PubMed

Abnormal autophagy, ubiquitination, inflammation and apoptosis are dependent upon lysosomal storage and are useful biomarkers of mucopolysaccharidosis VI.

Tessitore A, Pirozzi M, Auricchio A.

Pathogenetics. 2009 Jun 16;2(1):4.PMID: 19531206 [PubMed - in process]Free PMC ArticleFree textRelated citations

A block of autophagy in lysosomal storage disorders.

Settembre C, Fraldi A, Jahreiss L, Spampanato C, Venturi C, Medina D, de Pablo R, Tacchetti C, Rubinsztein DC, Ballabio A.

Hum Mol Genet. 2008 Jan 1;17(1):119-29. Epub 2007 Oct 3.PMID: 17913701 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

Autophagy, mitochondria and cell death in lysosomal storage diseases.

Kiselyov K, Jennigs JJ Jr, Rbaibi Y, Chu CT.

Autophagy. 2007 May-Jun;3(3):259-62. Epub 2007 May 23.PMID: 17329960 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Lysosomal storage diseases as disorders of autophagy.

Settembre C, Fraldi A, Rubinsztein DC, Ballabio A.

Autophagy. 2008 Jan 1;4(1):113-4. Epub 2007 Oct 30.PMID: 18000397 [PubMed - indexed for MEDLINE]Related citations

Drug-induced glycosaminoglycan storage: dose-dependent changes in the pattern of accumulated glycosaminoglycans in cultured bovine and human fibroblasts.

Fischer J.

Biochem Pharmacol. 1996 Nov 8;52(9):1331-7.PMID: 8937442 [PubMed - indexed for MEDLINE]Related citations

Biochemical, pathological, and skeletal improvement of mucopolysaccharidosis VI after gene transfer to liver but not to muscle.

Tessitore A, Faella A, O'Malley T, Cotugno G, Doria M, Kunieda T, Matarese G, Haskins M, Auricchio A.

Mol Ther. 2008 Jan;16(1):30-7. Epub 2007 Oct 23.PMID: 17955027 [PubMed - indexed for MEDLINE]Related citations

Lysosomal disorders: from storage to cellular damage.

Ballabio A, Gieselmann V.

Biochim Biophys Acta. 2009 Apr;1793(4):684-96. Epub 2008 Dec 8. Review.PMID: 19111581 [PubMed - indexed for MEDLINE]Related citations

Influence of X-ray on the autophagic-lysosomal system in rat pancreatic acini.

Telbisz A, Kovács AL, Somosy Z.

Micron. 2002;33(2):143-51.PMID: 11567883 [PubMed - indexed for MEDLINE]Related citations

Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease.

Walkley SU, Thrall MA, Haskins ME, Mitchell TW, Wenger DA, Brown DE, Dial S, Seim H.

Neuropathol Appl Neurobiol. 2005 Oct;31(5):536-44.PMID: 16150124 [PubMed - indexed for MEDLINE]Related citations

Lysosomal sulfate efflux following glycosaminoglycan degradation: measurements in enzyme-supplemented Maroteaux-Lamy syndrome fibroblasts and isolated lysosomes.

Harper GS, Rozaklis T, Bielicki J, Hopwood JJ.

Glycoconj J. 1993 Oct;10(5):407-15.PMID: 8298306 [PubMed - indexed for MEDLINE]Related citations

Characterization of dermatan sulfate in mucopolysaccharidosis VI. Evidence for the absence of hyaluronidase-like enzymes in human skin fibroblasts.

Klein U, von Figura K.

Biochim Biophys Acta. 1980 Jun 5;630(1):10-4.PMID: 6770909 [PubMed - indexed for MEDLINE]Related citations

Mucolipidosis type IV: the importance of functional lysosomes for efficient autophagy.

Vergarajauregui S, Puertollano R.

Autophagy. 2008 Aug 16;4(6):832-4. Epub 2008 Jul 8.PMID: 18635948 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Lysosomal myopathies: an excessive build-up in autophagosomes is too much to handle.

Malicdan MC, Noguchi S, Nonaka I, Saftig P, Nishino I.

Neuromuscul Disord. 2008 Jul;18(7):521-9. Epub 2008 May 27. Review.PMID: 18502640 [PubMed - indexed for MEDLINE]Related citations

[Protein degradation by autophagy]

Uchiyama Y.

Gan To Kagaku Ryoho. 2008 Jan;35(1):25-9. Japanese. PMID: 18195526 [PubMed - indexed for MEDLINE]Related citations

Aging: central role for autophagy and the lysosomal degradative system.

Rajawat YS, Hilioti Z, Bossis I.

Ageing Res Rev. 2009 Jul;8(3):199-213. Epub 2009 May 7. Review.PMID: 19427410 [PubMed - indexed for MEDLINE]Related citations

Prediction of neuropathology in mucopolysaccharidosis I patients.

Fuller M, Brooks DA, Evangelista M, Hein LK, Hopwood JJ, Meikle PJ.

Mol Genet Metab. 2005 Jan;84(1):18-24.PMID: 15639191 [PubMed - indexed for MEDLINE]Related citations

Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients.

Lin WD, Lin SP, Wang CH, Hwu WL, Chuang CK, Lin SJ, Tsai Y, Chen CP, Tsai FJ.

Clin Chim Acta. 2008 Aug;394(1-2):89-93. Epub 2008 Apr 27.PMID: 18486607 [PubMed - indexed for MEDLINE]Related citations

Mitochondrial Ca2+ homeostasis in lysosomal storage diseases.

Kiselyov K, Muallem S.

Cell Calcium. 2008 Jul;44(1):103-11. Epub 2008 Feb 1. Review.PMID: 18242695 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI.

Evers M, Saftig P, Schmidt P, Hafner A, McLoghlin DB, Schmahl W, Hess B, von Figura K, Peters C.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8214-9.PMID: 8710849 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Mitochondrial aberrations in mucolipidosis Type IV.

Jennings JJ Jr, Zhu JH, Rbaibi Y, Luo X, Chu CT, Kiselyov K.

J Biol Chem. 2006 Dec 22;281(51):39041-50. Epub 2006 Oct 20.PMID: 17056595 [PubMed - indexed for MEDLINE]Free ArticleRelated citations