Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. (Q37591118)

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scientific article published on 27 December 2013

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English	Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21.	scientific article published on 27 December 2013

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Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 (English)

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Stilianos Antonarakis

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Federico A Santoni

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Youssef Hibaoui

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Audrey Letourneau

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M Reza Sailani

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Sophie Dahoun

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Stefania Gimelli

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Michel Guipponi

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Marie Francoise Pelte

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Frédérique Béna

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27 December 2013

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EMBO Molecular Medicine

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describes a project that uses

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Twin-N-iPSCs line#8

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11 June 2022

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Reducing GABAA α5 receptor-mediated inhibition rescues functional and neuromorphological deficits in a mouse model of down syndrome.

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23 August 2017

Human pluripotent stem cells: applications and challenges in neurological diseases.

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OLIG2 over-expression impairs proliferation of human Down syndrome neural progenitors

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Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells

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The use of mouse models to understand and improve cognitive deficits in Down syndrome

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S100B and APP promote a gliocentric shift and impaired neurogenesis in Down syndrome neural progenitors

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Transient expression of Mnb/Dyrk1a couples cell cycle exit and differentiation of neuronal precursors by inducing p27KIP1 expression and suppressing NOTCH signaling

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DYRK1A protein kinase promotes quiescence and senescence through DREAM complex assembly

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Dyrk1A phosphorylates p53 and inhibits proliferation of embryonic neuronal cells

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Cognitive deficits and associated neurological complications in individuals with Down's syndrome

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Development of a sensitive non-radioactive protein kinase assay and its application for detecting DYRK activity in Xenopus laevis oocytes

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Dyrk1A overexpression inhibits proliferation and induces premature neuronal differentiation of neural progenitor cells

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REST and CoREST modulate neuronal subtype specification, maturation and maintenance

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A critical period in cortical interneuron neurogenesis in down syndrome revealed by human neural progenitor cells.

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The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

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Parkinson's disease patient-derived induced pluripotent stem cells free of viral reprogramming factors

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Green tea polyphenols rescue of brain defects induced by overexpression of DYRK1A.

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Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

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DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome

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Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly

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Notch regulates cell fate and dendrite morphology of newborn neurons in the postnatal dentate gyrus

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Alterations of neocortical pyramidal cell phenotype in the Ts65Dn mouse model of Down syndrome: effects of environmental enrichment

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Neuronal target genes of the neuron-restrictive silencer factor in neurospheres derived from fetuses with Down's syndrome: a gene expression study

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Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome

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A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region

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

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25 June 2018

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25 June 2018

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1 September 2018

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1 September 2018

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1 September 2018

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1 September 2018

Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice.

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1 September 2018

Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/- mouse

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1 September 2018

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1 September 2018

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1 September 2018

Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome.

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1 September 2018

Apoptosis-associated proteins p53 and APO-1/Fas (CD95) in brains of adult patients with Down syndrome.

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1 September 2018

Developmental changes of S-100 protein and glial fibrillary acidic protein in the brain in Down syndrome.

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1 September 2018

Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events

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21 January 2018

Clinical manifestations of the deletion of Down syndrome critical region including DYRK1A and KCNJ6

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12 December 2020

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P53- and CD95-associated apoptosis in neurodegenerative diseases

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12 December 2020

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Identifiers

10.1002/EMMM.201302848

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24375627%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24375627%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24375627%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

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