Intra-ER sorting of the peroxisomal membrane protein Pex3 relies on its luminal domain
Fakieh, Mohammad H, Drake, Peter J M, Lacey, Joanne, Munck, Joanne M, Motley, Alison M, Hettema, Ewald H
Published in Biology open (15.08.2013)
Published in Biology open (15.08.2013)
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Caenorhabditis elegans has a single pathway to target matrix proteins to peroxisomes
Motley, Alison M, Hettema, Ewald H, Ketting, Rene, Plasterk, Ronald, Tabak, Henk F
Published in EMBO reports (01.07.2000)
Published in EMBO reports (01.07.2000)
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Journal Article
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
Motley, Alison M, Hettema, Ewald H, Hogenhout, Eveline M, Brites, Pedro, ten Asbroek, Anneloor L.M.A, Wijburg, Frits A, Baas, Frank, Heijmans, Hugo S, Tabak, Henk F, Wanders, Ronald J.A, Distel, Ben
Published in Nature genetics (01.04.1997)
Published in Nature genetics (01.04.1997)
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Journal Article
dual function for Pex3p in peroxisome formation and inheritance
Munck, Joanne M, Motley, Alison M, Nuttall, James M, Hettema, Ewald H
Published in The Journal of cell biology (16.11.2009)
Published in The Journal of cell biology (16.11.2009)
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Journal Article
HIV-1 Nef-induced down-regulation of MHC class I requires AP-1 and clathrin but not PACS-1 and is impeded by AP-2
Lubben, Nienke B, Sahlender, Daniela A, Motley, Alison M, Lehner, Paul J, Benaroch, Philippe, Robinson, Margaret S
Published in Molecular biology of the cell (01.09.2007)
Published in Molecular biology of the cell (01.09.2007)
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Journal Article
Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata
Brites, Pedro, Motley, Alison M., Gressens, Pierre, Mooyer, Petra A.W., Ploegaert, Ingrid, Everts, Vincent, Evrard, Philippe, Carmeliet, Peter, Dewerchin, Mieke, Schoonjans, Luc, Duran, Marinus, Waterham, Hans R., Wanders, Ronald J.A., Baes, Myriam
Published in Human molecular genetics (15.09.2003)
Published in Human molecular genetics (15.09.2003)
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Journal Article
Mutational Spectrum in the PEX7 Gene and Functional Analysis of Mutant Alleles in 78 Patients with Rhizomelic Chondrodysplasia Punctata Type 1
Motley, Alison M., Brites, Pedro, Gerez, Lisya, Hogenhout, Eveline, Haasjes, Janet, Benne, Rob, Tabak, Henk F., Wanders, Ronald J.A., Waterham, Hans R.
Published in American journal of human genetics (01.03.2002)
Published in American journal of human genetics (01.03.2002)
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Journal Article
Functional Analysis of AP-2 α and μ2 Subunits
Motley, Alison M., Berg, Nicola, Taylor, Marcus J., Sahlender, Daniela A., Hirst, Jennifer, Owen, David J., Robinson, Margaret S.
Published in Molecular biology of the cell (01.12.2006)
Published in Molecular biology of the cell (01.12.2006)
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Journal Article
Functional analysis of AP-2 alpha and mu2 subunits
Motley, Alison M, Berg, Nicola, Taylor, Marcus J, Sahlender, Daniela A, Hirst, Jennifer, Owen, David J, Robinson, Margaret S
Published in Molecular biology of the cell (01.12.2006)
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Published in Molecular biology of the cell (01.12.2006)
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