Shuxia Chen
State Key Laboratory Of Genetic Engineering, Shanghai Key Laboratory Of Metabolic Remodeling And Health
Shanghai, 200438, China
Shanghai, 200438, China
Last Updated: 09/26/2026
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Found 8 publications
Phosphorylation of a conserved TBXT threonine residue is vital to vertebral development.
Journal: Science China. Life sciences
Published: February 14, 2025
A mutation in TBXT causes congenital vertebral malformations in humans and mice.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: March 05, 2023
Deleterious Rare Mutations of GLI1 Dysregulate Sonic Hedgehog Signaling in Human Congenital Heart Disease.
Journal: Frontiers in cardiovascular medicine
Published: October 19, 2021
Genetic variants of TBX6 and TBXT identified in patients with congenital scoliosis in Southern China.
Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society
Published: April 03, 2020
Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects.
Journal: Human mutation
Published: November 13, 2019
A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: December 21, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026