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

Evaluation value and mechanism of ADRB2 and FCER1B gene polymorphisms in preterm infants with congenital respiratory diseases.

Cellular and molecular biology (Noisy-le-Grand, France) - 10 Dec 2023

Liu Jiangyue, Zhu Qingwen, Jiang Hongru, Zhang Lingli, Cao Xian

Abstract excerpt

In this study, we observed the value of ADRB2 and FCER1B gene polymorphisms in evaluating congenital respiratory diseases in preterm infants (PTIs), analyzed their effects on airway smooth muscle cells (ASMCs), and preliminarily discussed the underlying mechanism. First, we placed 64 healthy PTIs (control group) and 45 PTIs with congenital respiratory diseases (research group) born at our hospital from April 2021...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Premature

Share to Polymorphism, Genetic

Share to Polymorphism, Single Nucleotide

Share to Receptors, Adrenergic, beta-2

Share to Receptors, IgE

Share to Respiratory Tract Diseases

Source

Identifiers

PMID: 38158688
DOI: 10.14715/cmb/2023.69.13.9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation value and mechanism of ADRB2 and FCER1B gene polymorphisms in preterm infants with congenital respiratory diseases.PMID 38158688Read ↗

Comprehensive analysis of characteristic genes of inflammation-related bronchopulmonary dysplasia based on bioinformatics methodsSemantic proximity Read ↗

Toward precision for bronchopulmonary dysplasia: Moving past current definitions.Semantic proximity Read ↗

Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role.Semantic proximity Read ↗

Risk factors of bronchopulmonary dysplasia in premature infants under 32 weeks of gestation: A retrospective case-control studySemantic proximity Read ↗

Establishment and efficiency analysis of the risk prediction model predicting the likelihood of bronchopulmonary dysplasia in preterm infants: A retrospective observational studySemantic proximity Read ↗

Identification of potential biomarkers in the peripheral blood of neonates with bronchopulmonary dysplasia using WGCNA and machine learning algorithmsSemantic proximity Read ↗

Role of Single Nucleotide Fibronectin Polymorphisms in Pathogenesis of Bronchopulmonary DysplasiaSemantic proximity Read ↗

Comprehensive Analysis of Long Non-coding RNA,miRNA，and mRNA-associated Competitive Endogenous RNA Networks in the Peripheral Blood of Preterm Infants with Bronchopulmonary DysplasiaSemantic proximity Read ↗

Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical InformationSemantic proximity Read ↗

Machine Learning Identification of Neutrophil Extracellular Trap-Related Genes as Potential Biomarkers and Therapeutic Targets for Bronchopulmonary DysplasiaSemantic proximity Read ↗

Establishment of Relational Model of Congenital Heart Disease Markers and GO Functional Analysis of the Association between Its Serum Markers and Susceptibility Genes.Semantic proximity Read ↗

Bronchopulmonary Dysplasia: Pathogenesis and PathophysiologySemantic proximity Read ↗

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