Xueqin F. Song

Shijiazhuang, China

Last Updated: 09/26/2026

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Found 71 publications

A Blood-Derived Factor Rescues ALS: Platelet Factor 4 Activates OPTN-Dependent Autophagy to Clear SOD1 Aggregates Independently of PINK1.

A Blood-Derived Factor Rescues ALS: Platelet Factor 4 Activates OPTN-Dependent Autophagy to Clear SOD1 Aggregates Independently of PINK1.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: May 06, 2026

Exercise-induced muscle injury in Duchenne muscular dystrophy: impaired mitophagy and altered PINK1-PARKIN pathway in mdx mice.

Exercise-induced muscle injury in Duchenne muscular dystrophy: impaired mitophagy and altered PINK1-PARKIN pathway in mdx mice.

Journal: Brain & development
Published: February 27, 2026

Elevated circulating cell-free mitochondrial DNA in fabry disease: insights into inflammatory activation.

Elevated circulating cell-free mitochondrial DNA in fabry disease: insights into inflammatory activation.

Journal: Frontiers in immunology
Published: September 15, 2025

PcabHLH58/PcabHLH151 regulates adventitious root development and nitrogen uptake in poplar.

PcabHLH58/PcabHLH151 regulates adventitious root development and nitrogen uptake in poplar.

Journal: Nature communications
Published: August 23, 2025

Coexistence of McArdle disease and hypokalemic periodic paralysis: A case report.

Coexistence of McArdle disease and hypokalemic periodic paralysis: A case report.

Journal: Medicina clinica
Published: August 21, 2025

Clinical, pathological and genetic characteristics of GNE myopathy: a single-center observational study.

Clinical, pathological and genetic characteristics of GNE myopathy: a single-center observational study.

Journal: BMC musculoskeletal disorders
Published: August 12, 2025

Clinical, pathological, and genetic characteristics of 23 DMD patients in northern China.

Clinical, pathological, and genetic characteristics of 23 DMD patients in northern China.

Journal: Orphanet journal of rare diseases
Published: August 10, 2025

SHMT2 deficiency disrupts transcriptional regulation through homocysteine-mediated suppression of histone lactylation in Huntington's disease models.

SHMT2 deficiency disrupts transcriptional regulation through homocysteine-mediated suppression of histone lactylation in Huntington's disease models.

Journal: The Journal of clinical investigation
Published: May 28, 2025

SRSF2 is upregulated in Duchenne muscular dystrophy and impairs myoblast autophagy by alternatively splicing HUWE1.

SRSF2 is upregulated in Duchenne muscular dystrophy and impairs myoblast autophagy by alternatively splicing HUWE1.

Journal: Neuromuscular disorders : NMD
Published: April 21, 2025

Poplar PdRabG3f inhibits root elongation and increases salt tolerance by enhancing endogenous abscisic acid synthesis.

Poplar PdRabG3f inhibits root elongation and increases salt tolerance by enhancing endogenous abscisic acid synthesis.

Journal: Plant physiology and biochemistry : PPB
Published: March 29, 2025

L-NAME improves the morphology and necrosis of skeletal muscle by activating PINK1-PARKIN mediated mitophagy in mdx mice.

L-NAME improves the morphology and necrosis of skeletal muscle by activating PINK1-PARKIN mediated mitophagy in mdx mice.

Journal: Brain & development
Published: February 16, 2025

Identification of VDAC1 as a mitochondria-related target of Duchenne muscular dystrophy based on bioinformatics analysis and in vitro experiments.

Identification of VDAC1 as a mitochondria-related target of Duchenne muscular dystrophy based on bioinformatics analysis and in vitro experiments.

Journal: International immunopharmacology
Published: February 10, 2025
Showing 1-12 of 71

Last Updated: 09/26/2026