Zobrazeno 1 - 10
of 51
pro vyhledávání: '"A. Aït-Ikhlef"'
Autor:
Kapetshi, Jimmy, Fausther-Bovendo, Hugues, Corbett, Cindi, Leung, Anders, Ait-Ikhlef, Kamal, Nsio, Justus, Aruna, Aaron, Ilunga, Benoit Kebela, Muyembe, Jean-Jacques, Formenty, Pierre, Kobinger, Gary P.
Publikováno v:
The Journal of Infectious Diseases, 2018 Dec . 218, S292-S296.
Externí odkaz:
https://www.jstor.org/stable/26576192
Autor:
El Messari, Saı̈d a, Aı̈t-Ikhlef, Ali b, Ambroise, Djennet-Hantaz a, b, Penicaud, Luc c, Arluison, Michel a, *
Publikováno v:
In Journal of Chemical Neuroanatomy 2002 24(4):225-242
Autor:
Blondet, Brigitte a, ∗, Carpentier, Gilles a, Aı̈t-Ikhlef, Ali b, Murawsky, Monique b, Rieger, François b
Publikováno v:
In Brain Research 2002 930(1):53-57
Publikováno v:
Brain Research. 930:53-57
The wobbler mutant mouse displays a recessively inherited neurological disease with degeneration of motoneurons and is considered to be an animal model for human motoneuron diseases. Mutant mice can be clinically recognised at about 3-4 weeks of age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d00ca3aa7cf4e95895afa43ac81bd572
https://doi.org/10.1016/s0006-8993(01)03405-9
https://doi.org/10.1016/s0006-8993(01)03405-9
Publikováno v:
Neuroscience Letters. 305:202-206
In neurodegenerative diseases, such as Alzheimer's disease or HIV encephalitis, neuronal DNA fragmentation has been observed at unexpected high frequencies, without definitive evidence for activation of an irreversible apoptotic pathway. The wobbler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea15459d7c6522bacf914d7f982f348
https://doi.org/10.1016/s0304-3940(01)01741-4
https://doi.org/10.1016/s0304-3940(01)01741-4
Publikováno v:
Journal of Neuroscience Research. 59:100-106
During late postnatal development, mice with the autosomal recessive wobbler mutation (wr/wr) develop motoneuron degeneration associated with astrogliosis in the spinal cord. In vitro, primary wobbler astrocytes are also affected, exhibiting abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991d1bf2bb17cad158d37325df3007b5
https://doi.org/10.1002/(sici)1097-4547(20000101)59:1<100::aid-jnr12>3.0.co
https://doi.org/10.1002/(sici)1097-4547(20000101)59:1<100::aid-jnr12>3.0.co
Autor:
A. Aït-Ikhlef, Monique Murawsky, François Rieger, Brigitte Blondet, Qiao Yan, Linxi Li, Lucien J. Houenou
Publikováno v:
Journal of the Neurological Sciences. 153:20-24
Several new neurotrophic factors have been recently identified and shown to prevent motoneuron death in vitro and in vivo. One such agent is brain-derived neurotrophic factor (BDNF). In this study, we tested BDNF on an animal model of early-onset mot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b5e991dbbe966bf40344bbabca046f4
https://doi.org/10.1016/s0022-510x(97)00171-8
https://doi.org/10.1016/s0022-510x(97)00171-8
Autor:
Monique Murawsky, François Rieger, A. Aït-Ikhlef, Brigitte Blondet, J.C. Martinou, D. Hantaz-Ambroise
Publikováno v:
Neuroscience Letters. 199:163-166
The wobbler mouse mutation, an autosomal recessive mutation, leads to motoneuron degeneration in early post-natal development. Transgenic mice in which neurons overexpress human bcl2 transgene have been generated: the overexpression of bcl2 reduces t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6137c2ee75e4a53f36cd632f8e006ecb
https://doi.org/10.1016/0304-3940(95)12061-8
https://doi.org/10.1016/0304-3940(95)12061-8
Autor:
Monique Murawsky, Brigitte Blondet, D. Hantaz-Ambroise, François Rieger, A. Aït-Ikhlef, Danièle Cambier
Publikováno v:
Neuroscience Letters. 183:179-182
Mice affected by the wobbler mutation are characterized by a muscular atrophy associated with motoneuron degeneration. As soon as the first clinical signs of the disease appear, reactive astrocytes, strongly glial fibrillary acidic protein (GFAP)-pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::280e12879273059416012c65bffbb164
https://doi.org/10.1016/0304-3940(94)11145-9
https://doi.org/10.1016/0304-3940(94)11145-9
Publikováno v:
Journal of chemical neuroanatomy. 24(4)
Following a previous immunocytochemical study of GLUT4 in the rat brain and spinal cord (J. Comp. Neurol. 399 (1998) 492), we now report the distribution and cellular expression of GLUT4 mRNA in the CNS using reverse transcription-polymerase chain re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50070fa19dd3d89eece9399685122ffe
https://pubmed.ncbi.nlm.nih.gov/12406499
https://pubmed.ncbi.nlm.nih.gov/12406499