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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.
Oncogene|January 1, 1990
Sensitization of transformed rat cells to parvovirus MVMp is restricted to specific oncogenesN Salomé, B van Hille, N Duponchel, 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.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 1, 1996
Developmental expression of laminin-5 and HD1 in the intestine: epithelial to mesenchymal shift for the laminin gamma-2 chain subunit depositionV Orian-Rousseau, D Aberdam, L Fontao, 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 Investigative Dermatology|January 29, 2000
Epidermolysis bullosa: novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophyF Rouan, L Pulkkinen, G Meneguzzi, et al.
The Journal of Biological Chemistry|August 15, 1997
Murine laminin alpha3A and alpha3B isoform chains are generated by usage of two promoters and alternative splicingO Ferrigno, T Virolle, M F Galliano, et al.
The Journal of Cell Biology|May 16, 2001
The short arm of the laminin gamma2 chain plays a pivotal role in the incorporation of laminin 5 into the extracellular matrix and in cell adhesionL Gagnoux-Palacios, M Allegra, F Spirito, et al.
Cell Death and Differentiation|February 23, 2013
CDC25A targeting by miR-483-3p decreases CCND-CDK4/6 assembly and contributes to cell cycle arrestT Bertero, C Gastaldi, I Bourget-Ponzio, et al.
Biochemical and Biophysical Research Communications|March 17, 1998
Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosaP Posteraro, S Sorvillo, L Gagnoux-Palacios, et al.
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