Evidence map›Paper›PMID 20179962›Full record

ReviewPflugers Archiv : European journal of physiology2010

Ryanodine receptor channelopathies.

Matthew J Betzenhauser, Andrew R Marks

Abstract readReview
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 137 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. The genetic landscape of pediatric postural orthostatic tachycardia syndrome.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
  8. Review
  9. Article
  10. Identification of Mutations of theJournal of Korean medical science · 2025
    Article
  11. Total syntheses of highly oxidativeBeilstein journal of organic chemistry · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Structural insights into the regulation of RyR1 by S100A1.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

4 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.

Matthew J BetzenhauserDepartment of Physiology, Clyde and Helen Wu Center for Molecular Cardiology, Columbia University College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032, USA.
Andrew R Marks
Columbia University · US

Funding

Molecular Basis of Sudden Cardiac DeathP01HL067849 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARKS, ANDREW ROBERT · 2001 to 2011
$15.0M
MOLECULAR BASIS OF HEART FAILURER01HL061503 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARKS, ANDREW ROBERT · 1998 to 2016
$6.5M
CARDIAC AND SKELETAL MUSCLE CALCIUM RELEASE CHANNELSR01HL056180 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF CUNY · PI MARKS, ANDREW ROBERT · 1996 to 2009
$4.0M
Regulation of cardiac ion channel function via allosteric modulatorsR01HL083418 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARKS, ANDREW ROBERT · 2006 to 2007
$841k
NHLBI NIH HHS HL 056180NHLBI NIH HHS HL 061503NHLBI NIH HHS HL 067849NHLBI NIH HHS HL 083418NHLBI NIH HHS P01 HL067849NHLBI NIH HHS R01 HL056180NHLBI NIH HHS R01 HL061503NHLBI NIH HHS R01 HL083418
6 · The paper itself

Abstract

Ryanodine receptors (RyR) are intracellular Ca2+-permeable channels that provide the sarcoplasmic reticulum Ca2+ release required for skeletal and cardiac muscle contractions. RyR1 underlies skeletal muscle contraction, and RyR2 fulfills this role in cardiac muscle. Over the past 20 years, numerous mutations in both RyR isoforms have been identified and linked to skeletal and cardiac diseases. Malignant hyperthermia, central core disease, and catecholaminergic polymorphic ventricular tachycardia have been genetically linked to mutations in either RyR1 or RyR2. Thus, RyR channelopathies are both of interest because they cause significant human diseases and provide model systems that can be studied to elucidate important structure-function relationships of these ion channels.

Indexed as

AnimalsCalciumChannelopathiesHumansMalignant HyperthermiaMiceMice, TransgenicMutationMyocardial ContractionMyopathy, Central CoreRyanodine Receptor Calcium Release ChannelSarcoplasmic ReticulumTachycardia, VentricularCalciumRyanodine Receptor Calcium Release Channel

Identifiers

PMID20179962
PMCPMC2885589
OpenAlexW1989056964

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.