Evidence map›Paper›PMID 7679508›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

MEF2C, a MADS/MEF2-family transcription factor expressed in a laminar distribution in cerebral cortex.

D Leifer, D Krainc, Y T Yu, J McDermott, R E Breitbart, J Heng, R L Neve, B Kosofsky, B Nadal-Ginard, S A Lipton

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
11.1field-weighted citation impact, top 1% 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

93 citing papers in PubMed, 238 citations in OpenAlex.

  1. Article
  2. Mef2c Controls Postnatal Callosal Axon Targeting by Regulating Sensitivity to Ephrin Repulsion.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  13. Peripheral Auditory Nerve Impairment in a Mouse Model of Syndromic Autism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  14. Review
  15. Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degeneration.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  16. Review
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33 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

10 authors at 1 institution in 1 country.

D LeiferDepartment of Neurology, Children's Hospital, Boston, MA.
D Krainc
Y T Yu
J McDermott
R E Breitbart
J Heng
R L Neve
B Kosofsky
B Nadal-Ginard
S A Lipton
Boston Children's Hospital · US

Funding

THY-1 IN MENTAL RETARDATION AND CNS REGENERATIONK11HD000888 · NICHD · YALE UNIVERSITY · PI LEIFER, DANA · 1989 to 1993
–
NEI NIH HHS EY06087NICHD NIH HHS HD00888
6 · The paper itself

Abstract

We have cloned cDNA encoding a human transcription factor that belongs to the MEF2 (myocyte-specific enhancer-binding factor 2) subfamily of the MADS (MCM1-agamous-deficiens-serum response factor) gene family. This factor, which we have named MEF2C, binds specifically to the MEF2 element and activates transcription via this element. Specific isoforms of this factor are found exclusively in brain and are robustly expressed by neurons in cerebral cortex. In situ hybridization indicates that the factor is expressed preferentially in certain neuronal layers of cortex and that expression declines during postnatal development. The unusual pattern of expression in brain suggests that this transcription factor may be important in the development of cortical architecture.

Indexed as

Multigene FamilyAmino Acid SequenceAnimalsbeta-GalactosidaseBlotting, NorthernBrainCerebral CortexChloramphenicol O-AcetyltransferaseCloning, MolecularDNADNA-Binding ProteinsFetusGene LibraryGenetic VectorsHumansMADS Domain Proteinsbeta-GalactosidaseChloramphenicol O-AcetyltransferaseDNADNA-Binding ProteinsMADS Domain ProteinsMEF2C protein, humanMEF2 Transcription FactorsMyogenic Regulatory FactorsRecombinant Fusion ProteinsRNATranscription Factors

Identifiers

PMID7679508
PMCPMC45911
OpenAlexW1978995496

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.