Cargando…

lncRNA ADAMTS9-AS1/circFN1 Competitively Binds to miR-206 to Elevate the Expression of ACTB, Thus Inducing Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease and can result in substantial disability. The current study explored the potentials of long noncoding RNA- (lncRNA-) circular RNA- (circRNA-) microRNA- (miRNA-) messenger RNA (mRNA) networks in HCM. Firstly, HCM-related microarray data w...

Descripción completa

Detalles Bibliográficos
Autores principales:	Feng, Wei, Han, Shuo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989615/ https://www.ncbi.nlm.nih.gov/pubmed/35401927 http://dx.doi.org/10.1155/2022/1450610

Ejemplares similares

circFN1 Mediates Sorafenib Resistance of Hepatocellular Carcinoma Cells by Sponging miR-1205 and Regulating E2F1 Expression
por: Yang, Cheng, et al.
Publicado: (2020)

Aberrant expressions of miRNA-206 target, FN1, in multifactorial Hirschsprung disease
por: Gunadi, et al.
Publicado: (2019)

ACTB and GAPDH appear at multiple SDS-PAGE positions, thus not suitable as reference genes for determining protein loading in techniques like Western blotting
por: Zhang, Keyin, et al.
Publicado: (2021)

Pseudogenes as Weaknesses of ACTB (Actb) and GAPDH (Gapdh) Used as Reference Genes in Reverse Transcription and Polymerase Chain Reactions
por: Sun, Yuan, et al.
Publicado: (2012)

Asymptomatic Apical Hypertrophic Cardiomyopathy in an Elite Competitive Athlete
por: Huang, Athena L., et al.
Publicado: (2022)

miR-206 inhibits FN1 expression and proliferation and promotes apoptosis of rat type II alveolar epithelial cells
por: Duan, Jun, et al.
Publicado: (2017)

Malignant epithelioid neoplasm of the ileum with ACTB-GLI1 fusion mimicking an adnexal mass
por: Marco, Ambrosio, et al.
Publicado: (2022)

Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
por: Latham, Sharissa L., et al.
Publicado: (2018)

ACTB Mutations Analysis and Genotype–Phenotype Correlation in Becker’s Nevus
por: Dai, Shangzhi, et al.
Publicado: (2021)

Why Is It Thus?
Publicado: (1897)

De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome
por: Rivière, Jean-Baptiste, et al.
Publicado: (2012)

Correction to: Malignant epithelioid neoplasm of the ileum with ACTB-GLI1 fusion mimicking an adnexal mass
por: Ambrosio, Marco, et al.
Publicado: (2022)

The circRNA circADAMTS6 promotes progression of ESCC and correlates with prognosis
por: Bu, Jing, et al.
Publicado: (2022)

Reversible Apical Hypertrophy in a Young Competitive Athlete with Familiar Hypertrophic Cardiomyopathy
por: Di Gioia, Giuseppe, et al.
Publicado: (2023)

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder
por: Cuvertino, Sara, et al.
Publicado: (2017)

Becker’s Naevus Syndrome with Breast Aplasia Due to Postzygotic Mutation of ACTB
por: RAMSPACHER, Jeanne, et al.
Publicado: (2022)

Implications for Collagen Binding from the Crystallographic Structure of Fibronectin (6)FnI(1–2)FnII(7)FnI
por: Erat, Michèle C., et al.
Publicado: (2010)

Hypertrophic cardiomyopathy
por: Antunes, Murillo de Oliveira, et al.
Publicado: (2020)

Hypertrophic Cardiomyopathy
por: Butt, Asra K., et al.
Publicado: (2023)

Microarray profiling of long non-coding RNA (lncRNA) associated with hypertrophic cardiomyopathy
por: Yang, Wei, et al.
Publicado: (2015)

Structure of unliganded membrane-proximal domains FN4-FN5-FN6 of DCC
por: Finci, Lorenzo I., et al.
Publicado: (2017)

Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
por: Latham, Sharissa L., et al.
Publicado: (2018)

Integrated proteome and malonylome analyses reveal the potential meaning of TLN1 and ACTB in end-stage renal disease
por: Tan, Ruqi, et al.
Publicado: (2023)

Hsa_circ_0000285 contributes to gastric cancer progression by upregulating FN1 through the inhibition of miR‐1278
por: Wang, Xue, et al.
Publicado: (2022)

The Feline Cardiomyopathies: 2. Hypertrophic cardiomyopathy
por: Kittleson, Mark D, et al.
Publicado: (2021)

Competitive endogenous network of circRNA, lncRNA, and miRNA in osteosarcoma chemoresistance
por: Qin, Shuang, et al.
Publicado: (2023)

Data Mining and Expression Analysis of Differential lncRNA ADAMTS9-AS1 in Prostate Cancer
por: Wan, Jiahui, et al.
Publicado: (2020)

Hypertrophic Obstructive Cardiomyopathy
por: Cohen, Lawrence S.
Publicado: (1972)

The genetics of hypertrophic cardiomyopathy
por: Akhtar, Mohammed, et al.
Publicado: (2018)

Disopyramide for Hypertrophic Cardiomyopathy
por: Sanchez-Nadales, Alejandro, et al.
Publicado: (2019)

T1 mapping in discrimination between hypertrophic and hypertensive cardiomyopathy
por: Hinojar, Rocio, et al.
Publicado: (2014)

Non-contrast T1rho CMR for hypertrophic cardiomyopathy
por: Wang, Chunhua, et al.
Publicado: (2015)

T(1) mapping for characterization of myocardial fibrosis in hypertrophic cardiomyopathy
por: Liu, Ying, et al.
Publicado: (2016)

TFRC and ACTB as the best reference genes to quantify Urokinase Plasminogen Activator in breast cancer
por: Majidzadeh-A, Keivan, et al.
Publicado: (2011)

Further delineation of putative ACTB loss‐of‐function variants: A 4‐patient series
por: Baumann, Matthias, et al.
Publicado: (2020)

Role of FN1 and GREB1 gene polymorphisms in endometriosis
por: Matalliotaki, Charoula, et al.
Publicado: (2019)

Corrigendum: Data Mining and Expression Analysis of Differential lncRNA ADAMTS9-AS1 in Prostate Cancer
por: Wan, Jiahui, et al.
Publicado: (2020)

Circ_0101692 knockdown retards the development of clear cell renal cell carcinoma through miR-384/FN1 pathway
por: Zhang, Huan, et al.
Publicado: (2023)

Native T1 is predictive of abnormal myocardial strain in hypertrophic cardiomyopathy
por: Jensen, Patrick J, et al.
Publicado: (2015)

Native T1 mapping in children and young adults with hypertrophic cardiomyopathy
por: Parekh, Keyur, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_rqn52taf3g6euoinal1tvbvv58