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Results: 1 to 20 of 118

Related Articles by Review for PubMed (Select 15495218)

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.

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
6.

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.

7.

[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
8.

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.

9.
10.

Keratins and the skin.

Fuchs E.

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

PMID:
8689554
11.

Keratin gene mutations in human skin disease.

Stevens HP, Rustin MH.

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

12.

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
13.

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
14.

Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.

McLean WH, Smith FJ, Cassidy AJ.

J Investig Dermatol Symp Proc. 2005 Oct;10(1):31-6. Review.

15.
16.

Genetic skin disorders of keratin.

Fuchs E.

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

PMID:
1281858
17.

Lessons from keratin transgenic and knockout mice.

Magin TM.

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

PMID:
9932492
18.

The molecular basis of human keratin disorders.

Arin MJ.

Hum Genet. 2009 May;125(4):355-73. doi: 10.1007/s00439-009-0646-5. Epub 2009 Feb 27. Review.

PMID:
19247691
19.

Keratin diseases.

Lane EB.

Curr Opin Genet Dev. 1994 Jun;4(3):412-8. Review.

PMID:
7522672
20.

Lessons from disorders of epidermal differentiation-associated keratins.

Ishida-Yamamoto A, Takahashi H, Iizuka H.

Histol Histopathol. 2002 Jan;17(1):331-8. Review.

PMID:
11813882
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