Zobrazeno 1 - 10
of 67
pro vyhledávání: 'Lüllmann-Rauch, Renate'
Autor:
Paul Saftig, Sönke Rudnik, Irm Hermans-Borgmeyer, Markus Glatzel, Thuy Linh Nguyen, Christian Bernreuther, Janna Schneppenheim, Bernd Schröder, Renate Lüllmann-Rauch
Publikováno v:
Oncotarget
// Thuy Linh Nguyen 1 , Janna Schneppenheim 2 , Sonke Rudnik 1 , Renate Lullmann-Rauch 2 , Christian Bernreuther 3 , Irm Hermans-Borgmeyer 4 , Markus Glatzel 3 , Paul Saftig 1 and Bernd Schroder 1 1 Biochemical Institute, Christian Albrechts Universi
Autor:
Gregor Martin, Radislav Sedlacek, Stefan Rose-John, Miryam Müller, R Barikbin, Sebastian Wetzel, Julia Köhn-Gaone, Olga Zbodakova, Renate Lüllmann-Rauch, Paul Saftig, Ivo Leuschner, Birte Wöhner, Gisa Tiegs, Juri Bergmann, Karel Chalupsky, Janina E.E. Tirnitz-Parker, Dirk Schmidt-Arras
Publikováno v:
Oncotarget
// Miryam Muller 1,* , Sebastian Wetzel 1,* , Julia Kohn-Gaone 2 , Karel Chalupsky 3 , Renate Lullmann-Rauch 4 , Roja Barikbin 5 , Juri Bergmann 1,6 , Birte Wohner 1 , Olga Zbodakova 3 , Ivo Leuschner 7 , Gregor Martin 3,9 , Gisa Tiegs 5 , Stefan Ros
Autor:
Renate Lüllmann-Rauch, Judith Blanz, Julia Mayerle, Ilya Gukovsky, Samuel W. French, Olga Vagin, Sudarshan R. Malla, Elmira Tokhtaeva, Iskandar Yakubov, Markus M. Lerch, Viola Oorschot, Matthias Sendler, Olga A. Mareninova, David W. Dawson, Judith Klumperman, Anna S. Gukovskaya
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology
Cellular and molecular gastroenterology and hepatology, vol 1, iss 6
ResearcherID
Cellular and Molecular Gastroenterology and Hepatology, Vol 1, Iss 6, Pp 678-694 (2015)
Cellular and molecular gastroenterology and hepatology, 1(6), 678. Elsevier Inc.
Cellular and molecular gastroenterology and hepatology, vol 1, iss 6
ResearcherID
Cellular and Molecular Gastroenterology and Hepatology, Vol 1, Iss 6, Pp 678-694 (2015)
Cellular and molecular gastroenterology and hepatology, 1(6), 678. Elsevier Inc.
Background & Aims: The pathogenic mechanism of pancreatitis is poorly understood. Recent evidence implicates defective autophagy in pancreatitis responses; however, the pathways mediating impaired autophagy in pancreas remain largely unknown. Here, w
PURPOSE. Retinal degeneration is a common feature of several lysosomal storage disorders, including the mucopolysaccharidoses, a group of metabolic disorders that is characterized by widespread accumulation of glycosaminoglycans due to lysosomal enzy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a899de0b25eb16d98389942cb29a949
https://pub.uni-bielefeld.de/record/2904124
https://pub.uni-bielefeld.de/record/2904124
Autor:
Rudi D'Hooge, Cecilia Weigelt, Volkmar Gieselmann, Claes Andersson, Carl Eistrup, Ulrich Matzner, Jens Fogh, Renate Lüllmann-Rauch, Stijn Stroobants
Publikováno v:
Molecular Therapy. 17(4):600-606
Inherited deficiencies of lysosomal hydrolases cause lysosomal storage diseases (LSDs) that are characterized by a progressive multisystemic pathology and premature death. Repeated intravenous injection of the active counterpart of the deficient enzy
Autor:
Hans Bockhardt, Renate Lüllmann-Rauch
Publikováno v:
Acta Pharmacologica et Toxicologica. 47:45-48
This study was aimed at the question of whether or not the antidepressant zimelidine, which is an amphiphilic cationic compound, can induce generalized lipidosis in animals. Rats were chronically treated with high oral doses (80 mg/kg) of the drug, a
Autor:
Stijn Stroobants, Paul Saftig, Renate Lüllmann-Rauch, Claes Andersson, Rudi D'Hooge, Meike Lüdemann, Jens Fogh, Willy Morelle, Judith Blanz, Helena Reuterwall, Jean Claude Michalski
Publikováno v:
Human Molecular Genetics. 17:3437-3445
Despite the progress in the treatment of lysosomal storage disorders (LSDs) mainly by enzyme replacement therapy, only limited success was reported in targeting the appropriate lysosomal enzyme into the brain. This prevents efficient clearance of neu
Autor:
Volkmar Gieselmann, Kerstin Khalaj Hedayati, Hariharasubramanian Ramakrishnan, Hans-Hilmar Goebel, Renate Lüllmann-Rauch, Simon Ngamli Fewou, Matthias Eckhardt, Carsten Wessig, Helena Maier
Publikováno v:
The Journal of Neuroscience. 27:9482-9490
Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder caused by the deficiency of arylsulfatase A (ASA). This results in accumulation of sulfated glycosphingolipids, mainly 3-O-sulfogalactosylceramide (sulfatide), in the nervous system a
Autor:
Ulrike Zimmermann, Eeva-Liisa Eskelinen, Paul Saftig, Michael Schwake, Renate Lüllmann-Rauch, Lukas Rüttiger, Cathrin Claussen, Jenny Schröder, Marlies Knipper
Publikováno v:
The Journal of Physiology. 576:73-86
Our previous studies revealed a critical role of the lysosomal membrane protein LIMP2 in the regulation of membrane transport processes in the endocytic pathway. Here we show that LIMP2-deficient mice display a progressive high-frequency hearing loss
Autor:
Peter Heimann, Thomas Dierks, Markus Damme, Steven U. Walkley, Tomo Sawada, Theresa Ortkras, Björn Kowalewski, Renate Lüllmann-Rauch
Publikováno v:
Human molecular genetics. 24(7)
Deficiency of arylsulfatase G (ARSG) leads to a lysosomal storage disease in mice resembling biochemical and pathological features of the mucopolysaccharidoses and particularly features of mucopolysaccharidosis type III (Sanfilippo syndrome). Here we