Zobrazeno 1 - 10 of 109 pro vyhledávání: '"Pierre L Roubertoux"'
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Akademický článek
Modulation of brain β-endorphin concentration by the specific part of the Y chromosome in mice.
Autor: Michel Botbol, Pierre L Roubertoux, Michèle Carlier, Séverine Trabado, Sylvie Brailly-Tabard, Fernando Perez-Diaz, Olivier Bonnot, Guillaume Bronsard, Sylvie Tordjman
Publikováno v: PLoS ONE, Vol 6, Iss 3, p e16704 (2011)
BackgroundSeveral studies in animal models suggest a possible effect of the specific part of the Y-chromosome (Y(NPAR)) on brain opioid, and more specifically on brain β-endorphin (BE). In humans, male prevalence is found in autistic disorder in whi
Externí odkaz: https://doaj.org/article/af60f39824ce4a61aae197ba43afcb73
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3
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot–Marie–Tooth disease 4H
Autor: Lara, El-Bazzal, Adeline, Ghata, Clothilde, Estève, Jihane, Gadacha, Patrice, Quintana, Christel, Castro, Nathalie, Roeckel-Trévisiol, Frédérique, Lembo, Nicolas, Lenfant, André, Mégarbané, Jean-Paul, Borg, Nicolas, Lévy, Marc, Bartoli, Yannick, Poitelon, Pierre L, Roubertoux, Valérie, Delague, Nathalie, Bernard-Marissal
Publikováno v: Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2022, ⟨10.1093/brain/awac402⟩
International audience; Charcot Marie Tooth disease is one of the most common inherited neurological disorders, affecting either axons from the motor and/or sensory neurons or Schwann cells of the peripheral nervous system, and caused by more than 10
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0782ce2aa538c788166fadb0e6d00695
https://amu.hal.science/hal-03977684
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5
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors
Autor: Michèle Carlier, Lucie Brosse, Pierre L. Roubertoux, Laurent Fasano, Mehdi Metwaly, Paolo Gubellini, Yasmine Belaidouni, Ahmed Fatmi, Pascal Salin, Dorian Chabbert, Jordan Molitor, Xavier Caubit, Lydia Kerkerian-Le Goff
Publikováno v: Translational Psychiatry
Translational Psychiatry, 2022, 12 (1), pp.106. ⟨10.1038/s41398-022-01865-6⟩
We previously linked TSHZ3 haploinsufficiency to autism spectrum disorder (ASD) and showed that embryonic or postnatal Tshz3 deletion in mice results in behavioral traits relevant to the two core domains of ASD, namely social interaction deficits and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186386d36fad341f1df311e5bfc98fc6
https://hal.science/hal-03388780
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6
Construct Validity and Cross Validity of a Test Battery Modeling Autism Spectrum Disorder (ASD) in Mice
Autor: Julie di Cristopharo, Pierre L. Roubertoux, Lydia Kerkerian-Le Goff, Adeline Ghata, Paolo Gubellini, Sylvie Tordjman, Michèle Carlier, Xavier Caubit, Laurent Fasano
Publikováno v: Behavior Genetics
Behavior Genetics, Springer Verlag, 2020, 50 (26-40), ⟨10.1007/s10519-019-09970-x⟩
Behavior Genetics, 2020, 50 (26-40), ⟨10.1007/s10519-019-09970-x⟩
Behavior Genetics, Springer Verlag, 2019, ⟨10.1007/s10519-019-09970-x⟩
International audience; Modeling in other organism species is one of the crucial stages in ascertaining the association between gene and psychiatric disorder. Testing Autism Spectrum Disorder (ASD) in mice is very popular but construct validity of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63994703d98cd83f5f252b991271be16
https://hal-amu.archives-ouvertes.fr/hal-02440792/document
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7
Postnatal Tshz3 deletion drives altered corticostriatal function and autism spectrum disorder-like behavior
Autor: Michèle Carlier, Pierre L. Roubertoux, Christina Frahm, Laurent Fasano, Mehdi Metwaly, Dany Severac, Paolo Gubellini, Alistair N. Garratt, Bernard Jacq, Ahmed Fatmi, Pascal Salin, Dorian Chabbert, Xavier Caubit, Bianca Habermann, Lydia Kerkerian-Le Goff, Emeric Dubois
Publikováno v: Biological Psychiatry
Biological Psychiatry, Elsevier, 2019, 86 (4), pp.274-285. ⟨10.1016/j.biopsych.2019.03.974⟩
Biological Psychiatry, 2019, 86 (4), pp.274-285. ⟨10.1016/j.biopsych.2019.03.974⟩
International audience; BACKGROUND: Heterozygous deletion of the TSHZ3 gene, encoding for the teashirt zinc-finger homeobox family member 3 (TSHZ3) transcription factor that is highly expressed in cortical projection neurons (CPNs), has been linked t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffbf5abb350369b7cee3b04f42362f43
http://edoc.mdc-berlin.de/18222/1/18222oa.pdf
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8
Repint of 'Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity'
Autor: R Canitano, George M. Anderson, Nathalie Coulon, Michel Botbol, Pierre L. Roubertoux, Sylvie Tordjman, David Cohen
Publikováno v: Neuroscience and Biobehavioral Reviews
Neuroscience and Biobehavioral Reviews, Elsevier, 2018, 89, pp.132-150. ⟨10.1016/j.neubiorev.2018.01.014⟩
Neuroscience and Biobehavioral Reviews, 2018, 89, pp.132-150. ⟨10.1016/j.neubiorev.2018.01.014⟩
Neuroscience and Biobehavioral Reviews, Elsevier, 2018, 89, pp.132-150. 〈10.1016/j.neubiorev.2018.01.014〉
International audience; Clinical and molecular genetics have advanced current knowledge on genetic disorders associated with autism. A review of diverse genetic disorders associated with autism is presented and for the first time discussed extensivel
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37aebae158540caa267f214d83db9f03
https://hal-amu.archives-ouvertes.fr/hal-01812461
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10
Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice
Autor: Adeline Ghata, Pierre L. Roubertoux, Pierre Cau, Julie di Christofaro, Michèle Carlier, Catherine Bartoli, Nathalie Baril, Christophe Scajola, Patrice Bourgeois, Sylvie Tordjman
Publikováno v: Behavior Genetics
Behavior Genetics, 2017, 47 (3), pp.305-322. ⟨10.1007/s10519-017-9835-5⟩
Behavior Genetics, Springer Verlag, 2017, 47 (3), pp.305-322. 〈10.1007/s10519-017-9835-5〉
Behavior Genetics, Springer Verlag, 2017, 47 (3), pp.305-322. ⟨10.1007/s10519-017-9835-5⟩
International audience; We hypothesize that the trisomy 21 (Down syndrome) is the additive and interactive outcome of the triple copy of different regions of HSA21. Because of the small number of patients with partial trisomy 21, we addressed the que
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8c813b2473c0e05557f1d503b0c2675
https://hal.science/hal-01614900/document
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