Evidence map›Paper›PMID 25934595›Full record

ReviewJournal of cardiac failure2015

Cardiomyopathy in a dish: using human inducible pluripotent stem cells to model inherited cardiomyopathies.

Forum Kamdar, Andre Klaassen Kamdar, Naoko Koyano-Nakagawa, Mary G Garry, Daniel J Garry

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cardiac failure, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-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

11 citing papers in PubMed, 20 citations in OpenAlex.

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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 1 institution in 1 country.

Forum KamdarCardiovascular Division and Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Andre Klaassen KamdarCardiovascular Division and Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Naoko Koyano-NakagawaCardiovascular Division and Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Mary G GarryCardiovascular Division and Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Daniel J GarryCardiovascular Division and Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota. Electronic address: garry@umn.edu.
University of Minnesota · US

Funding

Midwestern Progenitor Cell ConsortiumU01HL100407 · NHLBI · UNIVERSITY OF MINNESOTA · PI GARRY, DANIEL J., KYBA, MICHAEL · 2009 to 2015
$7.8M
Regulatory Mechanisms of Endothelial Development and RegenerationR01HL122576 · NHLBI · UNIVERSITY OF MINNESOTA · PI GARRY, DANIEL J. · 2014 to 2017
$1.5M
NHLBI NIH HHS R01 HL122576NHLBI NIH HHS R01HL122576NHLBI NIH HHS U01 HL100407NHLBI NIH HHS U01HL100407
6 · The paper itself

Abstract

Inherited cardiomyopathies, including hypertrophic cardiomyopathy, dilated cardiomyopathies, arrythmogenic right ventricular cardiomyopathy, and other inherited forms of heart failure, represent a unique set of genetically defined cardiovascular disease processes. Unraveling the molecular mechanisms of these deadly forms of human heart disease has been challenging, but recent groundbreaking scientific advances in stem cell technology have allowed for the generation of patient-specific human inducible stem cell (hiPSC)-derived cardiomyocytes (CMs). hiPSC-derived CMs retain the genetic blueprint of the patient, they can be maintained in culture, and they recapitulate the phenotypic characteristics of the disease in vitro, thus serving as a disease in a dish. This review provides an overview of in vitro modeling of inherited cardiomyopathies with the use of patient-specific hiPSC-derived CMs.

Indexed as

CardiomyopathiesModels, CardiovascularAnimalsHumansInduced Pluripotent Stem CellsMyocytes, CardiacCardiomyopathydisease modelsstem cells

Identifiers

PMID25934595
PMCPMC4554831
OpenAlexW1969743736

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.