Similar articles for PMID: 28126847

Year	Number of Results
1980	1
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1991	1
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2020	10
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2023	4
2024	0

1

Lipids regulate the hydrolysis of membrane bound glucosylceramide by lysosomal β-glucocerebrosidase.

Abdul-Hammed M, Breiden B, Schwarzmann G, Sandhoff K. Abdul-Hammed M, et al. J Lipid Res. 2017 Mar;58(3):563-577. doi: 10.1194/jlr.M073510. Epub 2017 Jan 26. J Lipid Res. 2017. PMID: 28126847 Free PMC article.

2

Lysosomal degradation on vesicular membrane surfaces. Enhanced glucosylceramide degradation by lysosomal anionic lipids and activators.

Wilkening G, Linke T, Sandhoff K. Wilkening G, et al. J Biol Chem. 1998 Nov 13;273(46):30271-8. doi: 10.1074/jbc.273.46.30271. J Biol Chem. 1998. PMID: 9804787 Free article.

3

Membrane lipids and their degradation compounds control GM2 catabolism at intralysosomal luminal vesicles.

Anheuser S, Breiden B, Sandhoff K. Anheuser S, et al. J Lipid Res. 2019 Jun;60(6):1099-1111. doi: 10.1194/jlr.M092551. Epub 2019 Apr 15. J Lipid Res. 2019. PMID: 30988135 Free PMC article.

4

Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease.

Hein LK, Duplock S, Fuller M. Hein LK, et al. J Lipid Res. 2013 Jun;54(6):1691-1697. doi: 10.1194/jlr.M038232. Epub 2013 Apr 6. J Lipid Res. 2013. PMID: 23564732 Free PMC article.

5

Phosphatidylcholine synthesis is elevated in neuronal models of Gaucher disease due to direct activation of CTP:phosphocholine cytidylyltransferase by glucosylceramide.

Bodennec J, Pelled D, Riebeling C, Trajkovic S, Futerman AH. Bodennec J, et al. FASEB J. 2002 Nov;16(13):1814-6. doi: 10.1096/fj.02-0149fje. Epub 2002 Sep 5. FASEB J. 2002. PMID: 12223447

6

Membrane lipids regulate ganglioside GM2 catabolism and GM2 activator protein activity.

Anheuser S, Breiden B, Schwarzmann G, Sandhoff K. Anheuser S, et al. J Lipid Res. 2015 Sep;56(9):1747-61. doi: 10.1194/jlr.M061036. Epub 2015 Jul 14. J Lipid Res. 2015. PMID: 26175473 Free PMC article.

7

Analysis of glucocerebrosidase activity using N-(1-[14C]hexanoyl)-D-erythroglucosylsphingosine demonstrates a correlation between levels of residual enzyme activity and the type of Gaucher disease.

Meivar-Levy I, Horowitz M, Futerman AH. Meivar-Levy I, et al. Biochem J. 1994 Oct 15;303 ( Pt 2)(Pt 2):377-82. doi: 10.1042/bj3030377. Biochem J. 1994. PMID: 7980395 Free PMC article.

8

GCase and LIMP2 Abnormalities in the Liver of Niemann Pick Type C Mice.

van der Lienden MJC, Aten J, Marques ARA, Waas ISE, Larsen PWB, Claessen N, van der Wel NN, Ottenhoff R, van Eijk M, Aerts JMFG. van der Lienden MJC, et al. Int J Mol Sci. 2021 Mar 3;22(5):2532. doi: 10.3390/ijms22052532. Int J Mol Sci. 2021. PMID: 33802460 Free PMC article.

9

Glucosylceramidase mass and subcellular localization are modulated by cholesterol in Niemann-Pick disease type C.

Salvioli R, Scarpa S, Ciaffoni F, Tatti M, Ramoni C, Vanier MT, Vaccaro AM. Salvioli R, et al. J Biol Chem. 2004 Apr 23;279(17):17674-80. doi: 10.1074/jbc.M313517200. Epub 2004 Feb 2. J Biol Chem. 2004. PMID: 14757764 Free article.

10

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions.

Yañez MJ, Marín T, Balboa E, Klein AD, Alvarez AR, Zanlungo S. Yañez MJ, et al. Biochim Biophys Acta Mol Basis Dis. 2020 Oct 1;1866(10):165875. doi: 10.1016/j.bbadis.2020.165875. Epub 2020 Jun 6. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32522631 Free article. Review.

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