Engel WK - Search Results

1

Luminescent conjugated oligothiophenes for sensitive fluorescent assignment of protein inclusion bodies.

Klingstedt T, Blechschmidt C, Nogalska A, Prokop S, Häggqvist B, Danielsson O, Engel WK, Askanas V, Heppner FL, Nilsson KP. Klingstedt T, et al. Among authors: engel wk. Chembiochem. 2013 Mar 18;14(5):607-16. doi: 10.1002/cbic.201200731. Epub 2013 Feb 28. Chembiochem. 2013. PMID: 23450708 Free PMC article.

2

Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. Neurology. 2006 Jan 24;66(2 Suppl 1):S39-48. doi: 10.1212/01.wnl.0000192128.13875.1e. Neurology. 2006. PMID: 16432144 Review.

3

Inclusion body myositis: a degenerative muscle disease associated with intra-muscle fiber multi-protein aggregates, proteasome inhibition, endoplasmic reticulum stress and decreased lysosomal degradation.

Askanas V, Engel WK, Nogalska A. Askanas V, et al. Among authors: engel wk. Brain Pathol. 2009 Jul;19(3):493-506. doi: 10.1111/j.1750-3639.2009.00290.x. Brain Pathol. 2009. PMID: 19563541 Free PMC article. Review.

4

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. Nogalska A, et al. Among authors: engel wk. Neurobiol Dis. 2012 Oct;48(1):141-9. doi: 10.1016/j.nbd.2012.06.008. Epub 2012 Jun 30. Neurobiol Dis. 2012. PMID: 22750528

5

Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.

Askanas V, Engel WK, Nogalska A. Askanas V, et al. Among authors: engel wk. Biochim Biophys Acta. 2015 Apr;1852(4):633-43. doi: 10.1016/j.bbadis.2014.09.005. Epub 2014 Sep 18. Biochim Biophys Acta. 2015. PMID: 25241263 Free article. Review.

6

Molecular pathology and pathogenesis of inclusion-body myositis.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. Microsc Res Tech. 2005 Jul;67(3-4):114-20. doi: 10.1002/jemt.20186. Microsc Res Tech. 2005. PMID: 16104000 Review.

7

Newest pathogenetic considerations in inclusion-body myositis: possible role of amyloid-beta, cholesterol, relation to aging and to Alzheimer's disease.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. Curr Rheumatol Rep. 2002 Oct;4(5):427-33. doi: 10.1007/s11926-002-0088-8. Curr Rheumatol Rep. 2002. PMID: 12217248 Review.

8

Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. Curr Opin Neurol. 2002 Oct;15(5):525-31. doi: 10.1097/00019052-200210000-00002. Curr Opin Neurol. 2002. PMID: 12351995 Review.

9

Unfolding story of inclusion-body myositis and myopathies: role of misfolded proteins, amyloid-beta, cholesterol, and aging.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. J Child Neurol. 2003 Mar;18(3):185-90. doi: 10.1177/08830738030180030401. J Child Neurol. 2003. PMID: 12731644

10

Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging.

Askanas V, Engel WK. Askanas V, et al. Among authors: engel wk. Curr Opin Rheumatol. 2003 Nov;15(6):737-44. doi: 10.1097/00002281-200311000-00009. Curr Opin Rheumatol. 2003. PMID: 14569203 Review.

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