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Anthony R Isles

Showing results (51-60 of 70) with videos related to

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Brain and Neuroscience Advances|September 21, 2020
Impairments in sensory-motor gating and information processing in a mouse model of <i>Ehmt1</i> haploinsufficiencyBrittany A Davis, François David, Ciara O'Regan, et al.
The European Journal of Neuroscience|June 5, 2015
Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndromeJennifer R Davies, Trevor Humby, Dominic M Dwyer, et al.
Genetics|March 23, 2018
Impulsive Choice in Mice Lacking Paternal Expression of <i>Grb10</i> Suggests Intragenomic Conflict in BehaviorClaire L Dent, Trevor Humby, Katie Lewis, et al.
Molecular Brain|December 10, 2016
Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT<sub>2C</sub> receptor mediated appetiteAlastair S Garfield, Jennifer R Davies, Luke K Burke, et al.
Molecular and Cellular Biology|March 31, 2005
Imprinted Nesp55 influences behavioral reactivity to novel environmentsAntonius Plagge, Anthony R Isles, Emma Gordon, et al.
Human Molecular Genetics|March 24, 2009
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviourChristine M Doe, Dinko Relkovic, Alastair S Garfield, et al.
Frontiers in Neuroscience|April 23, 2020
Unified Behavioral Scoring for Preclinical ModelsDavid J Harrison, Hugo D J Creeth, Hannah R Tyson, et al.
Human Molecular Genetics|June 8, 2021
Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspringDavid J Harrison, Hugo D J Creeth, Hannah R Tyson, et al.
Human Molecular Genetics|May 9, 2022
Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-functionNicholas E Clifton, Matthew L Bosworth, Niels Haan, et al.
The European Journal of Neuroscience|January 23, 2010
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndromeDinko Relkovic, Christine M Doe, Trevor Humby, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Brain and Neuroscience Advances|September 21, 2020
Impairments in sensory-motor gating and information processing in a mouse model of <i>Ehmt1</i> haploinsufficiencyBrittany A Davis, François David, Ciara O'Regan, et al.
The European Journal of Neuroscience|June 5, 2015
Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndromeJennifer R Davies, Trevor Humby, Dominic M Dwyer, et al.
Genetics|March 23, 2018
Impulsive Choice in Mice Lacking Paternal Expression of <i>Grb10</i> Suggests Intragenomic Conflict in BehaviorClaire L Dent, Trevor Humby, Katie Lewis, et al.
Molecular Brain|December 10, 2016
Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT<sub>2C</sub> receptor mediated appetiteAlastair S Garfield, Jennifer R Davies, Luke K Burke, et al.
Molecular and Cellular Biology|March 31, 2005
Imprinted Nesp55 influences behavioral reactivity to novel environmentsAntonius Plagge, Anthony R Isles, Emma Gordon, et al.
Human Molecular Genetics|March 24, 2009
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviourChristine M Doe, Dinko Relkovic, Alastair S Garfield, et al.
Frontiers in Neuroscience|April 23, 2020
Unified Behavioral Scoring for Preclinical ModelsDavid J Harrison, Hugo D J Creeth, Hannah R Tyson, et al.
Human Molecular Genetics|June 8, 2021
Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspringDavid J Harrison, Hugo D J Creeth, Hannah R Tyson, et al.
Human Molecular Genetics|May 9, 2022
Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-functionNicholas E Clifton, Matthew L Bosworth, Niels Haan, et al.
The European Journal of Neuroscience|January 23, 2010
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndromeDinko Relkovic, Christine M Doe, Trevor Humby, et al.
Pageof 7