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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....
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
American Physiological Society
2013
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| 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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