Page last updated: 2024-10-19

naphthalene and Cystic Fibrosis

naphthalene has been researched along with Cystic Fibrosis in 2 studies

Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carvalho-Oliveira, IM1
Charro, N1
Aarbiou, J1
Buijs-Offerman, RM1
Wilke, M1
Schettgen, T1
Kraus, T1
Titulaer, MK1
Burgers, P1
Luider, TM1
Penque, D1
Scholte, BJ1
Xie, W1
Fisher, JT1
Lynch, TJ1
Luo, M1
Evans, TI1
Neff, TL1
Zhou, W1
Zhang, Y1
Ou, Y1
Bunnett, NW1
Russo, AF1
Goodheart, MJ1
Parekh, KR1
Liu, X1
Engelhardt, JF1

Other Studies

2 other studies available for naphthalene and Cystic Fibrosis

ArticleYear
Proteomic analysis of naphthalene-induced airway epithelial injury and repair in a cystic fibrosis mouse model.
    Journal of proteome research, 2009, Volume: 8, Issue:7

    Topics: Animals; Cystic Fibrosis; Electrophoresis, Gel, Two-Dimensional; Epithelium; Lung; Male; Mice; Mice,

2009
CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice.
    The Journal of clinical investigation, 2011, Volume: 121, Issue:8

    Topics: Animals; Calcitonin Gene-Related Peptide; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane

2011