<i>mef2ca</i> and <i>mef2cb</i> Double Mutant Zebrafish Show Altered Craniofacial Phenotype and Motor Behaviour

<i>mef2ca</i> and <i>mef2cb</i> Double Mutant Zebrafish Show Altered Craniofacial Phenotype and Motor Behaviour

The transcription factor MEF2C is crucial in neuronal, cardiac, bone and cartilage molecular processes, as well as for craniofacial development. MEF2C was associated with the human disease MRD20, whose patients show abnormal neuronal and craniofacial development. Zebrafish <i>mef2ca</i>;...

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Bibliographic Details
Main Authors: Andreia Adrião, Sara Mariano, José Mariano, Paulo J. Gavaia, M. Leonor Cancela, Marta Vitorino, Natércia Conceição
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Biomolecules
Subjects:
Myocyte enhancer factor 2 (MEF2C)
autosomal dominant mental retardation syndrome-20 disease (MRD20)
MEF2C haploinsufficiency syndrome
zebrafish (<i>Danio rerio)</i>
craniofacial development
<i>Mef2c</i> mutants
Online Access:https://www.mdpi.com/2218-273X/13/5/805

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https://www.mdpi.com/2218-273X/13/5/805

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