Evidence map›Paper›PMID 15250821›Full record

ArticleThe Biochemical journal2004

Development of a chimaeric receptor approach to study signalling by tumour necrosis factor receptor family members.

Duorong Xu, Zhenqi Shi, Jay McDonald, George Pan, Xuemei Cao, Xueqing Yu, Xu Feng

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. SHP2 regulates osteoclastogenesis by promoting preosteoclast fusion.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  5. Article
  6. Article
  7. Molecular mechanisms of the biphasic effects of interferon-γ on osteoclastogenesis.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2012
    Article
  8. Article
  9. 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

7 authors at 2 institutions in 1 country.

Duorong XuDepartment of Pathology, University of Alabama at Birmingham, 1670 University Blvd., VH G046B, Birmingham, AL 35294, USA.
Zhenqi Shi
Jay McDonald
George Pan
Xuemei Cao
Xueqing Yu
Xu Feng
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

UAB Core Center for Musculoskeletal DisordersP30AR046031 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PONNAZHAGAN, SELVARANGAN · 2001 to 2010
$5.6M
RANK Signaling in Osteoclast Differentiation &FunctionR01AR047830 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FENG, XU · 2001 to 2016
$4.7M
NIAMS NIH HHS AR 47830NIAMS NIH HHS P30 AR046031NIAMS NIH HHS P30AR46031NIAMS NIH HHS R01 AR047830
6 · The paper itself

Abstract

Members of the tumour necrosis factor receptor family play a pivotal role in cell differentiation, function and apoptosis. However, signalling by many members of the family remains to be elucidated. In the present study, we developed a chimaeric receptor approach for studying signalling by receptors belonging to this family. The chimaeric receptor comprises the human Fas external domain linked to the transmembrane and cytoplasmic domains of a tumour necrosis factor receptor family member of interest. When the chimaera is expressed in mouse cells, the clustering of the chimaera induced by a human Fas-activating antibody activates the intracellular domain of the chimaera without affecting its endogenous counterpart. Since the antibody recognizes only human Fas, this approach can be used to dissect signalling by any tumour necrosis factor family member using any type of mouse cell including those endogenously expressing Fas. Moreover, we also showed that the chimaeric receptor approach can be used to study signalling at any stage of cell differentiation or function.

Indexed as

Signal TransductionAnimalsCell Differentiationfas ReceptorGlycoproteinsHumansMiceMultigene FamilyOsteoclastsOsteoprotegerinProtein Structure, TertiaryReceptors, Cytoplasmic and NuclearReceptors, Tumor Necrosis FactorRecombinant Fusion Proteinsfas ReceptorGlycoproteinsOsteoprotegerinReceptors, Cytoplasmic and NuclearReceptors, Tumor Necrosis FactorRecombinant Fusion ProteinsTNFRSF11B protein, humanTnfrsf11b protein, mouse

Identifiers

PMID15250821
PMCPMC1134062
OpenAlexW1993529140

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.