Peiqiang Li

Lanzhou, 730000, China

Last Updated: 09/26/2026

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Found 15 publications

Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.

Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.

Journal: Molecular therapy. Nucleic acids

Published: December 10, 2025

Mutation in MSH5 Causes Primary Ovarian Insufficiency and Successful Therapeutic Intervention by In Vitro Fertilisation.

Mutation in MSH5 Causes Primary Ovarian Insufficiency and Successful Therapeutic Intervention by In Vitro Fertilisation.

Journal: Journal of cellular and molecular medicine

Published: September 04, 2024

The potential up-regulation risk of 3' UTR SNP (rs10787760 G > A) for the VAX1 gene is associated with NSCLP in the northwest Chinese population.

The potential up-regulation risk of 3' UTR SNP (rs10787760 G > A) for the VAX1 gene is associated with NSCLP in the northwest Chinese population.

Journal: Gene

Published: September 21, 2023

Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.

Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.

Journal: Biomolecules

Published: April 25, 2023

Single-cell RNA sequencing reveals the transcriptomic characteristics of peripheral blood mononuclear cells in hepatitis B vaccine non-responders.

Single-cell RNA sequencing reveals the transcriptomic characteristics of peripheral blood mononuclear cells in hepatitis B vaccine non-responders.

Journal: Frontiers in immunology

Published: November 06, 2022

A novel mutation in the UBAP1 gene causing hereditary spastic paraplegia: A case report and overview of the genotype-phenotype correlation.

A novel mutation in the UBAP1 gene causing hereditary spastic paraplegia: A case report and overview of the genotype-phenotype correlation.

Journal: Frontiers in genetics

Published: May 05, 2022

Online and offline mixed teaching mode of medical genetics

Online and offline mixed teaching mode of medical genetics

Journal: Sheng wu gong cheng xue bao = Chinese journal of biotechnology

Published: September 02, 2021

Identification of Novel Single-Nucleotide Variants With Potential of Mediating Malfunction of MicroRNA in Congenital Heart Disease.

Identification of Novel Single-Nucleotide Variants With Potential of Mediating Malfunction of MicroRNA in Congenital Heart Disease.

Journal: Frontiers in cardiovascular medicine

Published: July 11, 2021

A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.

A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.

Journal: Fertility and sterility

Published: August 27, 2018

Decreased activity of RCAN1.4 is a potential risk factor for congenital heart disease in a Han Chinese population.

Decreased activity of RCAN1.4 is a potential risk factor for congenital heart disease in a Han Chinese population.

Journal: Protein & cell

Published: March 30, 2018

A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin.

A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin.

Journal: Oncotarget

Published: November 15, 2016

Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people.

Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people.

Journal: Clinical science (London, England : 1979)

Published: August 30, 2016

Showing 1-12 of 15

Last Updated: 09/26/2026