Nanopublications LDF server

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

• NP141490.RAR745VDkJQf0xmMwPNr9DYEcDkOQWAywKXsNnVQQYSkU130_assertion description "[The prevalence of factor V and prothrombin mutations in venous thrombosis patients was not significantly different from that in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141490.RAR745VDkJQf0xmMwPNr9DYEcDkOQWAywKXsNnVQQYSkU130_provenance.
• NP141491.RAYXZ_zUkcE5MwHqDvSiY4eIB4q9uinM-i9jbLY2Cka4g130_assertion description "[A mutation in the factor V gene, may contribute to the risk of both arterial and deep-vein thrombosis in patients with nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141491.RAYXZ_zUkcE5MwHqDvSiY4eIB4q9uinM-i9jbLY2Cka4g130_provenance.
• NP141493.RAfRI6Gh9c6b0L38GIzDzmkqf9eChRdGwyFnrJ3p1g4y4130_assertion description "[FV (HR2) plays a role as a risk factor for venous thrombosis in homozygous patients through an increased thrombin generation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141493.RAfRI6Gh9c6b0L38GIzDzmkqf9eChRdGwyFnrJ3p1g4y4130_provenance.
• NP141499.RAZKNdcUCubPjoK6aF-pf2EzxIhuy-32ntBlrkyrjGvlg130_assertion description "[The protein C system is physiologically important, and genetic defects affecting the system are the most common risk factors of venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141499.RAZKNdcUCubPjoK6aF-pf2EzxIhuy-32ntBlrkyrjGvlg130_provenance.
• NP141500.RAa2PON6nQDamROYHEWsUcMPCgwOpQ-34YW9CunZwMUpU130_assertion description "[K196E mutation is a genetic risk factor for deep vein thrombosis in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141500.RAa2PON6nQDamROYHEWsUcMPCgwOpQ-34YW9CunZwMUpU130_provenance.
• NP141504.RAU8Lz6vgu7nQP4rudsAuKFxqpEgU7jNWDduPbGe7cm5I130_assertion description "[Multivariate logistic regression analysis showed that IL-10 G13 and G10 alleles are independent risk factors for venous thrombosis/, IL-10 G10 allele is more frequent in recurrent disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141504.RAU8Lz6vgu7nQP4rudsAuKFxqpEgU7jNWDduPbGe7cm5I130_provenance.
• NP141510.RAaIPUIHxvxKQ5H3cG88pvqfHHJeDCujOw3k1kC1pzGyg130_assertion description "[The single base substitution of G to A at nucleotide 2709 was found in a proband with a family history of venous thrombosis/results in a substitution of 82 Ser by Asn, creating a new glycosylation site causing type I antithrombin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141510.RAaIPUIHxvxKQ5H3cG88pvqfHHJeDCujOw3k1kC1pzGyg130_provenance.
• NP141511.RAXbqtYkqe2mVxoH7j7aN0Bqy8LDGIT6T6a8YvX5zEpvU130_assertion description "[Five novel and two previously reported point mutations in the antithrombin gene causing venous thrombosis were identified; the novel L409P mutation is a type 2 pleiotropic effects (PE) deficiency and it is highly conserved among other serpins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141511.RAXbqtYkqe2mVxoH7j7aN0Bqy8LDGIT6T6a8YvX5zEpvU130_provenance.
• NP141512.RAc_4sGXCHmgnLv38bTGNBPQkUYwLKhpFvyKLgVTj1A5g130_assertion description "[Antithrombin A384S mutation is a prevalent genetic risk factor for venous thrombosis and is the most frequent cause of antithrombin deficiency in white populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141512.RAc_4sGXCHmgnLv38bTGNBPQkUYwLKhpFvyKLgVTj1A5g130_provenance.
• NP141519.RATQHIb9p4gO9jW80QkQIBREGwD5i1wdQuN5iXLGqW_ls130_assertion description "[the TFPI -33T- > C and -399C- > T polymorphisms are significantly associated with venous thrombosis in the presence of other risk factors, especially APS, and may be clinically relevant in patients who are prone to hypercoagulability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141519.RATQHIb9p4gO9jW80QkQIBREGwD5i1wdQuN5iXLGqW_ls130_provenance.
• NP141524.RAdyip-B7v3pHBf_ouXFRDZnLm280Mmp_oLY3hKXkNDN4130_assertion description "[The role played by FXII deficiency in the pathogenesis of venous thrombosis is minor, if any.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141524.RAdyip-B7v3pHBf_ouXFRDZnLm280Mmp_oLY3hKXkNDN4130_provenance.
• NP141527.RAa96y5cIK8MbwyFzKufF4EeX3xVx2XoyCRfshUaHrHZc130_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." NP141527.RAa96y5cIK8MbwyFzKufF4EeX3xVx2XoyCRfshUaHrHZc130_provenance.
• NP141529.RAQjukiQfoZcv7VNs8EiVmbnoBV39zr_mzxNYBaYcnKVA130_assertion description "[The MTRR 66GG genotype was found to be associated with 2.74-fold risk (95% CI: 1.73, 4.34) for deep vein thrombosis among South Indians/risk is increased further to 3.46-fold (95% CI: 1.38, 8.63) in the presence of the MTHFR 677CT/1298AC genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141529.RAQjukiQfoZcv7VNs8EiVmbnoBV39zr_mzxNYBaYcnKVA130_provenance.
• NP141531.RAT5WIX_5kYR5xIjfoBX9hKJXA5QV0lOAY3kXr02PcNes130_assertion description "[estrogen receptor alpha and beta gene polymorphisms may have a role in deep vein thrombosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141531.RAT5WIX_5kYR5xIjfoBX9hKJXA5QV0lOAY3kXr02PcNes130_provenance.
• NP141533.RASjGoESw21juy46-ePq8OmVA4xtY-9r6YcW_y0uu-hys130_assertion description "[thrombomodulin mutations, especially those with a haplotype consisting of 2729A > C and A455V missense mutation, affect sTM levels, and may be associated with deep vein thrombosis in Japanese ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141533.RASjGoESw21juy46-ePq8OmVA4xtY-9r6YcW_y0uu-hys130_provenance.
• NP141547.RAXXY-uXou-yZVQ9ZQ7Yt-INH96HBI4LM__qvZFHQu8vI130_assertion description "[We conclude that genetic approaches using PD-ECGF to target the myocardium are effective for alleviating chronic myocardial ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141547.RAXXY-uXou-yZVQ9ZQ7Yt-INH96HBI4LM__qvZFHQu8vI130_provenance.
• NP141554.RAe2Vq6bBdPFNeibk8P2yM0lLggH0x4own11iheMuQUMU130_assertion description "[The AA genotype of HMOX1 reduced the incidence of ischemic heart disease, possibly due to the expression level of HMOX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141554.RAe2Vq6bBdPFNeibk8P2yM0lLggH0x4own11iheMuQUMU130_provenance.
• NP141555.RAb3cJrx7dAd4J86zCsX5za4Y2hBh28DqYkCdIkdKSuPQ130_assertion description "[Increase in iPLA (2) and accumulation of membrane phospholipid-derived metabolites in HCAEC exposed to hypoxia or thrombin have important implications in inflammation and arrhythmogenesis in atherosclerosis/thrombosis and myocardial ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141555.RAb3cJrx7dAd4J86zCsX5za4Y2hBh28DqYkCdIkdKSuPQ130_provenance.
• NP141561.RAWFxZPPoGIrBCOimVtmD_ogX5fbyJhpG-gGQwrKV3bVg130_assertion description "[Study results suggest that the G-308A polymorphism is unlikely to be associated with the development of ischemic heart disease, whereas it might be a protective factor for ischemic stroke in Asians only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141561.RAWFxZPPoGIrBCOimVtmD_ogX5fbyJhpG-gGQwrKV3bVg130_provenance.
• NP141562.RASRJte13s8eXZhoul7BcaoNck14L7LjG_9TkZfdKAgZg130_assertion description "[The relationship between hemodynamic response to mental stress and mental stress-induced myocardial ischemia (MSIMI) and 5 common functional polymorphisms of beta1-adrenergic receptors (ADRB1) and beta2-adrenergic receptors (ADRB2) was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141562.RASRJte13s8eXZhoul7BcaoNck14L7LjG_9TkZfdKAgZg130_provenance.
• NP141567.RAQ5qhfCHf025vtIkyyaCY-PV4uB5GvR1hd8i4gAiB3_8130_assertion description "[The relationship between hemodynamic response to mental stress and mental stress-induced myocardial ischemia (MSIMI) and 5 common functional polymorphisms of beta1-adrenergic receptors (ADRB1) and beta2-adrenergic receptors (ADRB2) was investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141567.RAQ5qhfCHf025vtIkyyaCY-PV4uB5GvR1hd8i4gAiB3_8130_provenance.
• NP141570.RAek6LhGJotJT1ymKwUbQESxUrOzxpQPumjCoXcMm-79U130_assertion description "[ceramide-induced I (HERG) impairment may contribute to QT prolongation in prolonged myocardial ischemia, heart failure and diabetic cardiomyopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141570.RAek6LhGJotJT1ymKwUbQESxUrOzxpQPumjCoXcMm-79U130_provenance.
• NP141571.RAW9xb_tGaq9oHDDmQJcxDp9KPD6szvEBMU6LrPT30imo130_assertion description "[Isolation of 3 novel isoforms of AML 1 (RUNX1) with different transactivating function, that might be a regulatory element of the NCAM (CD56) overexpression in chronic myocardial ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141571.RAW9xb_tGaq9oHDDmQJcxDp9KPD6szvEBMU6LrPT30imo130_provenance.
• NP141574.RAWb2l6C6cOc_hC-1QwOSFSWUmUhHg4kFaM0cA8RWTpK8130_assertion description "[Both CA125 and brain natriuretic peptide (BNP) levels are significantly correlated with New York Heart Association (NYHA) class and outcome in patients with aortic stenosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141574.RAWb2l6C6cOc_hC-1QwOSFSWUmUhHg4kFaM0cA8RWTpK8130_provenance.
• NP141578.RAVgilqyvyZwwx_sELqzBXSTh7Zo-5U5uCVCbUW71_FpE130_assertion description "[RANKL-OPG pathway may regulate valvular calcification in calcific aortic stenosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141578.RAVgilqyvyZwwx_sELqzBXSTh7Zo-5U5uCVCbUW71_FpE130_provenance.
• NP141582.RAd8imelO_cadTfMjIRpw_GhIz8TldkuOb22ydaqTPqkE130_assertion description "[Both CA125 and brain natriuretic peptide (BNP) levels are significantly correlated with New York Heart Association (NYHA) class and outcome in patients with aortic stenosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141582.RAd8imelO_cadTfMjIRpw_GhIz8TldkuOb22ydaqTPqkE130_provenance.
• NP141589.RAf7PPDYrlp2N-HJpIuWr_3d8ycDYR8eDHGDYpm93z_Do130_assertion description "[High concentrations of MMP-9 found in patients with carotid stenosis and cerebral lesions suggest that MMP-9 assay could be useful in the evaluation of all carotid lesions to help identify those at highest risk of a neurologic event.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141589.RAf7PPDYrlp2N-HJpIuWr_3d8ycDYR8eDHGDYpm93z_Do130_provenance.
• NP141590.RAezd7j2S3ZTtaoX5JVYrUjt8wmojlxKgguiGkELoH1YU130_assertion description "[Elevated levels of MMP-9 iin carotid stenosis were associated with a 2-fold risk of ipsilateral stroke or cardiovascular death/may play an important role in the destabilization of atherosclerotic carotid plaques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141590.RAezd7j2S3ZTtaoX5JVYrUjt8wmojlxKgguiGkELoH1YU130_provenance.
• NP141592.RAQmWxXMUAr6_wXf6X63qi5l0sVlasoUw7NCWJ6aQrcm0130_assertion description "[Elevated C-reactive protein could serve as a marker for carotid stenosis but was not useful to identify plaques at risk for symptomatic conversion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141592.RAQmWxXMUAr6_wXf6X63qi5l0sVlasoUw7NCWJ6aQrcm0130_provenance.
• NP141597.RAdMoBnrlBTRl8e_xAqq_bdn2SLRKiURZweKskjTUUdUQ130_assertion description "[Demonstrated elevated serum OPN and OPG levels in patients with carotid stenosis and documented an independent association between these biochemical markers, pathology and carotid-induced symptomatology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141597.RAdMoBnrlBTRl8e_xAqq_bdn2SLRKiURZweKskjTUUdUQ130_provenance.
• NP141603.RAVhXLkY1Pb7PM9eNBSDYXKtg4cSslhaD3eHGS95_y1IE130_assertion description "[utations in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia and further demonstrates genotype-phenotype correlations in SPG6 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141603.RAVhXLkY1Pb7PM9eNBSDYXKtg4cSslhaD3eHGS95_y1IE130_provenance.
• NP141615.RAb5ri5-Td0-KPjfFuDx6hvqcVQut2guEmJMUZawRbQtE130_assertion description "[Mutations in the SPAST gene in 200 hereditary spastic paraplegia (HSP) patients and identified 47 different mutations, out of which 29 were novel mutations; the overall frequency of SPAST mutations in cohort was 28.5% (57/200).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141615.RAb5ri5-Td0-KPjfFuDx6hvqcVQut2guEmJMUZawRbQtE130_provenance.
• NP141628.RAYQWu7VkYWT1Em-_EH7WHwcgRg3PfrXgu5NMk1V0xqYM130_assertion description "[Seven families with six different SPG3A mutations were identified among 106 with autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141628.RAYQWu7VkYWT1Em-_EH7WHwcgRg3PfrXgu5NMk1V0xqYM130_provenance.
• NP141632.RAYiV12ym9sGN7otdHqMWH0uPqXcOgI7KEOT3kEItQSqQ130_assertion description "[Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141632.RAYiV12ym9sGN7otdHqMWH0uPqXcOgI7KEOT3kEItQSqQ130_provenance.
• NP141639.RAbsBDFmrYtVUbcxfC-0SzcWGLM36zmjBk-xkg-3XOjUc130_assertion description "[This study provides the first evidence of spartin subcellular localization and identifies it as the third mitochondrial protein implicated in hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141639.RAbsBDFmrYtVUbcxfC-0SzcWGLM36zmjBk-xkg-3XOjUc130_provenance.
• NP141645.RAbSzjLbb2KZQp7fCdmscnfGjIT_1WRwJ6qlg7eXqgdUM130_assertion description "[Dimerization act in hierarchical fashion, enabling WASP/WAVE proteins to integrate different classes of inputs to produce a wide range of cellular actin responses in Wiskoo Aldrich syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141645.RAbSzjLbb2KZQp7fCdmscnfGjIT_1WRwJ6qlg7eXqgdUM130_provenance.
• NP141651.RAazYyD-02PFnX8-jLPBe6sJ_CvfuzikFaRonoq8rp--M130_assertion description "[Chinese Wiskott-Aldrich Syndrome (WAS) patients had mutations involving exon 1 of the Wiskott-Aldrich syndrome protein (WASP) gene and none had the X-linked thrombocytopenia phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141651.RAazYyD-02PFnX8-jLPBe6sJ_CvfuzikFaRonoq8rp--M130_provenance.
• NP141666.RAYWkZyETI4O8PkNSDzsdbxlmpRteEX3h0_8B7i3pfC_c130_assertion description "[Treatment with interleukin-2 (IL-2) corrected the functional defects of NK cells by affecting their ability to bind to sensitive target cells and to accumulate F-actin in Wiskott-Aldrich syndrome cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141666.RAYWkZyETI4O8PkNSDzsdbxlmpRteEX3h0_8B7i3pfC_c130_provenance.
• NP141672.RATFoNj8Y7YPXm6Ab97FQL6Bo5FsDijz52yCl8mQWzX3A130_assertion description "[Results describe a quantitative model of allosteric regulation of the Wiskott-Aldrich syndrome protein (WASP) by the Rho GTPase Cdc42.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141672.RATFoNj8Y7YPXm6Ab97FQL6Bo5FsDijz52yCl8mQWzX3A130_provenance.
• NP141679.RATxaNuPiTMgUz7VimuRnq8YGGkwOBVgrEXsAVqm6IyEk130_assertion description "[Both autosomal dominant progressive external ophthalmoplegia and parkinsonism caused by mutations that directly affect the polymerase domain of polymerase gamma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141679.RATxaNuPiTMgUz7VimuRnq8YGGkwOBVgrEXsAVqm6IyEk130_provenance.
• NP141681.RAS0lHgWmVwPQvzsKslRZREcyGhtS_jwWihWy5q1Rqopo130_assertion description "[Mutation in DNA polymerase gamma is associated with progressive external ophthalmoplegia and parkinsonism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141681.RAS0lHgWmVwPQvzsKslRZREcyGhtS_jwWihWy5q1Rqopo130_provenance.
• NP141683.RAZVn_w-2TCRg4J8si11XL8x984pLfPWTQJZZvJx9he7o130_assertion description "[2 new heterozygous missense transitions (C2794T, G3151C) were found in the POLG gene in a family with an autosomal recessive syndrome: progressive external ophthalmoplegia, polyneuropathy, ataxia, sensorineural hearing loss, and affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141683.RAZVn_w-2TCRg4J8si11XL8x984pLfPWTQJZZvJx9he7o130_provenance.
• NP141686.RAcR2yt6psLSPcl0FoUrFv7-NIvcbNwHHwXGJncKLupHs130_assertion description "[MtDNA replication pausing is the consequence of Twinkle mutations that predisposes to progressive external ophthalmoplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141686.RAcR2yt6psLSPcl0FoUrFv7-NIvcbNwHHwXGJncKLupHs130_provenance.
• NP141690.RAcNyYY01CB8w4E9TVEAcldTrTkNKEVny04c7MMjRfEO0130_assertion description "[report a novel heterozygous C to A transversion at nucleotide 269 in the ANT1 gene in a German family with Progressive External Ophthalmoplegia, predicted to convert a highly conserved alanine at codon 90 to aspartic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141690.RAcNyYY01CB8w4E9TVEAcldTrTkNKEVny04c7MMjRfEO0130_provenance.
• NP141699.RAfZwMeaiNg79xBd6tCMtWl09NjZTlflXTAP-rrq69hY4130_assertion description "[This review summarizes the current state of research on the genetic polymorphisms of FMO3, with a focus on their clinical implications in gastrointestinal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141699.RAfZwMeaiNg79xBd6tCMtWl09NjZTlflXTAP-rrq69hY4130_provenance.
• NP141705.RAeocf2D82Q4KEuBmCP12toSN5gFS3wNAxY3VsEqZermQ130_assertion description "[MC4R mutation screen in bulimia nervosa patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141705.RAeocf2D82Q4KEuBmCP12toSN5gFS3wNAxY3VsEqZermQ130_provenance.
• NP141722.RAfb1Apt0DxpoupNgFpUEiOi4tzfDz0F64gWjov7p0QYM130_assertion description "[The authors found a correlation between CCND1 genotype and the age of onset of hepatoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141722.RAfb1Apt0DxpoupNgFpUEiOi4tzfDz0F64gWjov7p0QYM130_provenance.
• NP141735.RAc7VG5uo6SoD7472xZ1Je2eOYeY4QqAGiUtZpSbeN2KQ130_assertion description "[Homotypic cross-linking of neutrophil Fc gamma RIIIb results in significant release of alpha-defensins capable of recruiting mononuclear, dendritic, and T cells to antineutrophil cytoplasmic antibody (ANCA) -induced granuloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141735.RAc7VG5uo6SoD7472xZ1Je2eOYeY4QqAGiUtZpSbeN2KQ130_provenance.
• NP141740.RAYzuF7_PaD4UHNXbdY0Q0k3F0MMSf6WfACWcGr6NXKCI130_assertion description "[Tenascin-C expressed around granulomas in sarcoidosis, atypical mycobacteriosis, and tuberculosis of the lung and colocalized with the expression of myofibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141740.RAYzuF7_PaD4UHNXbdY0Q0k3F0MMSf6WfACWcGr6NXKCI130_provenance.
• NP141743.RAfjoLCGw8qmvPSe4KDFdmz4DqTT3AOlVg64S4HGwjhdE130_assertion description "[MMP-9 within tuberculous granuloma is associated with tissue destruction; monocytic cells packed together at the center of tuberculous granuloma exhibit strong cytoplasmic staining for MMP-9, but not TIMP-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141743.RAfjoLCGw8qmvPSe4KDFdmz4DqTT3AOlVg64S4HGwjhdE130_provenance.
• NP141745.RAYdMsjYmEdDFEzWd8vnZuwTHNalYzACp7UDEZfWC_G5A130_assertion description "[Postmortem brain tissue analysis demonstrates VEGFR1 localized as paracellular deposits in Durck's granulomas of patients with cerebral malaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141745.RAYdMsjYmEdDFEzWd8vnZuwTHNalYzACp7UDEZfWC_G5A130_provenance.
• NP141751.RAe8QvPyjVbmg1J7ok-iINLgkKaMG1GC5khh9znRgHwcs130_assertion description "[mechanisms by which PTPN22 confers susceptibility to Graves disease may, in part, be disease specific ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141751.RAe8QvPyjVbmg1J7ok-iINLgkKaMG1GC5khh9znRgHwcs130_provenance.
• NP141754.RAZHq1jHIyGjS6BcTsFvBQuqDk9X3ZeakBozg999eSLT0130_assertion description "[hyper-adiponectinemia is closely associated with increases in serum thyroid hormone levels and TSH receptor antibody in Basedow disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141754.RAZHq1jHIyGjS6BcTsFvBQuqDk9X3ZeakBozg999eSLT0130_provenance.
• NP141756.RAddaeHDhaqStG052DA1E13RGEffiH1WNYw7-OwwLB2bc130_assertion description "[Role of the CTLA-4 locus in the susceptibility to Graves disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141756.RAddaeHDhaqStG052DA1E13RGEffiH1WNYw7-OwwLB2bc130_provenance.
• NP141759.RAXIaw2-EYDnj8Biq007aLW1CBshRxVfCajYHCgejI5qg130_assertion description "[chemokine receptor CXCR6 was overexpressed in Th1 and Tc1 T lymphocytes compared with peripheral blood lymphocytes in Graves disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141759.RAXIaw2-EYDnj8Biq007aLW1CBshRxVfCajYHCgejI5qg130_provenance.
• NP141763.RAZaSSSfOzwFUYUfdpqjMeAFUiV6kt8c9NGblOd-c1ivo130_assertion description "[The reduction of CXCL10 levels after 131I treatment in Graves disease shows that the thyroid gland itself is the main source of circulating CXCL10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141763.RAZaSSSfOzwFUYUfdpqjMeAFUiV6kt8c9NGblOd-c1ivo130_provenance.
• NP141767.RAc_dNmdbvDoH4sFAgWTeLltixksUNTp3XTDfZAuweTU4130_assertion description "[evaluated the expression of Bcl-2, Bax and Bak in patients with Graves Disease (GD); findings suggest that the differential expression of Bcl-2 family proteins in both thyrocytes and lymphoid follicles may be involved in the pathology of GD ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141767.RAc_dNmdbvDoH4sFAgWTeLltixksUNTp3XTDfZAuweTU4130_provenance.
• NP141768.RARPh7tSPoyH_wGPYNRiK6PVLxb905pUIs8_nSuEn_Z78130_assertion description "[evaluated the expression of Bcl-2, Bax and Bak in patients with Graves Disease (GD); findings suggest that the differential expression of Bcl-2 family proteins in both thyrocytes and lymphoid follicles may be involved in the pathology of GD ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141768.RARPh7tSPoyH_wGPYNRiK6PVLxb905pUIs8_nSuEn_Z78130_provenance.
• NP141772.RAZSg-f6TEaoyMOJRlPqBhWFXAh1Yz7Z3p-Rsn_xnHnIE130_assertion description "[This gene has a predisposing effect for Graves disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141772.RAZSg-f6TEaoyMOJRlPqBhWFXAh1Yz7Z3p-Rsn_xnHnIE130_provenance.
• NP141775.RAUSFu-OQp2eGJQm_bVnhBv-si5-w5v93ggc8UBzMAx1M130_assertion description "[Analysis of HLA-DRB1 antigen and HLA-DQ antigens in Hashimoto thyroiditis and Graves disease reveals differences between the two.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141775.RAUSFu-OQp2eGJQm_bVnhBv-si5-w5v93ggc8UBzMAx1M130_provenance.
• NP141776.RAQ47BCBN2BSXyWq4fJ2kV4pze-p4dIAwtBBKovkJmQjc130_assertion description "[Our findings suggest that the changes in the expression of apoptotic proteins (Fas/FasL and caspase 8) in the thyroid gland of patients with autoimmune Graves Disease and Hashimoto's thyroiditis reflect their involvemetn in the pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141776.RAQ47BCBN2BSXyWq4fJ2kV4pze-p4dIAwtBBKovkJmQjc130_provenance.
• NP141777.RASOFvcq-oz1EXAKRZ4Gwaei_-iLUBCl9IlMaf_0O81ig130_assertion description "[results support the notion that CD40 C-1T polymorphism has a modest effect on genetic susceptibility to sporadic Graves disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141777.RASOFvcq-oz1EXAKRZ4Gwaei_-iLUBCl9IlMaf_0O81ig130_provenance.
• NP141783.RAblkYZXYEaAsTNLOdTueIwLnvtdVhJnmkVmjrx04DSZI130_assertion description "[Our results suggest that ADRB2 plays a role in susceptibility to Graves disease in humans ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141783.RAblkYZXYEaAsTNLOdTueIwLnvtdVhJnmkVmjrx04DSZI130_provenance.
• NP141786.RAaDvxcoAJD_hFQgMsRnxRP_KcarCpTjj9LsJlFypIkAg130_assertion description "[There is an association between CXCR6 genotype and progression from Pneumocystis carinii pneumonia to death in African-Americans with AIDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141786.RAaDvxcoAJD_hFQgMsRnxRP_KcarCpTjj9LsJlFypIkAg130_provenance.
• NP141788.RAW9ZpQpZRrfbOojWu6z9gCTpr4REBNAPmezdbsakGMgI130_assertion description "[Tumor suppressor genes p15 (INK4b), p14 (ARF) and p16 (INK4a) are located at the 9p21 locus in 26 cryopreserved neurofibromatosis type 1-related malignant peripheral nerve sheath tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141788.RAW9ZpQpZRrfbOojWu6z9gCTpr4REBNAPmezdbsakGMgI130_provenance.
• NP141791.RAU_IlZanGX03FUXk__Oag28-ZtIpIJjZ-aGn72BTZctQ130_assertion description "[MMP-13 may serve as a marker for progression of malignant peripheral nerve sheath tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141791.RAU_IlZanGX03FUXk__Oag28-ZtIpIJjZ-aGn72BTZctQ130_provenance.
• NP141793.RAYq6J_Gob412zdtU5blJL_FZfSyHdBO7NqXaczomIz6U130_assertion description "[Wild-type and mutant p53 are shown to differentially regulate MMP-13 expression in malignant peripheral nerve sheath tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141793.RAYq6J_Gob412zdtU5blJL_FZfSyHdBO7NqXaczomIz6U130_provenance.
• NP141801.RAQ533jMs5k34Kt9qOVvVTSmL_gPgp6M1_e08qW21if44130_assertion description "[The lack of NF2 alterations supports the hypothesis that GI schwannomas represent a morphologically and genetically distinct group of peripheral nerve sheath tumors that are different from conventional schwannomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141801.RAQ533jMs5k34Kt9qOVvVTSmL_gPgp6M1_e08qW21if44130_provenance.
• NP141802.RAUXyfBQnN3dsG_gqvPuZhI8YinncJF4m9I9z2Pq41WIg130_assertion description "[Nestin is more sensitive for malignant peripheral nerve sheath tumor (MPNST) than other neural markers, and immunostains for nestin in combination with other markers could be useful in the diagnosis of MPNST.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141802.RAUXyfBQnN3dsG_gqvPuZhI8YinncJF4m9I9z2Pq41WIg130_provenance.
• NP141804.RAXal7ALN4vj8MHZK3Eh7W8IKLeRxD0I0ofQJSvbbfPnY130_assertion description "[NF1 microdeletion individuals have a substantially higher lifetime risk for the development of malignant peripheral nerve sheath tumors than individuals with NF1 who do not have an NF1 microdeletion ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141804.RAXal7ALN4vj8MHZK3Eh7W8IKLeRxD0I0ofQJSvbbfPnY130_provenance.
• NP141805.RAaaZoLkIjEPMRsCRh3X3IU00-_CPPvHzhMSRYDXFkFVI130_assertion description "[Expression of IMP3 and p53 may be helpful biomarkers in the distinction of endometrial serous carcinoma from endometrioid adenocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141805.RAaaZoLkIjEPMRsCRh3X3IU00-_CPPvHzhMSRYDXFkFVI130_provenance.
• NP141811.RAaaPW7Gkfao6UFIE3TOSpq6wUevpONHxh47CLH-Fglsw130_assertion description "[Loss of hMLH1 and/or hMSH2 expression was found in nine of 15 microsatellite instability-high ovarian endometrioid carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141811.RAaaPW7Gkfao6UFIE3TOSpq6wUevpONHxh47CLH-Fglsw130_provenance.
• NP141815.RAWhukhpkaweVwwuVhcYkqdpYhclgPSzV3vDPoZPzeQQI130_assertion description "[Cyr61 is highly expressed in some endometrial cancer of endometrioid subtype/expression and positive lymph node metastases were independent prognostic factors for patients with endometrioid adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141815.RAWhukhpkaweVwwuVhcYkqdpYhclgPSzV3vDPoZPzeQQI130_provenance.
• NP141817.RAf0XLBqZp_7HlqKs8Sipx-6XVxszMXz37_17i-XqJN34130_assertion description "[Ezrin is de-expressed in endometriosis and endometrioid carcinoma compared with normal uterine epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141817.RAf0XLBqZp_7HlqKs8Sipx-6XVxszMXz37_17i-XqJN34130_provenance.
• NP141819.RAUxyT16eXH1uMR1fTpevhirMssWSareSOEcPixU2kT3g130_assertion description "[AQP1 may be involved in the tumorigenesis and progression of endometrioid adenocarcinoma by promoting angiogenesis, and AQP1 level may be both a tumor indicator and a new therapeutic target.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141819.RAUxyT16eXH1uMR1fTpevhirMssWSareSOEcPixU2kT3g130_provenance.
• NP141835.RAb6s9RdOzwT0QH91QF1RuM6gRvOo41UvNPVMRdDzeh-4130_assertion description "[The results indicated that the mutations in transcription regulator sequences of COL1A1 could cause idiopathic con-genital talipes equinovarus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141835.RAb6s9RdOzwT0QH91QF1RuM6gRvOo41UvNPVMRdDzeh-4130_provenance.
• NP141837.RAWoDUdC3sKcwIBK75mWTej1R5Tj1EWNIpz2Ts_etLRu8130_assertion description "[The increased glycolipid content in MDR1-transfected liver neoplasm cells is caused by a transcriptional up-regulation of the enzyme lactosylceramide synthase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141837.RAWoDUdC3sKcwIBK75mWTej1R5Tj1EWNIpz2Ts_etLRu8130_provenance.
• NP141845.RATQg4JVoQMLQeIGzOsMp6CoHjNj7VGfHbT3je2uP0B0s130_assertion description "[DLK1 was expressed in liver neoplasms/patients had a shorter survival time than DLK1-negative patients/regression analysis also showed that DLK1 is a risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141845.RATQg4JVoQMLQeIGzOsMp6CoHjNj7VGfHbT3je2uP0B0s130_provenance.
• NP141853.RAXAJwz8PTpku-7DubzSWUP_3ug_k9vAOL49FryWk6FsM130_assertion description "[Mosaic knockout mice lacking Bin1 exhibit lung and liver cancer, increased inflammation or premalignant lesions in prostate, and more progressive colon cancer/, Bin1 suppresses inflammation and cancer during aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141853.RAXAJwz8PTpku-7DubzSWUP_3ug_k9vAOL49FryWk6FsM130_provenance.
• NP141854.RAQjWJSzb3dNr4R4ia1vBKKciioMXcTk6S1FVSMUGnOyo130_assertion description "[AFP increase in patients with liver cancer was positively correlated with the infection of HBV and HCV/serum AFP elevation by the infection of HBV and HCV is one of mechanisms which lead to hepatocarcinogenesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141854.RAQjWJSzb3dNr4R4ia1vBKKciioMXcTk6S1FVSMUGnOyo130_provenance.
• NP141856.RAc1OCavRRGj_B1TJRH3cjZakhdZozh_lK6aUdlNDYgLQ130_assertion description "[In the liver cancer tissue, MT1F shows down-regulated expression that supports the inhibited function of MT1F in cancer growth ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141856.RAc1OCavRRGj_B1TJRH3cjZakhdZozh_lK6aUdlNDYgLQ130_provenance.
• NP141859.RAU2qkD5gh1zCg3qRxmyIFG09-FsgXjajZRXiMW1JZofA130_assertion description "[Polymorphism of this locus as related to the develpment of liver neoplasms in patients with chronic hepatitis C infection ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141859.RAU2qkD5gh1zCg3qRxmyIFG09-FsgXjajZRXiMW1JZofA130_provenance.
• NP141860.RAXFJ3-H6_XZrsPfeG5z1N3jxICMY-hPCNfMQQdRr2as4130_assertion description "[E2F1 may function as a critical antiapoptotic factor both in human and in rodent liver cancer through its ability to counteract c-Myc-driven apoptosis via activation of PIK3CA/Akt/mTOR and c-Myb/COX-2 pathways ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141860.RAXFJ3-H6_XZrsPfeG5z1N3jxICMY-hPCNfMQQdRr2as4130_provenance.
• NP141862.RAa1XtvkLzQpaBkMWYJUUjtm17nCSAtDWw8VxhPc7WKho130_assertion description "[in liver cancer modulation of CRBP-1 expression in HCCs contributes to tumor growth and progression via retinoid-mediated signaling and disruption of cellular vitamin A homeostasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141862.RAa1XtvkLzQpaBkMWYJUUjtm17nCSAtDWw8VxhPc7WKho130_provenance.
• NP141866.RAemJO4N6ChzkXPruHYYMozfiS4Al5hiNEoaioPHf7Sik130_assertion description "[A continuous rise of IL-6 and a transient elevation of IL-10 during liver cancer surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141866.RAemJO4N6ChzkXPruHYYMozfiS4Al5hiNEoaioPHf7Sik130_provenance.
• NP141868.RAZH-7IMof2P-1ZCUDKrCztRUtwsBbJjEV0O1Jc8qzOF8130_assertion description "[Knockdown of MMP-2 did not significantly alter the metastatic potential of the liver cancer cells but lead to a marked inhibition of metastatic foci growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141868.RAZH-7IMof2P-1ZCUDKrCztRUtwsBbJjEV0O1Jc8qzOF8130_provenance.
• NP141883.RAcRrCWZKU8U8azcMhUHXksXf136WJZoI7f3H_XaKfVcQ130_assertion description "[A novel full-length cDNA was cloned and differentiated, which was highly expressed in liver cancer tissues/HCCA3) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141883.RAcRrCWZKU8U8azcMhUHXksXf136WJZoI7f3H_XaKfVcQ130_provenance.
• NP141884.RAX0jUQ1XQyn6PcxlmHmkzwb7IYVb4B75CEBmzWpBX3cs130_assertion description "[expression of VEGFR-3 (S) is up-regulated in > 75% of hepatitis B x antigen positive hepatocellular carcinoma (HCC) nodules; HBxAg may short circuit VEGFR-3 (S) signaling in liver cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141884.RAX0jUQ1XQyn6PcxlmHmkzwb7IYVb4B75CEBmzWpBX3cs130_provenance.
• NP141891.RAZstrXuFXm42MPN1IFaxfYzbJ6TIUU1xjo9krmexE0uA130_assertion description "[GSDML may be a secretory or metabolic product involved in a secretory pathway, and changes in the regulation of GSDML splicing variant transcription and translation may be seen in the development and/or progression of gastrointestinal and hepatic cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141891.RAZstrXuFXm42MPN1IFaxfYzbJ6TIUU1xjo9krmexE0uA130_provenance.
• NP141892.RAQOa2X0F2TVz2PVgRviLpPxTm3-Z0EtFgVn9MU0TQQnI130_assertion description "[analysis of Wnt/beta-catenin and Myc signaling in liver cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141892.RAQOa2X0F2TVz2PVgRviLpPxTm3-Z0EtFgVn9MU0TQQnI130_provenance.
• NP141896.RAciM8_tc3Js58b6z4fTpBg6aVvoCG3a3pzNXxWEDoZdQ130_assertion description "[The detection of mutant p53 protein in hepatocellular cancer is corellated with clinicopathologic parameters and incidence of the liver neoplasms in Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141896.RAciM8_tc3Js58b6z4fTpBg6aVvoCG3a3pzNXxWEDoZdQ130_provenance.
• NP141899.RAZaRsC9Hk_-PDnCqjYef-JQMyEduGgbAxmaiVT63nVHk130_assertion description "[TGFB1 activates cytosolic phospholipase A2alpha (cPLA2alpha) -mediated prostaglandin E2 (PGE) 2/EP1 and peroxisome proliferator-activated receptor-gamma (PPAR-gamma)/Smad signaling pathways in human liver cancer cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141899.RAZaRsC9Hk_-PDnCqjYef-JQMyEduGgbAxmaiVT63nVHk130_provenance.
• NP141902.RAcv5fJzDO2v3Lj6HBSpRefxKQuoZLYfhAmaM64pNrp6I130_assertion description "[NDRG2 gene might express differently between normal tissues and cancer tissues, and might play an important role in the development of pancreatic cancer and liver cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141902.RAcv5fJzDO2v3Lj6HBSpRefxKQuoZLYfhAmaM64pNrp6I130_provenance.
• NP141919.RAUO0iZmHrLhm39JPJrHKnIPunfRt7F38aFmdw9olCACA130_assertion description "[Plasma adiponectin and leptin are expected as contributors related to dyslipidemia, suggesting these may be targets of prevention of vascular diseases in maintenance hemodialysis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141919.RAUO0iZmHrLhm39JPJrHKnIPunfRt7F38aFmdw9olCACA130_provenance.
• NP141925.RAXGbMODAI94b8DU0XLXL-DHjcj01pQrwoCWu4WdVbCaU130_assertion description "[High polyunsaturated fatty acid intakes were associated with atherogenic dyslipidemia in carriers of the minor T allele at the TCF7L2 single nucleotide polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141925.RAXGbMODAI94b8DU0XLXL-DHjcj01pQrwoCWu4WdVbCaU130_provenance.
• NP141926.RAW63x-CIxbqqU37Ho5be6R-9dFzF-HvJrIC1wZxuwGB0130_assertion description "[Lipoprotein lipase may represent a link between low adiponectin levels and dyslipidemia in both nondiabetic individuals and patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141926.RAW63x-CIxbqqU37Ho5be6R-9dFzF-HvJrIC1wZxuwGB0130_provenance.
• NP141931.RAcoW9Z8HloPkAbDEsy-lswDbt2kd--8fXR1Piheo9A_I130_assertion description "[LPL may represent a link between low adiponectin levels and dyslipidemia in both nondiabetic individuals and patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141931.RAcoW9Z8HloPkAbDEsy-lswDbt2kd--8fXR1Piheo9A_I130_provenance.
• NP141932.RAZCcOGFiQ3whubwlitdmUW43I5h2Z73qV-YFni0hVTbw130_assertion description "[Results show that the H- allele of LPL HindIII polymorphism might have a small effect on apoB levels in the Central European Caucasian population with dyslipidemia of metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141932.RAZCcOGFiQ3whubwlitdmUW43I5h2Z73qV-YFni0hVTbw130_provenance.
• NP141937.RAYRu73c7P01VuHE9HwaUBEmbW3pakvVlm5W80bVoOnEA130_assertion description "[Role of the SREBF-1 gene in genetic predisposition of metabolic diseases such as obesity, type 2 diabetes, and dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141937.RAYRu73c7P01VuHE9HwaUBEmbW3pakvVlm5W80bVoOnEA130_provenance.
• NP141939.RAaIC2PBLIeW7Cg9HqQhXfoIohGBkbwTMo_aMiE1ve9Jo130_assertion description "[This novel insight that thyroid hormone regulates LXR-alpha mRNA levels and promoter activity should shed light on a cross talk between LXR-alpha and TR-beta1 as a new therapeutic target against dyslipidemia and atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141939.RAaIC2PBLIeW7Cg9HqQhXfoIohGBkbwTMo_aMiE1ve9Jo130_provenance.

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