Evidence map›Paper›PMID 22582090›Full record

ArticleBiomolecular concepts2012

Regenerating proteins and their expression, regulation and signaling.

Abhirath Parikh, Anne-Fleur Stephan, Emmanuel S Tzanakakis

Abstract read
In one paragraph

Article in Biomolecular concepts, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

53 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Susceptibility of mice to primaryFrontiers in immunology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. [HTD4010 attenuates myocardial injury in mice with septic cardiomyopathy by promoting autophagyNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

3 authors.

Abhirath ParikhDepartment of Chemical and Biological Engineering, State University of New York at Buffalo, Buffalo, NY 14260.
Anne-Fleur Stephan
Emmanuel S Tzanakakis

Funding

Bioprocess for cardiac cell generation from human induced pluripotent stem cellsR01HL103709 · NHLBI · TUFTS UNIVERSITY MEDFORD · PI TZANAKAKIS, EMMANOUHL · 2011 to 2014
$1.5M
Scalable bioprocess for cardiomyocyte generation from human embryonic stem cellsR21HL092398 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI TZANAKAKIS, EMMANOUHL · 2008 to 2009
$452k
NHLBI NIH HHS R01 HL103709NHLBI NIH HHS R21 HL092398
6 · The paper itself

Abstract

The regenerating (Reg) protein family comprises C-type lectin-like proteins discovered independently during pancreatitis and pancreatic islet regeneration. However, an increasing number of studies provide evidence of participation of Reg proteins in the proliferation and differentiation of diverse cell types. Moreover, Reg family members are associated with various pathologies, including diabetes and forms of gastrointestinal cancer. These findings have led to the emergence of key roles for Reg proteins as anti-inflammatory, antiapoptotic and mitogenic agents in multiple physiologic and disease contexts. Yet, there are significant gaps in our knowledge regarding the regulation of expression of different Reg genes. In addition, the pathways relaying Reg-triggered signals, their targets and potential cross-talk with other cascades are still largely unknown. In this review, the expression patterns of different Reg members in the pancreas and extrapancreatic tissues are described. Moreover, factors known to modulate Reg levels in different cell types are discussed. Several signaling pathways, which have been implicated in conferring the effects of Reg ligands to date, are also delineated. Further efforts are necessary for elucidating the biological processes underlying the action of Reg proteins and their involvement in various maladies. Better understanding of the function of Reg genes and proteins will be beneficial in the design and development of therapies utilizing or targeting this protein group.

Identifiers

PMID22582090
PMCPMC3348543

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Registered trials

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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.