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Auteur Engel WK

Documents disponibles écrits par cet auteur (51)

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Article

Biochimica et biophysica acta, 1852, 4. Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy

Askanas V ; Engel WK ; Nogalska A | 2015

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Article

Journal of neuropathology and experimental neurology, 74, 6. Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy

Nogalska A, Auteur ; D'Agostino C ; Engel WK ; Cacciottolo M ; Asada S ; Mori K ; Askanas V | 2015

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En ligne

Article

Neurobiology of disease, 65. Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis

Nogalska A ; D'Agostino C ; Engel WK ; Askanas V | United States | 05/2014

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Article

Neuropathology and applied neurobiology, 39, 7. Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres

Cacciottolo M ; Nogalska A ; D'Agostino C ; Engel WK ; Askanas V | 2013

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Article

Neuromuscular disorders : NMD, 18, 9-10. In ALS, viral-dysmetabolic mechanisms acting via neuronal-nurturing cells (NNCs) could portend replacement therapy and should be sought by multitissue screening for rev-transcriptase (RT) and viral tracks (Poster)

Collectif ; Engel WK | 2008

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Article

Acta neuropathologica, 114, 5. NOGO is increased and binds to BACE1 in sporadic inclusion-body myositis and in AbetaPP-overexpressing cultured human muscle fibers

Wojcik S ; Engel WK ; Yan R ; McFerrin J ; Askanas V | 2007

Accès au résumé PubMed / to PubMed abstract

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Article

Current opinion in rheumatology, 19, 6. Inclusion-body myositis, a multifactorial muscle disease associated with aging : current concepts of pathogenesis

Askanas V ; Engel WK | 2007

Accès au résumé PubMed / to PubMed abstract

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Article

Experimental neurology, 240. Endoplasmic reticulum stress induces myostatin precursor protein and NF-kappaB in cultured human muscle fibers : relevance to inclusion body myositis

Nogalska A ; Wojcik S ; Engel WK ; McFerrin J ; Askanas V | 2007

Accès au résumé PubMed / to PubMed abstract

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Article

Neurology Parkin might play a novel role in the pathogenesis of sporadic inclusion-body myositis (s-IBM) (Abstract in 58th Annual Meeting of American Academy of Neurology)

58th Annual Meeting of American Academy of Neurology (April 1-8, 2006; San Diego (California)) ; Paciello O ; Wojcik S ; Engel WK ; Askanas V | 03/2006

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Article

Neurology Proteasome inhibition and endoplasmic reticulum (ER) stress influence aggregation and expression of valosin-containing peptide (VCP) in an inclusion-body-myopathy human-muscle tissue-culture (IBM-HM-TC) model (Abstract in 58th Annual Meeting of American Academy of Neurology)

58th Annual Meeting of American Academy of Neurology (April 1-8, 2006; San Diego (California)) ; McFerrin J ; Engel WK ; Askanas V | 03/2006

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Article

Microscopy research and technique, 67, 3-4. Molecular pathology and pathogenesis of inclusion-body myositis

Askanas V ; Engel WK | 2005

Accès au résumé PubMed / to PubMed abstract

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Article

Neurology Amyloid-beta42 is preferentially deposited in muscle biopsies of patients with sporadic inclusion-body myositis (s-IBM)

55th Annual Meeting program (American Academy of Neurology; March 29 - April 5, 2003; Honolulu, Hawaii) ; Vattemi G ; Checler F ; Engel WK ; Askanas V | 03/2003

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Article

Neurology The Val122IIe mutation in the transthyretin gene predisposes to accumulation of amyloid-beta (ABeta) and development of the inclusion-body myositis (IBM) phenotype in cultured human muscle fibers

55th Annual Meeting program (American Academy of Neurology; March 29 - April 5, 2003; Honolulu, Hawaii) ; McFerrin J ; Engel WK ; Vattemi G ; Askanas V | 03/2003

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Article

Current opinion in rheumatology, 15, 6. Proposed pathogenetic cascade of inclusion-body myositis : importance of amyloid-beta, misfolded proteins, predisposing genes, and aging

Askanas V ; Engel WK | 2003

Accès au résumé PubMed / to PubMed abstract

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Article

Neurology, 61, 2. Transthyretin Val122Ile, accumulated A-beta, and inclusion-body myositis aspects in cultured muscle

Askanas V ; Engel WK ; McFerrin J ; Vattemi G | 2003

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Article

Acta myologica, 21. Inclusion-body myositis : pathogenic role of amyloid-Beta, cholesterol, relation to aging and Alzheimer disease

Askanas V ; Engel WK | 12/2002

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Article

Acta myologica, 21. Newest pathogenic consideration in inclusion-body myositis : Importance of cholesterol and related mechanisms

Sixth Congress of the Mediterranean Society of Myology (May 23-26 2002; Corfu, Greece) ; Askanas V ; Engel WK | 04/2002

Abstract

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Article

Current opinion in neurology, 15. Inclusion-body myositis and myopathies : different etiologies, possibly similar pathogenic mechanisms

Askanas V ; Engel WK | 2002

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Article

Neurology, 58, 3. Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

Jaworska-Wilczynska M ; Wilczynski GM ; Engel WK ; Strickland DK ; Weisgraber KH ; Askanas V | 2002

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Article

NeuroReport, 12, 9. Novel cytoplasmic immunolocalization of RNA polymerase II in inclusion-body myositis muscle

Wilczynski GM ; Engel WK ; Askanas V | 07/2001

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Article

Neurology Novel proposed role of glycogen synthase kinase-3Beta (GSK-3Beta) in the pathogenesis of inclusion-body myositis (IBM)

Wilczynski GM ; Broccolini A ; Engel WK ; Askanas V | 04/2001

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Article

Annals of neurology, 48, 3. Late-juvenile sporadic inclusion body myositis : a newly recognized syndrome

Collectif ; Engel WK | 09/2000

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Article

American journal of pathology (The), 152, 4. 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 VMY ; Wisniewski T | 1998

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Article

Brain, 121, 6. Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies

Yang CC ; Alvarez RB ; Engel WK ; Heller SL ; Askanas V | 1998

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Publication AFM

Filaments and Myopathies : A symposium in honour of Fernando M.S Tomé (11-12 décembre 1998, Paris) : Actes de colloque

Collectif, Auteur ; Shelanski ML ; Askanas V ; Engel WK ; Argov Z ; Middleton L ; Hentati F ; Mikol J ; Bouchard JP ; Rouleau G ; Brais B ; Arahata K ; Blumen SC ; Fardeau M | AFM-TELETHON | 1998

Ce colloque a été organisé par l'AFM et l'institut de Myologie en collaboration avec : Le comité d'organisation : - Michel FARDEAU - Ketty SCHWARZ - Pascal GUCHENEY - J. Andoni URTIZBEREA

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Détail de l'auteur

Auteur Engel WK

Documents disponibles écrits par cet auteur (51)

Biochimica et biophysica acta, 1852, 4. Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy

Journal of neuropathology and experimental neurology, 74, 6. Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy

Neurobiology of disease, 65. Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis

Neuropathology and applied neurobiology, 39, 7. Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres

Neuromuscular disorders : NMD, 18, 9-10. In ALS, viral-dysmetabolic mechanisms acting via neuronal-nurturing cells (NNCs) could portend replacement therapy and should be sought by multitissue screening for rev-transcriptase (RT) and viral tracks (Poster)

Acta neuropathologica, 114, 5. NOGO is increased and binds to BACE1 in sporadic inclusion-body myositis and in AbetaPP-overexpressing cultured human muscle fibers

Current opinion in rheumatology, 19, 6. Inclusion-body myositis, a multifactorial muscle disease associated with aging : current concepts of pathogenesis

Experimental neurology, 240. Endoplasmic reticulum stress induces myostatin precursor protein and NF-kappaB in cultured human muscle fibers : relevance to inclusion body myositis

Neurology Parkin might play a novel role in the pathogenesis of sporadic inclusion-body myositis (s-IBM) (Abstract in 58th Annual Meeting of American Academy of Neurology)

Neurology Proteasome inhibition and endoplasmic reticulum (ER) stress influence aggregation and expression of valosin-containing peptide (VCP) in an inclusion-body-myopathy human-muscle tissue-culture (IBM-HM-TC) model (Abstract in 58th Annual Meeting of American Academy of Neurology)

Microscopy research and technique, 67, 3-4. Molecular pathology and pathogenesis of inclusion-body myositis

Neurology Amyloid-beta42 is preferentially deposited in muscle biopsies of patients with sporadic inclusion-body myositis (s-IBM)

Neurology The Val122IIe mutation in the transthyretin gene predisposes to accumulation of amyloid-beta (ABeta) and development of the inclusion-body myositis (IBM) phenotype in cultured human muscle fibers

Current opinion in rheumatology, 15, 6. Proposed pathogenetic cascade of inclusion-body myositis : importance of amyloid-beta, misfolded proteins, predisposing genes, and aging

Neurology, 61, 2. Transthyretin Val122Ile, accumulated A-beta, and inclusion-body myositis aspects in cultured muscle

Acta myologica, 21. Inclusion-body myositis : pathogenic role of amyloid-Beta, cholesterol, relation to aging and Alzheimer disease

Acta myologica, 21. Newest pathogenic consideration in inclusion-body myositis : Importance of cholesterol and related mechanisms

Current opinion in neurology, 15. Inclusion-body myositis and myopathies : different etiologies, possibly similar pathogenic mechanisms

Neurology, 58, 3. Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

NeuroReport, 12, 9. Novel cytoplasmic immunolocalization of RNA polymerase II in inclusion-body myositis muscle

Neurology Novel proposed role of glycogen synthase kinase-3Beta (GSK-3Beta) in the pathogenesis of inclusion-body myositis (IBM)

Annals of neurology, 48, 3. Late-juvenile sporadic inclusion body myositis : a newly recognized syndrome

American journal of pathology (The), 152, 4. 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

Brain, 121, 6. Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies

Filaments and Myopathies : A symposium in honour of Fernando M.S Tomé (11-12 décembre 1998, Paris) : Actes de colloque