Kevin C. Ess, M.D./Ph.D
Affiliations: | Vanderbilt University, Nashville, TN |
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Publications
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| Brown JA, Faley SL, Judge M, et al. (2023) Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit. Biorxiv : the Preprint Server For Biology |
| Chalkley ML, Mersfelder RB, Sundberg M, et al. (2023) Non-canonical functions of a mutant TSC2 protein in mitotic division. Plos One. 18: e0292086 |
| Klofas LK, Short BP, Snow JP, et al. (2020) DEPDC5 haploinsufficiency drives increased mTORC1 signaling and abnormal morphology in human iPSC-derived cortical neurons. Neurobiology of Disease. 104975 |
| Snow JP, Westlake G, Klofas LK, et al. (2020) Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotype. Neurobiology of Disease. 104881 |
| Xie Y, Ng NN, Safrina OS, et al. (2019) Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation. Neurobiology of Disease. 104627 |
| Gewin L, Summers ME, Harral JW, et al. (2019) Inactivation of in Abcg2 Lineage Derived Cells Drives the Appearance of Polycystic Lesions and Fibrosis in the Adult Kidney. American Journal of Physiology. Renal Physiology |
| Ess KC, Franz DN. (2019) Everolimus for cognition/autism in children with tuberous sclerosis complex: Definitive outcomes deferred. Neurology |
| Neal EH, Marinelli NA, Shi Y, et al. (2019) A Simplified, Fully Defined Differentiation Scheme for Producing Blood-Brain Barrier Endothelial Cells from Human iPSCs. Stem Cell Reports. 12: 1380-1388 |
| Short B, Kozek L, Harmsen H, et al. (2019) Cerebral aquaporin-4 expression is independent of seizures in tuberous sclerosis complex. Neurobiology of Disease |
| Simmons CQ, Thompson CH, Cawthon BE, et al. (2018) Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhood. Neurobiology of Disease. 115: 29-38 |