Chaochun Zou

China

Last Updated: 09/26/2026

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Found 32 publications

Childhood Ayme-Gripp syndrome: A case report.

Childhood Ayme-Gripp syndrome: A case report.

Journal: The Journal of international medical research
Published: May 31, 2026

Unravelling the Gut-Skin Axis in Chronic Urticaria: Dysbiosis, Metabolites and Immunological Mechanisms.

Unravelling the Gut-Skin Axis in Chronic Urticaria: Dysbiosis, Metabolites and Immunological Mechanisms.

Journal: Experimental dermatology
Published: February 03, 2026

Lamb-Shaffer syndrome in a Chinese adolescent: A case report.

Lamb-Shaffer syndrome in a Chinese adolescent: A case report.

Journal: Medicine
Published: August 25, 2025

A Cornelia de Lange syndrome NIPBL 5'-UTR mutation reduces cell proliferation in an in vitro model by downregulating RAD21 and β-catenin.

A Cornelia de Lange syndrome NIPBL 5'-UTR mutation reduces cell proliferation in an in vitro model by downregulating RAD21 and β-catenin.

Journal: Biomedical reports
Published: April 25, 2025

Corrigendum to "Vitamin C deficiency exacerbates diabetic glomerular injury through activation of transforming growth factor-β signaling" [BBA-General Subject, 1861 (2017) 2186-2195, on June 2017].

Corrigendum to "Vitamin C deficiency exacerbates diabetic glomerular injury through activation of transforming growth factor-β signaling" [BBA-General Subject, 1861 (2017) 2186-2195, on June 2017].

Journal: Biochimica et biophysica acta. General subjects
Published: January 03, 2024

Corrigendum to "High expression of Sonic hedgehog in allergic airway epithelia contributes to goblet cell metaplasia" [Mucosal Immunol. 11(5) (2018) 1306-1315].

Corrigendum to "High expression of Sonic hedgehog in allergic airway epithelia contributes to goblet cell metaplasia" [Mucosal Immunol. 11(5) (2018) 1306-1315].

Journal: Mucosal immunology
Published: October 20, 2023

Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).

Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).

Journal: Molecular genetics & genomic medicine
Published: October 09, 2023

Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China.

Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China.

Journal: Clinical genetics
Published: September 19, 2023

Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis.

Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis.

Journal: RNA biology
Published: July 05, 2023

Clinical manifestations in a Chinese girl with heterozygous de novo NAA10 variant c. 247C > T, p. (Arg83Cys): a case report.

Clinical manifestations in a Chinese girl with heterozygous de novo NAA10 variant c. 247C > T, p. (Arg83Cys): a case report.

Journal: Frontiers in pediatrics
Published: April 02, 2023

Health-related quality of life of children with Williams syndrome and caregivers in China.

Health-related quality of life of children with Williams syndrome and caregivers in China.

Journal: Frontiers in public health
Published: March 01, 2023

Phosphorylation of human glioma-associated oncogene 1 on Ser937 regulates Sonic Hedgehog signaling in medulloblastoma.

Phosphorylation of human glioma-associated oncogene 1 on Ser937 regulates Sonic Hedgehog signaling in medulloblastoma.

Journal: Nature communications
Published: November 08, 2022
Showing 1-12 of 32

Last Updated: 09/26/2026