Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Martine Chatelut"'
Autor:
Jacques Izopet, Jacqueline Puel, Francis Boudet, Marcel Miedougé, Lionel Rostaing, Karine Sandres-Sauné, Martine Chatelut, François Malecaze, Michel Abbal, Jean-Michel Mansuy
Publikováno v:
Journal of Medical Virology. 66:571-575
Prospective nucleic acid tests were carried out for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) using the COBAS Amplicor HIV-1 and HCV tests (Roche Diagnostics, Meylan, France) on potential organ (n=113) and cornea (n=368) donors i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::210ef0befd8da96f8c1ef25b1d0e5c02
https://doi.org/10.1002/jmv.2183
https://doi.org/10.1002/jmv.2183
Autor:
Robert Salvayre, Thierry Levade, Nathalie Andrieu-Abadie, Nathalie Augé, Jean-Pierre Jaffrézou, Bruno Ségui, Martine Chatelut
Publikováno v:
Chemistry and Physics of Lipids. 102:167-178
The ubiquitous sphingophospholipid sphingomyelin (SM) can be hydrolysed in human cells to ceramide by different sphingomyelinases (SMases). These enzymes exert a dual role, enabling not only the turnover of membrane SM and the degradation of exogenou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f56723b7956ffb1612818dc9d232391c
https://doi.org/10.1016/s0009-3084(99)00085-7
https://doi.org/10.1016/s0009-3084(99)00085-7
Autor:
Martine Chatelut, Jean-Claude Thiers, Guy Laurent, Isabelle Escargueil-Blanc, Thierry Levade, Pieraggi Mt, Nathalie Augé, Anne Nègre-Salvayre, Nathalie Andrieu-Abadie, Isabelle Lajoie-Mazenc, Robert Salvayre, Jean-Pierre Jaffrézou, Isabelle Suc
Publikováno v:
Journal of Biological Chemistry. 273:12893-12900
Proliferation of vascular smooth muscle cells (SMC) is a hallmark in the pathogenesis of atherosclerotic lesions. Mildly oxidized low density lipoproteins (UV-oxLDL), which are mitogenic to cultured AG-08133A SMC, activate the sphingomyelin (SM)-cera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4becf84b5cc8e0aee1253079c6f61b
https://doi.org/10.1074/jbc.273.21.12893
https://doi.org/10.1074/jbc.273.21.12893
Autor:
Martine Chatelut, Thierry Levade, Jean-Pierre Basile, Isabelle Redonnet-Vernhet, Robert Salvayre
Publikováno v:
Biochemical and Molecular Medicine. 62:42-49
The molecular defects in the LIPA gene encoding the lysosomal acid lipase (LAL) were investigated in two unrelated patients affected with cholesteryl ester storage disease (CESD), an autosomal recessive disorder associated with LAL-deficient activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9617b8b6d7210cf6728dbdb3fe43d986
https://doi.org/10.1006/bmme.1997.2626
https://doi.org/10.1006/bmme.1997.2626
Autor:
Marcel, Miédougé, Martine, Chatelut, Jean-Michel, Mansuy, Lionel, Rostaing, François, Malecaze, Karine, Sandres-Sauné, Francis, Boudet, Jacqueline, Puel, Michel, Abbal, Jacques, Izopet
Publikováno v:
Journal of medical virology. 66(4)
Prospective nucleic acid tests were carried out for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) using the COBAS Amplicor HIV-1 and HCV tests (Roche Diagnostics, Meylan, France) on potential organ (n=113) and cornea (n=368) donors i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6caa8d4389cbd47b35281a96897d1c8
https://pubmed.ncbi.nlm.nih.gov/11857539
https://pubmed.ncbi.nlm.nih.gov/11857539
Autor:
M C Vincent, Martine Chatelut, E Duchayne, S Roudani, C Demur, Robert Salvayre, Jean Tkaczuk, Jean Feunteun, Thierry Levade, Sylvie Caspar-Bauguil, Pieraggi Mt, Jean-Claude Thiers, P Laharrague, N Vacaresse, L Alibaud
Publikováno v:
Scandinavian journal of immunology. 48(6)
Human lymphocytes derived from the peripheral blood of a healthy woman were transfected with a plasmid carrying the simian virus 40 (SV40) large T antigen. The successfully transformed cells contained SV40 large T DNA and were negative for Epstein-Ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::351e4f43c928a48f4d6a405bdb442642
https://pubmed.ncbi.nlm.nih.gov/9874501
https://pubmed.ncbi.nlm.nih.gov/9874501
Autor:
Pierre J. Courtoy, Michèle Leruth, Thierry Levade, Shimon Gatt, Klaus Harzer, Arie Dagan, Sergio Marchesini, Martine Chatelut, Robert Salvayre
Publikováno v:
FEBS letters. 426(1)
Since the generation upon cell stimulation of the second messenger ceramide has been reported to occur in an endosomal/lysosomal compartment, we investigated whether ceramide formed in the lysosomes can escape this compartment. The metabolic fate of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ae4cf94cc59e148debbd2b5a161396c
https://pubmed.ncbi.nlm.nih.gov/9598987
https://pubmed.ncbi.nlm.nih.gov/9598987
Autor:
Thierry Levade, Helen Christomanou, Masao Hiraiwa, Barbara C. Paton, Martine Chatelut, John S. O'Brien, Klaus Harzer
Publikováno v:
FEBS letters. 417(3)
In loading tests using galactosylceramide which had been labelled with tritium in the ceramide moiety, living skin fibroblast lines derived from the original prosaposin-deficient patients had a markedly reduced capacity to degrade galactosylceramide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99f5bdf661d6cc9a527ccd18ebc8a35
https://pubmed.ncbi.nlm.nih.gov/9409731
https://pubmed.ncbi.nlm.nih.gov/9409731
Autor:
Thierry Levade, Pieraggi Mt, Helen Christomanou, Jean Feunteun, Robert Salvayre, Klaus Harzer, Martine Chatelut, Jean-Claude Thiers, Barbara C. Paton, Jean-Pierre Basile, John S. O'Brien, Yasuo Kishimoto
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 262(1-2)
Skin fibroblasts from patients with Farber disease (acid ceramidase deficiency) and from two siblings of the only known family affected with prosaposin deficiency were transformed by transfection with a plasmid carrying the SV40 large T antigen. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19c7b57516428a81ab25d103d2c61394
https://pubmed.ncbi.nlm.nih.gov/9204210
https://pubmed.ncbi.nlm.nih.gov/9204210
Autor:
Thierry Levade, Anthony H. Fensom, Jean-Pierre Basile, Robert Salvayre, Martine Chatelut, Klaus Harzer, Jean Feunteun
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 245(1)
Farber disease is an inborn lysosomal storage disorder characterized by accumulation of ceramide in the patient's tissues due to the deficient activity of acid ceramidase. Currently, confirmation of the diagnosis is performed in an extremely limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c740e0086b917aad157f8a901bfb778c
https://pubmed.ncbi.nlm.nih.gov/8646815
https://pubmed.ncbi.nlm.nih.gov/8646815