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Arx expansion mutation perturbs cortical development by augmenting apoptosis without activating innate immunity in a mouse model of X-linked infantile spasms syndrome
X-linked infantile spasms syndrome (ISSX) is a clinically devastating developmental epileptic encephalopathy with life-long impact. Arx((GCG)10+7), a mouse model of the most common triplet-repeat expansion mutation of ARX, exhibits neonatal spasms, electrographic phenotypes and abnormal migration of...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Dis Model Mech |
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| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Company of Biologists Ltd
2020
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7132796/ https://ncbi.nlm.nih.gov/pubmed/32033960 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.042515 |
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