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Journal of the American Academy of Dermatology|January 31, 2006
Clinicopathologic features of skin cancer in organ transplant recipients: a retrospective case-control seriesCatherine A Harwood, Charlotte M Proby, Jane M McGregor, et al.
Regulatory Toxicology and Pharmacology : RTP|December 29, 2009
Human uptake of persistent chemicals from contaminated soil: PCDD/Fs and PCBsRenate D Kimbrough, Constantine A Krouskas, M Leigh Carson, et al.
Molecular Ecology Resources|June 21, 2021
A robust sequencing assay of a thousand amplicons for the high-throughput population monitoring of Alpine ibex immunogeneticsCamille Kessler, Alice Brambilla, Dominique Waldvogel, et al.
Journal of Cell Science|November 1, 1989
Keratin expression in human mammary epithelial cells cultured from normal and malignant tissue: relation to in vivo phenotypes and influence of mediumJ Taylor-Papadimitriou, M Stampfer, J Bartek, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single familyD P Kelsell, A L Wilgoss, G Richard, et al.
Experimental Dermatology|October 28, 1999
Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratoderma to chromosome 12q11-q13: exclusion of the mapped type II keratinsD P Kelsell, H P Stevens, P E Purkis, et al.
The American Journal of Pathology|December 1, 1993
Keratin 17 expression as a marker for epithelial transformation in viral wartsC M Proby, L Churchill, P E Purkis, et al.
The Journal of General Virology|April 1, 1993
Characterization of factors involved in human papillomavirus type 16-mediated immortalization of oral keratinocytesC J Sexton, C M Proby, L Banks, et al.
In Vitro Cellular & Developmental Biology. Animal|February 24, 2007
Myoepithelial molecular markers in human breast carcinoma PMC42-LA cells are induced by extracellular matrix and stromal cellsStephanie C Lebret, Donald F Newgreen, Mark C Waltham, et al.
The Journal of Investigative Dermatology|December 1, 1991
Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14A Ishida-Yamamoto, J A McGrath, S J Chapman, et al.
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