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Peter C Kind

Showing results (61-70 of 77) with videos related to

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Science Translational Medicine|May 31, 2019
Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X SyndromeAntonis Asiminas, Adam D Jackson, Susana R Louros, et al.
Stem Cells (Dayton, Ohio)|January 15, 2016
Maturation and electrophysiological properties of human pluripotent stem cell-derived oligodendrocytesMatthew R Livesey, Dario Magnani, Elaine M Cleary, et al.
Neuron|May 15, 2012
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insultsMarc-André Martel, Tomás J Ryan, Karen F S Bell, et al.
Science Translational Medicine|September 21, 2012
Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofenChristina Henderson, Lasani Wijetunge, Mika Nakamoto Kinoshita, et al.
Cell Reports|August 14, 2020
Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X SyndromeSam A Booker, Laura Simões de Oliveira, Natasha J Anstey, et al.
Molecular Autism|June 21, 2020
Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patternsShreya Das Sharma, Rakhi Pal, Bharath Kumar Reddy, et al.
Cell Reports|October 26, 2018
The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal SequencesSean McKay, Tomás J Ryan, Jamie McQueen, et al.
Molecular Autism|July 19, 2022
Imbalance of flight-freeze responses and their cellular correlates in the Nlgn3<sup>-/y</sup> rat model of autismNatasha J Anstey, Vijayakumar Kapgal, Shashank Tiwari, et al.
Elife|October 4, 2016
Evidence for evolutionary divergence of activity-dependent gene expression in developing neuronsJing Qiu, Jamie McQueen, Bilada Bilican, et al.
Molecular Autism|June 14, 2024
Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorderLaura Simões de Oliveira, Heather E O'Leary, Sarfaraz Nawaz, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Science Translational Medicine|May 31, 2019
Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X SyndromeAntonis Asiminas, Adam D Jackson, Susana R Louros, et al.
Stem Cells (Dayton, Ohio)|January 15, 2016
Maturation and electrophysiological properties of human pluripotent stem cell-derived oligodendrocytesMatthew R Livesey, Dario Magnani, Elaine M Cleary, et al.
Neuron|May 15, 2012
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insultsMarc-André Martel, Tomás J Ryan, Karen F S Bell, et al.
Science Translational Medicine|September 21, 2012
Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofenChristina Henderson, Lasani Wijetunge, Mika Nakamoto Kinoshita, et al.
Cell Reports|August 14, 2020
Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X SyndromeSam A Booker, Laura Simões de Oliveira, Natasha J Anstey, et al.
Molecular Autism|June 21, 2020
Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patternsShreya Das Sharma, Rakhi Pal, Bharath Kumar Reddy, et al.
Cell Reports|October 26, 2018
The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal SequencesSean McKay, Tomás J Ryan, Jamie McQueen, et al.
Molecular Autism|July 19, 2022
Imbalance of flight-freeze responses and their cellular correlates in the Nlgn3<sup>-/y</sup> rat model of autismNatasha J Anstey, Vijayakumar Kapgal, Shashank Tiwari, et al.
Elife|October 4, 2016
Evidence for evolutionary divergence of activity-dependent gene expression in developing neuronsJing Qiu, Jamie McQueen, Bilada Bilican, et al.
Molecular Autism|June 14, 2024
Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorderLaura Simões de Oliveira, Heather E O'Leary, Sarfaraz Nawaz, et al.
Pageof 8