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Prolactin increases SMN expression and survival in a mouse model of severe spinal muscular atrophy via the STAT5 pathway

Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease that is characterized by the loss of motor neurons, resulting in progressive muscle atrophy. It is caused by the loss of functional survival motor neuron (SMN) protein due to mutations or deletion in the SMN1 gene. A p...

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Главные авторы: Farooq, Faraz, Molina, Francisco Abadía, Hadwen, Jeremiah, MacKenzie, Duncan, Witherspoon, Luke, Osmond, Matthew, Holcik, Martin, MacKenzie, Alex
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Clinical Investigation 2011
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3148738/
https://ncbi.nlm.nih.gov/pubmed/21785216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI46276
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