scholarly article | Q13442814 |
P356 | DOI | 10.1007/978-94-017-8914-1_26 |
P8608 | Fatcat ID | release_57ufnye2vzhdlcr2rtcbdd5n7u |
P932 | PMC publication ID | 4968566 |
P698 | PubMed publication ID | 25012388 |
P50 | author | Marco Ledri | Q59277168 |
P2093 | author name string | Ivan Soltesz | |
Merab Kokaia | |||
Esther Krook-Magnuson | |||
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Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy | Q34311339 | ||
Current status of gene therapy for brain tumors. | Q34318157 | ||
An integrated μLED optrode for optogenetic stimulation and electrical recording. | Q34411558 | ||
Cholecystokinin: a multi-functional molecular switch of neuronal circuits | Q34420892 | ||
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Standard antiepileptic drugs fail to block epileptiform activity in rat organotypic hippocampal slice cultures | Q36736095 | ||
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Tools, methods, and applications for optophysiology in neuroscience | Q37019105 | ||
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The therapeutic potential of focal cooling for neocortical epilepsy | Q37426955 | ||
Developmental mechanisms for the generation of telencephalic interneurons. | Q37864259 | ||
Basket cell dichotomy in microcircuit function | Q37971369 | ||
Complex single gene disorders and epilepsy. | Q38040446 | ||
Optogenetics in epilepsy | Q38110869 | ||
A neural circuit for spatial summation in visual cortex | Q39709858 | ||
Multiwaveguide implantable probe for light delivery to sets of distributed brain targets | Q41480429 | ||
A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing | Q42137770 | ||
A 3D glass optrode array for optical neural stimulation | Q42270039 | ||
Optogenetic silencing strategies differ in their effects on inhibitory synaptic transmission | Q42321485 | ||
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Efficient unsupervised algorithms for the detection of seizures in continuous EEG recordings from rats after brain injury | Q46841981 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | optogenetics | Q781492 |
lead | Q708 | ||
P304 | page(s) | 319-336 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | Advances in Experimental Medicine and Biology | Q4686385 |
P1476 | title | How might novel technologies such as optogenetics lead to better treatments in epilepsy? | |
P478 | volume | 813 |
Q34464281 | Beyond the hammer and the scalpel: selective circuit control for the epilepsies |
Q34948808 | Cerebellar Directed Optogenetic Intervention Inhibits Spontaneous Hippocampal Seizures in a Mouse Model of Temporal Lobe Epilepsy |
Q42405385 | DREADDnoughts Join in the Battle for Seizure Control |
Q26827783 | Future of seizure prediction and intervention: closing the loop |
Q47734973 | Hippocampal GABAergic Inhibitory Interneurons |
Q41266313 | In vivo evaluation of the dentate gate theory in epilepsy. |
Q28087559 | Neuroelectronics and Biooptics: Closed-Loop Technologies in Neurological Disorders |
Q35220504 | Resolution revolution: epilepsy dynamics at the microscale |
Q55440525 | Specificity, Versatility, and Continual Development: The Power of Optogenetics for Epilepsy Research. |
Q61449132 | The Role of BDNF in Peripheral Nerve Regeneration: Activity-Dependent Treatments and Val66Met |
Q33779967 | Zebrafish as an animal model in epilepsy studies with multichannel EEG recordings |
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