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Related Articles by Review for PubMed (Select 23393155)

1.

TFEB regulates lysosomal proteostasis.

Song W, Wang F, Savini M, Ake A, di Ronza A, Sardiello M, Segatori L.

Hum Mol Genet. 2013 May 15;22(10):1994-2009. doi: 10.1093/hmg/ddt052. Epub 2013 Feb 7.

2.

Gaucher disease.

Butters TD.

Curr Opin Chem Biol. 2007 Aug;11(4):412-8. Epub 2007 Jul 23. Review.

PMID:
17644022
3.

Gaucher disease paradigm: from ERAD to comorbidity.

Bendikov-Bar I, Horowitz M.

Hum Mutat. 2012 Oct;33(10):1398-407. doi: 10.1002/humu.22124. Epub 2012 Jun 11. Review.

PMID:
22623374
4.

Lysosomal integral membrane protein-2: a new player in lysosome-related pathology.

Gonzalez A, Valeiras M, Sidransky E, Tayebi N.

Mol Genet Metab. 2014 Feb;111(2):84-91. doi: 10.1016/j.ymgme.2013.12.005. Epub 2013 Dec 11. Review.

5.

Mutant GBA1 expression and synucleinopathy risk: first insights from cellular and mouse models.

Sardi SP, Singh P, Cheng SH, Shihabuddin LS, Schlossmacher MG.

Neurodegener Dis. 2012;10(1-4):195-202. doi: 10.1159/000335038. Epub 2012 Feb 9. Review.

PMID:
22327140
6.

Impairment of homeostasis in lysosomal storage disorders.

Segatori L.

IUBMB Life. 2014 Jul;66(7):472-7. doi: 10.1002/iub.1288. Epub 2014 Jul 18. Review.

PMID:
25044960
7.

Therapeutic strategies to ameliorate lysosomal storage disorders--a focus on Gaucher disease.

Sawkar AR, D'Haeze W, Kelly JW.

Cell Mol Life Sci. 2006 May;63(10):1179-92. Review.

PMID:
16568247
8.

Correction of lysosomal dysfunction as a therapeutic strategy for neurodegenerative diseases.

Boyd RE, Valenzano KJ.

Bioorg Med Chem Lett. 2014 Jul 15;24(14):3001-5. doi: 10.1016/j.bmcl.2014.04.108. Epub 2014 May 14. Review.

PMID:
24894562
9.

Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA).

Hruska KS, LaMarca ME, Scott CR, Sidransky E.

Hum Mutat. 2008 May;29(5):567-83. doi: 10.1002/humu.20676. Review.

PMID:
18338393
10.

What can cell biology tell us about heterogeneity in lysosomal storage diseases?

Gieselmann V.

Acta Paediatr Suppl. 2005 Mar;94(447):80-6; discussion 79. Review.

PMID:
15895717
11.

Mutations causing Gaucher disease.

Horowitz M, Zimran A.

Hum Mutat. 1994;3(1):1-11. Review.

PMID:
8118460
12.

Gaucher disease: Perspectives on a prototype lysosomal disease.

Zhao H, Grabowski GA.

Cell Mol Life Sci. 2002 Apr;59(4):694-707. Review.

PMID:
12022475
13.

Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond.

Shachar T, Lo Bianco C, Recchia A, Wiessner C, Raas-Rothschild A, Futerman AH.

Mov Disord. 2011 Aug 1;26(9):1593-604. doi: 10.1002/mds.23774. Epub 2011 May 26. Review.

PMID:
21618611
14.

Gaucher disease and other storage disorders.

Grabowski GA.

Hematology Am Soc Hematol Educ Program. 2012;2012:13-8. doi: 10.1182/asheducation-2012.1.13. 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.

The pathophysiology of GD - current understanding and rationale for existing and emerging therapeutic approaches.

Hughes DA, Pastores GM.

Wien Med Wochenschr. 2010 Dec;160(23-24):594-9. doi: 10.1007/s10354-010-0864-4. Review.

PMID:
21221911
17.

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.

18.

Using pharmacological chaperones to restore proteostasis.

Wang YJ, Di XJ, Mu TW.

Pharmacol Res. 2014 May;83:3-9. doi: 10.1016/j.phrs.2014.04.002. Epub 2014 Apr 18. Review.

19.

Signals from the lysosome: a control centre for cellular clearance and energy metabolism.

Settembre C, Fraldi A, Medina DL, Ballabio A.

Nat Rev Mol Cell Biol. 2013 May;14(5):283-96. doi: 10.1038/nrm3565. Review.

20.

The proteostasis boundary in misfolding diseases of membrane traffic.

Hutt DM, Powers ET, Balch WE.

FEBS Lett. 2009 Aug 20;583(16):2639-46. Review.

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