Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP172771.RAa2ONxnAHxoeQRXE-YKBHsCM7KPsFl5mYOjKpYj-beHM130_assertion description "[These observations suggest that alternative approaches to study CRP (perhaps using different pentraxins in the mouse model or using a rabbit model instead of a mouse model) are needed to evaluate the effects of pentraxins on atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172771.RAa2ONxnAHxoeQRXE-YKBHsCM7KPsFl5mYOjKpYj-beHM130_provenance.
- NP172772.RAd76mPWdTo_wa9Grz7-NiZlibGSE38AtvqI-yg0SdN7E130_assertion description "[The use of a DNA vaccine encoding the BCR/ABL fusion gene is thought to be a promising approach for patients with chronic myeloid leukemia (CML) to eradicate minimal residual disease after treatment with chemotherapy or targeted therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172772.RAd76mPWdTo_wa9Grz7-NiZlibGSE38AtvqI-yg0SdN7E130_provenance.
- NP172774.RAd57q2ILNTkupzaggfka8_cMrKkkMNl2WzQw4NWRDry8130_assertion description "[(4) OPN not only promotes arteriosclerosis but is also closely associated with arteriosteogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172774.RAd57q2ILNTkupzaggfka8_cMrKkkMNl2WzQw4NWRDry8130_provenance.
- NP172777.RAdKQwAxaJkZrpz7vTSibjP5XNpO3EM9MU4KwWsyN9h9g130_assertion description "[The present results show that the ObR is induced in endometriosis, and that leptin stimulates the growth of endometriotic epithelial cells through the JAK2/STAT3 and ERK pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172777.RAdKQwAxaJkZrpz7vTSibjP5XNpO3EM9MU4KwWsyN9h9g130_provenance.
- NP172778.RAQFfQgFY7KacMFlXXQ9NMz_Rb1RlfpsEASsQHgKPunDk130_assertion description "[The frequency of LRRK2 Gly2385Arg mutation in Hong Kong Chinese with early-onset (age < or =45 years) Parkinson's disease was identified and compared with late-onset patients (age >50 years) and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172778.RAQFfQgFY7KacMFlXXQ9NMz_Rb1RlfpsEASsQHgKPunDk130_provenance.
- NP172783.RAcFrxnIjjnU3zn0vC93HryXuPs9Gltwy5eLjbhlJK9eA130_assertion description "[Plasminogen activator inhibitor type 1 serum levels and 4G/5G gene polymorphism in morbidly obese Hispanic patients with non-alcoholic fatty liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172783.RAcFrxnIjjnU3zn0vC93HryXuPs9Gltwy5eLjbhlJK9eA130_provenance.
- NP172787.RAQtR6y0IsPvy_VtLuXn2aJKpfSCeqAzcWSQ2_e9JGcio130_assertion description "[Alagille syndrome (ALGS), also known as arteriohepatic dysplasia, is a multisystem disorder due to defects in components of the Notch signalling pathway, most commonly due to mutation in JAG1 (ALGS type 1), but in a small proportion of cases mutation in NOTCH2 (ALGS type 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172787.RAQtR6y0IsPvy_VtLuXn2aJKpfSCeqAzcWSQ2_e9JGcio130_provenance.
- NP172790.RAc0ro12LR3iN13ZKQR4jBFeoNiOZi4I4Nj7URSWfDVhY130_assertion description "[To determine the frequency distribution of K-ras-2 point mutation genotypes in pancreatic adenocarcinoma and to evaluate the effectiveness of K-ras-2 genotyping as a means to predict localized disease and potential long-term survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172790.RAc0ro12LR3iN13ZKQR4jBFeoNiOZi4I4Nj7URSWfDVhY130_provenance.
- NP172791.RAXq_KktiOf9XMUJ8xRF7k9VR-OstxDXd2yy5cIMogFKM130_assertion description "[Izabella and her partner sought pre-implantation genetic diagnosis (PGD) because Izabella had retinoblastoma due to a deletion in chromosome 13 and they want to have children not at genetic risk of retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172791.RAXq_KktiOf9XMUJ8xRF7k9VR-OstxDXd2yy5cIMogFKM130_provenance.
- NP172802.RAYEaGdfPdj6u8ntNoRPo52UrF3HA_UuRGOvuiQWhYPLk130_assertion description "[Plasma OPN levels appeared to correlate with tumor hypoxia in HNSCC patients and may serve as noninvasive tests to identify patients at high risk for tumor recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172802.RAYEaGdfPdj6u8ntNoRPo52UrF3HA_UuRGOvuiQWhYPLk130_provenance.
- NP172808.RAf2w9A7_N8P25d_ja8nAgeGv8B8FpiIhPgjA3cspFY1k130_assertion description "[These findings expose another facet of p53 functions unrelated to tumor suppression and render it a novel regulator of hepatic lipid metabolism and consequently of systemic lipid homeostasis and atherosclerosis development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172808.RAf2w9A7_N8P25d_ja8nAgeGv8B8FpiIhPgjA3cspFY1k130_provenance.
- NP172814.RARlpfyWaTuhKtTVCL6qqSP0hV6vp9ae4i8b9WpzPCWn0130_assertion description "[Among cirrhotic patients, males with the TIMP-1 372 T allele developed cirrhosis at a younger age, and patients who were homozygous for the higher-transcription TIMP-2 -418 G allele had significantly lower serum albumin concentrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172814.RARlpfyWaTuhKtTVCL6qqSP0hV6vp9ae4i8b9WpzPCWn0130_provenance.
- NP172815.RAaP9I1zxfqiTFoik2Pc3jmOnkXIp10nXTIhlrr8aS9Jc130_assertion description "[We examined the expression of tumor-suppressor protein p53 in a variety of laryngeal carcinomas from 43 patients (25 primary, 13 metastatic and 5 recurrent cases), 13 normal laryngeal tissues and 7 benign laryngeal nodule biopsy specimens, using the polyclonal antibody CM-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172815.RAaP9I1zxfqiTFoik2Pc3jmOnkXIp10nXTIhlrr8aS9Jc130_provenance.
- NP172819.RARON5JXqibhqtvQKjlpmiXW4pny_x7OzOGTc7LtLPGvo130_assertion description "[Investigation into thiol conjugation of transthyretin in hereditary transthyretin amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172819.RARON5JXqibhqtvQKjlpmiXW4pny_x7OzOGTc7LtLPGvo130_provenance.
- NP172821.RAW3UIhjLu4wRqzP5uQgzPNPxW6oVsZ31CLGXS5Y7koXA130_assertion description "[Genetic variations in TGFβ1, tPA, and ACE and radiation-induced thoracic toxicities in patients with non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172821.RAW3UIhjLu4wRqzP5uQgzPNPxW6oVsZ31CLGXS5Y7koXA130_provenance.
- NP172823.RAdeVJlkbO7IwcpC2wNd8agKDBABnr8ZcsmW5oXIABs1U130_assertion description "[Of great interest is the recent identification of novel Pi regulating genes, PHEX and FGF23, that play a role in the pathophysiology of inherited (X-linked hypophosphatemia and autosomal dominant hypophosphatemic rickets) and acquired (oncogenic hypophosphatemic rickets) disorders characterized by renal Pi wasting and associated skeletal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172823.RAdeVJlkbO7IwcpC2wNd8agKDBABnr8ZcsmW5oXIABs1U130_provenance.
- NP172824.RARiYdrLqbuW_GSYhXeUzGsuHG8DFjeQ0pU54Y7wvsimQ130_assertion description "[The present study evaluates evidence for linkage of schizophrenia to chromosome 6p24-p22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172824.RARiYdrLqbuW_GSYhXeUzGsuHG8DFjeQ0pU54Y7wvsimQ130_provenance.
- NP172829.RAeCPYTz_bdOhWSjxwyddi5Dg7GHBPrirX64crqGr_6v4130_assertion description "[The results also point to LEDGF/p75 as a potential contributor to cellular resistance to docetaxel-induced lysosomal destabilization and cell death, and an attractive candidate for molecular targeting in HRPC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172829.RAeCPYTz_bdOhWSjxwyddi5Dg7GHBPrirX64crqGr_6v4130_provenance.
- NP172831.RAR1dUNEUkC9_ohynuhW_HEtB4an_O86jCFnIIqbGQwW4130_assertion description "[These findings suggest that neither of these two polymorphisms is associated with suicide victims and it is unlikely that the 5-HT1A receptor gene is implicated in the susceptibility to suicide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172831.RAR1dUNEUkC9_ohynuhW_HEtB4an_O86jCFnIIqbGQwW4130_provenance.
- NP172833.RAfvn6YvwPQrfg_z_utlhdvX-p6Y08aUuBLUHXdibmb7g130_assertion description "[These include prevalent conditions such as Parkinson's disease (PD), dementia with Lewy bodies (DLB), and the Lewy body variant of Alzheimer's disease (LBVAD), as well as rarer conditions including multiple systems atrophy (MSA), and neurodegeneration with brain iron accumulation type-1 (NBIA-1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172833.RAfvn6YvwPQrfg_z_utlhdvX-p6Y08aUuBLUHXdibmb7g130_provenance.
- NP172838.RAa6WEuBTDvZoN7tZZTGLc8zgRYg0mot3NqcJhW0GRMUs130_assertion description "[We have used the comparative genomic hybridization (CGH) technique on 34 malignant mesotheliomas and 30 primary lung carcinomas (adenocarcinoma, including bronchoalveolar carcinoma and large-cell anaplastic carcinoma) to compare their copy number changes and to evaluate the use of CGH to distinguish between these two types of tumour.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172838.RAa6WEuBTDvZoN7tZZTGLc8zgRYg0mot3NqcJhW0GRMUs130_provenance.
- NP172850.RAfa5T_9R1opLFWOL19nlzD7Y0OhvBgzBSdxUj8HVrR7Q130_assertion description "[Using denaturing high-performance liquid chromatography and DNA sequencing, mutational analysis of 23 RyR2 exons previously implicated in CPVT1, comprehensive analysis of all translated exons in CASQ2 (CPVT2), KCNQ1 (LQT1), KCNH2 (LQT2), SCN5A (LQT3), KCNE1 (LQT5), KCNE2 (LQT6), and KCNJ2 (Andersen-Tawil syndrome [ATS1], also annotated LQT7), and analysis of 10 ANK2 exons implicated in LQT4 were performed on genomic DNA from 11 unrelated patients (8 females) referred to Mayo Clinic's Sudden Death Genomics Laboratory explicitly for CPVT genetic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172850.RAfa5T_9R1opLFWOL19nlzD7Y0OhvBgzBSdxUj8HVrR7Q130_provenance.
- NP172854.RAQMQOa4uZRil_hxn2Q9tGY1bHO-piAMItub2w5hDvURE130_assertion description "[These results indicate that the hsFRP gene probably functions as a tumor suppressor in normal cervical epithelium and down-regulation of hsFRP contributes to development of cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172854.RAQMQOa4uZRil_hxn2Q9tGY1bHO-piAMItub2w5hDvURE130_provenance.
- NP172859.RAV7Ma8S8J4iHA01V8kF6rzArdOw09L4e4FEwZFY8ockU130_assertion description "[Recent studies have established that two core members of the SWI/SNF chromatin remodeling complex, BRG1 and SNF5/INI1, possess tumor-suppressor activity in human and mouse cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172859.RAV7Ma8S8J4iHA01V8kF6rzArdOw09L4e4FEwZFY8ockU130_provenance.
- NP172866.RATy26WvlWHD7dBdB7aQEIeaTshpR2VBWKw6tYdjElNcY130_assertion description "[To determine the role of TFPI in the development of atherosclerosis, we bred mice which overexpress TFPI into the apolipoprotein E-deficient (apoE(-/-)) background.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172866.RATy26WvlWHD7dBdB7aQEIeaTshpR2VBWKw6tYdjElNcY130_provenance.
- NP172874.RAbZPQLsMJICgkTbbyz63ow86PgptuJKl-pNtXZsgrX6U130_assertion description "[We tested the hypothesis that exonic and/or promoter single nucleotide polymorphisms (SNPs) in the human 12/15-LOX gene (ALOX15) alter the risk of symptomatic coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172874.RAbZPQLsMJICgkTbbyz63ow86PgptuJKl-pNtXZsgrX6U130_provenance.
- NP172876.RAZIAPjBXtaWh7ujgotiD94CUQWr3RcvsOFNPCwwmytAM130_assertion description "[No cases of complete GH insensitivity syndrome (Laron syndrome) were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172876.RAZIAPjBXtaWh7ujgotiD94CUQWr3RcvsOFNPCwwmytAM130_provenance.
- NP172877.RAUWj9L9QntJKVlwsl9LIl-yh6fQW3vJSr5-Xq1fUeDjU130_assertion description "[In a case-control study, the authors compared the rates of 39 common cystic fibrosis-associated CFTR mutations between 949 white patients with pancreatic adenocarcinoma and 13,340 white controls from a clinical laboratory database for prenatal testing for CFTR mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172877.RAUWj9L9QntJKVlwsl9LIl-yh6fQW3vJSr5-Xq1fUeDjU130_provenance.
- NP172880.RAeM6PnWmGFzoLzNW8tamCWKRW8xCYrCDNrfwquYRV9vw130_assertion description "[Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172880.RAeM6PnWmGFzoLzNW8tamCWKRW8xCYrCDNrfwquYRV9vw130_provenance.
- NP172885.RAb1RiYt2h6cLHsI8nqaVHFY7bKbLD-byRk1dZLrz5ll0130_assertion description "[Expression of miR-126, miR-21, miR-375 and the potential targets NF-κB inhibitor alpha (IκBα, IKBA or NFKBIA), Polo-like kinase 2 (PLK2) and v-Crk sarcoma virus CT10 oncogene homolog (CRK) were assessed in 52 colonic biopsies from patients with active UC, inactive UC, irritable bowel syndrome (IBS) and from healthy subjects by quantitative RT-PCR and immunofluorescence analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172885.RAb1RiYt2h6cLHsI8nqaVHFY7bKbLD-byRk1dZLrz5ll0130_provenance.
- NP172887.RAaWz9fpZLL1w_RHrbr5YX0tux0vRI0Fuzs7qzHVsvieo130_assertion description "[RP3 appears to be the most centromeric of several positioned loci, including chronic granulomatous disease (CGD), McLeod phenotype (XK), and Duchenne muscular dystrophy (DMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172887.RAaWz9fpZLL1w_RHrbr5YX0tux0vRI0Fuzs7qzHVsvieo130_provenance.
- NP172890.RAYR4XRerDolnIlA8IcDUcesl2JcF5zyIvOLN5ZMhTw8A130_assertion description "[The diagnosis of MDS (n = 50) was based on the FAB criteria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172890.RAYR4XRerDolnIlA8IcDUcesl2JcF5zyIvOLN5ZMhTw8A130_provenance.
- NP172894.RAby818QnopsKt2WAT4MKRryAFx51TNQBK3-qldtnnGH8130_assertion description "[Detection and characterization of EWSR1/ATF1 and EWSR1/CREB1 chimeric transcripts in clear cell sarcoma (melanoma of soft parts).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172894.RAby818QnopsKt2WAT4MKRryAFx51TNQBK3-qldtnnGH8130_provenance.
- NP172896.RAfFcvQCONgnmy9OIyTWZTfsq0crLpge-rgUF_bpIR5oo130_assertion description "[Although low expression was present in testicular parenchyma with spermatogenesis, XIST was expressed at a higher level in parenchyma with carcinoma in situ, the precursor lesion of seminomas and nonseminomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172896.RAfFcvQCONgnmy9OIyTWZTfsq0crLpge-rgUF_bpIR5oo130_provenance.
- NP172898.RAY1gBR5st5_o87Sd8viKf64clG0Iv8FWdp-E5v7Y-SO4130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an autosomal, dominantly inherited neurodegenerative disease caused by an unstable CAG trinucleotide repeat expansion in the ataxin-1 gene located on chromosome 6p22-p23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172898.RAY1gBR5st5_o87Sd8viKf64clG0Iv8FWdp-E5v7Y-SO4130_provenance.
- NP172901.RAXy3oebUOkBJ3xGEdvoAvJX5ClrxOaHvefNB5z-x8jAM130_assertion description "[To further compare expression of HP-fVIII from an SIV-based lentiviral system, we constructed expression vectors containing the high expression transgene and a human elongation factor-1 alpha, cytomegalovirus (CMV) or phosphoglycerate kinase promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172901.RAXy3oebUOkBJ3xGEdvoAvJX5ClrxOaHvefNB5z-x8jAM130_provenance.
- NP172906.RAXgSd28SQq4oL9iYaDp07ILcPvPS5e3LL2bIv-txa7vQ130_assertion description "[This latter cell population has therefore been examined for chromosomal aberrations, using the in situ hybridization (ISH) procedure, making use of DNA probes for chromosomes 1, 7, 8, 9, 11, 12, 15, 17, and 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172906.RAXgSd28SQq4oL9iYaDp07ILcPvPS5e3LL2bIv-txa7vQ130_provenance.
- NP172908.RAVL14xeJcU8imOTGlL0Sz74EX09a5mW90ls-QYnbO4dI130_assertion description "[APOE HhaI polymorphism and APOE-C1 haplotypes showed no association with gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172908.RAVL14xeJcU8imOTGlL0Sz74EX09a5mW90ls-QYnbO4dI130_provenance.
- NP172910.RAVXn9iVmMd2XaVmtdw6RJ8oJ27T5EEZLt8NWkhX4fUAM130_assertion description "[An evaluation of the RPE signature genes in a recently completed AMD genomewide association (GWA) data set revealed that TIMP3, GRAMD3, PITPNA and CHRNA3 signature genes may have potential roles in AMD pathogenesis and deserve further examination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172910.RAVXn9iVmMd2XaVmtdw6RJ8oJ27T5EEZLt8NWkhX4fUAM130_provenance.
- NP172916.RAe93XS9JmQJjdNID2Gcd6zDdKEPdgStbc1pSJz_whoC8130_assertion description "[Minisatellite polymorphisms of the SLC6A19: susceptibility in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172916.RAe93XS9JmQJjdNID2Gcd6zDdKEPdgStbc1pSJz_whoC8130_provenance.
- NP172917.RAY6GnXFp6IgtnuALYQkEMKY9l4zFe_3DttzHiQpFD53g130_assertion description "[High expression of p73 mRNA and p73 protein in colorectal cancer may be involved in the progression of colorectal cancer and p73 mRNA and p73 protein may serve as a potential index to predict differentiation level and prognosis of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172917.RAY6GnXFp6IgtnuALYQkEMKY9l4zFe_3DttzHiQpFD53g130_provenance.
- NP172920.RATIdw0AykC1YeAGGWng9gzrbrFYCkP7pSqzaH8L9Dfy8130_assertion description "[All participants had a thrombotic workup that included the following: genetic markers: factor V Leiden G1691A and G20210A prothrombin mutations, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms; protein assays: protein C, protein S and antithrombin; other tests: blood typing and screening for hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172920.RATIdw0AykC1YeAGGWng9gzrbrFYCkP7pSqzaH8L9Dfy8130_provenance.
- NP172922.RAVG7rQux6waW12sx_5IMYjzCWO5O1Uph4MuU7svj034g130_assertion description "[The importance of HLA class I-restricted CD8 T-cell responses in the control of human immunodeficiency virus (HIV) infection is generally accepted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172922.RAVG7rQux6waW12sx_5IMYjzCWO5O1Uph4MuU7svj034g130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172928.RAYhrR8pdInEF31LbEbynESLAd-FzsHOOox_P7RnMeg70130_assertion description "[Analysis of these intermediates in CD34- cells from the bone marrow of patients with DBA harboring mutations in RPS19 revealed a pre-rRNA-processing defect similar to that observed in TF-1 cells where RPS19 expression was reduced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172928.RAYhrR8pdInEF31LbEbynESLAd-FzsHOOox_P7RnMeg70130_provenance.
- NP172929.RAdr90_cdONt1brVORTX8-Meg8G63BVbtyKuIXivPPuiE130_assertion description "[It has been hypothesized that the VDR-mediated signaling antagonizing TNF-α and IL-6 receptor-activated pro-inflammatory and proliferative intracellular pathways, may prevent development of IBD and colitis-associated colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172929.RAdr90_cdONt1brVORTX8-Meg8G63BVbtyKuIXivPPuiE130_provenance.
- NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_assertion description "[This study aims to investigate the genotype frequencies of GSTM1, GSTT1 and GSTM3 genes in 80 osteosarcoma patients and 160 normal control participants, and also the influence of these polymorphisms in the clinical outcome of osteosarcoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_provenance.
- NP172935.RAQZKVloddzjBOmPFQkXK5wess20vyUIxhZyz5MqF8vpo130_assertion description "[The human PAX-5 gene is located on chromosome 9 in region p13, which is involved in t(9;14)(pl3;q32) translocations recurring in small lymphocytic lymphomas of the plasmacytoid subtype and in derived large-cell lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172935.RAQZKVloddzjBOmPFQkXK5wess20vyUIxhZyz5MqF8vpo130_provenance.
- NP172946.RAXpqW_WBsWi5Azv5OXXof1bwE5kC45y-LDI6v6t4F6OI130_assertion description "[Together, these data suggest that a strong selective growth advantage for loss of PTEN and upregulation of PI3K/AKT, combined with the close proximity of PTEN to a large unstable segment of repeated DNA comprising SD17 and SD18, can lead to recurrent microdeletions of the PTEN gene in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172946.RAXpqW_WBsWi5Azv5OXXof1bwE5kC45y-LDI6v6t4F6OI130_provenance.
- NP172948.RAWDbU-qfH0VuvSW2Ye1vs8IJq4oHdZJ3JYZ03Jx_T8cU130_assertion description "[Patients with co-existing hereditary spherocytosis (HS) and UDP-glucuronosyltransferase 1A1 (UGT1A1) deficiency as Gilbert's syndrome (GS) have been reported, and previous studies have demonstrated an increased risk for developing gallstones in patients with co-inheritance of GS and HS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172948.RAWDbU-qfH0VuvSW2Ye1vs8IJq4oHdZJ3JYZ03Jx_T8cU130_provenance.
- NP172954.RATzD0bvBQ8D_VKSiKtgYItjOknpuoovsqqcQUqqIZmzM130_assertion description "[To elucidate the effect of the most widely used industrial phthalate, n-butyl benzyl phthalate (BBP), on cancer progression, we evaluated the results of BBP treatment using a whole human genome cDNA microarray and MetaCore software and selected candidate genes whose expression was changed by more than ten-fold by BBP compared with controls to analyze the signaling pathways in human breast cancer initiating cells (R2d).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172954.RATzD0bvBQ8D_VKSiKtgYItjOknpuoovsqqcQUqqIZmzM130_provenance.
- NP172955.RAQvtN_4-Joh3_46bbsPmPafRS1npV7yEjxTzIsx7qv44130_assertion description "[Using a mouse model of MYC-driven leukemia, we showed that, in addition to the well characterized BCL2 and BCLxl (BCL2L1), the other four family members -- BCLw (BCL2L2), BCLb (BCL2L10), BFL1 (BCL2A1) and MCL1 -- also cooperate with MYC to accelerate leukemogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172955.RAQvtN_4-Joh3_46bbsPmPafRS1npV7yEjxTzIsx7qv44130_provenance.
- NP172961.RAcTXNYYW5Twl9ECR73Zin7kM44hMa6Xqw3j2B8KPFeng130_assertion description "[These studies revealed that ALDH activity of patient breast tumor CSCs and cell lines correlates best with expression of another isoform, ALDH1A3, not ALDH1A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172961.RAcTXNYYW5Twl9ECR73Zin7kM44hMa6Xqw3j2B8KPFeng130_provenance.
- NP172963.RATbucWS8SKSj0hg_-WsV1-EhWk_9f4PXnym4mHPTFxjk130_assertion description "[The aim of this study was to determine the role of the hypertension associated angiotensin II type 1 receptor (AT1R) gene A1166C polymorphism in susceptibility to nephropathy in IDDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172963.RATbucWS8SKSj0hg_-WsV1-EhWk_9f4PXnym4mHPTFxjk130_provenance.
- NP172965.RAbqe1dwzF4BbHZGES8eAlBTwVBIjUyU_wEi21t_cKM3s130_assertion description "[The current study was undertaken to determine whether 1 mechanism by which group II sPLA2 might contribute to the progression of inflammation and atherosclerosis is by increasing the formation of biologically active oxidized phospholipids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172965.RAbqe1dwzF4BbHZGES8eAlBTwVBIjUyU_wEi21t_cKM3s130_provenance.
- NP172966.RAYy2W5YCgYzxA9EV_VLM-nyrtY1tTUkD2yLSXm91HzOw130_assertion description "[These data suggest that Ad-uPAR-MMP-9 shows its antitumor activity against both established and early phases of lung cancer metastases by causing the destruction of the tumor vasculature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172966.RAYy2W5YCgYzxA9EV_VLM-nyrtY1tTUkD2yLSXm91HzOw130_provenance.
- NP172967.RAYA0XhY_fTmvkV5XnhvmmVL6fBKRnBN7SWH4dOQkrW-w130_assertion description "[Polymorphism insertion/deletion of the ACE gene and ambulatory blood pressure circadian variability in essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172967.RAYA0XhY_fTmvkV5XnhvmmVL6fBKRnBN7SWH4dOQkrW-w130_provenance.
- NP172970.RASxQx0bIFpUUz7nj35nvuSXp01sw9yua56VGsqz2MmUI130_assertion description "[The proliferation-specific transcription factor Forkhead box M1 (FoxM1) acts as a master regulator of cancer cell growth and survival and plays an important role in the development of hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172970.RASxQx0bIFpUUz7nj35nvuSXp01sw9yua56VGsqz2MmUI130_provenance.
- NP172972.RAQjkBzpDZgnMRXgFaFNRmLWYjSauK66UjxrTX6xKKI90130_assertion description "[Mutations in the presenilin genes (PS-1 and PS-2) are linked to early onset familial Alzheimer's disease (AD), but the mechanisms by which these mutations cause the cognitive impairment characteristic of AD are unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172972.RAQjkBzpDZgnMRXgFaFNRmLWYjSauK66UjxrTX6xKKI90130_provenance.
- NP172974.RAWlvIhrQENhZhIE2Sf6DPHRSQb8Cv-HfNqYfXZotmH6I130_assertion description "[CCL2 protects prostate cancer PC3 cells from autophagic death via phosphatidylinositol 3-kinase/AKT-dependent survivin up-regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172974.RAWlvIhrQENhZhIE2Sf6DPHRSQb8Cv-HfNqYfXZotmH6I130_provenance.
- NP172975.RARkruJIljzv82WP4ELX0B4XAeW7nqoEuVEmep_sXDmvY130_assertion description "[Gastrin-releasing peptide (GRP; mammalian bombesin) is present in the neuroendocrine cells of human fetal lung and in small cell lung carcinomas (SCLCs), where it may act as a growth factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172975.RARkruJIljzv82WP4ELX0B4XAeW7nqoEuVEmep_sXDmvY130_provenance.
- NP172978.RAQuds4I-FAZLFZNEn_XPhYu8urj2JYZZSmLuK0vDDq5o130_assertion description "[`APC mutation-negative` FAP is genetically heterogeneous, and a combination of MLPA and SNuPE is able to link a considerable proportion (38%) to APC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172978.RAQuds4I-FAZLFZNEn_XPhYu8urj2JYZZSmLuK0vDDq5o130_provenance.
- NP172979.RAVYLUkEI0MLksOKjb38V_8gSZpvY2Av3ZCtzAc6OPWBw130_assertion description "[GCKR and PNPLA3 act together to convey susceptibility to fatty liver in obese youths.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172979.RAVYLUkEI0MLksOKjb38V_8gSZpvY2Av3ZCtzAc6OPWBw130_provenance.
- NP172981.RAe52E35aPS0xa9z88w9sHHKjWXiKUOCaYy1oS-5Kni7M130_assertion description "[In accord with these murine findings, IL-11 is selectively expressed in eosinophils and epithelial cells in patients with moderate and severe asthma where expression correlates directly with disease severity and inversely with FEV(1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172981.RAe52E35aPS0xa9z88w9sHHKjWXiKUOCaYy1oS-5Kni7M130_provenance.
- NP172982.RAfnqwJB-BXDmlMOjiWv8K_ZU8GG9FgP9i2gkOkIUg-ug130_assertion description "[An early step in the carcinogenesis of hereditary non-polyposis colorectal cancer (HNPCC) and some sporadic colorectal cancers (CRCs) is the acquisition of a 'mutator phenotype' resulting from defects in DNA mismatch repair (MMR) genes, which normally maintain genomic stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172982.RAfnqwJB-BXDmlMOjiWv8K_ZU8GG9FgP9i2gkOkIUg-ug130_provenance.
- NP172988.RAZIEDwYBnYo_4tiLmq4WClI4zgJayLnOchZHNPUlocFc130_assertion description "[We demonstrate marked down-regulation of ST8SIA2 gene expression across human brain development and show a significant haplotype×diagnosis effect on ST8SIA2 mRNA levels in adult cortex (ANOVA: F(1,87) = 6.031, P = 0.016).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172988.RAZIEDwYBnYo_4tiLmq4WClI4zgJayLnOchZHNPUlocFc130_provenance.
- NP172999.RAe7v4_FAtyOGA7Kc-T2-rHevkcLk7aFYoxvj6lRTHyBI130_assertion description "[Lack of association between prohibitin 3' untranslated region C-->T polymorphism and breast cancer in a Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172999.RAe7v4_FAtyOGA7Kc-T2-rHevkcLk7aFYoxvj6lRTHyBI130_provenance.
- NP173002.RAZ_Hp1HOJKFNKIjGFHzdhG2N6yD9ubyWlH0GXgFwYYg8130_assertion description "[In situ expression of connective tissue growth factor in human crescentic glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173002.RAZ_Hp1HOJKFNKIjGFHzdhG2N6yD9ubyWlH0GXgFwYYg8130_provenance.
- NP173003.RAYI6E2HHPZjKR6Z_bxVPvjHUR--82oSX0nCAuVLWMq-c130_assertion description "[In association with the onset and first 11 months of ANLL, the platelet count increased 10-fold to a peak of 750 x 10(9)/L, providing further evidence that the t(1;3)(p36;q21) translocation causes stimulation of thrombopoiesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173003.RAYI6E2HHPZjKR6Z_bxVPvjHUR--82oSX0nCAuVLWMq-c130_provenance.
- NP173004.RAWMeKyClh1Lu8xjBr5JqA8nkEvYoCR7DOsEDTl8EfNbo130_assertion description "[Expression of FABP7 was assessed during melanoma progression through assessment of various clinicopathology stages of primary tumor progression and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173004.RAWMeKyClh1Lu8xjBr5JqA8nkEvYoCR7DOsEDTl8EfNbo130_provenance.
- NP173005.RAfVBZ9xCtBG_yIzU2l-5DjzajKcHlm3DMs9n7HtGdk80130_assertion description "[We report on the second M-D family in which several clinically affected epsilon-sarcoglycan gene (SGCE) mutation carriers have seizures in addition to myoclonus and dystonia, adding to the evidence that epilepsy and EEG abnormalities may form part of the phenotypic spectrum of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173005.RAfVBZ9xCtBG_yIzU2l-5DjzajKcHlm3DMs9n7HtGdk80130_provenance.
- NP173013.RAfgsyOFpdDQquUlUhKsyvGv_afd-hb5AdcSQ5ODPDGL0130_assertion description "[Quantification of membrane and membrane-bound proteins in normal and malignant breast cancer cells isolated from the same patient with primary breast carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173013.RAfgsyOFpdDQquUlUhKsyvGv_afd-hb5AdcSQ5ODPDGL0130_provenance.
- NP173015.RAUc9f4rdPsCQYcNA-jSsPuoFJ1R-gGXU5WSREMPG6eZA130_assertion description "[Logistic regression analysis showed GSTT1 null and CYP2D6 poor metabolizer were risk factors in astrocytoma (odds ratio = 2.67 P = 0.0005 and odds ratio = 4.17 P = 0.0043, respectively) and meningioma (odds ratio = 4.52, P = 0.0001 and odds ratio = 4.90, P = 0.0132, respectively) when corrected for the other variables.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173015.RAUc9f4rdPsCQYcNA-jSsPuoFJ1R-gGXU5WSREMPG6eZA130_provenance.
- NP173019.RAVm7KstyKlnCK_Rl-iY_cTpf0EiG4q-tQrQE52XGJI9M130_assertion description "[The cell adhesion molecules CD44v6 and integrin-β1 are associated with the progression and metastasis of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173019.RAVm7KstyKlnCK_Rl-iY_cTpf0EiG4q-tQrQE52XGJI9M130_provenance.
- NP173022.RAU3xe73BxPeXSUs96L9L-o4dFUhCnnbStCEdNFIRTZtQ130_assertion description "[It has been revealed that GSTM1 null genotype or NAT2 slow acetylator genotype may be associated with a small increase in urothelial cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173022.RAU3xe73BxPeXSUs96L9L-o4dFUhCnnbStCEdNFIRTZtQ130_provenance.
- NP173024.RAamFETQvDq6VOz34OZ1Umc8OMRiTYThm-n48jc3ZxvWU130_assertion description "[In an ischemia/reperfusion model CTGF-TG hearts did not differ from controls.Our data suggest that CTGF itself does not induce cardiac fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173024.RAamFETQvDq6VOz34OZ1Umc8OMRiTYThm-n48jc3ZxvWU130_provenance.
- NP173025.RAYHd33OtcnQ01YQ7JCCWtULnuIGu_CPBUFjESvIVWwp4130_assertion description "[Patients with diverse cancers referred to the Clinical Center for Targeted Therapy were analyzed for PIK3CA and, if possible, KRAS mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173025.RAYHd33OtcnQ01YQ7JCCWtULnuIGu_CPBUFjESvIVWwp4130_provenance.
- NP173026.RAVxYyig_14wld6aSaVkZwULZvMslDjJ-5rX8aUveH2Ds130_assertion description "[These results demonstrated that PEDF could inhibit diabetes- or AGE-induced RAGE gene expression by blocking the superoxide-mediated NF-kappaB activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173026.RAVxYyig_14wld6aSaVkZwULZvMslDjJ-5rX8aUveH2Ds130_provenance.
- NP173029.RAVE2i0hH1KYIAHuUJJMJ2Ms6NVPW9QvDZDJnzqprmI1s130_assertion description "[Allele and genotype frequencies of single nucleotide polymorphisms for the following AMD-associated alleles were evaluated: risk alleles in complement factor H (CFH) gene (Y402H and IVS14) and LOC387715/HTRA1 gene on 10q26 (A69S) and protective alleles in CFH (IVS1, IVS6, and delCFHR1-3) and complement factor B loci (H9L and R32Q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173029.RAVE2i0hH1KYIAHuUJJMJ2Ms6NVPW9QvDZDJnzqprmI1s130_provenance.
- NP173031.RAX5VnhyiONYtbFBXu15rBgGv_RxocdRn9H3BqicZ4i1Q130_assertion description "[Putative apolipoprotein receptor gene (LRP, A2MR) is not rearranged in either myxoid liposarcoma or lipomas with translocations in 12q13-14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173031.RAX5VnhyiONYtbFBXu15rBgGv_RxocdRn9H3BqicZ4i1Q130_provenance.
- NP173042.RAZiJ0gYcCDs_yxyvlOXvct3x5vAhPwmoqlx6IPxausz0130_assertion description "[Patients with X-linked lymphoproliferative syndrome (XLP) experience excessive T cell proliferation after primary Epstein-Barr virus (EBV) infection, due to mutations in the signalling lymphocyte activation molecule (SLAM) associated protein (SAP) molecule.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173042.RAZiJ0gYcCDs_yxyvlOXvct3x5vAhPwmoqlx6IPxausz0130_provenance.
- NP173043.RARkbRaLQ04HOZNuvecXK-VIsJTd4_xoC9w4-pdWxJV40130_assertion description "[Interestingly, in samples obtained from seven patients at diagnosis, during induction chemotherapy, or relapse, the level of TEL-AML1 in peripheral blood (PB) and bone marrow (BM) was found to differ only by threefold, suggesting that MRD may be evaluated in PB samples in most patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173043.RARkbRaLQ04HOZNuvecXK-VIsJTd4_xoC9w4-pdWxJV40130_provenance.
- NP173048.RAcwphy8Ir44XdXmL_dL0kQM-SZrEwEF--b2MasmAKF_M130_assertion description "[Myeloma-osteoclast interactions stimulated the production of TRAP, cathepsin K, matrix metalloproteinase (MMP)-1, -9, and urokinase plasminogen activator (uPA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173048.RAcwphy8Ir44XdXmL_dL0kQM-SZrEwEF--b2MasmAKF_M130_provenance.
- NP173051.RAZzsXpbd5KyoQuYMvJDKk8Paxbzxni2WZqDDwg8_flDg130_assertion description "[The association of the C8orf13-BLK region with SLE was replicated in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173051.RAZzsXpbd5KyoQuYMvJDKk8Paxbzxni2WZqDDwg8_flDg130_provenance.
- NP173054.RAWrmMbWfyNbKmxt21O1DJxWhi9l5SALcJ0vJrkOFp-OE130_assertion description "[GHRH supplementation by delivery of human GHRH from a muscle-specific GHRH expression plasmid did not increase tumor progression in tumor-bearing nude mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173054.RAWrmMbWfyNbKmxt21O1DJxWhi9l5SALcJ0vJrkOFp-OE130_provenance.
- NP173058.RAX7uomVoTfvsrm3Kep-WrDFsIzX8NsHt75PZHKofZ5vw130_assertion description "[We also found a correlation between both DKK1 and RANKL or COOH-terminal telopeptides of type I collagen (CTX) serum levels in 21-OHD patients on cGC treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173058.RAX7uomVoTfvsrm3Kep-WrDFsIzX8NsHt75PZHKofZ5vw130_provenance.
- NP173064.RAVBMxKvjvQKHNdcHNwc0WzRp1LxxTNnGGg1yHr4S5vyg130_assertion description "[This finding was in keeping with their low-renin hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173064.RAVBMxKvjvQKHNdcHNwc0WzRp1LxxTNnGGg1yHr4S5vyg130_provenance.
- NP173066.RAY4xsFyrEEvF1du27wwIhvoxNG_NcF3gsYIJfypFAASg130_assertion description "[Primary immunodeficiency diseases (PID) are a heterogeneous group of inherited disorders of the immune system, predisposing individuals to recurrent infections, allergy, autoimmunity, and malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173066.RAY4xsFyrEEvF1du27wwIhvoxNG_NcF3gsYIJfypFAASg130_provenance.
- NP173067.RAVErhXrP6khyt2DrGGjGqb9W-zJ2vMaDWcBTJJY3baKc130_assertion description "[Non-alcoholic fatty liver disease (NAFLD) is one of the most frequent causes of abnormal liver function and correlates with central adiposity, obesity, insulin resistance, the metabolic syndrome and type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173067.RAVErhXrP6khyt2DrGGjGqb9W-zJ2vMaDWcBTJJY3baKc130_provenance.
- NP173068.RAY_uFjSCysvzro_kPVrqqhnSNK2mNGqaQeNnR5_jVYF8130_assertion description "[Phenotype analysis of NuMA-RARalpha+ mice demonstrated that these mice developed a myeloproliferative disease-like myeloid leukemia within 4 months of birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173068.RAY_uFjSCysvzro_kPVrqqhnSNK2mNGqaQeNnR5_jVYF8130_provenance.
- NP173069.RATUtkYI5w3ucNBmMA69QC-TJGk-xtkC3dKDaS6jHEdvg130_assertion description "[Secretory type II phospholipase A2 (PLA2G2A) expression status in colorectal carcinoma derived cell lines and in normal colonic mucosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173069.RATUtkYI5w3ucNBmMA69QC-TJGk-xtkC3dKDaS6jHEdvg130_provenance.
- NP173071.RAVxHWvqLwFGQalobxgbOuTZ1hO-rbM5mv7oSROtN0nZw130_assertion description "[We generated periostin(-/-) mice and found no morphologically abnormal cardiomyocyte phenotypes; however, after AMI, cardiac healing was impaired in these mice, resulting in cardiac rupture as a consequence of reduced myocardial stiffness caused by a reduced number of alpha smooth muscle actin-positive cells, impaired collagen fibril formation, and decreased phosphorylation of FAK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173071.RAVxHWvqLwFGQalobxgbOuTZ1hO-rbM5mv7oSROtN0nZw130_provenance.
- NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_assertion description "[More importantly, the CD133 gene signature identifies an aggressive subtype of GBM seen in younger patients with shorter survival who bear excessive genomic mutations as surveyed through the Cancer Genome Atlas Network GBM mutation spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_provenance.
- NP173075.RAfNGmPpAxUO92whAxref6Zi-Oh2xS2gOgmP9gjzoyYzE130_assertion description "[Serum cortisol and sex hormone binding globulin (SHBG) levels, body fat distribution and the role of genetic factors in obese females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173075.RAfNGmPpAxUO92whAxref6Zi-Oh2xS2gOgmP9gjzoyYzE130_provenance.
- NP173079.RAZsWlUueuwNQBmUBz-3jGePPsaQIsBHhFgbnjiVnLkj8130_assertion description "[Extensive overlap of the phenotypes of the sisters and 15 other patients with either syndrome and PCS confirms that these are either allelic conditions or the same disease--designated Roberts-SC phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173079.RAZsWlUueuwNQBmUBz-3jGePPsaQIsBHhFgbnjiVnLkj8130_provenance.
- NP173081.RAXq6yIS3XekSHej2XtIuAWqaKzIv83_Tl04G2r3NA4yk130_assertion description "[The prognostic value of the FAB classification, bone marrow histology, Bournemouth score, and chromosome findings was studied in 88 patients with primary myelodysplastic syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173081.RAXq6yIS3XekSHej2XtIuAWqaKzIv83_Tl04G2r3NA4yk130_provenance.
- NP173082.RARFGJk54jW_hUuSjMCxogVPU3_jp4c36OGmDd6Avt3n4130_assertion description "[Statistically significant differences were found between APL and NPM-mutated AML in CD33, CD13, CD2 and CD110 reactivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173082.RARFGJk54jW_hUuSjMCxogVPU3_jp4c36OGmDd6Avt3n4130_provenance.
- NP173084.RAceGDYwsSp8XsRieJGOZF-_sljce3FVBnVq0ENErCD6k130_assertion description "[(1) MicroRNA expression was investigated in normal (NL), chronic HBV hepatitis (CH), HBV-positive cirrhotic (CL), HBV-positive HCC and corresponding normal para-tumorous livers (NT) and hepatoma cells was evaluated with microRNA microarray and verified by real-time PCR, and microRNA-602 was selected for further study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173084.RAceGDYwsSp8XsRieJGOZF-_sljce3FVBnVq0ENErCD6k130_provenance.
- NP173086.RAcz3JX0tgazg3QMQjg4GEgRyn2KcK8W1OrApY6JpxMts130_assertion description "[Paraplegin mutations are a frequent cause of sporadic spastic paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173086.RAcz3JX0tgazg3QMQjg4GEgRyn2KcK8W1OrApY6JpxMts130_provenance.
- NP173089.RAbaauX2jbgviZ90aZXh_sQaCRsH6lwt2975E0ANdl3DE130_assertion description "[Association analysis revealed that plasma hTERT DNA levels were closely related to tumor size, portal vein cancer embolus and TNM stage (P=0.013, P=0.010, and P=0.029, respectively), but were not associated with lymph node metastasis, hepatitis B surface antigen, or α-fetoprotein (AFP) (all P > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173089.RAbaauX2jbgviZ90aZXh_sQaCRsH6lwt2975E0ANdl3DE130_provenance.