2026
preprint
OpenAlex
Amandine Aka, Joran Martin, Fanny Kopp, Teresa Bulfone et autres
ABSTRACT The primary cilium is a microtubule-based sensory organelle projecting from the plasma membrane of most mammalian cells. Genetic defects in ciliary components cause chronic kidney disease (CKD) characterized by heightened production of inflammatory and fibrogenic mediators by tubular epithelial cells. Yet, …
fr, de, us
(code pays fourni par la source)
2026
article
OpenAlex
Gilles R. Codo, Pauline Duchatelet, Gemma Martinez-Rivas, Alessio Lampis et autres
Unlike in humans, where apolipoprotein A-II amyloidosis (AApoAII) is a rare hereditary form, AApoAII is common in mice and considered as the most frequent amyloidosis type in aged animals. Especial...
fr
(code pays fourni par la source)
Accès ouvert
2026
article
OpenAlex
Nicolas Pautrat, Quentin Raimbourg, Camille Cohen
A 70-year-old man, originally from Cape Verde, residing in France since 2020 with frequent return visits, presented with fatigue, unintentional weight loss (15 kg over the past year), and a recent onset of febrile pancytopenia. Physical examination was unremarkable, with no evidence …
fr
(code pays fourni par la source)
2025
article
OpenAlex
Martin Nicol, Camille Cohen, Alexis Talbot, Mathilde Baudet et autres
Randall disease is characterized by organ’s deposits of immunoglobulin light chains due to a clonal plasma accumulation secreting monoclonal immunoglobulin chains. In Randall disease, immunoglobuli...
fr
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Accès ouvert
2025
article
OpenAlex
Samuel D. Chauvin, Anne Coutrot, Camille Cohen
enable us to identify signatures of senescence beyond histology, and potentially, without the need for invasive tissue sampling.soon join the ranks of specialties poised to benefit from senescence-directed precision medicine.
fr
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Accès ouvert
2025
article
OpenAlex
Caroline Abadie, Aldja Abderrahmane, Ouarda Abdous, Carine Abel et autres
Integrating genomic medicine into healthcare systems is a health policy challenge that requires continuously transferring scientific advances into clinics and ensuring equal access for patients. France was one of the first countries to integrate genome sequencing into clinical practice at a nationwide …
2024
article
OpenAlex
Noémie Senot, Jean Baptiste Gibier, Marion Rabant, Emmanuel Estève et autres
BACKGROUND: Kidney involvement, along with cardiac disease, is the most frequent manifestation of systemic AL amyloidosis, usually resulting in nephrotic-range proteinuria. Rarely, deposits predominantly or exclusively affect the intrarenal arterioles or arteries, with these vascular-limited forms following a distinct clinical course, but …
fr
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Accès ouvert
2024
conference-abstract
OpenAlex
Daren Yabi, Pierre-Édouard Debureaux, Zoé Van de Wyngaert, Pauline Caillard et autres
Introduction: Renal impairment is common during multiple myeloma (MM) and persistent reduction in kidney function strongly affects long term prognosis. Light chain cast nephropathy (LCCN) is the main mechanism involved in MM renal injury. With typical presentation (acute kidney injury with predominant …
fr
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Accès ouvert
2024
article
OpenAlex
Marie-Camille Lafargue, Jean–Paul Duong Van Huyen, Helmut G. Rennke, Marie Essig et autres
Introduction: The objective of this study was to describe kidney involvement in patients with myelodysplastic syndromes (MDS), their treatments, and outcomes. Methods: We conducted a multicenter retrospective study in seven centers, identifying MDS patients with acute kidney injury (AKI), chronic kidney disease …
fr, us
(code pays fourni par la source)
2024
preprint
OpenAlex
Simon Roubille, Tristan Escure, Franceline Juillard, Armelle Corpet et autres
Abstract Herpes simplex virus 1 (HSV-1) latently infected neurons show multiple patterns in the distribution of the viral genomes within the nucleus, at least in mouse models. One of the major patterns is characterized by the presence of quiescent HSV-1 genomes trapped …
fr, ca, pt
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Manal Mazloum, Brice Lapin, Amandine Viau, Rushdi Alghamdi et autres
Abstract Autosomal dominant polycystic kidney disease (ADPKD), which affects around 4 million patients worldwide, is characterized by the formation of multiple tubule derived cysts, which grossly enlarge both kidneys and progressively compromise renal function. ADPKD mainly results from mutations in PKD1 , …
fr, sa, de
(code pays fourni par la source)
2024
other
OpenAlex
Christophe Sirac, Gemma Martinez-Rivas, BENDER Sébastien, Camille Cohen