Cargando…

Association of Angio-LncRNAs MIAT rs1061540/MALAT1 rs3200401 Molecular Variants with Gensini Score in Coronary Artery Disease Patients Undergoing Angiography

Long non-coding RNAs (lncRNAs) have emerged as essential biomolecules with variable diagnostic and/or prognostic utility in several diseases, including coronary artery disease (CAD). We aimed for the first time to investigate the potential association of five angiogenesis-related lncRNAs (PUNISHER,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Elwazir, Mohamed Y., Hussein, Mohammad H., Toraih, Eman A., Al Ageeli, Essam, Esmaeel, Safya E., Fawzy, Manal S., Faisal, Salwa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773982/ https://www.ncbi.nlm.nih.gov/pubmed/35053285 http://dx.doi.org/10.3390/biom12010137

Ejemplares similares

Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
por: Ismail, Nesreen M., et al.
Publicado: (2022)

The Relationship between MALAT1 Polymorphism rs3200401 C > T and the Risk of Overall Cancer: A Meta-Analysis
por: Li, Keming, et al.
Publicado: (2022)

Angio-LncRs: LncRNAs that regulate angiogenesis and vascular disease
por: Yu, Bo, et al.
Publicado: (2018)

MicroRNA-17-92a-1 Host Gene (MIR17HG) Expression Signature and rs4284505 Variant Association with Alopecia Areata: A Case–Control Study
por: Faisal, Salwa, et al.
Publicado: (2022)

MicroRNA-499a (rs3746444A/G) gene variant and susceptibility to type 2 diabetes-associated end-stage renal disease
por: Fawzy, Manal S., et al.
Publicado: (2022)

Association of long non-coding RNA MIAT and MALAT1 expression profiles in peripheral blood of coronary artery disease patients with previous cardiac events
por: Toraih, Eman A., et al.
Publicado: (2019)

Migration/Differentiation-Associated LncRNA SENCR rs12420823*C/T: A Novel Gene Variant Can Predict Survival and Recurrence in Patients with Breast Cancer
por: Ageeli, Essam Al, et al.
Publicado: (2022)

Analysis of the autoimmune regulator (AIRE) gene variant rs2075876 (G/A) association with breast cancer susceptibility
por: Fawzy, Manal S., et al.
Publicado: (2020)

Quercetin Can Inhibit Angiogenesis via the Down Regulation of MALAT1 and MIAT LncRNAs in Human Umbilical Vein Endothelial Cells
por: Esteghlal, Somayeh, et al.
Publicado: (2021)

Analysis of microRNA-34a expression profile and rs2666433 variant in colorectal cancer: a pilot study
por: Fawzy, Manal S., et al.
Publicado: (2020)

Diagnostic and Prognostic Risk Assessment of Heat Shock Protein HSPA1B rs2763979 Gene Variant in Asthma
por: Faisal, Salwa, et al.
Publicado: (2022)

Association of VDBP rs4701 Variant, but not VDR/RXR-α Over-Expression with Bone Mineral Density in Pediatric Well-Chelated β-Thalassemia Patients
por: Sahmoud, Shaimaa, et al.
Publicado: (2020)

Association of microRNA-34a rs2666433 (A/G) Variant with Systemic Lupus Erythematosus in Female Patients: A Case-Control Study
por: Ismail, Nesreen M., et al.
Publicado: (2021)

Association of microRNA 17 host gene variant (rs4284505) with susceptibility and severity of systemic lupus erythematosus
por: Abdel‐Gawad, Abdelhady R., et al.
Publicado: (2020)

Analysis of MIR27A (rs11671784) Variant Association with Systemic Lupus Erythematous
por: Khired, Zenat Ahmed, et al.
Publicado: (2023)

Glutathione S-Transferase (GSTT1 rs17856199) and Nitric Oxide Synthase (NOS2 rs2297518) Genotype Combination as Potential Oxidative Stress-Related Molecular Markers for Type 2 Diabetes Mellitus
por: Gusti, Amani M T, et al.
Publicado: (2021)

PUNISHER rs12318065 C>A transversion: a putative somatic driver mutation for poor prognosis in colon cancer
por: Shaheen, Sameerah, et al.
Publicado: (2022)

MYD88, NFKB1, and IL6 transcripts overexpression are associated with poor outcomes and short survival in neonatal sepsis
por: AbdAllah, Nouran B., et al.
Publicado: (2021)

Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma
por: Toraih, Eman A., et al.
Publicado: (2017)

Matrix Metalloproteinase 9/microRNA-145 Ratio: Bridging Genomic and Immunological Variabilities in Thyroid Cancer
por: Toraih, Eman A., et al.
Publicado: (2023)

Prognostic Value of LINC-ROR (rs1942347) Variant in Patients with Colon Cancer Harboring BRAF Mutation: A Propensity Score-Matched Analysis
por: Shaalan, Aly A. M., et al.
Publicado: (2022)

Association of cyclin-dependent kinase inhibitor 2B antisense RNA 1 gene expression and rs2383207 variant with breast cancer risk and survival
por: Kattan, Shahad W., et al.
Publicado: (2021)

Association between genetic variants (rs920778, rs4759314, and rs217727) in LncRNAs and cervical cancer susceptibility in Chinese population: A systematic review and meta-analysis
por: Liu, Yi, et al.
Publicado: (2022)

Longevity-Related Gene Transcriptomic Signature in Glioblastoma Multiforme
por: Fawzy, Manal S., et al.
Publicado: (2018)

Long Non-Coding RNAs Gene Variants as Molecular Markers for Diabetic Retinopathy Risk and Response to Anti-VEGF Therapy
por: Mohammad, Hala M F, et al.
Publicado: (2021)

Long Non-Coding RNAs ANRIL and HOTAIR Upregulation is Associated with Survival in Neonates with Sepsis in a Neonatal Intensive Care Unit
por: AbdAllah, Nouran B, et al.
Publicado: (2022)

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population
por: Razavian, Takavar, et al.
Publicado: (2020)

Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
por: Maher, Shymaa Ahmed, et al.
Publicado: (2022)

Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia
por: Bănescu, Claudia, et al.
Publicado: (2019)

MALAT1 rs619586 A/G polymorphisms are associated with decreased risk of lung cancer
por: Chen, Ming, et al.
Publicado: (2021)

Unleash Multifunctional Role of miRNA Biogenesis Gene Variants (XPO5*rs34324334 and RAN*rs14035) with Susceptibility to Hepatocellular Carcinoma
por: Elsalahaty, Mohamed I., et al.
Publicado: (2023)

Analyzing Gensini Score as a Semi-Continuous Outcome
por: Kashani, Homa, et al.
Publicado: (2016)

Association between the Gensini Score and Carotid Artery Stenosis
por: Avci, Anil, et al.
Publicado: (2016)

The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
por: Che, Di, et al.
Publicado: (2019)

Meta-analysis of the association between MALAT1 rs619586 A>G polymorphism and cancer risk
por: Ni, Wenwen, et al.
Publicado: (2020)

Joint effects of paraoxonase 1 rs662 polymorphism and vitamins C/E intake on coronary artery disease severity (Gensini and SYNTAX scores) and lipid profile in patients undergoing coronary angiography
por: Darand, Mina, et al.
Publicado: (2023)

Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children
por: Buda, Piotr, et al.
Publicado: (2021)

Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus
por: Alfaifi, Mohammed, et al.
Publicado: (2021)

Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)
por: Raina, Jyotdeep Kour, et al.
Publicado: (2020)

Association of rs6983267 at 8q24, HULC rs7763881 polymorphisms and serum lncRNAs CCAT2 and HULC with colorectal cancer in Egyptian patients
por: Shaker, Olfat G., et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_8ofkp5uvpc3lhq6dmajbi0klr9