Evidence map›Paper›PMID 15489920›Full record

ReviewOncogene2004

Molecular interdiction of Src-family kinase signaling in hematopoietic cells.

Robert L Geahlen, Misty D Handley, Marietta L Harrison

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 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
1.1field-weighted citation impact, top 26% 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, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Nonreceptor tyrosine kinases in prostate cancer.Neoplasia (New York, N.Y.) · 2007
    Review
  8. Article
  9. Review
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 1 institution in 1 country.

Robert L GeahlenDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907, USA.
Misty D Handley
Marietta L Harrison
Purdue University West Lafayette · US

Funding

TYROSINE PROTEIN KINASES AND LYMPHOCYTE ACTIVATIONR01CA037372 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI GEAHLEN, ROBERT L · 1985 to 2011
$3.5M
P56LCK AND ASSOCIATED PROTEINSR01GM048099 · NIGMS · PURDUE UNIVERSITY WEST LAFAYETTE · PI HARRISON, MARIETTA L · 1992 to 2006
$1.5M
TRAINING IN DRUG AND CARCINOGEN-DNA INTERACTIONST32CA009634 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI BERGSTROM, DONALD E. · 1990 to 2006
$1.4M
NCI NIH HHS CA37372NCI NIH HHS T32CA09634NIGMS NIH HHS GM48099
6 · The paper itself

Abstract

The ability of Src-family kinases (SFKs) to mediate signaling from cell surface receptors in hematopoietic cells is a function of their catalytic activity, location and binding partners. Kinase activity is regulated in the cell by kinases and phosphatases that alter the state of phosphorylation of key tyrosine residues and by protein binding partners that stabilize the kinase in active or inactive conformations or localize the enzyme to specific subcellular or submembrane domains. Kinase activity and function can be modulated experimentally through the use of small molecule inhibitors designed to directly target catalytic or binding domains or regulate the location of the protein by altering its state of acylation.

Indexed as

AnimalsHematopoietic Stem CellsHumansMembrane MicrodomainsProtein BindingProtein Structure, TertiarySignal Transductionsrc-Family Kinasessrc-Family Kinases

Identifiers

PMID15489920
OpenAlexW1971160595

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.