Ge Bai
Hangzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
ANXA11 suppression restores muscular function in the mdx mouse model of Duchenne muscular dystrophy (DMD).
Journal: Nature communications
Published: April 08, 2025
S-acylation of TDP43 regulates its condensation in amyotrophic lateral sclerosis.
Journal: Molecular cell
Published: August 06, 2024
Biomolecular condensates and disease pathogenesis.
Journal: Science China. Life sciences
Published: May 01, 2024
Friend or foe: The role of stress granule in neurodegenerative disease.
Journal: Neuron
Published: December 01, 2023
A spatiotemporal barrier formed by Follistatin is required for left-right patterning.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 05, 2023
Uncovering the mystery of genetic heterogeneity in inherited peripheral neuropathies.
Journal: Life medicine
Published: April 24, 2023
CMT2D neuropathy is influenced by vitamin D-mediated environmental pathway.
Journal: Journal of molecular cell biology
Published: August 15, 2022
Netrin-3 Suppresses Diabetic Neuropathic Pain by Gating the Intra-epidermal Sprouting of Sensory Axons.
Journal: Neuroscience bulletin
Published: March 29, 2022
Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules.
Journal: Cell
Published: December 14, 2021
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.
Journal: Brain : a journal of neurology
Published: August 21, 2020
Identification and functional characterization of novel GDAP1 variants in Chinese patients with Charcot-Marie-Tooth disease.
Journal: Annals of clinical and translational neurology
Published: July 22, 2020
Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family.
Journal: Brain : a journal of neurology
Published: May 22, 2020
Last Updated: 09/26/2026