Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Lydie Guigand"'
Autor:
Thibaut Larcher, Aude Lafoux, Laurent Tesson, Séverine Remy, Virginie Thepenier, Virginie François, Caroline Le Guiner, Helicia Goubin, Maéva Dutilleul, Lydie Guigand, Gilles Toumaniantz, Anne De Cian, Charlotte Boix, Jean-Baptiste Renaud, Yan Cherel, Carine Giovannangeli, Jean-Paul Concordet, Ignacio Anegon, Corinne Huchet
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e110371 (2014)
A few animal models of Duchenne muscular dystrophy (DMD) are available, large ones such as pigs or dogs being expensive and difficult to handle. Mdx (X-linked muscular dystrophy) mice only partially mimic the human disease, with limited chronic muscu
Externí odkaz:
https://doaj.org/article/5360c456b3714a1faaa7b80cda6608fc
Autor:
Caroline Le Guiner, Knut Stieger, Alice Toromanoff, Mickaël Guilbaud, Alexandra Mendes-Madeira, Marie Devaux, Lydie Guigand, Yan Cherel, Philippe Moullier, Fabienne Rolling, Oumeya Adjali
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e102538 (2014)
Numerous studies have demonstrated the efficacy of the Adeno-Associated Virus (AAV)-based gene delivery platform in vivo. The control of transgene expression in many protocols is highly desirable for therapeutic applications and/or safety reasons. To
Externí odkaz:
https://doaj.org/article/ffab1b8d1e2d44658e04053f53d319fa
Autor:
Christel Gentil, Caroline Le Guiner, Sestina Falcone, Jean-Yves Hogrel, Cécile Peccate, Stéphanie Lorain, Sofia Benkhelifa-Ziyyat, Lydie Guigand, Marie Montus, Laurent Servais, Thomas Voit, France Piétri-Rouxel
At present, the clinically most advanced strategy to treat Duchenne muscular dystrophy (DMD) is the exon-skipping strategy. Whereas antisense oligonucleotide-based clinical trials are underway for DMD, it is essential to determine the dystrophin rest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab0d1564d66957b55cd490f3e001e35d
https://doi.org/10.1089/hum.2016.041
https://doi.org/10.1089/hum.2016.041
Autor:
Grégory Jouvion, Jack-Yves Deschamps, Laurence Dubreil, Isabelle Testault, Priscilla Orlando, Isabelle Leroux, Lydie Guigand, Stéphane Deleau, Bruno Delorme, Thibaut Larcher, Yan Cherel, Marine Carlus, Marine Theret, Karl Rouger, Marc Fiszman, Benoît Fornasari, Elisabeth Le Rumeur, Céline Zuber, Mireille Ledevin, Blandine Lieubeau, Caroline Le Guiner
Publikováno v:
American Journal of Pathology
American Journal of Pathology, American Society for Investigative Pathology, 2011, 179 (5), pp.2501-18. ⟨10.1016/j.ajpath.2011.07.022⟩
American Journal of Pathology, 2011, 179 (5), pp.2501-18. ⟨10.1016/j.ajpath.2011.07.022⟩
American Journal of Pathology, American Society for Investigative Pathology, 2011, 179 (5), pp.2501-18. ⟨10.1016/j.ajpath.2011.07.022⟩
American Journal of Pathology, 2011, 179 (5), pp.2501-18. ⟨10.1016/j.ajpath.2011.07.022⟩
Muscle Stem = MuStem; International audience; Duchenne muscular dystrophy (DMD) is a genetic progressive muscle disease resulting from the lack of dystrophin and without effective treatment. Adult stem cell populations have given new impetus to cell-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6c1df7b06b5bb39872c883b0da3d66
https://doi.org/10.1016/j.ajpath.2011.07.022
https://doi.org/10.1016/j.ajpath.2011.07.022
Autor:
Pierre Weiss, Lydie Guigand, Sophie Portron, Jérôme Amiaud, Claire Vinatier, Yan Cherel, Christophe Merceron, Martial Masson, Jérôme Guicheux
Publikováno v:
American Journal of Physiology-Cell Physiology
American Journal of Physiology-Cell Physiology, American Physiological Society, 2010, 298 (2), pp.C355-C364. ⟨10.1152/ajpcell.00398.2009⟩
American Journal of Physiology-Cell Physiology, American Physiological Society, 2010, 298 (2), pp.C355-C364. ⟨10.1152/ajpcell.00398.2009⟩
International audience; Human adipose tissue-derived stem cells (hATSC) have been contemplated as reparative cells for cartilage engineering. Chondrogenic differentiation of hATSC can be induced by an enriched culture medium and a three-dimensional e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa47baf4476b4778eebf2098cd06e651
https://doi.org/10.1152/ajpcell.00398.2009
https://doi.org/10.1152/ajpcell.00398.2009
Publikováno v:
Neuromuscular Disorders
Neuromuscular Disorders, Elsevier, 2005, 15 (2), pp.154-163. ⟨10.1016/j.nmd.2004.11.002⟩
Neuromuscular Disorders, Elsevier, 2005, 15 (2), pp.154-163. ⟨10.1016/j.nmd.2004.11.002⟩
Due to the abundance of muscle, intravascular administration seems required for efficient gene or cell therapy of muscular dystrophy. Here, we examined the skeletal muscle microvasculature to assess if it is altered with dystrophin deficiency. Image
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52cbfc27cfab89aa2a1d270cab07b803
https://doi.org/10.1016/j.nmd.2004.11.002
https://doi.org/10.1016/j.nmd.2004.11.002
Publikováno v:
Gene Therapy. 9:1037-1043
The recent identification of genes responsible for several muscle diseases, particularly inherited myopathies, has made gene transfer to pathologic muscle tissue an attractive research field. As early pathologic changes in myopathic muscle involve re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbc7d5fe8b568922e75caeb8f3bf335d
https://doi.org/10.1038/sj.gt.3301773
https://doi.org/10.1038/sj.gt.3301773
Autor:
Fabienne Rolling, Lydie Guigand, Alexandra Mendes-Madeira, Knut Stieger, Oumeya Adjali, Yan Cherel, Alice Toromanoff, Philippe Moullier, Caroline Le Guiner, Marie Devaux, Mickaël Guilbaud
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2014, 9 (9), pp.1-10
PLoS ONE, Public Library of Science, 2014, 9 (9), pp.1-10. ⟨10.1371/journal.pone.0102538⟩
PLoS ONE, Vol 9, Iss 9, p e102538 (2014)
PLoS ONE, Public Library of Science, 2014, 9 (9), pp.1-10
PLoS ONE, Public Library of Science, 2014, 9 (9), pp.1-10. ⟨10.1371/journal.pone.0102538⟩
PLoS ONE, Vol 9, Iss 9, p e102538 (2014)
Numerous studies have demonstrated the efficacy of the Adeno-Associated Virus (AAV)-based gene delivery platform in vivo. The control of transgene expression in many protocols is highly desirable for therapeutic applications and/or safety reasons. To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ef3310505c779317e919032ea9aa93
https://hal.archives-ouvertes.fr/hal-01131077
https://hal.archives-ouvertes.fr/hal-01131077
Autor:
Laurent Tesson, Helicia Goubin, Jean-Baptiste Renaud, Thibaut Larcher, Caroline Le Guiner, Yan Cherel, Carine Giovannangeli, Corinne Huchet, Maeva Dutilleul, Ignacio Anegon, Gilles Toumaniantz, Anne De Cian, Lydie Guigand, Jean-Paul Concordet, Séverine Remy, Charlotte Boix, A. Lafoux, Virginie François, Virginie Thepenier
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2014, 9 (10), 13 p. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, Vol 9, Iss 10, p e110371 (2014)
PLoS ONE, Public Library of Science, 2014, 9 (10), pp.e110371. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, 2014, 9 (10), 13 p. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, 2014, 9 (10), pp.e110371. ⟨10.1371/journal.pone.0110371⟩
Plos One 10 (9), 13 p.. (2014)
PLoS ONE, Public Library of Science, 2014, 9 (10), 13 p. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, Vol 9, Iss 10, p e110371 (2014)
PLoS ONE, Public Library of Science, 2014, 9 (10), pp.e110371. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, 2014, 9 (10), 13 p. ⟨10.1371/journal.pone.0110371⟩
PLoS ONE, 2014, 9 (10), pp.e110371. ⟨10.1371/journal.pone.0110371⟩
Plos One 10 (9), 13 p.. (2014)
International audience; A few animal models of Duchenne muscular dystrophy (DMD) are available, large ones such as pigs or dogs being expensive and difficult to handle. Mdx (X-linked muscular dystrophy) mice only partially mimic the human disease, wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03c4413cbd0bf7a3aecc2986c1e1475b
https://hal.archives-ouvertes.fr/hal-01190124/document
https://hal.archives-ouvertes.fr/hal-01190124/document
Publikováno v:
J. Vet. Anat.
J. Vet. Anat., 2014, 7 (1), pp.89-111
Journal of Veterinary Anatomy
Journal of Veterinary Anatomy, 2014, 7 (1), pp.89-111
J. Vet. Anat., 2014, 7 (1), pp.89-111
Journal of Veterinary Anatomy
Journal of Veterinary Anatomy, 2014, 7 (1), pp.89-111
Morphological features and chronology of myocytes changes after denervation were studied over 35 days period in 2 heavy (HW) and light-weight (LW) strains of 5-week-old male turkeys. Denervation caused progressive atrophy in posterior latissimu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e855d2a72d80ee4d22871114d5782221
https://hal.archives-ouvertes.fr/hal-01190007/document
https://hal.archives-ouvertes.fr/hal-01190007/document