Stephanie N Fox - Publications
Affiliations: | University of Alabama at Birmingham School of Medicine |
Year | Citation | Score | |||
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2021 | McMeekin LJ, Fox SN, Boas SM, Cowell RM. Dysregulation of PGC-1α-Dependent Transcriptional Programs in Neurological and Developmental Disorders: Therapeutic Challenges and Opportunities. Cells. 10. PMID 33572179 DOI: 10.3390/cells10020352 | 0.493 | |||
2020 | Schneeberger PE, Kortüm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D, Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M, Biskup S, et al. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder. Brain : a Journal of Neurology. PMID 32761064 DOI: 10.1093/Brain/Awaa204 | 0.359 | |||
2019 | Laszczyk AM, Nettles D, Pollock TA, Fox S, Garcia ML, Wang J, Quarles LD, King GD. FGF-23 Deficiency Impairs Hippocampal-Dependent Cognitive Function. Eneuro. 6. PMID 30911673 DOI: 10.1523/ENEURO.0469-18.2019 | 0.444 | |||
2018 | McMeekin LJ, Li Y, Fox SN, Rowe GC, Crossman DK, Day JJ, Li Y, Detloff PJ, Cowell RM. Cell-specific deletion of PGC-1α from medium spiny neurons causes transcriptional alterations and age-related motor impairment. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29491012 DOI: 10.1523/Jneurosci.0848-17.2018 | 0.499 | |||
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