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Roles of NR2F1 in Hippocampal Circuit Function and Mitochondrial Regulation: Insights into NR2F1-Related Neurodevelopmental Disorder

Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) is a rare neurodevelopmental disorder caused by pathogenic variants in the gene NR2F1, a nuclear transcriptional regulator with essential roles in brain development and neuronal function. While the clinical phenotype includes cognitive impairments, visual deficits, and autistic traits, the cellular ...
openaire   +1 more source

NR2F1‐AS1 regulated miR‐423‐5p/SOX12 to promote proliferation and invasion of papillary thyroid carcinoma

Journal of Cellular Biochemistry, 2020
Chuanjia Yang   +2 more
exaly  

lncRNA NR2F1‐AS1 promotes breast cancer angiogenesis through activating IGF‐1/IGF‐1R/ERK pathway

Journal of Cellular and Molecular Medicine, 2020
Tianfu Li, Nan Shao, Ying Lin
exaly  

NR2F1 haploinsufficiency is associated with optic atrophy, dysmorphism and global developmental delay

American Journal of Medical Genetics Part A, 2013
Hussam, Al-Kateb   +5 more
openaire   +2 more sources

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