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Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits

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Principles for the buffering of genetic variation

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Principles for the Buffering of Genetic Variation

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Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

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The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein.

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Dendritic Spine Structural Anomalies in Fragile-X Mental Retardation Syndrome

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Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes.

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Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome

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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

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Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain

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Of Mice and Mazes: Similarities Between Mice and Rats on Dry Land But Not Water Mazes

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Radial-maze performance and structural variation of the hippocampus in mice: a correlation with mossy fibre distribution

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The Drosophila easily shocked gene: A mutation in a phospholipid synthetic pathway causes seizure, neuronal failure, and paralysis

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Mildly impaired water maze performance in maleFmr1 knockout mice

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Hippocampal function required for nonspatial working memory

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Hippocampal mossy fibers and radial-maze learning in the mouse: A correlation with spatial working memory but not with non-spatial reference memory

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Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

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Fine structure of the human FMR1 gene

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FMR1 Knockout mice: A model to study fragile X mental retardation

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Ethopharmacological analysis of the effects of putative ‘anxiogenic’ agents in the mouse elevated plus-maze

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Complications associated with genetic background effects in research using knockout mice

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Behavioral responses to novelty and structural variation of the hippocampus in mice. II. Multivariate genetic analysis

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Correlations between radial-maze learning and structural variations of septum and hippocampus in rodents

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Intermale aggression and dark/light preference in ten inbred mouse strains

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Hippocampal mossy fiber distribution covaries with open-field habituation in the mouse

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Fragile X Syndrome: Diagnosis, Treatment and Research

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Covariations Between Hippocampal Mossy Fibres and Working and Reference Memory in Spatial and Non‐spatial Radial Maze Tasks in Mice

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Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes.

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Behavioral and Psychiatric Disorders in Adult Male Carriers of Fragile X

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Fragile X syndrome at the turn of the century

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Behavioral and neuroanatomical characterization of FVB/N inbred mice

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KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism

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Genetic Selection for Novelty-Induced Rearing Behavior in Mice Produces Changes in Hippocampal Mossy Fiber Distributions

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Further phenotypical characterisation of two substrains of C57BL/6J inbred mice differing by a spontaneous single-gene mutation

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Hippocampal mossy fiber distributions in mice selected for aggression

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Behavioural and neuroanatomical divergence between two sublines of C57BL/6J inbred mice

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The Fragile X Syndrome and Other Fragile Site Disorders

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Apolipoprotein E deficiency effects on learning in mice are dependent upon the background strain

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Chapter 4.8 Measuring aggression in the mouse

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Long‐term potentiation in the hippocampus of fragile X knockout mice

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A Mouse is Not Just a Mouse

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Chapter 4.1 Ethological approaches in behavioral neurogenetic research

Gerlai, R. T. (1999) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(99)80047-9 · Cited by 6 · see citing works

Untitled work

Miller (1999) · doi:10.1002/(sici)1096-8628(19990402)83:4

Untitled work

Turner (1996) · doi:10.1002/(sici)1096-8628(19960712)64:1

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic‐like behavior in mice

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Trinucleotide Repeat Disorders

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Assessment of spatial memory in mice

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Altered anxiety‐related and social behaviors in the <i>Fmr1</i> knockout mouse model of fragile X syndrome

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Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome

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Deficits in trace fear memory and long-term potentiation in a mouse model for fragile X syndrome

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Knockout mice: simple solutions to the problems of genetic background and flanking genes

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Reversal of Disease-Related Pathologies in the Fragile X Mouse Model by Selective Activation of GABA _B Receptors with Arbaclofen

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Social approach in genetically engineered mouse lines relevant to autism

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Modeling fragile X syndrome in the &lt;i&gt;Fmr1&lt;/i&gt; knockout mouse

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A phenotypic and molecular characterization of the <i>fmr1‐tm1Cgr</i> Fragile X mouse

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GSK3 Influences Social Preference and Anxiety-Related Behaviors during Social Interaction in a Mouse Model of Fragile X Syndrome and Autism

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Hippocampal pyramidal cells in adult Fmr1 knockout mice exhibit an immature-appearing profile of dendritic spines

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NCS-1 in the Dentate Gyrus Promotes Exploration, Synaptic Plasticity, and Rapid Acquisition of Spatial Memory

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Lithium ameliorates altered glycogen synthase kinase-3 and behavior in a mouse model of Fragile X syndrome

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Fragile X Protein FMRP Is Required for Homeostatic Plasticity and Regulation of Synaptic Strength by Retinoic Acid

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Social behavior deficits in the Fmr1 mutant mouse

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Expression profiling suggests underexpression of the GABAA receptor subunit δ in the fragile X knockout mouse model

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Cytisine, a partial agonist of high-affinity nicotinic acetylcholine receptors, has antidepressant-like properties in male C57BL/6J mice

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Object recognition impairment in Fmr1 knockout mice is reversed by amphetamine: involvement of dopamine in the medial prefrontal cortex

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Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins

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Glycogen Synthase Kinase-3 Inhibitors Reverse Deficits in Long-term Potentiation and Cognition in Fragile X Mice

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