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A selective 5-HT(1a) receptor agonist improves respiration in a mouse model of Rett syndrome

Rett syndrome is a neurological disorder caused by loss of function mutations in the gene that encodes the DNA binding protein methyl-CpG-binding protein 2 (Mecp2). A prominent feature of the syndrome is disturbances in respiration characterized by frequent apnea and an irregular interbreath cycle....

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Levitt, Erica S., Hunnicutt, Barbara J., Knopp, Sharon J., Williams, John T., Bissonnette, John M.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Physiological Society 2013
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3882741/
https://ncbi.nlm.nih.gov/pubmed/24092697
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/japplphysiol.00889.2013
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