Lista de obras - Simon P Brooks - Dominio Público Uruguay

A Longitudinal Motor Characterisation of the HdhQ111 Mouse Model of Huntington's Disease

artículo científico publicado en 2016

A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the HdhQ111 Mouse Model of Huntington's Disease

scientific article published on 04 October 2016

A novel extended sequence learning task (ESLeT) for rodents: validation and the effects of amphetamine, scopolamine and striatal lesions

artículo científico publicado en 2010

Age-dependent maintenance of motor control and corticostriatal innervation by death receptor 3.

artículo científico publicado en 2010

Assessment of Motor Coordination and Balance in Mice Using the Rotarod, Elevated Bridge, and Footprint Tests.

artículo científico publicado en 2012

Behavioural profiles of inbred mouse strains used as transgenic backgrounds. I: motor tests

artículo científico publicado en 2004

Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease.

artículo científico

Cognitive deficits in animal models of basal ganglia disorders.

artículo científico publicado en 2012

Cognitive training modifies disease symptoms in a mouse model of Huntington's disease

artículo científico publicado en 2016

Comparison of mHTT Antibodies in Huntington's Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development

artículo científico publicado en 2016

Corrigendum: Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease.

artículo científico publicado en 2017

Early onset deficits on the delayed alternation task in the Hdh(Q92) knock-in mouse model of Huntington's disease.

artículo científico publicado en 2011

Effects of corticosterone on place conditioning to ethanol.

artículo científico publicado en 2004

Effects of reinforcer sweetness and the D2/D3 antagonist raclopride on progressive ratio operant performance

scientific article published on 01 March 1995

Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model

artículo científico publicado en 2013

Gene expression and behaviour in mouse models of HD.

artículo científico publicado en 2011

Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdhQ111 Model of HD.

artículo científico publicado en 2015

Identification of novel alternative splicing events in the huntingtin gene and assessment of the functional consequences using structural protein homology modelling.

artículo científico publicado en 2014

In Vivo MRI Evidence that Neuropathology is Attenuated by Cognitive Enrichment in the Yac128 Huntington's Disease Mouse Model.

artículo científico publicado en 2015

Light and electron microscopic characterization of the evolution of cellular pathology in HdhQ92 Huntington's disease knock-in mice.

artículo científico publicado en 2011

Light and electron microscopic characterization of the evolution of cellular pathology in YAC128 Huntington's disease transgenic mice

artículo científico publicado en 2011

Light and electron microscopic characterization of the evolution of cellular pathology in the Hdh(CAG)150 Huntington's disease knock-in mouse.

artículo científico publicado en 2011

Light and electron microscopic characterization of the evolution of cellular pathology in the R6/1 Huntington's disease transgenic mice.

artículo científico publicado en 2011

Longitudinal analyses of operant performance on the serial implicit learning task (SILT) in the YAC128 Huntington's disease mouse line

artículo científico publicado en 2011

Longitudinal analysis of gene expression and behaviour in the HdhQ150 mouse model of Huntington's disease

artículo científico publicado en 2011

Longitudinal analysis of the behavioural phenotype in HdhQ92 Huntington's disease knock-in mice

artículo científico publicado en 2010

Longitudinal analysis of the behavioural phenotype in R6/1 (C57BL/6J) Huntington's disease transgenic mice

artículo científico publicado en 2011

Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice

artículo científico publicado en 2010

Low alcohol preference among the "high alcohol preference" C57/BL10 mice; factors affecting such preference.

artículo científico publicado en 2002

Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease

artículo científico publicado en 2017

Motor actions of eliprodil in the normal and monoamine-depleted mouse: a role in the treatment of Parkinson's disease?

artículo científico publicado en 1996

Mouse Models of Huntington's Disease

artículo científico publicado en 2015

Nimodipine prevents the effects of ethanol in tests of memory.

artículo científico publicado en 2002

Nimodipine prior to alcohol withdrawal prevents memory deficits during the abstinence phase.

artículo científico publicado en 2008

Operant Analysis of Fronto-striatal Function in Rodents

Optimising Golgi-Cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington's disease

artículo científico publicado en 2015

Practice, progress and future directions for physical therapies in Huntingtons disease

artículo científico publicado en 2012

Profiles of motor and cognitive impairment in the transgenic rat model of Huntington's disease.

artículo científico publicado en 2011

Proteomic changes in the brains of Huntington's disease mouse models reflect pathology and implicate mitochondrial changes

artículo científico publicado en 2011

Rule learning, visuospatial function and motor performance in the Hdh(Q92) knock-in mouse model of Huntington's disease.

artículo científico

Selective cognitive impairment in the YAC128 Huntington's disease mouse.

artículo científico publicado en 2011

Selective extra-dimensional set shifting deficit in a knock-in mouse model of Huntington's disease

scientific journal article

Selective increases in regional brain glucocorticoid: a novel effect of chronic alcohol.

artículo científico publicado en 2008

Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence

artículo científico publicado en 2015

Social defeat increases alcohol preference of C57BL/10 strain mice; effect prevented by a CCKB antagonist.

artículo científico publicado en 2005

Striatal lesions in the mouse disrupt acquisition and retention, but not implicit learning, in the SILT procedural motor learning task

artículo científico publicado en 2007

Subtle but progressive cognitive deficits in the female tgHD hemizygote rat as demonstrated by operant SILT performance.

artículo científico publicado en 2009

Tests to assess motor phenotype in mice: a user's guide

artículo científico publicado en 2009

The utilisation of operant delayed matching and non-matching to position for probing cognitive flexibility and working memory in mouse models of Huntington's disease

artículo científico publicado en 2015

Lista de obras de Simon P Brooks

A Longitudinal Motor Characterisation of the HdhQ111 Mouse Model of Huntington's Disease

A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the HdhQ111 Mouse Model of Huntington's Disease

A novel extended sequence learning task (ESLeT) for rodents: validation and the effects of amphetamine, scopolamine and striatal lesions

Age-dependent maintenance of motor control and corticostriatal innervation by death receptor 3.

Assessment of Motor Coordination and Balance in Mice Using the Rotarod, Elevated Bridge, and Footprint Tests.

Behavioural profiles of inbred mouse strains used as transgenic backgrounds. I: motor tests

Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease.

Cognitive deficits in animal models of basal ganglia disorders.

Cognitive training modifies disease symptoms in a mouse model of Huntington's disease

Comparison of mHTT Antibodies in Huntington's Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development

Corrigendum: Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease.

Early onset deficits on the delayed alternation task in the Hdh(Q92) knock-in mouse model of Huntington's disease.

Effects of corticosterone on place conditioning to ethanol.

Effects of reinforcer sweetness and the D2/D3 antagonist raclopride on progressive ratio operant performance

Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model

Gene expression and behaviour in mouse models of HD.

Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdhQ111 Model of HD.

Identification of novel alternative splicing events in the huntingtin gene and assessment of the functional consequences using structural protein homology modelling.

In Vivo MRI Evidence that Neuropathology is Attenuated by Cognitive Enrichment in the Yac128 Huntington's Disease Mouse Model.

Light and electron microscopic characterization of the evolution of cellular pathology in HdhQ92 Huntington's disease knock-in mice.

Light and electron microscopic characterization of the evolution of cellular pathology in YAC128 Huntington's disease transgenic mice

Light and electron microscopic characterization of the evolution of cellular pathology in the Hdh(CAG)150 Huntington's disease knock-in mouse.

Light and electron microscopic characterization of the evolution of cellular pathology in the R6/1 Huntington's disease transgenic mice.

Longitudinal analyses of operant performance on the serial implicit learning task (SILT) in the YAC128 Huntington's disease mouse line

Longitudinal analysis of gene expression and behaviour in the HdhQ150 mouse model of Huntington's disease

Longitudinal analysis of the behavioural phenotype in HdhQ92 Huntington's disease knock-in mice

Longitudinal analysis of the behavioural phenotype in R6/1 (C57BL/6J) Huntington's disease transgenic mice

Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice

Low alcohol preference among the "high alcohol preference" C57/BL10 mice; factors affecting such preference.

Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease

Motor actions of eliprodil in the normal and monoamine-depleted mouse: a role in the treatment of Parkinson's disease?

Mouse Models of Huntington's Disease

Nimodipine prevents the effects of ethanol in tests of memory.

Nimodipine prior to alcohol withdrawal prevents memory deficits during the abstinence phase.

Operant Analysis of Fronto-striatal Function in Rodents

Optimising Golgi-Cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington's disease

Practice, progress and future directions for physical therapies in Huntingtons disease

Profiles of motor and cognitive impairment in the transgenic rat model of Huntington's disease.

Proteomic changes in the brains of Huntington's disease mouse models reflect pathology and implicate mitochondrial changes

Rule learning, visuospatial function and motor performance in the Hdh(Q92) knock-in mouse model of Huntington's disease.

Selective cognitive impairment in the YAC128 Huntington's disease mouse.

Selective extra-dimensional set shifting deficit in a knock-in mouse model of Huntington's disease

Selective increases in regional brain glucocorticoid: a novel effect of chronic alcohol.

Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence

Social defeat increases alcohol preference of C57BL/10 strain mice; effect prevented by a CCKB antagonist.

Striatal lesions in the mouse disrupt acquisition and retention, but not implicit learning, in the SILT procedural motor learning task

Subtle but progressive cognitive deficits in the female tgHD hemizygote rat as demonstrated by operant SILT performance.

Tests to assess motor phenotype in mice: a user's guide

The utilisation of operant delayed matching and non-matching to position for probing cognitive flexibility and working memory in mouse models of Huntington's disease