Pawel M. Switonski

Poznan, WP, Poland

Last Updated: 09/26/2026

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Found 19 publications

Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats.

Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats.

Journal: RNA biology

Published: June 24, 2026

Spinocerebellar ataxia 27B (SCA27B)-a systematic review and a case report of a Polish family.

Spinocerebellar ataxia 27B (SCA27B)-a systematic review and a case report of a Polish family.

Journal: Journal of applied genetics

Published: February 11, 2025

Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients.

Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients.

Journal: Science translational medicine

Published: November 06, 2024

Antibody-assisted selective isolation of Purkinje cell nuclei from mouse cerebellar tissue.

Antibody-assisted selective isolation of Purkinje cell nuclei from mouse cerebellar tissue.

Journal: Cell reports methods

Published: December 19, 2023

Purkinje-Enriched snRNA-seq in SCA7 Cerebellum Reveals Zebrin Identity Loss as a Central Feature of Polyglutamine Ataxias.

Purkinje-Enriched snRNA-seq in SCA7 Cerebellum Reveals Zebrin Identity Loss as a Central Feature of Polyglutamine Ataxias.

Journal: bioRxiv : the preprint server for biology

Published: May 22, 2023

Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease models.

Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease models.

Journal: BMC biology

Published: September 06, 2022

Altered H3 histone acetylation impairs high-fidelity DNA repair to promote cerebellar degeneration in spinocerebellar ataxia type 7.

Altered H3 histone acetylation impairs high-fidelity DNA repair to promote cerebellar degeneration in spinocerebellar ataxia type 7.

Journal: Cell reports

Published: January 07, 2021

Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7.

Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7.

Journal: Disease models & mechanisms

Published: December 21, 2020

FairSubset: A tool to choose representative subsets of data for use with replicates or groups of different sample sizes.

FairSubset: A tool to choose representative subsets of data for use with replicates or groups of different sample sizes.

Journal: Journal of biological methods

Published: April 01, 2019

Nicotinamide Pathway-Dependent Sirt1 Activation Restores Calcium Homeostasis to Achieve Neuroprotection in Spinocerebellar Ataxia Type 7.

Nicotinamide Pathway-Dependent Sirt1 Activation Restores Calcium Homeostasis to Achieve Neuroprotection in Spinocerebellar Ataxia Type 7.

Journal: Neuron

Published: December 11, 2018

Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.

Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.

Journal: Cell reports

Published: April 25, 2018

Nuclear speckles are detention centers for transcripts containing expanded CAG repeats.

Nuclear speckles are detention centers for transcripts containing expanded CAG repeats.

Journal: Biochimica et biophysica acta

Published: April 06, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026