Laura Maschirow

ORCID: 0000-0002-7727-2544
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About
Contact & Profiles
Research Areas
  • IL-33, ST2, and ILC Pathways
  • Advanced Glycation End Products research
  • Immune Cell Function and Interaction
  • Cardiovascular Disease and Adiposity
  • Pediatric health and respiratory diseases
  • Autoimmune and Inflammatory Disorders Research
  • Adipokines, Inflammation, and Metabolic Diseases
  • Eosinophilic Esophagitis
  • Natural Antidiabetic Agents Studies
  • Diet and metabolism studies
  • Adipose Tissue and Metabolism
  • Clostridium difficile and Clostridium perfringens research
  • Pediatric Urology and Nephrology Studies
  • Gut microbiota and health
  • Atherosclerosis and Cardiovascular Diseases
  • Infant Nutrition and Health

Charité - Universitätsmedizin Berlin
2019-2024

Humboldt-Universität zu Berlin
2018-2023

Freie Universität Berlin
2018-2023

University of Potsdam
2013-2015

This study aims to increase understanding of the connection between oxidative stress and inflammation in diabetes disease progression provide a basis for investigating improved diagnostic possibilities, treatment prevention prediabetes.Differences level biochemical markers (erythrocyte GSH/GSSG urinary 8-isoprostane), (CRP, IL-6), endothelial dysfunction (plasma homocysteine, 8-hydroxy-2-deoxy-guanosine) coagulation/fibrinolysis (C5a, D-Dimer) were determined prediabetes control...

10.1016/j.clinbiochem.2015.02.015 article EN cc-by-nc-nd Clinical Biochemistry 2015-03-06
Ivo Röwekamp Laura Maschirow Anne Rabes Facundo Fiocca Vernengo Lutz Hamann and 95 more Gitta Anne Heinz Mir‐Farzin Mashreghi Sandra Caesar Miha Milek Alexandra Muniz Gomes da Fonseca Sandra-Maria Wienhold Geraldine Nouailles Ling Yao Soraya Mousavi Dunja Bruder Julia D. Boehme Monika Puzianowska‐Kuźnicka Dieter Beule Martin Witzenrath Max Löhning Christoph S. N. Klose Markus M. Heimesaat Andreas Diefenbach Bastian Opitz André Fuchs Maximilian Engelmann Gregor Paul Mousa Ayoub Katharina Groehl Katrin Riedl Daiana Stolz Wolfgang Bauer Eva Diehl-Wiesenecker Iris von Wunsch-Rolshoven Terue Noah Galtung Norbert Suttorp Martin Witzenrath Christian Wildberg Caitlin Pley Enrico Zessin Sibylle Schmager Bernhard Schaaf Julius Kremling Daniela Nickoleit-Bitzenberger Harun Azzaui Martin Hower Frederik Hempel Katharina Prebeg Kalina Popkirova Martin Kolditz Bernhard Schulte-Hubbert Simona Langner Gernot Rohde Carla Bellinghausen A Grünewaldt Adrian Endres Carlo Sala Frigerio B. Fiedler Marcus Panning Tobias Welte Isabell Pink Nora Drick T Fühner Mariet van’t Klooster T H Steinberg Grit Barten-Neiner W. Kröner Olesya Unruh Nina Adaskina Frank Eberhardt Christina Julius Thomas Illig Norman Klopp Mathias W. Pletz Benjamin T. Schleenvoigt Christina Bahrs Anne Moeser Juliane Ankert Urte Sommerwerck T Wintermantel Daniel Drömann P. Parschke Klaas Franzen Jan Rupp Frederike Waldeck Nadja Käding Christoph D. Spinner Johanna Erber Florian Voit Jochen Schneider Marco Falcone Giusy Tiseo David F. Heigener I. Hering Werner C. Albrich Frank Rassouli Benjamin Wirth Claus Neurohr Andreas Essig Steffen Stenger

IL-22 plays a critical role in defending against mucosal infections, but how production is regulated incompletely understood. Here, we show that mice lacking IL-33 or its receptor ST2 (IL-1RL1) were more resistant to Streptococcus pneumoniae lung infection than wild-type animals and single-nucleotide polymorphisms IL33 IL1RL1 associated with pneumococcal pneumonia humans. The effect of on S. was mediated by negative regulation innate lymphoid cells (ILCs) independent ILC2s as well IL-4 IL-13...

10.1073/pnas.2310864121 article EN Proceedings of the National Academy of Sciences 2024-05-23

ABSTRACT IL-22 plays a critical role in defending against mucosal infections, but how production is regulated incompletely understood. Here, we show that mice lacking IL-33 or its receptor ST2 (IL-1RL1) were more resistant to Streptococcus pneumoniae lung infection than wild-type animals, and single nucleotide polymorphisms IL33 IL1RL1 associated with pneumococcal pneumonia humans. The effect of on S. was mediated by negative regulation innate lymphoid cells (ILCs), independent ILC2s as well...

10.1101/2023.07.19.549679 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-07-19

Lange Zeit ging man von einer sterilen intrauterinen Fetalentwicklung aus. Dank neuer molekularbiologischer Methoden ist der Nachweis bakterieller DNA und die Bestimmung Bakterienstämmen möglich. Die Frage, ob fetale Darm bereits vorgeburtlich mit vitalen, kultivierbaren Bakterien besiedelt wird oder bakterielle lediglich via maternal-plazentarem Transfer in den fetalen gelangt, weiterhin ungeklärt. In einem Literaturreview konnten wir zeigen, dass bislang durchgeführten Studien insbesondere...

10.1055/s-0038-1671126 article DE Geburtshilfe und Frauenheilkunde 2018-09-20
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