Výsledky vyhledávání - "Tricoire Hervé"

Akademický článek

Autor: Monnier Véronique, Lasbleiz Christelle, Girardot Fabrice, Tricoire Hervé

Publikováno v: BMC Genomics, Vol 7, Iss 1, p 69 (2006)

Abstract Background During the last two decades progress in the genetics of aging in invertebrate models such as C. elegans and D. melanogaster has clearly demonstrated the existence of regulatory pathways that control the rate of aging in these orga

Externí odkaz: https://doaj.org/article/d9f97c8657ca44d1aa2499c5904809e6

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Akademický článek

Genome wide analysis of common and specific stress responses in adult drosophila melanogaster

Autor: Girardot Fabrice, Monnier Véronique, Tricoire Hervé

Publikováno v: BMC Genomics, Vol 5, Iss 1, p 74 (2004)

Abstract Background During their life, multicellular organisms are challenged with oxidative stress. It is generated by several reactive oxygen species (ROS), may limit lifespan and has been related to several human diseases. ROS can generate a wide

Externí odkaz: https://doaj.org/article/5b5b718e9eac42b2beddc9c72a33f170

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Akademický článek

Karyopherin α-3 is a key protein in the pathogenesis of spinocerebellar ataxia type 3 controlling the nuclear localization of ataxin-3

Autor: Sowa, Anna Sergeevna, Martin, Elodie, Martins, Inês Morgado, Schmidt, Jana, Depping, Reinhard, Weber, Jonasz Jeremiasz, Rother, Franziska, Hartmann, Enno, Bader, Michael, Riess, Olaf, Tricoire, Hervé, Schmidt, Thorsten

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 2018 Mar . 115(11), E2624-E2633.

Externí odkaz: https://www.jstor.org/stable/26508363

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Genetic Screen in Adult Drosophila Reveals That dCBP Depletion in Glial Cells Mitigates Huntington Disease Pathology through a Foxo-Dependent Pathway

Autor: Martin, Elodie, Heidari, Raheleh, Monnier, Véronique, Tricoire, Hervé

Publikováno v: International Journal of Molecular Sciences
International Journal of Molecular Sciences, 2021, 22 (8), ⟨10.3390/ijms22083884⟩
International Journal of Molecular Sciences, Vol 22, Iss 3884, p 3884 (2021)
Volume 22
Issue 8

International audience; Huntington's disease (HD) is a progressive and fatal autosomal dominant neurodegenerative disease caused by a CAG repeat expansion in the first exon of the huntingtin gene (HTT). In spite of considerable efforts, there is curr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ca3a0a8a9233a744dbbd61942ec1eb6b
https://pubmed.ncbi.nlm.nih.gov/33918672

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Chapitre 9: les autres modèles animaux alternatifs

Autor: Tricoire, Hervé, Geoffrois, L

Publikováno v: Quelles alternatives en expérimentation animale-Editions QUAE
Quelles alternatives en expérimentation animale-Editions QUAE, 2020

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8abd885f7db6a445ce16500d6e217729
https://hal.archives-ouvertes.fr/hal-03084862

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Akademický článek

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Akademický článek

A New, Discontinuous 2 Phases of Aging Model: Lessons from Drosophila melanogaster.

Autor: Tricoire, Hervé¹, Rera, Michael¹ michael.rera@univ-paris-diderot.fr

Publikováno v: PLoS ONE. 11/3/2015, Vol. 10 Issue 10, p1-14. 14p.

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Karyopherin α-3 is a key protein in the pathogenesis of spinocerebellar ataxia type 3 controlling the nuclear localization of ataxin-3

Autor: Tricoire, Hervé, Sowa, Anna Sergeevna, Martin, Elodie, Martins, Inês Morgado, Schmidt, Jana, Depping, Reinhard, Weber, Jonasz Jeremiasz, Rother, Franziska, Hartmann, Enno, Bader, Michael, Riess, Olaf, Tricoire, Hérvé, Schmidt, Thorsten

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2018, 115 (11), pp.E2624-E2633. ⟨10.1073/pnas.1716071115⟩

Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder caused by a CAG expansion in the ATXN3 gene leading to a polyglutamine expansion in the ataxin-3 protein. The nuclear presence and aggregation of expanded ataxin-3 are critical step

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a01047c00cc7883219354d5ac1e91954
https://hal.archives-ouvertes.fr/hal-02325731

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Identification of cardioprotective drugs by medium-scale in vivo pharmacological screening on a Drosophila cardiac model of Friedreich's ataxia

Autor: Tricoire, Hervé, Palandri, Amandine, Martin, Elodie, Russi, Maria, Rera, Michael, Tricoire, Hérvé, Monnier, Véronique

Publikováno v: Disease Models & Mechanisms
Disease Models & Mechanisms, Cambridge Company of Biologists, 2018, 11 (7), pp.dmm033811. ⟨10.1242/dmm.033811⟩
Disease Models & Mechanisms, Vol 11, Iss 7 (2018)
Disease Models & Mechanisms, 2018, 11 (7), pp.dmm033811. ⟨10.1242/dmm.033811⟩

Friedreich's ataxia (FA) is caused by reduced levels of frataxin, a highly conserved mitochondrial protein. There is currently no effective treatment for this disease, characterized by progressive neurodegeneration and cardiomyopathy, the latter bein

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2decee805047778ab53f0e2e3523244d
https://doi.org/10.1242/dmm.033811

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