Showing 1 - 13 results of 13 for search 'Sillence, D', query time: 0.05s
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Introduction: Glycosphingolipids in cell biology and disease. by Sillence, D, Platt, F
Published 2004Journal article -
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Glycosphingolipids in endocytic membrane transport. by Sillence, D, Platt, F
Published 2004Journal article -
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Storage diseases: new insights into sphingolipid functions. by Sillence, D, Platt, F
Published 2003Journal article -
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Glycosphingolipid storage leads to the enhanced degradation of the B cell receptor in Sandhoff disease mice. by te Vruchte, D, Jeans, A, Platt, F, Sillence, D
Published 2010Journal article -
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Glucosylceramide modulates membrane traffic along the endocytic pathway. by Sillence, D, Puri, V, Marks, D, Butters, T, Dwek, R, Pagano, R, Platt, F
Published 2002Journal article -
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The association of Shiga-like toxin with detergent-resistant membranes is modulated by glucosylceramide and is an essential requirement in the endoplasmic reticulum for a cytotoxic... by Smith, D, Sillence, D, Falguières, T, Jarvis, R, Johannes, L, Lord, J, Platt, F, Roberts, L
Published 2006Journal article -
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Accumulation of glycosphingolipids in Niemann-Pick C disease disrupts endosomal transport. by te Vruchte, D, Lloyd-Evans, E, Veldman, R, Neville, D, Dwek, R, Platt, F, van Blitterswijk, W, Sillence, D
Published 2004Journal article -
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Treatment with miglustat reverses the lipid-trafficking defect in Niemann-Pick disease type C. by Lachmann, R, te Vruchte, D, Lloyd-Evans, E, Reinkensmeier, G, Sillence, D, Fernandez-Guillen, L, Dwek, R, Butters, T, Cox, T, Platt, F
Published 2004Journal article -
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Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. by Lloyd-Evans, E, Morgan, A, He, X, Smith, D, Elliot-Smith, E, Sillence, D, Churchill, G, Schuchman, E, Galione, A, Platt, F
Published 2008Journal article -
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Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies. by Ilkovski, B, Pagnamenta, A, O'Grady, G, Kinoshita, T, Howard, M, Lek, M, Thomas, B, Turner, A, Christodoulou, J, Sillence, D, Knight, S, Popitsch, N, Keays, D, Anzilotti, C, Goriely, A, Waddell, L, Brilot, F, North, K, Kanzawa, N, Macarthur, D, Taylor, J, Kini, U, Murakami, Y, Clarke, N
Published 2015Journal article -
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Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias. by Le Goff, C, Mahaut, C, Wang, L, Allali, S, Abhyankar, A, Jensen, S, Zylberberg, L, Collod-Beroud, G, Bonnet, D, Alanay, Y, Brady, A, Cordier, M, Devriendt, K, Genevieve, D, Kiper, P, Kitoh, H, Krakow, D, Lynch, SA, Le Merrer, M, Mégarbane, A, Mortier, G, Odent, S, Polak, M, Rohrbach, M, Sillence, D
Published 2011Journal article -
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NAD deficiency, congenital malformations and niacin supplementation by Shi, H, Enriquez, A, Rapadas, M, Martin, E, Wang, R, Moreau, J, Lim, C, Szot, J, Ip, E, Hughes, J, Sugimoto, K, Humphreys, D, McInerney-Leo, A, Leo, P, Maghzal, G, Halliday, J, Smith, J, Colley, A, Mark, P, Collins, F, Sillence, D, Winlaw, D, Ho, J, Guillemin, G, Brown, M, Kikuchi, K, Thomas, P, Stocker, R, Giannoulatou, E, Chapman, G, Duncan, E, Sparrow, D, Dunwoodie, S
Published 2017Journal article