Evidence map›Paper›PMID 11336630›Full record

ReviewThe Biochemical journal2001

The marks, mechanisms and memory of epigenetic states in mammals.

V K Rakyan, J Preis, H D Morgan, E Whitelaw

Registry-linked trialAbstract readReview
In one paragraph

Review in The Biochemical journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00755677 (Exploring the Health Benefits Associated With Daily Pulse Consumption in Individuals With Peripheral Arterial Disease), which is not on this map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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.

NCT00755677 early_phase1completednot on this mapstarted 2007, after this paper: background citation

Exploring the Health Benefits Associated With Daily Pulse Consumption in Individuals With Peripheral Arterial Disease

TypeinterventionalSponsorSt. Boniface HospitalRan2007 to 2008Enrolled26ConditionsPeripheral Arterial DiseaseArmsPulses
3 · Its place in the literature

Who cites it

53 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The role of MeCP2 in learning and memory.Learning & memory (Cold Spring Harbor, N.Y.) · 2019
    Article
  10. Review
  11. Review
  12. Review
  13. Single nucleotide variations: biological impact and theoretical interpretation.Protein science : a publication of the Protein Society · 2014
    Review
  14. Epigenetics: a new way to look at kidney diseases.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2014
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors.

V K RakyanDepartment of Biochemistry, G08, University of Sydney, NSW 2006, Australia.
J Preis
H D Morgan
E Whitelaw

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well recognized that there is a surprising degree of phenotypic variation among genetically identical individuals, even when the environmental influences, in the strict sense of the word, are identical. Genetic textbooks acknowledge this fact and use different terms, such as 'intangible variation' or 'developmental noise', to describe it. We believe that this intangible variation results from the stochastic establishment of epigenetic modifications to the DNA nucleotide sequence. These modifications, which may involve cytosine methylation and chromatin remodelling, result in alterations in gene expression which, in turn, affects the phenotype of the organism. Recent evidence, from our work and that of others in mice, suggests that these epigenetic modifications, which in the past were thought to be cleared and reset on passage through the germline, may sometimes be inherited to the next generation. This is termed epigenetic inheritance, and while this process has been well recognized in plants, the recent findings in mice force us to consider the implications of this type of inheritance in mammals. At this stage we do not know how extensive this phenomenon is in humans, but it may well turn out to be the explanation for some diseases which appear to be sporadic or show only weak genetic linkage.

Indexed as

DNA MethylationGene Expression RegulationIntercellular Signaling Peptides and ProteinsRepressor ProteinsAgouti Signaling ProteinAnimalsAxin ProteinChromatinDosage Compensation, GeneticGenomic ImprintingMammalsMiceModels, GeneticProteinsAgouti Signaling ProteinAxin ProteinChromatinIntercellular Signaling Peptides and ProteinsProteinsRepressor Proteins

Identifiers

PMID11336630
PMCPMC1221806

What OpenQuestion holds

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Registered trials

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.