Evidence map›Paper›PMID 17853903›Full record

ReviewNature reviews. Immunology2007

Calcium signalling and cell-fate choice in B cells.

Andrew M Scharenberg, Lisa A Humphries, David J Rawlings

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

112 citing papers in PubMed, 223 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Exploration (Beijing, China) · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Pharmaceutical agent cetylpyridinium chloride inhibits immune mast cell function by interfering with calcium mobilization.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Disrupted CaCellular & molecular immunology · 2023
    Article
  20. Review

52 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

3 authors at 2 institutions in 1 country.

Andrew M ScharenbergDepartment of Pediatrics, University of Washington School of Medicine and Children's Hospital and Regional Medical Center, Suite 300, 307 Westlake Avenue, Seattle, Washington 98109, USA. andrewms@u.washington.edu
Lisa A Humphries
David J Rawlings
Seattle Children's Hospital · USUniversity of Washington · US

Funding

Regulation of Metal Ion Homeostasis by Channel KinasesP01GM078195 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FLEIG, ANDREA · 2007 to 2011
$8.7M
REGULATION OF B CELL DEVELOPMENT AND SIGNALING BY BTKR01HD037091 · NICHD · UNIVERSITY OF WASHINGTON · PI RAWLINGS, DAVID J · 1999 to 2008
$2.7M
MODEL FOR GENE THERAPY IN X LINKED AGAMMAGLOBULINEMIAR01CA081140 · NCI · UNIVERSITY OF WASHINGTON · PI RAWLINGS, DAVID J · 1999 to 2008
$2.7M
Molecular mechanisms of vertebrate Mg2+ homeostasisR01GM064316 · NIGMS · UNIVERSITY OF WASHINGTON · PI SCHARENBERG, ANDREW M. · 2001 to 2009
$2.5M
TSLP receptor in the regulation of cell developmentR01AI044259 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI ZIEGLER, STEVEN F · 1999 to 2010
$2.5M
ADP-ribose dependent calcium entry in the immune systemR01GM064091 · NIGMS · UNIVERSITY OF WASHINGTON · PI SCHARENBERG, ANDREW M · 2001 to 2005
$1.4M
ANALYSIS OF B-CELL RECEPTOR CALCIUM SIGNALINGR01AI045901 · NIAID · UNIVERSITY OF WASHINGTON · PI SCHARENBERG, ANDREW M · 2000 to 2004
$1.2M
NCI NIH HHS CA81140NCI NIH HHS R01 CA081140NHLBI NIH HHS HL07543NIAID NIH HHS AI044259NIAID NIH HHS AI45901NIAID NIH HHS R01 AI044259NIAID NIH HHS R01 AI045901NICHD NIH HHS HD37091NICHD NIH HHS R01 HD037091NIGMS NIH HHS GM64091NIGMS NIH HHS GM64316NIGMS NIH HHS P01 GM078195NIGMS NIH HHS R01 GM064091NIGMS NIH HHS R01 GM064316
6 · The paper itself

Abstract

Alterations in the cytosolic concentration of calcium ions (Ca2+) transmit information that is crucial for the development and function of B cells. Cytosolic Ca2+ concentration is determined by a balance of active transport and gradient-driven Ca2+ fluxes, both of which are subject to the influence of multiple receptors and environmental sensing pathways. Recent advances in genomics have allowed for the compilation of an increasingly comprehensive list of Ca2+ transporters and channels expressed by B cells. The increasing understanding of the function and regulation of these proteins has begun to shift the frontier of Ca2+ physiology in B cells from molecular analysis to determining how diverse inputs to cytosolic Ca2+ concentration are integrated in specific immunological contexts.

Indexed as

AnimalsB-LymphocytesCalciumCalcium SignalingCytosolHumansInositol 1,4,5-TrisphosphatePhospholipase C gammaReceptors, Antigen, B-CellCalciumInositol 1,4,5-TrisphosphatePhospholipase C gammaReceptors, Antigen, B-Cell

Identifiers

PMID17853903
PMCPMC2743935
OpenAlexW2011593699

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.