Xiao-jun Li

305 East Zhongshan Road
Nanjing, 210002, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

A mouse model for X-linked Alport syndrome induced by Del-ATGG in the Col4a5 gene.

A mouse model for X-linked Alport syndrome induced by Del-ATGG in the Col4a5 gene.

Journal: Frontiers in medicine

Published: November 05, 2022

Comparative Functional Analysis in vitro of 2 COL4A5 Splicing Mutations at the Same Site in 2 Unrelated Alport Syndrome Chinese Families.

Comparative Functional Analysis in vitro of 2 COL4A5 Splicing Mutations at the Same Site in 2 Unrelated Alport Syndrome Chinese Families.

Journal: Cytogenetic and genome research

Published: November 27, 2019

miR-212-5p exerts tumor promoter function by regulating the Id3/PI3K/Akt axis in lung adenocarcinoma cells.

miR-212-5p exerts tumor promoter function by regulating the Id3/PI3K/Akt axis in lung adenocarcinoma cells.

Journal: Journal of cellular physiology

Published: December 25, 2018

Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.

Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.

Journal: Cytogenetic and genome research

Published: November 22, 2017

Inhibitor of DNA binding 3 reverses cisplatin resistance in human lung adenocarcinoma cells by regulating the PI3K/Akt pathway.

Inhibitor of DNA binding 3 reverses cisplatin resistance in human lung adenocarcinoma cells by regulating the PI3K/Akt pathway.

Journal: Oncology letters

Published: March 09, 2017

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome.

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome.

Journal: PloS one

Published: November 25, 2016

Long noncoding RNA expression profile in fibroblast-like synoviocytes from patients with rheumatoid arthritis.

Long noncoding RNA expression profile in fibroblast-like synoviocytes from patients with rheumatoid arthritis.

Journal: Arthritis research & therapy

Published: June 11, 2016

Identification of citrullinated peptides in the synovial fluid of patients with rheumatoid arthritis using LC-MALDI-TOF/TOF.

Identification of citrullinated peptides in the synovial fluid of patients with rheumatoid arthritis using LC-MALDI-TOF/TOF.

Journal: Clinical rheumatology

Published: October 09, 2015

A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review.

A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review.

Journal: Molecular medicine reports

Published: September 29, 2014

A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria.

A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria.

Journal: Journal of genetics

Published: September 06, 2014

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report.

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report.

Journal: Molecular medicine reports

Published: May 29, 2014

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family.

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family.

Journal: BMC medical genetics

Published: May 04, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026