Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anita Le-Heron"'
Autor:
Lucy Sneezum, Kevin Eislmayr, Helene Dworak, Vitaly Sedlyarov, Anita Le Heron, Florian Ebner, Irmgard Fischer, Yoichiro Iwakura, Pavel Kovarik
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
The bioavailability of the major pro-inflammatory cytokines IL-1α and IL-1β is tightly controlled by transcription and post-translational processing to prevent hyperinflammation. The role of mRNA decay in maintenance of physiological IL-1 amounts r
Externí odkaz:
https://doaj.org/article/e77c6edfb5a14fc29a5f224721f77f84
Autor:
Audrey Bourdon, Virginie François, Liwen Zhang, Aude Lafoux, Bodvael Fraysse, Gilles Toumaniantz, Thibaut Larcher, Tiphaine Girard, Mireille Ledevin, Cyrielle Lebreton, Agnès Hivonnait, Anna Creismeas, Marine Allais, Basile Marie, Justine Guguin, Véronique Blouin, Séverine Remy, Ignacio Anegon, Corinne Huchet, Alberto Malerba, Betty Kao, Anita Le Heron, Philippe Moullier, George Dickson, Linda Popplewell, Oumeya Adjali, Federica Montanaro, Caroline Le Guiner
Publikováno v:
Gene Therapy. 29:520-535
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d9c1614fc49440d97af2761d82421d2
https://doi.org/10.1038/s41434-022-00317-6
https://doi.org/10.1038/s41434-022-00317-6
Autor:
Shanthi Herath, HH Abdul-Razak, Susan Jarmin, Marinee Chuah, Linda Popplewell, Chiara Sidoli, Ngoc Lu-Nguyen, Alberto Malerba, George Dickson, Thierry VandenDriessche, Anita Le Heron
Publikováno v:
Human Gene Therapy. 32:1138-1146
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease that affects 1:5,000 live male births and is characterized by muscle wasting. By the age of 13 years, affected individuals are often wheelchair bound and suffer from respiratory and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e4112daffd9550d891767f9f1b9911c
https://doi.org/10.1089/hum.2020.325
https://doi.org/10.1089/hum.2020.325
Autor:
Audrey, Bourdon, Virginie, François, Liwen, Zhang, Aude, Lafoux, Bodvael, Fraysse, Gilles, Toumaniantz, Thibaut, Larcher, Tiphaine, Girard, Mireille, Ledevin, Cyrielle, Lebreton, Agnès, Hivonnait, Anna, Creismeas, Marine, Allais, Basile, Marie, Justine, Guguin, Véronique, Blouin, Séverine, Remy, Ignacio, Anegon, Corinne, Huchet, Alberto, Malerba, Betty, Kao, Anita, Le Heron, Philippe, Moullier, George, Dickson, Linda, Popplewell, Oumeya, Adjali, Federica, Montanaro, Caroline, Le Guiner
Publikováno v:
Gene therapy. 29(9)
Duchenne muscular dystrophy (DMD) is a muscle wasting disorder caused by mutations in the gene encoding dystrophin. Gene therapy using micro-dystrophin (MD) transgenes and recombinant adeno-associated virus (rAAV) vectors hold great promise. To overc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::932d0ee578a32dab628daaac46e8bb2b
https://pubmed.ncbi.nlm.nih.gov/35449294
https://pubmed.ncbi.nlm.nih.gov/35449294
Autor:
Graham McClorey, Amédée Mollard, Stéphanie Lorain, Sofia Benkhelifa-Ziyyat, Susan Jarmin, Thomas Voit, Anita Le Heron, Maëva Le Hir, Laura Julien, Matthew J.A. Wood, Cécile Peccate, George Dickson
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2016, 25, pp.3555-3563. ⟨10.1093/hmg/ddw201⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25, pp.3555-3563. ⟨10.1093/hmg/ddw201⟩
Human Molecular Genetics, 2016, 25, pp.3555-3563. ⟨10.1093/hmg/ddw201⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25, pp.3555-3563. ⟨10.1093/hmg/ddw201⟩
International audience; In preclinical models for Duchenne muscular dystrophy, dystrophin restoration during adeno-associated virus (AAV)-U7-mediated exon-skipping therapy was shown to decrease drastically after six months in treated muscles. This de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7e4aa968cad10b8526c38947b77746a
https://hal.sorbonne-universite.fr/hal-01590933
https://hal.sorbonne-universite.fr/hal-01590933
Autor:
Klaudia Kawecka, Alberto Malerba, Michael Theodoulides, Takis Athanasopoulos, Hanna Kymalainen, Yalin Hasoglu, Susan Jarmin, Anita Le-Heron, Linda Popplewell, George Dickson
Publikováno v:
Current gene therapy. 15(4)
Duchenne muscular dystrophy (DMD), an X-linked inherited musclewasting disease primarily affecting young boys with prevalence of between1:3,500- 1:5,000, is a rare genetic disease caused by defects in the gene for dystrophin. Dystrophin protein is cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46579a6d32796838e68beea8e730e633
https://pubmed.ncbi.nlm.nih.gov/26159373
https://pubmed.ncbi.nlm.nih.gov/26159373
Autor:
Maria Gabriela Boza-Morán, Sara Bernal, Klaus Wanisch, Eduardo F. Tizzano, Rafael J. Yáñez-Muñoz, Anita Le Heron, Eva Also-Rallo, Jiing-Kuan Yee, Laura Alias, Mathilde Girard, Cécile V. Denis, Rebeca Martínez-Hernández
Publikováno v:
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by mutations in Survival Motor Neuron 1 (SMN1), leading to degeneration of alpha motor neurons (MNs) but also affecting other cell types. Induced pluripotent stem cell (iPSC)-derived hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::426581c77115e30ded3d69665dc6ae59
https://pubmed.ncbi.nlm.nih.gov/26114395
https://pubmed.ncbi.nlm.nih.gov/26114395