Microarray expression profiling identifies genes with altered expression in Adolescent Idiopathic Scoliosis

No abstract is available for this paper.

• Publication year

  2013

• Venue

  European spine journal

• Publication date

  2013-03-07

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00586-013-2728-2PMID 23467837PMCID PMC3676547
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

  2011cited by this paper
• Potential role of COMP as a biomarker for adolescent idiopathic scoliosis.

  2011cited by this paper
• Epigenetics: Principles and Practice

  2011cited by this paper
• New disease gene location and high genetic heterogeneity in idiopathic scoliosis

  2011cited by this paper
• Adolescent idiopathic scoliosis (AIS), environment, exposome and epigenetics: a molecular perspective of postnatal normal spinal growth and the etiopathogenesis of AIS with consideration of a network approach and possible implications for medical therapy

  2011cited by this paper
• MicroRNAs, epigenetics and disease.

  2010cited by this paper
• Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.

  2009cited by this paper
• Association of an ERAP1 ERAP2 haplotype with familial ankylosing spondylitis

  2009cited by this paper
• A novel locus for adolescent idiopathic scoliosis on chromosome 12p

  2009cited by this paper
• Estrogen cross‐talk with the melatonin signaling pathway in human osteoblasts derived from adolescent idiopathic scoliosis patients

  2008cited by this paper
• Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.

  2008cited by this paper
• Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel

  2007cited by this paper
• Melatonin Receptor 1B (MTNR1B) Gene Polymorphism Is Associated With the Occurrence of Adolescent Idiopathic Scoliosis

  2007cited by this paper
• Evidence of a linkage between matrilin-1 gene (MATN1) and idiopathic scoliosis

  2006cited by this paper
• Association of Estrogen Receptor Gene Polymorphisms With Susceptibility to Adolescent Idiopathic Scoliosis

  2006cited by this paper
• Idiopathic Scoliosis: Identification of Candidate Regions on Chromosome 19p13

  2006cited by this paper
• Knockdown of the complete Hox paralogous group 1 leads to dramatic hindbrain and neural crest defects

  2005cited by this paper
• Familial Idiopathic Scoliosis: Evidence of an X-Linked Susceptibility Locus

  2003cited by this paper
• Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11

  2002cited by this paper
• Sex steroids and the construction and conservation of the adult skeleton.

  2002cited by this paper
• Pseudoachondroplasia and multiple epiphyseal dysplasia: Mutation review, molecular interactions, and genotype to phenotype correlations

  2002cited by this paper
• A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3.

  2002cited by this paper
• Smad1 Domains Interacting with Hoxc-8 Induce Osteoblast Differentiation*

  2000cited by this paper
• Localization of Susceptibility to Familial Idiopathic Scoliosis

  2000cited by this paper
• Role of Pitx1 upstream of Tbx4 in specification of hindlimb identity.

  1999cited by this paper
• Mutation of HOXA13 in hand-foot-genital syndrome

  1997cited by this paper
• Melatonin: A Possible Role in Pathogenesis of Adolescent Idiopathic Scoliosis

  1996cited by this paper
• Gain of function mutations for paralogous Hox genes: implications for the evolution of Hox gene function.

  1995cited by this paper
• Levels of platelet calmodulin for the prediction of progression and severity of adolescent idiopathic scoliosis.

  1994cited by this paper
• Trunk Asymmetry, Posture, Growth, and Risk of Scoliosis: A Three-Year Follow-Up of Finnish Prepubertal School Children

  1993cited by this paper
• Moe's textbook of scoliosis and other spinal deformities

  1987cited by this paper
• The contribution of the intervertebral disk to the scoliotic deformity.

  1981cited by this paper
• A study of labyrinthine function in patients with adolescent idiopathic scoliosis. I. An electro-nystagmographic study.

  1979cited by this paper
• Posterior spinal fusion in scoliosis: indications, technique, and results.

  1979cited by this paper
• Posterior spinal fusion in scoliosis: indications, technique, and results.

  1979cited by this paper

• Large-scale mouse mutagenesis identifies novel genes affecting vertebral anatomy

  2026cites this paper
• Genome-wide profiling of circulating microRNAs in adolescent idiopathic scoliosis and their relation to spinal deformity severity, and disease pathophysiology

  2025cites this paper
• Local Expression of Epigenetic Candidate Biomarkers of Adolescent Idiopathic Scoliosis Progression

  2025cites this paper
• Methylation Profile of Cell-Free DNA as a Diagnostic Marker for Myocarditis

  2025cites this paper
• Identification of Epigenetic Biomarkers of Adolescent Idiopathic Scoliosis Progression: A Workflow to Assess Local Gene Expression

  2024cites this paper
• Preliminary Investigation into the Association between Scoliosis and Hypoxia: A Retrospective Cohort Study on the Impact of Eliminating Hypoxic Factors on Scoliosis Outcomes

  2024cites this paper
• Large-scale mouse mutagenesis identifies novel genes affecting vertebral development

  2024cites this paper
• Identification and validation of putative biomarkers by in silico analysis, mRNA expression and oxidative stress indicators for negative energy balance in buffaloes during transition period

  2024influential citation
• Etiopathogenesis of adolescent idiopathic scoliosis (AIS): Role of genetic and environmental factors

  2023cites this paper
• Advances in epigenetic research of adolescent idiopathic scoliosis and congenital scoliosis

  2023cites this paper
• Protein-protein interaction map in pre-eclampsia through the integration of hub genes, transcription factors and microRNAs

  2022cites this paper
• Idiopathic scoliosis as a multifactorial disease: systematic review of current literature

  2022cites this paper
• Upregulation of microRNA-96-5p is associated with adolescent idiopathic scoliosis and low bone mass phenotype

  2022cites this paper
• Idiopathic scoliosis: general characteristics and analysis of etiological theories (literature review)

  2021cites this paper
• Putative biomarkers for early detection of mastitis in cattle

  2020cites this paper
• Quantitation Analysis of PCDH10 Methylation In Adolescent Idiopathic Scoliosis Using Pyrosequencing Study.

  2020cites this paper
• Research progress on the etiology and pathogenesis of adolescent idiopathic scoliosis

  2020cites this paper
• Increased EEG alpha peak frequency in adolescents with idiopathic scoliosis during balance control in normal upright standing.

  2020cites this paper
• Clinical Observations and Treatment Approaches for Scoliosis in Prader–Willi Syndrome

  2020cites this paper
• Upregulation of cGMP‐dependent Protein Kinase (PRKG1) in the Development of Adolescent Idiopathic Scoliosis

  2020cites this paper
• Association of higher bone turnover with risk of curve progression in Adolescent Idiopathic Scoliosis.

  2020cites this paper
• Effets de l'estradiol et du chargement mécanique sur la régulation de la POC5 et du récepteur ADGRG7 dans la scoliose idiopathique

  2019cites this paper
• Asymmetric expression of GPR126 in the convex/concave side of the spine is associated with spinal skeletal malformation in adolescent idiopathic scoliosis population

  2019cites this paper
• Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome

  2019cites this paper
• Dissecting the mechanisms of bone loss in Gorham-Stout disease.

  2019cites this paper
• Cortical dynamics of sensorimotor information processing associated with balance control in adolescents with and without idiopathic scoliosis.

  2019cites this paper
• Abnormal PITX1 gene methylation in adolescent idiopathic scoliosis: a pilot study

  2018influential citation
• The 17β-estradiol induced upregulation of the adhesion G-protein coupled receptor (ADGRG7) is modulated by ESRα and SP1 complex

  2018cites this paper
• Quantitative Evaluation of MMP-9 and TIMP-1 Promoter Methylation in Chronic Periodontitis

  2018cites this paper
• The filamin-B–refilin axis – spatiotemporal regulators of the actin-cytoskeleton in development and disease

  2018cites this paper
• Quantitative evaluation of the relationship between COMP promoter methylation and the susceptibility and curve progression of adolescent idiopathic scoliosis

  2018cites this paper
• Aberrant miR‐145–5p/β‐catenin signal impairs osteocyte function in adolescent idiopathic scoliosis

  2018cites this paper
• Etiological Theories of Adolescent Idiopathic Scoliosis: Past and Present

  2017cites this paper
• DNA-Based Testing for Adolescent Idiopathic Scoliosis Policy

  2016cites this paper
• Genetics and pathogenesis of idiopathic scoliosis

  2016cites this paper
• Identification of Differential Genes Expression Profiles and Pathways of Bone Marrow Mesenchymal Stem Cells of Adolescent Idiopathic Scoliosis Patients by Microarray and Integrated Gene Network Analysis

  2016cites this paper
• FEP Medical Policy Manual

  2016cites this paper
• Screening for candidate genes related to breast cancer with cDNA microarray analysis

  2015cites this paper
• The Trk family of neurotrophin receptors is downregulated in the lumbar spines of rats with congenital kyphoscoliosis

  2015cites this paper
• Serum level of cartilage oligomeric matrix protein is lower in children with idiopathic scoliosis than in non-scoliotic controls

  2015cites this paper
• Mesenchymal Progenitors Aging Highlights a miR‐196 Switch Targeting HOXB7 as Master Regulator of Proliferation and Osteogenesis

  2015cites this paper
• Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations

  2014cites this paper
• DNA-Based Testing for Adolescent Idiopathic Scoliosis

  2012cites this paper