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Items: 1 to 20 of 122

1.

Keratins and skin disorders.

Lane EB, McLean WH.

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

PMID:
15495218
2.

The molecular genetics of keratin disorders.

Smith F.

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

PMID:
12688839
3.

Human keratin diseases: hereditary fragility of specific epithelial tissues.

Corden LD, McLean WH.

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

PMID:
9028791
4.

Genetic approaches to understanding the keratinopathies.

Bale SJ, DiGiovanna JJ.

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

PMID:
8973737
5.

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.

6.

[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
7.
8.

Keratins and the skin.

Fuchs E.

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

PMID:
8689554
9.

Keratin gene mutations in human skin disease.

Stevens HP, Rustin MH.

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

10.

The keratins and their disorders.

Rugg EL, Leigh IM.

Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):4-11. Review.

PMID:
15452838
11.

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
12.

Keratin gene mutations in disorders of human skin and its appendages.

Chamcheu JC, Siddiqui IA, Syed DN, Adhami VM, Liovic M, Mukhtar H.

Arch Biochem Biophys. 2011 Apr 15;508(2):123-37. doi: 10.1016/j.abb.2010.12.019. Epub 2010 Dec 19. Review.

13.

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.

14.

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
15.

Lessons from keratin transgenic and knockout mice.

Magin TM.

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

PMID:
9932492
16.

Genetic disorders of palm skin and nail.

McLean WH; Epithelial Genetics Group.

J Anat. 2003 Jan;202(1):133-41. Review.

17.

Keratins and skin disease.

Knöbel M, O'Toole EA, Smith FJ.

Cell Tissue Res. 2015 Jun;360(3):583-9. doi: 10.1007/s00441-014-2105-4. Epub 2015 Jan 27. Review.

PMID:
25620412
18.

Phenotypes, genotypes and their contribution to understanding keratin function.

Porter RM, Lane EB.

Trends Genet. 2003 May;19(5):278-85. Review.

PMID:
12711220
19.

Genetic skin disorders of keratin.

Fuchs E.

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

20.

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

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