Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Stephen A Murray"'
Autor:
Qi-Zhu Wu, Diane Fatkin, Nicolas Plachta, Anjana Chandran, Stephanie E. Simonds, Milena B. Furtado, Nadia Rosenthal, James T. Pearson, Christine Biben, David Willians, Taylor J. Willow, Gurpreet Kaur, Joelle Perera, Hieu T. Nim, Richard P. Harvey, Julia C. Wilmanns, Ekaterina Salimova, James M. Denegre, Olivia Hon, David M. Kaye, Mirana Ramialison, Stephen A. Murray, Mauro W. Costa, Michael A. Cowley
Mutations in the Nkx2-5 gene are a main cause of congenital heart disease. Several studies have addressed the phenotypic consequences of disrupting the Nkx2-5 gene locus, although animal models to date failed to recapitulate the full spectrum of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f696b31663b1143e8fa0f2aa2167515e
http://hdl.handle.net/10044/1/56521
http://hdl.handle.net/10044/1/56521
Autor:
Claire A. Walshe, Stephen M Murray, Claude H.T. Chan, Stephen A. Beers, Andrei Ivanov, Jekaterina Erenpreisa, Kerry L. Cox, Mark S. Cragg, Kathleen N. Potter, Tetyana Klymenko, Timothy M Illidge, Martin J. Glennie, Waleed Alduaij, Jamie Honeychurch
mAbs are becoming increasingly utilized in the treatment of lymphoid disorders. Although Fc-FcgammaR interactions are thought to account for much of their therapeutic effect, this does not explain why certain mAb specificities are more potent than ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24dafec2099dd337c52a583daa416bdf
https://europepmc.org/articles/PMC2719942/
https://europepmc.org/articles/PMC2719942/