59(1):86-90. doi: 10.1016/j.jaad.2008.02.031. Review.

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