Pulmonary FibrosisIdiopathic Pulmonary FibrosisFibrosisBleomycinCystic FibrosisLungHydroxyprolineLung Diseases, InterstitialBronchoalveolar Lavage FluidFibroblastsMyofibroblastsPulmonary AlveoliAlveolitis, Extrinsic AllergicCystic Fibrosis Transmembrane Conductance RegulatorCollagenCollagen DiseasesScleroderma, SystemicTransforming Growth Factor betaEndomyocardial FibrosisRespiratory Function TestsPeplomycinMice, Inbred C57BLDisease Models, AnimalTransforming Growth Factor beta1Lung TransplantationSarcoidosis, PulmonaryPulmonary EmphysemaAntibiotics, AntineoplasticLiver CirrhosisBronchoalveolar LavageHermanski-Pudlak SyndromePyridonesRetroperitoneal FibrosisAsbestosisLung DiseasesMacrophages, AlveolarPulmonary Surfactant-Associated Protein CVital CapacityPneumocytesAsbestosSeverity of Illness IndexIdiopathic Interstitial PneumoniasCollagen Type IIIDisease ProgressionLung InjuryCryptogenic Organizing PneumoniaCollagen Type IPulmonary Diffusing CapacityTime FactorsBiopsyMice, KnockoutRespiratory MucosaPneumoniaTomography, X-Ray ComputedTreatment OutcomeBiological MarkersSarcoidosisDyspneaRetrospective StudiesSilicon DioxideEpithelial CellsSilicosisRespiratory System AgentsHypertension, PulmonaryHSP47 Heat-Shock ProteinsImmunohistochemistryCells, CulturedSmad3 ProteinTotal Lung CapacityRNA, MessengerSymptom AssessmentConnective Tissue Growth FactorRadiation PneumonitisDepressionMucin-5BExtracellular MatrixPleural DiseasesSignal TransductionPulmonary Surfactant-Associated Protein AActinsProspective StudiesConnective Tissue DiseasesOral Submucous FibrosisCase-Control StudiesInflammationQuestionnairesAmbroxolForced Expiratory VolumeExpectorantsRespiratory AspirationEpithelial-Mesenchymal TransitionChronic DiseaseFollow-Up StudiesLiver Cirrhosis, ExperimentalSmad2 ProteinPrognosisRisk FactorsProcollagenGene Expression RegulationPhenotype