Asvin K. Lakkaraju
Zurich, ZH 8091, Switzerland
Last Updated: 09/26/2026
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Found 17 publications
Channel Activities of the Full-Length Prion and Truncated Proteins.
Journal: ACS chemical neuroscience
Published: December 14, 2023
Glial activation in prion diseases is selectively triggered by neuronal PrPSc.
Journal: Brain pathology (Zurich, Switzerland)
Published: December 07, 2021
A conformational switch controlling the toxicity of the prion protein.
Journal: Nature structural & molecular biology
Published: December 01, 2021
Calreticulin mutations affect its chaperone function and perturb the glycoproteome.
Journal: Cell reports
Published: July 08, 2021
Loss of PIKfyve drives the spongiform degeneration in prion diseases.
Journal: EMBO molecular medicine
Published: June 15, 2021
Soluble dimeric prion protein ligand activates Adgrg6 receptor but does not rescue early signs of demyelination in PrP-deficient mice.
Journal: PloS one
Published: July 31, 2020
Toward Therapy of Human Prion Diseases.
Journal: Annual review of pharmacology and toxicology
Published: September 30, 2017
Inhibition of group-I metabotropic glutamate receptors protects against prion toxicity.
Journal: PLoS pathogens
Published: September 08, 2017
GPR56/ADGRG1 regulates development and maintenance of peripheral myelin.
Journal: The Journal of experimental medicine
Published: October 09, 2016
The prion protein is an agonistic ligand of the G protein-coupled receptor Adgrg6.
Journal: Nature
Published: December 22, 2015
Last Updated: 09/26/2026