Evidence map›Paper›PMID 12177410›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Gene expression during the priming phase of liver regeneration after partial hepatectomy in mice.

Andrew I Su, Luca G Guidotti, John Paul Pezacki, Francis V Chisari, Peter G Schultz

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 213 citations in OpenAlex.

  1. Contradictory Role of Gadd45β in Liver Diseases.Journal of cellular and molecular medicine · 2024
    Pooled it
  2. Article
  3. Genomic repeats for single-cell molecular recording.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Role of Fibrinogen-like Protein 1 in Tumor Recurrence Following Hepatectomy.Journal of clinical and translational hepatology · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Therapeutic strategies to improve liver regeneration after hepatectomy.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  14. Review
  15. Article
  16. Gadd45 in the Liver: Signal Transduction and Transcriptional Mechanisms.Advances in experimental medicine and biology · 2022
    Article
  17. Genetic and Cellular Contributions to Liver Regeneration.Cold Spring Harbor perspectives in biology · 2021
    Article
  18. Article
  19. Article
  20. The liver matrisome - looking beyond collagens.JHEP reports : innovation in hepatology · 2020
    Review

20 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 2 countries.

Andrew I SuDepartment of Chemistry and Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Luca G Guidotti
John Paul Pezacki
Francis V Chisari
Peter G Schultz
Scripps Research Institute · USGenomics Institute of the Novartis Research Foundation · USNational Academies of Sciences, Engineering, and Medicine · USSteacie Institute for Molecular Sciences · CA

Funding

PATHOGENESIS OF HEPATITIS B VIRUS IN TRANSGENIC MICER01CA040489 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI CHISARI, FRANCIS VINCENT · 1985 to 2010
$7.7M
Regulation of HBV Replication by the Immune SystemR01AI040696 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI GUIDOTTI, LUCA G. · 1997 to 2012
$5.2M
PATHOGENESIS OF HEPATITIS B IN TRANSGENIC MICER37CA040489 · NCI · SCRIPPS RESEARCH INSTITUTE · PI CHISARI, FRANCIS VINCENT · 1990 to 1999
–
NCI NIH HHS CA40489NCI NIH HHS R01 CA040489NCI NIH HHS R37 CA040489NIAID NIH HHS AI40696NIAID NIH HHS R01 AI040696
6 · The paper itself

Abstract

Understanding the gene-expression patterns during liver regeneration may help to reveal how regenerative processes are initiated and controlled as well as shed new light onto processes that lead to liver disease. Using high-density oligonucleotide arrays, we have examined the gene-expression program in the livers of mice after partial hepatectomy. A time course was constructed for gene expression between 0 and 4 h after partial hepatectomy, corresponding to the priming phase of liver regeneration. The genomic program for liver regeneration involves transcription-factor generation, stress and inflammatory responses, cytoskeletal and extracellular matrix modification, and regulation of cell-cycle entry. The genome-wide changes that are observed provide a detailed and comprehensive map of the initial priming stage of liver regeneration.

Indexed as

Gene Expression RegulationHepatectomyAnimalsBase SequenceDNA PrimersEnzymesLiverLiver RegenerationMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisProteinsReverse Transcriptase Polymerase Chain ReactionTranscription FactorsDNA PrimersEnzymesProteinsTranscription Factors

Identifiers

PMID12177410
PMCPMC123230
OpenAlexW2102524715

What Socratic 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 Socratic graph.