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Role of Ostm1 Cytosolic Complex with Kinesin 5B in Intracellular Dispersion and Trafficking

In humans and in mice, mutations in the Ostm1 gene cause the most severe form of osteopetrosis, a major bone disease, and neuronal degeneration, both of which are associated with early death. To gain insight into Ostm1 function, we first investigated by sequence and biochemical analysis an immature...

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Detalhes bibliográficos
Publicado no:Mol Cell Biol
Main Authors: Pandruvada, Subramanya N. M., Beauregard, Janie, Benjannet, Suzanne, Pata, Monica, Lazure, Claude, Seidah, Nabil G., Vacher, Jean
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4719428/
https://ncbi.nlm.nih.gov/pubmed/26598607
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.00656-15
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