44 results on '"Askanas, Valerie"'
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2. Update on neuromuscular diseases: Pathology and molecular pathogenesis
3. Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis
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
5. Novel demonstration of conformationally modified tau in sporadic inclusion-body myositis muscle fibers
6. 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
7. Decreased SIRT1 deacetylase activity in sporadic inclusion-body myositis muscle fibers
8. Impaired Autophagy in Sporadic Inclusion-Body Myositis and in Endoplasmic Reticulum Stress-Provoked Cultured Human Muscle Fibers
9. Increased BACE1 mRNA and noncoding BACE1-antisense transcript in sporadic inclusion-body myositis muscle fibers—Possibly caused by endoplasmic reticulum stress
10. In inclusion-body myositis muscle fibers Parkinson-associated DJ-1 is increased and oxidized
11. Endoplasmic reticulum stress induces myostatin precursor protein and NF-κB in cultured human muscle fibers: Relevance to inclusion body myositis
12. AβPP-overexpression and proteasome inhibition increase αB-crystallin in cultured human muscle: Relevance to inclusion-body myositis
13. Proteasome Inhibition and Aggresome Formation in Sporadic Inclusion-Body Myositis and in Amyloid-β Precursor Protein-Overexpressing Cultured Human Muscle Fibers
14. Endoplasmic Reticulum Stress and Unfolded Protein Response in Inclusion Body Myositis Muscle
15. BACE1 and BACE2 in pathologic and normal human muscle
16. Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis
17. Mitochondrial DNA variants in inclusion body myositis
18. Cyclin-dependent kinase 5 colocalizes with phosphorylated tau in human inclusion-body myositis paired-helical filaments and may play a role in tau phosphorylation
19. Redox factor-1 in muscle biopsies of patients with inclusion-body myositis
20. Association of Active Extracellular Signal-Regulated Protein Kinase with Paired Helical Filaments of Inclusion-Body Myositis Muscle Suggests Its Role in Inclusion-Body Myositis Tau Phosphorylation
21. Alzheimer disease (AD) and inclusion-body myositis (IBM) ; Do the remarkable cytochemical similarities indicate similarities of molecular pathogenesis?
22. Paired Helical Filaments of Inclusion-Body Myositis Muscle Contain RNA and Survival Motor Neuron Protein
23. Does Overexpression of βAPP in Aging Muscle Have a Pathogenic Role and a Relevance to Alzheimer's Disease?
24. Immunolocalization of transcription factor NF-κB in inclusion-body myositis muscle and at normal human neuromuscular junctions
25. Immunolocalization of Nitric Oxide Synthases at the Postsynaptic Domain of Human and Rat Neuromuscular Junctions—Light and Electron Microscopic Studies
26. Expression of β-Amyloid Precursor Protein Gene Is Developmentally Regulated in Human Muscle Fibers in Vivo and in Vitro
27. Apolipoprotein E immunoreactive deposits in inclusion-body muscle diseases
28. Tropomodulin Is Highly Concentrated at the Postsynaptic Domain of Human and Rat Neuromuscular Junctions
29. Prion protein is strongly immunolocalized at the postsynaptic domain of human normal neuromuscular junctions
30. New organotypic model to culture the entire fetal rat spinal cord
31. Strong immunoreactivity of β-amyloid precursor protein, including the β-amyloid protein sequence, at human neuromuscular junctions
32. β-amyloid protein immunoreactivity in muscle of patients with inclusion-body myositis
33. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy
34. Acetylcholine receptors and acetylcholinesterase accumulate at the nerve-muscle contacts ofde novo grown human monolayer muscle cocultured with fetal rat spinal cord
35. Fibroblast growth factor, epidermal growth factor and insulin exert a neuronal-like influence on acetylcholine receptors in aneurally cultured human muscle
36. Effects of electrical stimulation and tetrodotoxin paralysis on expression of muscle-specific isozymes of four enzymes in aneurally cultured embryonic rat muscle
37. Developmental expression of the muscle-specific isozyme of phosphoglycerate mutase in human muscle cultured in monolayer and innervated by fetal rat spinal cord
38. Biochemical and morphological effects of 20,25-diazacholesterol on cultured muscle cells
39. Adrenomyeloneuropathy: Increased accumulation of very long chain fatty acid in cultured skeletal muscle
40. Systemic Manifestations of Gyrate Atrophy of the Choroid and Retina
41. Accumulation of CK-MM is impaired in innervated and contracting cultured muscle fibers of duchenne muscular dystrophy patients
42. Immunocytochemical localization of thymosin-α1 in thymic epithelial cells of normal and myasthenia gravis patients and in thymic cultures
43. Asynchronous regulation of muscle specific isozymes of creatine kinase, glycogen phosphorylase, lactic dehydrogenase and phosphoglycerate mutase in innervated and non-innervated cultured human muscle
44. Histochemistry of cultured aneural chick muscle. Morphological maturation without differentiation of fiber types
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