نتایج جستجو برای: pulmonary surfactant

تعداد نتایج: 243200  

Journal: :American journal of physiology. Lung cellular and molecular physiology 2006
Zhan Yin Linda Gonzales Venkatadri Kolla Nibedita Rath Yuzhen Zhang Min Min Lu Shioko Kimura Philip L Ballard Michael F Beers Jonathan A Epstein Edward E Morrisey

Hop is an unusual homeodomain protein that was first identified in the developing heart where it functions downstream of Nkx2.5 to modulate cardiac gene expression. Hop functions through interactions with histone deacetylase (HDAC) 2 to mediate repression of cardiac-specific genes, and recent studies show that HDAC activity and HDAC2 expression are decreased in people with chronic obstructive p...

2014
Heui Seung Jo

Respiratory distress syndrome (RDS) among preterm infants is typically due to a quantitative deficiency of pulmonary surfactant. Aside from the degree of prematurity, diverse environmental and genetic factors can affect the development of RDS. The variance of the risk of RDS in various races/ethnicities or monozygotic/dizygotic twins has suggested genetic influences on this disorder. So far, se...

Journal: :The Journal of Experimental Medicine 2008
Margarita Martinez-Moczygemba Minh L. Doan Okan Elidemir Leland L. Fan Sau Wai Cheung Jonathan T. Lei James P. Moore Ghamartaj Tavana Lora R. Lewis Yiming Zhu Donna M. Muzny Richard A. Gibbs David P. Huston

Pulmonary alveolar proteinosis (PAP) is a rare lung disorder in which surfactant-derived lipoproteins accumulate excessively within pulmonary alveoli, causing severe respiratory distress. The importance of granulocyte/macrophage colony-stimulating factor (GM-CSF) in the pathogenesis of PAP has been confirmed in humans and mice, wherein GM-CSF signaling is required for pulmonary alveolar macroph...

Journal: :Neonatology 2016
Giuseppe Buonocore Tore Curstedt Henry L Halliday Mikko Hallman Ola D Saugstad Christian P Speer

nia, meconium aspiration syndrome and congenital diaphragmatic hernia. Results from these studies may lead to a widening of the clinical indications for surfactant therapy, something that would have greatly pleased Bengt Robertson, in whose name the lecture was given. The second invited speaker was Robin H. Steinhorn from Washington, D.C., USA, who discussed advances in the pathogenesis and tre...

Journal: :Soft matter 2015
Eline Hermans M Saad Bhamla Peter Kao Gerald G Fuller Jan Vermant

The surfactant lining the walls of the alveoli in the lungs increases pulmonary compliance and prevents collapse of the lung at the end of expiration. In premature born infants, surfactant deficiency causes problems, and lung surfactant replacements are instilled to facilitate breathing. These pulmonary surfactants, which form complex structured fluid-fluid interfaces, need to spread with great...

Journal: :The European respiratory journal 1997
M Griese P Birrer A Demirsoy

Cystic fibrosis (CF) leads to a chronic inflammation of the airways with significant air flow limitations developing early in the course of the disease. As a well-functioning pulmonary surfactant is necessary to keep the alveoli and the small conducting airways open during expiration, we hypothesized that the biochemical and biophysical properties of surfactant may be impaired in CF. Bronchoalv...

Journal: :Cellular Physiology and Biochemistry 2010

Journal: :Pediatrics & Neonatology 2015

Journal: :European Respiratory Journal 1997

Journal: :Journal of Clinical Investigation 1990

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