Evidence map›Paper›PMID 15994457›Full record

ReviewMolecular interventions2005

Discovery and therapeutic promise of selective androgen receptor modulators.

Jiyun Chen, Juhyun Kim, James T Dalton

Abstract readReview
In one paragraph

Review in Molecular interventions, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Review
  2. Selective Androgen Receptor Modulators: An Emerging Liver Toxin.Journal of clinical and translational hepatology · 2023
    Review
  3. Article
  4. Article
  5. Drug Repurposing for Triple-Negative Breast Cancer.Journal of personalized medicine · 2020
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Evaluation of Resettin® on serum hormone levels in sedentary males.Journal of the International Society of Sports Nutrition · 2014
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Sex hormones, their receptors and bone health.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2008
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  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

3 authors.

Jiyun ChenDivision of Pharmaceutics, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, USA. chenjiyun@yahoo.com
Juhyun Kim
James T Dalton

Funding

Pharmacology of Nonsteroidal Androgen Receptor LigandsR01DK059800 · NIDDK · OHIO STATE UNIVERSITY · PI DALTON, JAMES T · 2000 to 2007
$2.2M
NIDDK NIH HHS R01 DK059800NIDDK NIH HHS R01 DK59800
6 · The paper itself

Abstract

Androgens are essential for male development and the maintenance of male secondary characteristics, such as bone mass, muscle mass, body composition, and spermatogenesis. The main disadvantages of steroidal androgens are their undesirable physicochemical and pharmacokinetic properties. The recent discovery of nonsteroidal selective androgen receptor modulators (SARMs) provides a promising alternative for testosterone replacement therapies with advantages including oral bioavailability, flexibility of structural modification, androgen receptor specificity, tissue selectivity, and the lack of steroid-related side effects.

Indexed as

Androgen Receptor AntagonistsDrug DesignAndrogensAnimalsHormone AntagonistsHumansReceptors, AndrogenStructure-Activity RelationshipAndrogen Receptor AntagonistsAndrogensHormone AntagonistsReceptors, Androgen

Identifiers

PMID15994457
PMCPMC2072877

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.