Zexiao Jia

发表

A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency

Hong Chen, Wendong Huang, Yaping Sun, 2019, Front. Genet..

Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.

Wendong Huang, Xufen Zhu, Aifu Lin, 2019, Mitochondrion.

AIFM1 variants associated with auditory neuropathy spectrum disorder cause apoptosis due to impaired apoptosis-inducing factor dimerization

J. Guan, Aifu Lin, Hui Zhou, 2023, Journal of Zhejiang University-SCIENCE B.

A novel NF2 splicing mutant causes neurofibromatosis type 2 via liquid-liquid phase separation with large tumor suppressor and Hippo pathway

Wenqi Wang, Aifu Lin, Dajiang Xie, 2022, iScience.

Drosophila Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial function

Xiaohang Yang, Hui-jun Zhou, Y. Qiu, 2019, Cell & Bioscience.

Drosophila Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial function

Xiaohang Yang, Hui-jun Zhou, Y. Qiu, 2019, Cell & Bioscience.

MAP3K1 Variant Causes Hyperactivation of Wnt4/β-Catenin/FOXL2 Signaling Contributing to 46,XY Disorders/Differences of Sex Development

Hui Zhou, Wendong Huang, Hong Chen, 2022, Frontiers in Genetics.

Impaired AIF-CHCHD4 interaction and mitochondrial calcium overload contribute to auditory neuropathy spectrum disorder in patient-iPSC-derived neurons with AIFM1 variant

J. Guan, Aifu Lin, Hui Zhou, 2023, Cell death & disease.