Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nelly Poulain"'
Autor:
Stéphanie Ngo, Jacques Blouin, Lubka T. Roumenina, Nelly Poulain, Véronique Frémeaux-Bacchi, Pauline Bordereau, Stéphane Roncelin, Marie-Agnès Dragon-Durey
Publikováno v:
Revue Francophone des Laboratoires. 2012:31-37
Resume Le systeme du complement est un ensemble de proteines qui participe aux mecanismes de defense naturels de l’hote contre l’infection, au maintien en solution et a l’elimination des complexes immuns. Compte tenu des fonctions du systeme du
Autor:
Stéphane Roncelin, Paula Vieira Martins, Pauline Bordereau, Véronique Frémeaux-Bacchi, Marie-Agnès Dragon-Durey, Stéphanie Ngo, Nelly Poulain, Jérémie Rosain
Publikováno v:
Annales de biologie clinique. 72(3)
The complement system is a complex system involving serum and membrane proteins interacting in a regulated manner. The complement system plays a major role in antibacterial immunity, in inflammation, and in immune complex processing. Therefore, defic
Autor:
Lubka T, Roumenina, Roxane, Roquigny, Caroline, Blanc, Nelly, Poulain, Stéphanie, Ngo, Marie-Agnès, Dragon-Durey, Véronique, Frémeaux-Bacchi
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1100
The atypical hemolytic uremic syndrome (aHUS) is a paradigm of a disease, caused by overactivation of the alternative complement pathway secondary to a not well-understood trigger event. About 60 % of the patients present genetic or acquired abnormal
Autor:
Marie-Agnès, Dragon-Durey, Caroline, Blanc, Lubka T, Roumenina, Nelly, Poulain, Stéphanie, Ngo, Pauline, Bordereau, Véronique, Frémeaux-Bacchi
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1100
Non-Shiga-toxin-associated hemolytic uremic syndrome (atypical HUS) is a rare form of thrombotic microangiopathy which associates hemolytic anemia, thrombocytopenia, and acute renal failure. In 10 % of cases the disease is linked to presence of autoa
Autor:
Pauline Bordereau, Véronique Frémeaux-Bacchi, Lubka T. Roumenina, Caroline Blanc, Stéphanie Ngo, Nelly Poulain, Marie-Agnès Dragon-Durey
Publikováno v:
The Complement System ISBN: 9781627037235
Non-Shiga-toxin-associated hemolytic uremic syndrome (atypical HUS) is a rare form of thrombotic microangiopathy which associates hemolytic anemia, thrombocytopenia, and acute renal failure. In 10 % of cases the disease is linked to presence of autoa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb527eab6874308900a626b94a68d5e7
https://doi.org/10.1007/978-1-62703-724-2_20
https://doi.org/10.1007/978-1-62703-724-2_20
Autor:
Nelly Poulain, Véronique Frémeaux-Bacchi, Stéphanie Ngo, Roxane Roquigny, Marie-Agnès Dragon-Durey, Lubka T. Roumenina, Caroline Blanc
Publikováno v:
The Complement System ISBN: 9781627037235
The atypical hemolytic uremic syndrome (aHUS) is a paradigm of a disease, caused by overactivation of the alternative complement pathway secondary to a not well-understood trigger event. About 60 % of the patients present genetic or acquired abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebe89e2a1ab24c3b4c798655c96bab8b
https://doi.org/10.1007/978-1-62703-724-2_19
https://doi.org/10.1007/978-1-62703-724-2_19