C Z. Yan-Chuanzhu
No. 107 West Wenhua Road
Jinan, 250012, China
Jinan, 250012, China
Last Updated: 09/26/2026
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Found 18 publications
Sex-associated neuroinflammatory and astrocytic responses in amyotrophic lateral sclerosis: evidence from clinical cohorts and a TDP-43 N390D mouse model.
Journal: Brain, behavior, and immunity
Published: December 01, 2025
Pbk positively regulates myoblast differentiation and muscle regeneration via enhancing AMPK/ULK1 mediated myogenic autophagy.
Journal: Journal of translational medicine
Published: June 08, 2025
Growth differentiation factor 15: a valuable biomarker for the diagnosis and prognosis of late-onset form of multiple Acyl-CoA dehydrogenation deficiency.
Journal: Orphanet journal of rare diseases
Published: December 26, 2024
Advances in the Differentiation of hiPSCs into Cerebellar Neuronal Cells.
Journal: Stem cell reviews and reports
Published: July 10, 2024
Queuine ameliorates impaired mitochondrial function caused by mt-tRNAAsn variants.
Journal: Journal of translational medicine
Published: June 09, 2024
Protein kinase R is highly expressed in dermatomyositis and promotes interferon-beta-induced muscle damage.
Journal: Annals of the rheumatic diseases
Published: May 02, 2024
Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE.
Journal: Journal of translational medicine
Published: February 20, 2024
Intracranial vasculopathy: an important organ damage in young adult patients with late-onset Pompe disease.
Journal: Orphanet journal of rare diseases
Published: December 12, 2023
A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene.
Journal: Journal of human genetics
Published: August 12, 2023
Combining idebenone and rosuvastatin prevents atherosclerosis by suppressing oxidative stress and NLRP3 inflammasome activation.
Journal: European journal of pharmacology
Published: February 12, 2023
Distinctive metabolic remodeling in TYMP deficiency beyond mitochondrial dysfunction.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: January 02, 2023
Migratory Rolandic Encephalopathy Caused by the Mitochondrial ND3 Variant.
Journal: Neurology
Published: October 30, 2021
Last Updated: 09/26/2026