Search Results - "Durussel, Fanny"

Loss of Ecrg4 improves calcium oxalate nephropathy by Daniela Cabuzu, Suresh K. Ramakrishnan, Matthias B. Moor, Dusan Harmacek, Muriel Auberson, Fanny Durussel, Olivier Bonny

“…Kidney stone is one of the most frequent urinary tract diseases, affecting 10% of the population and displaying a high recurrence rate. Kidney stones are the…”
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Multiomics reveals multilevel control of renal and systemic metabolism by the renal tubular circadian clock by Bignon, Yohan, Wigger, Leonore, Ansermet, Camille, Weger, Benjamin D, Lagarrigue, Sylviane, Centeno, Gabriel, Durussel, Fanny, Götz, Lou, Ibberson, Mark, Pradervand, Sylvain, Quadroni, Manfredo, Weger, Meltem, Amati, Francesca, Gachon, Frédéric, Firsov, Dmitri

“…Circadian rhythmicity in renal function suggests rhythmic adaptations in renal metabolism. To decipher the role of the circadian clock in renal metabolism, we…”
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Loss of Ecrg4 improves calcium oxalate nephropathy by Cabuzu, Daniela, Ramakrishnan, Suresh K, Moor, Matthias B, Harmacek, Dusan, Auberson, Muriel, Durussel, Fanny, Bonny, Olivier

“…Kidney stone is one of the most frequent urinary tract diseases, affecting 10% of the population and displaying a high recurrence rate. Kidney stones are the…”
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Renal FGF23 signaling depends on redox protein Memo1 and promotes orthovanadate-sensitive protein phosphotyrosyl phosphatase activity by Bartos, Katalin, Ramakrishnan, Suresh Krishna, Braga-Lagache, Sophie, Hänzi, Barbara, Durussel, Fanny, Prakash Sridharan, Arjun, Zhu, Yao, Sheehan, David, Hynes, Nancy E., Bonny, Olivier, Moor, Matthias B.

“…Memo1 deletion in mice causes premature aging and an unbalanced metabolism partially resembling Fgf23 and Klotho loss-of-function animals. We report a role for…”
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A novel transgenic mouse model highlights molecular disruptions involved in the pathogenesis of Dent disease 1 by Sakhi, Imene Bouchra, De Combiens, Elise, Frachon, Nadia, Durussel, Fanny, Brideau, Gaelle, Nemazanyy, Ivan, Frère, Perrine, Thévenod, Frank, Lee, Wing-Kee, Zeng, Qinghe, Klein, Christophe, Lourdel, Stéphane, Bignon, Yohan

“…[Display omitted] •Dent disease type 1 (DD1) is a rare inherited disorder induced by Clcn5 mutations.•We generated a clinically relevant DD1 transgenic mouse…”
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Redox-Dependent Bone Alkaline Phosphatase Dysfunction Drives Part of the Complex Bone Phenotype in Mice Deficient for Memo1 by Moor, Matthias B, Ramakrishnan, Suresh K, Legrand, Finola, Dolder, Silvia, Siegrist, Mark, Durussel, Fanny, Centeno, Gabriel, Firsov, Dmitri, Hynes, Nancy E, Hofstetter, Willy, Bonny, Olivier

“…Mediator of ErbB2-driven cell Motility 1 (MEMO1) is an intracellular redox protein that integrates growth factors signaling with the intracellular redox state…”
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