Yuanyuan Liu

Muenster, NW, Germany

Last Updated: 09/26/2026

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Found 19 publications

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

Journal: EBioMedicine

Published: August 28, 2025

Active LXR signaling, coupled with elevated mitochondrial and glycolytic metabolism contributes to GM-CSF-induced trained immunity.

Active LXR signaling, coupled with elevated mitochondrial and glycolytic metabolism contributes to GM-CSF-induced trained immunity.

Journal: Frontiers in immunology

Published: August 14, 2025

Deep Learning Reveals Liver MRI Features Associated With PNPLA3 I148M in Steatotic Liver Disease.

Deep Learning Reveals Liver MRI Features Associated With PNPLA3 I148M in Steatotic Liver Disease.

Journal: Liver international : official journal of the International Association for the Study of the Liver

Published: January 12, 2025

Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy.

Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: December 17, 2023

Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia.

Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia.

Journal: EBioMedicine

Published: June 01, 2023

Protocol for the induction of innate immune memory in human smooth muscle cells and endothelial cells in vitro.

Protocol for the induction of innate immune memory in human smooth muscle cells and endothelial cells in vitro.

Journal: STAR protocols

Published: April 17, 2023

Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype.

Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype.

Journal: Cerebral cortex (New York, N.Y. : 1991)

Published: November 01, 2022

Direct fluorescent labeling of NF186 and NaV1.6 in living primary neurons using bioorthogonal click chemistry.

Direct fluorescent labeling of NF186 and NaV1.6 in living primary neurons using bioorthogonal click chemistry.

Journal: Journal of cell science

Published: September 01, 2022

Reply: Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China.

Reply: Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China.

Journal: Brain : a journal of neurology

Published: January 18, 2022

Theoretical analysis of a contactless transportation system for cylindrical objects based on ultrasonic levitation.

Theoretical analysis of a contactless transportation system for cylindrical objects based on ultrasonic levitation.

Journal: The Journal of the Acoustical Society of America

Published: October 02, 2021

In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders.

In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders.

Journal: British journal of pharmacology

Published: August 20, 2021

A SCN8A variant associated with severe early onset epilepsy and developmental delay: Loss- or gain-of-function?

A SCN8A variant associated with severe early onset epilepsy and developmental delay: Loss- or gain-of-function?

Journal: Epilepsy research

Published: July 06, 2021

Showing 1-12 of 19

Last Updated: 09/26/2026