Zobrazeno 1 - 10
of 227
pro vyhledávání: '"M.-C. Lecomte"'
Publikováno v:
BioTechniques, Vol 22, Iss 3, Pp 430-434 (1997)
Externí odkaz:
https://doaj.org/article/3db99ab9ab234d2e83647ba1c3de84aa
Autor:
G. Nicolas, Desire Tshala-Katumbay, Victor Monterroso, A. L. Ramos, E. Couchi, Jill S. Wentzell, Doris Kretzschmar, Roman M. Kassa, M. C. Lecomte, Mihail S. Iordanov
Publikováno v:
Journal of Molecular Neuroscience. 47:631-638
We use 1,2-diacetylbenzene (1,2-DAB) to probe molecular mechanisms of proximal giant neurofilamentous axonopathy (PGNA), a pathological hallmark of amyotrophic lateral sclerosis. The spinal cord proteome of rodents displaying 1,2-DAB PGNA suggests a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb8929af2f11946a7e6199fbea0098c
https://doi.org/10.1007/s12031-011-9699-8
https://doi.org/10.1007/s12031-011-9699-8
Autor:
J. M. W. Quinn, M. C. Lecomte, S. L. Asplund, K. Sugita, T. J. Huang, T. Matsushita, C. Rahuel, M. Nees, A. Takagi, J. E Compston, H. Okada, M. T. Canciani, S. Bord, M. A. Scott, J. P. Cartron, C. Capoferri, R. E. Lewis, Y. Colin, S. Breit, T. Kojima, W. El Nemer, D. P. Kontoyiannis, A. Yoshioka, J. Takamatsu, E. Frith, E. Gauthier, E. Lee, M. E. Reid, M. Muckenthaler, M. Cole-Sinclair, J. W. Sentry, P. Gane, Y. Kroviarski, A. E. Kulozik, K. Yamamoto, G. Burgess, J. I. O. Craig, M. Pfoersich, M. T. Gillespie, T. Yamazaki, T. Murate, S. H. Kroft, M. Sugimoto, T. Adachi, C. Hagemeier, U. Schaefer, W.-J. Cheng, C. Le Van Kim, F. P. L. Lai, G. R. Halverson, D. C. Ireland, N. J. Karandikar, H.-G. Schneider, P. M. Mannucci, H. Saito, R. W. McKenna
Publikováno v:
British Journal of Haematology. 126
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfc1c59151a8e4179495e54c57d20a4e
https://doi.org/10.1111/j.1365-2141.2004.005016.x
https://doi.org/10.1111/j.1365-2141.2004.005016.x
Publikováno v:
European journal of biochemistry. 267(9)
The spectrin role(s) is (are) very important for the shape and the physical properties of red cells, such as deformability and resistance to mechanical stresses. Moreover a variety of spectrin diseases are known. We have previously demonstrated [Cors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::970605e6f082e63370084ed70930acdf
https://pubmed.ncbi.nlm.nih.gov/10785404
https://pubmed.ncbi.nlm.nih.gov/10785404
Publikováno v:
Blood. 93(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2fbe774a9a165a485ea6ea658397cd5a
https://pubmed.ncbi.nlm.nih.gov/10215350
https://pubmed.ncbi.nlm.nih.gov/10215350
Publikováno v:
Blood. 89(12)
An alpha-spectrin variant with increased susceptibility to tryptic digestion, alpha(II/47), was previously observed in a child with severe, recessively inherited, poikilocytic anemia. The molecular basis of this variant, spectrin St Claude, has now b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::10ffcd1ce424ea67fad6b39aa73d7d11
https://pubmed.ncbi.nlm.nih.gov/9192783
https://pubmed.ncbi.nlm.nih.gov/9192783
Autor:
S L, Le Bonniec, C, Fournier, C, Deregnaucourt, P, Grellier, D, Dhermy, M C, Lecomte, J, Schrevel
Publikováno v:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie. 319(11)
Many proteases play a crucial role in the Plasmodium intraerythrocytic life cycle. Spectrin depletion, one of the major events involved in parasite release from the red blood cell, results from proteolytic activities associated with the presence of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1feedb7cbef9b0d128cad068db0ce83
https://pubmed.ncbi.nlm.nih.gov/9033845
https://pubmed.ncbi.nlm.nih.gov/9033845
Autor:
M, Garbarz, L, Boulanger, S, Pedroni, M C, Lecomte, H, Gautero, C, Galand, P, Boivin, L, Feldman, D, Dhermy
Publikováno v:
Blood. 80(4)
An Argentinian family with hereditary elliptocytosis (HE) associated with a shortened beta-spectrin (Sp) chain was studied. As with most of the other shortened Sp beta-chains that have been described, this variant, called SpTandil, has impaired abili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::767e0344230525a13ac216b4fda7b496
https://pubmed.ncbi.nlm.nih.gov/1498324
https://pubmed.ncbi.nlm.nih.gov/1498324
Autor:
William T. Tse, Patrick G. Gallagher, Didier Dhermy, M. Garbarz, Theresa L. Coetzer, M C Lecomte, S K Ballas, A Baruchel, H S Zarkowsky, J Palek
We studied nine individuals from five unrelated families with alpha I/46-50a hereditary elliptocytosis (HE) or hereditary pyropoikilocytosis (HPP), including one of the original HHP probands first reported by Zarkowsky and colleagues (1975. Br. J. Ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57aaf1474424afcd88f0273183e37b17
https://europepmc.org/articles/PMC442935/
https://europepmc.org/articles/PMC442935/
Publikováno v:
Medicina. 52(2)
Using clinical, functional and biochemical criteria, we studied the red blood cell membrane of nine caucasic patients from four families with hereditary elliptocytosis (HE). From a clinical point of view, seven cases were classified as compensated mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc9737616c613ed771a0376b9346e708
https://pubmed.ncbi.nlm.nih.gov/1308902
https://pubmed.ncbi.nlm.nih.gov/1308902