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Peter L Oliver

Showing results (61-70 of 82) with videos related to

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Translational Psychiatry|November 16, 2021
Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cuesGauri Ang, Laurence A Brown, Shu K E Tam, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Translational Psychiatry|August 16, 2018
Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disordersGauri Ang, Laura E McKillop, Ross Purple, et al.
Redox Biology|April 26, 2019
Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageingLaura C D Pomatto, Patrick Y Sun, Kelsi Yu, et al.
Nucleic Acid Therapeutics|February 19, 2026
Investigating the Biophysical Properties and <i>In Vivo</i> Activity of 7',5'-Alpha-Bicyclo-DNA Phosphodiester Backbone Gapmer Antisense OligonucleotidesDamien Evequoz, Remya R Nair, Martina Cadeddu, et al.
Disease Models & Mechanisms|January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalitiesMichelle Stewart, Petrina Lau, Gareth Banks, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, et al.
Cell Reports|October 24, 2019
Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and BehaviorBenjamin H M Hunn, Siv Vingill, Sarah Threlfell, et al.
Human Molecular Genetics|October 19, 2018
The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neuronsMattéa J Finelli, Davide Aprile, Enrico Castroflorio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Translational Psychiatry|November 16, 2021
Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cuesGauri Ang, Laurence A Brown, Shu K E Tam, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Translational Psychiatry|August 16, 2018
Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disordersGauri Ang, Laura E McKillop, Ross Purple, et al.
Redox Biology|April 26, 2019
Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageingLaura C D Pomatto, Patrick Y Sun, Kelsi Yu, et al.
Nucleic Acid Therapeutics|February 19, 2026
Investigating the Biophysical Properties and <i>In Vivo</i> Activity of 7',5'-Alpha-Bicyclo-DNA Phosphodiester Backbone Gapmer Antisense OligonucleotidesDamien Evequoz, Remya R Nair, Martina Cadeddu, et al.
Disease Models & Mechanisms|January 30, 2019
Loss of <i>Frrs1l</i> disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalitiesMichelle Stewart, Petrina Lau, Gareth Banks, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, et al.
Cell Reports|October 24, 2019
Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and BehaviorBenjamin H M Hunn, Siv Vingill, Sarah Threlfell, et al.
Human Molecular Genetics|October 19, 2018
The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neuronsMattéa J Finelli, Davide Aprile, Enrico Castroflorio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Pageof 9