Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice. (Q30497997)

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English	Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice.	scientific article

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15 February 2020

Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice (English)

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15 February 2020

long-term potentiation

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Alexander M Kleschevnikov

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15 February 2020

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15 February 2020

Antonio Baldini

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Antonio Baldini

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15 February 2020

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Tao Yu

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15 February 2020

Chunhong Liu

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15 February 2020

Pavel Belichenko

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15 February 2020

Steven J Clapcote

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15 February 2020

Shaomin Li

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Annie Pao

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Allison R Bechard

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15 February 2020

Suhail Asrar

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15 February 2020

Rongqing Chen

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15 February 2020

Ni Fan

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15 February 2020

Zhengping Jia

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15 February 2020

Chu Chen

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15 February 2020

John C Roder

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15 February 2020

Bin Liu

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15 February 2020

William C Mobley

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15 February 2020

Y Eugene Yu

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15 February 2020

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26 October 2010

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15 February 2020

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15 February 2020

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15 February 2020

162-171

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15 February 2020

Olig1 and Olig2 triplication causes developmental brain defects in Down syndrome

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The role of SAP97 in synaptic glutamate receptor dynamics

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Behavioral deficits and subregion-specific suppression of LTP in mice expressing a population of mutant NMDA receptors throughout the hippocampus

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A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

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G protein-activated inwardly rectifying potassium channels mediate depotentiation of long-term potentiation.

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NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.

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An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes

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28 July 2018

Deficits in hippocampal CA1 LTP induced by TBS but not HFS in the Ts65Dn mouse: a model of Down syndrome.

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28 July 2018

Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome.

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Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

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The neuropsychology of Down syndrome: evidence for hippocampal dysfunction

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Identification and characterization of a synaptojanin 2 splice isoform predominantly expressed in nerve terminals

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Synaptojanin 2, a novel Rac1 effector that regulates clathrin-mediated endocytosis

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28 July 2018

Behavioral phenotype of individuals with Down syndrome

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Functional consequences of reduction in NMDA receptor glycine affinity in mice carrying targeted point mutations in the glycine binding site

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28 July 2018

Long-term potentiation--a decade of progress?

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28 July 2018

Altered long-term potentiation in the young and old Ts65Dn mouse, a model for Down Syndrome.

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28 July 2018

Synaptojanin 2, a novel synaptojanin isoform with a distinct targeting domain and expression pattern

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28 July 2018

Mice lacking metabotropic glutamate receptor 5 show impaired learning and reduced CA1 long-term potentiation (LTP) but normal CA3 LTP

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28 July 2018

Enhanced LTP in mice deficient in the AMPA receptor GluR2.

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Long-term depression in hippocampus

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A mouse model for Down syndrome exhibits learning and behaviour deficits.

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Improved national prevalence estimates for 18 selected major birth defects--United States, 1999-2001

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12 December 2020

based on heuristic

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10.1016/J.BRAINRES.2010.09.107

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15 February 2020

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15 February 2020

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15 February 2020

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