Evidence map›Paper›PMID 24958601›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2015

Epigenetics in kidney development and renal disease.

Gregory R Dressler, Sanjeevkumar R Patel

Open access · greenAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Sex-specific epigenetic programming in renal fibrosis and inflammation.American journal of physiology. Renal physiology · 2023
    Review
  5. Are Alterations in DNA Methylation Related to CKD Development?International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Sexual Dimorphism of Corticosteroid Signaling during Kidney Development.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Epigenetics of Renal Development and Disease.The Yale journal of biology and medicine · 2016
    Review
  17. Epigenetics mechanisms in renal development.Pediatric nephrology (Berlin, Germany) · 2016
    Review
  18. What is damaging the kidney in lupus nephritis?Nature reviews. Rheumatology · 2016
    Review
  19. Review
  20. Review
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.

Gregory R DresslerDepartment of Pathology, University of Michigan, Ann Arbor, Mich. Electronic address: dressler@umich.edu.
Sanjeevkumar R PatelDepartment of Internal Medicine, University of Michigan, Ann Arbor, Mich.
University of Michigan · US

Funding

Research Supplement to Promote Diversity in Health Related ResearchR01DK054740 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DRESSLER, GREGORY R · 1999 to 2024
$9.0M
Epigenetic Regulation of Kidney DevelopmentR01DK073722 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DRESSLER, GREGORY R · 2006 to 2020
$4.6M
Mechanism of Gene Repression in the KidneyR01DK082409 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PATEL, SANJEEVKUMAR R · 2009 to 2013
$1.5M
NIDDK NIH HHS DK073722NIDDK NIH HHS DK082409NIDDK NIH HHS R01 DK054740NIDDK NIH HHS R01 DK073722NIDDK NIH HHS R01 DK082409
6 · The paper itself

Abstract

The study of epigenetics is intimately linked and inseparable from developmental biology. Many of the genes that imprint epigenetic information on chromatin function during the specification of cell lineages in the developing embryo. These include the histone methyltransferases and their cofactors of the Polycomb and Trithorax gene families. How histone methylation is established and what regulates the tissue and locus specificity of histone methylation is an emerging area of research. The embryonic kidney is used as a model to understand how DNA-binding proteins can specify cell lineages and how such proteins interact directly with the histone methylation machinery to generate a unique epigenome for particular tissues and cell types. In adult tissues, histone methylation marks must be maintained for normal gene expression patterns. In chronic and acute renal disease, epigenetic marks are being characterized and correlated with the establishment of metabolic memory, in part to explain the persistence of pathologies even when optimal treatment modalities are used. Thus, the state of the epigenome in adult cells must be considered when attempting to alleviate or alter gene expression patterns in disease.

Indexed as

Epigenesis, GeneticAnimalsChromatin Assembly and DisassemblyGene Expression Regulation, DevelopmentalGenetic MarkersGenomic InstabilityHistonesHumansKidneyKidney DiseasesTranslational Research, BiomedicalGenetic MarkersHistones

Identifiers

PMID24958601
PMCPMC4256142
OpenAlexW2105691664

What OpenQuestion holds

Textmetadata
LicenceTDM
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.