Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hermann Joseph Gröne"'
Autor:
Peter P. Nawroth, Norbert Gretz, Tjeerd P. Sijmonsma, Johannes Backs, Gernot Poschet, Adam J. Rose, Rüdiger Hell, Eva-Maria Weis, Sven W. Sauer, Ralf H. Adams, Hermann-Joseph Gröne, Jacqueline Taylor, Stefanie E. Herberich, Iris Moll, Jürgen G. Okun, Stephan Herzig, Lorenz H. Lehmann, Markus Jabs, Giuseppina Federico, Roland M. Schmid, Hellmut G. Augustin, Andreas Fischer, Minhong Yan, Carolin Mogler
Publikováno v:
Circulation 137, 2592-2608 (2018)
Background: Nutrients are transported through endothelial cells before being metabolized in muscle cells. However, little is known about the regulation of endothelial transport processes. Notch signaling is a critical regulator of metabolism and angi
Autor:
Hermann Joseph Gröne, Reinhardt Fünfstück, Martin Busch, J. Gerth, Christoph C. Haufe, Günter Stein, Undine Ott, Sperschneider H
Publikováno v:
Medizinische Klinik. 97:547-552
Hintergrund: Thrombotische Mikroangiopathien treten selten im Zusammenhang mit einer Schwangerschaft auf. Pathogenetisch bestehen Ahnlichkeiten mit dem HELLP-Syndrom und der schweren Eklampsie.
Autor:
John Williams, Keshwar Baboolal, Hermann Joseph Gröne, Ulf Janssen, Stephen Riley, Jürgen Floege, Aled O. Phillips, Robert Steadman
Publikováno v:
American Journal of Kidney Diseases. 37:400-410
The aim of the current study was to characterize the effects of prolonged hyperglycemia on renal structure and function using a model of non-insulin-dependent diabetes mellitus: the Goto Kakizaki (GK) rat, which does not have confounding variables, s
Autor:
Hermann Joseph Gröne, Matthew D. Breyer, Martin Kömhoff, Nikola Jeck, Hannsjörg W. Seyberth, Rolf M. Nüsing
Publikováno v:
Kidney International. 58:2420-2424
Cyclooxygenase-2 expression is associated with the renal macula densa of patients with Bartter-like syndrome. Background Bartter-like syndrome (BLS) is a heterogeneous set of congenital tubular disorders that is associated with significant renal salt
Autor:
Hermann Joseph Gröne, J Zimmermann, Kai Olaf Netzer, Christoph Wanner, Andreas Gal, Ekkehart Heidbreder, Kai Lopau, L. Schramm
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 43(3)
Lowe syndrome, or oculocerebrorenal syndrome of Lowe (OCRL), is a rare X-chromosomal disorder characterized by renal dysfunction, congenital cataract, and, in the majority of cases, mental retardation. Although gradual loss of renal function has been
Autor:
Jens, Gerth, Martin, Busch, Undine, Ott, Hermann Joseph, Gröne, Christoph C, Haufe, Reinhardt, Fünfstück, Heide, Sperschneider, Günter, Stein
Publikováno v:
Medizinische Klinik (Munich, Germany : 1983). 97(9)
Thrombotic microangiopathies are diseases rarely associated with pregnancy. The pathogenesis might be related to severe preeclampsia and HELLP syndrome.In May 2000, we saw a 26-year-old primigravida in the 39th gestational week with worsening anemia,
Autor:
Søren Nielsen, Melanie Peters, Stefanie Weber, Karl-Heinz Grzeschik, Lene N. Nejsum, Hartmut Engel, Hermann-Joseph Gröne, Hannsjörg W. Seyberth, Karl P. Schlingmann, Rolf M. Nüsing, Martin Konrad
Publikováno v:
Europe PubMed Central
Weber, S, Schlingmann, K P, Peters, M, Nejsum, L N, Nielsen, S, Engel, H, Grzeschik, K H, Seyberth, H W, Grone, H J, Nusing, R & Konrad, M 2001, ' Primary gene structure and expression studies of rodent paracellin-1 ' Journal of the American Society of Nephrology, vol. 12, pp. 2664-2672 .
Weber, S, Schlingmann, K P, Peters, M, Nejsum, L N, Nielsen, S, Engel, H, Grzeschik, K H, Seyberth, H W, Gröne, H J, Nüsing, R & Konrad, M 2001, ' Primary gene structure and expression studies of rodent paracellin-1 ', Journal of the American Society of Nephrology, vol. 12, no. 12, pp. 2664-72 .
Aarhus University
Weber, S, Schlingmann, K P, Peters, M, Nejsum, L N, Nielsen, S, Engel, H, Grzeschik, K H, Seyberth, H W, Grone, H J, Nusing, R & Konrad, M 2001, ' Primary gene structure and expression studies of rodent paracellin-1 ' Journal of the American Society of Nephrology, vol. 12, pp. 2664-2672 .
Weber, S, Schlingmann, K P, Peters, M, Nejsum, L N, Nielsen, S, Engel, H, Grzeschik, K H, Seyberth, H W, Gröne, H J, Nüsing, R & Konrad, M 2001, ' Primary gene structure and expression studies of rodent paracellin-1 ', Journal of the American Society of Nephrology, vol. 12, no. 12, pp. 2664-72 .
Aarhus University
The novel member of the claudin multigene family, paracellin-1/claudin-16, encoded by the gene PCLN1, is a renal tight junction protein that is involved in the paracellular transport of magnesium and calcium in the thick ascending limb of Henle's loo
Autor:
Hermann Joseph Gröne, Hiroshi Kawachi, Ferdinand H. Bahlmann, Karl M. Koch, Tammo Ostendorf, Jürgen Floege, Fujio Shimizu, Uta Kunter, Nebojsa Janjic
Publikováno v:
Journal of the American Society of Nephrology : JASN. 12(5)
Glomerular mesangial cell proliferation and/or mesangial matrix accumulation characterizes many progressive renal diseases. Rats with progressive mesangioproliferative glomerulonephritis were treated from day 3 to day 7 after disease induction with a
Autor:
Ulf Janssen, Jürgen Floege, Georg Brabant, Tammo Ostendorf, Hermann Joseph Gröne, Uta Kunter, Hartmut Schmidt, Terezila Machado Coimbra
Publikováno v:
Kidney international. 57(1)
Early events leading to renal injury in obese Zucker (fatty) rats with type II diabetes. Background More than half of the new patients admitted to dialysis therapy in some centers are diagnosed with type IIb diabetes, that is, diabetes associated wit
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology. 19(9)
Abstract —Endothelial cell proliferation and migration may play a central role in angiogenesis, wound healing, and atherosclerosis. Although CXC chemokines can act on endothelial cells by influencing proliferation, an involvement of CC chemokines a