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- W2341296804 abstract "Microarrays are a powerful and effective tool that allows the detection of genome-wide gene expression differences between controls and disease conditions. They have been broadly applied to investigate the pathobiology of diverse forms of pulmonary hypertension, namely group 1, including patients with idiopathic pulmonary arterial hypertension, and group 3, including pulmonary hypertension associated with chronic lung diseases such as chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. To date, numerous human microarray studies have been conducted to analyse global (lung homogenate samples), compartment-specific (laser capture microdissection), cell type-specific (isolated primary cells) and circulating cell (peripheral blood) expression profiles. Combined, they provide important information on development, progression and the end-stage disease. In the future, system biology approaches, expression of noncoding RNAs that regulate coding RNAs, and direct comparison between animal models and human disease might be of importance." @default.
- W2341296804 created "2016-06-24" @default.
- W2341296804 creator A5016018148 @default.
- W2341296804 creator A5025485923 @default.
- W2341296804 creator A5039470820 @default.
- W2341296804 creator A5078385671 @default.
- W2341296804 date "2016-04-13" @default.
- W2341296804 modified "2023-10-12" @default.
- W2341296804 title "Microarray analysis in pulmonary hypertension" @default.
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- W2341296804 doi "https://doi.org/10.1183/13993003.02030-2015" @default.
- W2341296804 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5009873" @default.