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pick disease of the brain/protease

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8 rezultatov

Depletion of oxidative and endoplasmic reticulum stress regulators in Pick disease.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Both oxidative and endoplasmic reticulum (ER) stress is associated with multiple neurodegenerative, age-related diseases. The rare disorder Pick disease (PiD) shares some pathological hallmarks of other neurodegenerative diseases that may be related to oxidative stress. Importantly, activation of an

Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Niemann-Pick disease type C (NPC) is a lysosomal storage disorder characterized by liver disease and progressive neurodegeneration. Deficiency of either NPC1 or NPC2 leads to the accumulation of cholesterol and glycosphingolipids in late endosomes and early lysosomes. In order to identify

Genetics of Lipid-Storage Management in Caenorhabditis elegans Embryos.

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Prijava / prijava
Lipids play a pivotal role in embryogenesis as structural components of cellular membranes, as a source of energy, and as signaling molecules. On the basis of a collection of temperature-sensitive embryonic lethal mutants, a systematic database search, and a subsequent microscopic analysis of >300

U18666A-mediated apoptosis in cultured murine cortical neurons: role of caspases, calpains and kinases.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Studies have suggested that cholesterol imbalance in the brain might be related to the development of neurological disorders such as Alzheimer's disease and Niemann-Pick disease type C. Previously, we have reported that U18666A, a cholesterol transport-inhibiting agent, leads to apoptosis and

Potential pitfalls and solutions for use of fluorescent fusion proteins to study the lysosome.

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Prijava / prijava
Use of fusion protein tags to investigate lysosomal proteins can be complicated by the acidic, protease-rich environment of the lysosome. Potential artifacts include degradation or release of the tag and acid quenching of fluorescence. Tagging can also affect protein folding, glycosylation and/or
5H7, an anti-human class I MHC mAb that recognizes a monomorphic determinant of the alpha3 domain, profoundly inhibits T lymphocyte activation. The present study was designed to determine the role of programmed cell death in 5H7-mediated immune suppression. Incubation of PBMC with 5H7 mAb induced a

Seeding selectivity and ultrasensitive detection of tau aggregate conformers of Alzheimer disease.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Alzheimer disease (AD) and chronic traumatic encephalopathy (CTE) involve the abnormal accumulation in the brain of filaments composed of both three-repeat (3R) and four-repeat (4R) (3R/4R) tau isoforms. To probe the molecular basis for AD's tau filament propagation and to improve detection of tau

Protein targets of oxidative damage in human neurodegenerative diseases with abnormal protein aggregates.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Human neurodegenerative diseases with abnormal protein aggregates are associated with aberrant post-translational modifications, solubility, aggregation and fibril formation of selected proteins which cannot be degraded by cytosolic proteases, ubiquitin-protesome system and autophagy, and,
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