Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Roseline Poirier"'
Publikováno v:
Neurobiology of Disease, Vol 183, Iss , Pp 106163- (2023)
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and adaptive behaviors and represents a major medical issue. Although ID-patients develop behavioral problems and are diagnosed during childhood, most be
Externí odkaz:
https://doaj.org/article/eee0086b2a0f496686e6e1b82986cf6b
Autor:
Charlotte Castillon, Steeve Lunion, Nathalie Desvignes, André Hanauer, Serge Laroche, Roseline Poirier
Publikováno v:
Neurobiology of Disease, Vol 115, Iss , Pp 69-81 (2018)
Adult neurogenesis is involved in certain hippocampus-dependent cognitive functions and is linked to psychiatric diseases including intellectual disabilities. The Coffin-Lowry syndrome (CLS) is a developmental disorder caused by mutations in the Rsk2
Externí odkaz:
https://doaj.org/article/38b820d4632d43709f513d0229d759cb
Autor:
Céline Serrano, Morgane Dos Santos, Dimitri Kereselidze, Louison Beugnies, Philippe Lestaevel, Roseline Poirier, Christelle Durand
Publikováno v:
Biology, Vol 10, Iss 3, p 192 (2021)
The cognitive consequences of postnatal brain exposure to ionizing radiation (IR) at low to moderate doses in the adult are not fully established. Because of the advent of pediatric computed tomography scans used for head exploration, improving our k
Externí odkaz:
https://doaj.org/article/cdb432b808694d74b4e4dc6acda4b2a3
Autor:
Elise Morice, Séverine Farley, Roseline Poirier, Glenn Dallerac, Carine Chagneau, Solange Pannetier, André Hanauer, Sabrina Davis, Cyrille Vaillend, Serge Laroche
Publikováno v:
Neurobiology of Disease, Vol 58, Iss , Pp 156-168 (2013)
The Coffin–Lowry syndrome (CLS) is a syndromic form of intellectual disability caused by loss-of-function of the RSK2 serine/threonine kinase encoded by the rsk2 gene. Rsk2 knockout mice, a murine model of CLS, exhibit spatial learning and memory i
Externí odkaz:
https://doaj.org/article/77281fa05613408aa5d345f70f9bf238
Autor:
Roseline Poirier, Hélène Cheval, Caroline Mailhes, Sonia Garel, Patrick Charnay, Sabrina Davis, Serge Laroche
Publikováno v:
Frontiers in Neuroscience, Vol 2 (2008)
The different gene members of the Egr family of transcriptional regulators have often been considered to have related functions in brain, based on their co-expression in many cell-types and structures, the relatively high homology of the translated p
Externí odkaz:
https://doaj.org/article/ec5d5f45bb3a445da9eeae5521fd91dd
Autor:
Roseline Poirier, Hélène Cheval, Caroline Mailhes, Patrick Charnay, Sabrina Davis, Serge Laroche
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 1 (2007)
It is well established that Egr1/zif268, a member of the Egr family of transcription factors, is critical for the consolidation of several forms of memories. Recently, the Egr3 family member has also been implicated in learning and memory. Because Eg
Externí odkaz:
https://doaj.org/article/504c26c414ca42628e1e50906ab23337
Autor:
Marie-Stephanie Clerget-Froidevaux, Lamis Chamas, Isabelle Seugnet, Odessa Tanve, Roseline Poirier, Valerie Enderlin
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de6ab885f1faded42650c6db6ccefd34
https://doi.org/10.1530/endoabs.84.op-13-64
https://doi.org/10.1530/endoabs.84.op-13-64
Autor:
Lamis Chamas, Isabelle Seugnet, Roseline Poirier, Marie-Stéphanie Clerget-Froidevaux, Valérie Enderlin
Adult-onset hypothyroidism is associated with learning and cognitive dysfunctions, which may be related to alterations in synaptic plasticity. Local reduced levels of thyroid hormones (THs) may impair glia morphology and activity, and promote the inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d9050340ca1626c8a400af42527c0e3
https://doi.org/10.1101/2022.04.06.487389
https://doi.org/10.1101/2022.04.06.487389
Autor:
Cyrille Vaillend, Jean-Vianney Barnier, Serge Laroche, Sandrine Guyon, Laurine Gonzalez, Philippe Lestaevel, Kevin Da Silva, Christelle Durand, Roseline Poirier, Charlotte Castillon, Florence Domenichini
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1950-1968. ⟨10.1093/hmg/ddz296⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1950-1968. ⟨10.1093/hmg/ddz296⟩
The link between mutations associated with intellectual disability (ID) and the mechanisms underlying cognitive dysfunctions remains largely unknown. Here, we focused on PAK3, a serine/threonine kinase whose gene mutations cause X-linked ID. We gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d5da44e89511f6df88a00661b38de5
https://doi.org/10.1093/hmg/ddz296
https://doi.org/10.1093/hmg/ddz296
Autor:
Lamis Chamas, Isabelle Seugnet, Roseline Poirier, Marie-Stéphanie Clerget-Froidevaux, Valérie Enderlin
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 19; Pages: 11938
Adult-onset hypothyroidism is associated with learning and cognitive dysfunctions, which may be related to alterations in synaptic plasticity. Local reduced levels of thyroid hormones (THs) may impair glia morphology and activity, and promote the inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c33d996903180b328bcbaa94750e906
https://doi.org/10.3390/ijms231911938
https://doi.org/10.3390/ijms231911938