Ya-zhou Li
Shijiazhuang, China
Last Updated: 09/26/2026
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Found 9 publications
SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.
Journal: Communications biology
Published: October 09, 2024
Identification of novel variations in three cases with rare inherited neuromuscular disorder.
Journal: Experimental and therapeutic medicine
Published: December 18, 2023
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).
Journal: Molecular genetics & genomic medicine
Published: August 07, 2023
Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: December 16, 2021
Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis.
Journal: Frontiers in genetics
Published: August 24, 2021
Identification of novel variations in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
Journal: Molecular genetics & genomic medicine
Published: April 28, 2021
Therapeutic Effect Evaluation of Neuromuscular Electrical Stimulation With or Without Strengthening Exercise on Spastic Cerebral Palsy.
Journal: Clinical pediatrics
Published: October 10, 2017
External Fixator-assisted Ulnar Osteotomy: A Novel Technique to Treat Missed Monteggia Fracture in Children.
Journal: Orthopaedic surgery
Published: September 10, 2017
Effect of acupuncture on inflammatory cytokines expression of spastic cerebral palsy rats.
Journal: Asian Pacific journal of tropical medicine
Published: December 10, 2013
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Last Updated: 09/26/2026