Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Helene Guizouarn"'
Autor:
Helene Guizouarn, Gregory Barshtein
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/5a451b7db2f04dce9a43690c0dd5a962
Autor:
Helene Guizouarn, Gregory Barshtein
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/5bfabcfd1e3748478125e1d8a85c3ba3
Autor:
Achille Iolascon, Luigia De Falco, Franck Borgese, Maria Rosaria Esposito, Rosa Anna Avvisati, Pietro Izzo, Carmelo Piscopo, Helene Guizouarn, Andrea Biondani, Antonella Pantaleo, Lucia De Franceschi
Publikováno v:
Haematologica, Vol 94, Iss 8 (2009)
Background Stomatocytoses are a group of inherited autosomal dominant hemolytic anemias and include overhydrated hereditary stomatocytosis, dehydrated hereditary stomatocytosis, hereditary cryohydrocytosis and familial pseudohyperkalemia.Design and M
Externí odkaz:
https://doaj.org/article/9cca593df5394f18b9db1fc6786766ca
Autor:
Stefania Cannone, Maria Raffaella Greco, Tiago M. A. Carvalho, Helene Guizouarn, Olivier Soriani, Daria Di Molfetta, Richard Tomasini, Katrine Zeeberg, Stephan Joel Reshkin, Rosa Angela Cardone
Publikováno v:
Cancers
Cancers, 2022, 14 (15), ⟨10.3390/cancers14153737⟩
Cancers; Volume 14; Issue 15; Pages: 3737
Cancers, 2022, 14 (15), ⟨10.3390/cancers14153737⟩
Cancers; Volume 14; Issue 15; Pages: 3737
Simple Summary Here, we demonstrate for the first time that ECM composition cooperates with CAFs to jointly regulate/modulate the highly dynamic interactions between the CPC and CSC cell lines and establish a continuum between tumor initiation and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5e4d890d796fd1c1695a972c44b0bf
https://pubmed.ncbi.nlm.nih.gov/35954400
https://pubmed.ncbi.nlm.nih.gov/35954400
Autor:
Yohei Yamaguchi, Benoit Allegrini, Raphaël Rapetti-Mauss, Véronique Picard, Loïc Garçon, Peter Kohl, Olivier Soriani, Rémi Peyronnet, Hélène Guizouarn
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Hereditary Xerocytosis, a rare hemolytic anemia, is due to gain of function mutations in PIEZO1, a non-selective cation channel activated by mechanical stress. How these PIEZO1 mutations impair channel function and alter red blood cell (RBC) physiolo
Externí odkaz:
https://doaj.org/article/1d9a91a5bc6d474c92aa25835614ff12
Autor:
Leonid Livshits, Gregory Barshtein, Dan Arbell, Alexander Gural, Carina Levin, Hélène Guizouarn
Publikováno v:
Biomolecules, Vol 11, Iss 7, p 992 (2021)
Red blood cell (RBC) transfusion is one of the most common therapeutic procedures in modern medicine. Although frequently lifesaving, it often has deleterious side effects. RBC quality is one of the critical factors for transfusion efficacy and safet
Externí odkaz:
https://doaj.org/article/cda2b49d77bb49a0a9a13f6834f87c6c
Autor:
Raphaël Rapetti-Mauss, Véronique Picard, Corinne Guitton, Khaldoun Ghazal, Valérie Proulle, Catherine Badens, Olivier Soriani, Loïc Garçon, Hélène Guizouarn
Publikováno v:
Haematologica, Vol 102, Iss 10 (2017)
Externí odkaz:
https://doaj.org/article/2ee5ded7fbf34d9fa90f899b9717f24b
Publikováno v:
Haematologica, Vol 101, Iss 11 (2016)
Externí odkaz:
https://doaj.org/article/6d6cea14f2d64b14bf452728c86c9063
Publikováno v:
International Journal of Cell Biology, Vol 2011 (2011)
Missense mutations in the erythroid band 3 protein (Anion Exchanger 1) have been associated with hereditary stomatocytosis. Features of cation leaky red cells combined with functional expression of the mutated protein led to the conclusion that the A
Externí odkaz:
https://doaj.org/article/c22936974a514406aad6d1b43222ecf4