Microbiota and fungal-bacterial interactions in the cystic fibrosis lung

E Santos-Fernandez, L Martin-Souto… - FEMS Microbiology …, 2023 - academic.oup.com
The most common genetic hereditary disease affecting Caucasians is cystic fibrosis (CF),
which is caused by autosomal recessive mutations in the CFTR gene. The most serious …

[HTML][HTML] New insight in molecular detection of Mycobacterium tuberculosis

SMA Mousavi-Sagharchi, E Afrazeh… - AMB …, 2024 - amb-express.springeropen.com
Mycobacterium tuberculosis, the causative agent of tuberculosis, is a pathogenic bacterium
that has claimed millions of lives since the Middle Ages. According to the World Health …

Comparing Cytology Brushes for Optimal Human Nasal Epithelial Cell Collection: Implications for Airway Disease Diagnosis and Research

LK Fawcett, N Turgutoglu, KM Allan, Y Belessis… - Journal of Personalized …, 2023 - mdpi.com
Primary nasal epithelial cells and culture models are used as important diagnostic, research
and drug development tools for several airway diseases. Various instruments have been …

An integrated metaproteomics workflow for studying host-microbe dynamics in bronchoalveolar lavage samples applied to cystic fibrosis disease

ME Kruk, S Mehta, K Murray, LA Higgins, K Do… - …, 2024 - journals.asm.org
Airway microbiota are known to contribute to lung diseases, such as cystic fibrosis (CF), but
their contributions to pathogenesis are still unclear. To improve our understanding of host …

Exploring the dynamics of mixed-species biofilms involving Candida spp. and bacteria in cystic fibrosis

K Gourari-Bouzouina, Z Boucherit-Otmani… - Archives of …, 2024 - Springer
Cystic fibrosis (CF) is an inherited disease that results from mutations in the gene
responsible for the cystic fibrosis transmembrane conductance regulator (CFTR). The …

[PDF][PDF] Микробиологическая характеристика хронического риносинусита у детей с муковисцидозом в сравнении с другими локусами респираторного тракта

ДП Поляков, АЮ Воронкова… - Вопросы …, 2023 - researchgate.net
Пациенты и методы. Включены 94 пациента в возрасте от 2 до 18 лет с диагнозом
хронического риносинусита на фоне МВ, которые были подвергнуты …

Bacterial Mucin Degradation in the Cystic Fibrosis Airways: A Potential Regulator of P. aeruginosa Pathogenicity

AR Villarreal - 2023 - search.proquest.com
Cystic fibrosis (CF) is characterized by impaired mucociliary clearance, leading to mucus
accumulation and chronic bacterial respiratory infections. Pseudomonas aeruginosa (PA) is …

[PDF][PDF] Virulence mechanisms of the cystic fibrosis pathogen Achromobacter xylosoxidans

C Sahl - 2024 - portal.research.lu.se
Cystic fibrosis (CF) is a genetic disorder caused by mutations in the chloride channel cystic
fibrosis transmembrane conductance regulator (CFTR). The defective ion transport causes …

Role of Post-Transcriptional Dysregulation and Aberrant Microbiota in Obstructive Lung Disease

W Wang - 2023 - search.proquest.com
We leverage multi-omics approaches RNA-seq and 16S rRNA gene sequencing to
characterize non-coding RNAs and microbial community changes in diseases that affect the …

[HTML][HTML] МИКРОБИОТА НИЖНИХ ДЫХАТЕЛЬНЫХ ПУТЕЙ И ЕЁ ЧУВСТВИТЕЛЬНОСТЬ К АНТИБАКТЕРИАЛЬНЫМ ПРЕПАРАТАМ У БОЛЬНЫХ …

ЯЯ Яковлев, ОВ Бурнышева, МЛ Готлиб… - Мать и дитя в …, 2022 - cyberleninka.ru
Муковисцидоз–аутосомно-рецессивное заболевание, характеризуется поражением
всех экзокринных желёз, жизненно важных органов и систем. Нарушения функции …