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Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

Psychopharmacologia, 2009-06, Vol.204 (2), p.361-373

2009

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Histone Methylation Regulates Memory Formation

The Journal of neuroscience, 2010-03, Vol.30 (10), p.3589-3599

2010

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The stress-induced hyperthermia paradigm as a physiological animal model for anxiety: A review of pharmacological and genetic studies in the mouse

Neuroscience and biobehavioral reviews, 2007, Vol.31 (1), p.41-59

2007

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Group I metabotropic glutamate receptor antagonists alter select behaviors in a mouse model for fragile X syndrome

Psychopharmacologia, 2012-01, Vol.219 (1), p.47-58

2012

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Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses

Autism research, 2011-02, Vol.4 (1), p.40-56

2011

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Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression

Neuron (Cambridge, Mass.), 2006-08, Vol.51 (4), p.441-454

2006

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The use of behavioral test batteries: Effects of training history

Physiology & behavior, 2001-08, Vol.73 (5), p.705-717

2001

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A mouse model of the human Fragile X syndrome I304N mutation

PLoS genetics, 2009-12, Vol.5 (12), p.e1000758-e1000758

2009

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Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome

Behavioural brain research, 2011-10, Vol.223 (2), p.310-321

2011

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Simultaneous behavioral characterizations: Embracing complexity

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (52), p.20563-20564

Paylor, Richard

2008

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Removal of FKBP12 Enhances mTOR-Raptor Interactions, LTP, Memory, and Perseverative/Repetitive Behavior

Neuron (Cambridge, Mass.), 2008-12, Vol.60 (5), p.832-845

2008

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Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome

Psychopharmacology, 2011-09, Vol.217 (1), p.143-151

2011

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Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits

Human molecular genetics, 2012-07, Vol.21 (14), p.3083-3096

2012

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Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

Human molecular genetics, 2005-01, Vol.14 (2), p.205-220

2005

Volltextzugriff (PDF)

Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene

Behavioral neuroscience, 2008-06, Vol.122 (3), p.710-715

2008

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Applying the ARRIVE Guidelines to an In Vivo Database

PLoS biology, 2015-05, Vol.13 (5), p.e1002151-e1002151

2015

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Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

Human molecular genetics, 2016-08, Vol.25 (15), p.3284-3302

2016

Volltextzugriff (PDF)

A Long CAG Repeat in the Mouse Sca1 Locus Replicates SCA1 Features and Reveals the Impact of Protein Solubility on Selective Neurodegeneration

Neuron (Cambridge, Mass.), 2002-06, Vol.34 (6), p.905-919

2002

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The Modulation of Fragile X Behaviors by the Muscarinic M4 Antagonist, Tropicamide

Behavioral neuroscience, 2011-10, Vol.125 (5), p.783-790

2011

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Behavioral and physiological mouse assays for anxiety: a survey in nine mouse strains

Behavioural brain research, 2002-11, Vol.136 (2), p.489-501

2002

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Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

Proceedings of the National Academy of Sciences - PNAS, 2006-05, Vol.103 (20), p.7729-7734

2006

Volltextzugriff (PDF)

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

Nature genetics, 2003-09, Vol.35 (1), p.84-89

2003

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Onset and progression of behavioral and molecular phenotypes in a novel congenic R6/2 line exhibiting intergenerational CAG repeat stability

PloS one, 2011-12, Vol.6 (12), p.e28409

2011

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A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice

Hormones and behavior, 1997-06, Vol.31 (3), p.197-211

1997

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Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes

Human molecular genetics, 2007-08, Vol.16 (15), p.1802-1813

2007

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Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

Histone Methylation Regulates Memory Formation

The stress-induced hyperthermia paradigm as a physiological animal model for anxiety: A review of pharmacological and genetic studies in the mouse

Group I metabotropic glutamate receptor antagonists alter select behaviors in a mouse model for fragile X syndrome

Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses

Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression

The use of behavioral test batteries: Effects of training history

A mouse model of the human Fragile X syndrome I304N mutation

Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome

Simultaneous behavioral characterizations: Embracing complexity

Removal of FKBP12 Enhances mTOR-Raptor Interactions, LTP, Memory, and Perseverative/Repetitive Behavior

Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene

Applying the ARRIVE Guidelines to an In Vivo Database

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

A Long CAG Repeat in the Mouse Sca1 Locus Replicates SCA1 Features and Reveals the Impact of Protein Solubility on Selective Neurodegeneration

The Modulation of Fragile X Behaviors by the Muscarinic M4 Antagonist, Tropicamide

Behavioral and physiological mouse assays for anxiety: a survey in nine mouse strains

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

Onset and progression of behavioral and molecular phenotypes in a novel congenic R6/2 line exhibiting intergenerational CAG repeat stability

A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes

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