Zobrazeno 1 - 10
of 20
pro vyhledávání: '"R. Leijendekker"'
Autor:
Andrew J. Leigh-Brown, R. Leijendekker, Graça Raposo, Donald Innes, Philippe Benaroch, Marilyn Moore, Hans J. Geuze
Publikováno v:
Traffic. 3:718-729
Macrophages are important targets for HIV-1 infection and harbor the virions in an as yet unidentified organelle. To determine the location of HIV-1 in these cells, an extensive analysis of primary human macrophages infected in vitro with HIV-1 was c
Publikováno v:
Journal of Biological Chemistry. 273:25880-25888
UDP-galactose:ceramide galactosyltransferase (CGalT) transfers UDP-galactose to ceramide to form the glycosphingolipid galactosylceramide. Galactosylceramide is the major constituent of myelin and is also highly enriched in many epithelial cells, whe
Publikováno v:
The Journal of Cell Biology
Misfolded membrane proteins are rapidly degraded, often shortly after their synthesis and insertion in the endoplasmic reticulum (ER), but the exact location and mechanisms of breakdown remain unclear. We have exploited the requirement of MHC class I
Autor:
Graça Raposo, Jacques Neefjes, R. Leijendekker, Hans J. Geuze, Viola Oorschot, Peter J. Peters, Hidde L. Ploegh
Publikováno v:
The Journal of Experimental Medicine
In human B lymphoblastoid cell lines, the majority of major histocompatibility complex (MHC) class II heterodimers are located on the cell surface and in endocytic compartments, while invariant chain (Ii)-associated class II molecules represent biosy
Publikováno v:
The Journal of biological chemistry. 277(12)
The small GTPase rab4 is associated with early endosomes and regulates membrane recycling in fibroblasts. rab4 is present in epithelial cells; however, neither its localization nor function has been established in this cell type. We transfected Madin
Autor:
R. Leijendekker, Peter van der Sluijs, Lisya Gerez, Bas Nagelkerken, Marcel van Raak, Karin Mohrmann
Publikováno v:
Electrophoresis. 18(14)
Rab GTPases are localized on the cytoplasmic surface of most intracellular organelles where they play a role in the regulation of vesicular transport. As it has been difficult to detect endogenous rab proteins by morphological methods, their localiza
Autor:
Peter M.T. Deen, Michèle Lonergan, J.P.L. Rijss, C.H. van Os, K. Morgan, R. Leijendekker, P. van der Sluijs, M. Fujiwara, Erik-Jan Kamsteeg, Daniel G. Bichet, Marie-Françoise Arthus, S.M. Mulders
Publikováno v:
Journal of Clinical Investigation, 102, pp. 57-66
Journal of Clinical Investigation, 102, 57-66
Journal of Clinical Investigation, 102, 57-66
Mutations in the aquaporin-2 (AQP2) water channel gene cause autosomal recessive nephrogenic diabetes insipidus (NDI). Here we report the first patient with an autosomal dominant form of NDI, which is caused by a G866A transition in the AQP2 gene of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::788d1a3f2ba7951b3a9254de33fb9134
https://hdl.handle.net/2066/188746
https://hdl.handle.net/2066/188746
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