Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP177110.RAQEXOz3iZM2V9J-UmfG5B5jCKmUPDq_aVmC7kuHW1_DU130_assertion description "[Expression of proteins encoded by genes of a putative NF-kappaB signature, NF-kappaB p65, and TP53 were examined in HNSCC tissue specimens by immunostaining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177110.RAQEXOz3iZM2V9J-UmfG5B5jCKmUPDq_aVmC7kuHW1_DU130_provenance.
- NP177123.RASglaQLbg3c_SGKKVcIaFBbiGwI9DVx_Xuc0Yq1A2DWs130_assertion description "[Hierarchical clusterings of diffuse large B-cell lymphoma (DLBCL) based on gene expression signatures have previously been used to classify DLBCL into Germinal Center B-cell (GCB) and Activated B-cell (ABC) types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177123.RASglaQLbg3c_SGKKVcIaFBbiGwI9DVx_Xuc0Yq1A2DWs130_provenance.
- NP177124.RAeY8AxNJZQvW_rhTVIDnfXlPEcT9is8MJYD0e-Vt2RuM130_assertion description "[Thus, these studies contribute in vivo data in support of the hypothesis that PNH arises as a consequence of a pathological process that selects for hematopoietic stem cells that are GPI-AP-deficient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177124.RAeY8AxNJZQvW_rhTVIDnfXlPEcT9is8MJYD0e-Vt2RuM130_provenance.
- NP177125.RAUStAHC_4DuDk4jXHGYXeANvTEYy0yjZMjF8qT9y0v_w130_assertion description "[To examine whether polymorphism at the SAA loci is associated with the development of amyloid protein A (AA)-amyloidosis, we determined the genotypes at the SAA1 and SAA2 loci in 43 AA-amyloidosis patients (amyloidosis population) and 77 patients with rheumatoid arthritis (RA) who had been ill for less than 5 years (early RA population).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177125.RAUStAHC_4DuDk4jXHGYXeANvTEYy0yjZMjF8qT9y0v_w130_provenance.
- NP177141.RAadsjx41pOtJkuh1BMRyoiLlU1x0hODch9IS64ZQAu5M130_assertion description "[To suppress production of variant transthyretin (TTR) in the liver, we injected purified normal human TTR into patients with FAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177141.RAadsjx41pOtJkuh1BMRyoiLlU1x0hODch9IS64ZQAu5M130_provenance.
- NP177148.RAQVBtGf7dCjco4CUZ0YdkmpQdFOKpa-RRBYLqrBMl328130_assertion description "[Systematic study of association of four GABAergic genes: glutamic acid decarboxylase 1 gene, glutamic acid decarboxylase 2 gene, GABA(B) receptor 1 gene and GABA(A) receptor subunit beta2 gene, with schizophrenia using a universal DNA microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177148.RAQVBtGf7dCjco4CUZ0YdkmpQdFOKpa-RRBYLqrBMl328130_provenance.
- NP177152.RASAxTr-e6U6z_YuURhtKvfYqKJQMSIfi8Q18j1cU1-9A130_assertion description "[To determine whether the autosomal dominant Strudwick-type SEMD in a three-generation family, showing specific phenotypical features such as chest deformity, limb shortening, myopia and early-onset degenerative osteoarthrosis, might be caused by a novel COL2A1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177152.RASAxTr-e6U6z_YuURhtKvfYqKJQMSIfi8Q18j1cU1-9A130_provenance.
- NP177153.RAdrLGY_-SsWNIVrYRaGuwANBnblw2NQx4BohEoiAN3DM130_assertion description "[Indeed, 1p36/19q13 has been shown successively to predict increased chemosensitivity and better prognosis, to be associated with frontal location in brain and classic oligodendroglioma morphology, to be mutually exclusive with high-level gene amplification, to be actually whole chromosome arms 1p/19q codeletion, to mediate a t(1;19)(q10;p10) and to be associated with IDH mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177153.RAdrLGY_-SsWNIVrYRaGuwANBnblw2NQx4BohEoiAN3DM130_provenance.
- NP177165.RATTk-HmCKXJnw5UcmujukcWVigxo35Wf_CplCXn3Y2E8130_assertion description "[Two independent familial STS deletions, one of which is associated with a phenotype of ichthyosis plus ocular albinism (XI/OA1) and the other with nystagmus plus Rud syndrome, lack some but not all of the normal S232 PFGE fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177165.RATTk-HmCKXJnw5UcmujukcWVigxo35Wf_CplCXn3Y2E8130_provenance.
- NP177167.RATP9sRoIAXwf8E5dVynKW42YXolEpVsUyPaS6-DbZfeA130_assertion description "[This study examined aldehyde dehydrogense (ALDH2) gene status, alcohol dehydrogense (ADH2) gene status, conduct disorder, and alcohol dependence in Chinese, Korean, and White American college students.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177167.RATP9sRoIAXwf8E5dVynKW42YXolEpVsUyPaS6-DbZfeA130_provenance.
- NP177169.RASHIBwenOsDURed6O-p0oIzJ7WWpr5QgA8As0T_2f7CA130_assertion description "[Here we have investigated the functional contribution of ER stress to HD by targeting the expression of two main UPR transcription factors, XBP1 and ATF4 (activating transcription factor 4), in full-length mutant Huntingtin (mHtt) transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177169.RASHIBwenOsDURed6O-p0oIzJ7WWpr5QgA8As0T_2f7CA130_provenance.
- NP177170.RARtj37EdrHG9TpElD1h-ToXDdbL3djeICMQgSSRChyB8130_assertion description "[Late-onset familial neurohypophyseal diabetes insipidus due to a novel mutation in the AVP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177170.RARtj37EdrHG9TpElD1h-ToXDdbL3djeICMQgSSRChyB8130_provenance.
- NP177176.RAWAl4ZC614CGqsamQcQE71J5QGOmO7-swEqGt4wRckqo130_assertion description "[Furthermore, we show that the breakpoints, setting the centromeric amplicon boundaries, are within the CFS FRA7G region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177176.RAWAl4ZC614CGqsamQcQE71J5QGOmO7-swEqGt4wRckqo130_provenance.
- NP177180.RAYWFYajOv6KN_MvJU-dVSedaDBq8YMqMjGtjgweeRGjA130_assertion description "[Alpha-cardiac actin is one of the disease genes where different missense mutations have been found to cause either HCM or DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177180.RAYWFYajOv6KN_MvJU-dVSedaDBq8YMqMjGtjgweeRGjA130_provenance.
- NP177181.RAXa1ySk2k1Iup3mNUE7XNFgrQ60LFd1Yat9T3s8IK4uk130_assertion description "[A virus-directed enzyme prodrug therapy (VDEPT) strategy for lung cancer using a CYP2B6/NADPH-cytochrome P450 reductase fusion protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177181.RAXa1ySk2k1Iup3mNUE7XNFgrQ60LFd1Yat9T3s8IK4uk130_provenance.
- NP177188.RAaSFvdTdJMRDZQsEgCoa4NxqPKG0WQk-_P0GhLTy7aUU130_assertion description "[PKD2 depletion in pancreatic tumours inhibited tumour-driven blood vessel formation and tumour growth in the CAM and in orthotopic pancreatic cancer xenografts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177188.RAaSFvdTdJMRDZQsEgCoa4NxqPKG0WQk-_P0GhLTy7aUU130_provenance.
- NP177198.RATJEy6hx_W65v2IpQkrHTNhL207XcDlmIfhrp_ynHKZA130_assertion description "[We determined the association of CYP2C19 loss-of-function (*2) and gain-of-function (*17) allele status with platelet reactivity in 118 stented patients on DAPT ≥2 weeks and in 143 patients with stable coronary artery disease on aspirin therapy alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177198.RATJEy6hx_W65v2IpQkrHTNhL207XcDlmIfhrp_ynHKZA130_provenance.
- NP177200.RAU7ZWde_K2SKmq7BPGWc7oZT8p2HrWAHOJW05bPFy69k130_assertion description "[The aim of this study is to determine the status of p53 gene alteration in this distinct type of ovarian carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177200.RAU7ZWde_K2SKmq7BPGWc7oZT8p2HrWAHOJW05bPFy69k130_provenance.
- NP177201.RAasIU-od6NV4lJQPCEBZeQa5FFIQx7xzA_WMlBMORChM130_assertion description "[The expression of MRP-1/CD9 and KAI1/CD82 genes are useful indicators of a poor prognosis in breast cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177201.RAasIU-od6NV4lJQPCEBZeQa5FFIQx7xzA_WMlBMORChM130_provenance.
- NP177202.RAWQt145A451Dxe29t3WZGW5lFJ8cvrgUNSWb_zWXMMW4130_assertion description "[This study showed that ABCD2, ABCD3, and ABCD4 are less likely the disease-modifying genes, necessitating further studies to identify genes modifying ALD phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177202.RAWQt145A451Dxe29t3WZGW5lFJ8cvrgUNSWb_zWXMMW4130_provenance.
- NP177205.RAUTpH0G1M8YZQ7wyXtmPUj1qmNgiSOQ677q0rGMR4cng130_assertion description "[Here, we report that cardiac glycosides, which have been used for the treatment of cardiac failure for many years, sensitize lung cancer cells but not normal human peripheral blood mononuclear cells to Apo2L/TRAIL-induced apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177205.RAUTpH0G1M8YZQ7wyXtmPUj1qmNgiSOQ677q0rGMR4cng130_provenance.
- NP177211.RAWPQTqIVZu5THvuevay4rs5Jcly1xFWWdRYBr163KWWM130_assertion description "[The latter finding could be in line with the observation that CDKN2A/p16 inactivation is a step in the molecular pathway to tumor progression in oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177211.RAWPQTqIVZu5THvuevay4rs5Jcly1xFWWdRYBr163KWWM130_provenance.
- NP177215.RAdjj1YXbRDk9uOfmbptHpgVJIQjgGXqwdU6_fCdFqSAU130_assertion description "[This study shows that locus directed integration of model FMR1 CGG transgenes could be a new basic tool to further elucidating the basic molecular mechanisms behind transcriptional deregulation of the FMR1 gene in fragile X-syndrome and FXTAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177215.RAdjj1YXbRDk9uOfmbptHpgVJIQjgGXqwdU6_fCdFqSAU130_provenance.
- NP177217.RAe3wuHw-SZiPjDYYpVA4fQygRRuR_-ejQ6Ta7m5sJbSs130_assertion description "[Here we explored whether aberrant somatic hypermutation, leading to the acquisition of new mutations in PIM-1, PAX-5, RhoH/TTF and c-MYC genes, is involved in transformation from FL or B-CLL to DLBCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177217.RAe3wuHw-SZiPjDYYpVA4fQygRRuR_-ejQ6Ta7m5sJbSs130_provenance.
- NP177220.RAQKunWSmg-tBqTnlX_iE3Nx5XgnfvseLrYystgIUnAO4130_assertion description "[Furthermore, a number of single nucleotide polymorphism associations from GWA were located directly within VDR binding intervals, for example, rs13385731 associated with SLE and rs947474 associated with T1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177220.RAQKunWSmg-tBqTnlX_iE3Nx5XgnfvseLrYystgIUnAO4130_provenance.
- NP177229.RATcPq6Lvrr4nrOHs-WaBD-ekvsum88x9l9XkytWn57MU130_assertion description "[Shikonin affected NAT activity, gene expression (NAT1 mRNA), AF-DNA adducts formation and formation of NAT Ag-Ab in human bladder tumor T24 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177229.RATcPq6Lvrr4nrOHs-WaBD-ekvsum88x9l9XkytWn57MU130_provenance.
- NP177230.RARjt1bWvQaymKVTmrFB1sZFhURBpDvmGcRAiZ1Fel7dc130_assertion description "[The mean beta-arrestin 1 expression was unchanged in the cytosol of TTNs, in membranes and cytosol of CTNs and decreased in the membranes of TTNs compared to their surrounding tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177230.RARjt1bWvQaymKVTmrFB1sZFhURBpDvmGcRAiZ1Fel7dc130_provenance.
- NP177239.RAYSdv07EF--ulJTOoBQGTqYVMSacrNF9tUmLfQYXDCOs130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an inherited autosomal dominant vascular dysplasia caused by mutations in mainly the endoglin gene (ENG) or activin-like kinase receptor 1 (ALK1) gene (ACVRL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177239.RAYSdv07EF--ulJTOoBQGTqYVMSacrNF9tUmLfQYXDCOs130_provenance.
- NP177243.RAcoBFXxci8MSyfaPkYQUwSx7iuEVZm9V1REjZU1jN3G4130_assertion description "[Here, we report that knock-in mouse expressing humanized chimeric PrP demonstrated PrP(Sc) accumulations in follicular dendritic cells following human prion infections, including variant Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177243.RAcoBFXxci8MSyfaPkYQUwSx7iuEVZm9V1REjZU1jN3G4130_provenance.
- NP177250.RARxZJGzvzGkgZN0v0gG7lmVRFgb3C8DoPRvKTADZORPc130_assertion description "[The influence of the CYP2C19 LOF alleles (*2 and *3) on clopidogrel response and clinical outcomes in East Asians with acute myocardial infarction (AMI) has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177250.RARxZJGzvzGkgZN0v0gG7lmVRFgb3C8DoPRvKTADZORPc130_provenance.
- NP177253.RAfcSsvjV3m6_jr3-ATJ8QWDy_2Nxv0q5BdyXt52uip0o130_assertion description "[We now demonstrate that Ad.mda-7 decreases viability by induction of apoptosis in hormone-responsive (LNCaP) and hormone-independent (DU-145 and PC-3) human prostate carcinomas, without altering growth or survival in early-passage normal human prostate epithelial cells (HuPEC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177253.RAfcSsvjV3m6_jr3-ATJ8QWDy_2Nxv0q5BdyXt52uip0o130_provenance.
- NP177254.RAfjdiqBX6MIGZ3sO7L53zsPGXlhV_9cNN4thoDmOxMvM130_assertion description "[The negative effect of TGFbeta1 on ADAMTS-1, -5, -9, and -15 coupled with increases in their inhibitor, TIMP-3 may aid the accumulation of versican in the stromal compartment of the prostate in BPH and prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177254.RAfjdiqBX6MIGZ3sO7L53zsPGXlhV_9cNN4thoDmOxMvM130_provenance.
- NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion description "[The objectives of this study were: to determine plasma total homocysteine tHcy levels and the prevalence of hyperhomocysteinemia in children with type 1 diabetes, to determine correlates of plasma tHcy levels with nutritional factor such as serum folic acid and vitamin B12 levels, genetic factors as methylenetetrahydrofolate reductase MTHFR gene polymorphism (C677T and A1298C), to attempt to identify possible dependencies between tHcy and the degree of metabolic control, the duration of the disease and presence of complications, and also to determine the relationship between other coronary risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance.
- NP177263.RAePeXJwaMS4yzMlWYbh9JZMWpnCs9CYtAkYFUtCQqaJ4130_assertion description "[Recent large-scale cohort studies showed that Fc receptor-like 3 gene (FCRL3) single nucleotide polymorphism (SNP) and peptidylarginine deiminases citrullinating enzymes 4 gene (PADI4) haplotype were associated with autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177263.RAePeXJwaMS4yzMlWYbh9JZMWpnCs9CYtAkYFUtCQqaJ4130_provenance.
- NP177265.RAWpM4TUfINiHqeVUO5NNY5rj55CZZxIEz-GFZRo5kV3c130_assertion description "[Here we report a case of intragenic EGFR microdeletion in renal cell carcinoma (RCC) associated with the effect of treatment by gefitinib.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177265.RAWpM4TUfINiHqeVUO5NNY5rj55CZZxIEz-GFZRo5kV3c130_provenance.
- NP177271.RAYS0M9TMIqXqTYNuocaR2K4MDrGnLMraiEdYoJQM-o8w130_assertion description "[Levels of antibodies to all three SS-A/Ro antigens were significantly higher in mothers of children with CHB than in controls with SLE and primary SS (P = 0.0001-0.0014).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177271.RAYS0M9TMIqXqTYNuocaR2K4MDrGnLMraiEdYoJQM-o8w130_provenance.
- NP177280.RAcsUg6y5GVAF0EPYN2qGBDkJOrG1pSDHqJam_INSynWE130_assertion description "[Constitutive activation of ADAM10 has been implicated in the pathogenesis of several types of solid tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177280.RAcsUg6y5GVAF0EPYN2qGBDkJOrG1pSDHqJam_INSynWE130_provenance.
- NP177281.RAfskjO0-YMQsFC1zAbikPg3MlD26HcbqIQHkOZ2_pxSM130_assertion description "[Furthermore, the development of novel therapeutics targeting Akt1 or components of the PI3K/Akt pathway may enhance the management of carcinoid disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177281.RAfskjO0-YMQsFC1zAbikPg3MlD26HcbqIQHkOZ2_pxSM130_provenance.
- NP177282.RAY_mafcnE2DM-1AZcsg8sYp89vdOBXp7SJRXXvUDR-nk130_assertion description "[Increasing cyclooxygenase-2 (cox-2) gene expression in the progression of Barrett's esophagus to adenocarcinoma correlates with that of Bcl-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177282.RAY_mafcnE2DM-1AZcsg8sYp89vdOBXp7SJRXXvUDR-nk130_provenance.
- NP177283.RAdsqBGauTmDPUYI4_ohCdkxksF4YUZrnNFiezpxDPMyc130_assertion description "[Two other FGFRs, FGFR1 and FGFR3, also account for craniosynostoses of variable severity [Pfeiffer, Crouzon with acanthosis nigricans (a pre-malignant skin disorder), and Muenke syndromes].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177283.RAdsqBGauTmDPUYI4_ohCdkxksF4YUZrnNFiezpxDPMyc130_provenance.
- NP177290.RAcmoRUGUIk1nxKvnWUE9q8tE61EmjxJgHc_lhwBMLUxM130_assertion description "[Our results confirm the previous reports showing that the variant A allele of MPO has a protective effect against risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177290.RAcmoRUGUIk1nxKvnWUE9q8tE61EmjxJgHc_lhwBMLUxM130_provenance.
- NP177294.RAfCFYGDoIMvAJvzDnnZ1Wh-NvYPjXqHy16YLb4A-wVDM130_assertion description "[Taken together, these findings suggest that high expression of CXCR7 increases the risk of metastasis in post-resective HCC patients with relatively good differentiated tumors, potentially through upregulation of OPN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177294.RAfCFYGDoIMvAJvzDnnZ1Wh-NvYPjXqHy16YLb4A-wVDM130_provenance.
- NP177295.RARukRXfuoYOFKs98LuaTsN84exR_pG9aO8tPcxDiVbYM130_assertion description "[Increased melanoma growth and metastasis spreading in mice overexpressing placenta growth factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177295.RARukRXfuoYOFKs98LuaTsN84exR_pG9aO8tPcxDiVbYM130_provenance.
- NP177297.RAXPn2AHdoGvhYVp272zAlkdJDmCt66nVbskYLdEF9gI8130_assertion description "[Smoldering MM (SMM) is a MM precursor defined by an M-protein concentration >or= 3 g/dL and/or >or= 10% bone marrow plasma cells, in the absence of end-organ damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177297.RAXPn2AHdoGvhYVp272zAlkdJDmCt66nVbskYLdEF9gI8130_provenance.
- NP177298.RAfUpoF-jlpQ_GVazWLxp-FG1_rmC6mfa3COQlRs5yOv0130_assertion description "[LIPC and ABCA1 are related to intermediate and large drusen, as well as advanced AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177298.RAfUpoF-jlpQ_GVazWLxp-FG1_rmC6mfa3COQlRs5yOv0130_provenance.
- NP177301.RAQdVPlgjcWpjZYFjcHfQajxJJQvdyLgsM3oC9FpbebUs130_assertion description "[Decreased expression of fibronectin and MMP2 in lymph node metastases was further confirmed by real-time polymerase chain reaction assays performed on five additional specimen pairs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177301.RAQdVPlgjcWpjZYFjcHfQajxJJQvdyLgsM3oC9FpbebUs130_provenance.
- NP177302.RAbFWYhWSVptvGq46FGfDNEe7VGrvQUcT2kEOt5ZyEJ3s130_assertion description "[No association was found between polymorphisms of the coding region of LHR or FSHR genes and the development of OHSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177302.RAbFWYhWSVptvGq46FGfDNEe7VGrvQUcT2kEOt5ZyEJ3s130_provenance.
- NP177317.RAdXyVaX0E-SfHznFZi6TZa7YQ1piGju2Gym82NJTklQA130_assertion description "[We confirmed that carriers of an MMR gene mutation were at increased risk of a wide variety of cancers, including some cancers not previously recognized as being a result of MMR mutations, and found no evidence of an increased risk of cancer for their noncarrier relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177317.RAdXyVaX0E-SfHznFZi6TZa7YQ1piGju2Gym82NJTklQA130_provenance.
- NP177318.RAX-16d1IlxmWTyFfJ6C8g-Gu9etv5Uz_YEyCAybUiAn0130_assertion description "[Here, we report that dextran sodium sulfate (DSS)-induced colitis is accompanied by major shifts in the composition and function of the intestinal microbiota of STAT1(-/-) and wild-type mice, as determined by 454 pyrosequencing of bacterial 16S rRNA (gene) amplicons, metatranscriptomics and quantitative fluorescence in situ hybridization of selected phylotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177318.RAX-16d1IlxmWTyFfJ6C8g-Gu9etv5Uz_YEyCAybUiAn0130_provenance.
- NP177321.RAbejkqi3DQYm_bTMFVs0k5lcohKSJrnFVbNgLAjLuozo130_assertion description "[These results show that inhibitory agents of LINGO-1 activity can protect DA neurons against degeneration and indicate a role for the leucine-rich repeat protein LINGO-1 and related classes of proteins in the pathophysiological responses of midbrain DA neurons in PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177321.RAbejkqi3DQYm_bTMFVs0k5lcohKSJrnFVbNgLAjLuozo130_provenance.
- NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion description "[Although these traits are present at relatively high prevalence in the population, the magnitude of the increased thrombotic risk associated with these factors is substantially less than that related to inherited deficiency of the natural anticoagulant protein antithrombin, and somewhat less than the elevated risk with protein C and protein S deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance.
- NP177328.RAckPK8KGVzkfE8KxsAAhGzQVxthHq9oG42WoCqJZEXDo130_assertion description "[The effect of gentamicin-induced readthrough on a novel premature termination codon of CD18 leukocyte adhesion deficiency patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177328.RAckPK8KGVzkfE8KxsAAhGzQVxthHq9oG42WoCqJZEXDo130_provenance.
- NP177329.RAZZbyolEHUKVB-edICDF6xMxXYkqP5SI7FAeVoCqf7WM130_assertion description "[ASK1 resistant neuroblastoma is deficient in activation of p38 kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177329.RAZZbyolEHUKVB-edICDF6xMxXYkqP5SI7FAeVoCqf7WM130_provenance.
- NP177334.RAYJBxQYaOxBQQT6oURHZrAHSOk7WfgOs1eP9SJHalgqE130_assertion description "[Invasive primary tumors from a population-based sample of 107 cases of colorectal cancer diagnosed before age 45 years and tested for germ-line mutations in MLH1, MSH2, MSH6, and PMS2 and MMR protein expression were screened for MSI using the National Cancer Institute panel and an expanded 10-microsatellite marker panel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177334.RAYJBxQYaOxBQQT6oURHZrAHSOk7WfgOs1eP9SJHalgqE130_provenance.
- NP177339.RAaOypqXsqfTSVacHQxgIByRq4nOsThhU-auwRwb6icRk130_assertion description "[Using DNA samples collected at baseline in a prospective cohort of 14,916 initially healthy American men, we evaluated 3 AGER genetic variants: -429T>C, -374T>A, and Gly82Ser, among 600 white individuals who subsequently developed atherothrombotic event (incident myocardial infarction or ischemic stroke) and among 600 age- and smoking-matched white individuals who remained free of reported vascular disease during follow-up (controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177339.RAaOypqXsqfTSVacHQxgIByRq4nOsThhU-auwRwb6icRk130_provenance.
- NP177340.RAQdUbbknUZc7ajXkjCxp1gnBPiS_u07SPyVpHWT9PqF4130_assertion description "[In the present study we investigated the role of childhood traumas and 5-HTTLPR on measures of psychological resilience and depression in a sample of individuals at a high risk for psychological distress (763 male prisoners).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177340.RAQdUbbknUZc7ajXkjCxp1gnBPiS_u07SPyVpHWT9PqF4130_provenance.
- NP177345.RAXA1peWEdzrr-XKGOjZi9HTUaoqJHMcGnGKWExMPXmlc130_assertion description "[The BCL6 rearrangement was identified in 48% of NLPHL cases and was not detected in cHL cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177345.RAXA1peWEdzrr-XKGOjZi9HTUaoqJHMcGnGKWExMPXmlc130_provenance.
- NP177348.RAVorcGCFOgLelqAKsW7eSM4PJAMyQ4ej-vGgNedoNdlI130_assertion description "[Reduced ovarian cancer Dab2 histoscores correlated with high miR-187 levels and improved outcomes of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177348.RAVorcGCFOgLelqAKsW7eSM4PJAMyQ4ej-vGgNedoNdlI130_provenance.
- NP177352.RAYs_nBLNkbkXJBlcGjk-iL2X1BB7rcM6zAgRGtGagAQ0130_assertion description "[CYP1B1 mutations were found in 16 index patients with PCG (nine), POAG (three), JOAG (two), and ARS (two).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177352.RAYs_nBLNkbkXJBlcGjk-iL2X1BB7rcM6zAgRGtGagAQ0130_provenance.
- NP177353.RASH854yiLZrr-ztqfEBAFNkNaIIqROPc_X_qI7QLbeWE130_assertion description "[In contrast, neither normal germinal centre B-cells nor malignant cells of nodular lymphocyte-predominant Hodgkin's lymphoma, Burkitt lymphoma or diffuse large B-cell lymphoma expressed GATA-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177353.RASH854yiLZrr-ztqfEBAFNkNaIIqROPc_X_qI7QLbeWE130_provenance.
- NP177356.RAdGobNWd8c0zL2_c8FVQRhosripL3ZAuNc7VgZGbh4cs130_assertion description "[Polymorphism in ecto-nucleotide pyrophosphatase/phosphodiesterase 1 gene (ENPP1/PC-1) and early development of advanced diabetic nephropathy in type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177356.RAdGobNWd8c0zL2_c8FVQRhosripL3ZAuNc7VgZGbh4cs130_provenance.
- NP177359.RAdUZFg9Ep6YFAl-_ZF_pXBgCigeQvdNp7VN5pxSUsvDw130_assertion description "[Thioredoxin 2, a mitochondrion-specific thioredoxin whose role in diabetes was unknown, was suppressed in the aorta from rats with two weeks of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177359.RAdUZFg9Ep6YFAl-_ZF_pXBgCigeQvdNp7VN5pxSUsvDw130_provenance.
- NP177362.RAXE0xmZbQX7tyYlHlDVvdE5xBrlaPEqXr5F3KwmMlLA8130_assertion description "[To address whether a good disease outcome of NB was a consequence of high-level expression of a `favorable NB gene,` we examined the effect of EPHB6 on NB cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177362.RAXE0xmZbQX7tyYlHlDVvdE5xBrlaPEqXr5F3KwmMlLA8130_provenance.
- NP177364.RAQbWKZqbgaARRjaIvBCv3Xcms6vfPo2EKAUEJrNo0vLQ130_assertion description "[The BRAF genotype was correlated with the ability to concentrate (131)I and/or 2-[(18)F]fluoro-2-deoxi-d-glucose ((18)F-FDG) in the recurrent cancers, serum markers of recurrence, and patient outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177364.RAQbWKZqbgaARRjaIvBCv3Xcms6vfPo2EKAUEJrNo0vLQ130_provenance.
- NP177367.RAXjKn7UVNgBnMnY-9ZpcV56L0NQNe0umqxx3yWUZJWKA130_assertion description "[We investigated the alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia (T-ALL) and T-ALL cell lines by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis and direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177367.RAXjKn7UVNgBnMnY-9ZpcV56L0NQNe0umqxx3yWUZJWKA130_provenance.
- NP177371.RAbZsTe-G1DVEhL2Jdl7CFNsmdfIMxARm7FbQIWQpfiXM130_assertion description "[This review provides a background to the IMP protein family with an emphasis on human IMP2, followed by a closer look at the GWA studies to evaluate the significance, if any, of the proposed correlation between IMP2 and T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177371.RAbZsTe-G1DVEhL2Jdl7CFNsmdfIMxARm7FbQIWQpfiXM130_provenance.
- NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_assertion description "[Our study shows that -26 5' UTR polymorphism in BRCA2 can modulate the fine-tuned regulation of the multifunctional gene BRCA2 and renders risk or protection according to the genotype status in the sporadic form of breast cancer, which is further influenced by the germline genetic backgrounds of codon 72 polymorphism of p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_provenance.
- NP177383.RAenZSqpq_XErAvRg2UtrCg_KqHISRcL21a_i7Yu37RU8130_assertion description "[The Smith-Lemli-Opitz syndrome (SLOS), an autosomal recessive disorder associated with multiple developmental malformations, is caused by a large spectrum of mutations in the DHCR7 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177383.RAenZSqpq_XErAvRg2UtrCg_KqHISRcL21a_i7Yu37RU8130_provenance.
- NP177385.RAUNdhgO4qNzv1MjOMx59VaSTgbHFcH9KQBWeHwYU8AYY130_assertion description "[The survey, based on 74 unrelated kindreds, revealed that antithrombin III, protein C and protein S defects are the most frequent genetic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177385.RAUNdhgO4qNzv1MjOMx59VaSTgbHFcH9KQBWeHwYU8AYY130_provenance.
- NP177386.RASLJ5FGJ9aDVLvYOq2Fnxa7tVFH9jm02k_FiJmDvy-Hk130_assertion description "[In this review, we divide the osteochondrodysplasias into groups based on their genetic relationships, including mutations in various types of collagen, fibroblast growth factor, cartilage oligomeric matrix protein, parathyroid hormone receptor, the diastrophic dysplasia sulfate transporter, enzymes such as steroid sulfatases, transcription factor SOX9, and a cysteine proteinase, cathepsin K. We describe the major osteochondrodysplasias, define their causes and clinical manifestations, and provide the orthopaedic surgeon with an understanding of the underlying molecular defects as well as the anatomical aspects of these disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177386.RASLJ5FGJ9aDVLvYOq2Fnxa7tVFH9jm02k_FiJmDvy-Hk130_provenance.
- NP177387.RAUQRdYwkySvN2UJb1XCdFbnHKKjy-yMHmwQn8ri_Qrpk130_assertion description "[Using gastrocnemius muscles of mice overexpressing human mutant SOD1 (mutSOD1) at different disease stages, we found that the expression of a selected set of genes associated to muscle atrophy, MyoD, myogenin, atrogin-1, and transforming growth factor (TGF)β1, is up-regulated already at the presymptomatic stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177387.RAUQRdYwkySvN2UJb1XCdFbnHKKjy-yMHmwQn8ri_Qrpk130_provenance.
- NP177390.RAXcNWc2B2xW_FUebRXm4HYzdxIGr907zL-EkorgcZ4bs130_assertion description "[None of these three SNPs of TNRC9/LOC643714 gene is associated with individual susceptibility to breast cancer in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177390.RAXcNWc2B2xW_FUebRXm4HYzdxIGr907zL-EkorgcZ4bs130_provenance.
- NP177395.RAafKtx5DnfQhodPwFUdgOWo1j01EouVYKyqPmJGTaM4o130_assertion description "[The moderate to severe disease caused by E. chaffeensis in humans, first identified in 1986 and reported for more than 1,000 patients through 2000, represents a prototypical `emerging infection.` Knowledge of the biology and natural history of E. chaffeensis, and of the epidemiology, clinical features, and laboratory diagnosis of the zoonotic disease it causes (commonly referred to as human monocytic ehrlichiosis [HME]) has expanded considerably in the period since its discovery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177395.RAafKtx5DnfQhodPwFUdgOWo1j01EouVYKyqPmJGTaM4o130_provenance.
- NP177399.RAbEc7T1Oa3FY0tKjC0GzlrakX5tJQmGImpPlgLH7XOiQ130_assertion description "[To determine whether the sporadically occurring amplification of the oncogene erbB2/HER2 in gastrointestinal carcinomas is associated with additional changes of this sequence, DNA from 17 colorectal and 5 stomach carcinomas was analyzed for copy number, sequence rearrangement and DNA methylation by Southern blot hybridization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177399.RAbEc7T1Oa3FY0tKjC0GzlrakX5tJQmGImpPlgLH7XOiQ130_provenance.
- NP177402.RAZIWx8Snq4LxPIEIQMqRJS-_lM9HD6g6QylRu_t6elRo130_assertion description "[Activating KIR and HLA Bw4 ligands are associated to decreased susceptibility to pemphigus foliaceus, an autoimmune blistering skin disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177402.RAZIWx8Snq4LxPIEIQMqRJS-_lM9HD6g6QylRu_t6elRo130_provenance.
- NP177404.RAQ4gbnq561TjlzLQuQYX6iX-5UYRIXkJWlIKQzm2-hUA130_assertion description "[In this study, we compared EGFR and KRAS mutations in primary and unrelated metastatic lung adenocarcinomas from retrospectively collected clinical cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177404.RAQ4gbnq561TjlzLQuQYX6iX-5UYRIXkJWlIKQzm2-hUA130_provenance.
- NP177407.RAa-dsGsDj0sc2D4B5HP1qDvDu9dbm_0iu6CtfzIbx0pE130_assertion description "[Therefore, we examined the prevalence of 1958G>A polymorphism of MTHFD1 gene, encoding trifunctional folate enzyme 5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methenyltetrahydrofolate cyclohydrolase and 10-formyltetrahydrofolate synthetase (MTHFD1), and 2756A>G variant of methionine synthase (MTR) gene in patients with BD (n=200), schizophrenia (n=200) and in controls (n=300).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177407.RAa-dsGsDj0sc2D4B5HP1qDvDu9dbm_0iu6CtfzIbx0pE130_provenance.
- NP177408.RATFXEo7QmmWyr2h11vi-DoHCstkukWPgl_ppS7JAVI2g130_assertion description "[Repressive chromatin marks (H3K27me3) at the promoter were identified in CTNNA1-repressed AML cell lines and primary leukemias, with the most repressive state correlating with DNA methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177408.RATFXEo7QmmWyr2h11vi-DoHCstkukWPgl_ppS7JAVI2g130_provenance.
- NP177412.RAYov3OU2pxwbJhHOjG04KZJVnf5GzNedalgN4Lh2bK8A130_assertion description "[GST pi gene is frequently coamplified with INT2 and HSTF1 proto-oncogenes in human breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177412.RAYov3OU2pxwbJhHOjG04KZJVnf5GzNedalgN4Lh2bK8A130_provenance.
- NP177416.RAeNqBF6QihDMQJen-NdUTQsjYq4t_JOz38jVC0Goqo8M130_assertion description "[BLIN-2 has a clonal rearrangement of the Ig heavy chain locus, a dic(9;20) chromosomal abnormality, and a bi-allelic deletion of the p16(INK4a) and p19(ARF) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177416.RAeNqBF6QihDMQJen-NdUTQsjYq4t_JOz38jVC0Goqo8M130_provenance.
- NP177417.RAb86VlvIwSahZIVD6jPoZoAIRSOWC8whg9z1icvSozog130_assertion description "[Here, we report that genetically engineered mutants of severe acute respiratory syndrome coronavirus (SARS-CoV) and human coronavirus 229E (HCoV-229E) expressing ADRP-deficient macrodomains displayed an increased sensitivity to the antiviral effect of alpha interferon compared with their wild-type counterparts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177417.RAb86VlvIwSahZIVD6jPoZoAIRSOWC8whg9z1icvSozog130_provenance.
- NP177434.RAd4lWDWs6iUJ8ryyz5V2rbxqU3jAgmJ5zav-vTMWRSOk130_assertion description "[Breast cancer risk, dietary intake, and methylenetetrahydrofolate reductase (MTHFR)single nucleotide polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177434.RAd4lWDWs6iUJ8ryyz5V2rbxqU3jAgmJ5zav-vTMWRSOk130_provenance.
- NP177438.RAVPA8hbKIHEgXaKUic3UtyCrXuuGzrT6ttPKH7xd-DWM130_assertion description "[Metallo-β-lactamase genes such as bla(IMP), bla(VIM), bla(SPM), bla(GIM), and bla(SIM) and bla(OXA-50) were detected by polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177438.RAVPA8hbKIHEgXaKUic3UtyCrXuuGzrT6ttPKH7xd-DWM130_provenance.
- NP177440.RAS1y5db6YTxBkW70BNjahp9dgiFRW9a2DX0i7sK1eZm8130_assertion description "[The IRR for any early cardiovascular disease given a family history of premature noncardiovascular death was significantly lower, 1.12 (95% CI: 1.10 to 1.14) (p(cardiac vs. noncardiac) < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177440.RAS1y5db6YTxBkW70BNjahp9dgiFRW9a2DX0i7sK1eZm8130_provenance.
- NP177444.RAWs05z0u_v65woVf86Fip8XzYgyFWYixD2JDnajaGvrw130_assertion description "[Klotho, a gene related to a syndrome resembling human premature aging, functions in a negative regulatory circuit of vitamin D endocrine system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177444.RAWs05z0u_v65woVf86Fip8XzYgyFWYixD2JDnajaGvrw130_provenance.
- NP177447.RAR6YPnEgiqhm4XAOt9yvbA4WpyUqEY9KIwGjU9-N7LN8130_assertion description "[The AGE-RAGE system may thus participate in the development of diabetic microangiopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177447.RAR6YPnEgiqhm4XAOt9yvbA4WpyUqEY9KIwGjU9-N7LN8130_provenance.
- NP177448.RAX2GLHX51mRdBAeYWf4WuxCqWkE8WSUTOjHYJ6jHdlaA130_assertion description "[Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177448.RAX2GLHX51mRdBAeYWf4WuxCqWkE8WSUTOjHYJ6jHdlaA130_provenance.
- NP177449.RAdCOCou68ku0pehJKxNpqv1E6eD2un_m_C93co7HWSlw130_assertion description "[The ACT-AA polymorphism is not related to an increased risk of developing PD in the Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177449.RAdCOCou68ku0pehJKxNpqv1E6eD2un_m_C93co7HWSlw130_provenance.
- NP177457.RAWEHVc32ac1osn2jf7WoFzUu5Vl4TL7u2aHIvSv32IiM130_assertion description "[Angiotensin-converting enzyme is responsible for several vascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177457.RAWEHVc32ac1osn2jf7WoFzUu5Vl4TL7u2aHIvSv32IiM130_provenance.
- NP177458.RAUv9GGvJdr5nK-LNNb6x9Db6oCoqUfNR4sgETr2jOY_k130_assertion description "[The elevated levels of IL-22 suggest an association between this cytokine and immunopathology during tuberculosis-IRIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177458.RAUv9GGvJdr5nK-LNNb6x9Db6oCoqUfNR4sgETr2jOY_k130_provenance.
- NP177462.RAYotWbKk5WMCSbAgZpE8l3_ekit8qdORjk1HganAsOyM130_assertion description "[CXCR4 participates in several biological processes (bone marrow hematopoiesis, cardiogenesis, angiogenesis, neurogenesis) and is implicated in different clinical pathologic conditions (WHIM, HIV infection, tumor metastatization, autoimmunity).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177462.RAYotWbKk5WMCSbAgZpE8l3_ekit8qdORjk1HganAsOyM130_provenance.
- NP177466.RAZQwSLxc0hMmrD1seHYbd9UHMV6CrNhL4AIQmaAHT7dw130_assertion description "[Apolipoprotein E gene variants as a risk factor for coronary artery disease in type 2 diabetic Egyptian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177466.RAZQwSLxc0hMmrD1seHYbd9UHMV6CrNhL4AIQmaAHT7dw130_provenance.
- NP177468.RAQSP0tkaVrNAT2g-O_cHBFdQ8uZSLx2LhiDoUQD2qOIw130_assertion description "[A preliminary study of 3 adult control subjects and 4 children older than 12 years with CF verified that the new protocol was well tolerated and produced NPD measurements that did not differ significantly from those obtained with the standard protocol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177468.RAQSP0tkaVrNAT2g-O_cHBFdQ8uZSLx2LhiDoUQD2qOIw130_provenance.
- NP177474.RAdTfstEEanMhOT0qHlmUjD6bTCB_2TCSyxN8SrIMpEL8130_assertion description "[Although expression of PLU-1 in ce-1 cells is regulated by signaling from c-ErbB2, the gene is expressed in all the breast cancer cell lines examined, in cells cultured from primary breast cancers, and in the invasive and in situ components of primary breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177474.RAdTfstEEanMhOT0qHlmUjD6bTCB_2TCSyxN8SrIMpEL8130_provenance.
- NP177483.RAdbAvQhVo1lkUysnlrQtHB0toEHgrjdFTIovYZThAcug130_assertion description "[We have assessed 29 human primary breast carcinomas for both the presence of abnormal FHIT transcripts and the Fhit protein levels as compared with the normal breast epithelium of the same patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177483.RAdbAvQhVo1lkUysnlrQtHB0toEHgrjdFTIovYZThAcug130_provenance.
- NP177484.RAZhoFyzTBpU4v5wywuB0u7l6LxJ6XZ60ox_oBIKS3gKI130_assertion description "[A protocol for rapid mutation detection based on direct sequencing of large PCR-amplified genomic DNA fragments revealed a known TNNT2 mutation (Phe110Ile) in one of 30 FHC probands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177484.RAZhoFyzTBpU4v5wywuB0u7l6LxJ6XZ60ox_oBIKS3gKI130_provenance.
- NP177496.RAUJnaa9SJt84YOnpX21djdoogIaFlGAmfSFoyCkagQ9Y130_assertion description "[SGK1 contributes to metabolic syndrome and the pathophysiology of neurodegeneration, allergy, peptic ulcer, fibrosing disease and response to ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177496.RAUJnaa9SJt84YOnpX21djdoogIaFlGAmfSFoyCkagQ9Y130_provenance.
- NP177497.RARy1QS-rgdq_Hyu67RqyuIvk8LDvv1e_vny2JAtvY15Q130_assertion description "[Matrix metalloproteinase 9 (MMP-9) was selectively upregulated in the erythema migrans skin lesions of patients with acute Lyme disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177497.RARy1QS-rgdq_Hyu67RqyuIvk8LDvv1e_vny2JAtvY15Q130_provenance.
- NP177499.RAaRP1vLnTcLKWJ8vYu_2VLsLKIKqIKzhmpPktiNcOw4o130_assertion description "[Hep G2 cells carrying pHBV2CAT (similar to pHBV1CAT, but with the hepatitis B virus sequences in reverse orientation with respect to the CAT sequences) and pHBV3CAT (similar to pHBV2CAT, but hepatitis B virus sequences are separated from the CAT sequences by about 700 bases) also expressed CAT activity, but not as strongly as with pHBV1CAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177499.RAaRP1vLnTcLKWJ8vYu_2VLsLKIKqIKzhmpPktiNcOw4o130_provenance.
- NP177502.RAeUfXjbNMaEuTyy-CW3smEZmqvzFX4cb-E5TWOagLvn8130_assertion description "[In this study we examined the relationship of CD44 expression to somatic genetic events in the adenoma-carcinoma sequence: point mutation of K-ras in codons 12 and 13 and overexpression of p53 protein as a marker of gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177502.RAeUfXjbNMaEuTyy-CW3smEZmqvzFX4cb-E5TWOagLvn8130_provenance.