Evidence map›Paper›PMID 24825161›Full record

ReviewSmall GTPases2014

Rho-GTPases as key regulators of T lymphocyte biology.

Abdelhadi Saoudi, Sahar Kassem, Anne Dejean, Guillaume Gaud

Open access · bronzeAbstract readReview
In one paragraph

Review in Small GTPases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

49 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. TGF-βRII/IL-15 immunotherapeutic complex targets exhausted CD8Journal for immunotherapy of cancer · 2025
    Article
  6. Identification of Novel Kv1.3 Channel-Interacting Proteins Using Proximity Labelling in T-Cells.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Rac1 overexpression promotes Treg-derived cytokines to mediate choroidal neovascularization in wet age-related macular degeneration.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  13. A model for predicting bacteremia species based on host immune response.Frontiers in cellular and infection microbiology · 2025
    Article
  14. The role of actin cytoskeleton component Arp2/3 in inflammatory response.Frontiers in cell and developmental biology · 2025
    Review
  15. Article
  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 at 3 institutions in 1 country.

Abdelhadi SaoudiInserm; U1043; Toulouse, France; CNRS; U5282; Toulouse, France; Université de Toulouse; Centre de Physiopathologie de Toulouse Purpan; Toulouse, France.
Sahar KassemInserm; U1043; Toulouse, France; CNRS; U5282; Toulouse, France; Université de Toulouse; Centre de Physiopathologie de Toulouse Purpan; Toulouse, France.
Anne DejeanInserm; U1043; Toulouse, France; CNRS; U5282; Toulouse, France; Université de Toulouse; Centre de Physiopathologie de Toulouse Purpan; Toulouse, France.
Guillaume GaudInserm; U1043; Toulouse, France; CNRS; U5282; Toulouse, France; Université de Toulouse; Centre de Physiopathologie de Toulouse Purpan; Toulouse, France.
Université de Toulouse · FRCentre de Physiopathologie de Toulouse-Purpan · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rho-GTPases belong to the Ras superfamily and are crucial signal transducing proteins downstream of many receptors. In general, the Rho-GTPases function as molecular switches, cycling between inactive (GDP-bound) and active (GTP-bound) states. The activated GTP bound Rho-GTPases interact with a broad spectrum of effectors to regulate a plethora of biological pathways including cytoskeletal dynamics, motility, cytokinesis, cell growth, apoptosis, transcriptional activity and nuclear signaling. Recently, gene targeting in mice allowed the selective inactivation of different Rho-GTPases and has advanced our understanding of the physiological role of these proteins, particularly in the immune system. Particularly, these proteins are key signaling molecules in T lymphocytes, which are generated in the thymus and are major players in the immune system. The scope of this review is to discuss recent data obtained in Rho-GTPases deficient mice by focusing on the role-played by Rho-GTPases in T-lymphocyte development, migration, activation and differentiation.

Indexed as

AnimalsCell DifferentiationCell MovementCytokinesisReceptors, Antigen, T-Cellrho GTP-Binding ProteinsSignal TransductionSynapsesThymus GlandT-LymphocytesReceptors, Antigen, T-Cellrho GTP-Binding ProteinsRho-GTPasesT-cell developmentT-cell differentiationT-cell migration

Identifiers

PMID24825161
PMCPMC4160340
OpenAlexW1977230291

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.