Peter Crino
Affiliations: | University of Pennsylvania School of Medicine, Philadelphia, PA, United States |
Area:
Epilepsy (Tuberous Sclerosis)Google:
"Peter Crino"Mean distance: 18.18 (cluster 17)
Parents
Sign in to add mentor| Ladislav Volicer | grad student | Boston University | |
| James H. Eberwine | post-doc | University of Pennsylvania School of Medicine |
Children
Sign in to add trainee| Julie Chen | grad student | 2011- | Penn |
| Ksenia A. Orlova | grad student | 2009 | Penn |
| Victoria Tsai | grad student | 2008-2012 | Penn |
| Whitney E. Parker | grad student | 2007-2014 | Penn |
BETA: Related publications
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Publications
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| Elziny S, Sran S, Yoon H, et al. (2023) Loss of alters development of the mouse cerebral cortex. Biorxiv : the Preprint Server For Biology |
| Iffland PH, Everett ME, Cobb-Pitstick KM, et al. (2022) NPRL3 loss alters neuronal morphology, mTOR localization, cortical lamination, and seizure threshold. Brain : a Journal of Neurology |
| Terry BK, Park R, Cho SH, et al. (2022) Abnormal activation of yap/Taz contributes to the pathogenesis of tuberous sclerosis complex. Human Molecular Genetics |
| Dang LT, Vaid S, Lin G, et al. (2021) STRADA-mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiation. Developmental Neurobiology |
| Dang LT, Glanowska KM, Iffland Ii PH, et al. (2020) Multimodal Analysis of STRADA Function in Brain Development. Frontiers in Cellular Neuroscience. 14: 122 |
| Iffland PH, Baybis M, Barnes AE, et al. (2018) DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons. Neurobiology of Disease |
| Iffland PH, Crino PB. (2017) Focal Cortical Dysplasia: Gene Mutations, Cell Signaling, and Therapeutic Implications. Annual Review of Pathology. 12: 547-571 |
| Liu C, Russin J, Heck C, et al. (2016) Dysregulation of PINCH signaling in mesial temporal epilepsy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia |
| Crino PB. (2016) The mTOR signalling cascade: paving new roads to cure neurological disease. Nature Reviews. Neurology |
| Bhoj EJ, Li D, Harr M, et al. (2016) Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia. American Journal of Human Genetics |