Zobrazeno 1 - 10
of 128
pro vyhledávání: '"M. Espeel"'
Publikováno v:
Biology of the Cell. 90:641-652
The interaction of cells with extracellular matrix components contributes to their specific differentiation. We studied hepatic peroxisomes and their changing features during embryonic development, and we immunolocalized in the same tissue the extrac
Autor:
M ESPEEL
Publikováno v:
Hepatology. 22:497-504
Publikováno v:
Endocrine. 3:61-68
The secretion of 23 kDa prolactin by rat pituitary cells has been thoroughly investigated, but secretion of glycosylated rat prolactin is not currently known. This is mainly due to the lack of an antiserum which is solely specific for glycosylated ra
Autor:
M. Espeel, G. Van Limbergen
Publikováno v:
Diagnosis of human peroxisomal disorders ISBN: 9780792338550
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a232bb8728493d3e1ba6ca41479786
https://doi.org/10.1007/978-94-011-9635-2_12
https://doi.org/10.1007/978-94-011-9635-2_12
Autor:
J. G. Leroy, M. Espeel, J. F. Gadisseux, H. Mandel, M. Martinez, B. T. Poll-The, R. J. A. Wanders, F. Roels
Publikováno v:
Diagnosis of human peroxisomal disorders ISBN: 9780792338550
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d2ab90ee94e3fe70665a1b1fd7dbc88
https://doi.org/10.1007/978-94-011-9635-2_16
https://doi.org/10.1007/978-94-011-9635-2_16
Publikováno v:
The Journal of biological chemistry. 269(40)
The peroxisomal membrane appears to play a crucial role in transporting proteins into the organelle. Some human genetic disorders involving peroxisome biogenesis, such as Zellweger syndrome, may be caused by genetic defects of the import machinery lo
Autor:
M. Espeel, J. C. Heikoop, J. A. M. Smeitink, F. A. Beemer, D. De Craemer, M. Van Den Berg, T. Hashimoto, R. J. A. Wanders, R. B. H. Schutgens, B. T. Poll-The, F. Roels
Publikováno v:
Ultrastructural pathology, 17(6), 623-636. Informa Healthcare
In the liver biopsy from an 8.5-year-old girl with the biochemical characteristics of rhizomelic chondrodysplasia punctata (RCDP), but with normal limbs, normal catalase-containing peroxisomes were absent. Light microscopy after diaminobenzidine stai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e69f849a95933c2442910e312530d33
https://pure.amc.nl/en/publications/cytoplasmic-catalase-and-ghostlike-peroxisomes-in-the-liver-from-a-child-with-atypical-chondrodysplasia-punctata(fa3382f3-5033-4b7b-8068-ca48aa539040).html
https://pure.amc.nl/en/publications/cytoplasmic-catalase-and-ghostlike-peroxisomes-in-the-liver-from-a-child-with-atypical-chondrodysplasia-punctata(fa3382f3-5033-4b7b-8068-ca48aa539040).html
Akademický článek
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Autor:
M. Ferrara, Guido Tytgat, F. Barberani, F. Berger, A. Peracchia, M. Adler, G. Ghillebert, C. Bertrand, A. Franchini, S. Farella, S. Ponette, B. Gulbis, C. Jonas, Riflolfi Ruggero, T. Laporta, G. Costamagna, P. Rossi, C. Beyaert, J. F. Rey, M. Ambrogi, D. Carpinelli, M. Greff, W. Van Ganse, José Sahel, F. Pincione, J C Lemper, J. P. Meessen, Amadori Dino, M. Deltenre, R. Ribacchi, Y. Minaire, R. V. Buecino, J. Escourrou, Georges Coremans, A. Dell’ Anna, F. Buin, V. Masi, Ph. Marlière, K. Faucon, R. Castro, G. Vinciguerre, Jacques Reeders, L. Risa, M. Dal Fants, F. Silverstein, Zdenek Maratka, M. G. Mortilla, A. Neri, A. Russo, M. Baize, J. J. Van Den Oord, K. Geboes, J. X. Laurent, F. Senegas-Balas, R. Rossoni, M. Delhaye, P. Rozen, G. Miscusi, E. Cristallini, S. Shaneyfelt, J. C. Debongnie, H. Sarles, R. Lambert, I. Dell’Amico, L. Norberto, E. Aneona, D. Gilbert, Labadie M, L. Stessens, A. Verdier, J. Deviere, M. Bretagnolle, A. Hallstrom, Gaston Vantrappen, A. Burette, Ravaioli Alberto, X. Van Meerhaeghe, J Morobe, G. Giannone, C. De Boelpaepe, F. Roels, J. De Toeuf, B. Fontaniére, A. Cusumano, J. Janssens, J. Mudry, P Laurent, Paul Rutgeerts, L. Philippeth, A. Sicari, M. Lombardi, A. Vanneste, G. Legros, J. Battin, M. Espeel, B. Cola, A. Montori, A. Van Gossum, N. Soehendra, A. Liaras, A. Ribet, M. Cremer, Y. Philippart, P. Depelchin, P. Aertsen, M J. Bastié, G. De Wolf-Peeters, M. Van Gossum, G. Stevanato, A. Gulbis, M. De Reuck, G. P. Fatale, R. Troiani, J. M. Brunetaud, F. Ciolfi, F. Vicari, P M Bret, B. Dez Marez, L. Broeckaert, Robert Vanheuverzwyn, D. Polito, M. Buset, N. Bourgeois, D. Balas, F. Dunham, A. Van Laethem, Jules Haot, P. Spinelli, A. Fond, V. Maunoury, M. Jungers, M. Quenon, M. Piccione, D. Oselladore, B. Martella, A. Osmani, M. Delvaux, P. Van der Spek, A. Delia Spoletina, I. Kempeneers, J. M. Bondonny, G. A. Cora, B. Bouvet, Bernhard Tribukait, R. Giardino, L. Masoni, A. Mourin-Jouret, Liverani Marilena, C. Paris, A. Cornelis, J. M. Bidart, J. Papillon, M. Mayer, H. Lamouliatte
Publikováno v:
Acta Endoscopica. 15:63-116
Akademický článek
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