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Stereotaxic Infusion of Oligomeric Amyloid-beta into the Mouse Hippocampus
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IX International Symposium on Amyloidosis, July 15-21, 2001, Budapest, Hungary

Jean D Sipe1, Giampaolo Merlini, Martha Skinner

  • 1Tissue Engineering Study Section, Center for Scientific Review, National Institutes of Health, Bethesda, MD 20892-7814, USA. sipej@csr.nih.gov

Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis
|May 10, 2002
PubMed
Abstract

No abstract available in PubMed .

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Amyloid Fibrils03:03

Amyloid Fibrils

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. 
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Amyloid Fibrils03:03

Amyloid Fibrils

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, normally used to...

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