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

Association between PKA gene polymorphism and NTDs in high risk Chinese population in Shanxi.

International journal of clinical and experimental pathology - 1 Jan 2013

Wu Jian, Lu Xiaolin, Wang Zhen, Shangguan Shaofang, Chang Shaoyan, Li Rui, Wu Lihua, Bao Yihua, Niu Bo, Wang Li, Zhang Ting

Abstract excerpt

OBJECTIVE: This study aimed to investigate the single nucleotide polymorphisms (SNPs) of PKA and neural tube defects (NTDs) in Chinese population. METHOD: A total of 183 NTDs cases and 200 healthy controls were used in this study. 7 selected single nucleotide polymorphism (SNP) sites in the PKA gene were analyzed with MassArray high-throughput DNA analyzer with matrix-assisted laser desorption/ionization...

Read the complete abstract on PubMed

Topics

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

Share to Chi-Square Distribution
Share to Gestational Age

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Incidence

Share to Logistic Models

Share to Neural Tube Defects

Share to Odds Ratio

Share to Sex Factors

Share to Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Source

Open in PubMed Open full text

Identifiers

PMID: 24294386
PMCID: PMC3843280

Genes

PRKACB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between PKA gene polymorphism and NTDs in high risk Chinese population in Shanxi.PMID 24294386Read ↗

Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study.Semantic proximity Read ↗

Genes encoding catalytic subunits of protein kinase A and risk of spina bifida.Semantic proximity Read ↗

[Association of gene polymorphisms with the susceptibility of schizophrenia in Han Chinese population].Semantic proximity Read ↗

Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect.Semantic proximity Read ↗

Combined MECP2 duplication syndrome and ADNP syndrome in a Chinese boy: a case report and literature reviewSemantic proximity Read ↗

Association of genetic polymorphisms of VAX1, MAFB, and NTN1 with nonsyndromic cleft lip with or without cleft palate in Chinese population.Semantic proximity Read ↗

Association between ALDH1L1 gene polymorphism and neural tube defects in the Chinese Han population.Semantic proximity Read ↗

Phenotypic characterization of seven individuals with Marbach-Schaaf neurodevelopmental syndrome.Semantic proximity Read ↗

Polymorphism rs1052536 in Base Excision Repair Gene Is a Risk Factor in a High-Risk Area of Neural Tube Defects in China.Semantic proximity Read ↗

The correlation between SNPs within the gene of adrenergic receptor and neuropeptide Y and risk of cervical vertigo.Semantic proximity Read ↗

Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population.Semantic proximity Read ↗

Protein Kinase A in neurological disordersSemantic proximity Read ↗

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