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PubMed 17456529 Contribution of anti-cyclic citrullinated peptide antibody and rheumatoid factor to the diagnosis of arthropathy in haemochromatosis. OBJECTIVE: To investigate the prevalence of antibodies to cyclic c 1.35 KB 2015-12-25 4 3
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PubMed 15648059 Investigation of genes coding for inflammatory components in Parkinson's disease. Several findings obtained recently indicate that inflammation may contribute to the pathogenesis in Parkinson's diseas 1.33 KB 2015-11-22 4 9
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PubMed 21757251 Marsdenia tenacissima extract restored gefitinib sensitivity in resistant non-small cell lung cancer cells. Most non-small cell lung cancer (NSCLC) patients responding to gefitinib harbor activating m 1.67 KB 2015-11-26 6 3
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PubMed 16505253 SLC12A3 (solute carrier family 12 member [sodium/chloride] 3) polymorphisms are associated with end-stage renal disease in diabetic nephropathy. Diabetic nephropathy is the most common cause of end-st 1.36 KB 2015-11-19 3 3
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PubMed 11358390 Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis. More than 80% of the patients affected by hereditary hemochromatosis, a common inherited iron disorder, are homozygo 2.2 KB 2015-11-17 4 26
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PubMed 17585057 Common variation in the BRCA1 gene and prostate cancer risk. Rare inactivating mutations in the BRCA1 gene seem to play a limited role in prostate cancer. To our knowledge, however, no study has compr 1.7 KB 2015-11-23 6 5
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PubMed 24429876 Noninvasive detection of response and resistance in EGFR-mutant lung cancer using quantitative next-generation genotyping of cell-free plasma DNA. PURPOSE: Tumor genotyping using cell-free plasma DNA 1.89 KB 2015-11-27 7 14
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PubMed 15171721 Unfolded protein response is involved in the pathology of human congenital hypothyroid goiter and rat non-goitrous congenital hypothyroidism. The unfolded protein response (UPR) is an intracellular si 2.33 KB 2015-11-19 5 14
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PubMed 22844323 Interactions of miR-34b/c and TP53 polymorphisms on the risk of intracranial aneurysm. Several lines of evidence indicate that inflammatory processes play a key role in the happening and development o 1.28 KB 2015-11-26 7 10
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PubMed 18442119 Progranulin gene mutation with an unusual clinical and neuropathologic presentation. Progranulin gene (PGRN) mutations cause frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD- 1.28 KB 2015-11-24 6 5
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