Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Kai Olaf Netzer"'
Autor:
Sebastian Toncar, Thomas Schmiedeke, Thomas Vogl, Nils Pollak, Michael Leidig, Beatrix Büschges-Seraphin, Marianne Kleinert, Cord Schneuzer, Christina Klaeffling, Clemens Grupp, Christoph Blaser, Susanne Berweck, Rüdiger Götz, Stefan Fischer, Andreas Schmitt, Bettina Wirth, Frank Breunig, Markus Ketteler, Hendrick Witsch, Frank Strutz, Uwe Malzahn, Oliver Jung, Markus Schneider, Julian Gebhardt, Jan Goßmann, Mohamed Marwan, Holger Naujoks, Mara Dörken, L. Schramm, Ewelina Sobkowiak, Michael Heckel, Joanna Harazny, Arnfried Klingbeil, J Zimmermann, Maria Moritz, Heribert Fink, Raoul Zeltner, Patrick Biggar, Rolf Janka, Ahmet Cakmak, Stefan Büttner, Christoph Betz, Fabian Hammer, Heike Schneider, Sarah Rudolf, Beate Schamberger, Imke Reimer, Claudius Kleinert, Michael Brunner, Sabine Schütterle, Susanne Schwedler, Vera Krane, Thorsten Klink, Sophie Richter, Christian Ritter, Markus Schöffauer, Tilo Freiwald, Helmut Geiger, Ulrike Raff, Benjamin-Florian Koch, Renate Hammerstingl, Thomas Bochannek, Joachim Hoyer, Wolfgang Freisinger, Paul Würmell, Daniel Sollinger, Vladimir Vasiljuk, Michael Schmid, Clemens Reichert, Jens Lutz, Stefan Störk, Reinhard Schneider, Andrea Heyd-Schramm, Thomas Döltz, Brigitte Moye, Kai-Olaf Netzer, Kai-Uwe Eckardt, Jurij Ribel, Christoph Wanner, Julian Donhauser, Thorsten Walther, Julia Weinmann-Menke, Judith Kosowski
Publikováno v:
Kidney International. 95:983-991
Mineralocorticoid receptor antagonists have beneficial effects on left ventricular remodeling, cardiac fibrosis, and arrhythmia in heart failure, but efficacy and safety in dialysis patients is less clear. We evaluated the effect of spironolactone on
Type IV collagen alpha1-alpha6 chains have important roles in the assembly of basement membranes and are implicated in the pathogenesis of Goodpasture syndrome, an autoimmune disorder, and Alport syndrome, a hereditary renal disease. We report compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ca5d16f139e8d54fe680112d2018db2
https://ora.ox.ac.uk/objects/uuid:dac858b5-4e91-47ae-955a-97b548817dc1
https://ora.ox.ac.uk/objects/uuid:dac858b5-4e91-47ae-955a-97b548817dc1
Publikováno v:
Nephrology Dialysis Transplantation. 17:1218-1227
Background. Alport syndrome (AS) is a hereditary nephropathy characterized by progressive renal failure, hearing loss and ocular lesions. Numerous mutations of the COL4A5 gene encoding the a5-chain of type IV collagen have been described, establishin
Autor:
Hermann Haller, Jan T. Kielstein, Manfred Weber, Kai-Olaf Netzer, Udo Helmchen, Jürgen Floege
Publikováno v:
Nephrology Dialysis Transplantation. 16:2082-2085
chain of type IV collagen isthe pathogenetic basis for the development of anti-glomerular basement membrane (GBM) disease. InGoodpasture’s syndrome clinical involvement ofboth kidneys and lungs is present. In rare cases anassociation of Goodpasture
Autor:
Sripad Gunwar, Milton E. Noelken, Billy G. Hudson, Olga Bondar, Kai-Olaf Netzer, Yoshifumi Ninomiya, Yoshikazu Sado, Dorin-Bogdan Borza, Narinder Singh, Ariel Boutaud
Publikováno v:
Journal of Biological Chemistry. 275:30716-30724
The ultrafiltration function of the glomerular basement membrane (GBM) of the kidney is impaired in genetic and acquired diseases that affect type IV collagen. The GBM is composed of five (alpha1 to alpha5) of the six chains of type IV collagen, orga
Autor:
Oliver Gross, B. Ermisch, Matthias Brandis, L. B. Zimmerhackl, Kai-Olaf Netzer, Manfred Weber
Publikováno v:
Pediatric Nephrology. 14:758-761
Alport syndrome (AS) is a genetic disorder of basement membranes caused by mutations in type IV collagen genes that is characterized by chronic hematuria and progressive nephropathy leading to renal failure. The main extrarenal features include senso
Autor:
Anu Leinonen, Juan Saus, Dorin-Bogdan Borza, Parvin Todd, Kai-Olaf Netzer, Billy G. Hudson, Javier Cervera
Publikováno v:
Journal of Biological Chemistry. 275:6030-6037
Goodpasture (GP) disease is an autoimmune disorder in which autoantibodies against the α3(IV) chain of type IV collagen bind to the glomerular and alveolar basement membranes, causing progressive glomerulonephritis and pulmonary hemorrhage. Two majo
Autor:
Jan P. M. Langeveld, Anu Leinonen, Ariel Boutaud, Parvin Todd, Kai-Olaf Netzer, Dorin-Bogdan Borza, Sripad Gunwar, Billy G. Hudson
Publikováno v:
Journal of Biological Chemistry. 274:11267-11274
The Goodpasture (GP) autoantigen has been identified as the alpha3(IV) collagen chain, one of six homologous chains designated alpha1-alpha6 that comprise type IV collagen (Hudson, B. G., Reeders, S. T., and Tryggvason, K. (1993) J. Biol. Chem. 268,
Publikováno v:
Kidney International. 55:926-935
Goodpasture antigen: Expression of the full-length α3(IV) chain of collagen IV and localization of epitopes exclusively to the noncollagenous domain. Background Tissue injury in Goodpasture (GP) syndrome (rapidly progressive glomerular nephritis and
Autor:
Raghuram Kalluri, Eric G. Neilson, Kai Olaf Netzer, Manfred Weber, Mae Jane Sun, Billy G. Hudson
Publikováno v:
Kidney International. 45:721-726
Mutations in the COL4A5 gene encoding the alpha 5(IV) chain of type IV collagen have been implicated as the primary defect in X-linked Alport syndrome. Several kinds of mutations have been reported so far, spanning point mutations to complete gene de