Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

143
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
143
Chronic Bowel Disorders: Introduction01:17

Chronic Bowel Disorders: Introduction

390
Chronic bowel diseases are a group of long-term conditions affecting the digestive tract, characterized by inflammation and damage to the gut lining. These conditions primarily include irritable bowel syndrome and inflammatory bowel disease.
Irritable Bowel Syndrome (IBS) is a common disorder affecting the gastrointestinal tract. The distinctive feature is recurrent abdominal pain associated with altered bowel movements, manifesting as constipation, diarrhea, or fluctuating between both. The...
390
COPD: Management Using Bronchodilators and Corticosteroids01:26

COPD: Management Using Bronchodilators and Corticosteroids

182
Chronic obstructive pulmonary isease (COPD) involves a group of progressive lung disorders characterized by persistent airflow limitation and chronic respiratory symptoms. Asthma-COPD Overlap Syndrome (ACOS), encompassing features of both asthma and Chronic obstructive pulmonary disease (COPD), is a group of progressive lung disorders that includes chronic bronchitis, emphysema, and refractory (non-reversible) asthma. ACOS leads to complex clinical presentations that combine the inflammatory...
182
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

192
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
192
Pulmonary Tuberculosis V01:28

Pulmonary Tuberculosis V

170
Medical management of tuberculosis (TB) patients involves a comprehensive approach that includes diagnosis, treatment, and monitoring. The specific strategies can vary depending on the type of tuberculosis (latent or active), the patient's overall health status, and other considerations.
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
170
COPD: Pathogenesis and Clinical Features01:20

COPD: Pathogenesis and Clinical Features

235
Chronic obstructive pulmonary disease (COPD) is a group of lung conditions that progressively worsen over time, including chronic bronchitis and emphysema. This cluster of diseases collectively leads to a gradual and irreversible decline in lung function over time.
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...
235

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Bacterial taxa associated with lung cancer cases in Southeast Asians: a pilot case-control study.

Cellular oncology (Dordrecht, Netherlands)·2026
Same author

Targeting Inflammation in Bronchiectasis.

Drugs·2026
Same author

Single-bacterial cell insights into mechanisms of ceftriaxone resistance in Neisseria subflava.

Nature communications·2026
Same author

Lower airway dysbiosis in nontuberculous mycobacteria-positive bronchiectasis is associated with neutrophil extracellular trap-predominant severe phenotypes.

American journal of respiratory and critical care medicine·2026
Same author

Human airway organoids for bacterial-host interaction studies: methods, insights and translational promise.

Thorax·2026
Same author

Gut-lung microbial dynamics with lumacaftor/ivacaftor in children with cystic fibrosis: a prospective multicenter study.

Pediatric research·2026

相关实验视频

Updated: Jun 8, 2025

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes
03:53

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes

Published on: April 19, 2024

480

支气管切除菌的微生物组:当前的理解和治疗影响

Jayanth Kumar Narayana1, Micheál Mac Aogáin2,3, Philip M Hansbro4

  • 1Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.

Current opinion in pulmonary medicine
|November 4, 2024
PubMed
概括

呼吸道微生物组与支气管切除症有关,为诊断和治疗提供了新的可能性. 了解这些微生物群落可以带来更好的患者结果.

更多相关视频

The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections
06:57

The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections

Published on: May 8, 2017

9.2K
Design and Development of a Model to Study the Effect of Supplemental Oxygen on the Cystic Fibrosis Airway Microbiome
07:38

Design and Development of a Model to Study the Effect of Supplemental Oxygen on the Cystic Fibrosis Airway Microbiome

Published on: August 3, 2021

2.3K

相关实验视频

Last Updated: Jun 8, 2025

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes
03:53

Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes

Published on: April 19, 2024

480
The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections
06:57

The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections

Published on: May 8, 2017

9.2K
Design and Development of a Model to Study the Effect of Supplemental Oxygen on the Cystic Fibrosis Airway Microbiome
07:38

Design and Development of a Model to Study the Effect of Supplemental Oxygen on the Cystic Fibrosis Airway Microbiome

Published on: August 3, 2021

2.3K

科学领域:

  • 呼吸系统医学 呼吸系统医学
  • 微生物学 微生物学
  • 基因组学就是基因组学.

背景情况:

  • 支气管切除是一种未被认可的疾病,具有显著的异质性.
  • 最近的研究强调了呼吸道微生物群在支气管切除症表型中的作用.
  • 测序技术的进步使得微生物组的详细分析成为可能.

研究的目的:

  • 审查了解支气管病菌微生物群的近期进展.
  • 探索微生物组分析在支气管切除症临床决策中的潜力.
  • 突出诊断,分层和个性化干预的机会.

主要方法:

  • 审查最近的大规模,多中心和纵向临床研究.
  • 分析经典微生物学和整体微生物组测序的发现.
  • 微生物组数据与临床和生物数据集的整合.

主要成果:

  • 支气管切除症表现出多样化的微生物群概况,反映出疾病的异质性.
  • 关键的微生物标记物包括Pseudomonas aeruginosa和Haemophilus influenza. 这两种类型的微生物标记物.
  • 整体分析揭示了与其他细菌种群,真菌,病毒及其相互作用的关联.

结论:

  • 支气管切除菌的微生物组是一个关键的新兴研究领域.
  • 微生物组的洞察力对理解和治疗支气管切除症具有重大意义.
  • 进一步整合微生物组数据有望改善患者的治疗结果.