Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Marie-Françoise Arthus"'
Autor:
Pierre Bissonnette, Yoann Lussier, Jessica Matar, Alexandre Leduc‐Nadeau, Sandra Da Cal, Marie‐Françoise Arthus, Robert J. Unwin, Julia Steinke, Dharshan Rangaswamy, Daniel G. Bichet
Publikováno v:
Physiological Reports, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Aquaporin‐2 (AQP2) is a homotetrameric water channel responsible for the final water reuptake in the kidney. Disease‐causing AQP2 mutations induce nephrogenic diabetes insipidus (NDI), a condition that challenges the bodily water balance
Externí odkaz:
https://doaj.org/article/aa0c019621244c8c983c7ae83b1bb46e
Autor:
Michel Boutin, Pamela Lavoie, Iskren Menkovic, Amanda Toupin, Mona Abaoui, Maha Elidrissi-Elawad, Marie-Françoise Arthus, Carole Fortier, Claudia Ménard, Bruno Maranda, Daniel G. Bichet, Christiane Auray-Blais
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 17, p 6114 (2020)
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the GLA gene encoding the α-galactosidase A enzyme. This enzyme cleaves the last sugar unit of glycosphingolipids, including globotriaosylceramide (Gb3), globotriaosylsph
Externí odkaz:
https://doaj.org/article/fc8aa000ac284c6f90cac01d6cf85e64
Autor:
Marie Françoise Arthus, Sandra Da Cal, Alexandre Leduc-Nadeau, Daniel G. Bichet, Jessica Matar, Julia Steinke, Robert J. Unwin, Yoann Lussier, Dharshan Rangaswamy, Pierre Bissonnette
Publikováno v:
Physiological Reports
Physiological Reports, Vol 9, Iss 11, Pp n/a-n/a (2021)
Physiological Reports, Vol 9, Iss 11, Pp n/a-n/a (2021)
Aquaporin‐2 (AQP2) is a homotetrameric water channel responsible for the final water reuptake in the kidney. Disease‐causing AQP2 mutations induce nephrogenic diabetes insipidus (NDI), a condition that challenges the bodily water balance by produ
Autor:
Pamela Lavoie, Mona Abaoui, Daniel G. Bichet, Marie-Françoise Arthus, Michel Boutin, Claudia Ménard, Amanda Toupin, Bruno Maranda, Christiane Auray-Blais, Maha Elidrissi-Elawad, Carole Fortier, Iskren Menkovic
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 6114, p 6114 (2020)
Volume 21
Issue 17
International Journal of Molecular Sciences, Vol 21, Iss 6114, p 6114 (2020)
Volume 21
Issue 17
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the GLA gene encoding the &alpha
galactosidase A enzyme. This enzyme cleaves the last sugar unit of glycosphingolipids, including globotriaosylceramide (Gb3), globotr
galactosidase A enzyme. This enzyme cleaves the last sugar unit of glycosphingolipids, including globotriaosylceramide (Gb3), globotr
Autor:
Kaye LeMoine, Syed Wasim, Marie-Françoise Arthus, Michael West, Robin H. Lachmann, Larry D. Lynd, Daniel G. Bichet, Cheryl Rockman-Greenberg, Sandra Sirrs, Carla E. M. Hollak, Chantal F. Morel
Publikováno v:
Value in health, 24(2), 268-273. Elsevier Limited
Objectives Orphan medicinal products (OMPs) often receive market authorization under conditions imposed by regulators for ongoing postauthorization surveillance (PAS) to answer questions that remain at the time of market entry. This surveillance may
Autor:
Michel Boutin, Marie-Françoise Arthus, Pamela Lavoie, Carole Fortier, Christiane Auray-Blais, Mona Abaoui, Daniel G. Bichet, Claudia Ménard, Amanda Toupin
Publikováno v:
Analytica Chimica Acta. 1015:35-49
Fabry disease is an X-linked lysosomal storage disorder with marked variability in the phenotype and genotype. Glycosphingolipids such as globotriaosylceramide (Gb3) isoforms/analogs, globotriaosylsphingosine (lyso-Gb3) and analogs, and galabiosylcer
Autor:
Marie-Françoise Arthus, Wesley Hayes, Daniela Iancu, Daniel G. Bichet, Emma Ashton, Sonia Sharma, Robert Kleta, Detlef Bockenhauer, William van’t Hoff
Publikováno v:
Clinical Kidney Journal
Background Inherited nephrogenic diabetes insipidus (NDI) is a rare disorder characterized by impaired urinary concentrating ability. Little clinical data on long-term outcome exists. Method This was a single-centre retrospective medical record revie
Autor:
Marie-Françoise Arthus, Lise Bankir, Daniel G. Bichet, Sofia Enhörning, Dorinne Desposito, Olle Melander, Ronan Roussel, Catherine Chollet, Valérie Paradis, Christophe Magnan, Christopher Taveau, Isabelle Hainault, Nadine Bouby, Ludovic Waeckel, Erwann Philippe, Gilberto Velho, Fabienne Foufelle
Publikováno v:
Diabetologia. 58:1081-1090
High plasma copeptin, a marker of vasopressin (VP) secretion, has been shown to be associated with the metabolic syndrome and development of type 2 diabetes in humans. The present study was designed to determine the long-term influence of plasma VP c
Autor:
Amanda, Toupin, Pamela, Lavoie, Marie-Françoise, Arthus, Mona, Abaoui, Michel, Boutin, Carole, Fortier, Claudia, Ménard, Daniel G, Bichet, Christiane, Auray-Blais
Publikováno v:
Analytica chimica acta. 1015
Fabry disease is an X-linked lysosomal storage disorder with marked variability in the phenotype and genotype. Glycosphingolipids such as globotriaosylceramide (Gb
Autor:
Alexandre Leduc-Nadeau, Daniel G. Bichet, Jean-Yves Lapointe, Michèle Lonergan, Anatoly Tiulpakov, Yoann Lussier, Rafael Bedoya Perez, Marie-Françoise Arthus, Cécile Guyon, Pierre Bissonnette
Publikováno v:
American Journal of Physiology-Renal Physiology. 297:F489-F498
Aquaporin-2 (AQP2) is a water channel responsible for the final water reabsorption in renal collecting ducts. Alterations in AQP2 function induce nephrogenic diabetes insipidus (NDI), a condition characterized by severe polyuria and polydipsia. Three