Results 71 to 80 of about 2,097 (184)

Normal mucus formation requires cAMP-dependent HCO3- secretion and Ca2+-mediated mucin exocytosis. [PDF]

open access: yes, 2013
  Evidence from the pathology in cystic fibrosis (CF) and recent results in vitro indicate that HCO3- is required for gel-forming mucins to form the mucus that protects epithelial surfaces.
Garcia, Mary Abigail S   +2 more
core   +1 more source

Learning from each other: ABC transporter regulation by protein phosphorylation in plant and mammalian systems [PDF]

open access: yes, 2015
The ABC (ATP-binding cassette) transporter family in higher plants is highly expanded compared with those of mammalians. Moreover, some members of the plant ABCB subfamily display very high substrate specificity compared with their mammalian ...
Aryal, Bibek   +2 more
core   +1 more source

NTIBIOTICS SENSITIVITY OF STAPHYLOCOCCUS AUREUS, PSEUDOMONAS AERUGINOSA AND BACTERIA OF BURKHOLDERIA CEPACIA COMPLEX, PERSISTING IN LUNGS OF PATIENTS WITH MUCOVISCIDOSIS (MV)

open access: yesЖурнал микробиологии, эпидемиологии и иммунобиологии, 2015
Aim. Study the spectrum of resistance to antibiotics and its variability of Staphylococcus aureus, Pseudomonas aeruginosa and Вurkholderia cepacia complex (BCC), persisting in lungs of MV patients. Materials and methods. 312 strains of S.
L. R Avetisyan   +10 more
doaj  

Use of inhaled tobramycin in patients with cystic fibrosis

open access: yesТерапевтический архив, 2010
The results of a few studies evaluating the efficacy and safety of nebulized tobramycin solution used in patients with cystic fibrosis have been published to date. Pulmonary deposition of inhaled tobramycin and its lung produced concentrations are rather
A G Chermensky, M E Gembitskaya
doaj  

IMMUNE PREVENTION OF RESPIRATORY-SYNCYTIAL VIRAL INFECTION: 15 YEARS OF WORLD EXPERIENCE

open access: yesПедиатрическая фармакология, 2013
The article is dedicated to one of the most important issues of modern neonatology – prevention of respiratory-syncytial virus infection, which is a frequent cause of bronchiolites and pneumoniae in infants and neonates, especially premature infants. The
E. S. Keshishyan
doaj   +1 more source

Cystic Fibrosis Atypical Forms Presentation: Edema, Anemia and Skin Lesions

open access: yesRevista Finlay, 2021
Cystic fibrosis or mucoviscidosis is the most common genetic disease in the Caucasian race characterized by thickening of secretions due to abnormal ion transport of epithelial cells, manifested with pancreatic insufficiency, progressive lung disease ...
Chabelys de la Caridad Rodríguez Membrides   +2 more
doaj   +2 more sources

Expanded carrier screening: A current perspective [PDF]

open access: yes, 2018
Prenatal carrier screening has expanded to include a large number of genes offered to all couples considering pregnancy or with an ongoing pregnancy.
Al-Kouatly, Hb   +12 more
core   +1 more source

Ubiquitin C-terminal hydrolase L1 (UCH-L1):Structure, distribution and roles in brain function and dysfunction [PDF]

open access: yes, 2016
Ubiquitin C-terminal hydrolase L1 (UCH-L1) is an extremely abundant protein in the brain where, remarkably, it is estimated to make up 1–5% of total neuronal protein.
Bishop, Paul, Henley, Jeremy, Rocca, Dan
core   +3 more sources

Immunomodifying effects of macrolides: areas of possible clinical use in pulmonology

open access: yesТерапевтический архив, 2011
The review is devoted to non-antibacterial effects of macrolides in patients with respiratory diseases: bronchial asthma, bronchoectasis, chronic obstructive pulmonary disease, chronic rhinosinusitis, mucoviscidosis, diffuse bronchiolithiasis, severe flu,
Aleksandr Igorevich Sinopal'nikov   +1 more
doaj  

Abstract

open access: yes
JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

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