Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Jean Marie Warter"'
Publikováno v:
Neurobiology of Disease, Vol 8, Iss 4, Pp 626-635 (2001)
Sensory neuropathies are frequently associated with diabetes or with antimitotic treatments in humans suffering from cancer, and are in this case the most important limitation to the use of antimitotic drugs. For this reason, there is a need to estab
Externí odkaz:
https://doaj.org/article/2e839d93a05a454881268208240c9bca
Publikováno v:
Neurobiology of Disease, Vol 8, Iss 3, Pp 447-458 (2001)
The frissonnant (fri) mutation is an autosomic recessive mutation which spontaneously appeared in the stock of C3H mice. fri mutant mice have locomotor instability and rapid tremor. Since tremor ceases when mutant mice have sleep or are anaesthetized
Externí odkaz:
https://doaj.org/article/fb8494878ed04c85a8646ae98fdd2124
Autor:
Philippe F. Kennel, Paul Fonteneau, Elisabeth Martin, Jean-Marc Schmidt, Mimoun Azzouz, Jacques Borg, Jean-Louis Guenet, Henning Schmalbruch, Jean-Marie Warter, Philippe Poindron
Publikováno v:
Neurobiology of Disease, Vol 3, Iss 2, Pp 137-147 (1996)
The mouse autosomal recessive mutation progressive motor neuronopathy (pmn) results in early onset motor neuron disease with rapidly progressive hindlimb paralysis, severe muscular wasting, and death at around 6 weeks of age. This mutant provides opp
Externí odkaz:
https://doaj.org/article/e479a197653d4eb091b69aa009a1136f
Autor:
Christian Marescaux, Jean de Barry, François Sellal, Jean-Marie Danion, Agnes Janoshazi, Jean Marie Warter
Publikováno v:
Neurobiology of Aging. 27:245-251
There is a growing evidence of early changes of blood cells in Alzheimer's disease (AD). We have developed an original novel method for quantifying the alteration of protein kinase C (PKC) by its fluorescence spectrum: by using Fim-1, a specific fluo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a426a783ebe543c948e9dbb57540a72
https://doi.org/10.1016/j.neurobiolaging.2005.02.009
https://doi.org/10.1016/j.neurobiolaging.2005.02.009
Autor:
André Muller, Jean-Louis Kuntz, Jacques Kopferschmitt, Christian Brandt, Marie-Thérèse Haeringer, Jean-Marie Warter, Christian Rempp, Pierre Meyer, Jean Sibilia
Publikováno v:
Douleurs : Evaluation - Diagnostic - Traitement. 6:151-159
Resume Objectifs de l’etude La ketamine a faibles doses en intraveineux a des effets anti-hyperalgesiants. L’objectif principal est de verifier si elle est efficace sur le syndrome douloureux des patients atteints de fibromyalgie. Les objectifs s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f4c96cb919de63615048725423e95c2
https://doi.org/10.1016/s1624-5687(05)80252-5
https://doi.org/10.1016/s1624-5687(05)80252-5
Autor:
Yves Lombard, Vincent Laporte, Christine Tranchant, Jean-Marie Warter, Rachel Levy-Benezra, Philippe Poindron
Publikováno v:
Journal of Leukocyte Biology. 76:451-461
Artificial diffuse and amyloid core of neuritic plaques [β-amyloid peptide (Aβ) deposits] could be prepared using heat-killed yeast particles opsonized with Aβ 1–40 or Aβ 1–42 peptides. Interaction and fate of these artificial deposits with m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd6091c78c68ac60a1e4888d45b8a2ab
https://doi.org/10.1189/jlb.1203620
https://doi.org/10.1189/jlb.1203620
Autor:
Jean-Marie Warter, Stéphanie Wagner, Philippe Poindron, Olivier M. Dorchies, Herrade Stoeckel, Kenneth Takeda
Publikováno v:
Pfl�gers Archiv European Journal of Physiology. 447:14-22
Under normal conditions in situ, muscle fibers and motoneurons, the main partners of motor units, are strongly dependent on each other. This interdependence hinders ex vivo studies of neuromuscular disorders where nervous or muscular components are c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deb18f615b851f4b44a958698a27fca3
https://doi.org/10.1007/s00424-003-1135-7
https://doi.org/10.1007/s00424-003-1135-7
Autor:
Eliane Lampert, Florence Ribera, Christine Tranchant, Jean-Marie Warter, Joffrey Zoll, Jean Lonsdorfer, Andoni Echaniz-Laguna
Publikováno v:
Annals of Neurology. 52:623-627
Evidence implicating mitochondrial dysfunction in the central nervous system of patients with sporadic amyotrophic lateral sclerosis (SALS) has recently been accumulating. In contrast, data on mitochondrial function in skeletal muscle in SALS are sca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afa795de08be8a3c56eb49f3c46e7550
https://doi.org/10.1002/ana.10357
https://doi.org/10.1002/ana.10357
Publikováno v:
Analytical Letters. 35:1135-1148
Spinal muscular atrophy (SMA) is a lethal autosomal recessive disease. SMA is characterized by degeneration of motor neurons in the spinal cord, causing progressive weakness of the limbs and trunk, followed by muscle atrophy. The gene most highly ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89b6de11d01ff8b6575e37753e769831
https://doi.org/10.1081/al-120005963
https://doi.org/10.1081/al-120005963
Autor:
Joffrey Zoll, Jean-Marie Warter, Philippe Poindron, Florence Ribera, Nathalie Leclerc, J. Borg, Eliane Lampert
Publikováno v:
Neuromuscular Disorders. 11:722-727
Cases of familial amyotrophic lateral sclerosis (FALS) are associated with mutations in cytosolic copper, zinc superoxide dismutase (SOD1). Total SOD activity and functional mitochondrial properties were studied in muscles and nervous tissues of cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69229e95a0b581cfa7c54b553ecc02da
https://doi.org/10.1016/s0960-8966(01)00240-1
https://doi.org/10.1016/s0960-8966(01)00240-1