Evidence map›Paper›PMID 8118099›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1993

The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32.

B Drouet, L Garcia, D Simon-Chazottes, M G Mattei, J L Guénet, A Schwartz, G Varadi, M Pinçon-Raymond

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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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

8 authors at 5 institutions in 2 countries.

B DrouetGroupe de Biologie, Développement et Régénération du Système Neuromusculaire, INSERM U. 153, Paris, France.
L Garcia
D Simon-Chazottes
M G Mattei
J L Guénet
A Schwartz
G Varadi
M Pinçon-Raymond
Institut Pasteur · FRHôpital d'Enfants · FRInstitut du Fer à Moulin · FRUniversity of Cincinnati · USUniversity of Cincinnati Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using both chromosomal in situ hybridization and molecular techniques, we report the genetic localization of the gene coding for the alpha 1 subunit of the skeletal slow Ca2+ current channel/DHP receptor gene (Cchl1a3) on human Chromosome (Chr) 1 (1q31-1q32 region) and on mouse Chr 1 (region (F-G)). On the basis of single-strand conformation polymorphism (SSCP-PCR) analysis in an interspecific backcross, we have determined that the Cchl1a3 = mdg (muscular dysgenesis) locus is very closely linked to the myogenin (Myog) locus.

Indexed as

Chromosomes, Human, Pair 1AnimalsBase SequenceBone and BonesCalcium ChannelsCalcium Channels, L-TypeChromosome MappingCrosses, GeneticDNA PrimersHumansIn Situ HybridizationMiceMice, Inbred C57BLMolecular Sequence DataMuridaeMuscle ProteinsCalcium ChannelsCalcium Channels, L-TypeDNA PrimersMuscle ProteinsReceptors, Cholinergic

Identifiers

PMID8118099
OpenAlexW2039877630

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.