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Kateryna Pysanenko

Showing results (11-20 of 14) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 24, 2012
Differential distribution of glycine receptor subtypes at the rat calyx of Held synapseBohdana Hruskova, Johana Trojanova, Akos Kulik, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2022
ISL1 is necessary for auditory neuron development and contributes toward tonotopic organizationIva Filova, Kateryna Pysanenko, Mitra Tavakoli, et al.
Neurobiology of Disease|February 6, 2025
Binding of HCN channels to GABA<sub>B</sub> receptors in dopamine neurons of the VTA limits synaptic inhibition and prevents the development of anxietyEnrique Pérez-Garci, Kateryna Pysanenko, Giorgio Rizzi, et al.
Nature Communications|July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 24, 2012
Differential distribution of glycine receptor subtypes at the rat calyx of Held synapseBohdana Hruskova, Johana Trojanova, Akos Kulik, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2022
ISL1 is necessary for auditory neuron development and contributes toward tonotopic organizationIva Filova, Kateryna Pysanenko, Mitra Tavakoli, et al.
Neurobiology of Disease|February 6, 2025
Binding of HCN channels to GABA<sub>B</sub> receptors in dopamine neurons of the VTA limits synaptic inhibition and prevents the development of anxietyEnrique Pérez-Garci, Kateryna Pysanenko, Giorgio Rizzi, et al.
Nature Communications|July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
Pageof 2