Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Matthieu Bourderioux"'
Autor:
Parisa Bayat, Charlotte Rambaud, Bernard Priem, Matthieu Bourderioux, Mélanie Bilong, Salomé Poyer, Manuela Pastoriza-Gallego, Abdelghani Oukhaled, Jérôme Mathé, Régis Daniel
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-12 (2022)
Glycosaminoglycans (GAGs) are highly anionic functional polysaccharides with subtle structural variations that are very difficult to differentiate. Here the authors demonstrate proof-of-concept single-molecule detection by nanopore, taking a first st
Externí odkaz:
https://doaj.org/article/18b1c60b9c0f4531816fb57c2e5cef8d
Autor:
Régis Daniel, Matthieu Bourderioux, Murielle Jérôme, Parisa Bayat, Mélanie Bilong, Alexandre Giuliani
Publikováno v:
Glycobiology
Glycobiology, Oxford University Press (OUP), 2021, 31 (7), pp.751-761. ⟨10.1093/glycob/cwab004⟩
Glycobiology, 2021, 31 (7), pp.751-761. ⟨10.1093/glycob/cwab004⟩
Glycobiology, Oxford University Press (OUP), 2021, 31 (7), pp.751-761. ⟨10.1093/glycob/cwab004⟩
Glycobiology, 2021, 31 (7), pp.751-761. ⟨10.1093/glycob/cwab004⟩
Mammalian hyaluronidases are endo-N-acetyl-D-hexosaminidases involved in the catabolism of hyaluronic acid (HA) but their role in the catabolism of chondroitin sulfate (CS) is also examined. HA and CS are glycosaminoglycans implicated in several phys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4337fcaca9d6d5c1c397abb5b6697e93
https://hal-univ-evry.archives-ouvertes.fr/hal-03103354/document
https://hal-univ-evry.archives-ouvertes.fr/hal-03103354/document
Autor:
Cerina Chhuon, Matthieu Bourderioux, Isabelle Sermet-Gaudelus, Virginie Rollet-Cohen, Sophie Guérin-Pfyffer, Ida Chiara Guerrera, Thao Nguyen-Khoa, Aleksander Edelman, Joanna Lipecka, Alain Schmitt, Myriam Mesbahi, Vincent Jung
Publikováno v:
Journal of Proteomics
Journal of Proteomics, Elsevier, 2018, 185, ⟨10.1016/J.JPROT.2018.07.001⟩
Journal of Proteomics, 2018, 185, ⟨10.1016/J.JPROT.2018.07.001⟩
Journal of Proteomics, Elsevier, 2018, 185, ⟨10.1016/J.JPROT.2018.07.001⟩
Journal of Proteomics, 2018, 185, ⟨10.1016/J.JPROT.2018.07.001⟩
Cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) are pulmonary genetic disorders associated with inflammation and heterogeneous progression of the lung disease. We hypothesized that respiratory exosomes, nanovesicles circulating in the respi
Akademický článek
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Autor:
Aleksander Edelman, Joanna Lipecka, Marie-Andrée Bessard, Ida Chiara Guerrera, Peter van Endert, Matthieu Bourderioux, Cerina Chhuon
Publikováno v:
Proteomics. 16(13)
Efficient protein solubilization using detergents is required for in-depth proteome analysis, but successful LC-MS/MS analysis greatly depends on proper detergents removal. A commonly used sample processing method is the filter-aided sample preparati
Autor:
Marta Walczak, Danielle Tondelier, Estelle Escudier, Cerina Chhuon, Bertrand Knebelmann, Soumeya Bekri, Ida Chiara Guerrera, Aleksander Edelman, Ludovic Jeanson, Thao Nguyen-Khoa, Matthieu Bourderioux, Mario Ollero, Bernard Escudier
Publikováno v:
Journal of proteome research. 14(1)
Cystinuria is a purely renal, rare genetic disease caused by mutations in cystine transporter genes and characterized by defective cystine reabsorption leading to kidney stones. In 14% of cases, patients undergo nephrectomy, but given the difficulty
Autor:
Claudia Bich, Alain Brunelle, Emilie L. Saussereau, Janine Fritsch, Aleksander Edelman, Nicolas Desbenoit, Mario Ollero, Matthieu Bourderioux
Publikováno v:
International Journal of Biochemistry and Cell Biology
International Journal of Biochemistry and Cell Biology, Elsevier, 2014, 52, pp.77-82. ⟨10.1016/j.biocel.2014.01.026⟩
International Journal of Biochemistry and Cell Biology, Elsevier, 2014, 52, pp.77-82. 〈10.1016/j.biocel.2014.01.026〉
International Journal of Biochemistry and Cell Biology, Elsevier, 2014, 52, pp.77-82. ⟨10.1016/j.biocel.2014.01.026⟩
International Journal of Biochemistry and Cell Biology, Elsevier, 2014, 52, pp.77-82. 〈10.1016/j.biocel.2014.01.026〉
International audience; : A consistent body of research has linked cystic fibrosis (CF) with variations in the tissue and fluid content in a number of lipid molecules. However, little is known about the spatial localization of those variations. We ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d196fbc22f540ecba8ebf9f65cb71c0f
https://hal.archives-ouvertes.fr/hal-00995365
https://hal.archives-ouvertes.fr/hal-00995365