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Results: 1 to 20 of 100

1.

Autophagy-lysosome pathway associated neuropathology and axonal degeneration in the brains of alpha-galactosidase A-deficient mice.

Nelson MP, Tse TE, O'Quinn DB, Percival SM, Jaimes EA, Warnock DG, Shacka JJ.

Acta Neuropathol Commun. 2014 Feb 14;2:20. doi: 10.1186/2051-5960-2-20.

PMID:
24529306
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Disruption of the autophagy-lysosome pathway is involved in neuropathology of the nclf mouse model of neuronal ceroid lipofuscinosis.

Thelen M, Damme M, Schweizer M, Hagel C, Wong AM, Cooper JD, Braulke T, Galliciotti G.

PLoS One. 2012;7(4):e35493. doi: 10.1371/journal.pone.0035493. Epub 2012 Apr 20. Erratum in: PLoS One. 2012;7(5): doi/10.1371/annotation/a4b06d46-8eb9-4d15-a15a-41bf4b5ccb8b. Daμμe, Markus [corrected to Damme, Markus]..

PMID:
22536393
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Cathepsin D deficiency induces persistent neurodegeneration in the absence of Bax-dependent apoptosis.

Shacka JJ, Klocke BJ, Young C, Shibata M, Olney JW, Uchiyama Y, Saftig P, Roth KA.

J Neurosci. 2007 Feb 21;27(8):2081-90.

PMID:
17314303
[PubMed - indexed for MEDLINE]
Free Article
4.

Selective molecular alterations in the autophagy pathway in patients with Lewy body disease and in models of alpha-synucleinopathy.

Crews L, Spencer B, Desplats P, Patrick C, Paulino A, Rockenstein E, Hansen L, Adame A, Galasko D, Masliah E.

PLoS One. 2010 Feb 19;5(2):e9313. doi: 10.1371/journal.pone.0009313.

PMID:
20174468
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Localization of MAP1-LC3 in vulnerable neurons and Lewy bodies in brains of patients with dementia with Lewy bodies.

Higashi S, Moore DJ, Minegishi M, Kasanuki K, Fujishiro H, Kabuta T, Togo T, Katsuse O, Uchikado H, Furukawa Y, Hino H, Kosaka K, Sato K, Arai H, Wada K, Iseki E.

J Neuropathol Exp Neurol. 2011 Apr;70(4):264-80. doi: 10.1097/NEN.0b013e318211c86a.

PMID:
21412173
[PubMed - indexed for MEDLINE]
6.

Disrupted autophagy leads to dopaminergic axon and dendrite degeneration and promotes presynaptic accumulation of α-synuclein and LRRK2 in the brain.

Friedman LG, Lachenmayer ML, Wang J, He L, Poulose SM, Komatsu M, Holstein GR, Yue Z.

J Neurosci. 2012 May 30;32(22):7585-93. doi: 10.1523/JNEUROSCI.5809-11.2012.

PMID:
22649237
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Kidney histologic alterations in α-Galactosidase-deficient mice.

Valbuena C, Oliveira JP, Carneiro F, Relvas S, Ganhão M, Sá-Miranda MC, Rodrigues LG.

Virchows Arch. 2011 Apr;458(4):477-86. doi: 10.1007/s00428-011-1051-8. Epub 2011 Feb 16.

PMID:
21328014
[PubMed - indexed for MEDLINE]
8.

alpha-Galactosidase A deficient mice: a model of Fabry disease.

Ohshima T, Murray GJ, Swaim WD, Longenecker G, Quirk JM, Cardarelli CO, Sugimoto Y, Pastan I, Gottesman MM, Brady RO, Kulkarni AB.

Proc Natl Acad Sci U S A. 1997 Mar 18;94(6):2540-4.

PMID:
9122231
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transfer.

Ziegler RJ, Yew NS, Li C, Cherry M, Berthelette P, Romanczuk H, Ioannou YA, Zeidner KM, Desnick RJ, Cheng SH.

Hum Gene Ther. 1999 Jul 1;10(10):1667-82.

PMID:
10428212
[PubMed - indexed for MEDLINE]
10.

Anderson-Fabry disease: a multiorgan disease.

Tuttolomondo A, Pecoraro R, Simonetta I, Miceli S, Pinto A, Licata G.

Curr Pharm Des. 2013;19(33):5974-96. Review.

PMID:
23448451
[PubMed - indexed for MEDLINE]
11.

Neurophysiological, behavioral and morphological abnormalities in the Fabry knockout mice.

Rodrigues LG, Ferraz MJ, Rodrigues D, Pais-Vieira M, Lima D, Brady RO, Sousa MM, Sá-Miranda MC.

Neurobiol Dis. 2009 Jan;33(1):48-56. doi: 10.1016/j.nbd.2008.09.001. Epub 2008 Sep 23.

PMID:
18848893
[PubMed - indexed for MEDLINE]
12.

Induction of autophagy in axonal dystrophy and degeneration.

Wang QJ, Ding Y, Kohtz DS, Mizushima N, Cristea IM, Rout MP, Chait BT, Zhong Y, Heintz N, Yue Z.

J Neurosci. 2006 Aug 2;26(31):8057-68. Erratum in: J Neurosci. 2006 Aug 15;26(33):1 p preceding 8409. Kohtz, Stave [corrected to Kohtz, D Stave].

PMID:
16885219
[PubMed - indexed for MEDLINE]
Free Article
13.

Regional deficiencies in chaperone-mediated autophagy underlie α-synuclein aggregation and neurodegeneration.

Malkus KA, Ischiropoulos H.

Neurobiol Dis. 2012 Jun;46(3):732-44. doi: 10.1016/j.nbd.2012.03.017. Epub 2012 Mar 9.

PMID:
22426402
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Normal hearing in alpha-galactosidase A-deficient mice, the mouse model for Fabry disease.

Noben-Trauth K, Neely H, Brady RO.

Hear Res. 2007 Dec;234(1-2):10-4. Epub 2007 Sep 14.

PMID:
17933476
[PubMed - indexed for MEDLINE]
15.

Lysosomal delivery of therapeutic enzymes in cell models of Fabry disease.

Marchesan D, Cox TM, Deegan PB.

J Inherit Metab Dis. 2012 Nov;35(6):1107-17. doi: 10.1007/s10545-012-9472-3. Epub 2012 Mar 24.

PMID:
22450713
[PubMed - indexed for MEDLINE]
16.

Caveolin-associated accumulation of globotriaosylceramide in the vascular endothelium of alpha-galactosidase A null mice.

Shu L, Shayman JA.

J Biol Chem. 2007 Jul 20;282(29):20960-7. Epub 2007 May 29.

PMID:
17535804
[PubMed - indexed for MEDLINE]
Free Article
17.

Distinct effects of methamphetamine on autophagy-lysosome and ubiquitin-proteasome systems in HL-1 cultured mouse atrial cardiomyocytes.

Funakoshi-Hirose I, Aki T, Unuma K, Funakoshi T, Noritake K, Uemura K.

Toxicology. 2013 Oct 4;312:74-82. doi: 10.1016/j.tox.2013.07.016. Epub 2013 Aug 7.

PMID:
23933405
[PubMed - indexed for MEDLINE]
18.

The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice.

Alves S, Cormier-Dequaire F, Marinello M, Marais T, Muriel MP, Beaumatin F, Charbonnier-Beaupel F, Tahiri K, Seilhean D, El Hachimi K, Ruberg M, Stevanin G, Barkats M, den Dunnen W, Priault M, Brice A, Durr A, Corvol JC, Sittler A.

Acta Neuropathol. 2014 Nov;128(5):705-22. doi: 10.1007/s00401-014-1289-8. Epub 2014 May 24.

PMID:
24859968
[PubMed - in process]
19.

Beclin 1 gene transfer activates autophagy and ameliorates the neurodegenerative pathology in alpha-synuclein models of Parkinson's and Lewy body diseases.

Spencer B, Potkar R, Trejo M, Rockenstein E, Patrick C, Gindi R, Adame A, Wyss-Coray T, Masliah E.

J Neurosci. 2009 Oct 28;29(43):13578-88. doi: 10.1523/JNEUROSCI.4390-09.2009.

PMID:
19864570
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Autophagosome maturation is impaired in Fabry disease.

Chévrier M, Brakch N, Céline L, Genty D, Ramdani Y, Moll S, Djavaheri-Mergny M, Brasse-Lagnel C, Annie Laquerrière AL, Barbey F, Bekri S.

Autophagy. 2010 Jul;6(5):589-99. doi: 10.4161/auto.6.5.11943. Epub 2010 Jul 1.

PMID:
20431343
[PubMed - indexed for MEDLINE]
Free Article
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