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Meeting at the crossroads: common mechanisms in Fragile X and Down syndrome
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Europe PubMed Central
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4090020
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
title
Meeting at the crossroads: common mechanisms in Fragile X and Down syndrome
(English)
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stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
main subject
Down syndrome
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author
Kyung-Tai Min
series ordinal
4
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Europe PubMed Central
PMC publication ID
4090020
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
author name string
Karen T Chang
series ordinal
1
1 reference
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Europe PubMed Central
PMC publication ID
4090020
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
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23 February 2020
Hyunah Ro
series ordinal
2
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Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
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23 February 2020
Wei Wang
series ordinal
3
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4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
publication date
25 September 2013
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Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
published in
Trends in Neurosciences
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stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
volume
36
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
issue
12
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Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
page(s)
685-694
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Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
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Elongation factor 2 and fragile X mental retardation protein control the dynamic translation of Arc/Arg3.1 essential for mGluR-LTD
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Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome
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A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
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FMRP mediates mGluR5-dependent translation of amyloid precursor protein
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Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs
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Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation
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The challenge of Down syndrome
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5 July 2018
Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression
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5 July 2018
Dendritic pathology in mental retardation: from molecular genetics to neurobiology.
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5 July 2018
RCAN1 (DSCR1 or Adapt78) stimulates expression of GSK-3beta.
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5 July 2018
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.
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5 July 2018
The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction
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5 July 2018
Dendritic spine abnormalities in amyloid precursor protein transgenic mice demonstrated by gene transfer and intravital multiphoton microscopy
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5 July 2018
From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
The mGluR theory of fragile X mental retardation
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
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5 July 2018
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
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5 July 2018
GSK-3 kinases enhance calcineurin signaling by phosphorylation of RCNs
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
The Drosophila homolog of Down's syndrome critical region 1 gene regulates learning: implications for mental retardation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
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5 July 2018
Ubiquitination regulates PSD-95 degradation and AMPA receptor surface expression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Mnb/Dyrk1A is transiently expressed and asymmetrically segregated in neural progenitor cells at the transition to neurogenic divisions.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Altered synaptic plasticity in a mouse model of fragile X mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Dendritic spine structural anomalies in fragile-X mental retardation syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
A conserved family of calcineurin regulators.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
DSCR1, overexpressed in Down syndrome, is an inhibitor of calcineurin-mediated signaling pathways
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Altered long-term potentiation in the young and old Ts65Dn mouse, a model for Down Syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Dendritic and histochemical development and ageing in patients with Down's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
minibrain: a new protein kinase family involved in postembryonic neurogenesis in Drosophila
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Amyloid A4 protein and its precursor in Down's syndrome and Alzheimer's disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Down's syndrome and Alzheimer's disease: dendritic spine counts in the hippocampus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
Pyramidal cell abnormalities in the motor cortex of a child with Down's syndrome. A Golgi study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
5 July 2018
DSCAM contributes to dendrite arborization and spine formation in the developing cerebral cortex
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
p38α MAP kinase phosphorylates RCAN1 and regulates its interaction with calcineurin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Dyrk1A influences neuronal morphogenesis through regulation of cytoskeletal dynamics in mammalian cortical neurons.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Hypersensitivity to mGluR5 and ERK1/2 leads to excessive protein synthesis in the hippocampus of a mouse model of fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Gamma-secretase inhibition reduces spine density in vivo via an amyloid precursor protein-dependent pathway.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Age-associated motor and visuo-spatial learning phenotype in Dyrk1A heterozygous mutant mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Defining mechanisms of actin polymerization and depolymerization during dendritic spine morphogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Phosphorylation of FMRP inhibits association with Dicer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
FMRP acts as a key messenger for dopamine modulation in the forebrain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Chronic pentylenetetrazole but not donepezil treatment rescues spatial cognition in Ts65Dn mice, a model for Down syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
The Down syndrome critical region protein RCAN1 regulates long-term potentiation and memory via inhibition of phosphatase signaling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Renaming the DSCR1/Adapt78 gene family as RCAN: regulators of calcineurin.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Selective dendritic degeneration of medium spiny neurons in dementia with Lewy bodies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
DYRK1A BAC transgenic mice show altered synaptic plasticity with learning and memory defects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Metabotropic receptor-dependent long-term depression persists in the absence of protein synthesis in the mouse model of fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/- mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
The mRNA for elongation factor 1alpha is localized in dendrites and translated in response to treatments that induce long-term depression.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Dendritic spine abnormalities in the occipital cortex of C57BL/6 Fmr1 knockout mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Sequence of abnormal dendritic spine development in primary somatosensory cortex of a mouse model of the fragile X mental retardation syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Developmental switch in synaptic mechanisms of hippocampal metabotropic glutamate receptor-dependent long-term depression.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Synaptic structural abnormalities in the Ts65Dn mouse model of Down Syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Dendrite and dendritic spine alterations in Alzheimer models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Deficits of neuronal density in CA1 and synaptic density in the dentate gyrus, CA3 and CA1, in a mouse model of Down syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Apolipoprotein E isoform-specific regulation of dendritic spine morphology in apolipoprotein E transgenic mice and Alzheimer's disease patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Synaptic deficit in the temporal cortex of partial trisomy 16 (Ts65Dn) mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090020
retrieved
29 October 2018
Identifiers
DOI
10.1016/J.TINS.2013.08.007
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
Fatcat ID
release_opzfzqwtwbc7zpuitayyg4zyyi
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/opzfzqwtwbc7zpuitayyg4zyyi
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PMC publication ID
4090020
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
PubMed publication ID
24075449
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090020
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24075449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
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