V. Nalesso

发表

Training and aging modulate the loss‐of‐balance phenotype observed in a new ENU‐induced allele of Otopetrin1

Y. Hérault, J. Bizot, N. Messaddeq, 2005, Biology of the cell.

KIT is required for hepatic function during mouse post-natal development

H. Fuchs, Y. Hérault, M. D. de Angelis, 2007, BMC Developmental Biology.

Missense Mutation in the Second RNA Binding Domain Reveals a Role for Prkra (PACT/RAX) during Skull Development

Y. Hérault, C. Chevalier, C. White, 2011, PloS one.

DMM017814 623..634

Y. Hérault, D. Dembélé, A. Duchon, 2015 .

A 16p11.2 deletion mouse model displays quantitatively and qualitatively different behaviours in sociability and social novelty over short- and long-term observation

Y. Hérault, F. de Chaumont, V. Brault, 2022, bioRxiv.

Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

Y. Hérault, M. Potier, A. Duchon, 2022, bioRxiv.

Ts 66 Yah , a refined Ts 65 Dn DS mouse model , unravels genetic 1 interaction between regions homologous to Human chromosome 21 2 and the Scaf 8-Pde 10 a genetic interval

Y. Hérault, M. Potier, A. Duchon, 2022 .

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

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

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

Y. Hérault, D. Dembélé, A. Duchon, 2015, Disease Models & Mechanisms.

The DNA methyltransferase DNMT3C protects male germ cells from transposon activity

Y. Hérault, Aurélie Teissandier, D. Bourc’his, 2016, Science.

Localization of the 3' IgH locus elements that effect long-distance regulation of class switch recombination.

A. Khamlichi, E. Pinaud, M. Le Bert, 2001, Immunity.

Cognition and Hippocampal Plasticity in the Mouse Is Altered by Monosomy of a Genomic Region Implicated in Down Syndrome

Stylianos E. Antonarakis, Yann Herault, Mara Dierssen, 2014, Genetics.

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

Y. Hérault, H. Meziane, J. Armspach, 2021, Human molecular genetics.

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

Y. Hérault, H. Meziane, J. Armspach, 2020, bioRxiv.

Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models

Y. Hérault, C. Chevalier, M. Birling, 2020, bioRxiv.

Changes in social behaviour with alterations of MAPK3 and KCTD13/CUL3 pathways in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders

Y. Hérault, J. Concordet, L. Tesson, 2023, bioRxiv.

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

Y. Hérault, A. Sharp, A. Duchon, 2011, Mammalian Genome.

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

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

Towards Preclinical Validation of Arbaclofen (R-baclofen) Treatment for 16p11.2 Deletion Syndrome

Y. Hérault, M. Schaffler, T. Tsukahara, 2023, bioRxiv.

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model

Y. Hérault, A. Sharp, D. Dembélé, 2012, PLoS genetics.

Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders

Y. Hérault, J. Concordet, L. Tesson, 2023, Frontiers in Neuroscience.

Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

Y. Hérault, M. Potier, A. Duchon, 2022, Disease Models & Mechanisms.

Towards Preclinical Validation of Arbaclofen (R-baclofen) Treatment for 16p11.2 Deletion Syndrome

S. R. Datta, Brigitta B. Gundersen, M. Schaffler, 2023, bioRxiv.