Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Amandine Viau"'
Autor:
Marceau Quatredeniers, Alice S. Serafin, Alexandre Benmerah, Antonio Rausell, Sophie Saunier, Amandine Viau
Publikováno v:
Scientific Data, Vol 10, Iss 1, Pp 1-23 (2023)
Abstract While the amount of studies involving single-cell or single-nucleus RNA-sequencing technologies grows exponentially within the biomedical research area, the kidney field requires reference transcriptomic signatures to allocate each cluster i
Externí odkaz:
https://doaj.org/article/9de29832527c4a2e9b6ba65ccb4e4984
Autor:
Sebastian Friedrich, Hannah Müller, Caroline Riesterer, Hannah Schüller, Katja Friedrich, Carlotta Leonie Wörner, Tilman Busch, Amandine Viau, E. Wolfgang Kuehn, Michael Köttgen, Alexis Hofherr
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Abstract Autosomal dominant polycystic kidney disease (ADPKD) affects more than 12 million people worldwide. Mutations in PKD1 and PKD2 cause cyst formation through unknown mechanisms. To unravel the pathogenic mechanisms in ADPKD, multiple studies h
Externí odkaz:
https://doaj.org/article/26259eef2f0a4eac970d8c986bd2bb91
Autor:
Jérémy Magescas, Lucie Sengmanivong, Amandine Viau, Adeline Mayeux, Tien Dang, Martine Burtin, Ulf J. Nilsson, Hakon Leffler, Françoise Poirier, Fabiola Terzi, Delphine Delacour
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Glycosylation is critical for the regulation of several cellular processes. One glycosylation pathway, the unusual O-linked β-N-acetylglucosamine glycosylation (O-GlcNAcylation) has been shown to be required for proper mitosis, likely throu
Externí odkaz:
https://doaj.org/article/c6d69700b2e14178b5342c6ead7e8f61
Autor:
Khalil El Karoui, Amandine Viau, Olivier Dellis, Alessia Bagattin, Clément Nguyen, William Baron, Martine Burtin, Mélanie Broueilh, Laurence Heidet, Géraldine Mollet, Anne Druilhe, Corinne Antignac, Bertrand Knebelmann, Gérard Friedlander, Frank Bienaimé, Morgan Gallazzini, Fabiola Terzi
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016)
Proteinuria promotes chronic kidney disease progression. Karoui et al. show that proteinuria stimulates overexpression of iron transporting protein lipocalin-2 via Ca2+release-induced ER stress, which leads to tubular apoptosis, and that inhibition o
Externí odkaz:
https://doaj.org/article/84d6beb4c2bc4aa9bafacf3ebe31468b
Autor:
Amandine Viau, Gerd Walz, Esben Lorentzen, Heike Janusch, Athina Ganner, Fruzsina Kotsis, Albrecht Kramer-Zucker, Christopher Boehlke, Roland Nitschke, Daniel Epting, Yujie Li, Elke Neumann-Haefelin, E. Wolfgang Kuehn
Publikováno v:
Kotsis, F, Janusch, H, Li, Y, Viau, A, Epting, D, Kramer-Zucker, A, Walz, G, Nitschke, R, Lorentzen, E, Ganner, A, Neumann-Haefelin, E, Kuehn, E W & Boehlke, C 2021, ' Ift88, but not Kif3a, is required for establishment of the periciliary membrane compartment ', Biochemical and Biophysical Research Communications, vol. 584, pp. 19-25 . https://doi.org/10.1016/j.bbrc.2021.10.075
The primary cilium is a sensory organelle at the cell surface with integral functions in cell signaling. It contains a microtubular axoneme that is rooted in the basal body (BB) and serves as a scaffold for the movement of intraflagellar transport (I
Autor:
Roman Pichler, Ludovica Rizzo, Kevin Tröndle, Michaela Bühler, Hanna Brucker, Anna-Lena Müller, Kelli Grand, Silvia Farè, Amandine Viau, Michael M. Kaminski, E. Wolfgang Kuehn, Fritz Koch, Stefan Zimmermann, Peter Koltay, Soeren S. Lienkamp
Publikováno v:
Biomaterials. 291
Renal tubular cells frequently lose differentiation markers and physiological properties when propagated in conventional cell culture conditions. Embedding cells in 3D microenvironments or controlling their 3D assembly by bioprinting can enhance thei
Publikováno v:
The FASEB Journal. 36
Autor:
Hugo, Garcia, Alice S, Serafin, Flora, Silbermann, Esther, Porée, Amandine, Viau, Clémentine, Mahaut, Katy, Billot, Éléonore, Birgy, Meriem, Garfa-Traore, Stéphanie, Roy, Salomé, Ceccarelli, Manon, Mehraz, Pamela C, Rodriguez, Bérangère, Deleglise, Laetitia, Furio, Fabienne, Jabot-Hanin, Nicolas, Cagnard, Elaine, Del Nery, Marc, Fila, Soraya, Sin-Monnot, Corinne, Antignac, Stanislas, Lyonnet, Pauline, Krug, Rémi, Salomon, Jean-Philippe, Annereau, Alexandre, Benmerah, Marion, Delous, Luis, Briseño-Roa, Sophie, Saunier
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(18)
Nephronophthisis (NPH) is an autosomal recessive tubulointerstitial nephropathy belonging to the ciliopathy disorders and known as the most common cause of hereditary end-stage renal disease in children. Yet, no curative treatment is available. The m
Autor:
E. Wolfgang Kuehn, Amandine Viau, Alexis Hofherr, Tilman Busch, Anusha Venkatraman, Lukas Peintner, Christoph Borner, Alexander Voronov, Astrid Waeldin, Michael Köttgen
Publikováno v:
Autophagy
Mutations in the PKD1 gene result in autosomal dominant polycystic kidney disease (ADPKD), the most common monogenetic cause of end-stage renal disease (ESRD) in humans. Previous reports suggested that PKD1, together with PKD2/polycystin-2, may funct
Autor:
Hugo Garcia, Alice Serafin, Flora Silbermann, Esther Poree, Clémentine Mahaut, Amandine Viau, Katy Billot, Éléonore Birgy, Meriem Garfa-Traore, Stéphanie Roy, Salomé Cecarelli, Manon Mehraz, Pamela C. Rodriguez, Bérangère Deleglise, Laetitia Furio, Fabienne Jabot-Hanin, Nicolas Cagnard, Elaine Del Nery, Marc Fila, Soraya Sin-Monnot, Corinne Antignac, Stanislas Lyonnet, Pauline Krug, Rémi Salomon, Jean-Philippe Annereau, Alexandre Benmerah, Marion Delous, Luis Briseño-Roa, Sophie Saunier
SummaryNephronophthisis (NPH) is an autosomal recessive tubulointerstitial nephropathy belonging to the ciliopathy disorders and known as the most common cause of hereditary end-stage renal disease in children. Yet, no curative treatment is available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1220b1f23a9be5c30f8c38126be9b93f
https://doi.org/10.1101/2022.01.21.477191
https://doi.org/10.1101/2022.01.21.477191