[HTML][HTML] Knowledge mapping of idiopathic scoliosis genes and research hotspots (2002–2022): a bibliometric analysis
L Ru, H Zheng, W Lian, S Zhao, Q Fan - Frontiers in Pediatrics, 2023 - ncbi.nlm.nih.gov
Background The etiology of idiopathic scoliosis (IS) remains unclear. Gene-based studies
on genetic etiology and molecular mechanisms have improved our understanding of IS and …
on genetic etiology and molecular mechanisms have improved our understanding of IS and …
Estrogen receptor type 1 and type 2 presence in paravertebral skeletal muscles: expression level and relation to phenotype in children with idiopathic scoliosis
T Kotwicki, M Tomaszewski, M Andrusiewicz, A Śliwa… - Genes, 2022 - mdpi.com
The study aimed to detect the presence and assess the expression levels of the estrogen
receptors type 1 (ESR1) and type 2 (ESR2) within paravertebral skeletal muscles of female …
receptors type 1 (ESR1) and type 2 (ESR2) within paravertebral skeletal muscles of female …
FTO-dependent m6A regulates muscle fiber remodeling in an NFATC1–YTHDF2 dependent manner
W Wang, X Du, M Luo, N Yang - Clinical Epigenetics, 2023 - Springer
Background Adolescent idiopathic scoliosis (AIS) is characterized by low lean mass without
vertebral deformity. The cause-and-effect relationship between scoliosis and paraspinal …
vertebral deformity. The cause-and-effect relationship between scoliosis and paraspinal …
Basonuclin-2 regulates extracellular matrix production and degradation
Epithelial–mesenchymal transition is essential for tissue patterning and organization. It
involves both regulation of cell motility and alterations in the composition and organization of …
involves both regulation of cell motility and alterations in the composition and organization of …
COMPARATIVE ANALYSIS OF THE UTS2R RS11654140 (T> C) POLYMORPHISM DISTRIBUTION IN PATIENTS WITH ADOLESCENT IDIOPATHIC SCOLIOSIS AND …
KG Buslov, SE Khalchitsky, AN Filippova - 2022 - elibrary.ru
Background: Polymorphic variant of UTS2R (rs11654140) have recently been reported as a
potential contributor to the susceptibility of adolescent idiopathic scoliosis (AIS) in the …
potential contributor to the susceptibility of adolescent idiopathic scoliosis (AIS) in the …
[PDF][PDF] COMPARATIVE ANALYSIS OF THE RS1800449 (LOX G473A) GENETIC POLYMORPHISM FREQUENCY DISTRIBUTION AMONG PATIENTS WITH …
BK Grigorevich, KS Egorovich… - UAE–RUSSIA …, 2023 - scholar.archive.org
Introduction. The aim of the study was to determine the association between the single
nucleotide genetic polyorphism rs1800449 in the lysyl oxidase gene (LOX G473A) and the …
nucleotide genetic polyorphism rs1800449 in the lysyl oxidase gene (LOX G473A) and the …