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Pcsk5 is required in the early cranio-cardiac mesoderm for heart development
BACKGROUND: Loss of proprotein convertase subtilisin/kexin type 5 (Pcsk5) results in multiple developmental anomalies including cardiac malformations, caudal regression, pre-sacral mass, renal agenesis, anteroposterior patterning defects, and tracheo-oesophageal and anorectal malformations, and is a...
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| Publicat a: | BMC Dev Biol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5407003/ https://ncbi.nlm.nih.gov/pubmed/28446132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12861-017-0148-y |
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