Nalesso Valérie - Institut de Génétique Biologie Moléculaire et Cellulaire - UMR 7104 - U1258, Université de Strasbourg

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论文共 23 篇作者统计合作学者相似作者

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Cognitive and molecular characterization of the Ts66Yah murine model of Down syndrome: deepening on hippocampal changes associated with genotype and aging

Chiara Lanzillotta,Monika Rataj Baniowska,Francesca Prestia, Chiara Sette,Valérie Nalesso,Marzia Perluigi,Eugenio Barone,Arnaud Duchon,Antonella Tramutola,Yann Herault,Fabio Di Domenico

biorxiv（2024）

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Shaping Down Syndrome Brain Cognitive and Molecular Changes Due to Aging Using Adult Animals from the Ts66Yah Murine Model

Chiara Lanzillotta,Monika Rataj Baniowska,Francesca Prestia, Chiara Sette,Valerie Nalesso,Marzia Perluigi,Eugenio Barone,Arnaud Duchon,Antonella Tramutola,Yann Herault,Fabio Di Domenico

NEUROBIOLOGY OF DISEASE (2024)

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Day-to-day Spontaneous Social Behaviours is Quantitatively and Qualitatively Affected in a 16p11.2 Deletion Mouse Model

Anna Rusu,Claire Chevalier,Fabrice de Chaumont,Valerie Nalesso,Veronique Brault,Yann Herault,Elodie Ey

FRONTIERS IN BEHAVIORAL NEUROSCIENCE (2023)

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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

Sandra Martin Lorenzo,Maria Del Mar Muniz Moreno, Helin Atas, Marion Pellen,Valérie Nalesso,Wolfgang Raffelsberger,Geraldine Prevost,Loic Lindner,Marie-Christine Birling,Séverine Menoret,Laurent Tesson,Luc Negroni,Jean-Paul Concordet,Ignacio Anegon,Yann Herault

FRONTIERS IN NEUROSCIENCE (2023): 1148683

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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

Sandra Martin Lorenzo,Maria del Mar Muniz Moreno, Helin Atas, Marion Pellen,Valerie Nalesso,Wolfgang Raffelsberger,Geraldine Prevost,Loic Lindner,Marie-Christine Birling,Severine Menoret, Laurent Tesson,Luc Negroni,Jean-Paul Concordet, Ignacio Anegon,Yann Herault

FRONTIERS IN NEUROSCIENCE (2023)

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

Brigitta B. Gundersen, William T. O’Brien,Melanie D Schaffler, Maria N. Schultz,Tatsuya Tsukahara,Sandra Martín Lorenzo,Valérie Nalesso, Alice H Luo Clayton,Ted Abel,Jacqueline N. Crawley,Sandeep Robert Datta,Yann Hérault

bioRxiv (Cold Spring Harbor Laboratory) (2023)

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Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations

Maria Victoria HINCKELMANN,Aline Dubos, Victorine Artot,Gabrielle Rudolf,Thu Lan Nguyen,Peggy Tilly,Valerie Nalesso,Maria del Mar Muniz Moreno,Marie-Christine Birling,Juliette Godin,Veronique Brault,Yann Herault

biorxiv（2023）

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A 16p11.2 Deletion Mouse Model Displays Quantitatively and Qualitatively Different Behaviours in Sociability and Social Novelty over Short- and Long-Term Observation

Anna Rusu,Claire Chevalier, Fabrice Chaumont,Valérie Nalesso, Véronique Brault,Yann Hérault,Elodie Ey

crossref（2022）

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Ts66Yah, a Mouse Model of Down Syndrome with Improved Construct and Face Validity

Arnaud Duchon,Maria del Mar Muniz Moreno,Claire Chevalier,Valerie Nalesso,Philippe Andre,Marta Fructuoso-Castellar,Mary Mondino,Chrystelle Po,Vincent Noblet,Marie-Christine Birling,Marie-Claude Potier,Yann Herault

Disease models & mechanisms（2022）

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Ts66Yah, an Upgraded Ts65Dn Mouse Model for Down Syndrome, for Only the Region Homologous to Human Chromosome 21

Arnaud Duchon,Maria del Mar Muñiz Moreno,Claire Chevalier,Valérie Nalesso,Philippe Andre,Marta Fructuoso-Castellar,Mary Mondino,Chrystelle Po,Vincent Noblet,Marie-Christine Birling,Marie-Claude Potier,Yann Herault

Disease Models & Mechanisms（2022）

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