Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Florence Robriquet"'
Autor:
Camila F. Almeida, Florence Robriquet, Tatyana A. Vetter, Nianyuan Huang, Reid Neinast, Lumariz Hernandez-Rosario, Dhanarajan Rajakumar, W. David Arnold, Kim L. McBride, Kevin M. Flanigan, Robert B. Weiss, Nicolas Wein
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Myotonic dystrophy type 1 (DM1) is the most common form of muscular dystrophy in adults and affects mainly the skeletal muscle, heart, and brain. DM1 is caused by a CTG repeat expansion in the 3′UTR region of the DMPK gene that sequesters musclebli
Externí odkaz:
https://doaj.org/article/64f77f1950614b9e88620a368751f95d
Autor:
Florence Robriquet, Aurélie Lardenois, Candice Babarit, Thibaut Larcher, Laurence Dubreil, Isabelle Leroux, Céline Zuber, Mireille Ledevin, Jack-Yves Deschamps, Yves Fromes, Yan Cherel, Laetitia Guevel, Karl Rouger
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0123336 (2015)
Several adult stem cell populations exhibit myogenic regenerative potential, thus representing attractive candidates for therapeutic approaches of neuromuscular diseases such as Duchenne Muscular Dystrophy (DMD). We have recently shown that systemic
Externí odkaz:
https://doaj.org/article/326afcc66b9241d0aa7718770ea0975c
Autor:
Mathias Vilaine, Céline Garrec, Pierre Lindenbaum, Sophie Couvé, Mathilde Pacault, Laurence Heidet, Stéphane Bézieau, Celeste Bento, David Hoogewijs, Helene Dreau, Yannick Arlot-Bonnemains, Nelly Burnichon, Marion Lenglet, Richard van Wijk, Maria-Luigia Randi, Alexandre Buffet, Florence Robriquet, Fabrice Airaud, Holger Cario, Nicolas Janin, Melissa M. Pentony, Erika Kvikstad, Stéphane Richard, Karim Bouchireb, Antonis Kattamis, Jean-Michaël Mazzella, Carme Camps, Sylvie Job, Sophie Ferlicot, Anne Couturier, Richard Redon, Maria Caterina Putti, Thomas Besnard, Joachim R. Göthert, Klaus-Michael Debatin, Betty Gardie, Sophie Deveaux, Franck Chesnel, Solenne Dumont, Jenny C. Taylor, Marine Cornec, Bin Tean Teh, François Girodon, Vincent Bours, Sophie Gad, Anne-Paule Gimenez-Roqueplo, Sabine Irtan, Klaus Schwarz, Elpis Mantadakis, Samantha J. L. Knight, Brigitte Bressac-de Paillerets
Publikováno v:
Blood
Blood, 2018, 132 (5), pp.469-483. ⟨10.1182/blood-2018-03-838235⟩
Blood, American Society of Hematology, 2018, 132 (5), pp.469-483. ⟨10.1182/blood-2018-03-838235⟩
Blood, Vol. 132, no.5, p. 469-483 (2018)
Blood, 2018, 132 (5), pp.469-483. ⟨10.1182/blood-2018-03-838235⟩
Blood, American Society of Hematology, 2018, 132 (5), pp.469-483. ⟨10.1182/blood-2018-03-838235⟩
Blood, Vol. 132, no.5, p. 469-483 (2018)
International audience; Chuvash polycythemia is an autosomal recessive form of erythrocytosis associated with a homozygous p.Arg200Trp mutation in the von Hippel-Lindau (VHL) gene. Since this discovery, additional VHL mutations have been identified i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0880746e10359614471af0a533de25b
https://hal.science/hal-01833917
https://hal.science/hal-01833917
Autor:
Marion, Lenglet, Florence, Robriquet, Klaus, Schwarz, Carme, Camps, Anne, Couturier, David, Hoogewijs, Alexandre, Buffet, Samantha J L, Knight, Sophie, Gad, Sophie, Couvé, Franck, Chesnel, Mathilde, Pacault, Pierre, Lindenbaum, Sylvie, Job, Solenne, Dumont, Thomas, Besnard, Marine, Cornec, Helene, Dreau, Melissa, Pentony, Erika, Kvikstad, Sophie, Deveaux, Nelly, Burnichon, Sophie, Ferlicot, Mathias, Vilaine, Jean-Michaël, Mazzella, Fabrice, Airaud, Céline, Garrec, Laurence, Heidet, Sabine, Irtan, Elpis, Mantadakis, Karim, Bouchireb, Klaus-Michael, Debatin, Richard, Redon, Stéphane, Bezieau, Brigitte, Bressac-de Paillerets, Bin Tean, Teh, François, Girodon, Maria-Luigia, Randi, Maria Caterina, Putti, Vincent, Bours, Richard, Van Wijk, Joachim R, Göthert, Antonis, Kattamis, Nicolas, Janin, Celeste, Bento, Jenny C, Taylor, Yannick, Arlot-Bonnemains, Stéphane, Richard, Anne-Paule, Gimenez-Roqueplo, Holger, Cario, Betty, Gardie
Publikováno v:
Blood. 132(5)
Chuvash polycythemia is an autosomal recessive form of erythrocytosis associated with a homozygous p.Arg200Trp mutation in the von Hippel-Lindau (
Autor:
Mireille Ledevin, Bruno Delorme, Laurence Dubreil, Lucie Chabrand, Gillian Butler-Browne, Armelle Magot, Yann Péréon, Sabrina Viau, Karl Rouger, Laëtitia Guével, Blandine Lieubeau, Florence Robriquet, Candice Babarit, Elisa Negroni, Vincent Mouly, Isabelle Leroux, Chantal Thorin, Antoine Hamel, Cindy Schleder, Charlotte Saury, Judith Lorant
Publikováno v:
Molecular Therapy
Molecular Therapy, Cell Press, 2018, 26 (2), ⟨10.1016/j.ymthe.2017.10.013⟩
Molecular Therapy, 2018, 26 (2), ⟨10.1016/j.ymthe.2017.10.013⟩
Molecular Therapy, Nature Publishing Group, 2017, ⟨10.1016/j.ymthe.2017.10.013⟩
Molecular Therapy, Cell Press, 2018, 26 (2), ⟨10.1016/j.ymthe.2017.10.013⟩
Molecular Therapy, 2018, 26 (2), ⟨10.1016/j.ymthe.2017.10.013⟩
Molecular Therapy, Nature Publishing Group, 2017, ⟨10.1016/j.ymthe.2017.10.013⟩
After intra-arterial delivery in the dystrophic dog, allogeneic muscle-derived stem cells, termed MuStem cells, contribute to long-term stabilization of the clinical status and preservation of the muscle regenerative process. However, it remains unkn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1de191d6b2dbfee3ec1768766f5d9d14
https://hal.archives-ouvertes.fr/hal-01673455/document
https://hal.archives-ouvertes.fr/hal-01673455/document
Autor:
Lisa Oliver, Peter J. Ratcliffe, Betty Gardie, Jiannis Ragoussis, Peppi Koivunen, Valérie Trichet, Claire Vinatier, Ines Batinic-Haberle, Judith V.M.G. Bovée, Johanna Myllyharju, Florence Robriquet
Publikováno v:
Hypoxia
Hypoxia, DovePress, 2017, 5, [Epub ahead of print]
Hypoxia, DovePress, 2017, 5, pp.11-20. ⟨10.2147/HP.S127042⟩
Hypoxia, 2017, 5, pp.11-20. ⟨10.2147/HP.S127042⟩
Hypoxia, Vol Volume 5, Pp 11-20 (2017)
Hypoxic Signaling
Hypoxic Signaling, 5, 11-20
Hypoxia, DovePress, 2017, 5, [Epub ahead of print]
Hypoxia, DovePress, 2017, 5, pp.11-20. ⟨10.2147/HP.S127042⟩
Hypoxia, 2017, 5, pp.11-20. ⟨10.2147/HP.S127042⟩
Hypoxia, Vol Volume 5, Pp 11-20 (2017)
Hypoxic Signaling
Hypoxic Signaling, 5, 11-20
Peter Ratcliffe,1,2 Peppi Koivunen,3 Johanna Myllyharju,3 Jiannis Ragoussis,4 Judith VMG Bovée,5 Ines Batinic-Haberle,6 Claire Vinatier,7 Valérie Trichet,8 Florence Robriquet,9 Lisa Oliver,9 Betty Gardie9,10 1Target Discovery Institute, University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::150a71aad5c45cfe6c0472d3befb4e9d
https://ora.ox.ac.uk/objects/uuid:d9b0c77f-dad1-4937-b6a9-4b8779e39394
https://ora.ox.ac.uk/objects/uuid:d9b0c77f-dad1-4937-b6a9-4b8779e39394
Autor:
Karl Rouger, Candice Babarit, Thibaut Larcher, Florence Robriquet, Laurence Dubreil, Hélicia Goubin, Laëtitia Guével, Mireille Ledevin
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, BioMed Central, 2016, 17 (1), pp.209. ⟨10.1186/s12891-016-1060-5⟩
BMC Musculoskeletal Disorders 1 (17), 209. (2016)
BMC Musculoskeletal Disorders, BioMed Central, 2016, 17 (1), pp.209. ⟨10.1186/s12891-016-1060-5⟩
BMC Musculoskeletal Disorders 1 (17), 209. (2016)
Background Duchenne muscular dystrophy (DMD) is an X-linked muscle disease that leads to fibre necrosis and progressive paralysis. At present, DMD remains a lethal disease without any effective treatment, requiring a better understanding of the patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab0ef1049d080e9204927ca3d7423c1f
https://hal.archives-ouvertes.fr/hal-01321085
https://hal.archives-ouvertes.fr/hal-01321085