Miao B. He

Key Laboratory Of Environmental Stress And Chronic Disease Control & Prevention
Shenyang, 110122, China

Last Updated: 09/26/2026

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Found 193 publications

ALG14 variants contribute to a congenital disorder of glycosylation characterized by congenital myasthenia and epilepsy.

ALG14 variants contribute to a congenital disorder of glycosylation characterized by congenital myasthenia and epilepsy.

Journal: HGG advances
Published: June 02, 2026

The Clean Transit Paradox: Elevated Particle Exposure and Health Impacts in Subway Microenvironments.

The Clean Transit Paradox: Elevated Particle Exposure and Health Impacts in Subway Microenvironments.

Journal: Environmental science & technology
Published: May 21, 2026

Regulatory role of protein lactylation in tumor metastasis: mechanisms and emerging therapeutic strategies.

Regulatory role of protein lactylation in tumor metastasis: mechanisms and emerging therapeutic strategies.

Journal: Journal of advanced research
Published: March 16, 2026

Combined intratracheal instillation of trace emerging pollutants induced testicular damage.

Combined intratracheal instillation of trace emerging pollutants induced testicular damage.

Journal: Ecotoxicology and environmental safety
Published: February 01, 2026

A patient with a rare metabolic disease and myo-inositol administration leading to a new treatment for epilepsy.

A patient with a rare metabolic disease and myo-inositol administration leading to a new treatment for epilepsy.

Journal: Molecular genetics and metabolism
Published: January 19, 2026

Taurine attenuates diabetic nephropathy by suppressing the HMGB1/TLR4/MyD88/NF-κB axis in mice.

Taurine attenuates diabetic nephropathy by suppressing the HMGB1/TLR4/MyD88/NF-κB axis in mice.

Journal: International immunopharmacology
Published: December 22, 2025

Sodium butyrate induces mitochondrial pathway apoptosis in liver cancer via ATF4/SLC7A11-mediated ferroptosis.

Sodium butyrate induces mitochondrial pathway apoptosis in liver cancer via ATF4/SLC7A11-mediated ferroptosis.

Journal: PloS one
Published: December 06, 2025

L-fucose supplementation in a patient with global hypofucosylation and a mono-allelic variant in SLC35C1: Clinical improvement and assessment of biomarkers.

L-fucose supplementation in a patient with global hypofucosylation and a mono-allelic variant in SLC35C1: Clinical improvement and assessment of biomarkers.

Journal: Molecular genetics and metabolism
Published: November 28, 2025

A homozygous nonsense variant in the oligosaccharyltransferase complex gene, RPN1, causes a congenital disorder of glycosylation.

A homozygous nonsense variant in the oligosaccharyltransferase complex gene, RPN1, causes a congenital disorder of glycosylation.

Journal: HGG advances
Published: November 17, 2025

Expanded characterization of glycosylation abnormalities and galactose therapy in a patient with CCDC115-CDG using semi-quantitative N-glycan analysis of total and fractionated plasma glycoproteins, in response to Geerts et al. [1].

Expanded characterization of glycosylation abnormalities and galactose therapy in a patient with CCDC115-CDG using semi-quantitative N-glycan analysis of total and fractionated plasma glycoproteins, in response to Geerts et al. [1].

Journal: Molecular genetics and metabolism
Published: November 14, 2025

SCYL1 deficiency and intrafamilial variability: Two cases from Kuwait.

SCYL1 deficiency and intrafamilial variability: Two cases from Kuwait.

Journal: Molecular genetics and metabolism reports
Published: September 07, 2025

Investigating Elevated Glutaric Acid in Early Infancy.

Investigating Elevated Glutaric Acid in Early Infancy.

Journal: The journal of applied laboratory medicine
Published: September 02, 2025
Showing 1-12 of 193

Last Updated: 09/26/2026