Evidence map›Paper›PMID 42162556›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

3D Chromatin Architecture During Early Development: New Methods and New Findings.

Eduardo Blanco-Olais, Karina Jácome-López, Rosario Pérez-Molina, Mayra Furlan-Magaril

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Eduardo Blanco-OlaisMolecular Genetics Department, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
Karina Jácome-LópezMolecular Genetics Department, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
Rosario Pérez-MolinaMolecular Genetics Department, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
Mayra Furlan-MagarilMolecular Genetics Department, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico. mfurlan@ifc.unam.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies on genome spatial organization have increased considerably in the past few decades, allowing for the detailed characterization of diverse genomic topological landscapes. Chromatin interactions between promoters and regulatory elements are crucial in controlling gene regulation during development, resulting in specific gene expression profiles characterized by transcript dosage and their distribution in time and space. Here, we describe both proximity-ligation-based and non-proximity-ligation-based new technologies, as well as their exciting findings in pluripotent cells and early embryogenesis. We also discuss examples of chromatin conformation disruption in disease and cancer.

Indexed as

ChromatinEmbryonic DevelopmentAnimalsChromatin Assembly and DisassemblyGene Expression Regulation, DevelopmentalHumansPromoter Regions, GeneticChromatinChromatin architectureDistal regulatory elementsGenome topology

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.