Zobrazeno 1 - 10
of 146
pro vyhledávání: '"B Pellat"'
Publikováno v:
IEEE Journal of Solid-State Circuits. 43:1372-1383
An integrated 2.4 GHz CMOS receiver front-end according to the IEEE 802.15.4 standard is presented in this paper. It integrates the overall RF part, from the balun up to the first stage of the channel filter, as well as the cells for the LO signal co
Publikováno v:
Oral Microbiology and Immunology. 21:197-200
Background: As antigen-presenting cells, Langerhans cells may play an important role in the initiation and maintenance of periodontal disease. This study is the first report that extends our knowledge of the expression of matrix metalloproteinases an
Autor:
D. Stania, L. Maman, Anne-Laure Ejeil, Antoine Lafont, S. Igondjo-Tchen, S. M. Dridi, F. Gaultier, D. Dohan, B. Pellat, G. Godeau, Bruno Gogly, C. B. Wierzba
Publikováno v:
Archives of Dermatological Research. 296:220-225
Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are considered to be drug-induced diseases, and are characterized by extensive mucocutaneous disorder and epidermal necrosis which result in the detachment of the epidermis. Inactive
Autor:
B. Pellat, C. Chaussain Miller, Louis Dubertret, Alexis Desmoulière, Corinne Lebreton-Decoster, Bernard Coulomb, G. Godeau
Publikováno v:
Experimental Dermatology. 12:403-411
The aim of this work was to validate an image analysis method, based on cell nuclei form factor determination, for counting fibroblasts within human dermis. We first used reconstructed dermal equivalents in which fibroblasts can also be counted direc
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 15:305-311
Publikováno v:
Gerontology. 44:318-323
Background: A quantitative study of dermal and arterial elastic fibers as a function of age was carried out by computerized image analysis. Objective: We investigated whether any parallelism can be established between the morphometric parameters of e
Publikováno v:
Blood. 91:319-323
The molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome is the presence of a mutation in the iron-responsive element (IRE) of the L ferritin gene, located on chromosome 19q13.3-13.4. Two mutations have been repor
Publikováno v:
Cell Adhesion and Communication. 3:273-281
Elastin-derived peptides (kappa-elastin: kappa E, mean molecular mass: 75 kDa), either coated onto plastic dishes or added to culture media (0.26 to 1.33 nM) stimulated the growth of human skin fibroblasts (HSF) strains obtained from different donors
Autor:
A. Chryssostalis, I Rosa Hezode, H. Hagège, C. Barrault, T Lons, D. Gillot, M. Chousterman, B. Pellat, A.C. Lesage
Publikováno v:
Endoscopy. 41
Autor:
I Rosa Hezode, P Cattan, H. Hagège, C. Barrault, A. Chryssostalis, C. Grateau, M. Soulier, B. Pellat, D. Gillot, T Lons, A.C. Lesage
Publikováno v:
Endoscopy. 41