Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sabina Schmitt-Grohe"'
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
Akademický článek
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Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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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
Publikováno v:
Europe PubMed Central
Severe adverse events were evaluated in a comparative efficacy trial in Germany in infants who received either the Lederle/Takeda acellular pertussis component DTP (DTaP) vaccine, the Lederle whole-cell component DTP (DTP) or DT vaccine. Vaccinees re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b0cbf111d79b07aa712713ee7028415c
https://pubmed.ncbi.nlm.nih.gov/9272335
https://pubmed.ncbi.nlm.nih.gov/9272335
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