Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Willem P. Vermeulen"'
Publikováno v:
Molecular Membrane Biology. 13:95-102
Decreasing the size of the outer leaflet pool of phosphatidylethanolamine (PE) in the erythrocyte membrane by treatment of intact cells with either phospholipase A2, or trinitrobenzenesulphonic acid (TNBS), causes a corresponding decrease in Mg(2+)-A
Autor:
Ben Roelofsen, Jacob J. Briedé, J.A.F. Op den Kamp, R.J. Kraaijenhagen, G. Bunt, Willem P. Vermeulen
Publikováno v:
British Journal of Haematology, 90(1), 56-64. Wiley
Hereditary spherocytosis (HS) is a congenital haemolytic anaemia which is characterized by a great variety of structural defects in the red cell's membrane skeleton and/or deficiencies in particular membrane (skeletal) proteins. Enhanced (Mg2+)-depen
Autor:
Ben Roelofsen, Esther Middelkoop, Willem P. Vermeulen, J.A.F. Op den Kamp, Alexander J. Smith
Publikováno v:
Molecular Dynamics of Biomembranes ISBN: 9783642647079
Shortly after its discovery in the early seventies, the phenomenon of an asymmetric distribution of phospholipids in the red cell and other plasma membranes raised questions regarding its generation and maintenance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe978923cb96f747d6910b3839529b9
https://doi.org/10.1007/978-3-642-61126-1_29
https://doi.org/10.1007/978-3-642-61126-1_29