Results 31 to 40 of about 21,621 (295)

Author Correction: Mapping histone modifications in low cell number and single cells using antibody-guided chromatin tagmentation (ACT-seq)

open access: yesNature Communications, 2020
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Benjamin Carter   +6 more
doaj   +1 more source

melRNA-seq for Expression Analysis of SINE RNAs and Other Medium-Length Non-Coding RNAs

open access: yesMobile DNA, 2021
Background Small interspersed elements (SINEs) are transcribed by RNA polymerase III (Pol III) to produce RNAs typically 100–500 nucleotides in length.
Yoshinobu Mori, Kenji Ichiyanagi
doaj   +1 more source

Epigenome-wide association studies: current knowledge, strategies and recommendations

open access: yesClinical Epigenetics, 2021
The aetiology and pathophysiology of complex diseases are driven by the interaction between genetic and environmental factors. The variability in risk and outcomes in these diseases are incompletely explained by genetics or environmental risk factors ...
M. Campagna   +7 more
semanticscholar   +1 more source

Mapping histone modifications in low cell number and single cells using antibody-guided chromatin tagmentation (ACT-seq)

open access: yesNature Communications, 2019
The authors introduce ACT-seq: a Tn5-based method for rapidly profiling epigenetic marks in bulk-cell and single-cell samples. ACT-seq avoids many laborious or time-consuming steps required for similar techniques including chromatin fragmentation and end
Benjamin Carter   +6 more
doaj   +1 more source

A systematic review of childhood maltreatment and DNA methylation: candidate gene and epigenome-wide approaches

open access: yesTranslational Psychiatry, 2021
Childhood maltreatment is a major risk factor for chronic and severe mental and physical health problems across the lifespan. Increasing evidence supports the hypothesis that maltreatment is associated with epigenetic changes that may subsequently serve ...
S. Parade   +5 more
semanticscholar   +1 more source

Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons

open access: yesbioRxiv, 2022
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by loss-of-function heterozygous mutations of Methyl CpG-binding Protein 2 (MECP2) on the X chromosome in girls.
Junming Qian   +9 more
semanticscholar   +1 more source

The Epigenome in Neurodevelopmental Disorders [PDF]

open access: yesFrontiers in Neuroscience, 2021
Neurodevelopmental diseases (NDDs), such as autism spectrum disorders, epilepsy, and schizophrenia, are characterized by diverse facets of neurological and psychiatric symptoms, differing in etiology, onset and severity. Such symptoms include mental delay, cognitive and language impairments, or restrictions to adaptive and social behavior. Nevertheless,
Julia Reichard   +3 more
openaire   +5 more sources

The epigenomics of sarcoma

open access: yesNature Reviews Cancer, 2020
Epigenetic regulation is critical to physiological control of development, cell fate, cell proliferation, genomic integrity, and fundamentally, transcriptional regulation. This epigenetic control occurs at multiple levels including through DNA methylation, histone modification, nucleosome remodeling, and modulation of the three-dimensional chromatin ...
Jamie S.E. Yu   +8 more
openaire   +4 more sources

Captive rearing effects on the methylome of Atlantic salmon after oceanic migration: Sex‐specificity and intergenerational stability

open access: yesMolecular Ecology Resources, EarlyView., 2023
Abstract Captive rearing in salmon hatcheries can have considerable impacts on both fish phenotype and fitness within a single generation, even in the absence of genetic change. Evidence for hatchery‐induced changes in DNA methylation is becoming abundant, though questions remain on the sex‐specificity of these effects, their persistence until spawning
Clare J. Venney   +6 more
wiley   +1 more source

Epigenetic alterations in TRAMP mice: epigenome DNA methylation profiling using MeDIP-seq

open access: yesCell & Bioscience, 2018
Purpose We investigated the genomic DNA methylation profile of prostate cancer in transgenic adenocarcinoma of the mouse prostate (TRAMP) cancer model and to analyze the crosstalk among targeted genes and the related functional pathways. Methods Prostate
Wenji Li   +11 more
doaj   +1 more source

Home - About - Disclaimer - Privacy