Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Sabina Schmitt"'
Autor:
Georges P. Schmartz, Jacqueline Rehner, Madline P. Gund, Verena Keller, Leidy-Alejandra G. Molano, Stefan Rupf, Matthias Hannig, Tim Berger, Elias Flockerzi, Berthold Seitz, Sara Fleser, Sabina Schmitt-Grohé, Sandra Kalefack, Michael Zemlin, Michael Kunz, Felix Götzinger, Caroline Gevaerd, Thomas Vogt, Jörg Reichrath, Lisa Diehl, Anne Hecksteden, Tim Meyer, Christian Herr, Alexey Gurevich, Daniel Krug, Julian Hegemann, Kenan Bozhueyuek, Tobias A. M. Gulder, Chengzhang Fu, Christine Beemelmanns, Jörn M. Schattenberg, Olga V. Kalinina, Anouck Becker, Marcus Unger, Nicole Ludwig, Martina Seibert, Marie-Louise Stein, Nikolas Loka Hanna, Marie-Christin Martin, Felix Mahfoud, Marcin Krawczyk, Sören L. Becker, Rolf Müller, Robert Bals, Andreas Keller
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract The human microbiome emerges as a promising reservoir for diagnostic markers and therapeutics. Since host-associated microbiomes at various body sites differ and diseases do not occur in isolation, a comprehensive analysis strategy highlight
Externí odkaz:
https://doaj.org/article/ebb47b78b5394a2ca2f41acd3fc0cf2a
Autor:
Sivagurunathan Sutharsan, Stefanie Dillenhoefer, Matthias Welsner, Florian Stehling, Folke Brinkmann, Manuel Burkhart, Helmut Ellemunter, Anna-Maria Dittrich, Christina Smaczny, Olaf Eickmeier, Matthias Kappler, Carsten Schwarz, Sarah Sieber, Susanne Naehrig, Lutz Naehrlich, Klaus Tenbrock, Claus Pfannenstiel, Dirk Steffen, Jochen Meister, Britta Welzenbach, Anette Scharschinger, Markus Kratz, Maike Pincus, Tobias Tenenbaum, Mirjam Stahl, Kerstin Landwehr, Stefanie Dillenhöfer, Hans Kössel, Petra Kaiser, Manfred Käding, Simone Stolz, Stefan Blaas, Jutta Hammermann, Monika Gappa, Antje Schuster, Dana Spittel, Sabine Zirlik, Sabina Schmitt, Joachim Bargon, Malte Cremer, Sebastian Fähndrich, Andrea Heinzmann, Lutz Nährlich, Stefan Kuhnert, Sebastian Schmidt, Bettina Wollschläger, Anna Nolde, Inka Held, Wolfgang Kamin, Felix C. Ringshausen, Sabine Wege, Olaf Sommerburg, Norbert Geier, Sara Lisa Fleser, Heinrike Wilkens, Michael Lorenz, Paul Vöhringer, Martin Schebek, Christian Timke, Ingrid Bobis, Thomas Nüßlein, Doris Dieninghoff, Ernst Rietschel, Bastian Klinkhammer, Freerk Prenzel, Alexandra Wald, Axel Kempa, Eva Lücke, Ines Adams, Krystyna Poplawska, Simone Lehmkühler, Monika Bauck, Anne Pfülb, Rainald Fischer, Gudrun Schopper, Susanne Nährig, Matthias Griese, Jörg Grosse, Peter Küster, Birte KinderHolger Köster, Susanne Büsing, Margarethe Pohl, Andreas Artlich, Alexander Kiefer, Manfred Ballmann, Nikola Gjorgjevski, Markus A. Rose, Friederike Ruf, Rolf Mahlberg, Wolfgang Thomas, Ute Graepler, Sebastian Bode, hilipp Meyn, Josef Rosenecker, Cordula Koerner, Klaus-Michael Keller, Tina Teßmer, Helge Hebestreit, Gerhild Lohse
Publikováno v:
The Lancet Regional Health. Europe, Vol 32, Iss , Pp 100690- (2023)
Summary: Background: Treatment with elexacaftor/tezacaftor/ivacaftor (ETI) improves multiple clinical outcomes in people with cystic fibrosis (pwCF) with at least one F508del allele. This study evaluated the real-world impact of ETI on lung function,
Externí odkaz:
https://doaj.org/article/cb7f1132ad9145b4909f1a838def4b95
Autor:
Joern Pascal Laubach, Michael Ludwig, Tabea Horn, Olaf Eickmeier, Christina Smaczny, Ralf Schubert, Stefan Zielen, Christof Majoor, Malik Aydin, Alexander Schnell, Sabina Schmitt-Grohé
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 7, p 138 (2023)
Background: High TGFβ1-producing variants cause severe clinical disease in F508del homozygous patients. Lately, we showed that a single nucleotide polymorphism (SNP), rs41266431, in the GJA4 gene modifies the disease severity of cystic fibrosis (CF)
Externí odkaz:
https://doaj.org/article/16d181019809414886fb939000eab2b6
Autor:
Alisa Bär, Sabina Schmitt-Grohé, Jürgen Held, Julia Lubig, Gregor Hanslik, Fabian B. Fahlbusch, Heiko Reutter, Joachim Woelfle, Adriana van der Donk, Maria Schleier, Tobias Hepp, Patrick Morhart
Publikováno v:
Antibiotics, Vol 12, Iss 2, p 189 (2023)
(1) Background: Since 2013, weekly screening for multidrug-resistant Gram-negative (MDRGN) bacteria has been performed in German neonatal intensive care units (NICU). National guidelines recommend considering these colonization analyses for antibioti
Externí odkaz:
https://doaj.org/article/bed19d7ac0794289a7d85263459f880b
Autor:
Joern Pascal Laubach, Michael Ludwig, Tabea Horn, Olaf Eickmeier, Christina Smaczny, Ralf Schubert, Stefan Zielen, Christof Majoor, Malik Aydin, Sabina Schmitt-Grohé
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 27, Iss 6, p 168 (2022)
Background: Recently, we provided evidence that a single nucleotide polymorphism (SNP), rs41266431, on the gap junction protein alpha 4 (GJA4) gene, acts as a modifier for clinical disease severity in patients with cystic fibrosis (CF). These feature
Externí odkaz:
https://doaj.org/article/bddf1121be364e7b93eb602a821f7985
Autor:
Tabea Horn, Michael Ludwig, Olaf Eickmeier, Anne H. Neerinex, Anke H. Maitland-van der Zee, Christina Smaczny, Thomas O. F. Wagner, Ralf Schubert, Stefan Zielen, Christof Majoor, Lieuwe D. Bos, Sabina Schmitt-Grohé
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundLung disease phenotype varies widely even in the F508del (homozygous) genotype. Leukocyte-driven inflammation is important for pulmonary disease pathogenesis in cystic fibrosis (CF). Blood cytokines correlate negatively with pulmonary funct
Externí odkaz:
https://doaj.org/article/2ab698d1b93c4ae189b24ff5e33b561e
Autor:
Carsten Schwarz, Claudia Brandt, Elisabeth Antweiler, Alexander Krannich, Doris Staab, Sabina Schmitt-Grohé, Rainald Fischer, Dominik Hartl, Anja Thronicke, Kathrin Tintelnot
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171485 (2017)
BACKGROUND:An increasing rate of respiratory colonization and infection in cystic fibrosis (CF) is caused by fungi of the Scedosporium apiospermum species complex or Lomentospora prolificans (Sac-Lp). These fungi rank second among the filamentous fun
Externí odkaz:
https://doaj.org/article/897f9b7e656a4a1594cf503b7c761275
Publikováno v:
Klinische Pädiatrie.
Autor:
Christina Tremel, Renate Ruppel, Julia Sobel, Sabina Schmitt-Grohé, Joachim Wölfle, Folke Brinkmann
Publikováno v:
Klinische Pädiatrie.
Publikováno v:
Der Pneumologe. 16:19-26
Durch Einfuhrung des Neugeborenenscreenings optimiert sich der Therapiebeginn der Cystischen Fibrose (CF) in das Sauglingsalter. Schon in diesem Alter beginnen die entzundlichen Prozesse in den Atemwegen. Spezifisch fur die Erkrankung ist eine anhalt