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Dermatologic Clinics|May 8, 2010
Transmission electron microscopy for the diagnosis of epidermolysis bullosaRobin A J Eady, Patricia J C Dopping-HepenstalExperimental Dermatology|August 22, 2003
Desmosomes exhibit site-specific features in human palm skinHong Wan, Patricia J C Dopping-Hepenstal, Matthew J Gratian, et al.The Journal of Investigative Dermatology|May 20, 2006
Complete maternal isodisomy of chromosome 3 in a child with recessive dystrophic epidermolysis bullosa but no other phenotypic abnormalitiesHiva Fassihi, Liu Lu, Vesarat Wessagowit, et al.Acta Dermato-Venereologica|March 31, 2011
Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosaNoor Almaani, Lu Liu, Patricia J C Dopping-Hepenstal, et al.The Journal of Investigative Dermatology|April 4, 2008
Potential of fibroblast cell therapy for recessive dystrophic epidermolysis bullosaTracy Wong, Luke Gammon, Lu Liu, et al.Neuromuscular Disorders : NMD|July 14, 2010
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectinKatharine Forrest, Jemima E Mellerio, Stephanie Robb, et al.Journal of Cell Science|July 4, 2003
Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stabilityAndrew P South, Hong Wan, Michael G Stone, et al.The Journal of Investigative Dermatology|January 29, 2005
LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosumAkemi Ishida-Yamamoto, Céline Deraison, Chrystelle Bonnart, et al.Journal of Medical Genetics|November 30, 2010
The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagenPeter C van den Akker, Jemima E Mellerio, Anna E Martinez, et al.The Journal of Investigative Dermatology|February 5, 2010
Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in childrenRita M Cabral, Lu Liu, Carol Hogan, et al.Pageof 2