260 related articles for article (PubMed ID: 25241263)
1. Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.
Askanas V; Engel WK; Nogalska A
Biochim Biophys Acta; 2015 Apr; 1852(4):633-43. PubMed ID: 25241263
[TBL] [Abstract][Full Text] [Related]
2. Sporadic inclusion-body myositis: conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau.
Askanas V; Engel WK
Presse Med; 2011 Apr; 40(4 Pt 2):e219-35. PubMed ID: 21392932
[TBL] [Abstract][Full Text] [Related]
3. Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis.
Askanas V; Engel WK; Nogalska A
J Neuropathol Exp Neurol; 2012 Aug; 71(8):680-93. PubMed ID: 22805774
[TBL] [Abstract][Full Text] [Related]
4. Inclusion-body myositis: muscle-fiber molecular pathology and possible pathogenic significance of its similarity to Alzheimer's and Parkinson's disease brains.
Askanas V; Engel WK
Acta Neuropathol; 2008 Dec; 116(6):583-95. PubMed ID: 18974994
[TBL] [Abstract][Full Text] [Related]
5. Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy.
Askanas V; Engel WK; Yang CC; Alvarez RB; Lee VM; Wisniewski T
Am J Pathol; 1998 Apr; 152(4):889-95. PubMed ID: 9546349
[TBL] [Abstract][Full Text] [Related]
6. Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition.
Askanas V; Engel WK
Neurology; 2006 Jan; 66(2 Suppl 1):S39-48. PubMed ID: 16432144
[TBL] [Abstract][Full Text] [Related]
7. 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.
Nogalska A; Terracciano C; D'Agostino C; King Engel W; Askanas V
Acta Neuropathol; 2009 Sep; 118(3):407-13. PubMed ID: 19557423
[TBL] [Abstract][Full Text] [Related]
8. Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis.
Vattemi G; Nogalska A; King Engel W; D'Agostino C; Checler F; Askanas V
Acta Neuropathol; 2009 May; 117(5):569-74. PubMed ID: 19280202
[TBL] [Abstract][Full Text] [Related]
9. Molecular pathology and pathogenesis of inclusion-body myositis.
Askanas V; Engel WK
Microsc Res Tech; 2005 Jul; 67(3-4):114-20. PubMed ID: 16104000
[TBL] [Abstract][Full Text] [Related]
10. Novel demonstration of conformationally modified tau in sporadic inclusion-body myositis muscle fibers.
Nogalska A; D'Agostino C; Engel WK; Askanas V
Neurosci Lett; 2011 Oct; 503(3):229-33. PubMed ID: 21896314
[TBL] [Abstract][Full Text] [Related]
11. Inclusion-body myositis: newest concepts of pathogenesis and relation to aging and Alzheimer disease.
Askanas V; Engel WK
J Neuropathol Exp Neurol; 2001 Jan; 60(1):1-14. PubMed ID: 11202170
[TBL] [Abstract][Full Text] [Related]
12. Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging.
Askanas V; Engel WK
Curr Opin Rheumatol; 2003 Nov; 15(6):737-44. PubMed ID: 14569203
[TBL] [Abstract][Full Text] [Related]
13. Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging.
Askanas V; Engel WK
Scand J Rheumatol; 1998; 27(6):389-405. PubMed ID: 9855208
[TBL] [Abstract][Full Text] [Related]
14. Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres.
Cacciottolo M; Nogalska A; D'Agostino C; Engel WK; Askanas V
Neuropathol Appl Neurobiol; 2013 Dec; 39(7):750-61. PubMed ID: 23452232
[TBL] [Abstract][Full Text] [Related]
15. Increased BACE1 mRNA and noncoding BACE1-antisense transcript in sporadic inclusion-body myositis muscle fibers--possibly caused by endoplasmic reticulum stress.
Nogalska A; Engel WK; Askanas V
Neurosci Lett; 2010 May; 474(3):140-143. PubMed ID: 20236612
[TBL] [Abstract][Full Text] [Related]
16. Activation of the γ-secretase complex and presence of γ-secretase-activating protein may contribute to Aβ42 production in sporadic inclusion-body myositis muscle fibers.
Nogalska A; D'Agostino C; Engel WK; Askanas V
Neurobiol Dis; 2012 Oct; 48(1):141-9. PubMed ID: 22750528
[TBL] [Abstract][Full Text] [Related]
17. Novel demonstration of amyloid-β oligomers in sporadic inclusion-body myositis muscle fibers.
Nogalska A; D'Agostino C; Engel WK; Klein WL; Askanas V
Acta Neuropathol; 2010 Nov; 120(5):661-6. PubMed ID: 20711838
[TBL] [Abstract][Full Text] [Related]
18. Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis.
D'Agostino C; Nogalska A; Cacciottolo M; Engel WK; Askanas V
Acta Neuropathol; 2011 Nov; 122(5):627-36. PubMed ID: 21935636
[TBL] [Abstract][Full Text] [Related]
19. Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers.
Fratta P; Engel WK; Van Leeuwen FW; Hol EM; Vattemi G; Askanas V
Neurology; 2004 Sep; 63(6):1114-7. PubMed ID: 15452314
[TBL] [Abstract][Full Text] [Related]
20. Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced cultured human muscle fibers.
Nogalska A; Engel WK; McFerrin J; Kokame K; Komano H; Askanas V
J Neurochem; 2006 Mar; 96(5):1491-9. PubMed ID: 16441512
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
