Evidence map›Paper›PMID 27729899›Full record

ArticleFrontiers in endocrinology2016

TSH Receptor Signaling Abrogation by a Novel Small Molecule.

Rauf Latif, Ronald B Realubit, Charles Karan, Mihaly Mezei, Terry F Davies

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Current concepts regarding Graves' orbitopathy.Journal of internal medicine · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Rauf LatifThyroid Research Unit, James J. Peters VA Medical Center, Icahn School of Medicine at Mount Sinai , New York, NY , USA.
Ronald B RealubitSulzberger Columbia Genome Center, Columbia University , New York, NY , USA.
Charles KaranSulzberger Columbia Genome Center, Columbia University , New York, NY , USA.
Mihaly MezeiDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai , New York, NY , USA.
Terry F DaviesThyroid Research Unit, James J. Peters VA Medical Center, Icahn School of Medicine at Mount Sinai , New York, NY , USA.
Columbia University · USIcahn School of Medicine at Mount Sinai · USJames J. Peters VA Medical Center · US

Funding

Small Molecules and Antibodies Interacting at the TSH ReceptorR01DK069713 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAVIES, TERRY FRANCIS · 2006 to 2019
$5.6M
TSH RECEPTOR MULTIMERIZATIONI01BX000800 · VA · JAMES J PETERS VA MEDICAL CENTER · PI DAVIES, TERRY FRANCIS · 2011 to 2025
–
BLRD VA I01 BX000800NIDDK NIH HHS R01 DK069713
6 · The paper itself

Abstract

Pathological activation of the thyroid-stimulating hormone receptor (TSHR) is caused by thyroid-stimulating antibodies in patients with Graves' disease (GD) or by somatic and rare genomic mutations that enhance constitutive activation of the receptor influencing both G protein and non-G protein signaling. Potential selective small molecule antagonists represent novel therapeutic compounds for abrogation of such abnormal TSHR signaling. In this study, we describe the identification and

Indexed as

antagonistsmall moleculeTSH receptor

Identifiers

PMID27729899
PMCPMC5037132
OpenAlexW2525024148

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.