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1.
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders.
Cells
; 12(10)2023 05 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-37408271
2.
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro.
Nat Commun
; 12(1): 2897, 2021 05 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-34006844
3.
Phenotypic Screen with TSC-Deficient Neurons Reveals Heat-Shock Machinery as a Druggable Pathway for mTORC1 and Reduced Cilia.
Cell Rep
; 31(12): 107780, 2020 06 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-32579942
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