Jiuxiang X. Wang
Hefei, 230000, China
Last Updated: 09/26/2026
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Found 15 publications
SIAH1-Mediated Ubiquitination and Degradation of TRIB3 Modulate Osteogenic and Adipogenic Differentiation.
Journal: Stem cells international
Published: January 13, 2026
Case Report: A rare case of bone destructive sacrococcygeal chordoma presenting as anal distension.
Journal: Frontiers in oncology
Published: July 24, 2025
Analysis of clinical phenotype and ATP7B variants characteristics of 337 patients with hepatolenticular degeneration in Anhui province
Journal: Zhonghua yi xue za zhi
Published: April 13, 2025
Association between obesity measurement indexes and symptomatic knee osteoarthritis among the Chinese population: analysis from a nationwide longitudinal study.
Journal: BMC musculoskeletal disorders
Published: August 15, 2024
Clinical and genetic characterization of patients with late onset Wilson's disease.
Journal: NPJ genomic medicine
Published: February 20, 2024
Discussion on the Mechanism of Gandoufumu Decoction Attenuates Liver Damage of Wilson's Disease by Inhibiting Autophagy through the PI3K/Akt/mTOR Pathway Based on Network Pharmacology and Experimental Verification.
Journal: Mediators of inflammation
Published: December 08, 2022
Clinical manifestations and genetic analysis of a newborn with Arboleda-Tham syndrome.
Journal: Frontiers in genetics
Published: July 09, 2022
Association between osteoporosis or osteopenia and taking antiplatelet agents in general US population of NHANES.
Journal: Frontiers in endocrinology
Published: May 16, 2022
Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein-Associated Neurodegeneration.
Journal: Frontiers in genetics
Published: January 11, 2022
Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.
Journal: Neuro-degenerative diseases
Published: December 18, 2021
Study on the Mechanism of Compound Kidney-Invigorating Granule for Osteoporosis based on Network Pharmacology and Experimental Verification.
Journal: Evidence-based complementary and alternative medicine : eCAM
Published: April 16, 2021
Identification of mutations in the ATP7B gene in 14 Wilson disease children: Case series.
Journal: Medicine
Published: December 19, 2020
Last Updated: 09/26/2026