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

Correlation of the predisposition of Chinese children to cerebral palsy with nucleotide variation in pri-miR-124 that alters the non-canonical apoptosis pathway.

Acta pharmacologica Sinica - 1 Sept 2018

Li Hui, Wang Xiu-Li, Wu Yan-Qiu, Liu Xiu-Mei, Li Ai-Min

Abstract excerpt

Cerebral palsy is a group of non-progressive motor impairment syndromes caused by brain lesions during development. Herein, we investigated the relationship between nucleotide variations in a miRNA coding region and the predisposition of Chinese children to cerebral palsy. A total of 233 CP patients and 256 healthy participants were enrolled, and 60 children were selected from each group for plasma miRNA...

Read the complete abstract on PubMed

Topics

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

Share to Beclin-1
Share to Cerebral Palsy

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Down-Regulation

Share to HEK293 Cells

Share to MicroRNAs

Share to Microtubule-Associated Proteins

Share to RNA Precursors

Share to Up-Regulation

Source

Open in PubMed Open full text

Identifiers

PMID: 29770797
DOI: 10.1038/aps.2017.211
PMCID: PMC6289373

Genes

BECN1
ITGB1
LAMC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Correlation of the predisposition of Chinese children to cerebral palsy with nucleotide variation in pri-miR-124 that alters the non-canonical apoptosis pathway.PMID 29770797Read ↗

A SNP site in pri-miR-124 changes mature miR-124 expression but no contribution to Alzheimer's disease in a Mongolian population.Semantic proximity Read ↗

MicroRNAs serve as prediction and treatment-response biomarkers of attention-deficit/hyperactivity disorder and promote the differentiation of neuronal cells by repressing the apoptosis pathwaySemantic proximity Read ↗

Exome-wide association study identified genetic variants contributing to the risk of cerebral palsySemantic proximity Read ↗

Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.Semantic proximity Read ↗

Genetic variants in the HLA region contribute to the risk of cerebral palsy.Semantic proximity Read ↗

Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families.Semantic proximity Read ↗

TNF-α and MTHFR Polymorphisms Associated with Cerebral Palsy in Chinese Infants.Semantic proximity Read ↗

Blood-Bourne MicroRNA Biomarker Evaluation in Attention-Deficit/Hyperactivity Disorder of Han Chinese Individuals: An Exploratory StudySemantic proximity Read ↗

MicroRNA-124 rs531564 Polymorphism and Cancer Risk: A Meta-analysis.Semantic proximity Read ↗

miR-124 and VAMP3 Act Antagonistically in Human Neuroblastoma.Semantic proximity Read ↗

Genetic association study of adaptor protein complex 4 with cerebral palsy in a Han Chinese population.Semantic proximity Read ↗

Association between the p73 G4C14-to-A4T14 polymorphism and risk of nasopharyngeal carcinoma: a case-control and family-based study.Semantic proximity Read ↗

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