Found: 10
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Keratins (K16 and K17) as markers of keratinocyte hyperproliferation in psoriasis <em>in vivo</em> and <em>in vitro</em>.
- Published in:
- British Journal of Dermatology, 1995, v. 133, n. 4, p. 501, doi. 10.1111/j.1365-2133.1995.tb02696.x
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- Publication type:
- Article
Cloning, sequencing and chromosomal localization of human keratin 17.
- Published in:
- 1990
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- Publication type:
- Abstract
The effect of topically applied progesterone on sebum excretion rate.
- Published in:
- British Journal of Dermatology, 1979, v. 100, n. 6, p. 687, doi. 10.1111/j.1365-2133.1979.tb08073.x
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- Publication type:
- Article
Tolerance to the anti-seborrhoeic effect of topically applied progesterone.
- Published in:
- British Journal of Dermatology, 1978, v. 98, p. 9, doi. 10.1111/j.1365-2133.1978.tb13580.x
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- Publication type:
- Article
Epidermolysis bullosa simplex due to KRT5 mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamine N-oxide in cultured primary keratinocytes.
- Published in:
- British Journal of Dermatology, 2010, v. 162, n. 5, p. 980, doi. 10.1111/j.1365-2133.2009.09615.x
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- Publication type:
- Article
Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex.
- Published in:
- British Journal of Dermatology, 2006, v. 155, n. 1, p. 201, doi. 10.1111/j.1365-2133.2006.07269.x
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- Publication type:
- Article
Photosensitive Smith–Lemli–Opitz syndrome is not caused by a single gene mutation: analysis of the gene encoding 7-dehydrocholesterol reductase in five U.K. families.
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- British Journal of Dermatology, 2005, v. 153, n. 4, p. 774, doi. 10.1111/j.1365-2133.2005.06761.x
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- Publication type:
- Article
A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype.
- Published in:
- 2004
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- Publication type:
- Other
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma.
- Published in:
- Experimental Dermatology, 1999, v. 8, n. 2, p. 120, doi. 10.1111/j.1600-0625.1999.tb00358.x
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- Publication type:
- Article
Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot.
- Published in:
- Experimental Dermatology, 1999, v. 8, n. 2, p. 115, doi. 10.1111/j.1600-0625.1999.tb00357.x
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- Publication type:
- Article