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The Journal of Cell Biology|May 1, 1995
Transforming growth factor-beta 1 modulates beta 1 and beta 5 integrin receptors and induces the de novo expression of the alpha v beta 6 heterodimer in normal human keratinocytes: implications for wound healingG Zambruno, P C Marchisio, A Marconi, et al.The British Journal of Dermatology|January 30, 2004
Characterization of the ultraviolet B and X-ray response of primary cultured epidermal cells from patients with disseminated superficial actinic porokeratosisM D'Errico, M Teson, A Calcagnile, et al.Dermatologica|January 1, 1987
Antigenic thymus-epidermis relationships. Reactivity of a panel of anti-thymic cell monoclonal antibodies on human keratinocytes and Langerhans cellsD Schmitt, G Zambruno, M J Staquet, et al.The Journal of Investigative Dermatology|September 21, 2001
Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: effects on laminin-5 assembly, secretion, and depositionD Castiglia, P Posteraro, F Spirito, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Beta 1 and beta 3 integrin upregulation in rapidly progressive glomerulonephritisA Baraldi, G Zambruno, L Furci, et al.Clinical Genetics|August 12, 2009
Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosisD Castiglia, M Castori, E Pisaneschi, et al.Experimental Dermatology|January 7, 2004
Novel and recurrent mutations in the integrin beta 4 subunit gene causing lethal junctional epidermolysis bullosa with pyloric atresiaS Iacovacci, S Cicuzza, T Odorisio, et al.The Journal of Investigative Dermatology|November 6, 1998
Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosaM Terracina, P Posteraro, M Schubert, et al.The British Journal of Dermatology|March 23, 2010
Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10C Covaciu, M Castori, N De Luca, et al.The British Journal of Dermatology|January 3, 2013
Induction of senescence pathways in Kindler syndrome primary keratinocytesE Piccinni, G Di Zenzo, R Maurelli, et al.Pageof 12