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February 15, 2019 (v1)Journal articleUploaded on: December 3, 2022
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July 18, 2019 (v1)Journal articleMouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome
Optic nerve atrophy represents the most common form of hereditary optic neuropathies leading to vision impairment. The recently described Bosch-Boonstra-Schaaf optic atrophy (BBSOA) syndrome denotes an autosomal dominant genetic form of neuropathy caused by mutations or deletions in the NR2F1 gene. Herein, we describe a mouse model...
Uploaded on: December 4, 2022 -
June 23, 2020 (v1)Journal article
The formation of functional cortical maps in the cerebral cortex results from a timely regulated interaction between intrinsic genetic mechanisms and electrical activity. To understand how transcriptional regulation influences network activity and neuronal excitability within the neocortex, we used mice deficient for Nr2f1 (also known as...
Uploaded on: December 4, 2022