heme has been researched along with Cystic Fibrosis in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Glasser, NR; Hunter, RC; Liou, TG; Newman, DK | 1 |
| Butt, AT; Thomas, MS | 1 |
| Callaghan, M; McClean, S; Sá-Correia, I; Thomas, M; Tyrrell, J; Whelan, N; Wright, C | 1 |
| Cunnion, KM; Hair, PS; Krishna, NK; Sass, LA | 1 |
| Chotirmall, SH; Cosgrove, S; Greene, CM; McElvaney, NG | 1 |
1 review(s) available for heme and Cystic Fibrosis
| Article | Year |
|---|---|
Iron Acquisition Mechanisms and Their Role in the Virulence of
Topics: Animals; Burkholderia; Burkholderia gladioli; Burkholderia Infections; Burkholderia mallei; Burkholderia pseudomallei; Computational Biology; Cystic Fibrosis; Ferritins; Glanders; Heme; Horses; Humans; Iron; Lactoferrin; Lung; Melioidosis; Siderophores; Virulence | 2017 |
4 other study(ies) available for heme and Cystic Fibrosis
| Article | Year |
|---|---|
Refinement of metabolite detection in cystic fibrosis sputum reveals heme correlates with lung function decline.
Topics: Adult; Cystic Fibrosis; Female; Heme; Humans; Lung; Male; Sputum | 2019 |
Investigation of the multifaceted iron acquisition strategies of Burkholderia cenocepacia.
Topics: Adaptation, Physiological; Burkholderia cenocepacia; Burkholderia Infections; Cystic Fibrosis; Gene Expression; Gene Expression Regulation, Bacterial; Genes, Bacterial; Heme; Humans; Iron; Pneumonia, Bacterial; Pseudomonas aeruginosa; Pseudomonas Infections; Siderophores; Transcriptional Activation | 2015 |
Inhibition of Myeloperoxidase Activity in Cystic Fibrosis Sputum by Peptide Inhibitor of Complement C1 (PIC1).
Topics: Aniline Compounds; Antioxidants; Benzidines; Complement C1 Inhibitor Protein; Cystic Fibrosis; Heme; Humans; Neutrophils; Oxidation-Reduction; Peroxidase; Sputum | 2017 |
Pulmonary proteases in the cystic fibrosis lung induce interleukin 8 expression from bronchial epithelial cells via a heme/meprin/epidermal growth factor receptor/Toll-like receptor pathway.
Topics: Bronchoalveolar Lavage Fluid; Cell Line; Cystic Fibrosis; Epithelial Cells; ErbB Receptors; Heme; Hemoglobins; Humans; Interleukin-10; Interleukin-8; Leukocyte Elastase; Metalloendopeptidases; Myeloblastin; Peptide Hydrolases; Pneumonia, Bacterial; Pseudomonas aeruginosa; Pseudomonas Infections; Respiratory Mucosa; Serine Endopeptidases; Signal Transduction; Toll-Like Receptors | 2011 |