Publications
L’une des missions de la FRH est de diffuser les résultats des recherches effectuées dans le domaine du handicap. Voici un recueil de publications en lien avec cette large thématique. N’hésitez pas à nous faire suivre vos publications.
Ergebnisse 37 – 48 von 75 werden angezeigt
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DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
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Cognition and Hippocampal Plasticity in the Mouse Is Altered by Monosomy of a Genomic Region Implicated in Down Syndrome
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Human chromosome 21 gene expression atlas in the mouse
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Nineteen Additional Unpredicted Transcripts from Human Chromosome 21
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Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an Adult With Mosaic Down Syndrome Model Accelerated Neuronal Ageing and Neurodegeneration
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Genotype-phenotype correlation in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21
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Domains of genome-wide gene expression dysregulation in Down’s syndrome
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Investigation of the molecular mechanisms underlying Down syndrome phenotypes
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Mouse models for Down Syndrome-Associated Developmental Cognitive Disabilities
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Prevalence and risk of Down syndrome in monozygotic and dizygotic multiple pregnancies in Europe : implication for prenatal screening
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Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21
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Allocentric spatial learning and memory deficits in Down syndrome