Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
Mauro S. Porcel de Peralta(Consejo Nacional de Investigaciones Científicas y Técnicas), Nora B. Calcaterra(Consejo Nacional de Investigaciones Científicas y Técnicas), Gabriela Coux(Consejo Nacional de Investigaciones Científicas y Técnicas), Valeria S. Mouguelar(Consejo Nacional de Investigaciones Científicas y Técnicas), Maria Rita Passos‐Bueno(Universidade de São Paulo), María Antonella Sdrigotti(Consejo Nacional de Investigaciones Científicas y Técnicas), Roberto D. Fanganiello(Université Laval), Felipe Augusto André Ishiy(Dassault Systèmes (Canada))
Cited by 40
Related Papers
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
|Nature Genetics|2022|613
Reconstruction of Large Cranial Defects in Nonimmunosuppressed Experimental Design With Human Dental Pulp Stem Cells
|Journal of Craniofacial Surgery|2008|228
Genetics of Craniosynostosis: Genes, Syndromes, Mutations and Genotype-Phenotype Correlations
|Frontiers of oral physiology/Frontiers of oral biology|2008|161
Syndromes of the first and second pharyngeal arches: A review
|American Journal of Medical Genetics Part A|2009|116
New Source of Muscle-Derived Stem Cells with Potential for Alveolar Bone Reconstruction in Cleft Lip and/or Palate Patients
|Tissue Engineering Part A|2008|95