Master regulators of skeletal muscle lineage development and pluripotent stem cells differentiation

J Esteves de Lima, F Relaix - Cell Regeneration, 2021 - Springer
In vertebrates, the skeletal muscles of the body and their associated stem cells originate
from muscle progenitor cells, during development. The specification of the muscles of the …

Tissue cross talks governing limb muscle development and regeneration

F Helmbacher, S Stricker - Seminars in Cell & Developmental Biology, 2020 - Elsevier
For decades, limb development has been a paradigm of three-dimensional patterning.
Moreover, as the limb muscles and the other tissues of the limb's musculoskeletal system …

Muscle precursor cell movements in zebrafish are dynamic and require Six family genes

JC Talbot, EM Teets, D Ratnayake, PQ Duy… - …, 2019 - journals.biologists.com
Muscle precursors need to be correctly positioned during embryonic development for proper
body movement. In zebrafish, a subset of hypaxial muscle precursors from the anterior …

The susceptibility and potential functions of the LBX1 gene in adolescent idiopathic Scoliosis

M Luo, Y Zhang, S Huang, Y Song - Frontiers in Genetics, 2021 - frontiersin.org
Genome-wide association studies have identified many susceptibility genes for adolescent
idiopathic scoliosis (AIS). However, most of the results are hard to be replicated in multi …

Paraspinal muscle ladybird homeobox 1 (LBX1) in adolescent idiopathic scoliosis: a cross-sectional study

W Jennings, M Hou, D Perterson, P Missiuna… - The Spine Journal, 2019 - Elsevier
BACKGROUND CONTEXT Adolescent idiopathic scoliosis (AIS) is the leading cause of
spinal deformity in adolescents globally. Recent evidence from genome-wide association …

Idiopathic scoliosis families highlight actin-based and microtubule-based cellular projections and extracellular matrix in disease etiology

EE Baschal, EA Terhune, CI Wethey… - G3: Genes …, 2018 - academic.oup.com
Idiopathic scoliosis (IS) is a structural lateral spinal curvature of≥ 10° that affects up to 3% of
otherwise healthy children and can lead to life-long problems in severe cases. It is well …

Asymmetric expression of Wnt/B-catenin pathway in AIS: primary or secondary to the curve?

L Xu, Z Dai, C Xia, Z Wu, Z Feng, X Sun, Z Liu, Y Qiu… - Spine, 2020 - journals.lww.com
Study Design. A prospective case-control study. Objectives. To investigate whether the
asymmetric changes are primary or secondary to spinal deformity. Summary of Background …

Characterization of a novel Lbx1 mouse loss of function strain

L Decourtye, JA McCallum-Loudeac… - Differentiation, 2022 - Elsevier
Abstract Adolescent Idiopathic Scoliosis (AIS) is the most common type of spine deformity
affecting 2–3% of the population worldwide. The etiology of this disease is still poorly …

[HTML][HTML] Fibroblast growth factor 8: Multifaceted Role in Development and Developmental Disorder

H Yin, L Duan, Z Wang, L Liu, J Shen - Genes & Diseases, 2025 - Elsevier
Abstract Fibroblast growth factor 8 (FGF8), a secreted signaling molecule, involves in
regulating cell survival, proliferation, migration, and differentiation. It exhibits a highly …

Abrogation of LBX1 in skeletal muscle results in hypoplastic limbs and progressive kyphosis in mice

Y Matsuhashi, K Horiuchi, T Nakagawa… - Journal of …, 2023 - Wiley Online Library
LBX1 is a gene located near a single‐nucleotide polymorphism, rs11190870, which is
highly associated with susceptibility to adolescent idiopathic scoliosis. However, the …