Cargando…

Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees

Genetic polymorphisms can shape the global landscape of DNA methylation, by either changing substrates for DNA methyltransferases or altering the DNA binding affinity of cis-regulatory proteins. The interactions between CpG methylation and genetic polymorphisms have been previously investigated by m...

Descripción completa

Detalles Bibliográficos
Autores principales:	Plongthongkum, Nongluk, van Eijk, Kristel R., de Jong, Simone, Wang, Tina, Sul, Jae Hoon, Boks, Marco P. M., Kahn, René S., Fung, Ho-Lim, Ophoff, Roel A., Zhang, Kun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096397/ https://www.ncbi.nlm.nih.gov/pubmed/25019935 http://dx.doi.org/10.1371/journal.pone.0099313

Ejemplares similares

Aging effects on DNA methylation modules in human brain and blood tissue
por: Horvath, Steve, et al.
Publicado: (2012)

Library-free Methylation Sequencing with Bisulfite Padlock Probes
por: Diep, Dinh, et al.
Publicado: (2012)

Identification of methylation haplotype blocks aids in deconvolution of heterogeneous tissue samples and tumor tissue-of-origin mapping from plasma DNA
por: Guo, Shicheng, et al.
Publicado: (2017)

Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
por: van Eijk, Kristel R, et al.
Publicado: (2012)

The Relationship of DNA Methylation with Age, Gender and Genotype in Twins and Healthy Controls
por: Boks, Marco P., et al.
Publicado: (2009)

Lithium Use during Pregnancy and the Risk of Miscarriage
por: Poels, Eline M. P., et al.
Publicado: (2020)

Powerful eQTL mapping through low-coverage RNA sequencing
por: Schwarz, Tommer, et al.
Publicado: (2022)

Nuclear Pedigree Criteria of Suspected HNPCC
por: Kładny, Józef, et al.
Publicado: (2003)

Cell type deconvolution of bulk blood RNA-Seq to reveal biological insights of neuropsychiatric disorders
por: Boltz, Toni, et al.
Publicado: (2023)

Utilization of Receptor-Binding Domain of SARS-CoV-2 Spike Protein Expressed in Escherichia coli for the Development of Neutralizing Antibody Assay
por: Tantiwiwat, Termsak, et al.
Publicado: (2022)

Computational design of novel nanobodies targeting the receptor binding domain of variants of concern of SARS-CoV-2
por: Longsompurana, Phoomintara, et al.
Publicado: (2023)

“Forward Genetics” as a Method to Maximize Power and Cost-Efficiency in Studies of Human Complex Traits
por: Boks, M. P. M., et al.
Publicado: (2010)

Methylome Analysis of Two Xanthomonas spp. Using Single-Molecule Real-Time Sequencing
por: Seong, Hoon Je, et al.
Publicado: (2016)

Methylome evolution in plants
por: Vidalis, Amaryllis, et al.
Publicado: (2016)

The association between antibodies to neurotropic pathogens and bipolar disorder: A study in the Dutch Bipolar (DB) Cohort and meta-analysis
por: Snijders, Gijsje J. L. J., et al.
Publicado: (2019)

Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis
por: Derks, Eske M., et al.
Publicado: (2012)

Correction: Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis
por: Derks, Eske M., et al.
Publicado: (2013)

The role of ABCA7 in Alzheimer’s disease: evidence from genomics, transcriptomics and methylomics
por: De Roeck, Arne, et al.
Publicado: (2019)

Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto’s thyroiditis
por: Gong, Licheng, et al.
Publicado: (2018)

Erratum to: Methylome Evolution in plants
por: Vidalis, Amaryllis, et al.
Publicado: (2017)

A Gene Co-Expression Network in Whole Blood of Schizophrenia Patients Is Independent of Antipsychotic-Use and Enriched for Brain-Expressed Genes
por: de Jong, Simone, et al.
Publicado: (2012)

Adenomatous Polyposis Coli Gene Mutations in 22 Chinese Pedigrees with Familial Adenomatous Polyposis
por: Wang, Dan, et al.
Publicado: (2019)

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates
por: Sul, Jae Hoon, et al.
Publicado: (2020)

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
por: McLaughlin, Russell L., et al.
Publicado: (2017)

O12.1. EXAMINING THE NEUROBIOLOGICAL IMPACT OF CHILDHOOD TRAUMA: AN IMPORTANT ROLE FOR FRONTAL AND INSULAR REGIONS
por: Begemann, Marieke, et al.
Publicado: (2018)

Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder
por: Chubick, Alex, et al.
Publicado: (2023)

Parasites and Their Pedigree
Publicado: (1884)

Rules for resolving Mendelian inconsistencies in nuclear pedigrees typed for two-allele markers
por: Khan, Sajjad Ahmad, et al.
Publicado: (2017)

A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
por: Zhou, Yunguo, et al.
Publicado: (2023)

A single-nucleus RNA-sequencing pipeline to decipher the molecular anatomy and pathophysiology of human kidneys
por: Lake, Blue B., et al.
Publicado: (2019)

The Landscape of Genomic Imprinting at the Porcine SGCE/PEG10 Locus from Methylome and Transcriptome of Parthenogenetic Embryos
por: Ahn, Jinsoo, et al.
Publicado: (2020)

A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication
por: Zhuang, Jianlong, et al.
Publicado: (2019)

Nuclear Pedigree Criteria for the Identification of Individuals Suspected to be at Risk of an Inherited Predisposition to Renal Cancer
por: Tołoczko-Grabarek, Aleksandra, et al.
Publicado: (2005)

Nuclear Pedigree Criteria for the Identification of Individuals Suspected to Be at Risk of an Inherited Predisposition to Gastric Cancer
por: Gawdis-Wojnarska, Beata, et al.
Publicado: (2004)

Clinicopathological characteristics and postoperative prognosis of patients with nuclear pedigree of esophageal squamous cell carcinoma
por: Wei, Meng Xia, et al.
Publicado: (2023)

Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cells
por: Abeni, Edoardo, et al.
Publicado: (2017)

A Hæmophilic Pedigree
por: Macnicol, Malcolm
Publicado: (1910)

Pedigree Go Fish
por: Osier, Michael V.
Publicado: (2017)

The Pedigree of the Central Incisor
por: Thompson, A. H.
Publicado: (1893)

Exploring the cancer methylome
por: Berman, Benjamin P, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_4d25gpo0vvhdc40s4hvh4veehh