Zongcai Liu
9 Jinsui Rd
Guangzhou, 510623, China
Guangzhou, 510623, China
Last Updated: 09/26/2026
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Found 14 publications
Evaluation of efficacy and safety of AAV8-ΔC4ATP7B gene therapy in a mutant mouse model of Wilson's disease.
Journal: Molecular therapy. Methods & clinical development
Published: September 16, 2024
Natural history and outcome of nonketotic hyperglycinemia in China.
Journal: Frontiers in neurology
Published: May 30, 2024
METTL14-Mediated Bim mRNA m6A Modification Augments Osimertinib Sensitivity in EGFR-Mutant NSCLC Cells.
Journal: Molecular cancer research : MCR
Published: December 07, 2023
Circ-FOXO3 inhibits triple-negative breast cancer growth and metastasis via regulating WHSC1-H3K36me2-Zeb2 axis.
Journal: Cellular signalling
Published: November 28, 2023
Poliovirus receptor (PVR) mediates carboplatin-induced PD-L1 expression in non-small-cell lung cancer cells.
Journal: Biochimica et biophysica acta. General subjects
Published: March 27, 2023
Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children.
Journal: BMC gastroenterology
Published: July 11, 2021
The EGFR-P38 MAPK axis up-regulates PD-L1 through miR-675-5p and down-regulates HLA-ABC via hexokinase-2 in hepatocellular carcinoma cells.
Journal: Cancer communications (London, England)
Published: May 06, 2020
Enhanced histone H3 acetylation of the PD-L1 promoter via the COP1/c-Jun/HDAC3 axis is required for PD-L1 expression in drug-resistant cancer cells.
Journal: Journal of experimental & clinical cancer research : CR
Published: October 17, 2019
Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review.
Journal: BMC musculoskeletal disorders
Published: October 08, 2019
Clinical features and mutational analysis in 114 young children with Wilson disease from South China.
Journal: American journal of medical genetics. Part A
Published: February 04, 2019
A novel GTPCH deficiency mouse model exhibiting tetrahydrobiopterin-related metabolic disturbance and infancy-onset motor impairments.
Journal: Metabolism: clinical and experimental
Published: December 07, 2018
Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China.
Journal: American journal of medical genetics. Part A
Published: November 08, 2017
Last Updated: 09/26/2026