Pingping F. Jiang

Hangzhou, 310052, China

Last Updated: 09/26/2026

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Found 51 publications

Exosome-Based Proteomic Profiling for Biomarker Discovery in Pediatric Fabry Disease: Insights into Early Diagnosis Monitoring.

Exosome-Based Proteomic Profiling for Biomarker Discovery in Pediatric Fabry Disease: Insights into Early Diagnosis Monitoring.

Journal: Biomedicines

Published: September 24, 2025

XPNPEP2 regulates angiogenesis via modulation of mitochondrial function through SLC25A6.

XPNPEP2 regulates angiogenesis via modulation of mitochondrial function through SLC25A6.

Journal: Frontiers in cell and developmental biology

Published: September 03, 2025

Structural dynamics of the mitochondrial ADP/ATP carrier support an asymmetric transport mechanism.

Structural dynamics of the mitochondrial ADP/ATP carrier support an asymmetric transport mechanism.

Journal: International journal of biological macromolecules

Published: August 16, 2025

Delayed excitability recovery and downregulation of neurodevelopmental pathways contribute to phenotypic differences in KCNQ2-related disorders.

Delayed excitability recovery and downregulation of neurodevelopmental pathways contribute to phenotypic differences in KCNQ2-related disorders.

Journal: Epilepsia

Published: April 09, 2025

Loss of MTX2 causes mitochondrial dysfunction, podocyte injury, nephrotic proteinuria and glomerulopathy in mice and patients.

Loss of MTX2 causes mitochondrial dysfunction, podocyte injury, nephrotic proteinuria and glomerulopathy in mice and patients.

Journal: International journal of biological sciences

Published: September 07, 2023

Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1.

Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1.

Journal: iScience

Published: January 11, 2023

Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China.

Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China.

Journal: Frontiers in cell and developmental biology

Published: October 01, 2022

Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Journal: Orphanet journal of rare diseases

Published: December 08, 2021

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Journal: JCI insight

Published: December 08, 2021

Mosaic PKHD1 in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.

Mosaic PKHD1 in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.

Journal: Frontiers in medicine

Published: July 17, 2021

Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Journal: Orphanet journal of rare diseases

Published: July 15, 2021

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.

Journal: Investigative ophthalmology & visual science

Published: June 22, 2021

Showing 1-12 of 51

Last Updated: 09/26/2026