Evidence map›Paper›PMID 19247306›Full record

ReviewNature reviews. Drug discovery2009

The FGF family: biology, pathophysiology and therapy.

Andrew Beenken, Moosa Mohammadi

Abstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 944 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
944citing papers in PubMed, 3 pooled it
39.4field-weighted citation impact, top 1% 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

944 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,895 citations in OpenAlex.

  1. Pooled it
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  12. Journal of thoracic disease · 2026
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884 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

2 authors at 1 institution in 1 country.

Andrew BeenkenDepartment of Pharmacology, New York University School of Medicine, New York, New York 10016, USA. Andrew.Beenken@med.nyu.edu
Moosa Mohammadi
New York University · US

Funding

MECHANISMS OF FGF RECEPTOR REGULATION AND SIGNALINGR01DE013686 · NIDCR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOHAMMADI, MOOSA · 2000 to 2020
$12.3M
Training in Pharmacological SciencesT32GM066704 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BACH, ERIKA A · 2004 to 2018
$2.6M
NIDCR NIH HHS R01 DE013686NIDCR NIH HHS R01-DE13686NIGMS NIH HHS T32 GM066704NIGMS NIH HHS T32-GM066704-05
6 · The paper itself

Abstract

The family of fibroblast growth factors (FGFs) regulates a plethora of developmental processes, including brain patterning, branching morphogenesis and limb development. Several mitogenic, cytoprotective and angiogenic therapeutic applications of FGFs are already being explored, and the recent discovery of the crucial roles of the endocrine-acting FGF19 subfamily in bile acid, glucose and phosphate homeostasis has sparked renewed interest in the pharmacological potential of this family. This Review discusses traditional applications of recombinant FGFs and small-molecule FGF receptor kinase inhibitors in the treatment of cancer and cardiovascular disease and their emerging potential in the treatment of metabolic syndrome and hypophosphataemic diseases.

Indexed as

AnimalsCardiovascular DiseasesFibroblast Growth FactorsHomeostasisHumansHypophosphatemiaMetabolic SyndromeNeoplasmsReceptors, Fibroblast Growth FactorFGF19 protein, humanFibroblast Growth FactorsReceptors, Fibroblast Growth Factor

Identifiers

PMID19247306
PMCPMC3684054
OpenAlexW2027239974

What OpenQuestion holds

Textmetadata
LicenceTDM
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.