Imperial College London

DrJonathanBaker

Faculty of MedicineNational Heart & Lung Institute

Honorary Senior Research Fellow
 
 
 
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Contact

 

+44 (0)20 7594 7790jonathan.baker

 
 
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Location

 

223Guy Scadding BuildingRoyal Brompton Campus

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Summary

 

Publications

Citation

BibTex format

@article{Baker:2018:10.1165/rcmb.2018-0187ED,
author = {Baker, JR},
doi = {10.1165/rcmb.2018-0187ED},
journal = {American Journal of Respiratory Cell and Molecular Biology},
pages = {412--414},
title = {Sirtuin-1: a new potential therapeutic target for rhinosinusitis? Who 'nose'?},
url = {http://dx.doi.org/10.1165/rcmb.2018-0187ED},
volume = {59},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Chronic rhinosinusitis is one of the most common upper respiratory tract diseases. In the USA chronic rhinosinusitis has a high prevalence, with around 12% of the population having the disease, and therefore as a consequence the disease has a high health cost burden (1). Chronic rhinosinusitis is classified as an inflammatory nasal disease in which the nasal cavities become inflamed and swollen. The disease can be divided into two distinct disease phenotypes: Chronic rhinosinusitis without nasal polyps (CRSsNP) and Chronic rhinosinusitis with nasal polyps(CRSwNP) (2). One of the major clinical differences between the two subsets of disease is that CRSwNP patients form nasal polyps within their nasal cavities, with these being described as inflammatory lesions of sinonasal tissue which further narrow this space (3). This leads to symptoms of nasal congestion, rhinorrhoea and facial pressure or pain that is of duration of 12 weeks or longer (3). CRSwNP is believed to be a disease of eosinophilia, with an impaired sinonasal epithelial barrier that causes hypersensitivity to inhaled pathogens and particulates, as well as increased permeability, exacerbating the recruitment of inflammatory cells in response to the stimulus.
AU - Baker,JR
DO - 10.1165/rcmb.2018-0187ED
EP - 414
PY - 2018///
SN - 1044-1549
SP - 412
TI - Sirtuin-1: a new potential therapeutic target for rhinosinusitis? Who 'nose'?
T2 - American Journal of Respiratory Cell and Molecular Biology
UR - http://dx.doi.org/10.1165/rcmb.2018-0187ED
UR - https://www.ncbi.nlm.nih.gov/pubmed/29995434
UR - https://www.atsjournals.org/doi/abs/10.1165/rcmb.2018-0187ED
UR - http://hdl.handle.net/10044/1/62302
VL - 59
ER -