Xuan Yang

Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels.

Hala Sakkal-Alkaddour, L Zhang, Xuan Yang et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 84 citations · Full text

Type Ii 3, Gynecology, Type Ii +16

Systematic discovery of mutation-directed neo-protein-protein interactions in cancer

Xiulei Mo, Qiankun Niu, Andrei A. Ivanov et al. · Cell · 2022 · 69 citations · Full text

Tumor Biology, Somatic Variant, Interactomics +6

Hypomorph mutation-directed small-molecule protein-protein interaction inducers to restore mutant SMAD4-suppressed TGF-β signaling

Cong Tang, Xiulei Mo, Qiankun Niu et al. · Cell chemical biology · 2020 · 38 citations · Full text

Molecular Physiology, Signal Transduction, Signaling Pathway +8

Phase Engineering of Intermetallic PtBi₂ Nanoplates for Formic Acid Electrochemical Oxidation

Xianbiao Fu, Hongjian Li, Aoni Xu et al. · Nano Letters · 2023 · 30 citations

A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.

L Zhang, Hala Sakkal-Alkaddour, Ying Chang et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 29 citations · Full text

Adrenal Gland, Codon 318, Developmental Biology +14