Detalhe da pesquisa
1.
Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.
Biochim Biophys Acta
; 1852(4): 633-43, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25241263
2.
Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-ß42 in an in vitro-model of inclusion-body myositis.
Neurobiol Dis
; 65: 93-101, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24472798
3.
Luminescent conjugated oligothiophenes for sensitive fluorescent assignment of protein inclusion bodies.
Chembiochem
; 14(5): 607-16, 2013 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23450708
4.
Activation of the γ-secretase complex and presence of γ-secretase-activating protein may contribute to Aß42 production in sporadic inclusion-body myositis muscle fibers.
Neurobiol Dis
; 48(1): 141-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22750528
5.
Update on neuromuscular diseases: Pathology and molecular pathogenesis.
Biochim Biophys Acta
; 1852(4): 561-2, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25585262
6.
Impaired autophagy in sporadic inclusion-body myositis and in endoplasmic reticulum stress-provoked cultured human muscle fibers.
Am J Pathol
; 177(3): 1377-87, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20616343
7.
Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis.
Acta Neuropathol
; 122(5): 627-36, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21935636
8.
In AbetaPP-overexpressing cultured human muscle fibers proteasome inhibition enhances phosphorylation of AbetaPP751 and GSK3beta activation: effects mitigated by lithium and apparently relevant to sporadic inclusion-body myositis.
J Neurochem
; 112(2): 389-96, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19878439
9.
Novel demonstration of amyloid-ß oligomers in sporadic inclusion-body myositis muscle fibers.
Acta Neuropathol
; 120(5): 661-6, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20711838
10.
Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis.
Acta Neuropathol
; 117(5): 569-74, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19280202
11.
p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis.
Acta Neuropathol
; 118(3): 407-13, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557423
12.
In inclusion-body myositis muscle fibers Parkinson-associated DJ-1 is increased and oxidized.
Free Radic Biol Med
; 45(6): 773-9, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18601999
13.
Inclusion-body myositis: muscle-fiber molecular pathology and possible pathogenic significance of its similarity to Alzheimer's and Parkinson's disease brains.
Acta Neuropathol
; 116(6): 583-95, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18974994
14.
Dysferlin is a newly identified binding partner of AßPP and it co-aggregates with amyloid-ß42 within sporadic inclusion-body myositis (s-IBM) muscle fibers.
Acta Neuropathol
; 126(5): 781-3, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24091414
15.
AbetaPP-overexpression and proteasome inhibition increase alphaB-crystallin in cultured human muscle: relevance to inclusion-body myositis.
Neuromuscul Disord
; 16(12): 839-44, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17056255
16.
Molecular pathology and pathogenesis of inclusion-body myositis.
Microsc Res Tech
; 67(3-4): 114-20, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16104000
17.
Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy.
J Neuropathol Exp Neurol
; 74(6): 538-46, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25978849
18.
Unfolding story of inclusion-body myositis and myopathies: role of misfolded proteins, amyloid-beta, cholesterol, and aging.
J Child Neurol
; 18(3): 185-90, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12731644
19.
Expression of Nogo-A in human muscle fibers is not specific for amyotrophic lateral sclerosis.
Ann Neurol
; 62(6): 676-7; author reply 677, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17894379
20.
Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis.
J Neuropathol Exp Neurol
; 71(8): 680-93, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22805774