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Blood Transcriptomics Predicts Progression of Pulmonary Fibrosis and Associated Natural Killer Cells
37/37 checkable references clean · checked 2026-07-25
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
2 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 37 checked references that resolve
resolves10.1164/rccm.2009-040GL
An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management
resolves10.1164/rccm.201105-0840OC
Forced Vital Capacity in Patients with Idiopathic Pulmonary Fibrosis: Test Properties and Minimal Clinically Important Difference
resolves10.1056/NEJMp1500526
Forced Vital Capacity in Idiopathic Pulmonary Fibrosis — FDA Review of Pirfenidone and Nintedanib
resolves10.1164/rccm.201508-1546OC
Predictors of Mortality Poorly Predict Common Measures of Disease Progression in Idiopathic Pulmonary Fibrosis
resolves10.1126/scitranslmed.3005964
Peripheral Blood Mononuclear Cell Gene Expression Profiles Predict Poor Outcome in Idiopathic Pulmonary Fibrosis
resolves10.1016/S2213-2600(17)30349-1
Validation of a 52-gene risk profile for outcome prediction in patients with idiopathic pulmonary fibrosis: an international, multicentre, cohort study
resolves10.1371/journal.pone.0037708
The Peripheral Blood Transcriptome Identifies the Presence and Extent of Disease in Idiopathic Pulmonary Fibrosis
resolves10.1155/2016/4759040
Comparative Study of Circulating MMP-7, CCL18, KL-6, SP-A, and SP-D as Disease Markers of Idiopathic Pulmonary Fibrosis
resolves10.1016/S2213-2600(18)30185-1
Prognostic and predictive biomarkers for patients with idiopathic pulmonary fibrosis treated with pirfenidone: post-hoc assessment of the CAPACITY and ASCEND trials
resolves10.1152/ajplung.00139.2012
Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis
resolves10.1164/ajrccm.165.2.ats01
American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias
resolves10.1111/j.2517-6161.1995.tb02031.x
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
resolves10.18637/jss.v033.i01
Regularization Paths for Generalized Linear Models via Coordinate Descent
resolves10.18637/jss.v039.i05
Regularization Paths for Cox's Proportional Hazards Model via Coordinate Descent
resolves10.1111/j.1467-9868.2011.01004.x
Strong Rules for Discarding Predictors in Lasso-Type Problems
resolves10.1186/1471-2105-12-77
pROC: an open-source package for R and S+ to analyze and compare ROC curves
resolves10.18637/jss.v061.i08
<b>OptimalCutpoints</b>: An<i>R</i>Package for Selecting Optimal Cutpoints in Diagnostic Tests
resolves10.1164/rccm.201202-0314OC
A Placebo-Controlled Randomized Trial of Warfarin in Idiopathic Pulmonary Fibrosis
resolves10.1056/NEJMoa1113354
Prednisone, Azathioprine, and
<i>N</i>
-Acetylcysteine for Pulmonary Fibrosis
resolves10.1056/NEJMoa1002110
A Controlled Trial of Sildenafil in Advanced Idiopathic Pulmonary Fibrosis
resolves10.1056/NEJMoa1402582
A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
resolves10.1164/ajrccm.185.12.1329
Plasma Proteins for Risk Prediction in Idiopathic Pulmonary Fibrosis
resolves10.1164/rccm.201804-0761OC
Prognosticating Outcomes in Interstitial Lung Disease by Mediastinal Lymph Node Assessment. An Observational Cohort Study with Independent Validation
resolves10.1097/01.LAB.0000032380.82232.67
Abnormal Re-epithelialization and Lung Remodeling in Idiopathic Pulmonary Fibrosis: The Role of ΔN-p63
resolves10.3389/fimmu.2016.00591
The Role of Lymphocytes in Radiotherapy-Induced Adverse Late Effects in the Lung
resolves10.1016/S2213-2600(17)30430-7
An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study
resolves10.3389/fimmu.2018.01869
Natural Killer Cells: Development, Maturation, and Clinical Utilization
resolves10.1016/j.cell.2020.01.022
Tissue Determinants of Human NK Cell Development, Function, and Residence
resolves10.1016/j.cyto.2013.12.003
Peripheral depletion of NK cells and imbalance of the Treg/Th17 axis in idiopathic pulmonary fibrosis patients
resolves10.1007/s00439-009-0666-1
MICA polymorphisms and decreased expression of the MICA receptor NKG2D contribute to idiopathic pulmonary fibrosis susceptibility
resolves10.1513/AnnalsATS.201502-088AW
Viruses in Idiopathic Pulmonary Fibrosis. Etiology and Exacerbation
resolves10.1164/rccm.201607-1525OC
Microbes Are Associated with Host Innate Immune Response in Idiopathic Pulmonary Fibrosis
resolves10.3389/fimmu.2017.00301
Immunoregulatory Role of NK Cells in Tissue Inflammation and Regeneration
The 2 references without a DOI — listed, not checked
no DOI — not checkedShort-term longitudinal gene expression changes predict forced vital capacity decline in idiopathic pulmonary fibrosis [abstract]
no DOI — not checkedLinear models and empirical bayes methods for assessing differential expression in microarray experiments
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