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Neurobiology of Disease|December 2, 2019
Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutationYunyao Xie, Nathan N Ng, Olga S Safrina, et al.
Human Molecular Genetics|January 29, 2025
Human TSC2 mutant cells exhibit aberrations in early neurodevelopment accompanied by changes in the DNA MethylomeMary-Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA MethylomeMary-Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, et al.
Annals of Neurology|October 22, 2005
A common pattern of persistent gene activation in human neocortical epileptic fociSanjay N Rakhade, Bin Yao, Sharlin Ahmed, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2014
Metabolic costs and evolutionary implications of human brain developmentChristopher W Kuzawa, Harry T Chugani, Lawrence I Grossman, et al.
Neurobiology of Disease|May 13, 2019
Cerebral aquaporin-4 expression is independent of seizures in tuberous sclerosis complexBrittany Short, Lindsay Kozek, Hannah Harmsen, et al.
Biorxiv : the Preprint Server for Biology|April 15, 2024
Regulation of fatty acid delivery to metastases by tumor endotheliumDeanna N Edwards, Shan Wang, Wenqiang Song, et al.
Epilepsia|March 5, 2003
Quantitative interictal subdural EEG analyses in children with neocortical epilepsyEishi Asano, Otto Muzik, Aashit Shah, et al.
Annals of Neurology|August 2, 2003
Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy modelMichael Wong, Kevin C Ess, Erik J Uhlmann, et al.
Bioengineering (Basel, Switzerland)|March 27, 2024
Contractile and Genetic Characterization of Cardiac Constructs Engineered from Human Induced Pluripotent Stem Cells: Modeling of Tuberous Sclerosis Complex and the Effects of RapamycinVeniamin Y Sidorov, Tatiana N Sidorova, Philip C Samson, et al.
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