Evidence map›Paper›PMID 16636683›Full record

ReviewThe pharmacogenomics journal2007

Pharmacogenetics of the human beta-adrenergic receptors.

M R G Taylor

Abstract readReview
PubMed Publisher
In one paragraph

Review in The pharmacogenomics journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

50 citing papers in PubMed, 107 citations in OpenAlex.

  1. Trial
  2. βJournal of clinical pharmacology · 2019
    Trial
  3. Trial
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  6. Review
  7. Article
  8. Review
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  14. Article
  15. Article
  16. Glucose Metabolism in Burns-What Happens?International journal of molecular sciences · 2021
    Review
  17. Cerebrovascular and neurological perspectives on adrenoceptor and calcium channel modulating pharmacotherapies.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Review
  18. Association of Genetic Variances inSports (Basel, Switzerland) · 2021
    Article
  19. Activation of βArchives of pharmacal research · 2021
    Review
  20. Article
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

1 author at 1 institution in 1 country.

M R G TaylorAdult Medical Genetics Program, University of Colorado at Denver and Health Sciences, Aurora, CO 80045, USA. matthew.taylor@uchsc.edu
University of Colorado Denver · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The beta-adrenergic receptors (ADRBs) are cell surface receptors that play central roles in the sympathetic nervous system. Pharmacological targeting of two of these receptors, ADRB1 and ADRB2, represents a widely used therapeutic approach for common and important diseases including asthma, hypertension and heart failure. Genetic variation in both ADRB1 and ADRB2 has been linked to both in vitro and clinical disease phenotypes. More recently, interest has shifted to studies that explore potential interaction between variation in ADRBs and medications directed at these important receptors. This paper reviews the current state of knowledge and understanding of ADRB genetic variation and explores the likely direction of future studies in this area.

Indexed as

PharmacogeneticsHumansPolymorphism, GeneticReceptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Receptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2

Identifiers

PMID16636683
OpenAlexW2095237667

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.