Cargando…

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)

Ventricular Septal Defect (VSD), the most common congenital heart defect, is characterized by a hole in the septum between the right and left ventricles. The pathogenesis of VSD is unknown in most clinical cases. There is a paucity of data relevant to epigenetic changes in VSD. The placenta is a fet...

Descripción completa

Detalles Bibliográficos
Autores principales:	Radhakrishna, Uppala, Albayrak, Samet, Zafra, Rita, Baraa, Alosh, Vishweswaraiah, Sangeetha, Veerappa, Avinash M., Mahishi, Deepthi, Saiyed, Nazia, Mishra, Nitish K., Guda, Chittibabu, Ali-Fehmi, Rouba, Bahado-Singh, Ray O.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2019
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428297/ https://www.ncbi.nlm.nih.gov/pubmed/30897084 http://dx.doi.org/10.1371/journal.pone.0200229

Ejemplares similares

Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF)
por: Radhakrishna, Uppala, et al.
Publicado: (2018)

Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy
por: Bahado-Singh, Ray O., et al.
Publicado: (2019)

Placental DNA methylation changes and the early prediction of autism in full-term newborns
por: Bahado-Singh, Ray O., et al.
Publicado: (2021)

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia
por: Vishweswaraiah, Sangeetha, et al.
Publicado: (2019)

Precision Oncology: Artificial Intelligence and DNA Methylation Analysis of Circulating Cell-Free DNA for Lung Cancer Detection
por: Bahado-Singh, Ray, et al.
Publicado: (2022)

Alzheimer’s Precision Neurology: Epigenetics of Cytochrome P450 Genes in Circulating Cell-Free DNA for Disease Prediction and Mechanism
por: Bahado-Singh, Ray O., et al.
Publicado: (2023)

Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome
por: Radhakrishna, Uppala, et al.
Publicado: (2023)

Precision gynecologic oncology: circulating cell free DNA epigenomic analysis, artificial intelligence and the accurate detection of ovarian cancer
por: Bahado-Singh, Ray O., et al.
Publicado: (2022)

Transcatheter Ventricular Septal Defect (VSD) Creation for Restrictive VSD in Double-Outlet Right Ventricle
por: Lin, C. Huie, et al.
Publicado: (2012)

Differential methylation of microRNA encoding genes may contribute to high myopia
por: Swierkowska, Joanna, et al.
Publicado: (2023)

Endovascular closure of MINOCA-caused ventricular septal defect (VSD)
por: Petrov, Ivo Spasov, et al.
Publicado: (2021)

Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS)
por: Radhakrishna, Uppala, et al.
Publicado: (2016)

Decreased Levels of DNA Methylation in the PCDHA Gene Cluster as a Risk Factor for Early-Onset High Myopia in Young Children
por: Swierkowska, Joanna, et al.
Publicado: (2022)

Risk factor analysis for adverse prognosis of the fetal ventricular septal defect (VSD)
por: Shan, Wang, et al.
Publicado: (2023)

Integrative Analysis Unveils the Correlation of Aminoacyl-tRNA Biosynthesis Metabolites with the Methylation of the SEPSECS Gene in Huntington’s Disease Brain Tissue
por: Vishweswaraiah, Sangeetha, et al.
Publicado: (2023)

Percutaneous closure of congenital Gerbode defect using Nit-Occlud(®) Lê VSD coil
por: Phan, Quang T, et al.
Publicado: (2017)

Application of VSD technique in adults with chronic osteomyelitis of the extremities combined with soft tissue defects
por: Zhang, Xinling, et al.
Publicado: (2022)

An Updated Mutation Spectrum of the γ-Secretase Complex: Novel NCSTN Gene Mutation in an Indian Family with Hidradenitis Suppurativa and Acne Conglobata
por: Ratnamala, Uppala, et al.
Publicado: (2023)

Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers
por: Vishweswaraiah, Sangeetha, et al.
Publicado: (2015)

A Case of a Ventricular Septal Defect (VSD) Leading to a Left Ventricular Aneurysm
por: Moreira, Matheus, et al.
Publicado: (2022)

Precision oncology: Artificial intelligence, circulating cell‐free DNA, and the minimally invasive detection of pancreatic cancer—A pilot study
por: Bahado‐Singh, Ray O., et al.
Publicado: (2023)

Comparative Analysis of Differentially Expressed miRNAs and their Downstream mRNAs in Ovarian Cancer and its Associated Endometriosis
por: Wu, Richard Licheng, et al.
Publicado: (2015)

Unravelling the Complexity of Human Olfactory Receptor Repertoire by Copy Number Analysis across Population Using High Resolution Arrays
por: Veerappa, Avinash M., et al.
Publicado: (2013)

Cytogenomic profiling of breast cancer brain metastases reveals potential for repurposing targeted therapeutics
por: Bollig-Fischer, Aliccia, et al.
Publicado: (2015)

Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes
por: Veerappa, Avinash M., et al.
Publicado: (2015)

Perventricular Muscular Ventricular Septal Defect (VSD) Closure under Epicardial Echocardiography Guidance: A Case Report
por: Molaei, Akbar, et al.
Publicado: (2017)

Artificial Intelligence and Circulating Cell-Free DNA Methylation Profiling: Mechanism and Detection of Alzheimer’s Disease
por: Bahado-Singh, Ray O., et al.
Publicado: (2022)

ECHOCARDIOGRAPHY FOR RESIDUAL VSD
por: Kapoor, Poonam Malhotra
Publicado: (2016)

Artificial intelligence and leukocyte epigenomics: Evaluation and prediction of late-onset Alzheimer’s disease
por: Bahado-Singh, Ray O., et al.
Publicado: (2021)

Genome-wide DNA methylation analysis reveals molecular subtypes of pancreatic cancer
por: Mishra, Nitish Kumar, et al.
Publicado: (2017)

Ventricular Septal Defect in an Octogenarian: A Case Report of VSD Surgical Repair Concomitant with Coronary Artery Bypass and Valvular Surgery
por: Tayama, Eiki, et al.
Publicado: (2012)

Closure of a Prosthetic Mitral Valve Paravalvular Leak Using a Ventricular Septal Defect (VSD) Amplatzer Occluder Device
por: Oladiran, Oreoluwa, et al.
Publicado: (2021)

Undiagnosed sub-valvular aortic stenosis with an associated Ventricular Septal Defect (VSD) presenting late in a multi-parous woman
por: Appiah, Lambert Tetteh, et al.
Publicado: (2023)

Methylated Cytochrome P450 and the Solute Carrier Family of Genes Correlate With Perturbations in Bile Acid Metabolism in Parkinson’s Disease
por: Vishweswaraiah, Sangeetha, et al.
Publicado: (2022)

Long-term outcome of perimembranous VSD closure using the Nit-Occlud® Lê VSD coil system
por: Kozlik-Feldmann, Rainer, et al.
Publicado: (2020)

First report of polymorphisms in MTRR, GATA4, VEGF, and ISL1 genes in Pakistani children with isolated ventricular septal defects (VSD)
por: Sarwar, Sumbal, et al.
Publicado: (2021)

Survival Analysis of Multi-Omics Data Identifies Potential Prognostic Markers of Pancreatic Ductal Adenocarcinoma
por: Mishra, Nitish Kumar, et al.
Publicado: (2019)

Prognostic value of biomarkers in the tumor microenvironment of pancreatic ductal adenocarcinoma
por: Mishra, Nitish K., et al.
Publicado: (2020)

Pan-Cancer Analysis of Human Kinome Gene Expression and Promoter DNA Methylation Identifies Dark Kinase Biomarkers in Multiple Cancers
por: Southekal, Siddesh, et al.
Publicado: (2021)

Becoming a Teenager after Early Surgical Ventricular Septal Defect (VSD) Repair: Longitudinal Biopsychological Data on Mental Health and Maternal Involvement
por: Lang, Laura, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_qnln7q88qi9qh327vorj4phgfp