Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP148385.RAaVyKnudxUsPdCCYQ0et91iOb5VqtxFn3iIdZLYjxLvg130_assertion description "[There are pronounced tubulointerstitial HSPG alterations in primary kidney disease, which may affect the inflammatory response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148385.RAaVyKnudxUsPdCCYQ0et91iOb5VqtxFn3iIdZLYjxLvg130_provenance.
- NP148390.RAQSuGhrUCmp-3tNlh9ZgXxzFgv3qvwIv0tgyzSk1kh6A130_assertion description "[In this population, neither heterozygosity nor homozygosity for the 677C-- > T and 1298A-- > C variants in MTHFR was associated with placental abruption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148390.RAQSuGhrUCmp-3tNlh9ZgXxzFgv3qvwIv0tgyzSk1kh6A130_provenance.
- NP148392.RAdtKuiu2nnGXRZlLd5biADsD7gQZH7ks_A2CMsoTua34130_assertion description "[A FV Leiden/methylenetetrahydrofolate reductase (MTHFR) T677T double genotype increases the risk for placental abruption ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148392.RAdtKuiu2nnGXRZlLd5biADsD7gQZH7ks_A2CMsoTua34130_provenance.
- NP148394.RAf0_TVLhQ0Ev8pA79lpbJwyQOL6EXiojJVHQL8aUKqX4130_assertion description "[The Glu298Asp variant of eNOS is associated with an increased risk for abruptio placentae in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148394.RAf0_TVLhQ0Ev8pA79lpbJwyQOL6EXiojJVHQL8aUKqX4130_provenance.
- NP148395.RAWP5R6BD40GGtGrANxyMpLdsVB_rvQQ1i8WrlkvjgvD8130_assertion description "[metallothionein in decidual cells seems to be responsible for the proper coexistence between decidual cells and activated immune cells that infiltrate both eutopic and ectopic decidua during cesarean section and placental abruption ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148395.RAWP5R6BD40GGtGrANxyMpLdsVB_rvQQ1i8WrlkvjgvD8130_provenance.
- NP148400.RAQRrWJ5WT6t0kTaiSEqwHb9ynKOoA1p0S6lmqQmXKQQw130_assertion description "[There was familial aggregation of ischemic stroke and a difference in degree of familial clustering between stroke subtypes/authors also found that the PDE4D gene is significantly associated with small-vessel infarction in inbred individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148400.RAQRrWJ5WT6t0kTaiSEqwHb9ynKOoA1p0S6lmqQmXKQQw130_provenance.
- NP148401.RAa-SE2PB69e3Vvv_cWhs5HZp4CJQn08mvqY1DOX1P3Aw130_assertion description "[Studies that employ genome-wide linkage scans with hundreds of small nuclear families have identified new susceptibility genes for coronary artery disease and myocardiaI infarction, including PDE4D (encoding phosphodiesterase 4D) for ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148401.RAa-SE2PB69e3Vvv_cWhs5HZp4CJQn08mvqY1DOX1P3Aw130_provenance.
- NP148402.RAQDP_LRGXlVnPEfq33cfFxgJJuTIOSyL0VGmiqu9G1G8130_assertion description "[Genome-wide association studies identified significant association for myocardiaI infarction with the LTA gene (encoding lymphotoxin-alpha) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148402.RAQDP_LRGXlVnPEfq33cfFxgJJuTIOSyL0VGmiqu9G1G8130_provenance.
- NP148414.RAVaQNiZz7XfKN2aCLTH3fEuRpcw1o9AQheV5AnVK62QU130_assertion description "[The results showed that conjunctival nevi, similar to skin nevi, have a high frequency of oncogenic BRAF mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148414.RAVaQNiZz7XfKN2aCLTH3fEuRpcw1o9AQheV5AnVK62QU130_provenance.
- NP148417.RATf03k76NVxVu9KsXbQYPKWET9zvzQClz9HQfP3ph-x8130_assertion description "[Mosaicism of FGFR3 caused an epidermal nevus syndrome with cerebral involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148417.RATf03k76NVxVu9KsXbQYPKWET9zvzQClz9HQfP3ph-x8130_provenance.
- NP148422.RASCSUgXXPoQs3kG3p7eJL1PVUu8qjp78So6w3CHlO_Xo130_assertion description "[XAF1 expression in melanoma tissues was significantly reduced compared with benign melanocytic nevi ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148422.RASCSUgXXPoQs3kG3p7eJL1PVUu8qjp78So6w3CHlO_Xo130_provenance.
- NP148423.RAXAHUs0yBIfnoj6vnarCCTo-ty_DWDQYUQ7pQH_MyJcg130_assertion description "[BRAF mutation is associated with melanoma and melanocytic nevi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148423.RAXAHUs0yBIfnoj6vnarCCTo-ty_DWDQYUQ7pQH_MyJcg130_provenance.
- NP148424.RAW-QjkAdKfm-ry5H28B70nfojstS-rdV-p5r2SDTIWRA130_assertion description "[BRAF mutation does not seem to be sufficient to produce MAPK activation in melanocytic nevi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148424.RAW-QjkAdKfm-ry5H28B70nfojstS-rdV-p5r2SDTIWRA130_provenance.
- NP148436.RAc-C51jkJMEiIqBNmVGfjc8m37kxemuorz8Pi_7ZTQIw130_assertion description "[Sata showed lower levels of STS mRNA for polycystic ovarian syndrome endometria without treatment and with endometrial hyperplasia compared to control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148436.RAc-C51jkJMEiIqBNmVGfjc8m37kxemuorz8Pi_7ZTQIw130_provenance.
- NP148438.RAQGfxspUYt9TJ316axzQ3NTdI9-5q2DZhpPSuzpa7En8130_assertion description "[uteroglobin expression is regulated by progesterone in the normal endometrium but regulation by progesterone receptor is lost in endometrial hyperplasia and carcinoma according to acquirement of tumorigenesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148438.RAQGfxspUYt9TJ316axzQ3NTdI9-5q2DZhpPSuzpa7En8130_provenance.
- NP148439.RAS0LSp2nlvmphXZkYf6qelGjSJJ3reLzHPJmKB6y2nsE130_assertion description "[Findings show that in endometrial hyperplasia and low-grade endometrioid endometrial carcinoma, coordinate increase in cdc25B and phosphorylated ER-alpha occurs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148439.RAS0LSp2nlvmphXZkYf6qelGjSJJ3reLzHPJmKB6y2nsE130_provenance.
- NP148440.RAaYNDg0OQAS5sFQcRvJwlie6x1hlzYuZe4ckTTcx8svE130_assertion description "[Patients harbouring G3-endometrioid endometrial carcinomas had significantly higher TFF3 serum concentration by ELISA when compared with healthy patients or patients harbouring endometrial hyperplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148440.RAaYNDg0OQAS5sFQcRvJwlie6x1hlzYuZe4ckTTcx8svE130_provenance.
- NP148444.RAbidCFkJDRILZY-fE6NxXLhANPbS1BhS0Ez-pNc46cfY130_assertion description "[study performed to determine the status of K-ras-2 in liver angiosarcomas (LAS) from workers occupationally exposed to vinyl chloride ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148444.RAbidCFkJDRILZY-fE6NxXLhANPbS1BhS0Ez-pNc46cfY130_provenance.
- NP148451.RAYhCENCfMZjnzM8xko5eQZnJ4xcZTTauif-vay5-vhLU130_assertion description "[LYVE-1 does not seem to be a reliable marker for proliferating infantile hemangiomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148451.RAYhCENCfMZjnzM8xko5eQZnJ4xcZTTauif-vay5-vhLU130_provenance.
- NP148452.RAaGapiZSXCt9u_YYHlKiMIifewfQ6vHslKsde3hFBJ_I130_assertion description "[Tie2 mRNA and protein were up-regulated in the pathogenesis of hemangioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148452.RAaGapiZSXCt9u_YYHlKiMIifewfQ6vHslKsde3hFBJ_I130_provenance.
- NP148454.RAdriBftsbwr0xftsrfrehG1QXQFzzDLLDHphPfyjSltM130_assertion description "[the defective TGFBR2 expression might contribute to the carcinogenesis and/or development of large cell carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148454.RAdriBftsbwr0xftsrfrehG1QXQFzzDLLDHphPfyjSltM130_provenance.
- NP148455.RAWk-PAztT9VvzNiLOYysdIppucIsyrq6CAFMpYWAg24Y130_assertion description "[FHIT was more highly expressed in large cell carcinomas and adenocarcinomas, and higher in females than males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148455.RAWk-PAztT9VvzNiLOYysdIppucIsyrq6CAFMpYWAg24Y130_provenance.
- NP148458.RAecaBulo4ZFBCR6HYas0cqIYAr3t7k2GdVrpPCGnGQxM130_assertion description "[there is an inverse relationship between Kras2 activation and RASSF1A promoter methylation in the majority of human lung adenocarcinomas and large cell carcinomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148458.RAecaBulo4ZFBCR6HYas0cqIYAr3t7k2GdVrpPCGnGQxM130_provenance.
- NP148461.RAa8THlmsMnCThcNTT8Ikw1SAeaqzH2NRmZhtzdLH_sfc130_assertion description "[there is an inverse relationship between Kras2 activation and RASSF1A promoter methylation in the majority of human lung adenocarcinomas and large cell carcinomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148461.RAa8THlmsMnCThcNTT8Ikw1SAeaqzH2NRmZhtzdLH_sfc130_provenance.
- NP148469.RAawSEAnIMoobMaGGAebU5-WUXQWAJLTXuiIj8OdIokg0130_assertion description "[Microsatellite instability with absent hMLH1 expression plays a role in the development of poorly differentiated adenocarcinoma and microsatellite-unstable mucinous carcinoma in the elderly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148469.RAawSEAnIMoobMaGGAebU5-WUXQWAJLTXuiIj8OdIokg0130_provenance.
- NP148471.RAVwHeTC1HBehphYzFh7d9x7477rD80MY8B6pkmKLXwuU130_assertion description "[Ectopic expression of a GlcNAc 6-O-sulfotransferase, GlcNAc6ST-2, in colonic mucinous adenocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148471.RAVwHeTC1HBehphYzFh7d9x7477rD80MY8B6pkmKLXwuU130_provenance.
- NP148477.RAR6wa-e6omWXWIhhnPdk4eBVEewgs07vraUZST7vQ2Dc130_assertion description "[p53 protein was estimated by immunohistochemistry of beta-catenin and p53 proteins in colorecta mucinous carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148477.RAR6wa-e6omWXWIhhnPdk4eBVEewgs07vraUZST7vQ2Dc130_provenance.
- NP148484.RAb8nX_DD9TqGe4E5DCUtB3gju-M6j0J2IXj4A_g9YLCU130_assertion description "[results suggest that microsatellite instability and p53 mutations are involved in tumor progression of dermatofibrosarcoma protuberans to fibrosarcoma as early and late events, respectively ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148484.RAb8nX_DD9TqGe4E5DCUtB3gju-M6j0J2IXj4A_g9YLCU130_provenance.
- NP148489.RAfYYYOohSm03I4olwxVQmGDYVgedKqYYpeAd8GXp7ezc130_assertion description "[Interleukin 1beta polymorphisms increase risk of hypochlorhydria and atrophic gastritis and reduce risk of duodenal ulcer recurrence in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148489.RAfYYYOohSm03I4olwxVQmGDYVgedKqYYpeAd8GXp7ezc130_provenance.
- NP148495.RAQLSZrEfCI2sGo8QuWCfJQ2fx9xXMGFcqzEDHhp9NhIk130_assertion description "[mRNA expression in atrophic gastritis before and after Helicobacter pylori eradication ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148495.RAQLSZrEfCI2sGo8QuWCfJQ2fx9xXMGFcqzEDHhp9NhIk130_provenance.
- NP148497.RAblRwLa4rSF0CH6aeSVXxv64lLFFE7SAr5GxdM9rnTIU130_assertion description "[Decreased expression of the Shh pathway in atrophic gastritis and gastric cancer might reflect altered differentiation processes within the gastric unit and contributes to the development of gastric atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148497.RAblRwLa4rSF0CH6aeSVXxv64lLFFE7SAr5GxdM9rnTIU130_provenance.
- NP148503.RAeDtRfx-uaOBdU912zsT5rGaiKjslT3o3gkX5hBjx8lg130_assertion description "[Comparative study in the expression of p53, EGFR, TGF-alpha, and cyclin D1 in verrucous carcinoma, verrucous hyperplasia, and squamous cell carcinoma of head and neck region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148503.RAeDtRfx-uaOBdU912zsT5rGaiKjslT3o3gkX5hBjx8lg130_provenance.
- NP148505.RAT1cxy5NaIcG-re7gLttS4JceizkLJ3j_QnE0mh3pRLE130_assertion description "[Gene-gene interaction between GATA3 and IL13 polymorphisms can influence the risk of childhood rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148505.RAT1cxy5NaIcG-re7gLttS4JceizkLJ3j_QnE0mh3pRLE130_provenance.
- NP148507.RAfPU3DfktMDPzKzRmmexGGd12sQz0LYw4b-0MLt3gWGE130_assertion description "[Increased expression of iNOS might have a role in the development of allergic inflammation in upper and lower airways and in comorbidity of allergic rhinitis and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148507.RAfPU3DfktMDPzKzRmmexGGd12sQz0LYw4b-0MLt3gWGE130_provenance.
- NP148509.RAR2yeB7RV0pEEQM3rj_dXJJ3SCrhjcUMCmwu69v1XNMc130_assertion description "[Suggest S100A7 polymorphisms are associated with allergic rhinitis in Swedish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148509.RAR2yeB7RV0pEEQM3rj_dXJJ3SCrhjcUMCmwu69v1XNMc130_provenance.
- NP148510.RAb9hjccaz6BPOT1GkHppWi2Bse14lZuEcqawrtAksUAE130_assertion description "[Interleukin-18 polymorphisms are associated with allergic rhinitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148510.RAb9hjccaz6BPOT1GkHppWi2Bse14lZuEcqawrtAksUAE130_provenance.
- NP148514.RAWT4bhDgKMVMgGl06914-AQ5ZCRDY_TkY7YOsgsEX5t4130_assertion description "[Carriers of MBL gene variant alleles (MBLva) might be one of the host-related genetic factors involved in atopic disorders, namely allergic rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148514.RAWT4bhDgKMVMgGl06914-AQ5ZCRDY_TkY7YOsgsEX5t4130_provenance.
- NP148515.RAWAPx4zn5g5sLbGkIdbBaQmX3aOYiQIrAX61IaaDd7fk130_assertion description "[Gene-gene interaction between GATA3 and IL13 polymorphisms can influence the risk of childhood rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148515.RAWAPx4zn5g5sLbGkIdbBaQmX3aOYiQIrAX61IaaDd7fk130_provenance.
- NP148522.RAciQT36j1IzY8fpLDvsFFP1LiCLWcGijF7ykoBksCw8s130_assertion description "[Reduction in anti-inflammatory activity by CC16 may contribute to the pathogenesis of allergic rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148522.RAciQT36j1IzY8fpLDvsFFP1LiCLWcGijF7ykoBksCw8s130_provenance.
- NP148527.RARQP7pGUq0ihy16M2wLfVGFVMLwXd0FpdEPZSQoHHnT4130_assertion description "[The study results indicated that the -403 and -28 alleles in the RANTES promoter region belong to the predictor gene set for allergic rhinitis and could be used in genomic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148527.RARQP7pGUq0ihy16M2wLfVGFVMLwXd0FpdEPZSQoHHnT4130_provenance.
- NP148528.RAaQDInhvLOjxve3-d8TyLWQHs3ZKLxj2MVk2-nQdmPTY130_assertion description "[Stronger immunoreactivity for PAR-2 was observed in allergic rhinitis nasal mucosa as compared with normal nasal mucosa/results suggest that PAR-2 may be involved in allergic nasal inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148528.RAaQDInhvLOjxve3-d8TyLWQHs3ZKLxj2MVk2-nQdmPTY130_provenance.
- NP148529.RAftJp__vY9h_v8_kQ4XY9cTJMh5IOm4uJqulS6k5zAN0130_assertion description "[increased circulating levels in symptomatic allergic rhinitis and asthmatic patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148529.RAftJp__vY9h_v8_kQ4XY9cTJMh5IOm4uJqulS6k5zAN0130_provenance.
- NP148530.RAcOaHpqbKYggq4nbqsqKVpuTqYyReTXOF-tje708Yrms130_assertion description "[Study shows that Fc gammaRIIa gene 131R allele represents an important genetic risk factor for bronchial asthma and allergic rhinitis susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148530.RAcOaHpqbKYggq4nbqsqKVpuTqYyReTXOF-tje708Yrms130_provenance.
- NP148533.RAS5MQw3DfujycKUKyvQAfq5S70nAlSrhG_g3tYfx5YpE130_assertion description "[the changes in cytokeratin 8/18 in hepatocytes might be one of the sources of pathogenesis of de novo autoimmune hepatitis after liver transplantation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148533.RAS5MQw3DfujycKUKyvQAfq5S70nAlSrhG_g3tYfx5YpE130_provenance.
- NP148534.RAVBs2GEOq-oPx2ubK_Dt2Q9Sy1IQAuAARKLYdxT-m4Gw130_assertion description "[Genetic mismatch can be considered a risk factor for de novo autoimmune hepatitis in liver transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148534.RAVBs2GEOq-oPx2ubK_Dt2Q9Sy1IQAuAARKLYdxT-m4Gw130_provenance.
- NP148535.RAbi5w3urLMP9n3dW99DqUUpNV48uCoE7cN6RcmUoh3Eg130_assertion description "[Susceptibility to type 1 Autoimmune hepatitis in Japanese patients is not influenced by FcgammaRIIA, FcgammaRIIB, or FCRL3 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148535.RAbi5w3urLMP9n3dW99DqUUpNV48uCoE7cN6RcmUoh3Eg130_provenance.
- NP148538.RAd-rw8vmIcSlYvBVU5ME4REolEPfp2OUY1hHpDDA-abQ130_assertion description "[Report human hepatic met-enkephalin and delta opioid receptor-1 immunoreactivities in viral and autoimmune hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148538.RAd-rw8vmIcSlYvBVU5ME4REolEPfp2OUY1hHpDDA-abQ130_provenance.
- NP148541.RAW8KaNuFgqQBA_xklwZZXzOy0Jca4mcWoPKIfPPsmkic130_assertion description "[Hepatitis C positive/LKM1+ sera recognize a specific conformational epitope on cytochrome 2 D6 between amino acids 254 to 288, the region that contains the major linear epitope in type 2 autoimmune hepatitis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148541.RAW8KaNuFgqQBA_xklwZZXzOy0Jca4mcWoPKIfPPsmkic130_provenance.
- NP148543.RAcDbhvWbSakg7aH6N-JKGHNJa9tsZKH35LXg1kGcu0HA130_assertion description "[HLA DRB1*0301 was associated with an increased risk of autoimmune hepatitis type 1 in this study in Thailand.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148543.RAcDbhvWbSakg7aH6N-JKGHNJa9tsZKH35LXg1kGcu0HA130_provenance.
- NP148546.RAVF1K6IFPxxb3z2bcqcONua6J1SlIW_gX4WuAT52y6_c130_assertion description "[The most influential gene on type 1 autoimmune hepatitis pathogenesis in Japanese is the HLA-DRB1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148546.RAVF1K6IFPxxb3z2bcqcONua6J1SlIW_gX4WuAT52y6_c130_provenance.
- NP148550.RAcygi9vNB8CQygAtHce7EtwFVzf-LSVTEyu1dhJEY99s130_assertion description "[Anti-CYP2D6 antibodies detected by quantitative radioligand assay and relation to antibodies to liver-specific arginase in patients with autoimmune hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148550.RAcygi9vNB8CQygAtHce7EtwFVzf-LSVTEyu1dhJEY99s130_provenance.
- NP148552.RAaxdpbXvLW0jlpnklCvg6JVG1p4Z8GUGEHDByW4JMU34130_assertion description "[the changes in cytokeratin 8/18 in hepatocytes might be one of the sources of pathogenesis of de novo autoimmune hepatitis after liver transplantation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148552.RAaxdpbXvLW0jlpnklCvg6JVG1p4Z8GUGEHDByW4JMU34130_provenance.
- NP148557.RAYBbsytGcNbbccdJoXZ1MG1rTAZS0U5DvJoi6EL2PQc0130_assertion description "[ghrelin stimulates ACTH secretion directly from human tumoural corticotrophs, as well as normal rat pituitary; marked ACTH release elicited by ghrelin in patients with Cushing's disease is due, at least in part, to its action on the pituitary tumour ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148557.RAYBbsytGcNbbccdJoXZ1MG1rTAZS0U5DvJoi6EL2PQc0130_provenance.
- NP148558.RASDNEjBuRai3jGWf6k2S3m2J94R6y1T9k8_jdoFH-VCQ130_assertion description "[Brg1 and HDAC2 have roles in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148558.RASDNEjBuRai3jGWf6k2S3m2J94R6y1T9k8_jdoFH-VCQ130_provenance.
- NP148570.RASd4RNpUP3_zoXjWV0MXMpGjjsHWTSap5Wb6ESfdq2ng130_assertion description "[Data show that serum procalcitonin might be of value for distinguishing between infected and non-infected foot ulcers in subgroups of diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148570.RASd4RNpUP3_zoXjWV0MXMpGjjsHWTSap5Wb6ESfdq2ng130_provenance.
- NP148574.RAdm7eG_3YgGvTfdvB9RiolpQNsxkIF74pO3RA8wid7Pw130_assertion description "[present in diabetic foot ulcers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148574.RAdm7eG_3YgGvTfdvB9RiolpQNsxkIF74pO3RA8wid7Pw130_provenance.
- NP148576.RAWF8qSrQH_zZDdSbLZipNYYog7A0KkGDZ5PBhDEkbj7A130_assertion description "[present in diabetic foot ulcer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148576.RAWF8qSrQH_zZDdSbLZipNYYog7A0KkGDZ5PBhDEkbj7A130_provenance.
- NP148578.RAW9AE9EuDegi1YnjB_GC-O9Fwrkvx29ZdwZwa9SSX_Gs130_assertion description "[EGFR mutations in carcinogenesis of lung adenocarcinoma: distinct pathological subtypes with different EGFR mutations: homozygous deletion in exon 19 in the papillary adenocarcinoma and a point mutation of L858R in exon 21 in the tubular adenocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148578.RAW9AE9EuDegi1YnjB_GC-O9Fwrkvx29ZdwZwa9SSX_Gs130_provenance.
- NP148579.RAc8vuqqtsEsBWfhEAbxskITFWHXGZv1SoDiSmvdH9lgM130_assertion description "[Increased expression of protease-activated receptor 2 is associated with papillary adenocarcinoma of the gallbladder ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148579.RAc8vuqqtsEsBWfhEAbxskITFWHXGZv1SoDiSmvdH9lgM130_provenance.
- NP148591.RAeYsoEMesdbxHUgzy-ynzlFaDn2SrLqIUyKlBHKhv0-4130_assertion description "[EGFR protein is up-regulated in the inverted papilloma, and both synchronous and metachronous carcinoma with inverted papilloma of the nasal cavity, suggesting EGFR is involved in the transformation from inverted papilloma to squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148591.RAeYsoEMesdbxHUgzy-ynzlFaDn2SrLqIUyKlBHKhv0-4130_provenance.
- NP148592.RARmgp-Qq9mJigY1cx70B8UusA1XMLS0NXjabGwZZmTx0130_assertion description "[Changes in p53 expression seen in urothelial and sinonasal inverted papillomas suggest they may share common evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148592.RARmgp-Qq9mJigY1cx70B8UusA1XMLS0NXjabGwZZmTx0130_provenance.
- NP148593.RAchXwlYP25sNEeitMV6ddVjuCVmx9jkx39FGZm8dhfCE130_assertion description "[An inflammation-dependent EGF-R cascade causes overproduction of the gel-forming mucin MUC5AC, which accumulates in cholesterol gallstone disease/ability to interrupt this cascade is of potential interest in the prevention of cholesterol gallstones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148593.RAchXwlYP25sNEeitMV6ddVjuCVmx9jkx39FGZm8dhfCE130_provenance.
- NP148597.RASOklTszVnXzm3mtiIUh-gQ_RTjKjAfMe_txwate85-M130_assertion description "[MUC5AC is over-expressed in gallstone disease, despite the decrease in the expression of EGFR mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148597.RASOklTszVnXzm3mtiIUh-gQ_RTjKjAfMe_txwate85-M130_provenance.
- NP148607.RAdem0-qwIE8hbzkDiRmh686m_XVZiqZkb3TAxb2TE49A130_assertion description "[An insertion allele is found to be associated with gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148607.RAdem0-qwIE8hbzkDiRmh686m_XVZiqZkb3TAxb2TE49A130_provenance.
- NP148611.RAUWEQG5YLNvvG1ULONlwEnLEjKAN8HXJ9QAkmnK829w8130_assertion description "[APOC1 HpaI polymorphism is associated with gallstone disease and shows gender-specific differences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148611.RAUWEQG5YLNvvG1ULONlwEnLEjKAN8HXJ9QAkmnK829w8130_provenance.
- NP148612.RAXYgQWrHkvrmoxbM6uEFAQnhI6GsB8nPuYCfhdXoXA20130_assertion description "[The ADRB3 Trp64Arg polymorphism is associated with gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148612.RAXYgQWrHkvrmoxbM6uEFAQnhI6GsB8nPuYCfhdXoXA20130_provenance.
- NP148619.RATeiPFhuhrreqJXcggmnEY3xq5diIPkRHak2C1HNcnHY130_assertion description "[Bcl-x was associated with increased survival in thymic neoplasms/: Bax ratio was also associated with survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148619.RATeiPFhuhrreqJXcggmnEY3xq5diIPkRHak2C1HNcnHY130_provenance.
- NP148620.RAUTXxCGLNedKvqO2iMhMNxX44U9uOsWyAcXm9v_0PRhk130_assertion description "[we have shown an increased expression of ErbB-2 vestibular schwannomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148620.RAUTXxCGLNedKvqO2iMhMNxX44U9uOsWyAcXm9v_0PRhk130_provenance.
- NP148634.RAZaXXWnPGh18HajUyCUe2SJz81V0L5ADy3jS7zoHQ8U8130_assertion description "[Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148634.RAZaXXWnPGh18HajUyCUe2SJz81V0L5ADy3jS7zoHQ8U8130_provenance.
- NP148638.RAdaeWQpMZIXl-LUJ9N_UnzH3W7XPpcEqHqqo2HSI-hR8130_assertion description "[Coexpression of HIF-1alpha and CAIX in the epithelium in phyllodes tumors points to epithelial hypoxia, most probably caused by relatively distant blood vessels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148638.RAdaeWQpMZIXl-LUJ9N_UnzH3W7XPpcEqHqqo2HSI-hR8130_provenance.
- NP148644.RAYD9qC843S1pWf2NKB2TERGT8AjXuPjCDZxm2vjIeiNM130_assertion description "[Data show that alpha (1) -microglobulin/bikunin precursor specifically interacts with the ORF3 protein of hepatitis E virus and has a direct role in enhancing alpha (1) microglobulin export from the hepatocyte.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148644.RAYD9qC843S1pWf2NKB2TERGT8AjXuPjCDZxm2vjIeiNM130_provenance.
- NP148649.RAXhfv5f4pE5ww1oRziS5VJZaDH72N2MXTZIbLA77Q4fw130_assertion description "[Results suggest that MCP-1/CCL2 and IP-10/CXCL10 produced by astrocytes may activate astrocytes in an autocrine or paracrine manner and direct reactive gliosis followed by migration and activation of microglia/macrophages in demyelinating lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148649.RAXhfv5f4pE5ww1oRziS5VJZaDH72N2MXTZIbLA77Q4fw130_provenance.
- NP148658.RAfPj0cGeWyvhpT1P12b6ElURtgEMFCKnsvdjvvJMP1NI130_assertion description "[The prothrombin G20210A variant was not detected in either the cerebral venous and sinus thrombosis patients or the healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148658.RAfPj0cGeWyvhpT1P12b6ElURtgEMFCKnsvdjvvJMP1NI130_provenance.
- NP148669.RAfs_ht8PFkqeQvOje14ZYYUPGrK2X6ZCUUP_i1F6SwDk130_assertion description "[during the acute phase of stroke/transient ischemic attack, individuals with the AG/GG genotype had significantly elevated CRP concentrations as opposed to those with the AA genotype (2.02 +/- 1.59 vs.1.73 +/- 1.69 mg/l, P = 0.027) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148669.RAfs_ht8PFkqeQvOje14ZYYUPGrK2X6ZCUUP_i1F6SwDk130_provenance.
- NP148671.RAV0BbfCNd-oVVw29ggV80P9rrcxtvoCalHS-M8xqj2Xw130_assertion description "[The HLA-G genotype, homozygous for the presence of the 14 bp sequence in exon 8, was significantly associated with reduced fertility with respect to unsuccessful IVF treatments and increased risk of recurrent miscarriage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148671.RAV0BbfCNd-oVVw29ggV80P9rrcxtvoCalHS-M8xqj2Xw130_provenance.
- NP148672.RAbib7B5IV_4yx2-SeGU70v7HGbfLoLiN6bNWL2Ro9yVo130_assertion description "[Single nucleotide mutation associated with habitual abortion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148672.RAbib7B5IV_4yx2-SeGU70v7HGbfLoLiN6bNWL2Ro9yVo130_provenance.
- NP148676.RAeGs5GMK6IRf8Nk9M4nro5QiotMSumzC4SMoo6eAmGP4130_assertion description "[Some of SNPs found in the factor V gene may predispose women to acquired activated protein C resistance and recurrent miscarriage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148676.RAeGs5GMK6IRf8Nk9M4nro5QiotMSumzC4SMoo6eAmGP4130_provenance.
- NP148677.RAVkDr6Y24Y5nwifLo6eatI3oN5geXFQYoJDH3-nZ0Aj8130_assertion description "[Case Report: Activated protein C concentrate treatment for skin necrosis under warfarin treatment in severe genetic protein C deficiency combined with prothrombin mutation and factor V Leiden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148677.RAVkDr6Y24Y5nwifLo6eatI3oN5geXFQYoJDH3-nZ0Aj8130_provenance.
- NP148681.RAUyraCl0RLjmvF1V6vPavTk4Gd6Vms8IO_YTv5PU85zE130_assertion description "[Case Report: Activated protein C concentrate treatment for skin necrosis under warfarin treatment in severe genetic protein C deficiency combined with prothrombin mutation and factor V Leiden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148681.RAUyraCl0RLjmvF1V6vPavTk4Gd6Vms8IO_YTv5PU85zE130_provenance.
- NP148683.RAcFEnvnd3vOjqKs33T6A-B0e1V4pgArUqfcNNUq_Sp4Y130_assertion description "[Smoking-induced vascular endothelium injury reduces activated protein C in a cigarette smoke dose-dependent manner, leading to activated protein C deficiency hypercoagulability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148683.RAcFEnvnd3vOjqKs33T6A-B0e1V4pgArUqfcNNUq_Sp4Y130_provenance.
- NP148688.RASJ13Tp4f99LmMQcDELSdFHf_-XRk_7LoF-zrk_Fg7PA130_assertion description "[Hyperhomocysteinemia, a risk factor for coronary diseases, can be caused by genetic mutations in BHMT2 metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148688.RASJ13Tp4f99LmMQcDELSdFHf_-XRk_7LoF-zrk_Fg7PA130_provenance.
- NP148690.RAfN2UxK-3ghbMsx8KvIp9AVC7deIr3-aa9YSOtqSHCL4130_assertion description "[Mesenteric venous thrombosis with bowel infarction and hyperhomocysteinemia due to homozygous methylenetetrahydrofolate reductase C677T genotype (Case Report).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148690.RAfN2UxK-3ghbMsx8KvIp9AVC7deIr3-aa9YSOtqSHCL4130_provenance.
- NP148693.RAQ8uEP80ScDiDtoZLVhBlYySXiMeerbfS1nB5wexSFcQ130_assertion description "[Report on coexistence of prothrombin G20210A, factor V-Leiden, and homozygous MTHFR C677T with hyperhomocysteinemia in livedoid vasculopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148693.RAQ8uEP80ScDiDtoZLVhBlYySXiMeerbfS1nB5wexSFcQ130_provenance.
- NP148694.RAbwJbJW_QxVdpEpRb7UReTKMft5dNkhLAP9WQZ2_7PNk130_assertion description "[hyperhomocysteinemia is significantly related to the severity of CAD independent on MTHFR polymorphism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148694.RAbwJbJW_QxVdpEpRb7UReTKMft5dNkhLAP9WQZ2_7PNk130_provenance.
- NP148696.RAfOPCMmdO6KicUhgwHKmGEPxwvqfCWzYmMor1Qy9DF5U130_assertion description "[If hyperhomocysteinemia is important in the pathogenesis of glaucoma, this study does not support a role for MTHFR polymorphisms in this context.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148696.RAfOPCMmdO6KicUhgwHKmGEPxwvqfCWzYmMor1Qy9DF5U130_provenance.
- NP148699.RAXP3E6E7i4eZRlyH0ob0MliwQmnTIUo4AaRfJHDQ-Xns130_assertion description "[study evaluated the importance of the polymorphisms in the MTHFR, MTRR, and CBS genes for hyperhomocysteinemia, considering B12 and folate levels; results confirm that genetic interactions can influence on the homocysteine status ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148699.RAXP3E6E7i4eZRlyH0ob0MliwQmnTIUo4AaRfJHDQ-Xns130_provenance.
- NP148708.RAX9NZ__zEyLssYc9R6iFYy0NbyN3vCqfGQ1LVy0XQ30Y130_assertion description "[An effective risk factor was found when the polymorphisms of the ACE genes = and hyperhomocysteinemia were associated with risk of chronic kidnen allograft dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148708.RAX9NZ__zEyLssYc9R6iFYy0NbyN3vCqfGQ1LVy0XQ30Y130_provenance.
- NP148709.RAfaL_AQ7EADWCrRm-jWsS_HAZVNQa-pN37K1SHaoRlqY130_assertion description "[betaine-homocysteine methyltransferase (BHMT) transgenic mice are resistant to alcohol or high methionine low folate diet -induced hyperhomocysteinemia and liver steatosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148709.RAfaL_AQ7EADWCrRm-jWsS_HAZVNQa-pN37K1SHaoRlqY130_provenance.
- NP148718.RAaPgGylI2ZcQ9rOS4eszKiV161Qt1sjURHcJap0ElUzM130_assertion description "[metallothionein measured in renal specimens from cadaver kidneys was restricted to tubular cells with no differences between controls and patients with death due to chronic diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148718.RAaPgGylI2ZcQ9rOS4eszKiV161Qt1sjURHcJap0ElUzM130_provenance.
- NP148719.RAabspekFxVVFzCJ22Vbyo-YW8vvN2KrmZ0FAeOC1qfzM130_assertion description "[Serum amyloid A appears to be important mediator of inflammatory process, possibly contributing to pool of IL-8 produced in chronic diseases, which may play a role in degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148719.RAabspekFxVVFzCJ22Vbyo-YW8vvN2KrmZ0FAeOC1qfzM130_provenance.
- NP148720.RAeabliBmEwdeJ0eiiN2-cm4PIvad_CfOBzfdpjHgTRBE130_assertion description "[EPO levels increased incompensatively in anemia of chronic disease (ACD) children, which may be a cause of ACD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148720.RAeabliBmEwdeJ0eiiN2-cm4PIvad_CfOBzfdpjHgTRBE130_provenance.
- NP148725.RAVW4pUT7avMUXhMISv25ofFINoKCPEdgu-jlSB0hVqlc130_assertion description "[in the investigated Finnish pedigree with hereditary pancreatitis, the PRSS1 mutation R122H is linked with chronic disease; although the SPINK1 mutation (N34S) was also observed in two individuals, it was not linked with the disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148725.RAVW4pUT7avMUXhMISv25ofFINoKCPEdgu-jlSB0hVqlc130_provenance.
- NP148728.RAbgVvMiflr3nIE5ulGh8gX8xSeiR-D6O9I1_ChV1f9yY130_assertion description "[Results partly confirm previous findings of a significant gene-environment interaction of SLC6A4, indicating higher mental vulnerability to social stress and chronic disease/sample characteristics and risk were highly different from previous studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148728.RAbgVvMiflr3nIE5ulGh8gX8xSeiR-D6O9I1_ChV1f9yY130_provenance.
- NP148729.RAQwUCcey3YnsPHovHoFhQZgRElkBRUa9THwO6iBpon2Y130_assertion description "[Among patients with chronic illness, carriers of the s allele of 5-HTTLPR are more vulnerable to depression, perceived stress, and high norepinephrine secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148729.RAQwUCcey3YnsPHovHoFhQZgRElkBRUa9THwO6iBpon2Y130_provenance.
- NP148730.RAdjjB7o5XQ-HZLPW5BO-W8sM2qLqqn_LybGssLNiRjeU130_assertion description "[Serum amyloid A appears to be important mediator of inflammatory process, possibly contributing to pool of IL-8 produced in chronic diseases, which may play a role in degenerative diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148730.RAdjjB7o5XQ-HZLPW5BO-W8sM2qLqqn_LybGssLNiRjeU130_provenance.
- NP148738.RAXUeO_HbHsmz9kT-7_de-3zNtVIeGEBtVz9U56rLys0o130_assertion description "[a difference in genotype frequencies of the V249I and T280M polymorphisms in CX (3) CR1 between peripheral arterial disease patients and controls could not be detected ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148738.RAXUeO_HbHsmz9kT-7_de-3zNtVIeGEBtVz9U56rLys0o130_provenance.
- NP148748.RAcTCAKYKqX1SDYntn7ldbmxA5TxnE4IpWHPJXpifx5qU130_assertion description "[None of the examined NRP1 polymorphisms showed a difference in their allelic distribution between leg ulcer patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148748.RAcTCAKYKqX1SDYntn7ldbmxA5TxnE4IpWHPJXpifx5qU130_provenance.
- NP148754.RAT-oSOxyWwqCZTMckTEJcaoep8dcBwyOTEzqB8TNNMac130_assertion description "[analysis of the clinical manifestations, laboratory phenotype and genotype of congenital factor X deficiency in families ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148754.RAT-oSOxyWwqCZTMckTEJcaoep8dcBwyOTEzqB8TNNMac130_provenance.
- NP148756.RAR-udFSoL2oUT-8JFxsFfZBmCIDD0eDbV6n-6yMV1jgY130_assertion description "[Among patients admitted to the PICU with a meningococcal infection, those with the variant allele of the beta-adrenergic receptor gene-1 at locus 389 were more likely to have a high pediatric risk of mortality score on admission ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148756.RAR-udFSoL2oUT-8JFxsFfZBmCIDD0eDbV6n-6yMV1jgY130_provenance.
- NP148761.RAa0UIeh-mJU67JYgCxY8kVwQHKpkFpRtbqI-VVQsbLkw130_assertion description "[Adult-onset type II citrullinemia is caused by mutations of the SLC25A13 gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148761.RAa0UIeh-mJU67JYgCxY8kVwQHKpkFpRtbqI-VVQsbLkw130_provenance.