Lista de obras - Arnaud Duchon - Dominio Público Uruguay

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

scientific article published on 26 September 2009

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

artículo científico publicado en 2015

Controlled somatic and germline copy number variation in the mouse model

artículo científico publicado en 2010

DYRK1A overexpression decreases plasma lecithin:cholesterol acyltransferase activity and apolipoprotein A-I levels

artículo científico publicado en 2013

DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome

artículo científico publicado en 2016

DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinase

artículo científico publicado en 2009

Deletion of the App-Runx1 region in mice models human partial monosomy 21.

artículo científico publicado en 2015

Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome

artículo científico publicado en 2015

Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humans

artículo científico publicado en 2013

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

artículo científico publicado en 2014

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome

artículo científico publicado en 2011

Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination

artículo científico publicado en 2008

Long-lasting correction of in vivo LTP and cognitive deficits of mice modelling Down syndrome with an α5-selective GABAA inverse agonist

artículo científico publicado en 2020

Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organization

artículo científico publicado en 2006

Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses

artículo científico publicado en 2007

Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models

artículo científico publicado en 2021

Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.

artículo científico publicado en 2015

Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models.

artículo científico publicado en 2015

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

artículo científico publicado en 2019

TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis

artículo científico publicado en 2019

The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model

artículo científico publicado en 2012

The in vivo Down syndrome genomic library in mouse

artículo científico publicado en 2012

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

artículo científico publicado en 2010

Lista de obras de Arnaud Duchon

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

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

Controlled somatic and germline copy number variation in the mouse model

DYRK1A overexpression decreases plasma lecithin:cholesterol acyltransferase activity and apolipoprotein A-I levels

DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome

DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinase

Deletion of the App-Runx1 region in mice models human partial monosomy 21.

Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome

Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humans

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome

Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination

Long-lasting correction of in vivo LTP and cognitive deficits of mice modelling Down syndrome with an α5-selective GABAA inverse agonist

Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organization

Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses

Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models

Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.

Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models.

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis

The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model

The in vivo Down syndrome genomic library in mouse

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