Shasha Zhang

Lanzhou, 730000, China

Last Updated: 09/26/2026

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Found 13 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

Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.

Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.

Journal: Biomolecules

Published: April 25, 2023

Decreased lipid levels in adult with congenital heart disease: a systematic review and Meta-analysis.

Decreased lipid levels in adult with congenital heart disease: a systematic review and Meta-analysis.

Journal: BMC cardiovascular disorders

Published: March 06, 2023

Aberrant Cyclin D1 splicing in cancer: from molecular mechanism to therapeutic modulation.

Aberrant Cyclin D1 splicing in cancer: from molecular mechanism to therapeutic modulation.

Journal: Cell death & disease

Published: November 30, 2022

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

Influence of cyclin D1 splicing variants expression on breast cancer chemoresistance via CDK4/CyclinD1-pRB-E2F1 pathway.

Influence of cyclin D1 splicing variants expression on breast cancer chemoresistance via CDK4/CyclinD1-pRB-E2F1 pathway.

Journal: Journal of cellular and molecular medicine

Published: August 21, 2022

A novel PTEN mutant caused by polymorphism in cis-regulatory elements is involved in chemosensitivity in breast cancer.

A novel PTEN mutant caused by polymorphism in cis-regulatory elements is involved in chemosensitivity in breast cancer.

Journal: American journal of cancer research

Published: August 17, 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

CCN1 gene polymorphisms associated with congenital heart disease susceptibility in Northwest Chinese population from different high-altitude areas.

CCN1 gene polymorphisms associated with congenital heart disease susceptibility in Northwest Chinese population from different high-altitude areas.

Journal: Environmental science and pollution research international

Published: February 26, 2021

A SNP involved in alternative splicing of ABCB1 is associated with clopidogrel resistance in coronary heart disease in Chinese population.

A SNP involved in alternative splicing of ABCB1 is associated with clopidogrel resistance in coronary heart disease in Chinese population.

Journal: Aging

Published: July 02, 2020

Both Light-Induced SA Accumulation and ETI Mediators Contribute to the Cell Death Regulated by BAK1 and BKK1.

Both Light-Induced SA Accumulation and ETI Mediators Contribute to the Cell Death Regulated by BAK1 and BKK1.

Journal: Frontiers in plant science

Published: March 01, 2017

Identification and Characterization of Multiple Intermediate Alleles of the Key Genes Regulating Brassinosteroid Biosynthesis Pathways.

Identification and Characterization of Multiple Intermediate Alleles of the Key Genes Regulating Brassinosteroid Biosynthesis Pathways.

Journal: Frontiers in plant science

Published: July 21, 2016

Showing 1-12 of 13

Last Updated: 09/26/2026