18 results on '"Sripathy, Srinidhi Rao"'
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2. TCF4 Mutations Disrupt Synaptic Function Through Dysregulation of RIMBP2 in Patient-Derived Cortical Neurons
3. Evaluation of Nav1.8 as a therapeutic target for Pitt Hopkins Syndrome
4. CaPTure: Calcium PeakToolbox for analysis of in vitro calcium imaging data
5. A myelin-related transcriptomic profile is shared by Pitt–Hopkins syndrome models and human autism spectrum disorder
6. 302. Investigating the Impact of Common Genetic Risk Variants for Schizophrenia on Neuronal Function Elucidates Relationships Between Cellular Phenotypes, Clinical Status and Cognitive Performance
7. 301. Pro-Myelinating Drugs Promote Functional Recovery in an ASD Mouse Model of Pitt-Hopkins Syndrome
8. Promyelinating drugs promote functional recovery in an autism spectrum disorder mouse model of Pitt–Hopkins syndrome
9. Consensus molecular environment of schizophrenia risk genes in coexpression networks shifting across age and brain regions
10. TCF4 mutations disrupt synaptic function through dysregulation of RIMBP2 in patient-derived cortical neurons
11. Evaluation of Nav1.8 as a therapeutic target for Pitt Hopkins Syndrome
12. Clemastine fumarate enhances myelination and promotes functional recovery in a syndromic ASD mouse model of Pitt-Hopkins Syndrome
13. Schizophrenia Risk Genes Converge into Shifting Co-Expression Networks Across Brain Development, Ageing and Brain Regions
14. Electrophysiological measures from human iPSC-derived neurons are associated with schizophrenia clinical status and predict individual cognitive performance
15. TH71. ELECTROPHYSIOLOGICAL MEASURES FROM HUMAN IPSC-DERIVED NEURONS ARE ASSOCIATED WITH SCHIZOPHRENIA CLINICAL STATUS AND PREDICT INDIVIDUAL COGNITIVE PERFORMANCE
16. CaPTure: Calcium PeakToolbox for analysis of in vitro calcium imaging data
17. Electrophysiological measures from human iPSC-derived neurons are associated with schizophrenia clinical status and predict individual cognitive performance
18. TCF4 mutations disrupt synaptic function through dysregulation of RIMBP2 in patient-derived cortical neurons.
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