Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes

Biallelic mutations in the gene encoding centrosomal CDK5RAP2 lead to autosomal recessive primary microcephaly (MCPH), a disorder characterized by pronounced reduction in volume of otherwise architectonical normal brains and intellectual deficit. The current model for the microcephaly phenotype in M...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Cell Cycle
Autors principals: Kraemer, Nadine, Ravindran, Ethiraj, Zaqout, Sami, Neubert, Gerda, Schindler, Detlev, Ninnemann, Olaf, Gräf, Ralph, Seiler, Andrea EM, Kaindl, Angela M
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 2015
Matèries:
Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4613649/
https://ncbi.nlm.nih.gov/pubmed/25942099
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384101.2015.1044169
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars