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Results: 1-9 |
Results: 9
Cell-cell junctions in acantholytic diseases - Junction proteins in nonimmune and autoimmune acantholysis
Authors: Kowalewski, C Mackiewicz, W Schmitt, D Jablonska, S Haftek, M
Citation: C. Kowalewski et al., Cell-cell junctions in acantholytic diseases - Junction proteins in nonimmune and autoimmune acantholysis, ARCH DERM R, 293(1-2), 2001, pp. 1-11
Topically applied vitamin C enhances the mRNA level of collagens I and III, their processing enzymes and tissue inhibitor of matrix metalloproteinase1 in the human dermis
Authors: Nusgens, BV Humbert, P Rougier, A Colige, AC Haftek, M Lambert, CA Richard, A Creidi, P Lapiere, CM
Citation: Bv. Nusgens et al., Topically applied vitamin C enhances the mRNA level of collagens I and III, their processing enzymes and tissue inhibitor of matrix metalloproteinase1 in the human dermis, J INVES DER, 116(6), 2001, pp. 853-859
Refined characterization of corneodesmosin proteolysis during terminal differentiation of human epidermis and its relationship to desquamation
Authors: Simon, M Jonca, N Guerrin, M Haftek, M Bernard, D Caubet, C Egelrud, T Schmidt, R Serre, G
Citation: M. Simon et al., Refined characterization of corneodesmosin proteolysis during terminal differentiation of human epidermis and its relationship to desquamation, J BIOL CHEM, 276(23), 2001, pp. 20292-20299
Penetration of human metastatic melanoma cells through an authentic dermal-epidermal junction is associated with dissolution of native collagen typesIV and VII
Authors: Bechetoille, N Haftek, M Staquet, MJ Cochran, AJ Schmitt, D Berthier-Vergnes, O
Citation: N. Bechetoille et al., Penetration of human metastatic melanoma cells through an authentic dermal-epidermal junction is associated with dissolution of native collagen typesIV and VII, MELANOMA RE, 10(5), 2000, pp. 427-434
Acquired peeling skin syndrome in an adult.
Authors: Causeret, AS Grezard, P Haftek, M Roth, B Forestier, JY Perrot, H
Citation: As. Causeret et al., Acquired peeling skin syndrome in an adult., ANN DER VEN, 127(2), 2000, pp. 194-197
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome
Authors: Whittock, NV Haftek, M Angoulvant, N Wolf, F Perrot, H Eady, RAJ McGrath, JA
Citation: Nv. Whittock et al., Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome, J INVES DER, 115(3), 2000, pp. 368-374
Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome
Authors: Martin, L Toutain, A Guillen, C Haftek, M Machet, MC Toledano, C Arbeille, B Lorette, G Rotig, A Vaillant, L
Citation: L. Martin et al., Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome, BR J DERM, 143(4), 2000, pp. 876-883
Modulation of a fibrotic process induced by transforming growth factor beta-1 in dermal equivalents
Authors: Gentilhomme, E Neveux, Y Lebeau, J Desmouliere, A Bergier, J Schmitt, D Haftek, M
Citation: E. Gentilhomme et al., Modulation of a fibrotic process induced by transforming growth factor beta-1 in dermal equivalents, CELL BIOL T, 15(4), 1999, pp. 229-238
Internalization of gap junctions in benign familial pemphigus (Hailey-Hailey disease) and keratosis follicularis (Darier's disease)
Authors: Haftek, M Kowalewski, C Mesnil, M Blaszczyk, M Schmitt, D
Citation: M. Haftek et al., Internalization of gap junctions in benign familial pemphigus (Hailey-Hailey disease) and keratosis follicularis (Darier's disease), BR J DERM, 141(2), 1999, pp. 224-230
Risultati: 1-9 |