Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP144775.RAet5sz08pTt5vqWC-S0Y6MEeXfkLpFhVwRBWGcSXw3Gg130_assertion description "[identified an antigen recognized on a human non-small-cell lung carcinoma by a cytotoxic T lymphocyte clone derived from autologous tumor-infiltrating lymphocytes/antigenic peptide is presented by HLA-A2 and is encoded by the CALCA gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144775.RAet5sz08pTt5vqWC-S0Y6MEeXfkLpFhVwRBWGcSXw3Gg130_provenance.
- NP144777.RAX6dTFlrCTj0lARCKdhVPbH2juGhi5MkIa8mvXrZ-aFw130_assertion description "[expression is closely related to invasiveness and metastasis in non-small-cell lung carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144777.RAX6dTFlrCTj0lARCKdhVPbH2juGhi5MkIa8mvXrZ-aFw130_provenance.
- NP144778.RAegHLRX8cTg928_dOM9cl1J5u3x0vw5gBvYPd4J5PWGs130_assertion description "[Signaling pathways involved in PTGS2 induction by hepatocyte growth factor in non-small-cell lung carcinoma are reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144778.RAegHLRX8cTg928_dOM9cl1J5u3x0vw5gBvYPd4J5PWGs130_provenance.
- NP144782.RAQyQmb6H4Rov3sg43x1b56BIQ0lMNM9W5hGqFHh04K5c130_assertion description "[Crucial participants in tumour invasion and metastases are matrix metalloproteinases, tissue inhibitor of metalloproteinase inhibitors and cellular adhesion molecules/play roles in tumour invasion and metastasis in non-small-cell lung carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144782.RAQyQmb6H4Rov3sg43x1b56BIQ0lMNM9W5hGqFHh04K5c130_provenance.
- NP144785.RAQu0ZeCPeEzMg8NSOtp0-7uDRWUsS9kwC_8EA19VRXt4130_assertion description "[Elevated levels of hMTH1 protein is asociated with non-small-cell lung carcinomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144785.RAQu0ZeCPeEzMg8NSOtp0-7uDRWUsS9kwC_8EA19VRXt4130_provenance.
- NP144790.RAV2l0HTSnUQzD2BDIKwApsNURJPn_Nw7vz7bftqySm_Q130_assertion description "[GSTN1 polymorphism is associated with increased risk for small cell carcinoma in smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144790.RAV2l0HTSnUQzD2BDIKwApsNURJPn_Nw7vz7bftqySm_Q130_provenance.
- NP144792.RAV5puyoZkPo3PdJcg7gCt4_gaQ8yG9KfgHRaxl6dRiCI130_assertion description "[A significant proportion (27%) of small cell carcinomas of the urinary bladder expressed c-kit, suggesting that it may prove useful as a therapeutic target in small cell carcinoma of the urinary bladder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144792.RAV5puyoZkPo3PdJcg7gCt4_gaQ8yG9KfgHRaxl6dRiCI130_provenance.
- NP144794.RAfIyDYCPPrd2Zz91ZDGL06DHn_nxFjzcWOTK4OaDNXSU130_assertion description "[results suggest that p16 is up-regulated or accumulated in small cell carcinomas (SmCCs) of the uterine cervix, probably caused by infection with human papillomavirus; p14 inactivation is of high prevalence in SmCCs ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144794.RAfIyDYCPPrd2Zz91ZDGL06DHn_nxFjzcWOTK4OaDNXSU130_provenance.
- NP144795.RAVeIhZStbzi09U5di0Yablwbqf6SCr4hUaovrYcjfjmA130_assertion description "[MASH1 is a useful adjunct marker for differentiating small cell carcinoma of the lung from Merkel cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144795.RAVeIhZStbzi09U5di0Yablwbqf6SCr4hUaovrYcjfjmA130_provenance.
- NP144797.RAczPnlBuvsv4UrqKGVQKXrqOC5a0FV-s9p5Hska8tV44130_assertion description "[Immunohistochemical detection of KOC expression may be a useful diagnostic tool for distinguishing between small cell carcinoma and carcinoid tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144797.RAczPnlBuvsv4UrqKGVQKXrqOC5a0FV-s9p5Hska8tV44130_provenance.
- NP144806.RAcscvClM_dmksi8wSd_oY4ZOd76-22HFDrmlxdE3tEqw130_assertion description "[PKP2 mutation in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) correlates with earlier onset of symptoms and arrhythmia/experience implanted cardioverter/defibrillator (ICD) interventions irrespective of classic risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144806.RAcscvClM_dmksi8wSd_oY4ZOd76-22HFDrmlxdE3tEqw130_provenance.
- NP144810.RAa4WaLopusWSIbr7BHqByJtaH2MI99_1PzO6XwImGTR8130_assertion description "[The missense mutation of MYH7 may lead to Myosin storage myopathy with cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144810.RAa4WaLopusWSIbr7BHqByJtaH2MI99_1PzO6XwImGTR8130_provenance.
- NP144814.RAQxi7hYrSGTN8Rs07nHLuDmomKgJ6Pts81gjB7hekcMk130_assertion description "[the the kallikrein-kinin system has roles in intramyocardial inflammation, endothelial dysfunction and oxidative stress in diabetic cardiomyopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144814.RAQxi7hYrSGTN8Rs07nHLuDmomKgJ6Pts81gjB7hekcMk130_provenance.
- NP144824.RAat_9RjIS28rVXLNaX9pbITsf_G6k4x_77EcHEp4hhZY130_assertion description "[The researchers identified a nonsense Q312X mutation in the hemojuvelin gene that increases ferritin levels and leads to juvenile hemochromatosis that is associated with severe cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144824.RAat_9RjIS28rVXLNaX9pbITsf_G6k4x_77EcHEp4hhZY130_provenance.
- NP144844.RAWPBZjstyTSBvvZWG0iwDUyIhgfWdl8x0tJSIh32oG-g130_assertion description "[IgG antibodies to TpnI are increased in a significant number of patients with both idiopathic dilated and ischemic cardiomyopathy, yet it appears that these autoantibodies cannot bind heart muscle cells or influence [Ca2+]i transients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144844.RAWPBZjstyTSBvvZWG0iwDUyIhgfWdl8x0tJSIh32oG-g130_provenance.
- NP144849.RAa30VhBcuyj-RmhwjChAcQ5t4VFze5G_lZ09Y3K-rY_I130_assertion description "[Polymorphosm in beta1-adrenergic receptors determine improvement in left ventricular systolic function in nonischemic cardiomyopathy patients with heart failure after chronic treatment with carvedilol ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144849.RAa30VhBcuyj-RmhwjChAcQ5t4VFze5G_lZ09Y3K-rY_I130_provenance.
- NP144853.RAQDLGn_YfepAFkNRYOrwaCBJBww-u2nXHlT_Xh4HQAy4130_assertion description "[results show no significant differences either between Chagas disease cardiomyopathy (CCC) and asymptomatic patients, or among CCC patients according to severity of cardiomyopathy with respect to TNFa or -308 TNF promoter polymorphisms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144853.RAQDLGn_YfepAFkNRYOrwaCBJBww-u2nXHlT_Xh4HQAy4130_provenance.
- NP144855.RAfD8Yi2YiuP_TlPQziqqXama6YpreGPWjAf3crZFvn3s130_assertion description "[AP-2alpha as a novel cardiac regulator implicated in the activation of apoptosis in idiopathic-dilated cardiomyopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144855.RAfD8Yi2YiuP_TlPQziqqXama6YpreGPWjAf3crZFvn3s130_provenance.
- NP144856.RAT6KL_qyv_ckThUZZBpp2aaITxzigsB1H2tVuiuMpcyI130_assertion description "[Recent studies have elucidated the function of the PGC-1 coactivators in different tissues and have highlighted the implications of PGC-1 dysregulation in diseases such as diabetes, obesity, cardiomyopathy, or neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144856.RAT6KL_qyv_ckThUZZBpp2aaITxzigsB1H2tVuiuMpcyI130_provenance.
- NP144859.RAUnQyCk6OtOw7ibAnC-fWTcbOXdGDFarG8G1uI8valOA130_assertion description "[p38 alpha MAP kinase is one of the critical downstream signals for development of cardiomyopathy following chronic beta 2-adrenergic receptor stimulation in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144859.RAUnQyCk6OtOw7ibAnC-fWTcbOXdGDFarG8G1uI8valOA130_provenance.
- NP144862.RAeAL8Gv8Te0S9t50dJy9rA_Tca85fWtDiIlMxjbL6GuE130_assertion description "[EGFR may have a role in recurrence of rectal cancer after radiotherapy and surgery ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144862.RAeAL8Gv8Te0S9t50dJy9rA_Tca85fWtDiIlMxjbL6GuE130_provenance.
- NP144864.RARnTmllnehA7pNOAgyM9gOFi1IMsmHR1b3FJnpaGaQkQ130_assertion description "[MTHFR 677T-1298A haplotype in genomic DNA has the potential to be a predictive marker of tumor response in rectal cancer patients submitted to preoperative chemoradiotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144864.RARnTmllnehA7pNOAgyM9gOFi1IMsmHR1b3FJnpaGaQkQ130_provenance.
- NP144866.RAa8KdKmCLeDzR7wU6ALsm9NFQfYuGa6sXldEMM4OIRbg130_assertion description "[E-cadherin is hypermethylated and shows low expression in colon and rectal neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144866.RAa8KdKmCLeDzR7wU6ALsm9NFQfYuGa6sXldEMM4OIRbg130_provenance.
- NP144872.RAVv26V9ExtEh85_6vgM3Pqu3_hHgy4CtHTIlVCBzeiNo130_assertion description "[Expression of bcl (2) was present in only 5 cases or rectal cancer with the postchemotherapy changes being not significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144872.RAVv26V9ExtEh85_6vgM3Pqu3_hHgy4CtHTIlVCBzeiNo130_provenance.
- NP144876.RASW8iLj8IzuWFzRkRCBxXOllBr-TGrT5iHTrTiUrVW0A130_assertion description "[Cetuximab-based chemoradiotherapy increased PDGFRbeta levels in patients with rectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144876.RASW8iLj8IzuWFzRkRCBxXOllBr-TGrT5iHTrTiUrVW0A130_provenance.
- NP144881.RAWhgmskLu05LhJpPbI0Tmf7YaSFlcTYesrl1JaXGa9Qk130_assertion description "[The CYP2E1 c2/c2 genotype increases susceptibility to rectal cancer and the gene-environmental interactions between the CYP2E1 polymorphism and smoking or alcohol drinking exist for colorectal neoplasia in general.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144881.RAWhgmskLu05LhJpPbI0Tmf7YaSFlcTYesrl1JaXGa9Qk130_provenance.
- NP144896.RAd-KgWJQmkzXLmkto1y1joLzLgJGHNLl3Z8a6g1M5hCc130_assertion description "[Data show that beta-catenin is overexpressed in Kaposi sarcoma and primary effusion lymphoma, and that this overexpression is regulated by the Kaposi's sarcoma-associated herpesvirus (KSHV) latency-associated nuclear antigen LANA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144896.RAd-KgWJQmkzXLmkto1y1joLzLgJGHNLl3Z8a6g1M5hCc130_provenance.
- NP144900.RAdDg9xtJuZXFN8cxPQ03NIVhE5hm8xLXXAkY-pc8fBOc130_assertion description "[In vitro, primary effusion lymphoma -induced angiogenesis is dependent on VEGF and VEGF receptors/, although PEL cells produce VEGF and bFGF transcripts, they only secrete VEGF in vitro ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144900.RAdDg9xtJuZXFN8cxPQ03NIVhE5hm8xLXXAkY-pc8fBOc130_provenance.
- NP144905.RAUmVdmxFl-DB0eR2ftFCt3CkOuIqRpy3FA_jHEK4v3Mc130_assertion description "[POLG polymorphism may be a contributing factor in the pathogenesis of testicular germ cell cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144905.RAUmVdmxFl-DB0eR2ftFCt3CkOuIqRpy3FA_jHEK4v3Mc130_provenance.
- NP144909.RAU549pBaOMA6lGpK46pqm3q5Y42c1KLLSLc482GB-Nrk130_assertion description "[TSPY has been used as a marker for identifying germ cells at risk for neoplastic transformation in gonadoblastoma and testicular germ cell tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144909.RAU549pBaOMA6lGpK46pqm3q5Y42c1KLLSLc482GB-Nrk130_provenance.
- NP144918.RASY74h3qTgn34aUy0QdqSkTShhg1zrRej5wYvX4-z8Sg130_assertion description "[The variant, p/, found in only one case of testiciular germ cell tumor, is within a known functional domain of DND1 and is highly conserved through evolution; mutations in DND1 make, at most, a very small contribution to TGCT susceptibility ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144918.RASY74h3qTgn34aUy0QdqSkTShhg1zrRej5wYvX4-z8Sg130_provenance.
- NP144919.RAYktbuyE3juoAPn03QevpNH9cZb3rLQT4U7f5ze3CeRY130_assertion description "[XRCC1 Arg399Gln polymorphism may genetically modify the development and progression of testicular germ cell tumors through genomic instability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144919.RAYktbuyE3juoAPn03QevpNH9cZb3rLQT4U7f5ze3CeRY130_provenance.
- NP144920.RAV7ygy_OxKRmA9CgbB7TP-uOQ-8x5vjNo1yGibwhYeCA130_assertion description "[FNBP2 gene was linked to IKBKE and NORE1 genes on human chromosome 1q32.1/mRNA was expressed in melanoma, germ cell tumors, chondrosarcoma and retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144920.RAV7ygy_OxKRmA9CgbB7TP-uOQ-8x5vjNo1yGibwhYeCA130_provenance.
- NP144923.RAZsn1BLh-_2kRmgdDAAa22DvVgCsYtf_wA2tMx2VbLD0130_assertion description "[POU5F1 (OCT3/4) identifies cells with pluripotent potential in human germ cell tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144923.RAZsn1BLh-_2kRmgdDAAa22DvVgCsYtf_wA2tMx2VbLD0130_provenance.
- NP144925.RAfFlzhl23HM01v12ojUqGON-jQVOF7KHCkGX-BPtwugg130_assertion description "[The KIT-phosphatidylinositol 3-kinase-Akt protein pathway is constitutively activated in testicular germ cell tumors, due to overexpression of KIT protein and/or gain-of-function mutations in the c-kit gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144925.RAfFlzhl23HM01v12ojUqGON-jQVOF7KHCkGX-BPtwugg130_provenance.
- NP144926.RAUc4HokOKBAoxa_85irSqKIg-OS-T2kD7g6p40b9r3_w130_assertion description "[Further understanding of KIT signaling in testicular germ cell tumors may lead to novel therapeutic approaches for these tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144926.RAUc4HokOKBAoxa_85irSqKIg-OS-T2kD7g6p40b9r3_w130_provenance.
- NP144928.RAbDzj2u4bQhDk2lKJd61l1ji8jZ0gruH4jxOHXIf1A1M130_assertion description "[may play a role in malignant transformation of oral submucous fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144928.RAbDzj2u4bQhDk2lKJd61l1ji8jZ0gruH4jxOHXIf1A1M130_provenance.
- NP144930.RAWuoRiENbHsv4pMUoV58UmRpreVU2ceEvdFFO_rsMYtg130_assertion description "[evidence for overexpression in oral submucous fibrosis and its regulation by arecoline in oral fibroblasts ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144930.RAWuoRiENbHsv4pMUoV58UmRpreVU2ceEvdFFO_rsMYtg130_provenance.
- NP144933.RATVSB0brEnPF5Q5RWnOpicCKbn3gp5XDOdRxrV8TdDPc130_assertion description "[among adenocarcinomas, nonmucinous and mucinous bronchioloalveolar carcinoma components were significantly associated with EGFR and K-ras gene mutations, respectively ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144933.RATVSB0brEnPF5Q5RWnOpicCKbn3gp5XDOdRxrV8TdDPc130_provenance.
- NP144935.RAUX4RGcqM2j3n-Xw6dFmQXu-yx6P_1rdc4mv8BSuimdc130_assertion description "[EGFR mutation is associated with Long-lasting complete remission with tyrosine kinase inhibitor in bronchioloalveolar carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144935.RAUX4RGcqM2j3n-Xw6dFmQXu-yx6P_1rdc4mv8BSuimdc130_provenance.
- NP144938.RAXGzqsJIE-T5oY1ooYCckWIDKtNqa5BIh47G_bNYmLvY130_assertion description "[LAT1 expression may increase with the upregulation of metabolic activity and cell proliferation in high-grade atypical adenomatous hyperplasia and bronchioloalveolar carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144938.RAXGzqsJIE-T5oY1ooYCckWIDKtNqa5BIh47G_bNYmLvY130_provenance.
- NP144940.RAVbQNRQgiEtL1wIiGzCFZYmsRyQhyapFYch8bJ3Hqk2U130_assertion description "[Biliary epithelial cell antibodies via induction of TLR2 and TLR3, as well as inflammatory cytokine and chemokine production may induce epithelial cell inflammatory responses to bacterial components and contribute to posttransplantation cholangitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144940.RAVbQNRQgiEtL1wIiGzCFZYmsRyQhyapFYch8bJ3Hqk2U130_provenance.
- NP144945.RAf-c8uy6-N7JgeB2PPXRBVGxHwrEOe402bKoE_7nV1wU130_assertion description "[activated by the LTR from Moloney murine and feline leukemia viruses (Mo-MuLV and FeLV) via TLR3 dependent pathway ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144945.RAf-c8uy6-N7JgeB2PPXRBVGxHwrEOe402bKoE_7nV1wU130_provenance.
- NP144948.RAbtivSEtvUPWPm_bFpmFB8xnKaWRDn2hEQakE7nag0R8130_assertion description "[TLR3 and 9 as well as IFN-beta and TNF-alpha are expressed in verruca and molluscum contagiosum skin lesions and may play a pivotal role in cutaneous innate immune responses ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144948.RAbtivSEtvUPWPm_bFpmFB8xnKaWRDn2hEQakE7nag0R8130_provenance.
- NP144949.RAXuaUZh8bTOxb_Ctmq9hKfG5rOePdOqIlQCLLhatFNIk130_assertion description "[TLR3 and 9 as well as IFN-beta and TNF-alpha are expressed in verruca and molluscum contagiosum skin lesions and may play a pivotal role in cutaneous innate immune responses ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144949.RAXuaUZh8bTOxb_Ctmq9hKfG5rOePdOqIlQCLLhatFNIk130_provenance.
- NP144950.RAeuaqQR0t24cMKoRDy__kqrB0AP5GURsPvLEFsiP88JE130_assertion description "[Activation of Omi/HtrA2-mediated cell death is a potential mechanism for the tumor suppressive activity of WARTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144950.RAeuaqQR0t24cMKoRDy__kqrB0AP5GURsPvLEFsiP88JE130_provenance.
- NP144963.RAQcDSUB-9bYzq0-hES3BZ4qBQNahKI6imaXcLhA0GmlQ130_assertion description "[In summary, the presented data support the idea that adiponectin might be of critical relevance for cytokine regulation in obesity and fatty liver diseases affecting primarily macrophage functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144963.RAQcDSUB-9bYzq0-hES3BZ4qBQNahKI6imaXcLhA0GmlQ130_provenance.
- NP144975.RAQ6XD317unWQqI6ZjAhYDMlpZdjawQ6lXsIY0peiX2z4130_assertion description "[In obese patients with NAFLD (nonalcoholic fatty liver disease), OSA (obstructive sleep apnea) was associated with elevated alanine aminotransferase levels and a trend toward histologic evidence of progressive liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144975.RAQ6XD317unWQqI6ZjAhYDMlpZdjawQ6lXsIY0peiX2z4130_provenance.
- NP144980.RAWP1xmfDc0ChVXwmt7j9D1c1tO-mIUFYvC9jrm4Azn6Q130_assertion description "[In patients with chronic hepatitis c, adiponectin and receptors (AdipoR1 and AdipoR2) play a role in hepatic inflammation in both sexes and liver steatosis in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144980.RAWP1xmfDc0ChVXwmt7j9D1c1tO-mIUFYvC9jrm4Azn6Q130_provenance.
- NP144984.RAVqxs7ptmSsofYMwae3APWLRWQ8SL-3vFTMjgbBUNKBE130_assertion description "[Fas antagonism by Met is abrogated in human fatty liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144984.RAVqxs7ptmSsofYMwae3APWLRWQ8SL-3vFTMjgbBUNKBE130_provenance.
- NP144985.RARvVXDznASrNOZJA6esd7vu6iCZeFijzmYL9NRi8jGCg130_assertion description "[in nonalcoholic fatty liver disease, insulin signaling via IRS-1 causes the up-regulation of SREBP1-c, leading to the increased synthesis of fatty acids ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144985.RARvVXDznASrNOZJA6esd7vu6iCZeFijzmYL9NRi8jGCg130_provenance.
- NP144986.RAb8hijd7PFKGELcaWcdFV3zKndcNhIxvBZlH4OM84kgY130_assertion description "[Transgenic SHR overexpressing SREBP-1a is nonobese rat model of fatty liver, disordered glucose and lipid metabolism, and hypertension/model for studying pathogenesis and treatment of metabolic syndrome associated with hepatic steatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144986.RAb8hijd7PFKGELcaWcdFV3zKndcNhIxvBZlH4OM84kgY130_provenance.
- NP144988.RAa3foduMlR8S4LZiZJMwyPxqSQztogYvmtHV82e0DZSg130_assertion description "[FXR agonists and/or modulators may prove to be clinically useful for treating non-alcoholic fatty liver.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144988.RAa3foduMlR8S4LZiZJMwyPxqSQztogYvmtHV82e0DZSg130_provenance.
- NP144990.RAQIU7Sau9E4nJ2x3A6FbtQkj6P3nvWAyMP8hnnQ2m3tk130_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." NP144990.RAQIU7Sau9E4nJ2x3A6FbtQkj6P3nvWAyMP8hnnQ2m3tk130_provenance.
- NP144995.RAQHYZ7LGDlDwBJgp1fJ4UeRstAQb3O3F6z23pV2MHxa0130_assertion description "[We review the literature regarding the prevalence, hepatic distribution and possible therapeutic implications of iron overload in chronic hepatitis C, hepatitis B, alcoholic and non-alcoholic fatty liver diseases and porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144995.RAQHYZ7LGDlDwBJgp1fJ4UeRstAQb3O3F6z23pV2MHxa0130_provenance.
- NP145001.RAb7cXDIOAJj9YLD2g05YMX30iUtB6nG4A5ipskCDL2zI130_assertion description "[The mild iron overload associated with heterozygosity for C282Y HFE mutation confers susceptibility to nonalcoholic fatty liver disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145001.RAb7cXDIOAJj9YLD2g05YMX30iUtB6nG4A5ipskCDL2zI130_provenance.
- NP145005.RAbBR9TZx3H49EO0cjTWfU8D2ZvC4jyf1WJZKbLJrNzZw130_assertion description "[elevated production of IL-1alpha and TNF-alpha by in vitro stimulated whole blood cell cultures occurs in non-alcoholic fatty liver disease obese patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145005.RAbBR9TZx3H49EO0cjTWfU8D2ZvC4jyf1WJZKbLJrNzZw130_provenance.
- NP145011.RAY7Q2hN5sk0Sc0EnAoY4KzpMrt6HEwxyj0bUiYIu-7c4130_assertion description "[Despite similar total calcium contents, lower SERCA and PMCA activities were found in sacs associated with hydrocele compared to those associated with undescended testis suggest a difference among the levels of cytosolic calcium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145011.RAY7Q2hN5sk0Sc0EnAoY4KzpMrt6HEwxyj0bUiYIu-7c4130_provenance.
- NP145016.RAfYdpfiOsTe6g9AS9EHPF0eaeOgfXOSgUQXOQp7UqEjk130_assertion description "[T222P mutation cannot be considered either causative or a susceptibility factor for cryptorchidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145016.RAfYdpfiOsTe6g9AS9EHPF0eaeOgfXOSgUQXOQp7UqEjk130_provenance.
- NP145020.RAQ4Yg68wlhADPd3nwtzReY7LGfJ5oBwCxiqrDhXSupSE130_assertion description "[autocrine TGF-beta/Smad signaling is involved in contractility and matrix gene expression of fibroblasts from normal and hypertrophic scars; Smad7 inhibits these processes and may exert beneficial effects on excessive scar formation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145020.RAQ4Yg68wlhADPd3nwtzReY7LGfJ5oBwCxiqrDhXSupSE130_provenance.
- NP145023.RAd1o6H0fzJwifD3QCwuXBpQsC_NHbeMWjUzK1WIJzHW8130_assertion description "[The levels of p53 protein elevated in keloid, hypertrophic scar and white and hard hypertrophic scar ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145023.RAd1o6H0fzJwifD3QCwuXBpQsC_NHbeMWjUzK1WIJzHW8130_provenance.
- NP145033.RAVuFvSo0vOLUX5cduu39mJwNiEww7sa6nAsrCVxD1tpw130_assertion description "[Very rare CAV1 frameshift mutations appear to be associated with atypical lipodystrophy and hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145033.RAVuFvSo0vOLUX5cduu39mJwNiEww7sa6nAsrCVxD1tpw130_provenance.
- NP145034.RAWW8OGCTyR76AuSA1_MblaRbLPm575NAZG2P9ip9oksY130_assertion description "[Congenital lipodystrophy patients with Seipin mutations have a more severe lack of body fat, which affects both metabolically active and mechanical adipose tissue, compared with patients with mutations in the AGPAT2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145034.RAWW8OGCTyR76AuSA1_MblaRbLPm575NAZG2P9ip9oksY130_provenance.
- NP145049.RATYYV6ga5WWVaBn2bCdbdKwD-r6DmGSYiRurXjZ143go130_assertion description "[polymorphisms in the human SHP1 gene; found no rare SHP1 coding sequence variants that were exclusive to patients with lipodystrophy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145049.RATYYV6ga5WWVaBn2bCdbdKwD-r6DmGSYiRurXjZ143go130_provenance.
- NP145050.RAexi3Y5gwDISJSu1bWnKe43T9zc-D8ojaH84B4-u85RE130_assertion description "[both patients had markedly increased neck fat content, specifically surrounding the trachea.The association with sleep apnea might be related to the repartitioning of adipose tissue in patients with this type of lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145050.RAexi3Y5gwDISJSu1bWnKe43T9zc-D8ojaH84B4-u85RE130_provenance.
- NP145053.RASIRxxnITj8lzqMpOLJTIzRZzifEcluzyzhdV6bFSryU130_assertion description "[data suggest that the -238 promoter region TNF-alpha gene polymorphism is a determinant in the development of HIV-related lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145053.RASIRxxnITj8lzqMpOLJTIzRZzifEcluzyzhdV6bFSryU130_provenance.
- NP145055.RAaTnx_yqCB3wwQniNkqLuKARJyNkEpZ64vYje_Yvx5fI130_assertion description "[These data suggest that selected genes of the SLC28 and SLC29 families are not only targets of HIV-1 infection, but might also contribute to the development of adipose tissue alterations leading to lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145055.RAaTnx_yqCB3wwQniNkqLuKARJyNkEpZ64vYje_Yvx5fI130_provenance.
- NP145058.RAQTWzV4se0V5grdnINjq8AssV7ztFCselZQtWDqpgZ-I130_assertion description "[mutations in AGPAT2 or Seipin may have roles in Berardinelli-Seip congenital lipodystrophy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145058.RAQTWzV4se0V5grdnINjq8AssV7ztFCselZQtWDqpgZ-I130_provenance.
- NP145063.RAatfXwbt7HO1jhcBW7fYlIQw41EMo_3RgEYyjyg8B7JY130_assertion description "[A new subtype of congenital generalized lipodystrophy is not associated with the BSCL2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145063.RAatfXwbt7HO1jhcBW7fYlIQw41EMo_3RgEYyjyg8B7JY130_provenance.
- NP145064.RAXnH3eBQF7lLYCu27N0i6nNZn1i1r6rr2qRnkeYzcWHs130_assertion description "[A new subtype of congenital generalized lipodystrophy is not associated with the AGPAT2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145064.RAXnH3eBQF7lLYCu27N0i6nNZn1i1r6rr2qRnkeYzcWHs130_provenance.
- NP145065.RAeV6MSMFW3AxgSz_ATdIpKMlANq8tufldMi10cMS9oCo130_assertion description "[AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145065.RAeV6MSMFW3AxgSz_ATdIpKMlANq8tufldMi10cMS9oCo130_provenance.
- NP145066.RAUhwF1tHb5SirmzYj7iXf897QIy1JtrITUdKeves820U130_assertion description "[mutations in AGPAT2 or Seipin may have roles in Berardinelli-Seip congenital lipodystrophy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145066.RAUhwF1tHb5SirmzYj7iXf897QIy1JtrITUdKeves820U130_provenance.
- NP145071.RAQBC3rjMdKzTh7V6u7jHP3i63hOEVaxtsTZh18Ca1q6U130_assertion description "[Effects of deleting a tripeptide sequence observed in muscular dystrophy patients on the conformation of peptides corresponding to the scaffolding domain of caveolin-3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145071.RAQBC3rjMdKzTh7V6u7jHP3i63hOEVaxtsTZh18Ca1q6U130_provenance.
- NP145072.RAYp_uhF6bCvZFekbTgrlHsFWtRy4SrQxMhW-k5txlxVE130_assertion description "[Finding its mutation is useful for genetic diagnosis of type2 limb-gardle muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145072.RAYp_uhF6bCvZFekbTgrlHsFWtRy4SrQxMhW-k5txlxVE130_provenance.
- NP145074.RAShN8xlsaiBvqvLAaJFJPFvhi81ItOYABj67K54ESXzo130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the MEB locus, in three Tunisian patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145074.RAShN8xlsaiBvqvLAaJFJPFvhi81ItOYABj67K54ESXzo130_provenance.
- NP145088.RASk3xqaLOpFyc--WLzoKjZDLWMfBjHFL8OnZ0gn-0jLA130_assertion description "[A new SEPN1 point mutation, 943g- > A causing G315S was found in a rigid spine muscular dystrophy patient with cor pulmonale.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145088.RASk3xqaLOpFyc--WLzoKjZDLWMfBjHFL8OnZ0gn-0jLA130_provenance.
- NP145089.RAVRWePHlLnhI7JJ2pSlhvTusHcWO7YRXvZIAP8CLkuH8130_assertion description "[Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145089.RAVRWePHlLnhI7JJ2pSlhvTusHcWO7YRXvZIAP8CLkuH8130_provenance.
- NP145095.RASwrHBlOLJ83jeMlS0uxFdmIuQ2iQYuw6Ez_VXrww_6E130_assertion description "[two unrelated Mexican children with congenital muscular dystrophy who each have the identical, novel 1387A > G, N463D mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145095.RASwrHBlOLJ83jeMlS0uxFdmIuQ2iQYuw6Ez_VXrww_6E130_provenance.
- NP145099.RAZgFqUmhdzVEpw-gn-49NZ4hx_QobPh7I_jgX9FwtJyQ130_assertion description "[Homozygous deletion of the SMN1 gene in a Vietnamese spinal muscular dystrophy patient was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145099.RAZgFqUmhdzVEpw-gn-49NZ4hx_QobPh7I_jgX9FwtJyQ130_provenance.
- NP145100.RAXp6oG1qhJqdnUBgdlLyT85PmxY1xgN6fRjB2zBm4t50130_assertion description "[Biochemical analysis revealed altered glycosylation and decreased laminin-binding activity of alpha-dystroglycan in congenital muscular dystrophy.we focus on the molecular pathomechanism and diverging clinical phenotypes of alpha-dystroglycanopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145100.RAXp6oG1qhJqdnUBgdlLyT85PmxY1xgN6fRjB2zBm4t50130_provenance.
- NP145108.RAYvuAfOk5mUoBFrTYKwqeH2kDK8iEVE_RjxY4Xqu5eTQ130_assertion description "[Cytoplasmic localization of dysferlin correlates with fiber regeneration in a subset of muscular dystrophy patients/also identified patients with forms of LGMD and with abnormal dysferlin localization that doesn't correlate with fiber regeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145108.RAYvuAfOk5mUoBFrTYKwqeH2kDK8iEVE_RjxY4Xqu5eTQ130_provenance.
- NP145109.RASI6a7D2OWrVMRAcs8KxyCgEmTX8kylMwozasKjhQewg130_assertion description "[annexin A1 and A2 may have roles in dysferlin deficiency and in muscular dystrophies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145109.RASI6a7D2OWrVMRAcs8KxyCgEmTX8kylMwozasKjhQewg130_provenance.
- NP145115.RAXdUfx6oNuAq6XWUnD2U8FOOPk8VyAKt3J8c6VIvT9k4130_assertion description "[annexin A1 and A2 may have roles in dysferlin deficiency and in muscular dystrophies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145115.RAXdUfx6oNuAq6XWUnD2U8FOOPk8VyAKt3J8c6VIvT9k4130_provenance.
- NP145118.RAQ0U6lp0lhnFmi9w4voHS70Ba1UGUOP3H75mfaCt7ybk130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2 locus in three Tunisian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145118.RAQ0U6lp0lhnFmi9w4voHS70Ba1UGUOP3H75mfaCt7ybk130_provenance.
- NP145122.RAV9q_bhKcxC3WdsfvR0LIrBKvFn6zhQejlvcu3HWIbW4130_assertion description "[DNA analysis can be used to provide accurate prenatal diagnosis of thecongenital muscular dystrophy, and have an essential role in genetic counseling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145122.RAV9q_bhKcxC3WdsfvR0LIrBKvFn6zhQejlvcu3HWIbW4130_provenance.
- NP145129.RARHXXKtrUWDVGyvQTpVyQoaSUgMWxn9sKoHlHUnpW--M130_assertion description "[the lamin a-emerin complex might have a role in muscular dystrophy and cardiomyopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145129.RARHXXKtrUWDVGyvQTpVyQoaSUgMWxn9sKoHlHUnpW--M130_provenance.
- NP145131.RAVBpBh63_XKLXOBOpsOc40_nCwNc4DCJAfBc8JlJTkHA130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the CMD1B locus in three Tunisian patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145131.RAVBpBh63_XKLXOBOpsOc40_nCwNc4DCJAfBc8JlJTkHA130_provenance.
- NP145142.RAZuM1ztaqeJ3O8xL4-Gnf0FGgXbYeA2wN57b76Yj-de4130_assertion description "[nuclear extracts from murine erythroleukemia cells to purify a protein complex that binds the HPFH -198 gamma-globin gene promoter ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145142.RAZuM1ztaqeJ3O8xL4-Gnf0FGgXbYeA2wN57b76Yj-de4130_provenance.
- NP145143.RAQv7fvktV06IhVbVU47RiCfqUHNeUmzFlgzb9tKp1RL8130_assertion description "[TRB2-Mcl-1 axis plays an important role in survival factor withdrawal-induced apoptosis of TF-1 erythroleukemia cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145143.RAQv7fvktV06IhVbVU47RiCfqUHNeUmzFlgzb9tKp1RL8130_provenance.
- NP145154.RAd-2Fw54pJRIGG-1OHy8h980j0lXdcx_nCF0CsE0V3L0130_assertion description "[CD44 ligation triggers a novel caspase-independent cell death pathway via calpain-dependent AIF release in erythroleukemia cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145154.RAd-2Fw54pJRIGG-1OHy8h980j0lXdcx_nCF0CsE0V3L0130_provenance.
- NP145167.RAYnjzcEfgrEMsWWg-g0LJ3zQ0u2I7IhFYbnJpCk5h6lE130_assertion description "[FOXP2 is disrupted by a translocation in CS, a child with severe speech/language disorder/, a point mutation, altering a critical residue of the forkhead domain, segregates with speech/language deficits in all 15 affected members of family KE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145167.RAYnjzcEfgrEMsWWg-g0LJ3zQ0u2I7IhFYbnJpCk5h6lE130_provenance.
- NP145169.RARSWeqUmSs7O8g70K68n2GQe9C8fm_4Hfkmjk4Waz6EE130_assertion description "[Mutant and wild type FOXP2 heterodimers in the nucleus or FOXP2 R553H in the cytoplasm may underlie the pathogenesis of the autosomal dominant speech/language disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145169.RARSWeqUmSs7O8g70K68n2GQe9C8fm_4Hfkmjk4Waz6EE130_provenance.
- NP145178.RAUTUKD1P12hTfccZ81VpqTXhU4OoAn_2a719x4JvKbwk130_assertion description "[Novel and known missense mutations of XLRS1 gene in the diagnosis retinoschisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145178.RAUTUKD1P12hTfccZ81VpqTXhU4OoAn_2a719x4JvKbwk130_provenance.
- NP145179.RAcPfJGxT05oFSMl5I5t9bVJ1sTXE7NBOa6FhrAutCUGE130_assertion description "[Electroretinographic findings in three family members with X-linked juvenile retinoschisis associated with a novel Pro192Thr missense mutation of the XLRS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145179.RAcPfJGxT05oFSMl5I5t9bVJ1sTXE7NBOa6FhrAutCUGE130_provenance.
- NP145185.RAdTqYzYDyN4I6XJYiLjViga4UR9BKvTQRXYLH_dI_DO8130_assertion description "[MEFV protein mutations are associated with Familial Mediterranean fever ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145185.RAdTqYzYDyN4I6XJYiLjViga4UR9BKvTQRXYLH_dI_DO8130_provenance.
- NP145186.RAcf8RDos0m0u1hQoWxtnsxiVsuBkrgQQa4ySmTInh1cc130_assertion description "[MEFV protein mutations are associated with Familial Mediterranean fever ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145186.RAcf8RDos0m0u1hQoWxtnsxiVsuBkrgQQa4ySmTInh1cc130_provenance.
- NP145190.RAZjD6OWhTzX8RQLcnqbendc6nKw61agntm8SQntgaBTg130_assertion description "[MEFV mutations occur in Japanese familial Mediterranean fever (FMF) patients though FMF is rare in Japan; genetic analyses on 14 Japanese FMF patients in this study revealed that E148Q and M694I are frequent alleles ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145190.RAZjD6OWhTzX8RQLcnqbendc6nKw61agntm8SQntgaBTg130_provenance.
- NP145193.RAQO1gnDQMa187ebj8oaAzIHYRFWlWQWXfV5h2zxcjPEU130_assertion description "[spectrum of the MEFV mutations among our sampled Lebanese Familial Mediterranean Fever patients shows the high heterogeneity at the allelic level when compared to Arab and non-Arab populations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145193.RAQO1gnDQMa187ebj8oaAzIHYRFWlWQWXfV5h2zxcjPEU130_provenance.
- NP145194.RAfk0Brp1io4HIwlN2tIAPK3z71Qpq66a5IAf6zojVJ94130_assertion description "[Reduced expression of the MEFV gene is associated with inflammation and that it may be one of the pathogenic mechanisms of the attacks of inflammation in familial Mediterranean fever patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145194.RAfk0Brp1io4HIwlN2tIAPK3z71Qpq66a5IAf6zojVJ94130_provenance.
- NP145197.RAWdjTISJuUwByIT_iE8KXSF7f2M0Xc3SKtRYvgVl3RvI130_assertion description "[ABCC6 is unlikely to be a modifier gene for familial Mediterranean fever severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145197.RAWdjTISJuUwByIT_iE8KXSF7f2M0Xc3SKtRYvgVl3RvI130_provenance.