Evidence map›Paper›PMID 19802523›Full record

ArticleMolecular and cellular biochemistry2010

Modulation of chromatin by MARs and MAR binding oncogenic transcription factor SMAR1.

Kiran K Nakka, Samit Chattopadhyay

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 86% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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 at 1 institution in 1 country.

Kiran K NakkaNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune, 411007, Maharashtra, India.
Samit Chattopadhyay
National Centre for Cell Science · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The orchestration of the events in the cell during the progression of the cell cycle is modulated by various phenomenon which are regulated by structural modules of the cell. The nucleus is a major hub for all these regulatory units which harbour the nuclear matrix, matrix proteins and chromatin. The histone modifications etch a complex code on the chromatin and the matrix proteins in consort with the histone code regulate the gene expression. SMAR1 is a matrix attachment region binding protein that interacts with chromatin modulators like HDAC1, Sin3A and causes chromatin condensation. SMAR1 modulates the chromatin at the Vbeta locus and plays a prominent role in V(D)J recombination. Such indispensable function of SMAR1 by the modulation of chromatin in the context of malignancy and V(D)J recombination emphasizes that MAR binding proteins regulate the complex events of the cell and perturbed expression causes disease conditions.

Indexed as

Gene Expression RegulationAcetylationAnimalsCell Cycle ProteinsChromatinCyclin D1DNA-Binding ProteinsHistone Deacetylase 1HistonesHumansMatrix Attachment Region Binding ProteinsMatrix Attachment RegionsMethylationNuclear MatrixNuclear Matrix-Associated ProteinsNuclear ProteinsBANP protein, humanCell Cycle ProteinsChromatinCyclin D1DNA-Binding ProteinsHistone Deacetylase 1HistonesMatrix Attachment Region Binding ProteinsNuclear Matrix-Associated ProteinsNuclear Proteins

Identifiers

PMID19802523
OpenAlexW2075151455

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.