Evidence map›Paper›PMID 39546207›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

An Optimized Adaptation of DamID for NGS Applications.

Karen L Reddy, Xianrong Wong

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Karen L ReddyDepartment of Biological Chemistry and Center for Epigenetics, Johns Hopkins University of Medicine, Baltimore, MD, USA. kreddy4@jhmi.edu.
Xianrong WongSidney Kimmel Cancer Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA. xianrong_wong@asrl.a-star.edu.sg.

Funding

Differential Regulation and Roles of A-type Lamins in Early G1R01GM132427 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI REDDY, KAREN LYNN, WILSON, KATHERINE L · 2020 to 2023
$2.4M
NIGMS NIH HHS R01 GM132427
6 · The paper itself

Abstract

Recent studies have implicated higher-order genome organization in the regulation of genes and cellular state. Lamina-Associated Domains (LADs) are regions of heterochromatin associated with the nuclear envelope and the nuclear lamina, a protein network involved in both nuclear organization and genome structure. LADs are developmentally regulated, and their dysregulation is associated with several diseases and pathological states, including cancer and premature aging. In addition to LADs, other nuclear protein compartments appear to scaffold or support unique chromatin environments to affect gene expression. These revelations carry profound implications for our comprehension of developmental processes and the pathogenesis of various diseases, especially given the numerous disorders already directly associated with, for example, mutations in lamin and INM proteins. This spatial compartmentalization of chromatin subtypes to unique protein compartments has led to the adoption of proximity-labeling methods, such as DamID (DNA Adenine Methyltransferase Identification), to identify these unique chromatin compartments.

Indexed as

ChromatinHigh-Throughput Nucleotide SequencingDNA MethylationHeterochromatinHumansNuclear LaminaSite-Specific DNA-Methyltransferase (Adenine-Specific)ChromatinHeterochromatinSite-Specific DNA-Methyltransferase (Adenine-Specific)ChromatinDamID sequencingEpigeneticsGenome OrganizationLamina-Associated Domains (LADs)

Identifiers

PMID39546207

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.