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pro vyhledávání: '"Michel Fontés"'
Autor:
Michel Fontés
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 12, p 3807 (2018)
Peripheral neuropathies are subdivided into acquired and hereditary transmitted disorders. [...]
Externí odkaz:
https://doaj.org/article/a94beae2efca427fbd226df24965da91
Autor:
Sophie Belin, Ferdinand Kaya, Ghislaine Duisit, Sarah Giacometti, Joseph Ciccolini, Michel Fontés
Publikováno v:
PLoS ONE, Vol 4, Iss 2, p e4409 (2009)
BACKGROUND: Ascorbic acid (AA), or Vitamin C, is most well known as a nutritional supplement with antioxidant properties. Recently, we demonstrated that high concentrations of AA act on PMP22 gene expression and partially correct the Charcot-Marie-To
Externí odkaz:
https://doaj.org/article/c5a1f1d1e19d4193b2f995b0adcb30c4
Autor:
Vincent Béringue, Annick Le Dur, Philippe Tixador, Fabienne Reine, Laurence Lepourry, Armand Perret-Liaudet, Stéphane Haïk, Jean-Luc Vilotte, Michel Fontés, Hubert Laude
Publikováno v:
PLoS ONE, Vol 3, Iss 1, p e1419 (2008)
BackgroundThe evolution of the variant Creutzfeldt-Jakob disease (vCJD) epidemic is hazardous to predict due to uncertainty in ascertaining the prevalence of infection and because the disease might remain asymptomatic or produce an alternate, sporadi
Externí odkaz:
https://doaj.org/article/e7f0eade8b06464f8dd4852ff4d632c8
Akademický článek
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Autor:
Martin Krahn, Anne-Marie Imbert, Cecile Zaupa, Catherine Badens, Christian Chabannon, Alberto L. Epstein, Michel Fontés
Publikováno v:
Molecular Therapy. 9:S305
Top of pageAbstract Amplicons are promising helper-dependent HSV-1-derived vectors that allow the transfer and expression of large DNA fragments into dividing and quiescent cells. Their capacity to transduce human hematopoietic progenitors has been p
Autor:
Nicolas Lévy, Rafaëlle Bernard-Bronsard, Anne-Marie Lossi, Laurence Colleaux, Carlos Cardoso, Laurent Villard, Michel Fontés
Publikováno v:
Human Mutation. 14:448
Autor:
Pierre Miniou, Michel Fontes
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 6755 (2021)
Charcot–Marie–Tooth disease (CMT) is the most frequent hereditary peripheral neuropathies. It is subdivided in two main groups, demyelinating (CMT1) and axonal (CMT2). CMT1 forms are the most frequent. The goal of this review is to present publis
Externí odkaz:
https://doaj.org/article/30c23986efa04d6c81c75339a5153874
Autor:
Marion Sallée, Michel Fontès, Laurence Louis, Claire Cérini, Philippe Brunet, Stéphane Burtey
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82702 (2013)
BACKGROUND: The control of gene expression in the course of chronic kidney disease (CKD) is not well addressed. Alternative splicing is a common way to increase complexity of proteins. More than 90% of human transcripts are alternatively spliced. We
Externí odkaz:
https://doaj.org/article/ae13aa2e97e042469f1e05c796432b49