Zobrazeno 1 - 5
of 5
pro vyhledávání: '"François Monjaret"'
Autor:
Sylvie Juliant, Anne Harduin-Lepers, François Monjaret, Béatrice Catieau, Marie-Luce Violet, Pierre Cérutti, Annick Ozil, Martine Duonor-Cérutti
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e110422 (2014)
The core alpha1,6-fucosyltransferase (FUT8) catalyzes the transfer of a fucosyl moiety from GDP-fucose to the innermost asparagine-linked N-acetylglucosamine residue of glycoproteins. In mammals, this glycosylation has an important function in many f
Externí odkaz:
https://doaj.org/article/3c5f7d53abfa483095ad24e4c66f574b
Autor:
Sandra Ortiz-Cuaran, Lucas Michon, Marion Godefroy, Joyce Levy, Osman Osman, Maxime Boussageon, Aurélie Swalduz, Maurice Pérol, Bruno Russias, François Monjaret, Pierre Saintigny
Publikováno v:
Cancer Research. 82:3478-3478
The pleura is a frequent metastatic site during the evolution of cancers, which can lead to a symptomatic accumulation of pleural fluid that contains tumor and immune cells. To improve patients’ comfort this fluid is removed via chest draining, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7674225f17e0a03c3fd8cf6b39f72b26
https://doi.org/10.1158/1538-7445.am2022-3478
https://doi.org/10.1158/1538-7445.am2022-3478
Autor:
Florence Le Roy, Isabelle Richard, François Monjaret, Nathalie Bourg, Carinne Roudaut, Laurence Suel, Karine Charton
Publikováno v:
Molecular Therapy
Molecular Therapy, Nature Publishing Group, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
Molecular Therapy, Cell Press, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
Molecular Therapy, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
Molecular Therapy, Nature Publishing Group, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
Molecular Therapy, Cell Press, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
Molecular Therapy, 2014, 22 (6), pp.1176-1187. ⟨10.1038/mt.2014.35⟩
International audience; Muscular dystrophies are a group of genetically distinct diseases for which no treatment exists. While gene transfer approach is being tested for several of these diseases, such strategies can be hampered when the size of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63c4508b17e05d357b960ecb7354034a
https://doi.org/10.1038/mt.2014.35
https://doi.org/10.1038/mt.2014.35
Autor:
Amelie Argento, Mathieu Fernandes, Sébastien Degot, François Monjaret, Eve Duchemin-Pelletier, Joanne Young
Publikováno v:
Journal of laboratory automation. 21(2)
Adoption of spheroids within high-content screening (HCS) has lagged behind high-throughput screening (HTS) due to issues with running complex assays on large three-dimensional (3D) structures.To enable multiplexed imaging and analysis of spheroids,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1459ac4b8c0aa21f428465008627994b
https://pubmed.ncbi.nlm.nih.gov/26385905
https://pubmed.ncbi.nlm.nih.gov/26385905
Autor:
Nathalie Daniele, François Monjaret, Anne Tarrade, Anna Vihola, Jaakko Sarparanta, Bjarne Udd, Isabelle Richard, Evelyne Gicquel, Karine Charton, Carinne Roudaut
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2010, 19 (23), pp.4608-4624. ⟨10.1093/hmg/ddq388⟩
Human Molecular Genetics, Oxford University Press (OUP), 2010, 19 (23), pp.4608-4624. ⟨10.1093/hmg/ddq388⟩
Human Molecular Genetics, 2010, 19 (23), pp.4608-4624. ⟨10.1093/hmg/ddq388⟩
Human Molecular Genetics, Oxford University Press (OUP), 2010, 19 (23), pp.4608-4624. ⟨10.1093/hmg/ddq388⟩
International audience; The dominant tibial muscular dystrophy (TMD) and recessive limb-girdle muscular dystrophy 2J are allelicdisorders caused by mutations in the C-terminus of titin, a giant sarcomeric protein. Both clinical presentationswere init
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d35560a1faf1aa6de20c3d1100bf709d
https://hal-univ-evry.archives-ouvertes.fr/hal-02321460
https://hal-univ-evry.archives-ouvertes.fr/hal-02321460
