Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP37562.RARNqbcj1VkLCyAbRdwPzqRe_H6DLLrsHoF4J61pjPS80130_assertion description "[Hyperglycemia in streptozotocin-induced diabetic rat increases infarct size associated with low levels of myocardial HO-1 during ischemia/reperfusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37562.RARNqbcj1VkLCyAbRdwPzqRe_H6DLLrsHoF4J61pjPS80130_provenance.
- NP37563.RAU_WfuByr1xUYgDxYaKojY3ArYGPzZcbJITNQCd0okns130_assertion description "[Expression of heme oxygenase-1 protein and messenger RNA in permanent cerebral ischemia in rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37563.RAU_WfuByr1xUYgDxYaKojY3ArYGPzZcbJITNQCd0okns130_provenance.
- NP37568.RAdTN_8UwRf1-ZtKoZVEfa3BSYXgkljKpEhnAXiDBZE8A130_assertion description "[The serpin protease-nexin 1 is present in rat aortic smooth muscle cells and is upregulated in L-NAME hypertensive rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37568.RAdTN_8UwRf1-ZtKoZVEfa3BSYXgkljKpEhnAXiDBZE8A130_provenance.
- NP37574.RAXC5cn7I9jrs-07cT3Bcry1MwlMvU3nPMH4NAGzE65Us130_assertion description "[Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37574.RAXC5cn7I9jrs-07cT3Bcry1MwlMvU3nPMH4NAGzE65Us130_provenance.
- NP37581.RAWQsf_nUvdHxjBz6CmqnJE2iDWmdc1cLChmK0LvkE3I0130_assertion description "[The expression of somatostatin receptors in the hippocampus of pilocarpine-induced rat epilepsy model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37581.RAWQsf_nUvdHxjBz6CmqnJE2iDWmdc1cLChmK0LvkE3I0130_provenance.
- NP37585.RAR7DZMe-3hMTr0omkRRmV3PaBX2A3RILzok3-20xWYUw130_assertion description "[Blockage of JAK/STAT signalling attenuates renal ischaemia-reperfusion injury in rat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37585.RAR7DZMe-3hMTr0omkRRmV3PaBX2A3RILzok3-20xWYUw130_provenance.
- NP37588.RAcyVnMUOWuYQQpMz4hQMM7EGwmoJ00927NOQeWQNd_KQ130_assertion description "[Proliferation and apoptosis in PhIP-induced rat mammary gland carcinomas with elevated phosphotyrosine-STAT5a.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37588.RAcyVnMUOWuYQQpMz4hQMM7EGwmoJ00927NOQeWQNd_KQ130_provenance.
- NP37589.RAU5KFUwU3bMHmBC7UQHtrqyWD5heNV4hzID9MY3K6kbw130_assertion description "[Possible role of Stat5a in rat mammary gland carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37589.RAU5KFUwU3bMHmBC7UQHtrqyWD5heNV4hzID9MY3K6kbw130_provenance.
- NP37591.RAdlospmhTJQdt04gVFj6cO-tbTUg2oz-CPWUy_ohuQC0130_assertion description "[Increased estrogen sulfation of estradiol 17beta-D-glucuronide in metastatic tumor rat livers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37591.RAdlospmhTJQdt04gVFj6cO-tbTUg2oz-CPWUy_ohuQC0130_provenance.
- NP37600.RAUdN4wGXRfg_3r4QmuLeq9NlVMe7M2Qo_gMk4vszGagw130_assertion description "[Role of retinoid-X receptor-alpha in the suppression of rat bile acid coenzyme A-amino acid N-acyltransferase in liver during sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37600.RAUdN4wGXRfg_3r4QmuLeq9NlVMe7M2Qo_gMk4vszGagw130_provenance.
- NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_assertion description "[Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47931.RAfCc_yNMQPlyNh11mmfZvmhlk9RaKiPdPgAghdBTuIzA130_provenance.
- NP47932.RAYueNIWkBoKhMipK02VYeDPjfb6HtmGWZ8F2LxnYRq2E130_assertion description "[Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47932.RAYueNIWkBoKhMipK02VYeDPjfb6HtmGWZ8F2LxnYRq2E130_provenance.
- NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_assertion description "[To evaluate the contribution of SCA alleles to idiopathic RLS we investigated the CAG repeat length at the SCA1, SCA2, SCA3, SCA6, SCA7, and SCA17 loci in 215 patients who fulfilled the clinical criteria of RLS and presented periodic leg movements in sleep (PLMS) in polysomnographic recording.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_provenance.
- NP47940.RARaoyP5rGe6s92XIC_yQHMGIbda1pL9f-ERR8miZKn0Q130_assertion description "[This study appears to be the first report describing the PD phenotype in association with an expanded allele in the TATA-binding protein gene and suggests that SCA8 may also be a cause of typical PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47940.RARaoyP5rGe6s92XIC_yQHMGIbda1pL9f-ERR8miZKn0Q130_provenance.
- NP47943.RAXq2NuK__wcWIbGoSiOEyjatg3ja7UqJy41OrUPp04O8130_assertion description "[Thus, mutations of SCA2 or SCA3 did not play a major role in familial or early-onset PD in our study cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47943.RAXq2NuK__wcWIbGoSiOEyjatg3ja7UqJy41OrUPp04O8130_provenance.
- NP47945.RAQ4Ixe92k2-ciwbJQ8QztO0vPGQ05YClBkxpRYZ9VL0M130_assertion description "[Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47945.RAQ4Ixe92k2-ciwbJQ8QztO0vPGQ05YClBkxpRYZ9VL0M130_provenance.
- NP47948.RAbJsp03Ya6Lff0D1iB57bwK0juGCvH9hjap_zY2ZYx5E130_assertion description "[These intragenic polymorphisms can be useful for (1) the study of the origin of the MJD mutation(s), (2) the study of recombination events, (3) distinction of chromosomes with alleles of identical (CAG)n size in genetic tests (homoallelism), (4) the study of genetic modifiers in the region flanking the MJD1 gene, and (5) association studies in other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47948.RAbJsp03Ya6Lff0D1iB57bwK0juGCvH9hjap_zY2ZYx5E130_provenance.
- NP47950.RAZVkUWkajAl3TUx3pLXXdluw6ZZ2FQOrVb8hvXeUo5QY130_assertion description "[The CAG trinucleotide polymorphism of the MJD1 gene was analyzed by recombinant DNA technology and DNA sequencing in 35 spinocerebellar ataxia 3/Machado-Joseph disease (SCA3/MJD) patients from Mainland China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47950.RAZVkUWkajAl3TUx3pLXXdluw6ZZ2FQOrVb8hvXeUo5QY130_provenance.
- NP47955.RAYtbzfXZ719X_Mb52ty4Bbi2fNfqybLRzMikoR8rq94E130_assertion description "[The data presented here provide further support for the association between schizophrenia and CAG repeat number polymorphism in SCA1 gene. The significant increase of the mean number of CAG repeats in schizophrenics was found also in the MJD1/SCA3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47955.RAYtbzfXZ719X_Mb52ty4Bbi2fNfqybLRzMikoR8rq94E130_provenance.
- NP47963.RAfw9DgGnZl_CKqekG4FTQgReXWbPYNPQ5pbg-wJBbFo8130_assertion description "[Molecular analysis of CAG repeats at five different spinocerebellar ataxia loci: correlation and alternative explanations for disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47963.RAfw9DgGnZl_CKqekG4FTQgReXWbPYNPQ5pbg-wJBbFo8130_provenance.
- NP47972.RAem1QtOxuJE7PEgEJ6I6Z1BSV7IT34y1nt7vuKMXXLhk130_assertion description "[Development of a high-resolution melting method for the screening of Wilson disease-related ATP7B gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47972.RAem1QtOxuJE7PEgEJ6I6Z1BSV7IT34y1nt7vuKMXXLhk130_provenance.
- NP47975.RAT6ENjrdfYOPiVGD6oHc88urYLHH7EGgN3oasBOaW3X8130_assertion description "[Wilson disease (WD) is an autosomal recessive inherited disorder of copper metabolism that is caused by mutations in the ATP7B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47975.RAT6ENjrdfYOPiVGD6oHc88urYLHH7EGgN3oasBOaW3X8130_provenance.
- NP47976.RAUpsIrmBN2eo4AmKFgNsBfv1Zkdx61As6jHUJL9c7FLU130_assertion description "[Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47976.RAUpsIrmBN2eo4AmKFgNsBfv1Zkdx61As6jHUJL9c7FLU130_provenance.
- NP47978.RAfH0eXWkJjZ7HDqpoEF4InQuBDuUedKvTDjUrFPYqv38130_assertion description "[Taken together, we have provided further evidence that the His1069Gln mutation is the prevalent ATP7B mutation in central-european WD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47978.RAfH0eXWkJjZ7HDqpoEF4InQuBDuUedKvTDjUrFPYqv38130_provenance.
- NP48003.RAaNyKD6zpPoiiIF_IfyYVcsmrY9zPAvIEd-JuXF3LzIU130_assertion description "[Identification of 33 polymorphisms in the adipocyte-derived leucine aminopeptidase (ALAP) gene and possible association with hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48003.RAaNyKD6zpPoiiIF_IfyYVcsmrY9zPAvIEd-JuXF3LzIU130_provenance.
- NP48005.RARyJe1m19UUHw1oyyFdKc0a1NZ3IRtxnF7AmnOR7chNc130_assertion description "[ AhRR codon 185 polymorphism was associated with susceptibility to and severity of endometriosis in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48005.RARyJe1m19UUHw1oyyFdKc0a1NZ3IRtxnF7AmnOR7chNc130_provenance.
- NP48015.RASvcEUXxAW1N6v24M8WDD7h9YT1llODaVmwJ4it8neyY130_assertion description "[Increased risk of breast cancer in women bearing a combination of large CAG and GGN repeats in the exon 1 of the androgen receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48015.RASvcEUXxAW1N6v24M8WDD7h9YT1llODaVmwJ4it8neyY130_provenance.
- NP48034.RAWgCNrnA7P76DFHnoJXr1oq2buppUSUh7Go5XTWJI3g4130_assertion description "[Investigation of hormone receptor genes in migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48034.RAWgCNrnA7P76DFHnoJXr1oq2buppUSUh7Go5XTWJI3g4130_provenance.
- NP48036.RAUFc8XV4PZ2g-2IbaR-HGF59ohDDc7xabaFzTflRtorc130_assertion description "[Association of endometriosis risk and genetic polymorphisms involving sex steroid biosynthesis and their receptors: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48036.RAUFc8XV4PZ2g-2IbaR-HGF59ohDDc7xabaFzTflRtorc130_provenance.
- NP48038.RAW-l_hWkxJ3BfB_yo4dx-ct8DMT7_YBdaAwMQ-Vx_EFI130_assertion description "[Association of repeat polymorphisms in the estrogen receptors alpha, beta, and androgen receptor genes with knee osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48038.RAW-l_hWkxJ3BfB_yo4dx-ct8DMT7_YBdaAwMQ-Vx_EFI130_provenance.
- NP48041.RAWnNt7GdSJCNWz8B2AgUdi8B2U4Y8MeqI6w35BRlj7B8130_assertion description "[To study that possibility, we have genotyped both CAG and GGN polymorphisms of the AR gene in tumor tissue genomic DNA from a series of 204 consecutive patients with EC, and analyzed the results with regard to the pathological features and clinical outcome of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48041.RAWnNt7GdSJCNWz8B2AgUdi8B2U4Y8MeqI6w35BRlj7B8130_provenance.
- NP48045.RAQXHzxV1So5TEJiUo1CrDt9w8GQ2u5Mesex9SeQv32SU130_assertion description "[Forty one male breast cancer samples were studied, including one sample from a man with spinal and bulbar muscular atrophy (SBMA), which is caused by an AR CAG repeat expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48045.RAQXHzxV1So5TEJiUo1CrDt9w8GQ2u5Mesex9SeQv32SU130_provenance.
- NP48054.RAcHUjGBk-9vdjqyY9QoZU_6VDCY9pi5znu1Y14gkjGLg130_assertion description "[An androgen receptor mutation in the direct vicinity of the proposed C-terminal alpha-helix of the ligand binding domain containing the AF-2 transcriptional activating function core is associated with complete androgen insensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48054.RAcHUjGBk-9vdjqyY9QoZU_6VDCY9pi5znu1Y14gkjGLg130_provenance.
- NP48062.RAUxFZsNZCPN0_bCj5jepld6pvovjpcVFDaRi06sn9Wm4130_assertion description "[Novel polymorphisms of the amyloid precursor protein (APP) gene in Chinese/Taiwanese patients with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48062.RAUxFZsNZCPN0_bCj5jepld6pvovjpcVFDaRi06sn9Wm4130_provenance.
- NP48063.RAR0-u9BsJVW5ORXFeSqJdnS-OiAzZgSa9MuQDw9opcJ0130_assertion description "[Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48063.RAR0-u9BsJVW5ORXFeSqJdnS-OiAzZgSa9MuQDw9opcJ0130_provenance.
- NP48064.RASkfKzafevxyf0LCn1nJUgcZpTCcdagPcZhMYE-A40fA130_assertion description "[Promoter polymorphisms which modulate APP expression may increase susceptibility to Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48064.RASkfKzafevxyf0LCn1nJUgcZpTCcdagPcZhMYE-A40fA130_provenance.
- NP48065.RAeSLvyQ6H3yNZOEUZxSHpH0WsE00tLOarngUXe1MZsnY130_assertion description "[Prevalence of pathogenic mutations in an Italian clinical series of patients with familial dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48065.RAeSLvyQ6H3yNZOEUZxSHpH0WsE00tLOarngUXe1MZsnY130_provenance.
- NP48066.RAeSCilTs8afcORV57tT1DzjAMNwZ7TWYBFRHmtT_T4PU130_assertion description "[Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48066.RAeSCilTs8afcORV57tT1DzjAMNwZ7TWYBFRHmtT_T4PU130_provenance.
- NP48074.RAbCChCwo9MzxtChsLSBwFC0yglkAsPTPuS3HAw_6AJhM130_assertion description "[ Our results suggest that the G341A (Ser88Asn) polymorphism might be associated with increased risk of PICH in a Chinese population. The association appeared to be mediated by the generation of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48074.RAbCChCwo9MzxtChsLSBwFC0yglkAsPTPuS3HAw_6AJhM130_provenance.
- NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_assertion description "[ The prevalence of mutations in the fifth domain of beta2GPI in these patients with SLE and/or APS were similar to those previously reported for the general population. Heterozygosity for either mutation does not influence the incidence of aPL, but in patients with SLE, the mutation at exon 8 may predispose to thrombosis as an independent factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_provenance.
- NP48081.RARDudCKhPiKJG2Z-tK4cGjilzscYHxIt1BAVMf6h_g5c130_assertion description "[Effect of apolipoprotein E polymorphism and apolipoprotein A-1 gene promoter polymorphism on lipid parameters and premature coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48081.RARDudCKhPiKJG2Z-tK4cGjilzscYHxIt1BAVMf6h_g5c130_provenance.
- NP48087.RATssvdqgwcaasMyxk9sq9vlwoFwUsJh7ggDVsIxonbw4130_assertion description "[Joint effect of hypertension and APOE genotype on CSF biomarkers for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48087.RATssvdqgwcaasMyxk9sq9vlwoFwUsJh7ggDVsIxonbw4130_provenance.
- NP48097.RATH2dVKc7r5L84f5qQgXhhAdwLLxGVNZBVIZp_2nCV-w130_assertion description "[Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48097.RATH2dVKc7r5L84f5qQgXhhAdwLLxGVNZBVIZp_2nCV-w130_provenance.
- NP48098.RAWx8q4JQuAiLwdqdFnydJPzveRb-o0qeCGFvfSBH1oF4130_assertion description "[Molecular genetics of microvascular disease in diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48098.RAWx8q4JQuAiLwdqdFnydJPzveRb-o0qeCGFvfSBH1oF4130_provenance.
- NP48100.RAUHiX2ddhQoEOThCdd9nRKTgYF6wmb0X86H8yLOFqJUY130_assertion description "[Apolipoprotein E (apoE - e2, e3, e4 alleles) plays a role in the regulation of lipid metabolism, with the e4 considered to be a risk factor for coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48100.RAUHiX2ddhQoEOThCdd9nRKTgYF6wmb0X86H8yLOFqJUY130_provenance.
- NP48101.RAcTXlOJetn6GGwvmwp5nGMnDkQLUF8zmDX26MIC78H_Y130_assertion description "[Apolipoprotein E gene polymorphism effects triglycerides but not CAD risk in Caucasian women younger than 65 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48101.RAcTXlOJetn6GGwvmwp5nGMnDkQLUF8zmDX26MIC78H_Y130_provenance.
- NP48102.RAUG8I-ct9kfWas9iar4IliECSF1qWXjwGJe_4eRWceqo130_assertion description "[Multivariate logistic regression analysis, with adjustment for age, body mass index, and the prevalence of smoking and hyperuricemia, revealed that the -219G-->T polymorphism of the apolipoprotein E gene in low-risk men, the -1171/5A-->6A polymorphism of the stromelysin-1 gene in low-risk women, the 1019C-->T polymorphism of the connexin 37 gene in high-risk men, and the 3932T-->C polymorphism of the apolipoprotein E gene in high-risk women were significantly associated with CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48102.RAUG8I-ct9kfWas9iar4IliECSF1qWXjwGJe_4eRWceqo130_provenance.
- NP48108.RAcyYXeM9j_H1qKhLA_LR-ZhYXPuebzr4BE02Gf3JrMlI130_assertion description "[Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48108.RAcyYXeM9j_H1qKhLA_LR-ZhYXPuebzr4BE02Gf3JrMlI130_provenance.
- NP48111.RAa5Cx8oQn_TRO9-07BoMQz2yXdhLeVHoWHPncBhosDdY130_assertion description "[Po-husk, apart from lowering LDL-C, also reduced TG, TG related to certain gene variants, TC, Apo B-100, oxLDL, insulin-resistance and systolic BP in mild-moderate hypercholesterolaemic individuals. Thus, the target patients to receive Po-husk would be those who present a cluster of various CVD risk factors, such as metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48111.RAa5Cx8oQn_TRO9-07BoMQz2yXdhLeVHoWHPncBhosDdY130_provenance.
- NP48114.RARatJO3x8s9zTGZc11BGZVjSnlCWFVbkE9PeSMGw_mqM130_assertion description "[Pharmacogenetic study of apolipoprotein E, cholesteryl ester transfer protein and hepatic lipase genes and simvastatin therapy in Brazilian subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48114.RARatJO3x8s9zTGZc11BGZVjSnlCWFVbkE9PeSMGw_mqM130_provenance.
- NP48116.RARl-zRbKugm6quk9KC0CTbwlBkcSA4eZYKocaPazXFo4130_assertion description "[Effects of ezetimibe on lipids and lipoproteins in patients with hypercholesterolemia and different apolipoprotein E genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48116.RARl-zRbKugm6quk9KC0CTbwlBkcSA4eZYKocaPazXFo4130_provenance.
- NP48122.RATDl-xk-mp3Fa5vZEOm6X_qiHOWkl4ihEdY3sYi6YO2M130_assertion description "[The results suggest that APOE epsilon4 and heavy drinking and heavy smoking lower the age of onset for AD in an additive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48122.RATDl-xk-mp3Fa5vZEOm6X_qiHOWkl4ihEdY3sYi6YO2M130_provenance.
- NP48123.RAVxMFMk6cjt6eWRKz6MTmdnAl5fcMp39RXJVpIouK4x8130_assertion description "[Using phylogenetic analysis, we have identified a polymorphic poly-T variant, rs10524523, in the translocase of outer mitochondrial membrane 40 homolog (TOMM40) gene that provides greatly increased precision in the estimation of age of LOAD onset for APOE 3 carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48123.RAVxMFMk6cjt6eWRKz6MTmdnAl5fcMp39RXJVpIouK4x8130_provenance.
- NP48125.RAYloqUC6nfZ8C1eyUvZhAqR4Hyl27JLfSGtiIYGbPwd0130_assertion description "[Although the effect of apolipoprotein E (APOE) varepsilon4 on the brain is well-studied, less is known about the effect of family history of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48125.RAYloqUC6nfZ8C1eyUvZhAqR4Hyl27JLfSGtiIYGbPwd0130_provenance.
- NP48133.RAVohx5ruFJWN2skaIw3QD5FVl0EAIkP6hX-t6eClIHdo130_assertion description "[LPL 447X-containing genotypes (447X+) were significantly decreased in DN patients 18.6 vs 25.6%, odds ratio (OR) = 0.66, p = 0.02, as were APOE epsilon3/epsilon3 genotypes (64.8 vs 73.1%, OR = 0.68, p = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48133.RAVohx5ruFJWN2skaIw3QD5FVl0EAIkP6hX-t6eClIHdo130_provenance.
- NP48147.RAc3PxHcHqWkU6zAtJhnIhoslvC4tEbbDxJcqDNrU8qb8130_assertion description "[Stratified for apolipoprotein E genotype, the odds ratios for IHD in 9Asn (with -93G) heterozygotes and homozygotes combined vs. noncarriers were 2.6 (CI, 1.2-5.5) among epsilon32 individuals and 2.4 (CI, 1.4-4.1) among epsilon43 individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48147.RAc3PxHcHqWkU6zAtJhnIhoslvC4tEbbDxJcqDNrU8qb8130_provenance.
- NP48150.RAasvAApFi2puM_K65fwd6YQppPWS6sgtkkG1A32Hra9I130_assertion description "[To investigate the relationship between gallbladder stone disease (GSD) and single nucleotide polymorphisms of cholesterol 7alpha-hydroxylase (CYP7A) gene promoter, apolipoprotein (APO) B gene exon 26, APOE gene exon 4 or microsatellite polymorphism of low density lipoprotein receptor (LDLR) gene exon 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48150.RAasvAApFi2puM_K65fwd6YQppPWS6sgtkkG1A32Hra9I130_provenance.
- NP48152.RAUnLL0UeXqaFf5S-VgRP-Z8mMzU6VJB0V-Pt9WF8iQuQ130_assertion description "[Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48152.RAUnLL0UeXqaFf5S-VgRP-Z8mMzU6VJB0V-Pt9WF8iQuQ130_provenance.
- NP48160.RAWsqvqBdqO1pTMdNnAsCU9kOwCvdae4cG27paRk77vNc130_assertion description "[Apolipoprotein E gene polymorphism and serum lipid levels in the Guangxi Hei Yi Zhuang and Han populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48160.RAWsqvqBdqO1pTMdNnAsCU9kOwCvdae4cG27paRk77vNc130_provenance.
- NP48161.RAZh3qcYLWIE8yAE19j7EoT5KHF6No53tK1PBuXzOex1U130_assertion description "[Postprandial lipemia is modified by the presence of the APOB-516C/T polymorphism in a healthy Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48161.RAZh3qcYLWIE8yAE19j7EoT5KHF6No53tK1PBuXzOex1U130_provenance.
- NP48169.RAWo2b_xFGKqoOml6aBDpPiSbMf7JB_0QQyQMpoudEybk130_assertion description "[Apolipoprotein E gene polymorphism and colorectal cancer: gender-specific modulation of risk and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48169.RAWo2b_xFGKqoOml6aBDpPiSbMf7JB_0QQyQMpoudEybk130_provenance.
- NP48174.RAb54nc7iLTGeWxZwbj1cWJNeX9LNrdPbrOQT_ixdMDTw130_assertion description "[Apolipoprotein E (apoE) polymorphism plays a significant role in the development of atherosclerosis and cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48174.RAb54nc7iLTGeWxZwbj1cWJNeX9LNrdPbrOQT_ixdMDTw130_provenance.
- NP48178.RARnXXh9oAGjdy5dOgfVfUw6LAqj2dYyDW4O5N72uqKac130_assertion description "[Apolipoprotein E polymorphism in relation to plasma lipid levels and other risk factors of atherosclerosis in two ethnic groups from Slovakia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48178.RARnXXh9oAGjdy5dOgfVfUw6LAqj2dYyDW4O5N72uqKac130_provenance.
- NP48179.RAYYDu-JH1L8uEzuDc1DaZbq2G86QTglK2v9cuDnMolj4130_assertion description "[Relations of APOE promoter polymorphisms to LDL cholesterol and markers of subclinical atherosclerosis in young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48179.RAYYDu-JH1L8uEzuDc1DaZbq2G86QTglK2v9cuDnMolj4130_provenance.
- NP48183.RARV_y7a9ckzRgrHsFYmT6FSWPocT52b4jS_Jo-h1nNsU130_assertion description "[To examine if the genes encoding complement factor H (CFH), apolipoprotein E (APOE), and elongation of very-long-chain fatty acids-like 4 (ELOVL4) confer risk of neovascular age-related macular degeneration (AMD) in an independent or interactive manner when controlling for smoking exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48183.RARV_y7a9ckzRgrHsFYmT6FSWPocT52b4jS_Jo-h1nNsU130_provenance.
- NP48188.RAX1IfCcHYr_fPG1l6pRLp17CM4i7PFbVNDl80rS-ETmc130_assertion description "[The apolipoprotein E polymorphism in age related macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48188.RAX1IfCcHYr_fPG1l6pRLp17CM4i7PFbVNDl80rS-ETmc130_provenance.
- NP48189.RASK33dKwGdllw7pXyNIuOC9aVFjiwRqAjUJizqyWkz18130_assertion description "[Interestingly, the effect of TLR4, APOE and ABCA1 variants on AMD susceptibility was opposite to that of association with atherosclerosis risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48189.RASK33dKwGdllw7pXyNIuOC9aVFjiwRqAjUJizqyWkz18130_provenance.
- NP48190.RAUrQA1-gn_kKCZtwLMCZIZ-aEsKCmNMaIg96EBNbQQr4130_assertion description "[This study is cross-sectional, therefore it cannot determine whether abnormal gray matter volume is a state marker or trait marker of RLOD with ApoE epsilon4 allele carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48190.RAUrQA1-gn_kKCZtwLMCZIZ-aEsKCmNMaIg96EBNbQQr4130_provenance.
- NP48192.RAdiDBlP16T2yWQKU6-0QbMisuYdvqZbdMcbyrMBFfxsU130_assertion description "[Associations between AD and/or depression to gene polymorphisms APO E (epsilon4), choline acetyltransferase (ChAT) 4G to A, serotonin-transporter gene promoter-length, dopamine-D4-receptor, ciliary-neurotrophic-factor-null mutation and brain-derived neurotrophic factor (C270T) and to various known factors were analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48192.RAdiDBlP16T2yWQKU6-0QbMisuYdvqZbdMcbyrMBFfxsU130_provenance.
- NP48193.RAcI0Jo-bmmHYRrdKuDKbogxPnVg34jbh-5R8jWp0Pc74130_assertion description "[Depression is common in multiple sclerosis (MS) and the role of ApoE alleles is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48193.RAcI0Jo-bmmHYRrdKuDKbogxPnVg34jbh-5R8jWp0Pc74130_provenance.
- NP48196.RAes1L2nMpr0kSNG47URlBO15B0heqjasIIi6AnQo-9-M130_assertion description "[Major depression is an important comorbidity in Alzheimer's disease, which is definitely associated with the apolipoprotein E (apo E) polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48196.RAes1L2nMpr0kSNG47URlBO15B0heqjasIIi6AnQo-9-M130_provenance.
- NP48201.RAfFAttlj550iw4u_A9OG7u8TXoOp4uz2SihdA5TYH4E8130_assertion description "[To investigate the role of Apolipoprotein E alleles in Parkinson disease and Parkinson disease dementia, we have determined Apolipoprotein E genotypes in a group of patients with Parkinson disease (n = 95) and compared them with those of healthy control participants (n = 73).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48201.RAfFAttlj550iw4u_A9OG7u8TXoOp4uz2SihdA5TYH4E8130_provenance.
- NP48205.RAVTm8D1e4Uj82fSsIPx2vsQfaoNdxKPhYOFNj07tpAdI130_assertion description "[Previous studies investigating the association between apolipoprotein E (APOE) genotypes and Parkinson disease (PD) have yielded conflicting results, and only a few have addressed APOE as a possible determinant of PD pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48205.RAVTm8D1e4Uj82fSsIPx2vsQfaoNdxKPhYOFNj07tpAdI130_provenance.
- NP48206.RAZJmVx8phYdkjVv_d0H6vFTURTvTXdI9vqu4_gH0RF4M130_assertion description "[Assessment of apolipoprotein E genotype in Parkinson disease patients with and without dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48206.RAZJmVx8phYdkjVv_d0H6vFTURTvTXdI9vqu4_gH0RF4M130_provenance.
- NP48211.RAZn2iMJAX0u2Vl-YRt5kMJSfCrIRK-5Gk6Jgw2GxCNvE130_assertion description "[Study on apolipoprotein E gene polymorphism in Chinese type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48211.RAZn2iMJAX0u2Vl-YRt5kMJSfCrIRK-5Gk6Jgw2GxCNvE130_provenance.
- NP48212.RAYWbBqO805Lo5G2iF1ox5iULTwCtDsdV0HJWyoBeBIRI130_assertion description "[We performed apoE genotyping in 765 individuals with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48212.RAYWbBqO805Lo5G2iF1ox5iULTwCtDsdV0HJWyoBeBIRI130_provenance.
- NP48216.RAZ71KlWmUI1nW7SFsPX78Awwzw9I1XJbbCzy73rQUAko130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48216.RAZ71KlWmUI1nW7SFsPX78Awwzw9I1XJbbCzy73rQUAko130_provenance.
- NP48217.RAS0BYtVRoT6Bp8nvTHnSfZ9vpz_cAVPodWRq6BntrBgU130_assertion description "[Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48217.RAS0BYtVRoT6Bp8nvTHnSfZ9vpz_cAVPodWRq6BntrBgU130_provenance.
- NP48219.RAdJiKDT5MTPcw2CZ4wrGPTCd9xXtCubBwUnZaXYlZycA130_assertion description "[Accumulating evidence suggests that genetic factors such as apolipoprotein E (APOE), can act in different ways in the pathogenesis of cerebral amyloid angiopathy (CAA) and Alzheimer's disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48219.RAdJiKDT5MTPcw2CZ4wrGPTCd9xXtCubBwUnZaXYlZycA130_provenance.
- NP48220.RAU_CGtzngLvCYfAganrugY-5R4PalQML9iaiZ7JnDfb0130_assertion description "[We determined the relationship between capCAA and larger vessel CAA, amyloid (A) plaques, neurofibrillary changes, inflammation, and apolipoprotein E (APOE) in 22 cases of dyshoric capCAA using immunohistochemistry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48220.RAU_CGtzngLvCYfAganrugY-5R4PalQML9iaiZ7JnDfb0130_provenance.
- NP48223.RAR3jb_txDrRIIpTxGF3Tko7hM8cecjehA9FvIa5DDYpA130_assertion description "[Our data suggest that LRP8 R952Q variant may have an additive effect to APOE epsilon2/epsilon3/epsilon4 genotype in determining ApoE concentrations and risk of MI in an Italian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48223.RAR3jb_txDrRIIpTxGF3Tko7hM8cecjehA9FvIa5DDYpA130_provenance.
- NP48224.RASc2cB-UBYOl-9NtCPycR2HODUP34LJpedkzyzn-u-Ho130_assertion description "[We identified four genetic risk sets for acute myocardial infarction (AMI) from information on functional gene variants that favor inflammation or modulate cholesterol metabolism: IL6 -174 G/C, TNF -308 G/A, IL10 -1082 G/A, SERPINA3 -51 G/T, IFNG +874 T/A, HMGCR -911 C/A, and APOE epsilon2/3/4; 316 patients and 461 healthy subjects, all Italian.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48224.RASc2cB-UBYOl-9NtCPycR2HODUP34LJpedkzyzn-u-Ho130_provenance.
- NP48225.RASH0U7C3vVYRg_0QG2GxfbZ6UfPoNnytgzqz3HHc3L-4130_assertion description "[Effect of apolipoprotein E genotype and saturated fat intake on plasma lipids and myocardial infarction in the Central Valley of Costa Rica.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48225.RASH0U7C3vVYRg_0QG2GxfbZ6UfPoNnytgzqz3HHc3L-4130_provenance.
- NP48227.RAYTd_pyeET8sy4pc5YdEzFkgU2Y8-UoN4tM-_e7smLrU130_assertion description "[We compared apoE gene polymorphism in a group of patients with angiographically confirmed CAD but not MI CAD/MI (-)-group, n = 143 and a group of age and sex-matched CAD patients who had experienced a non-fatal Ml CAD/MI (+)-group, n = 124.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48227.RAYTd_pyeET8sy4pc5YdEzFkgU2Y8-UoN4tM-_e7smLrU130_provenance.
- NP48231.RAfQoGYbX5Babw1VFntde8A8GTIX6vtKgSdDje8hg9YRw130_assertion description "[Cerebral ischaemia is a potent stimulus for expression of genes that may influence recovery.We investigated whether functional polymorphisms in the apolipoprotein E (APOE), insulin-like growth factor-1 (IGF-1), tumor necrosis factor-A (TNF-A), interleukin-1A (IL-1A), interleukin-1B (IL-1B), and interleukin-6 (IL-6) genes are related with outcome after aneurysmal SAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48231.RAfQoGYbX5Babw1VFntde8A8GTIX6vtKgSdDje8hg9YRw130_provenance.
- NP48233.RAWKCvqeCVM5OQ15sH94rJenWP9GPr5eu2zxClzT6CXhc130_assertion description "[Psychosocial and neurocognitive performance after spontaneous nonaneurysmal subarachnoid hemorrhage related to the APOE-epsilon4 genotype: a prospective 5-year follow-up study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48233.RAWKCvqeCVM5OQ15sH94rJenWP9GPr5eu2zxClzT6CXhc130_provenance.
- NP48236.RAXQ8ZjClJlaYeIZTFGgMeg4QsmTmNtiLYwpQ9prurdbo130_assertion description "[Apolipoprotein E polymorphism and neuropsychological outcome following subarachnoid haemorrhage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48236.RAXQ8ZjClJlaYeIZTFGgMeg4QsmTmNtiLYwpQ9prurdbo130_provenance.
- NP48238.RARTnVYl3_Z1_x65v7QAQe3oGXNZm55EYFiIwFZ2veCWg130_assertion description "[This study suggests a role of the APOE gene in the etiology of aneurysmal SAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48238.RARTnVYl3_Z1_x65v7QAQe3oGXNZm55EYFiIwFZ2veCWg130_provenance.
- NP48240.RAXg02lcEi2AmeAH1jVPrTf1hG-bGiykYIUIaO7izHfW4130_assertion description "[The absence of a relation between apolipoprotein E genotypes and the severity of multiple sclerosis in Mexican patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48240.RAXg02lcEi2AmeAH1jVPrTf1hG-bGiykYIUIaO7izHfW4130_provenance.
- NP48244.RAQ9fPymLMwngkV8Gc51qKp1AI0pLLR0KHK5n9-ZVYhcE130_assertion description "[APOE genotypes in African American female multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48244.RAQ9fPymLMwngkV8Gc51qKp1AI0pLLR0KHK5n9-ZVYhcE130_provenance.
- NP48249.RAZPlTOzDi8ACSgvjgKX661elCc8HPAmhDMTMAF-6Rbh8130_assertion description "[Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48249.RAZPlTOzDi8ACSgvjgKX661elCc8HPAmhDMTMAF-6Rbh8130_provenance.
- NP48250.RAclreNkkqP3sc5-EDbPzWZNUnsoNunHqkNv6VTtr68LI130_assertion description "[This cross-sectional study showed a synergistic effect between the intron 4 polymorphism or T(-786)-->C polymorphism of the eNOS gene and the apoE polymorphism with respect to risk for carotid atherosclerosis in nondiabetic hemodialysis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48250.RAclreNkkqP3sc5-EDbPzWZNUnsoNunHqkNv6VTtr68LI130_provenance.
- NP48259.RAZzzusTnMOy6IMwmfDWHm-mB_4Vor6nns2YiDM_3woCk130_assertion description "[Apolipoprotein E gene polymorphism in cerebrovascular disease: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48259.RAZzzusTnMOy6IMwmfDWHm-mB_4Vor6nns2YiDM_3woCk130_provenance.
- NP48261.RAXzh16m993YNH8FISoYjOdIiHHxX72_GRSeNN7TzWylo130_assertion description "[Apolipoprotein E genotypic frequencies among Down syndrome patients imply early unsuccessful aging for ApoE4 carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48261.RAXzh16m993YNH8FISoYjOdIiHHxX72_GRSeNN7TzWylo130_provenance.
- NP48265.RAZcIKNyuCZlSqrF4vwrc1vRrQnwSmipUtQ0eAH7NVGNU130_assertion description "[Significant associations were found between carriers of the minor alleles of APOE-epsilon2, FABP2-A54T, UCP1-L229M, LPL-HindIII, LPL-S447X and LPL-T1973C, patients bearing a combination of LPL-D9N, LPL-N291S and LPL-P207L and obesity-related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48265.RAZcIKNyuCZlSqrF4vwrc1vRrQnwSmipUtQ0eAH7NVGNU130_provenance.
- NP48266.RAc_4U0Jr7R1D-kKGJOb3oA-lsvEQb9kipYFgu17j7zAc130_assertion description "[Association of cholesteryl ester transfer protein (TaqIB) and apolipoprotein E (HhaI) gene variants with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48266.RAc_4U0Jr7R1D-kKGJOb3oA-lsvEQb9kipYFgu17j7zAc130_provenance.
- NP48269.RAVLpG6Y0gs1XCKPNlj1elIRKG1LaHfm8rMOH5VK79JoQ130_assertion description "[Serum lipid and blood pressure responses to quercetin vary in overweight patients by apolipoprotein E genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48269.RAVLpG6Y0gs1XCKPNlj1elIRKG1LaHfm8rMOH5VK79JoQ130_provenance.
- NP48281.RAeO1H5iV0bjRJRNplW4KYXSzPUYHZNDOsINBBNj3UhuQ130_assertion description "[NSAID use and dementia risk in the Cardiovascular Health Study: role of APOE and NSAID type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48281.RAeO1H5iV0bjRJRNplW4KYXSzPUYHZNDOsINBBNj3UhuQ130_provenance.
- NP48282.RAYNwnO0Tc7UZDDZknP7X5bslT35gLu-FLE-vKvdCgzpY130_assertion description "[In our cohort, the APOE genotype does not constitute a risk factor for developing POAG, even in patients with normal-tension glaucoma.Clinical Relevance Apolipoprotein E polymorphisms do not appear to be contributory to POAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48282.RAYNwnO0Tc7UZDDZknP7X5bslT35gLu-FLE-vKvdCgzpY130_provenance.
- NP48284.RAbpEFYf1IGayR2cLXYCTWKRU6XnMDkocrPD03dbnTORE130_assertion description "[ APOE genotype did not influence susceptibility to Guillain-Barr??yndrome or recovery from it. This may be because our sample size of 91 was not sufficiently large to detect small differences in recovery associated with different APOE genotypes, or because cholesterol transportation is not a crucial rate limiting step in peripheral nerve regeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48284.RAbpEFYf1IGayR2cLXYCTWKRU6XnMDkocrPD03dbnTORE130_provenance.