Evidence map›Paper›PMID 15146233›Full record

ReviewThe Journal of clinical investigation2004

Dissecting the functional role of different isoforms of the L-type Ca2+ channel.

Emmanuel Bourinet, Matteo E Mangoni, Joël Nargeot

Abstract readReviewComment
In one paragraph

Review in The Journal of clinical investigation, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Emmanuel BourinetDépartement de Physiologie, Laboratoire de Génomique Fonctionnelle, Centre National de la Recherche Scientifique Unité Propre de Recherche 2580, Montpellier, France. Emmanuel.Bourinet@igh.cnrs.fr
Matteo E Mangoni
Joël Nargeot
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There currently exist a great number of different mouse lines in which the activity of a particular gene of interest has been inactivated or enhanced. However, it is also possible to insert specific mutations in a gene so that the pharmacological sensitivity of the gene product is altered. An example of such an approach shows how the abolition of the sensitivity of an L-type Ca(2+) channel isoform to dihydropyridines allows the investigation of the physiological role of these channels in different tissues.

Indexed as

AffectAnimalsCalcium Channels, L-TypeDihydropyridinesHeartHumansInsulinInsulin SecretionMiceModels, MolecularProtein IsoformsCalcium Channels, L-TypeDihydropyridinesInsulinProtein Isoforms

Identifiers

PMID15146233
PMCPMC406536
OpenAlexW2091116305

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.