Yangyang Yao
Key Laboratory Of Endocrine Glucose & Lipids Metabolism And Brain Aging
Jinan, 250021, China
Jinan, 250021, China
Last Updated: 09/26/2026
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Found 9 publications
Treatment with Minicircle DNA Expressing a FGF23 Fragment in a Clinically relevant Mouse Model of X-Linked Hypophosphatemic Rickets.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: May 16, 2025
Endoplasmic reticulum stress and autophagy as potential therapeutic targets in SERPINF1 mutation-induced type VI osteogenesis imperfecta.
Journal: Life sciences
Published: January 16, 2025
The role of the cartilaginous to osseous acetabular angle ratio in children with developmental dysplasia of the hip.
Journal: Frontiers in pediatrics
Published: December 01, 2023
The health-care utilization and economic burden in patients with genetic skeletal disorders.
Journal: Orphanet journal of rare diseases
Published: November 13, 2023
Characterization of Novel PHEX Variants in X-linked Hypophosphatemic Rickets and Genotype-PHEX Activity Correlation.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 12, 2023
Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: November 30, 2021
Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations.
Journal: Oxidative medicine and cellular longevity
Published: October 30, 2021
A standard set of outcome measures for the comprehensive assessment of osteogenesis imperfecta.
Journal: Orphanet journal of rare diseases
Published: July 03, 2020
Characterization of a novel COL10A1 variant associated with Schmid-type metaphyseal chondrodysplasia and a literature review.
Journal: Molecular genetics & genomic medicine
Published: May 30, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026