Langping Gao

Hangzhou, China

Last Updated: 09/26/2026

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Found 13 publications

Metabolic Profiling Reveals Organ-Specific Molecular Pathologies and Aging-Associated Biomarkers in Progeroid Laminopathy.

Metabolic Profiling Reveals Organ-Specific Molecular Pathologies and Aging-Associated Biomarkers in Progeroid Laminopathy.

Journal: Smart medicine

Published: February 10, 2026

Disease pathogenicity in Hutchinson-Gilford progeria syndrome mice: insights from lung-associated alterations.

Disease pathogenicity in Hutchinson-Gilford progeria syndrome mice: insights from lung-associated alterations.

Journal: Molecular medicine (Cambridge, Mass.)

Published: August 16, 2024

Identification of a novel GRHPR mutation in primary hyperoxaluria type 2 and establishment of patient-derived iPSC line.

Identification of a novel GRHPR mutation in primary hyperoxaluria type 2 and establishment of patient-derived iPSC line.

Journal: Human cell

Published: August 11, 2024

The Pathogenesis of Nephrotic Syndrome: A Perspective from B Cells.

The Pathogenesis of Nephrotic Syndrome: A Perspective from B Cells.

Journal: Kidney diseases (Basel, Switzerland)

Published: April 18, 2024

Comparison of Two Representative Methods for Differentiation of Human Induced Pluripotent Stem Cells into Mesenchymal Stromal Cells.

Comparison of Two Representative Methods for Differentiation of Human Induced Pluripotent Stem Cells into Mesenchymal Stromal Cells.

Journal: Journal of visualized experiments : JoVE

Published: November 06, 2023

Lipidomic profiles in serum and urine in children with steroid sensitive nephrotic syndrome.

Lipidomic profiles in serum and urine in children with steroid sensitive nephrotic syndrome.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: October 24, 2023

Generating Kidney Organoids in Suspension from Induced Pluripotent Stem Cells.

Generating Kidney Organoids in Suspension from Induced Pluripotent Stem Cells.

Journal: Journal of visualized experiments : JoVE

Published: September 07, 2023

Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents.

Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents.

Journal: International journal of biological macromolecules

Published: June 13, 2023

A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations.

A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations.

Journal: Vaccines

Published: April 30, 2023

Low skeletal muscle mass as an early sign in children with fabry disease.

Low skeletal muscle mass as an early sign in children with fabry disease.

Journal: Orphanet journal of rare diseases

Published: April 20, 2023

Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.

Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.

Journal: European journal of clinical investigation

Published: December 13, 2022

Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with GLA N215S mutation: Case report and literature review.

Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with GLA N215S mutation: Case report and literature review.

Journal: Heliyon

Published: November 30, 2022

Showing 1-12 of 13

Last Updated: 09/26/2026