Aderonke Sofoluwe
Overview
Explore the profile of Aderonke Sofoluwe including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
119
Followers
0
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Recent Articles
1.
Hussein S, Sofoluwe A, Paleja A, Duhme-Klair A, Thomas M
Microbiology (Reading)
. 2024 Jan;
170(1).
PMID: 38189440
One of the mechanisms employed by the opportunistic pathogen to acquire the essential element iron is the production and release of two ferric iron chelating compounds (siderophores), ornibactin and pyochelin....
2.
Immune response of polarized cystic fibrosis airway epithelial cells infected with Influenza A virus
Sofoluwe A, Zoso A, Bacchetta M, Lemeille S, Chanson M
J Cyst Fibros
. 2020 Sep;
20(4):655-663.
PMID: 32873524
Background: Cystic fibrosis (CF), a genetic disease caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is characterized by dysfunction of the immune response in the airway...
3.
Sofoluwe A, Bacchetta M, Badaoui M, Kwak B, Chanson M
Sci Rep
. 2019 Nov;
9(1):16556.
PMID: 31719610
Neutrophils are the first immune cells to kill invading microbes at sites of infection using a variety of processes, including the release of proteases, phagocytosis and the production of neutrophil...
4.
Zoso A, Sofoluwe A, Bacchetta M, Chanson M
Sci Data
. 2019 Oct;
6(1):240.
PMID: 31664037
Pathological remodeling of the airway epithelium is commonly observed in Cystic Fibrosis (CF). The different cell types that constitute the airway epithelium are regenerated upon injury to restore integrity and...
5.
Hagemeijer M, Siegwart D, Strug L, Cebotaru L, Torres M, Sofoluwe A, et al.
J Cyst Fibros
. 2017 Dec;
17(2S):S46-S51.
PMID: 29275953
Translational research efforts in cystic fibrosis (CF) aim to develop therapies for all subjects with CF. To reach this goal new therapies need to be developed that target multiple aspects...
6.
Rosen B, Chanson M, Gawenis L, Liu J, Sofoluwe A, Zoso A, et al.
J Cyst Fibros
. 2017 Sep;
17(2S):S28-S34.
PMID: 28939349
The cystic fibrosis (CF) field is the beneficiary of five species of animal models that lack functional cystic fibrosis transmembrane conductance regulator (CFTR) channel. These models are rapidly informing mechanisms...
7.
Shastri S, Spiewak H, Sofoluwe A, Eidsvaag V, Asghar A, Pereira T, et al.
Plasmid
. 2016 Nov;
89:49-56.
PMID: 27825973
To elucidate the function of a gene in bacteria it is vital that targeted gene inactivation (allelic replacement) can be achieved. Allelic replacement is often carried out by disruption of...