Yujing Gao

436 Cambridge Science Park
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 12 publications

U7 small nuclear RNA splice-switching therapeutics for STMN2 and UNC13A in Amyotrophic Lateral Sclerosis.

U7 small nuclear RNA splice-switching therapeutics for STMN2 and UNC13A in Amyotrophic Lateral Sclerosis.

Journal: bioRxiv : the preprint server for biology
Published: December 15, 2025

Altered Inflammatory Signature in a C9ORF72 -ALS iPSC-Derived Motor Neuron and Microglia Coculture Model.

Altered Inflammatory Signature in a C9ORF72 -ALS iPSC-Derived Motor Neuron and Microglia Coculture Model.

Journal: Glia
Published: May 02, 2025

The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1.

The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1.

Journal: Science advances
Published: June 26, 2024

Correction to: ASK1 is a novel molecular target for preventing aminoglycoside‑induced hair cell death.

Correction to: ASK1 is a novel molecular target for preventing aminoglycoside‑induced hair cell death.

Journal: Journal of molecular medicine (Berlin, Germany)
Published: May 10, 2022

ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death.

ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death.

Journal: Journal of molecular medicine (Berlin, Germany)
Published: June 09, 2021

Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort.

Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort.

Journal: Frontiers in neurology
Published: February 01, 2020

Distribution of Parkinson's disease associated RAB39B in mouse brain tissue.

Distribution of Parkinson's disease associated RAB39B in mouse brain tissue.

Journal: Molecular brain
Published: December 03, 2019

Clinical and Neuropathological Features Associated With Loss of RAB39B.

Clinical and Neuropathological Features Associated With Loss of RAB39B.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 07, 2019

Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder.

Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder.

Journal: Stem cell research
Published: June 01, 2019

Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease.

Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease.

Journal: Stem cell research
Published: January 24, 2018

The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.

The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 05, 2017

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

Journal: American journal of human genetics
Published: September 22, 2014
Showing 1-12 of 12

Last Updated: 09/26/2026