Výsledky vyhledávání - "Camille Fédou"

Akademický článek

Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease

Autor: Camille Fédou, Benjamin Breuil, Igor Golovko, Stéphane Decramer, Pedro Magalhães, Françoise Muller, Sophie Dreux, Petra Zürbig, Julie Klein, Joost P. Schanstra, Bénédicte Buffin-Meyer

Publikováno v: Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)

Abstract Production of amniotic fluid (AF) is view as predominately driven by excretion of fetal urine (FU). However, the origin of AF peptides, often considered as potential biomarkers of developmental diseases, has never been investigated. Here, we

Externí odkaz: https://doaj.org/article/428622a5f2e3402e83de58ba284e7d13

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Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrity

Publikováno v: Journal of Pathology
Journal of Pathology, Wiley, In press, Online ahead of print. ⟨10.1002/path.5703⟩
Journal of Pathology, Wiley, 2021, ⟨10.1002/path.5703⟩
Journal of Pathology, In press, Online ahead of print. ⟨10.1002/path.5703⟩

International audience; Congenital anomalies of the kidney and the urinary tract (CAKUT) are the first cause of chronic kidney disease in childhood. Several genetic and environmental origins are associated with CAKUT, but most pathogenic pathways rem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3609f57c547f85c357ebfbf85c2b8412
https://www.hal.inserm.fr/inserm-03268515

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The low affinity p75 neurotrophin receptor is down-regulated in congenital anomalies of the kidney and the urinary tract: Possible involvement in early nephrogenesis

Autor: Ophélie Lescat, Camille Fédou, Patrick Blader, Jean Sébastien Saulnier-Blache, Julie Klein, Joost P. Schanstra, Guylène Feuillet, Marie Buléon, Bénédicte Buffin-Meyer, Eric Neau, Stéphane Decramer, Julie Batut, Melinda Alves, Benjamin Breuil

Publikováno v: Biochemical and Biophysical Research Communications
Biochemical and Biophysical Research Communications, Elsevier, 2020, 533 (4), pp.786-791. ⟨10.1016/j.bbrc.2020.09.084⟩

Congenital Anomalies of the Kidney and of the Urinary Tract (CAKUT) cover a broad range of disorders including abnormal kidney development caused by defective nephrogenesis. Here we explored the possible involvement of the low affinity p75 neurotroph

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b0e1a9b326bbf1efe84ad6b62c3f51
https://hal.archives-ouvertes.fr/hal-03268519

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Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease

Autor: Romain Favre, Marie-Pierre Lavocat, Bernard Boudailliez, Charlotte Lucas, Camille Fédou, Jean-Sebastien Saulnier Blache, Anne-Sophie Weingertner, Blandine Hougas, Joost P. Schanstra, Pascal Gaucherand, Sylvie Cloarec, Julie Batut, Catherine Noel, J. Gondry, Philippe Eckart, Norbert Winer, Benjamin Breuil, Gérard Champion, Jean-Baptiste Benevent, Franck Perrotin, Christophe Vayssière, Florence Biquard, Harald Mischak, Gwenaelle Le Bouar, Jérôme Massardier, Françoise Conte Auriol, Pedro Magalhães, Sophie Martin, Jean-Paul Bory, Sophie Collardeau-Frachon, Eve Mousty, Lucie Bessenay, Corinne Floch, Julie Klein, Amelie Ryckewaert, Elisabeth Simon, Alain Martin, Guylène Bourdat-Michel, Marie-Françoise Froute, Franz Schaefer, Pascale Marcorelles, Stéphane Decramer, Nabila Moussaoui, Franck Boizard, Marie-Christine Manca-Pellissier, Mariannick Maupin-Hyvonnet, Marion Groussolles, Jean-Marie Delbosc, Guylène Feuillet, Anke Raaijmakers, François Nobili, Sophie Taque, Petra Zürbig, Vincent Guigonis, Audrey Casemayou, Patrick Blader, An Hindryckx, Luc Decatte, Karel Allegaert, Ophélie Lescat, Eric Neau, Odile Basmaison, Emma Allain-Launay, Agnes Sartor, Jean-Loup Bascands, Claudine Le Vaillant, Hélène Laurichesse Delmas, Bénédicte Buffin-Meyer, Nadia Lounis, Anne-Hélène Saliou, Véronique Baudouin, Elena Levtchenko, Maryse Fiorenza, Christine Pietrement, Valérie Goua, Marina Merveille, Laurent Bidat, Yves Aubard, Alexandra Benachi, Sylvie Kessler, Loic De Parscau, Jean-François Oury, Fabienne Prieur

Publikováno v: Kidney International
Kidney International, Nature Publishing Group, 2020, ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2020, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩

Although a rare disease, bilateral congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of end stage kidney disease in children. Ultrasound-based prenatal prediction of postnatal kidney survival in CAKUT pregnancies is f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d5ca47946f8c92399914c953f494aee
https://hal.archives-ouvertes.fr/hal-03063759

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Identification de la Plastine-3 comme nouvel acteur du développement rénal

Autor: Odile Burlet-Schiltz, Julie Klein, Bénédicte Buffin-Meyer, Ophélie Lescat, Stéphane Decramer, Jean-Sébastien Saulnier-Blache, Mylène Camus, Camille Fédou, J.P. Schanstra, Guylène Feuillet

Publikováno v: Néphrologie & Thérapeutique. 16:258

Introduction L’analyse omique de l’urine est consideree comme une biopsie liquide du rein qui a revolutionne la comprehension des maladies renales. Les malformations congenitales du rein et du tractus urinaire (CAKUT) sont des maladies genetiquem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::32df01c3fcaff149e6c4934b9c988808
https://doi.org/10.1016/j.nephro.2020.07.027

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