| scholarly article | Q13442814 |
| P50 | author | Elizabeth M. C. Fisher | Q21259007 |
| P2093 | author name string | Lesley Vanes | |
| Victor L J Tybulewicz | |||
| Hervé Daniel | |||
| Micaela Galante | |||
| Timothy V P Bliss | |||
| Elise Morice | |||
| Harsha Jani | |||
| P2860 | cites work | Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice | Q28506073 |
| TARP subtypes differentially and dose-dependently control synaptic AMPA receptor gating | Q28578675 | ||
| Place navigation impaired in rats with hippocampal lesions | Q29547869 | ||
| Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning | Q29616330 | ||
| Behavioral phenotype of individuals with Down syndrome | Q33971581 | ||
| Cerebellum-dependent learning: the role of multiple plasticity mechanisms | Q33979383 | ||
| An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes | Q33990273 | ||
| A new form of cerebellar long-term potentiation is postsynaptic and depends on nitric oxide but not cAMP. | Q34032867 | ||
| Pattern-dependent, simultaneous plasticity differentially transforms the input-output relationship of a feedforward circuit | Q34078423 | ||
| Down's syndrome | Q34191091 | ||
| Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice | Q34325156 | ||
| Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1. | Q34326346 | ||
| Study of somatic chromosomes from 9 mongoloid children | Q34539314 | ||
| staggerer phenotype in retinoid-related orphan receptor alpha-deficient mice. | Q36014244 | ||
| The power of comparative and developmental studies for mouse models of Down syndrome | Q36021399 | ||
| Time and tide in cerebellar memory formation | Q36306839 | ||
| Motor development and neuropsychological patterns in persons with Down syndrome | Q36408507 | ||
| Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome | Q36693574 | ||
| Down syndrome gene dosage imbalance on cerebellum development | Q36780326 | ||
| Preservation of long-term memory and synaptic plasticity despite short-term impairments in the Tc1 mouse model of Down syndrome | Q36826500 | ||
| Down syndrome: cognitive phenotype | Q36957694 | ||
| Early onset of stabilizing strategies for gait and obstacles: older adults with Down syndrome. | Q37079511 | ||
| The hyperactive syndrome: metanalysis of genetic alterations, pharmacological treatments and brain lesions which increase locomotor activity | Q37227281 | ||
| Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities | Q37394402 | ||
| The consequences of chromosome imbalance | Q37866119 | ||
| Weak hand preference in children with down syndrome is associated with language deficits. | Q38391655 | ||
| The neuropsychology of Down syndrome: evidence for hippocampal dysfunction | Q38520897 | ||
| Long-term depression | Q38613310 | ||
| Intradendritic release of calcium induced by glutamate in cerebellar purkinje cells | Q39243559 | ||
| Two families of TARP isoforms that have distinct effects on the kinetic properties of AMPA receptors and synaptic currents | Q40078473 | ||
| Deficits in hippocampal CA1 LTP induced by TBS but not HFS in the Ts65Dn mouse: a model of Down syndrome. | Q40418155 | ||
| Evidence for a multiple innervation of Purkinje cells by climbing fibers in the immature rat cerebellum | Q41789494 | ||
| Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome. | Q42467654 | ||
| Hippocampal hypocellularity in the Ts65Dn mouse originates early in development | Q42497958 | ||
| Behavioral assessment of the Ts65Dn mouse, a model for Down syndrome: altered behavior in the elevated plus maze and open field | Q42640762 | ||
| Random response fluctuations lead to spurious paired-pulse facilitation. | Q43819962 | ||
| Neuroanatomy of Down's syndrome: a high-resolution MRI study. | Q44080496 | ||
| Spatial memory and hippocampal function | Q44136977 | ||
| Differences among eight inbred strains of mice in motor ability and motor learning on a rotorod | Q44572107 | ||
| Synapses between parallel fibres and stellate cells express long-term changes in synaptic efficacy in rat cerebellum | Q44655914 | ||
| Phenotypic expression of the targeted null-mutation in the dopamine transporter gene varies as a function of the genetic background | Q44971583 | ||
| Experimental parameters affecting the Morris water maze performance of a mouse model of Down syndrome. | Q45012063 | ||
| Constitutive hyperdopaminergia is functionally associated with reduced behavioral lateralization | Q45049158 | ||
| Synaptic structural abnormalities in the Ts65Dn mouse model of Down Syndrome. | Q46035669 | ||
| Hippocampectomy impairs the memory of recently, but not remotely, acquired trace eyeblink conditioned responses | Q46100838 | ||
| Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships | Q46464782 | ||
| Cyclic AMP mediates a presynaptic form of LTP at cerebellar parallel fiber synapses | Q46533972 | ||
| Cbln1 is essential for synaptic integrity and plasticity in the cerebellum | Q46761725 | ||
| Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome | Q46866532 | ||
| Regulation of long-term depression and climbing fiber territory by glutamate receptor delta2 at parallel fiber synapses through its C-terminal domain in cerebellar Purkinje cells | Q46918316 | ||
| Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes. | Q47367835 | ||
| Early impairment of synaptic plasticity in patients with Down's syndrome. | Q48222350 | ||
| MRI volumes of the hippocampus and amygdala in adults with Down's syndrome with and without dementia | Q48238093 | ||
| Chronobiometry of behavioral activity in the Ts65Dn model of Down syndrome. | Q48347577 | ||
| Thigmotactic responses in an open-field | Q48358117 | ||
| Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of Down syndrome. | Q48365245 | ||
| alphaCaMKII Is essential for cerebellar LTD and motor learning | Q48418590 | ||
| Differences in behavioural test battery performance between mice with hippocampal and cerebellar lesions. | Q48438489 | ||
| Down syndrome mouse models are looking up. | Q48553448 | ||
| Laterality in persons with intellectual disability. I--do patients with trisomy 21 and Williams-Beuren syndrome differ from typically developing persons? | Q48594670 | ||
| Reimpressed selective breeding for lateralization of handedness in mice | Q48623898 | ||
| Down syndrome: MR quantification of brain structures and comparison with normal control subjects | Q48627913 | ||
| Stability of multiple innervation of Purkinje cells by climbing fibers in the agranular cerebellum of old rats X-irradiated at birth | Q48663205 | ||
| Spontaneous stereotypy in an animal model of Down syndrome: Ts65Dn mice | Q48705924 | ||
| An assessment of handedness in mice | Q48755012 | ||
| Persistent multiple climbing fiber innervation of cerebellar Purkinje cells in mice lacking mGluR1. | Q48819879 | ||
| Determinants of the time course of facilitation at the granule cell to Purkinje cell synapse. | Q48917451 | ||
| Amygdala and hippocampal volumes in children with Down syndrome: a high-resolution MRI study | Q48923372 | ||
| Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells | Q48969810 | ||
| Motor learning in Ts65Dn mice, a model for Down syndrome | Q49099435 | ||
| Mental health, behaviour and intellectual abilities of people with Down syndrome. | Q50302513 | ||
| Neuroanatomic correlates of autism and stereotypy in children with Down syndrome | Q50310207 | ||
| Cerebellar volume in adults with Down syndrome. | Q50972443 | ||
| A behavioral assessment of Ts65Dn mice: a putative Down syndrome model. | Q51120668 | ||
| Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. | Q51979051 | ||
| Altered long-term potentiation in the young and old Ts65Dn mouse, a model for Down Syndrome. | Q51995807 | ||
| Early learning and adaptive behaviour in toddlers with Down syndrome: evidence for an emerging behavioural phenotype? | Q52011548 | ||
| A mouse model for Down syndrome exhibits learning and behaviour deficits. | Q52013436 | ||
| Language, cognition, and short-term memory in individuals with Down syndrome. | Q52016314 | ||
| Motor dysfunction in a mouse model for Down syndrome. | Q52029981 | ||
| Deficits of neuronal density in CA1 and synaptic density in the dentate gyrus, CA3 and CA1, in a mouse model of Down syndrome. | Q52087699 | ||
| The preparation of reach to grasp movements in adults with Down syndrome. | Q52126347 | ||
| Long-term depression of the cerebellar climbing fiber--Purkinje neuron synapse. | Q52167905 | ||
| Motor and perceptual-motor competence in children with Down syndrome: variation in performance with age. | Q52169894 | ||
| Pairing of pre- and postsynaptic activities in cerebellar Purkinje cells induces long-term changes in synaptic efficacy in vitro. | Q54306360 | ||
| Laterality in persons with intellectual disability II. Hand, foot, ear, and eye laterality in persons with Trisomy 21 and Williams-Beuren syndrome | Q58198912 | ||
| Multiple innervation of cerebellar Purkinje cells by climbing fibres in staggerer mutant mouse | Q59069761 | ||
| Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry. | Q64982861 | ||
| Ontogenesis of olivocerebellar relationships. I. Studies by intracellular recordings of the multiple innervation of Purkinje cells by climbing fibers in the developing rat cerebellum | Q71121168 | ||
| Fate of the multiple innervation of cerebellar Purkinje cells by climbing fibers in immature control, x-irradiated and hypothyroid rats | Q71507253 | ||
| Movement disorder in Down's syndrome: a possible marker of the severity of mental handicap | Q71545721 | ||
| Characterization of sensorimotor performance, reproductive and aggressive behaviors in segmental trisomic 16 (Ts65Dn) mice | Q71712838 | ||
| Activation of presynaptic cAMP-dependent protein kinase is required for induction of cerebellar long-term potentiation | Q73212192 | ||
| Differential maturation of climbing fiber innervation in cerebellar vermis | Q79971023 | ||
| Joint stiffness and gait pattern evaluation in children with Down syndrome | Q81212852 | ||
| Abnormal synaptic plasticity in the Ts1Cje segmental trisomy 16 mouse model of Down syndrome | Q81916542 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 8 | |
| P921 | main subject | Down syndrome | Q47715 |
| P304 | page(s) | 1449-1463 | |
| P577 | publication date | 2009-01-29 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome | |
| P478 | volume | 18 |
| Q37423613 | A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome |
| Q48883998 | A role for myosin Va in cerebellar plasticity and motor learning: a possible mechanism underlying neurological disorder in myosin Va disease |
| Q47690390 | A third copy of the Down syndrome cell adhesion molecule (Dscam) causes synaptic and locomotor dysfunction in Drosophila |
| Q35859514 | Altered regulation of tau phosphorylation in a mouse model of down syndrome aging |
| Q55163408 | Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. |
| Q37543845 | Aneuploidy: from a physiological mechanism of variance to Down syndrome |
| Q64250457 | CD200-CD200R1 inhibitory signaling prevents spontaneous bacterial infection and promotes resolution of neuroinflammation and recovery after stroke |
| Q89081232 | Cerebellar synapse properties and cerebellum-dependent motor and non-motor performance in Dp71-null mice |
| Q34980227 | Chronic up-regulation of the SHH pathway normalizes some developmental effects of trisomy in Ts65Dn mice |
| Q54968002 | Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model. |
| Q26777254 | Dissecting Alzheimer disease in Down syndrome using mouse models |
| Q33816076 | Dissociation of Down syndrome and Alzheimer's disease effects with imaging |
| Q28543589 | Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome |
| Q27300997 | Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues |
| Q36681400 | Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21. |
| Q37347649 | Down syndrome: from understanding the neurobiology to therapy |
| Q22241596 | Down syndrome: searching for the genetic culprits |
| Q48287894 | Down syndrome: the brain in trisomic mode |
| Q34559285 | Dyrk1A is dynamically expressed on subsets of motor neurons and in the neuromuscular junction: possible role in Down syndrome |
| Q36141440 | Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome. |
| Q34114019 | Generation of a panel of antibodies against proteins encoded on human chromosome 21. |
| Q24634111 | Impaired locomotor learning and altered cerebellar synaptic plasticity in pep-19/PCP4-null mice |
| Q36075008 | Increased excitability and altered action potential waveform in cerebellar granule neurons of the Ts65Dn mouse model of Down syndrome |
| Q37912174 | Is it possible to improve neurodevelopmental abnormalities in Down syndrome? |
| Q34676133 | Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome |
| Q26863005 | Mouse models of Down syndrome as a tool to unravel the causes of mental disabilities |
| Q55363878 | Mouse models of aneuploidy. |
| Q92304592 | OLIG2 Drives Abnormal Neurodevelopmental Phenotypes in Human iPSC-Based Organoid and Chimeric Mouse Models of Down Syndrome |
| Q33788720 | Perturbed hematopoiesis in the Tc1 mouse model of Down syndrome |
| Q34278418 | Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows |
| Q37510955 | Preventative and therapeutic effects of a GABA transporter 1 inhibitor administered systemically in a mouse model of paclitaxel-induced neuropathic pain |
| Q36795890 | Selective inhibition of alpha/beta-hydrolase domain 6 attenuates neurodegeneration, alleviates blood brain barrier breakdown, and improves functional recovery in a mouse model of traumatic brain injury |
| Q35538343 | Sleep-like behavior and 24-h rhythm disruption in the Tc1 mouse model of Down syndrome |
| Q53667436 | The roles of motor activity and environmental enrichment in intellectual disability. |
| Q36662954 | The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome |
| Q45181313 | Three-dimensional synaptic ultrastructure in the dentate gyrus and hippocampal area CA3 in the Ts65Dn mouse model of Down syndrome |
| Q35053865 | Timing of muscle response to a sudden leg perturbation: comparison between adolescents and adults with Down syndrome |
| Q35740129 | Trisomy 21 and early brain development |
| Q37045414 | Weaker control of the electrical properties of cerebellar granule cells by tonically active GABAA receptors in the Ts65Dn mouse model of Down's syndrome. |
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