Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Etienne Sauvageau"'
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract AP-1 is a clathrin adaptor recruited to the trans-Golgi Network where it can interact with specific signals found in the cytosolic tail of cargo proteins to incorporate them into clathrin-coated vesicles for trafficking. The small G protein
Externí odkaz:
https://doaj.org/article/5c25b839927c4dc981e9a61bf3574f94
Publikováno v:
Biochemical Journal. 478:2339-2357
CLN5 is a soluble endolysosomal protein whose function is poorly understood. Mutations in this protein cause a rare neurodegenerative disease, Neuronal Ceroid Lipofuscinosis. We previously found that depletion of CLN5 leads to dysfunctional retromer,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20e3047c7f87c4d15688e90f1a73469
https://doi.org/10.1042/bcj20210171
https://doi.org/10.1042/bcj20210171
Autor:
Etienne Sauvageau, Stephane Lefrancois
Publikováno v:
The Biochemist. 41:36-40
The Beginner's Guides are an ongoing series of articles in the magazine, each one covering a key technique and offering the scientifically literate but not necessarily expert audience a background briefing on the underlying science of a technique tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d05b793d3f31c8280449cada650cf7c
https://doi.org/10.1042/bio04106036
https://doi.org/10.1042/bio04106036
CLN5 is a soluble endolysosomal protein whose function is poorly understood. Mutations in this protein cause a rare neurodegenerative disease, Neuronal Ceroid Lipofuscinosis. We previously found that depletion of CLN5 leads to dysfunctional retromer,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bceef2982e1bec4e3199f8cc893718f
https://doi.org/10.1101/2020.12.24.423824
https://doi.org/10.1101/2020.12.24.423824
Autor:
Guido Hermey, Graziana Modica, Abuzar Kaleem, Etienne Sauvageau, Seda Yasa, Stephane Lefrancois
Publikováno v:
Journal of Cell Science.
Mutations in CLN3 are a cause of juvenile neuronal ceroid lipofuscinosis (JNCL), also known as Batten disease. Clinical manifestations include cognitive regression, progressive loss of vision and motor function, epileptic seizures and a significantly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c859944f455940a50786ef9ed7dd70de
https://doi.org/10.1242/jcs.234047
https://doi.org/10.1242/jcs.234047
Autor:
Mohammad Mehdi, Haghdoost, Etienne, Sauvageau, Paul, Oguadinma, Hoang-Van, Tran, Stephane, Lefrancois, Annie, Castonguay
Publikováno v:
Journal of inorganic biochemistry. 210
The Cu-catalyzed click conjugation of an azide-functionalized vitamin B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d4baaac30def79b32b95c4244d413229
https://pubmed.ncbi.nlm.nih.gov/32763615
https://pubmed.ncbi.nlm.nih.gov/32763615
Autor:
Abuzar Kaleem, Seda Yasa, Etienne Sauvageau, Stephane Lefrancois, Guido Hermey, Graziana Modica
Mutations in CLN3 are a cause of juvenile NCL (JNCL), also known as Batten Disease. Clinical manifestations includes cognitive regression, progressive loss of vision and motor function, epileptic seizures, and a significantly reduced lifespan. CLN3 l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb491f5471c6c922c8074a559765475c
https://doi.org/10.1101/634915
https://doi.org/10.1101/634915
Autor:
Hoang-Van Tran, Etienne Sauvageau, Paul Oguadinma, Annie Castonguay, Stephane Lefrancois, Mohammad Mehdi Haghdoost
Publikováno v:
Journal of Inorganic Biochemistry. 210:111105
The Cu-catalyzed click conjugation of an azide-functionalized vitamin B12 (cobalamin) and an alkyne-labeled 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) led to the formation of a highly stable fluorescent BODIPY-labeled vitamin B12 (λex/λem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a0f8527502bbc6fa0ebe44409ed2a80
https://doi.org/10.1016/j.jinorgbio.2020.111105
https://doi.org/10.1016/j.jinorgbio.2020.111105
Autor:
Graziana Modica, Stephane Lefrancois, Olga Skorobogata, Christopher M. Yip, Adriano Vissa, Peter K. Kim, Etienne Sauvageau, Hugo Wurtele
Publikováno v:
Journal of Cell Science
Journal of Cell Science, Company of Biologists, 2017, 130 (15), pp.2579-2590. ⟨10.1242/jcs.199729⟩
Journal of Cell Science, Company of Biologists, 2017, 130 (15), pp.2579-2590. ⟨10.1242/jcs.199729⟩
International audience; Retromer is a multimeric protein complex that mediates endosome-to-trans-Golgi network (TGN) and endosome-to-plasma membrane trafficking of integral membrane proteins. Dysfunction of this complex has been linked to Alzheimer's
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7ea55021578fbf7976461c396f15c9b
https://hal-riip.archives-ouvertes.fr/pasteur-01574605
https://hal-riip.archives-ouvertes.fr/pasteur-01574605
Autor:
Regina Fluhrer, Etienne Sauvageau, Santiago Costantino, Martina Haug-Kröper, Javier Mazzaferri, Karine Dumaresq-Doiron, Felix Jules, Stephane Lefrancois
Publikováno v:
Experimental Cell Research
Experimental Cell Research, Elsevier, 2017, ⟨10.1016/j.yexcr.2017.04.024⟩
Experimental cell research 357(1), 40-50 (2017). doi:10.1016/j.yexcr.2017.04.024
Experimental Cell Research, Elsevier, 2017, ⟨10.1016/j.yexcr.2017.04.024⟩
Experimental cell research 357(1), 40-50 (2017). doi:10.1016/j.yexcr.2017.04.024
International audience; The Neuronal ceroid lipofuscinoses (NCLs) are a group of recessive disorders of childhood with overlapping symptoms including vision loss, ataxia, cognitive regression and premature death. 14 different genes have been linked t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2025acac2c030e49186cb6128d9e9d7e
https://hal-riip.archives-ouvertes.fr/pasteur-01534650
https://hal-riip.archives-ouvertes.fr/pasteur-01534650