Serial bronchoscopic lung lavage in pulmonary alveolar proteinosis under local anesthesia
Lung India, 2015 Pulmonary alveolar proteinosis (PAP) is a rare disease, characterized by alveolar accumulation of surfactant composed of proteins and lipids due to defective surfactant clearance by alveolar macrophages.
K Rennis Davis +3 more
doaj +1 more source
Can somatic GATA2 mutation mimic germ line GATA2 mutation? [PDF]
, 2018 Somatic GATA2 mutation is associated with immunodeficiency and pulmonary alveolar proteinosis in a patient with myeloproliferative ...
Collin, M +7 more
core
Von Hippel-Lindau protein is required for optimal alveolar macrophage terminal differentiation, self-renewal, and function [PDF]
, 2018 The rapid transit from hypoxia to normoxia in the lung that follows the first breath in newborn mice coincides with alveolar macrophage (AM) differentiation.
Brandi, Paola +12 more
core +4 more sources
Responsive liquid metal materials towards unstructured environment
Responsive Materials, Volume 4, Issue 1, February 2026.Room‐temperature liquid metals integrate conductivity, deformability, and interfacial dynamics, enabling robust performance in unstructured environments. This review highlights key properties, requirements, and applications across in vivo, underwater, natural, space, and radiation settings, with advances in sensing, actuation, thermal regulation, and ...
Bo Yuan +5 more
wiley +1 more source
Alveolar macrophages in pulmonary alveolar proteinosis: origin, function, and therapeutic strategies
Frontiers in Immunology, 2023 Pulmonary alveolar proteinosis (PAP) is a rare pulmonary disorder that is characterized by the abnormal accumulation of surfactant within the alveoli. Alveolar macrophages (AMs) have been identified as playing a pivotal role in the pathogenesis of PAP ...
Xinmei Huang +7 more
doaj +1 more source
Pulmonary alveolar proteinosis - a case report [PDF]
, 2014 Efst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinnPróteinútfellingar í lungnablöðrum (pulmonary alveolar proteinosis, PAP) eru oftast af óþekktum orsökum en meingerð sjúkdómsins er rakin til skertrar átfrumuvirkni í ...
Eyþór Björnsson +7 more
core
From the definition of Silicosis at the 1930 Johannesburg conference to the blurred boundaries between pneumoconioses, sarcoidosis and pulmonary alveolar proteinosis (PAP) [PDF]
, 2015 The 1930 International Labour Office Conference on silicosis in Johannesburg identified silicosis by setting a medicolegal framework to its nosology: as with other occupational illnesses, its medical content was fixed under economic pressure.
Catinon, Mickaël +4 more
core +3 more sources
Pulmonary alveolar proteinosis after lung transplantation
Respirology Case Reports, 2020 We report the case of a 69‐year‐old man five‐month post double lung transplant for idiopathic pulmonary fibrosis (IPF) who presented with progressive breathlessness, loss of lung function, and diffuse ground glass shadowing on the chest computed ...
Chandima Divithotawela +4 more
doaj +1 more source
Macrophages and lipid metabolism [PDF]
, 2018 Distinct macrophage populations throughout the body display highly heterogeneous transcriptional and epigenetic programs. Recent research has highlighted that these profiles enable the different macrophage populations to perform distinct functions as ...
Remmerie, Anneleen, Scott, Charlotte
core +1 more source
Clinical &Translational Immunology, Volume 15, Issue 1, 2026.In this study, we analysed the immune responses of blood‐derived monocyte macrophages and iPSC‐derived macrophages following BCG/HKMT infection. We found that iPSC‐derived macrophages displayed a markedly stronger activation profile, including faster migration, increased reactive oxygen species production, elevated apoptosis marker expression and ...
Daniela Paasch +17 more
wiley +1 more source