Cargando…

Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington disease

Huntington disease is an inherited neurodegenerative disorder characterized by motor, cognitive, psychiatric and metabolic symptoms. We recently published a study describing that the BACHD rat model of HD shows an obesity phenotype, which might affect their motivation to perform food-based behaviora...

Descripción completa

Detalles Bibliográficos
Autores principales:	Clemensson, Erik Karl Håkan, Clemensson, Laura Emily, Fabry, Benedikt, Riess, Olaf, Nguyen, Huu Phuc
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342229/ https://www.ncbi.nlm.nih.gov/pubmed/28273120 http://dx.doi.org/10.1371/journal.pone.0173232

Ejemplares similares

Correction: Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington disease
por: Clemensson, Erik Karl Håkan, et al.
Publicado: (2019)

The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory
por: Clemensson, Erik Karl Håkan, et al.
Publicado: (2017)

The BACHD Rat Model of Huntington Disease Shows Specific Deficits in a Test Battery of Motor Function
por: Manfré, Giuseppe, et al.
Publicado: (2017)

Reduced Motivation in the BACHD Rat Model of Huntington Disease Is Dependent on the Choice of Food Deprivation Strategy
por: Jansson, Erik Karl Håkan, et al.
Publicado: (2014)

Reduced cell size, chromosomal aberration and altered proliferation rates are characteristics and confounding factors in the STHdh cell model of Huntington disease
por: Singer, Elisabeth, et al.
Publicado: (2017)

The Alteration of Emotion Regulation Precedes the Deficits in Interval Timing in the BACHD Rat Model for Huntington Disease
por: Garces, Daniel, et al.
Publicado: (2018)

Reversal Learning and Associative Memory Impairments in a BACHD Rat Model for Huntington Disease
por: Abada, Yah-se K., et al.
Publicado: (2013)

Environment-dependent striatal gene expression in the BACHD rat model for Huntington disease
por: Novati, Arianna, et al.
Publicado: (2018)

Sex Differences in Sleep Phenotypes in the BACHD Mouse Model of Huntington’s Disease
por: Chiem, Emily, et al.
Publicado: (2023)

Assessment of Motor Function, Sensory Motor Gating and Recognition Memory in a Novel BACHD Transgenic Rat Model for Huntington Disease
por: Abada, Yah-se K., et al.
Publicado: (2013)

Differential Cellular Balance of Olfactory and Vomeronasal Epithelia in a Transgenic BACHD Rat Model of Huntington’s Disease
por: Krysewski, Lina-Marielle, et al.
Publicado: (2022)

Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington disease
por: Teo, Roy Tang Yi, et al.
Publicado: (2016)

Cardiac Dysfunction in the BACHD Mouse Model of Huntington’s Disease
por: Schroeder, Analyne M., et al.
Publicado: (2016)

Sexual behavior and testis morphology in the BACHD rat model
por: Novati, Arianna, et al.
Publicado: (2018)

Baroreceptor reflex dysfunction in the BACHD mouse model of Huntington’s disease.
por: Schroeder, Analyne M., et al.
Publicado: (2011)

Sex Differences in Circadian Dysfunction in the BACHD Mouse Model of Huntington’s Disease
por: Kuljis, Dika A., et al.
Publicado: (2016)

BACHD Mice Recapitulate the Striatal Parvalbuminergic Interneuron Loss Found in Huntington’s Disease
por: Rallapalle, Vyshnavi, et al.
Publicado: (2021)

Effects of mutant huntingtin inactivation on Huntington disease‐related behaviours in the BACHD mouse model
por: Cheong, Rachel Y., et al.
Publicado: (2021)

Targeted Genetic Reduction of Mutant Huntingtin Lessens Cardiac Pathology in the BACHD Mouse Model of Huntington's Disease
por: Park, Saemi, et al.
Publicado: (2021)

Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients
por: Tsai, Yu-Chun, et al.
Publicado: (2012)

Effects of Deletion of Mutant Huntingtin in Steroidogenic Factor 1 Neurons on the Psychiatric and Metabolic Phenotype in the BACHD Mouse Model of Huntington Disease
por: Baldo, Barbara, et al.
Publicado: (2014)

Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease
por: Che, Hong Van B, et al.
Publicado: (2011)

Dietary ketosis improves circadian dysfunction as well as motor symptoms in the BACHD mouse model of Huntington’s disease
por: Whittaker, Daniel S., et al.
Publicado: (2022)

A small molecule p75(NTR) ligand normalizes signalling and reduces Huntington’s disease phenotypes in R6/2 and BACHD mice
por: Simmons, Danielle A., et al.
Publicado: (2016)

Metabolic and behavioral effects of mutant huntingtin deletion in Sim1 neurons in the BACHD mouse model of Huntington’s disease
por: Soylu-Kucharz, Rana, et al.
Publicado: (2016)

Structural and functional features of medium spiny neurons in the BACHDΔN17 mouse model of Huntington’s Disease
por: Goodliffe, Joseph, et al.
Publicado: (2020)

High-Throughput Sequencing of BACHD Mice Reveals Upregulation of Neuroprotective miRNAs at the Pre-Symptomatic Stage of Huntington’s Disease
por: Olmo, Isabella G., et al.
Publicado: (2021)

BACHD rats expressing full-length mutant huntingtin exhibit differences in social behavior compared to wild-type littermates
por: Manfré, Giuseppe, et al.
Publicado: (2018)

The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients
por: Metzger, Silke, et al.
Publicado: (2013)

The calpain-suppressing effects of olesoxime in Huntington's disease
por: Weber, Jonasz J., et al.
Publicado: (2016)

Dynamic nuclear envelope phenotype in rats overexpressing mutated human torsinA protein
por: Yu-Taeger, Libo, et al.
Publicado: (2018)

Impaired Decision Making and Loss of Inhibitory-Control in a Rat Model of Huntington Disease
por: El Massioui, Nicole, et al.
Publicado: (2016)

Expression of Mutant Huntingtin in Leptin Receptor-Expressing Neurons Does Not Control the Metabolic and Psychiatric Phenotype of the BACHD Mouse
por: Lundh, Sofia Hult, et al.
Publicado: (2012)

The Guanine Nucleotide Exchange Factor Kalirin-7 Is a Novel Synphilin-1 Interacting Protein and Modifies Synphilin-1 Aggregate Transport and Formation
por: Tsai, Yu-Chun, et al.
Publicado: (2012)

Reduction in Subventricular Zone-Derived Olfactory Bulb Neurogenesis in a Rat Model of Huntington’s Disease Is Accompanied by Striatal Invasion of Neuroblasts
por: Kandasamy, Mahesh, et al.
Publicado: (2015)

The Cognitive Effects of Statins are Modified by Age
por: Alsehli, Ahmed M., et al.
Publicado: (2020)

Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease Animals
por: Yu-Taeger, Libo, et al.
Publicado: (2022)

Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease
por: Yu-Taeger, Libo, et al.
Publicado: (2019)

The Effects of Statins on Cognitive Performance Are Mediated by Low-Density Lipoprotein, C-Reactive Protein, and Blood Glucose Concentrations
por: Gentreau, Mélissa, et al.
Publicado: (2023)

Cerebellar Soluble Mutant Ataxin-3 Level Decreases during Disease Progression in Spinocerebellar Ataxia Type 3 Mice
por: Nguyen, Huu Phuc, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_39fjh4mdpb2a7aor8aomqv76pr