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Human Molecular Genetics|September 15, 1999
Splicing modulation of integrin beta4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageingS Chavanas, Y Gache, J Vailly, et al.The Journal of Investigative Dermatology|July 1, 1997
A homozygous in-frame deletion in the collagenous domain of bullous pemphigoid antigen BP180 (type XVII collagen) causes generalized atrophic benign epidermolysis bullosaS Chavanas, Y Gache, G Tadini, et al.The Journal of Clinical Investigation|May 15, 1996
Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophyY Gache, S Chavanas, J P Lacour, et al.Experimental Cell Research|April 2, 1998
Role of the bullous pemphigoid antigen 180 (BP180) in the assembly of hemidesmosomes and cell adhesion--reexpression of BP180 in generalized atrophic benign epidermolysis bullosa keratinocytesL Borradori, S Chavanas, R Q Schaapveld, et al.The Journal of Biological Chemistry|March 30, 2001
Reduced expression of the epithelial adhesion ligand laminin 5 in the skin causes intradermal tissue separationF Spirito, S Chavanas, C Prost-Squarcioni, et al.The Journal of Clinical Investigation|November 15, 1996
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophyS Chavanas, L Pulkkinen, Y Gache, et al.Cellular and Molecular Life Sciences : CMLS|August 11, 2005
The peptidylarginine deiminases expressed in human epidermis differ in their substrate specificities and subcellular locationsM C Méchin, M Enji, R Nachat, et al.International Journal of Cosmetic Science|May 21, 2008
Update on peptidylarginine deiminases and deimination in skin physiology and severe human diseasesM-C Méchin, M Sebbag, J Arnaud, et al.Nature Genetics|September 7, 2001
Gene polymorphism in Netherton and common atopic diseaseA J Walley, S Chavanas, M F Moffatt, et al.Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.Pageof 2