Evidence map›Paper›PMID 28377980›Full record

ArticleBone reports2017

The metabolic bone disease associated with the

Julia M Hum, Erica L Clinkenbeard, Colin Ip, Taryn A Cass, Matt Allen, Kenneth E White

Open access · goldAbstract read
In one paragraph

Article in Bone reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Non-Classical Effects of FGF23: Molecular and Clinical Features.International journal of molecular sciences · 2024
    Review
  2. Article
  3. Review
  4. Regulation of FGF23: Beyond Bone.Current osteoporosis reports · 2021
    Review
  5. Article
  6. Congenital Conditions of Hypophosphatemia in Children.Calcified tissue international · 2021
    Review
  7. 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

6 authors at 2 institutions in 1 country.

Julia M HumDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Erica L ClinkenbeardDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Colin IpDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Taryn A CassDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Matt AllenDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Kenneth E WhiteDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · US

Funding

BASIC SCIENCE STUDIES ON GENE THERAPY OF BLOOD DISEASEST32HL007910 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Roland W. Herzog, Reuben Kapur · 1999 to 2026
$7.6M
FGF-23 REGULATION OF PHOSPHATE HOMEOSTASISR01DK063934 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WHITE, KENNETH E · 2003 to 2015
$3.8M
Control of FGF23 Bioactivity via Circulating alpha-KlothoR01DK095784 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI WHITE, KENNETH E · 2013 to 2017
$1.7M
Novel mediators of FGF23 bioactivityR21AR070329 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI WHITE, KENNETH E · 2016 to 2017
$381k
Role of iron and hypoxia sensing in FGF23-dependent metabolic bone diseaseF32AR065389 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI CLINKENBEARD, ERICA L · 2014 to 2016
$183k
NHLBI NIH HHS T32 HL007910NIAMS NIH HHS F32 AR065389NIAMS NIH HHS R21 AR070329NIDDK NIH HHS R01 DK063934NIDDK NIH HHS R01 DK095784
6 · The paper itself

Abstract

Fibroblast growth factor-23 (FGF23) controls key responses to systemic phosphate increases through its phosphaturic actions on the kidney. In addition to stimulation by phosphate, FGF23 positively responds to iron deficiency anemia and hypoxia in rodent models and in humans. The disorder X-linked hypophosphatemia (XLH) is characterized by elevated FGF23 in concert with an intrinsic bone mineralization defect. Indeed, the

Indexed as

FGF23Hypoxia inducible factor-1αPhosphateX-linked hypophosphatemia

Identifiers

PMID28377980
PMCPMC5365303
OpenAlexW2574954873

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.