Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Lack of association between the promoter polymorphism of the MTNR1A gene and adolescent idiopathic scoliosis.

Spine - 15 Sept 2008

Qiu Xu-Sheng, Tang Nelson L S, Yeung Hiu-Yan, Cheng Jack C Y, Qiu Yong

Abstract excerpt

STUDY DESIGN: A genetic association study to investigate variation of the melatonin receptor 1A (MTNR1A) gene in adolescent idiopathic scoliosis (AIS) patients. OBJECTIVE: To determine whether the MTNR1A gene promoter polymorphism is associated with the predisposition and/or disease severity of A...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Gene Expression Regulation
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Polymorphism, Single Nucleotide

Share to Radiography

Share to Scoliosis

Source

Identifiers

PMID: 18794763
DOI: 10.1097/BRS.0b013e31817e0424

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18794763-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of association between the promoter polymorphism of the MTNR1A gene and adolescent idiopathic scoliosis.PMID 18794763Read ↗

[Effect of genetic polymorphism of MTNR1A gene on adolescent idiopathic scoliosis].Semantic proximity Read ↗

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.Semantic proximity Read ↗

Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population.Semantic proximity Read ↗

The role of melatonin receptor 1B gene (MTNR1B) in adolescent idiopathic scoliosis--a genetic association study.Semantic proximity Read ↗

The polymorphisms of melatonin receptor 1B gene (MTNR1B) (rs4753426 and rs10830963) and susceptibility to adolescent idiopathic scoliosis: a meta-analysis.Semantic proximity Read ↗

Genetic variants in melatonin synthesis and signaling pathway are not associated with adolescent idiopathic scoliosis.Semantic proximity Read ↗

The Association of rs4753426 Polymorphism in the Melatonin Receptor 1B (MTNR1B) Gene and Susceptibility to Adolescent Idiopathic Scoliosis: A Systematic Review and Meta-analysis.Semantic proximity Read ↗

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population.Semantic proximity Read ↗

Lack of association between DSCAM gene polymorphisms and adolescent idiopathic scoliosis susceptibility in a Chinese Han population.Semantic proximity Read ↗

[Association between polymorphism of Matrilin-1 gene (MATN1) with susceptibility to adolescent idiopathic scoliosis].Semantic proximity Read ↗

Single Nucleotide Polymorphisms and Adolescent Idiopathic Scoliosis: A Systematic Review and Meta-Analysis of the Literature.Semantic proximity Read ↗

Potential genetic markers predicting the outcome of brace treatment in patients with adolescent idiopathic scoliosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.