Carregant...

Discovery, Synthesis and Biological Evaluation of Novel SMN Protein Modulators

Spinal Muscular Atrophy (SMA) is an autosomal recessive disorder affecting the expression or function of survival motor neuron protein (SMN) due to the homozygous deletion or rare point mutations in the survival motor neuron gene 1 (SMN1). The human genome includes a second nearly identical gene cal...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Xiao, Jingbo, Marugan, Juan J., Zheng, Wei, Titus, Steve, Southall, Noel, Cherry, Jonathan J., Evans, Matthew, Androphy, Elliot J., Austin, Christopher P.
Format: Artigo
Idioma:Inglês
Publicat: 2011
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3174349/
https://ncbi.nlm.nih.gov/pubmed/21819082
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm200497t
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!