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Cell|February 21, 1997
Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversionM F Jonkman, H Scheffer, R Stulp, et al.American Journal of Human Genetics|June 1, 1997
Three novel homozygous point mutations and a new polymorphism in the COL17A1 gene: relation to biological and clinical phenotypes of junctional epidermolysis bullosaH Schumann, N Hammami-Hauasli, L Pulkkinen, et al.The Histochemical Journal|July 23, 1999
Hemidesmosomal molecular changes in dermatitis herpetiformis; decreased expression of BP230 and plectin/HD1 in uninvolved skinT Leivo, J Lohi, A L Kariniemi, et al.The British Journal of Dermatology|March 20, 2002
Cicatricial pemphigoid with circulating autoantibodies to beta4 integrin, bullous pemphigoid 180 and bullous pemphigoid 230M Leverkus, K Bhol, Y Hirako, et al.Gut|February 18, 2006
Hepatic stellate cells express synemin, a protein bridging intermediate filaments to focal adhesionsN Uyama, L Zhao, E Van Rossen, et al.Journal of Cell Science|January 1, 1997
The subcellular distribution of the high molecular mass protein, HD1, is determined by the cytoplasmic domain of the integrin beta 4 subunitP Sánchez-Aparicio, A M Martínez de Velasco, C M Niessen, et al.Archives of Dermatology|February 1, 1996
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiencyM F Jonkman, M C de Jong, K Heeres, et al.The Journal of Clinical Investigation|March 1, 1995
180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosaM F Jonkman, M C de Jong, K Heeres, et al.Muscle & Nerve|September 13, 2006
Plectin defects in epidermolysis bullosa simplex with muscular dystrophyJ R McMillan, M Akiyama, F Rouan, et al.Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.Pageof 7