Claudia Scheckel

Zurich, ZH, Switzerland

Last Updated: 09/26/2026

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Found 13 publications

Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle.

Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle.

Journal: PLoS pathogens

Published: June 19, 2024

Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons.

Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons.

Journal: eLife

Published: September 10, 2020

Soluble dimeric prion protein ligand activates Adgrg6 receptor but does not rescue early signs of demyelination in PrP-deficient mice.

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

Genome-wide transcriptomics identifies an early preclinical signature of prion infection.

Genome-wide transcriptomics identifies an early preclinical signature of prion infection.

Journal: PLoS pathogens

Published: May 18, 2020

A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ.

A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ.

Journal: Neuron

Published: December 06, 2019

Genome-wide identification of microRNAs regulating the human prion protein.

Genome-wide identification of microRNAs regulating the human prion protein.

Journal: Brain pathology (Zurich, Switzerland)

Published: September 15, 2018

A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ.

A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ.

Journal: Neuron

Published: September 10, 2018

Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.

Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.

Journal: Nature genetics

Published: August 03, 2018

Prions, prionoids and protein misfolding disorders.

Prions, prionoids and protein misfolding disorders.

Journal: Nature reviews. Genetics

Published: May 02, 2018

Regulatory consequences of neuronal ELAV-like protein binding to coding and non-coding RNAs in human brain.

Regulatory consequences of neuronal ELAV-like protein binding to coding and non-coding RNAs in human brain.

Journal: eLife

Published: July 28, 2015

Microexons--tiny but mighty.

Microexons--tiny but mighty.

Journal: The EMBO journal

Published: December 24, 2014

Functional characterization of C. elegans Y-box-binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes.

Functional characterization of C. elegans Y-box-binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes.

Journal: Nucleic acids research

Published: November 08, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026