Misfolded Proteins
Misfolded proteins activate Factor XII in humans, leading to kallikrein formation without initiating coagulation
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Blumenstock, Sonja (2017): Misfolded proteins affect synaptic plasticity and network activity: studies in mouse models of neurodegenerative diseases. Dissertation, LMU München: Fakultät für Biologie
141
Vibration Characteristics of Misfolded Proteins and Their Consquences
6
Selection of misfolded CFTR for proteasomal degradation by sequential Quality Control checkpoints
165
The ER Glycoprotein Quality Control System
15
Parkin, PINK1, and DJ 1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation
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The prion hypothesis in Parkinson's disease: Braak to the future
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Enhancement of proteasomal function protects against cardiac proteinopathy and ischemia/reperfusion injury in mice
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AAA-ATPase p97 suppresses apoptotic and autophagy-associated cell death in rheumatoid arthritis synovial fibroblasts
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The elusive physiologic role of Factor XII
5
Effect of Genetic Variation in a Drosophila Model of Diabetes-Associated Misfolded Human Proinsulin
27
Untangling the Prion-Like Misfolding Mechanism for Neurodegenerative Diseases
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Disorders of FZ-CRD; insights towards FZ-CRD folding and therapeutic landscape
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S nitrosylation of the thioredoxin like domains of protein disulphide isomerase and its role in neurodegenerative conditions
8
Unfolded protein response in cancer: the Physician's perspective
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Quantitative methods in neuropathology
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Unscrambling an egg: protein disaggregation by AAA+ proteins
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Protein quality control in the bacterial periplasm
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Airborne Magnetite and Iron Rich Pollution Nanoparticles:Potential Neurotoxicants and Environmental Risk Factors for Neurodegenerative Disease, Including Alzheimer's Disease
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Endoplasmic reticulum stress: cell life and death decisions
10