Cargando…

Effect of 9p21.3 (lncRNA and CDKN2A/2B) variant on lipid profile

BACKGROUND: Several 9p21.3 variants, such as rs1333049, rs4977574, rs10757274, rs10757278, and rs10811661, identified from recent genome-wide association studies (GWASs) are reported to be associated with coronary artery disease (CAD) susceptibility but independent of dyslipidemia. This study invest...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wei, Baozhu, Liu, Yang, Li, Hang, Peng, Yuanyuan, Luo, Zhi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Cardiovascular Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489913/ https://www.ncbi.nlm.nih.gov/pubmed/36158791 http://dx.doi.org/10.3389/fcvm.2022.946289

Ejemplares similares

Systematic Review and Meta-Analysis of SERPINE1 4G/5G Insertion/Deletion Variant With Circulating Lipid Levels
por: Luo, Zhi, et al.
Publicado: (2022)

Deletion of the murine ortholog of human 9p21.3 locus promotes atherosclerosis by increasing macrophage proinflammatory activity
por: Kettunen, Sanna, et al.
Publicado: (2023)

Roles of the Chr.9p21.3 ANRIL Locus in Regulating Inflammation and Implications for Anti-Inflammatory Drug Target Identification
por: Aarabi, Ghazal, et al.
Publicado: (2018)

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A
por: Vijayakrishnan, Jayaram, et al.
Publicado: (2015)

A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology
por: Hungate, Eric A., et al.
Publicado: (2016)

A Functional Variant on 9p21.3 Related to Glioma Risk Affects Enhancer Activity and Modulates Expression of CDKN2B‐AS1
por: Ali, Mourad Wagdy, et al.
Publicado: (2021)

A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects
por: Cheng, Liangping, et al.
Publicado: (2020)

The role of lncRNA-mediated pyroptosis in cardiovascular diseases
por: Hu, Bo, et al.
Publicado: (2023)

9p21.3 Microdeletion involving CDKN2A/2B in a young patient with multiple primary cancers and review of the literature
por: Jensen, Marlene Richter, et al.
Publicado: (2022)

Long Noncoding RNA ANRIL: Lnc-ing Genetic Variation at the Chromosome 9p21 Locus to Molecular Mechanisms of Atherosclerosis
por: Holdt, Lesca M., et al.
Publicado: (2018)

Integrated analysis of the lncRNA-miRNA-mRNA network based on competing endogenous RNA in atrial fibrillation
por: Wang, Manman, et al.
Publicado: (2023)

Correlation of Long Non-coding RNA LncRNA-FA2H-2 With Inflammatory Markers in the Peripheral Blood of Patients With Coronary Heart Disease
por: Guo, Fengxia, et al.
Publicado: (2021)

mRNA, lncRNA, and circRNA expression profiles in a new aortic dissection murine model induced by hypoxia and Ang II
por: Li, Yuanyuan, et al.
Publicado: (2022)

Corrigendum: Correlation of Long Non-coding RNA LncRNA-FA2H-2 With Inflammatory Markers in the Peripheral Blood of Patients With Coronary Heart Disease
por: Guo, Fengxia, et al.
Publicado: (2021)

Elevated Expression of lncRNA MEG3 Induces Endothelial Dysfunction on HUVECs of IVF Born Offspring via Epigenetic Regulation
por: Jiang, Ying, et al.
Publicado: (2022)

Percutaneous coronary intervention in a patient with homozygous RNF213 variant
por: Yashima, Fumiaki, et al.
Publicado: (2022)

Dominant role of CDKN2B/p15INK4B of 9p21.3 tumor suppressor hub in inhibition of cell-cycle and glycolysis
por: Xia, Yong, et al.
Publicado: (2021)

Identification of key genes for hypertrophic cardiomyopathy using integrated network analysis of differential lncRNA and gene expression
por: Cao, Jing, et al.
Publicado: (2022)

lncRNA LOC100911717-targeting GAP43-mediated sympathetic remodeling after myocardial infarction in rats
por: Li, Pingjiang, et al.
Publicado: (2023)

Construction and Analysis of the lncRNA-miRNA-mRNA Network Based on Competing Endogenous RNA in Atrial Fibrillation
por: Ke, Xiangyu, et al.
Publicado: (2022)

Knockdown of lncRNA ENST00000609755.1 Confers Protection Against Early oxLDL-Induced Coronary Heart Disease
por: Sun, Yi, et al.
Publicado: (2021)

Transcriptome Sequencing Data Reveal LncRNA-miRNA-mRNA Regulatory Network in Calcified Aortic Valve Disease
por: Huang, Kai, et al.
Publicado: (2022)

Bioinformatics analysis of lncRNA-related ceRNA networks in the peripheral blood lymphocytes of Kazakh patients with essential hypertension in Xinjiang
por: Wang, Yan, et al.
Publicado: (2023)

LncRNA PVT1 Knockdown Ameliorates Myocardial Ischemia Reperfusion Damage via Suppressing Gasdermin D-Mediated Pyroptosis in Cardiomyocytes
por: Li, Cuizhi, et al.
Publicado: (2021)

ZMYND8 suppresses MAPT213 LncRNA transcription to promote neuronal differentiation
por: Adhikary, Santanu, et al.
Publicado: (2022)

ANRIL: A lncRNA at the CDKN2A/B Locus With Roles in Cancer and Metabolic Disease
por: Kong, Yahui, et al.
Publicado: (2018)

A New lncRNA, APTR, Associates with and Represses the CDKN1A/p21 Promoter by Recruiting Polycomb Proteins
por: Negishi, Masamitsu, et al.
Publicado: (2014)

Novel lncRNA-miRNA-mRNA Competing Endogenous RNA Triple Networks Associated Programmed Cell Death in Heart Failure
por: Zheng, Yu, et al.
Publicado: (2021)

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient
por: Yuan, Zhuang-Zhuang, et al.
Publicado: (2020)

Effect of TRIB1 Variant on Lipid Profile and Coronary Artery Disease: A Systematic Review and Meta-Analysis
por: Wei, Baozhu, et al.
Publicado: (2023)

CARF (CDKN2AIP) Regulates Hepatic Lipid Metabolism and Protects Against Development of Non-Alcoholic Fatty Liver Diseases
por: Hasan, Kamrul M, et al.
Publicado: (2021)

LncRNA TUG1 Regulates Proliferation of Cardiac Fibroblast via the miR-29b-3p/TGF-β1 Axis
por: Guo, Yini, et al.
Publicado: (2021)

The Exosomal lncRNA KLF3-AS1 From Ischemic Cardiomyocytes Mediates IGF-1 Secretion by MSCs to Rescue Myocardial Ischemia-Reperfusion Injury
por: Chen, Gecai, et al.
Publicado: (2021)

Overexpressed lncRNA ROR Promotes the Biological Characteristics of ox-LDL-Induced HUVECs via the let-7b-5p/HOXA1 Axis in Atherosclerosis
por: Yu, Cong, et al.
Publicado: (2021)

Deficiency of a novel lncRNA-HRAT protects against myocardial ischemia reperfusion injury by targeting miR-370-3p/RNF41 pathway
por: Zheng, Xinbin, et al.
Publicado: (2022)

Clinical significance of the series of CYP2C9*non3 variants, an unignorable predictor of warfarin sensitivity in Chinese population
por: Wang, Dongxu, et al.
Publicado: (2022)

A Common Variant in the CDKN2B Gene on Chromosome 9p21 Protects Against Coronary Artery Disease in Americans of African Ancestry: CDKN2B Gene Variant and CAD in African Americans
por: Kral, Brian G., et al.
Publicado: (2011)

Upregulation of the Long Non-coding RNA LINC01480 Is Associated With Immune Infiltration in Coronary Artery Disease Based on an Immune-Related lncRNA-mRNA Co-expression Network
por: Xiong, Ting, et al.
Publicado: (2022)

The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease
por: Temel, Şehime Gülsün, et al.
Publicado: (2019)

lncRNA CDKN2B-AS1 Could Be an Indicator to Identify Prognosis and Status of Immune Microenvironment in Thyroid Cancer
por: Xue, Cheng, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_gs6euvdf7pk6ikotes8fa6ackp