Jukka T. Puolivali

Charles River
Kuopio, Finland

Last Updated: 09/26/2026

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Found 22 publications

Expression of human A53T alpha-synuclein without endogenous rat alpha-synuclein fails to elicit Parkinson's disease-related phenotypes in a novel humanized rat model.

Expression of human A53T alpha-synuclein without endogenous rat alpha-synuclein fails to elicit Parkinson's disease-related phenotypes in a novel humanized rat model.

Journal: PloS one

Published: June 13, 2025

Targeting a Novel Site in Exon 51 with Antisense Oligonucleotides Induces Enhanced Exon Skipping in a Mouse Model of Duchenne Muscular Dystrophy.

Targeting a Novel Site in Exon 51 with Antisense Oligonucleotides Induces Enhanced Exon Skipping in a Mouse Model of Duchenne Muscular Dystrophy.

Journal: Nucleic acid therapeutics

Published: February 07, 2025

BMN 351-Induced Exon Skipping and Dystrophin Expression in Skeletal and Cardiac Muscle Lead to Preservation of Motor Function in a Mouse Model of Exon 51 Skip-Amenable Duchenne Muscular Dystrophy.

BMN 351-Induced Exon Skipping and Dystrophin Expression in Skeletal and Cardiac Muscle Lead to Preservation of Motor Function in a Mouse Model of Exon 51 Skip-Amenable Duchenne Muscular Dystrophy.

Journal: Nucleic acid therapeutics

Published: February 07, 2025

Physiological and behavioural implications of the portosystemic shunt in C57Bl/6J mice.

Physiological and behavioural implications of the portosystemic shunt in C57Bl/6J mice.

Journal: The Journal of physiology

Published: July 05, 2024

Next Generation Exon 51 Skipping Antisense Oligonucleotides for Duchenne Muscular Dystrophy.

Next Generation Exon 51 Skipping Antisense Oligonucleotides for Duchenne Muscular Dystrophy.

Journal: Nucleic acid therapeutics

Published: April 10, 2023

Vertigoheel promotes rodent cognitive performance in multiple memory tests.

Vertigoheel promotes rodent cognitive performance in multiple memory tests.

Journal: Frontiers in neuroscience

Published: March 09, 2023

Detailed genetic and functional analysis of the hDMDdel52/mdx mouse model.

Detailed genetic and functional analysis of the hDMDdel52/mdx mouse model.

Journal: PloS one

Published: May 14, 2020

Rapid and robust patterns of spontaneous locomotor deficits in mouse models of Huntington's disease.

Rapid and robust patterns of spontaneous locomotor deficits in mouse models of Huntington's disease.

Journal: PloS one

Published: April 18, 2020

Using a State-of-the-Art Toolbox to Evaluate Molecular and Functional Readouts of Antisense Oligonucleotide-Induced Exon Skipping in mdx Mice.

Using a State-of-the-Art Toolbox to Evaluate Molecular and Functional Readouts of Antisense Oligonucleotide-Induced Exon Skipping in mdx Mice.

Journal: Nucleic acid therapeutics

Published: December 11, 2019

A multimodal approach to identify clinically relevant biomarkers to comprehensively monitor disease progression in a mouse model of pediatric neurodegenerative disease.

A multimodal approach to identify clinically relevant biomarkers to comprehensively monitor disease progression in a mouse model of pediatric neurodegenerative disease.

Journal: Progress in neurobiology

Published: June 19, 2019

Suppression of Mutant Protein Expression in SCA3 and SCA1 Mice Using a CAG Repeat-Targeting Antisense Oligonucleotide.

Suppression of Mutant Protein Expression in SCA3 and SCA1 Mice Using a CAG Repeat-Targeting Antisense Oligonucleotide.

Journal: Molecular therapy. Nucleic acids

Published: May 21, 2019

Impaired Performance of the Q175 Mouse Model of Huntington's Disease in the Touch Screen Paired Associates Learning Task.

Impaired Performance of the Q175 Mouse Model of Huntington's Disease in the Touch Screen Paired Associates Learning Task.

Journal: Frontiers in behavioral neuroscience

Published: July 09, 2018

Showing 1-12 of 22

Last Updated: 09/26/2026