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Related Concept Videos

Amyloid Fibrils03:03

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
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Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
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Evaluation of the Impact of Protein Aggregation on Cellular Oxidative Stress in Yeast
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Wild-type opsin does not aggregate with a misfolded opsin mutant

Megan Gragg1, Tae Gyun Kim1, Scott Howell1

  • 1Department of Ophthalmology and Visual Sciences, Case Western Reserve University, Cleveland, OH 44106, USA.

Biochimica Et Biophysica Acta
|April 28, 2016
PubMed
Summary

No abstract available in PubMed .

Keywords:
Conformational diseaseG protein-coupled receptorProtein aggregationProtein misfoldingRetinal degeneration

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