Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Valérie Nalesso

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Molecular Autism|January 13, 2021
Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse modelsSandra Martin Lorenzo, Valérie Nalesso, Claire Chevalier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndromeArnaud Duchon, Matthieu Raveau, Claire Chevalier, et al.
Frontiers in Behavioral Neuroscience|January 4, 2024
Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse modelAnna Rusu, Claire Chevalier, Fabrice de Chaumont, et al.
Science (New York, N.Y.)|November 19, 2016
The DNA methyltransferase DNMT3C protects male germ cells from transposon activityJoan Barau, Aurélie Teissandier, Natasha Zamudio, et al.
Biology of the Cell|February 26, 2005
Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1Vanessa Besson, Valérie Nalesso, Alexandre Herpin, et al.
Disease Models & Mechanisms|June 3, 2015
Deletion of the App-Runx1 region in mice models human partial monosomy 21Thomas Arbogast, Matthieu Raveau, Claire Chevalier, et al.
Plos Genetics|June 14, 2012
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse modelMatthieu Raveau, Jacques M Lignon, Valérie Nalesso, et al.
Genetics|April 23, 2014
Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndromeIgnasi Sahún, Damien Marechal, Patricia Lopes Pereira, et al.
Plos One|December 24, 2011
Missense mutation in the second RNA binding domain reveals a role for Prkra (PACT/RAX) during skull developmentBenjamin K Dickerman, Christine L White, Claire Chevalier, et al.
Neurobiology of Disease|May 5, 2024
Shaping down syndrome brain cognitive and molecular changes due to aging using adult animals from the Ts66Yah murine modelChiara Lanzillotta, Monika Rataj Baniowska, Francesca Prestia, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Molecular Autism|January 13, 2021
Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse modelsSandra Martin Lorenzo, Valérie Nalesso, Claire Chevalier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndromeArnaud Duchon, Matthieu Raveau, Claire Chevalier, et al.
Frontiers in Behavioral Neuroscience|January 4, 2024
Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse modelAnna Rusu, Claire Chevalier, Fabrice de Chaumont, et al.
Science (New York, N.Y.)|November 19, 2016
The DNA methyltransferase DNMT3C protects male germ cells from transposon activityJoan Barau, Aurélie Teissandier, Natasha Zamudio, et al.
Biology of the Cell|February 26, 2005
Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1Vanessa Besson, Valérie Nalesso, Alexandre Herpin, et al.
Disease Models & Mechanisms|June 3, 2015
Deletion of the App-Runx1 region in mice models human partial monosomy 21Thomas Arbogast, Matthieu Raveau, Claire Chevalier, et al.
Plos Genetics|June 14, 2012
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse modelMatthieu Raveau, Jacques M Lignon, Valérie Nalesso, et al.
Genetics|April 23, 2014
Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndromeIgnasi Sahún, Damien Marechal, Patricia Lopes Pereira, et al.
Plos One|December 24, 2011
Missense mutation in the second RNA binding domain reveals a role for Prkra (PACT/RAX) during skull developmentBenjamin K Dickerman, Christine L White, Claire Chevalier, et al.
Neurobiology of Disease|May 5, 2024
Shaping down syndrome brain cognitive and molecular changes due to aging using adult animals from the Ts66Yah murine modelChiara Lanzillotta, Monika Rataj Baniowska, Francesca Prestia, et al.
Pageof 2