Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Jean M. Delabar"'
Autor:
Jean M. Delabar, Julien Lagarde, Marta Fructuoso, Ammara Mohammad, Michel Bottlaender, Eric Doran, Ira Lott, Isabelle Rivals, Frederic A. Schmitt, Elizabeth Head, Marie Sarazin, Marie-Claude Potier
Publikováno v:
Translational Psychiatry, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Early markers are needed for more effective prevention of Alzheimer’s disease. We previously showed that individuals with Alzheimer’s disease have decreased plasma DYRK1A levels compared to controls. We assessed DYRK1A in the plasma of c
Externí odkaz:
https://doaj.org/article/5d6a3bb197104b249fcbd404915e0cfc
Autor:
Jean M. Delabar, Marion Ortner, Stephanie Simon, Anne Wijkhuisen, Cecile Feraudet‐Tarisse, Jonathan Pegon, Emma Vidal, Yael Hirschberg, Bruno Dubois, Marie‐Claude Potier
Publikováno v:
Alzheimer’s & Dementia: Translational Research & Clinical Interventions, Vol 6, Iss 1, Pp n/a-n/a (2020)
Abstract Introduction An effective therapy has not yet been developed for Alzheimer's disease (AD), in part because pathological changes occur years before clinical symptoms manifest. We recently showed that decreased plasma DYRK1A identifies individ
Externí odkaz:
https://doaj.org/article/78824974b0234847bd01a264b6d1fc28
Autor:
Yann Herault, Jean M. Delabar, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz, Eugene Yu, Veronique Brault
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 10, Pp 1165-1186 (2017)
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Down-syndrome-related features has been developed to understand this complex human chromosomal disorder. These mouse models have been important for dete
Externí odkaz:
https://doaj.org/article/790ab10207ce407489ca7bf4394b9b77
Autor:
Sònia Najas, Juan Arranz, Pamela A. Lochhead, Anne L. Ashford, David Oxley, Jean M. Delabar, Simon J. Cook, María José Barallobre, Maria L. Arbonés
Publikováno v:
EBioMedicine, Vol 2, Iss 2, Pp 120-134 (2015)
Alterations in cerebral cortex connectivity lead to intellectual disability and in Down syndrome, this is associated with a deficit in cortical neurons that arises during prenatal development. However, the pathogenic mechanisms that cause this defici
Externí odkaz:
https://doaj.org/article/2e2616fe74d7438690f9863488a1d0a7
Autor:
Fayçal Guedj, Patricia Lopes Pereira, Sonia Najas, Maria-Jose Barallobre, Caroline Chabert, Benoit Souchet, Catherine Sebrie, Catherine Verney, Yann Herault, Mariona Arbones, Jean M. Delabar
Publikováno v:
Neurobiology of Disease, Vol 46, Iss 1, Pp 190-203 (2012)
Copy number variation in a small region of chromosome 21 containing DYRK1A produces morphological and cognitive alterations in human. In mouse models, haploinsufficiency results in microcephaly, and a human DYRK1A gain-of-function model (three allele
Externí odkaz:
https://doaj.org/article/db3d5b2c8d124690bf6c0cdc300b6366
Autor:
Fayçal Guedj, Patricia Lopes Pereira, Sonia Najas, Maria-Jose Barallobre, Caroline Chabert, Benoit Souchet, Catherine Sebrie, Catherine Verney, Yann Herault, Mariona Arbones, Jean M. Delabar
Publikováno v:
Neurobiology of Disease, Vol 47, Iss 2, Pp 294- (2012)
Externí odkaz:
https://doaj.org/article/67b1996ba157405a88f4a92f84058155
Autor:
Maria L. Arbonés, Aurore Thomazeau, Akiko Nakano-Kobayashi, Masatoshi Hagiwara, Jean M. Delabar
Publikováno v:
Pharmacology and Therapeutics
Pharmacology and Therapeutics, Elsevier, 2019, 194, pp.199-221. ⟨10.1016/j.pharmthera.2018.09.010⟩
Pharmacology and Therapeutics, Elsevier, 2019, 194, pp.199-221. ⟨10.1016/j.pharmthera.2018.09.010⟩
The dosage of the serine threonine kinase DYRK1A is critical in the central nervous system (CNS) during development and aging. This review analyzes the functions of this kinase by considering its interacting partners and pathways. The role of DYRK1A
Autor:
Eugene Yu, Elizabeth M. C. Fisher, Yann Herault, Jean M. Delabar, Victor L. J. Tybulewicz, Véronique Brault
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, 2017, 23 (3), pp.578-589. ⟨10.1242/dmm.029728⟩
Disease Models & Mechanisms, Cambridge Company of Biologists, 2017, 23 (3), pp.578-589. ⟨10.1242/dmm.029728⟩
Disease Models & Mechanisms, Vol 10, Iss 10, Pp 1165-1186 (2017)
Disease Models & Mechanisms, 2017, 23 (3), pp.578-589. ⟨10.1242/dmm.029728⟩
Disease Models & Mechanisms, Cambridge Company of Biologists, 2017, 23 (3), pp.578-589. ⟨10.1242/dmm.029728⟩
Disease Models & Mechanisms, Vol 10, Iss 10, Pp 1165-1186 (2017)
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Down-syndrome-related features has been developed to understand this complex human chromosomal disorder. These mouse models have been important for dete
Autor:
Anne Badel, Maria L. Arbonés, A. C. Camproux, Jean-Louis Paul, P. Lamourette, Foudil Lamari, Stéphanie Simon, Marie-Claude Potier, Nathalie Janel, Cécile Feraudet-Tarisse, Jean M. Delabar, Bruno Dubois, Julien Lagarde, Panagiotis Alexopoulos, Marie Sarazin
Publikováno v:
Translational Psychiatry
Translational Psychiatry, Nature Pub. Group, 2017, 7, pp.e1154. ⟨10.1038/tp.2017.123⟩
Translational Psychiatry, 2017, 7, pp.e1154. ⟨10.1038/tp.2017.123⟩
Translational Psychiatry, 2017, 7, pp.e1154. 〈10.1038/tp.2017.123〉
Digital.CSIC. Repositorio Institucional del CSIC
instname
Translational Psychiatry, Nature Pub. Group, 2017, 7, pp.e1154. ⟨10.1038/tp.2017.123⟩
Translational Psychiatry, 2017, 7, pp.e1154. ⟨10.1038/tp.2017.123⟩
Translational Psychiatry, 2017, 7, pp.e1154. 〈10.1038/tp.2017.123〉
Digital.CSIC. Repositorio Institucional del CSIC
instname
Early identification of Alzheimer’s disease (AD) risk factors would aid development of interventions to delay the onset of dementia, but current biomarkers are invasive and/or costly to assess. Validated plasma biomarkers would circumvent these cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f79094776d60309b8ce82a86a591d1
https://hal.sorbonne-universite.fr/hal-01556869
https://hal.sorbonne-universite.fr/hal-01556869
Publikováno v:
Brain research. 1646
Down syndrome, or trisomy 21, has been modeled with various trisomic and transgenic mice to help understand the consequences of an altered gene dosage in brain development and function. Though Down syndrome has been associated with premature aging, l