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10.1164/rccm.201408-1452OC

http://scihub22266oqcxt.onion/10.1164/rccm.201408-1452OC
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C4315819!4315819!25333685
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suck abstract from ncbi


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pmid25333685      Am+J+Respir+Crit+Care+Med 2014 ; 190 (11): 1263-72
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  • Relationship of DNA Methylation and Gene Expression in Idiopathic Pulmonary Fibrosis #MMPMID25333685
  • Yang IV; Pedersen BS; Rabinovich E; Hennessy CE; Davidson EJ; Murphy E; Guardela BJ; Tedrow JR; Zhang Y; Singh MK; Correll M; Schwarz MI; Geraci M; Sciurba FC; Quackenbush J; Spira A; Kaminski N; Schwartz DA
  • Am J Respir Crit Care Med 2014[Dec]; 190 (11): 1263-72 PMID25333685show ga
  • Rationale: Idiopathic pulmonary fibrosis (IPF) is an untreatable and often fatal lung disease that is increasing in prevalence and is caused by complex interactions between genetic and environmental factors. Epigenetic mechanisms control gene expression and are likely to regulate the IPF transcriptome.Objectives: To identify methylation marks that modify gene expression in IPF lung.Methods: We assessed DNA methylation (comprehensive high-throughput arrays for relative methylation arrays [CHARM]) and gene expression (Agilent gene expression arrays) in 94 patients with IPF and 67 control subjects, and performed integrative genomic analyses to define methylation?gene expression relationships in IPF lung. We validated methylation changes by a targeted analysis (Epityper), and performed functional validation of one of the genes identified by our analysis.Measurements and Main Results: We identified 2,130 differentially methylated regions (DMRs; <5% false discovery rate), of which 738 are associated with significant changes in gene expression and enriched for expected inverse relationship between methylation and expression (P?
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