Idiopathic Pulmonary FibrosisPulmonary FibrosisBleomycinLung Diseases, InterstitialLungFibrosisCystic FibrosisBronchoalveolar Lavage FluidAlveolitis, Extrinsic AllergicIdiopathic Interstitial PneumoniasSarcoidosis, PulmonaryPulmonary AlveoliRespiratory Function TestsLung TransplantationFibroblastsMyofibroblastsHydroxyprolinePyridonesCryptogenic Organizing PneumoniaBronchoalveolar LavagePulmonary Diffusing CapacityPneumocytesPulmonary Surfactant-Associated Protein CRespiratory System AgentsVital CapacitySarcoidosisCollagen DiseasesRespiratory AspirationTransforming Growth Factor beta1Total Lung CapacityTransforming Growth Factor betaCollagenMucin-5BPulmonary Surfactant-Associated Protein ABiopsyLung DiseasesDyspneaDisease ProgressionPulmonary EmphysemaHypertension, PulmonaryMacrophages, AlveolarScleroderma, SystemicRespiratory MucosaTomography, X-Ray ComputedAntibiotics, AntineoplasticMice, Inbred C57BLPulmonary Surfactant-Associated Protein DLung InjuryRetrospective StudiesDisease Models, AnimalBiological MarkersPrimary Graft DysfunctionHSP47 Heat-Shock ProteinsConnective Tissue DiseasesPrednisoloneCase-Control StudiesEpithelial CellsPrognosisCollagen Type IDiagnostic Techniques, Respiratory SystemHemoperfusionPulmonary MedicineImmunohistochemistryTherapeutic IrrigationCystic Fibrosis Transmembrane Conductance RegulatorSeverity of Illness IndexPneumoniaEpithelial-Mesenchymal TransitionExpectorantsAcetylcysteineEndomyocardial FibrosisEmphysemaPulmonary Gas ExchangeCells, CulturedTelomeraseTreatment OutcomeRetroperitoneal FibrosisPeplomycinMatrix Metalloproteinase 7RNA, MessengerScoliosisTelomere ShorteningProton TherapyAcute DiseaseCiliary Neurotrophic Factor Receptor alpha SubunitPredictive Value of TestsCollagen Type VAnti-Inflammatory AgentsConnective Tissue Growth FactorExercise TestDyskeratosis CongenitaMice, KnockoutArthritis, JuvenileEnzyme-Linked Immunosorbent AssayExtracellular MatrixActinsSmad3 ProteinSignal TransductionPurpura, Thrombocytopenic, IdiopathicLiver Cirrhosis