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10.1186/ar3701

http://scihub22266oqcxt.onion/10.1186/ar3701
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22364570!3392812!22364570
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suck abstract from ncbi

pmid22364570      Arthritis+Res+Ther 2012 ; 14 (1): 204
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  • Contributions of mass spectrometry-based proteomics to defining cellular mechanisms and diagnostic markers for systemic lupus erythematosus #MMPMID22364570
  • Korte EA; Gaffney PM; Powell DW
  • Arthritis Res Ther 2012[Feb]; 14 (1): 204 PMID22364570show ga
  • Systematic lupus erythematosus (SLE) is a complex disease for which molecular diagnostics are limited and pathogenesis is not clearly understood. Important information is provided in this regard by identification and characterization of more specific molecular and cellular targets in SLE immune cells and target tissue and markers of early-onset and effective response to treatment of SLE complications. In recent years, advances in proteomic technologies and applications have facilitated such discoveries. Here we provide a review of insights into SLE pathogenesis, diagnosis and treatment that have been provided by mass spectrometry-based proteomic approaches.
  • |Biomarkers/analysis/*metabolism[MESH]
  • |Humans[MESH]
  • |Lupus Erythematosus, Systemic/diagnosis/*metabolism/therapy[MESH]
  • |Mass Spectrometry/*methods[MESH]
  • |Proteome/analysis/metabolism[MESH]
  • |Proteomics/*methods[MESH]
  • |Reproducibility of Results[MESH]


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