| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HIPO.10005 |
| 10.1002/HIPO.10005.ABS | ||
| P698 | PubMed publication ID | 11918286 |
| P50 | author | Wim Crusio | Q120981 |
| Sanne de Wit | Q87605920 | ||
| Frans Sluyter | Q108055796 | ||
| P2093 | author name string | Ben A Oostra | |
| Yann S Mineur | |||
| Ben A. Oostra | |||
| Yann S. Mineur | |||
| P2860 | cites work | Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis | Q24323108 |
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| Apolipoprotein E deficiency effects on learning in mice are dependent upon the background strain | Q31925840 | ||
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| Synaptic synthesis of the Fragile X protein: possible involvement in synapse maturation and elimination | Q48233677 | ||
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| Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. | Q48351859 | ||
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| Mildly impaired water maze performance in male Fmr1 knockout mice. | Q48818692 | ||
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| Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function. | Q51083891 | ||
| Ethopharmacological analysis of the effects of putative 'anxiogenic' agents in the mouse elevated plus-maze. | Q51119657 | ||
| KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism. | Q52034009 | ||
| Covariations between hippocampal mossy fibres and working and reference memory in spatial and non-spatial radial maze tasks in mice. | Q52060884 | ||
| Of mice and mazes: similarities between mice and rats on dry land but not water mazes. | Q52199312 | ||
| Transgenic mouse model for the fragile X syndrome. | Q52200260 | ||
| Behavioral and psychiatric disorders in adult male carriers of fragile X. | Q53728865 | ||
| Long-term potentiation in the hippocampus of fragile X knockout mice | Q57828486 | ||
| Intermale aggression and dark/light preference in ten inbred mouse strains | Q57897044 | ||
| Strain-dependent epithelial defects in mice lacking the EGF receptor | Q58326927 | ||
| Prevalence of fragile X syndrome | Q71578926 | ||
| The fragile X syndrome and other fragile site disorders | Q74790217 | ||
| The fragile X syndrome | Q74809876 | ||
| P433 | issue | 1 | |
| P921 | main subject | cognitive neuroscience | Q1138951 |
| knockout mouse | Q1364740 | ||
| P304 | page(s) | 39-46 | |
| P577 | publication date | 2002-01-01 | |
| P1433 | published in | Hippocampus | Q5768411 |
| P1476 | title | Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse | |
| Behavioral and neuroanatomical characterization of theFmr1 knockout mouse | |||
| P478 | volume | 12 |
| Q38500580 | A mouse model of fragile X syndrome exhibits heightened arousal and/or emotion following errors or reversal of contingencies. |
| Q50307286 | A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse. |
| Q34505148 | A presynaptic role for FMRP during protein synthesis-dependent long-term plasticity in Aplysia. |
| Q36937876 | Advances in behavioral genetics: mouse models of autism |
| Q51022589 | Age-related changes in climbing behavior and neural circuit physiology in Drosophila. |
| Q38458914 | Aggression in non-human vertebrates: Genetic mechanisms and molecular pathways. |
| Q40376074 | Altered Connectivity and Synapse Maturation of the Hippocampal Mossy Fiber Pathway in a Mouse Model of the Fragile X Syndrome. |
| Q50344832 | Analysis of FMR1 deletion in a subpopulation of post-mitotic neurons in mouse cortex and hippocampus. |
| Q35121791 | Animal models of mental retardation: from gene to cognitive function. |
| Q30469044 | Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders |
| Q35741152 | Anxiety in mice: a principal component analysis study |
| Q34137676 | Assessment of spatial memory in mice. |
| Q30442883 | Auditory processing in fragile x syndrome |
| Q36990260 | Behavioral Phenotype of Fmr1 Knock-Out Mice during Active Phase in an Altered Light/Dark Cycle. |
| Q30403591 | Behavioral analysis of male and female Fmr1 knockout mice on C57BL/6 background |
| Q48640185 | Behavioral and neurochemical alterations in mice lacking the RNA-binding protein translin. |
| Q44473103 | Brief report: altered social behavior in isolation-reared Fmr1 knockout mice |
| Q35035766 | Changes in sensitivity of reward and motor behavior to dopaminergic, glutamatergic, and cholinergic drugs in a mouse model of fragile X syndrome |
| Q30458768 | Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders |
| Q35962611 | Cytisine, a partial agonist of high-affinity nicotinic acetylcholine receptors, has antidepressant-like properties in male C57BL/6J mice |
| Q47795409 | Decreased home cage movement and oromotor impairments in adult Fmr1-KO mice. |
| Q47069991 | Defective neuronal development in the mushroom bodies of Drosophila fragile X mental retardation 1 mutants. |
| Q42482484 | Deficits in trace fear memory and long-term potentiation in a mouse model for fragile X syndrome. |
| Q36207550 | Developmental characteristics of dendritic spines in the dentate gyrus of Fmr1 knockout mice. |
| Q30493672 | Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon |
| Q34973856 | Dissociation of social and nonsocial anxiety in a mouse model of fragile X syndrome |
| Q33676486 | Distinctive behavioral and cellular responses to fluoxetine in the mouse model for Fragile X syndrome |
| Q41497643 | Dopamine Release and Uptake Impairments and Behavioral Alterations Observed in Mice that Model Fragile X Mental Retardation Syndrome |
| Q35906775 | Dynamics of subcellular proteomes during brain development |
| Q38978791 | Dysregulated mTORC1-Dependent Translational Control: From Brain Disorders to Psychoactive Drugs |
| Q60932961 | Effects of Voluntary Exercise on Cell Proliferation and Neurogenesis in the Dentate Gyrus of Adult FMR1 Knockout Mice |
| Q26829152 | Emerging pharmacologic treatment options for fragile X syndrome |
| Q33914148 | Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome. |
| Q35018423 | Epigenetic regulation of neuronal dendrite and dendritic spine development |
| Q34142731 | Evidence of reactive astrocytes but not peripheral immune system activation in a mouse model of Fragile X syndrome |
| Q35073511 | Expansion of the dentate mossy fiber-CA3 projection in the brain-derived neurotrophic factor-enriched mouse hippocampus |
| Q34276734 | Extinction of an instrumental response: a cognitive behavioral assay in Fmr1 knockout mice |
| Q40295553 | Fmr1 knockout mice are impaired in a leverpress escape/avoidance task |
| Q42226635 | Fragile X protein FMRP is required for homeostatic plasticity and regulation of synaptic strength by retinoic acid |
| Q26865162 | Fragile X syndrome and targeted treatment trials |
| Q54782597 | Fragile X syndrome: From protein function to therapy. |
| Q38162720 | Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development |
| Q27339352 | Functional magnetic resonance imaging in awake transgenic fragile X rats: evidence of dysregulation in reward processing in the mesolimbic/habenular neural circuit |
| Q33543082 | GSK3 influences social preference and anxiety-related behaviors during social interaction in a mouse model of fragile X syndrome and autism. |
| Q35125117 | Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome |
| Q46075544 | Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies |
| Q21135541 | Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice |
| Q37417156 | Glycogen synthase kinase-3 inhibitors reverse deficits in long-term potentiation and cognition in fragile X mice |
| Q35492486 | Glycogen synthase kinase-3: a promising therapeutic target for fragile x syndrome |
| Q34280548 | Hippocampal Y2 receptor-mediated mossy fiber plasticity is implicated in nicotine abstinence-related social anxiety-like behavior in an outbred rat model of the novelty-seeking phenotype |
| Q91850695 | Home-cage hypoactivity in mouse genetic models of autism spectrum disorder |
| Q39024323 | Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome |
| Q30557514 | Hyperactivity, perseveration and increased responding during attentional rule acquisition in the Fragile X mouse model |
| Q30428162 | IL1RAPL1 knockout mice show spine density decrease, learning deficiency, hyperactivity and reduced anxiety-like behaviours |
| Q33655637 | Imbalanced pattern completion vs. separation in cognitive disease: network simulations of synaptic pathologies predict a personalized therapeutics strategy |
| Q34134816 | Knockout mice: simple solutions to the problems of genetic background and flanking genes |
| Q26866506 | Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us. |
| Q47070046 | Learning and memory deficits consequent to reduction of the fragile X mental retardation protein result from metabotropic glutamate receptor-mediated inhibition of cAMP signaling in Drosophila. |
| Q24529151 | Learning spatial orientation tasks in the radial-maze and structural variation in the hippocampus in inbred mice |
| Q33607288 | Lithium ameliorates altered glycogen synthase kinase-3 and behavior in a mouse model of fragile X syndrome. |
| Q37416780 | Lithium treatment alleviates impaired cognition in a mouse model of fragile X syndrome |
| Q92104948 | MeCP2 Deficiency Disrupts Kainate-Induced Presynaptic Plasticity in the Mossy Fiber Projections in the Hippocampus |
| Q30420595 | Modeling fragile X syndrome in the Fmr1 knockout mouse |
| Q47358832 | NS-Pten knockout mice show sex- and age-specific differences in ultrasonic vocalizations |
| Q47551363 | Negative Effects of Chronic Rapamycin Treatment on Behavior in a Mouse Model of Fragile X Syndrome. |
| Q34817846 | Neuroimaging endophenotypes in animal models of autism spectrum disorders: lost or found in translation? |
| Q35076945 | Of mice and the fragile X syndrome. |
| Q36805389 | Olfactory discrimination learning in mice lacking the fragile X mental retardation protein |
| Q35009426 | Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders |
| Q55155951 | Paradoxical effect of baclofen on social behavior in the fragile X syndrome mouse model. |
| Q51012749 | Phenotypic changes in calbindin D28K immunoreactivity in the hippocampus of Fmr1 knockout mice. |
| Q30851354 | Phf8 loss confers resistance to depression-like and anxiety-like behaviors in mice |
| Q48104405 | Potential Involvement of Impaired BKCa Channel Function in Sensory Defensiveness and Some Behavioral Disturbances Induced by Unfamiliar Environment in a Mouse Model of Fragile X Syndrome |
| Q38708008 | Prefrontal Cortex Dysfunction in Fragile X Mice Depends on the Continued Absence of Fragile X Mental Retardation Protein in the Adult Brain. |
| Q24810315 | Prenatal exposure to alcohol does not affect radial maze learning and hippocampal mossy fiber sizes in three inbred strains of mouse |
| Q45192998 | Presynaptic FMR1 genotype influences the degree of synaptic connectivity in a mosaic mouse model of fragile X syndrome. |
| Q40667152 | Programming social behavior by the maternal fragile X protein. |
| Q34431654 | Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule |
| Q90600697 | Reversal learning paradigm reveals deficits in cognitive flexibility in the Fmr1 knockout male mouse |
| Q42512974 | Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen. |
| Q36350291 | Self-directed exploration provides a Ncs1-dependent learning bonus |
| Q29618044 | Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice |
| Q37138180 | Social approach in genetically engineered mouse lines relevant to autism |
| Q30603928 | Spaced training rescues memory and ERK1/2 signaling in fragile X syndrome model mice |
| Q51828032 | Spatiotemporal expression of PSD-95 in Fmr1 knockout mice brain. |
| Q47711512 | Spectral and temporal properties of calls reveal deficits in ultrasonic vocalizations of adult Fmr1 knockout mice |
| Q30401824 | Stem cells and modeling of autism spectrum disorders |
| Q34140855 | Sub-strains of Drosophila Canton-S differ markedly in their locomotor behavior |
| Q37398536 | Sub-synaptic, multiplexed analysis of proteins reveals Fragile X related protein 2 is mislocalized in Fmr1 KO synapses |
| Q38070017 | Synaptic retinoic acid signaling and homeostatic synaptic plasticity |
| Q30461456 | The GABA(A) receptor agonist THIP ameliorates specific behavioral deficits in the mouse model of fragile X syndrome |
| Q37359934 | The fragile X mental retardation protein in circadian rhythmicity and memory consolidation |
| Q35550078 | Understanding fragile X syndrome: insights from animal models |
| Q92662989 | Understanding intellectual disability and autism spectrum disorders from common mouse models: synapses to behaviour |
| Q52592966 | Utility of the Hebb-Williams Maze Paradigm for Translational Research in Fragile X Syndrome: A Direct Comparison of Mice and Humans. |
| Q24613049 | What can we learn about autism from studying fragile X syndrome? |
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