Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Sandra, Habbig"'
Autor:
Florian Erger, Deborah Nörling, Domenica Borchert, Esther Leenen, Sandra Habbig, Michael S. Wiesener, Malte P. Bartram, Andrea Wenzel, Christian Becker, Mohammad R. Toliat, Peter Nürnberg, Bodo B. Beck, Janine Altmüller
Publikováno v:
Genome Medicine, Vol 12, Iss 1, Pp 1-14 (2020)
Abstract Cell-free DNA (cfDNA) analysis has become essential in cancer diagnostics and prenatal testing. We present cfNOMe, a two-in-one method of measuring cfDNA cytosine methylation and nucleosome occupancy in a single assay using non-disruptive en
Externí odkaz:
https://doaj.org/article/bb52488d1ce849fc9f9bf985ae8ef595
Autor:
Rukshana Shroff, Aysun Bayazit, Constantinos J. Stefanidis, Varvara Askiti, Karolis Azukaitis, Nur Canpolat, Ayse Agbas, Ali Anarat, Bilal Aoun, Sevcan Bakkaloglu, Devina Bhowruth, Dagmara Borzych-Dużałka, Ipek Kaplan Bulut, Rainer Büscher, Claire Dempster, Ali Duzova, Sandra Habbig, Wesley Hayes, Shivram Hegde, Saoussen Krid, Christoph Licht, Mieczyslaw Litwin, Mark Mayes, Sevgi Mir, Rose Nemec, Lukasz Obrycki, Fabio Paglialonga, Stefano Picca, Bruno Ranchin, Charlotte Samaille, Mohan Shenoy, Manish Sinha, Colette Smith, Brankica Spasojevic, Enrico Vidal, Karel Vondrák, Alev Yilmaz, Ariane Zaloszyc, Michel Fischbach, Franz Schaefer, Claus Peter Schmitt
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Cardiovascular disease is prevalent in children on dialysis and accounts for almost 30% of all deaths. Randomised trials in adults suggest that haemodiafiltration (HDF) with high convection volumes is associated with reduced cardi
Externí odkaz:
https://doaj.org/article/300f2ede815f4448a33ee1186a0d9d0a
Autor:
Claudia Dafinger, Markus M. Rinschen, Lori Borgal, Carolin Ehrenberg, Sander G. Basten, Mareike Franke, Martin Höhne, Manfred Rauh, Heike Göbel, Wilhelm Bloch, F. Thomas Wunderlich, Dorien J. M. Peters, Dirk Tasche, Tripti Mishra, Sandra Habbig, Jörg Dötsch, Roman-Ulrich Müller, Jens C. Brüning, Thorsten Persigehl, Rachel H. Giles, Thomas Benzing, Bernhard Schermer, Max C. Liebau
Publikováno v:
Experimental and Molecular Medicine, Vol 50, Iss 6, Pp 1-17 (2018)
Cell cilia: Protein crucial for function identified A protein involved in building and maintaining thin protrusions from cell surfaces called cilia is implicated in “ciliopathies”, diseases in which ciliary function is disrupted. These include po
Externí odkaz:
https://doaj.org/article/8de13e7b325345b1995d5f539ec1dcfd
Autor:
Maximilian Stich, Veronica Di Cristanziano, Burkhard Tönshoff, Lutz Thorsten Weber, Jörg Dötsch, Marian Theodor Rammer, Susanne Rieger, Eva Heger, Sven F. Garbade, Kathrin Burgmaier, Louise Benning, Claudius Speer, Sandra Habbig, Sophie Haumann
Publikováno v:
Pediatric Nephrology. 38:1935-1948
Background Data on humoral immune response to standard COVID-19 vaccination are scarce in adolescent patients and lacking for children below 12 years of age with chronic kidney disease including kidney transplant recipients. Methods We therefore inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a224994804923666900dfc20a87c37c
https://doi.org/10.1007/s00467-022-05806-9
https://doi.org/10.1007/s00467-022-05806-9
Autor:
Markus, Schmidt, Sylvia, Stracke, Uwe, Schneider, Bettina, Kuschel, Thorsten, Feldkamp, Sandra, Habbig, Karoline, Mayer-Pickel, Andreas, Hartung, Birgit, Bader, Julia, Weinmann-Menke, Uwe, Korst, Frank, Vom Dorp, Ute Margaretha, Schäfer-Graf
Publikováno v:
Geburtshilfe Frauenheilkd
Aim As diagnostic and therapeutic options have improved in recent years, women with limited renal function of varying etiologies are now able to become pregnant. Depending on the extent of disease and the patientsʼ comorbidities, the care of these w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a43810a79f85ab3db5d0f708596a976d
https://doi.org/10.1055/a-1765-4157
https://doi.org/10.1055/a-1765-4157
Autor:
Fei Zhao, Sara Afonso, Susanne Lindner, Andrea Hartmann, Ina Löschmann, Bo Nilsson, Kristina N. Ekdahl, Lutz T. Weber, Sandra Habbig, Gesa Schalk, Michael Kirschfink, Peter F. Zipfel, Christine Skerka
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
C3 glomerulopathy (C3G) is a severe kidney disease, which is caused by defective regulation of the alternative complement pathway. Disease pathogenesis is heterogeneous and is caused by both autoimmune and genetic factors. Here we characterized IgG a
Externí odkaz:
https://doaj.org/article/5d550f1fe1af4ecaa888ba08162e924f
Autor:
Lioba Ester, Inês Cabrita, Michel Ventzke, Marita Christodoulou, Francesca Fabretti, Thomas Benzing, Sandra Habbig, Bernhard Schermer
BackgroundMutations in genes encoding nuclear pore proteins (NUPs) cause steroid-resistant nephrotic syndrome (SRNS) and focal and segmental glomerulosclerosis (FSGS). The mechanisms of how NUP deficiency may cause podocyte dysfunction and failure of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24c680373b1218855074bdd1cf40a474
https://doi.org/10.1101/2023.03.07.531564
https://doi.org/10.1101/2023.03.07.531564
Autor:
Sarina Kim Butzer, Sandra Habbig, Katrin Mehler, Sophie Haumann, Meike Meyer, Norma Jung, André Oberthür
Publikováno v:
Pediatric Infectious Disease Journal. 42:e61-e63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::110fcbe40d292c6441bf96208513a7bf
https://doi.org/10.1097/inf.0000000000003781
https://doi.org/10.1097/inf.0000000000003781
Publikováno v:
Der Nephrologe. 17:148-156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ff4035ca2218e49fa6bae36b5711d8b
https://doi.org/10.1007/s11560-021-00555-6
https://doi.org/10.1007/s11560-021-00555-6
Autor:
Jun Oh, Lars Pape, Rafael Schild, Jens König, Sandra Habbig, Martin Pohl, Stefanie Weber, Peter Hoyer
Publikováno v:
Nieren- und Hochdruckkrankheiten. 50:353-399
We present two cases of infants admitted with febrile COVID19 infection and developing atypical hemolytic uremic syndrome (aHUS) during the first week of hospitalization. aHUS is a rare disease due to uncontrolled activation of the complement system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33db7e8b3f70e6c992ca8d2cbc89e8c9
https://doi.org/10.5414/nhx02212
https://doi.org/10.5414/nhx02212