Xiaodan Chen

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

F. Ning, Haifang Wang, C. Zeng, 2021, Cancer communications.

Novel mutations in a Chinese family with two patients with succinic semialdehyde dehydrogenase deficiency

Hao Hu, Yunting Lin, Li Liu, 2020, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

A novel variant in SLC16A2 associated with typical Allan-Herndon-Dudley syndrome: a case report

C. Zeng, Xiaodan Chen, Li Liu, 2022, BMC Pediatrics.

Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China

C. Zeng, Li Liu, Zongcai Liu, 2018, American journal of medical genetics. Part A.

Human iPSC-derived neural stem cells with ALDH5A1 mutation as a model of succinic semialdehyde dehydrogenase deficiency

Chengcheng Zhou, Yan-na Cai, Xiaodan Chen, 2022, BMC neuroscience.

The effect and mechanism of inhibiting glucose-6-phosphate dehydrogenase activity on the proliferation of Plasmodium falciparum.

Weiying Jiang, Z. Fang, Xiaodan Chen, 2017, Biochimica et biophysica acta. Molecular cell research.

A comprehensive analysis of membrane and morphology of erythrocytes from patients with glucose-6-phosphate dehydrogenase deficiency.

Xiaoying Lin, Weiying Jiang, Z. Fang, 2016, Journal of structural biology.

Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome

R. Du, Wen Zhang, Yunting Lin, 2023, Frontiers in Genetics.

The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant

Xiaojing Li, Yunting Lin, Zhikun Lu, 2022, Clinical Genetics.

Congenital cataract with LSS gene mutations: a new case report

Xiaodan Chen, Li Liu, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Novel compound heterozygous variant of GJA8 gene in two siblings with congenital cataract mimics an autosomal recessive trait

Yunting Lin, Li Liu, Xiaodan Chen, 2022, European journal of ophthalmology.