Zobrazeno 1 - 10
of 75
pro vyhledávání: '"polycystin deficiency"'
Autor:
Lorthioir, Aurélien, Joannidès, Robinson, Rémy-Jouet, Isabelle, Fréguin-Bouilland, Caroline, Iacob, Michèle, Roche, Clothilde, Monteil, Christelle, Lucas, Danièle, Renet, Sylvanie, Audrézet, Marie-Pierre, Godin, Michel, Richard, Vincent, Thuillez, Christian, Guerrot, Dominique, Bellien, Jérémy *
Publikováno v:
In Kidney International February 2015 87(2):465-472
Autor:
A. Lorthioir, R. Joannidès, I. Rémy-Jouet, C. Fréguin-Bouilland, M. Iacob, C. Monteil, D. Lucas, M.P. Audrezet, D. Guerrot, V. Richard, C. Thuillez, M. Godin, J. Bellien
Publikováno v:
Artery Research, Vol 7, Iss 10 (2013)
Objectives: Autosomal dominant polycystic kidney disease (ADPKD) is due to mutations in genes PKD1 and PKD2 encoding polycystin-1 and -2, which transduce flow variations into cellular signals in the renal epithelium but also in vascular endothelium.
Externí odkaz:
https://doaj.org/article/cb2a46650cc145418a9d5407a85393e6
Autor:
M.-P. Audrézet, Danièle Lucas, Michel Godin, Christelle Monteil, Christian Thuillez, Aurelien Lorthioir, Vincent Richard, Sylvanie Renet, Robinson Joannides, Clothilde Roche, Dominique Guerrot, Isabelle Remy-Jouet, Caroline Freguin-Bouilland, Michele Iacob, Jeremy Bellien
Publikováno v:
Kidney International
Kidney International, Nature Publishing Group, 2015, 87 (2), pp.465-472. ⟨10.1038/ki.2014.241⟩
Kidney International, Nature Publishing Group, 2015, 87 (2), pp.465-472. ⟨10.1038/ki.2014.241⟩
International audience; Autosomal dominant polycystic kidney disease (ADPKD) is a renal hereditary disorder associated with increased cardiovascular mortality, due to mutations in polycystin-1 and polycystin-2 genes. Endothelial polycystin-deficient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa7fc7b86483e05725642939d3399bba
https://www.hal.inserm.fr/inserm-02296634/document
https://www.hal.inserm.fr/inserm-02296634/document
Autor:
Lorthioir, A., Joannidès, R., Rémy-Jouet, I., Fréguin-Bouilland, C., Iacob, M., Monteil, C., Lucas, D., Audrezet, M.P., Guerrot, D., Richard, V., Thuillez, C., Godin, M., Bellien, J.
Publikováno v:
In Artery Research September 2013 7(3-4):136-137
Autor:
Jeremy Bellien, Isabelle Remy-Jouet, Michele Iacob, Aurélien Lorthioir, Christelle Monteil, Danièle Lucas, Michel Godin, Christian Thuillez, C. Freguin-Bouilland, M.P. Audrezet, Dominique Guerrot, Robinson Joannides, Vincent Richard
Publikováno v:
Artery Research, Vol 7, Iss 10 (2013)
Objectives: Autosomal dominant polycystic kidney disease (ADPKD) is due to mutations in genes PKD1 and PKD2 encoding polycystin-1 and -2, which transduce flow variations into cellular signals in the renal epithelium but also in vascular endothelium.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c6bf417155b468acfbdffbfe7782329
https://doi.org/10.1016/j.artres.2013.10.124
https://doi.org/10.1016/j.artres.2013.10.124
Autor:
Dumont, Audrey 1, 2, 3, Hamzaoui, Mouad 4, Groussard, Déborah 1, Iacob, Michèle 2, Bertrand, Dominique 4, Remy-Jouet, Isabelle 1, Hanoy, Mélanie 4, Le Roy, Frank 4, Chevalier, Laurence 5, Enzensperger, Christoph 6, Arndt, Hans-Dieter 6, Renet, Sylvanie 1, Dumesnil, Anaïs 1, Lévêque, Emilie 7, Duflot, Thomas 1, 2, Brunel, Valéry 8, Michel-Després, Aurore 9, Audrézet, Marie-Pierre 9, Richard, Vincent 2, 3, Joannidès, Robinson 1, 2, Guerrot, Dominique 1, 3, 4, Bellien, Jérémy 1, 2, 3, ∗
Publikováno v:
In Kidney International December 2024 106(6):1158-1169
Autor:
Schellekens, Pieter1,2 Pieter.schellekens@uzleuven.be, Roosens, Willem3, Meyts, Isabelle4,5, Vennekens, Rudi6, Bammens, Bert1,2, Mekahli, Djalila3,7
Publikováno v:
Pediatric Nephrology. Nov2021, Vol. 36 Issue 11, p3505-3514. 10p. 2 Diagrams, 1 Chart.
Publikováno v:
Clinical Kidney Journal
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Cardiovascular (CV) complications are the major cause of death in autosomal-dominant polycystic kidney disease (ADPKD) patients. Hypertension is common in these patients even before the onset of renal insufficiency. Blood pressure (BP) elevation is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::bfea01abd3643920b414b9095bb961da
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10665
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10665
Autor:
Raina, Rupesh1,2 rraina@akronchildrens.org, Shah, Raghav1, Hong, Gordon3, Bhatt, Girish C.4, Abboud, Brian3, Jain, Rohit1, Chanchlani, Rahul5, Sethi, Siddharth Kumar6
Publikováno v:
Pediatric Nephrology. Sep2023, Vol. 38 Issue 9, p2957-2972. 16p. 2 Diagrams, 10 Charts, 5 Graphs.
Autor:
Sagar, Priyanka S.1,2 (AUTHOR), Munt, Alexandra1,2 (AUTHOR), Saravanabavan, Sayanthooran1,2 (AUTHOR), Vahedi, Farnoosh Asghar1,2 (AUTHOR), Elhindi, James3 (AUTHOR), Nguyen, Beatrice1 (AUTHOR), Chau, Katrina4,5 (AUTHOR), Harris, David C.1,2 (AUTHOR), Lee, Vincent2,6 (AUTHOR), Sud, Kamal6,7 (AUTHOR), Wong, Nikki6,7 (AUTHOR), Rangan, Gopala K.1,2 (AUTHOR) g.rangan@sydney.edu.au
Publikováno v:
Trials. 7/29/2023, Vol. 24 Issue 1, p1-12. 12p. 2 Diagrams, 1 Chart.