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Items: 1 to 20 of 61

1.

Pathogenic cascades in lysosomal disease-Why so complex?

Walkley SU.

J Inherit Metab Dis. 2009 Apr;32(2):181-9. doi: 10.1007/s10545-008-1040-5. Epub 2009 Jan 7. Review.

2.

Pathogenic mechanisms in lysosomal disease: a reappraisal of the role of the lysosome.

Walkley SU.

Acta Paediatr. 2007 Apr;96(455):26-32. Review.

PMID:
17391436
3.

Cellular pathology of lysosomal storage disorders.

Walkley SU.

Brain Pathol. 1998 Jan;8(1):175-93. Review.

PMID:
9458175
4.

The cell biology of disease: lysosomal storage disorders: the cellular impact of lysosomal dysfunction.

Platt FM, Boland B, van der Spoel AC.

J Cell Biol. 2012 Nov 26;199(5):723-34. doi: 10.1083/jcb.201208152. Review.

5.

The cellular pathology of lysosomal diseases.

Cox TM, Cachón-González MB.

J Pathol. 2012 Jan;226(2):241-54. doi: 10.1002/path.3021. Review.

PMID:
21990005
6.

Autophagy, lipophagy and lysosomal lipid storage disorders.

Ward C, Martinez-Lopez N, Otten EG, Carroll B, Maetzel D, Singh R, Sarkar S, Korolchuk VI.

Biochim Biophys Acta. 2016 Apr;1861(4):269-84. doi: 10.1016/j.bbalip.2016.01.006. Epub 2016 Jan 14. Review.

7.

Lysosomal storage disorders.

Vellodi A.

Br J Haematol. 2005 Feb;128(4):413-31. Review.

PMID:
15686451
8.

Lysosomal storage disease: revealing lysosomal function and physiology.

Parkinson-Lawrence EJ, Shandala T, Prodoehl M, Plew R, Borlace GN, Brooks DA.

Physiology (Bethesda). 2010 Apr;25(2):102-15. doi: 10.1152/physiol.00041.2009. Review.

PMID:
20430954
9.

Secondary accumulation of gangliosides in lysosomal storage disorders.

Walkley SU.

Semin Cell Dev Biol. 2004 Aug;15(4):433-44. Review.

PMID:
15207833
10.

Sphingolipid lysosomal storage disorders.

Platt FM.

Nature. 2014 Jun 5;510(7503):68-75. doi: 10.1038/nature13476. Review.

PMID:
24899306
11.

Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders.

Plotegher N, Duchen MR.

Trends Mol Med. 2017 Feb;23(2):116-134. doi: 10.1016/j.molmed.2016.12.003. Epub 2017 Jan 19. Review.

PMID:
28111024
12.

A shortcut to the lysosome: the mannose-6-phosphate-independent pathway.

Coutinho MF, Prata MJ, Alves S.

Mol Genet Metab. 2012 Nov;107(3):257-66. doi: 10.1016/j.ymgme.2012.07.012. Epub 2012 Jul 20. Review.

PMID:
22884962
13.

The lysosome: from waste bag to potential therapeutic target.

Appelqvist H, Wäster P, Kågedal K, Öllinger K.

J Mol Cell Biol. 2013 Aug;5(4):214-26. doi: 10.1093/jmcb/mjt022. Review.

PMID:
23918283
14.

Lysosomal lipid storage diseases.

Schulze H, Sandhoff K.

Cold Spring Harb Perspect Biol. 2011 Jun 1;3(6). pii: a004804. doi: 10.1101/cshperspect.a004804. Review.

15.

Common and uncommon pathogenic cascades in lysosomal storage diseases.

Vitner EB, Platt FM, Futerman AH.

J Biol Chem. 2010 Jul 2;285(27):20423-7. doi: 10.1074/jbc.R110.134452. Epub 2010 Apr 29. Review.

16.

Drug induced phospholipidosis: an acquired lysosomal storage disorder.

Shayman JA, Abe A.

Biochim Biophys Acta. 2013 Mar;1831(3):602-11. doi: 10.1016/j.bbalip.2012.08.013. Epub 2012 Aug 30. Review.

17.

Carbohydrate-Processing Enzymes of the Lysosome: Diseases Caused by Misfolded Mutants and Sugar Mimetics as Correcting Pharmacological Chaperones.

Stütz AE, Wrodnigg TM.

Adv Carbohydr Chem Biochem. 2016;73:225-302. doi: 10.1016/bs.accb.2016.08.002. Epub 2016 Oct 17. Review.

PMID:
27816107
18.

Autophagy and human disease: emerging themes.

Schneider JL, Cuervo AM.

Curr Opin Genet Dev. 2014 Jun;26:16-23. doi: 10.1016/j.gde.2014.04.003. Epub 2014 Jun 5. Review.

19.

Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis.

Jeyakumar M, Butters TD, Dwek RA, Platt FM.

Neuropathol Appl Neurobiol. 2002 Oct;28(5):343-57. Review.

PMID:
12366816
20.

Pathophysiology of neuropathic lysosomal storage disorders.

Bellettato CM, Scarpa M.

J Inherit Metab Dis. 2010 Aug;33(4):347-62. doi: 10.1007/s10545-010-9075-9. Epub 2010 Apr 29. Review.

PMID:
20429032

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