Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Jean-Pierre Cartron"'
Autor:
Samer Al-Samir, Dominique Goossens, Jean-Pierre Cartron, Søren Nielsen, Frank Scherbarth, Stephan Steinlechner, Gerolf Gros, Volker Endeward
Publikováno v:
Frontiers in Physiology, Vol 7 (2016)
We have measured maximal oxygen consumption (V’O2,max) of mice lacking one or two of the established mouse red-cell CO2 channels AQP1, AQP9 and Rhag. We intended to study whether these proteins, by acting as channels for O2, determine O2 exchange i
Externí odkaz:
https://doaj.org/article/179539f0bf1848789c341528ea1121e6
Autor:
Dominique Goossens, Nelly da Silva, Sylvain Metral, Ulrich Cortes, Isabelle Callebaut, Julien Picot, Isabelle Mouro-Chanteloup, Jean-Pierre Cartron
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80460 (2013)
Anti-RhD prophylaxis of haemolytic disease of the fetus and newborn (HDFN) is highly effective, but as the suppressive mechanism remains uncertain, a mouse model would be of interest. Here we have generated transgenic mice expressing human RhAG and R
Externí odkaz:
https://doaj.org/article/e1291796dd0d4b67bd6d3d34c0b50523
Autor:
Marie-Marcelle Trinh-Trang-Tan, Camilo Vilela-Lamego, Julien Picot, Marie-Paule Wautier, Jean-Pierre Cartron
Publikováno v:
Haematologica, Vol 95, Iss 5 (2010)
Background Abnormal adhesiveness of red blood cells to endothelium has been implicated in vaso-occlusive crisis of sickle cell disease. The present study examined whether the SAD mouse model exhibits the same abnormalities of red blood cell adhesion
Externí odkaz:
https://doaj.org/article/3178d5f0931649eb95bfc4b06f9fa632
Autor:
Marie-Hélène Odièvre, Viviane Bony, Malika Benkerrou, Claudine Lapouméroulie, Corinne Alberti, Rolande Ducrocq, Evelyne Jacqz-Aigrain, Jacques Elion, Jean-Pierre Cartron
Publikováno v:
Haematologica, Vol 93, Iss 4 (2008)
Background We investigated adhesion receptor levels on red blood cells, reticulocytes and erythroid progenitors from children with sickle cell disease treated or not with hydroxyurea.Design and Methods Four groups of patients were investigated: (i) c
Externí odkaz:
https://doaj.org/article/ded5bbb238fd47ee9e5580894717dc44
Autor:
Bérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar, Thankam S Nair, Lucy Yang, Seyve Landry, Guy Laiguillon, Claudine Giroux‐Lathuile, Sophie Anselme‐Martin, Hanane El Kenz, Olivier Hermine, Narla Mohandas, Jean Pierre Cartron, Yves Colin, Olivier Detante, Raphaël Marlu, Caroline Le Van Kim, Thomas E Carey, Slim Azouzi, Thierry Peyrard
Publikováno v:
EMBO Molecular Medicine. 15
Autor:
Farsad Eskandary, Nicolas Kozakowski, Jean‐Pierre Cartron, Yves Colin Aronovicz, Georg A. Böhmig, Alexander Kainz, Johannes Kläger, Stephan Segerer, Heinz Regele
Publikováno v:
Transplant International
Gene expression profiling of renal allograft biopsies revealed the Duffy antigen receptor for chemokines (DARC) as being strikingly upregulated in antibody‐mediated rejection (ABMR). DARC has previously been shown to be associated with endothelial
Autor:
Bérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar, Thankam S. Nair, Lucy Yang, Guy Laiguillon, Sophie Anselme-Martin, Claudine Giroux-Lathuile, Hanane El Kenz, Olivier Hermine, Narla Mohandas, Jean Pierre Cartron, Yves Colin, Olivier Detante, Caroline Le Van Kim, Thomas E. Carey, Slim Azouzi, Thierry Peyrard
Recent genome-wide association and murine studies identified the human neutrophil antigen -3a/b polymorphism (HNA-3a/b) in SLC44A2 (rs2288904-G/A) as a risk factor in venous thromboembolism (VTE). The choline transporter-like protein CTL2 encoded by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b45c4f9ce442f24816f4dac1fef89f4
https://doi.org/10.1101/2022.05.13.22273920
https://doi.org/10.1101/2022.05.13.22273920
Autor:
Christophe Chenet, Yasmine Mammasse, Rachel Petermann, Damien Drubay, Jean-Pierre Cartron, Corinne Martageix, William Vainchenker
Publikováno v:
British Journal of Haematology. 190:787-798
Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is the consequence of platelet destruction by maternal alloantibodies against fetal human platelet antigens (HPA). This may result in intracranial haemorrhages (ICH) or even fetal death. Currentl
Autor:
Gaël Nicolas, Thierry Peyrard, Mahmoud Mikdar, Slim Azouzi, Patrick Mayeux, Christine Bole-Feysot, Alexandra Willemetz, Olivier Hermine, Cédric Vrignaud, Marc Cloutier, Emilie-Fleur Gautier, Alexandre Raneri, Virginie Salnot, Maryse St-Louis, Caroline Le Van Kim, Jessica Constanzo-Yanez, Jean-Pierre Cartron, Gabriele Jedlitschky, Nancy Robitaille, Carole Éthier, Patricia Hermand, Patrick Nitschke, Yves Colin
Publikováno v:
Blood
Blood, 2019, 135 (6), pp.441-448. ⟨10.1182/blood.2019002320⟩
Blood, American Society of Hematology, 2019, 135 (6), pp.441-448. ⟨10.1182/blood.2019002320⟩
Blood, 2019, 135 (6), pp.441-448. ⟨10.1182/blood.2019002320⟩
Blood, American Society of Hematology, 2019, 135 (6), pp.441-448. ⟨10.1182/blood.2019002320⟩
The rare PEL-negative phenotype is one of the last blood groups with an unknown genetic basis. By combining whole-exome sequencing and comparative global proteomic investigations, we found a large deletion in the ABCC4/MRP4 gene encoding an ATP-bindi
Autor:
Karine Siquier, Thierry Peyrard, Berengere Koehl, Nicole Chemlay, Giulia Barcia, Hisham Megahed, Cécile Masson, Samer Wehbi, Yves Colin, Slim Azouzi, Vincent Cantagrel, Caroline Le Van Kim, Romain Duval, Gaël Nicolas, Alexandra Willemetz, Stanislas Lyonnet, Yoshiko Murakami, Olivier Hermine, Marie Hully, Taroh Kinoshita, Jean-Pierre Cartron, Mahmoud Mikdar, Cedric Vrignaud, Agnès Rötig
Publikováno v:
Transfusion Clinique et Biologique. 28:S30
Le phenotype erythrocytaire Emm- a ete decrit en 1973 mais reste l’un des derniers groupes sanguins de base genetique inconnue (antigene de prevalence elevee de la serie 901). Il avait ete propose qu’Emm serait porte par une proteine ancree a la