SH3-Binding Glutamic Acid Rich-Deficiency Augments Apoptosis in Neonatal Rat Cardiomyocytes

Congenital heart disease (CHD) is one of the most common birth defects in humans, present in around 40% of newborns with Down’s syndrome (DS). The SH3 domain-binding glutamic acid-rich (SH3BGR) gene, which maps to the DS region, belongs to a gene family encoding a cluster of small thioredoxin-like p...

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Detalles Bibliográficos
Autores principales: Deshpande, Anushka, Borlepawar, Ankush, Rosskopf, Alexandra, Frank, Derk, Frey, Norbert, Rangrez, Ashraf Yusuf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541172/
https://www.ncbi.nlm.nih.gov/pubmed/34681711
http://dx.doi.org/10.3390/ijms222011042

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541172/
https://www.ncbi.nlm.nih.gov/pubmed/34681711
http://dx.doi.org/10.3390/ijms222011042

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