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RSC Advances|May 2, 2022
Systematic laboratory approach to produce Mg-rich carbonates at low temperatureZulfa Ali Al Disi, Nabil Zouari, Essam Attia, et al.
Human Molecular Genetics|September 1, 2022
Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over timeInga Dunsche, Ellen L Raddatz, Haide Ismer, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2011
T(H)17 cells mediate pulmonary collateral primingMelanie Albrecht, Hui-Chen Chen, Paula Preston-Hurlburt, et al.
European Radiology|August 7, 2023
Effect of CFTR modulator therapy with elexacaftor/tezacaftor/ivacaftor on pulmonary ventilation derived by 3D phase-resolved functional lung MRI in cystic fibrosis patientsFilip Klimeš, Andreas Voskrebenzev, Marcel Gutberlet, et al.
The Science of the Total Environment|April 28, 2018
Phosphorus retention and internal loading in the Bay of Quinte, Lake Ontario, using diagenetic modellingPhuong T K Doan, Sue B Watson, Stefan Markovic, et al.
Scientific Reports|August 5, 2023
Variability of blue carbon storage in arid evaporitic environment of two coastal Sabkhas or mudflatsZulfa Ali Al Disi, Khaled Naja, Sankaran Rajendran, et al.
The European Respiratory Journal|December 11, 2020
IL-17A from innate and adaptive lymphocytes contributes to inflammation and damage in cystic fibrosis lung diseaseMatthias Hagner, Melanie Albrecht, Matteo Guerra, et al.
Microbiology Spectrum|July 13, 2026
Effects of elexacaftor/tezacaftor/ivacaftor on the nasal microbial metagenome in cystic fibrosisTom L Hertramph, Marie Dorda, Sophia T Pallenberg, et al.
Frontiers in Medicine|January 23, 2023
TRACK-CF prospective cohort study: Understanding early cystic fibrosis lung diseaseEva Steinke, Olaf Sommerburg, Simon Y Graeber, et al.
Plant Physiology|March 20, 2019
A Cytosolic Bypass and G6P Shunt in Plants Lacking Peroxisomal Hydroxypyruvate ReductaseJiying Li, Sarathi M Weraduwage, Alyssa L Preiser, et al.
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