Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP146196.RAmlZt1c7tDLgAOpzHaOraibJm781LlsO5xK1R2xHyCfk130_assertion description "[Genetic variation in leukotriene pathway members and their receptors confer an increased risk of ischemic stroke in 2 independent populations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146196.RAmlZt1c7tDLgAOpzHaOraibJm781LlsO5xK1R2xHyCfk130_provenance.
- NP146197.RApe7v7DD6VnE_uht8T9Y98SC7z_Nr0IukYYSNP0sdRIs130_assertion description "[Overall, the results of this study indicated that decreased serum PON1 activity should be considered as a risk factor for ischemic stroke in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146197.RApe7v7DD6VnE_uht8T9Y98SC7z_Nr0IukYYSNP0sdRIs130_provenance.
- NP146198.RAqL6CCrm6QXr3osz85-KtvnW6h6mtAZRWb6VVS1E4M-4130_assertion description "[C311S polymorphism of PON2 has no significant correlation with stroke in Han people of Chinese Hunan area and allele C/S is not an independent risk factor for stroke, neither is G148A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146198.RAqL6CCrm6QXr3osz85-KtvnW6h6mtAZRWb6VVS1E4M-4130_provenance.
- NP146199.RAreDpx0Z04w-D5IPKReeJ5ysi-xVpSeNynHjstzCDhns130_assertion description "[genotypes with the C allele of the PON2 gene C311S polymorphism is a risk factor for large vessel disease stroke in a Polish population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146199.RAreDpx0Z04w-D5IPKReeJ5ysi-xVpSeNynHjstzCDhns130_provenance.
- NP146210.RAnTQCx_N-9fdoFXGajeRSsYKRYE-2lKk5z4qv3PAZQM4130_assertion description "[in the Mediterranean populations the PT 20210 mutation, but not FV Leiden, is a risk factor for cryptogenic stroke in young adults ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146210.RAnTQCx_N-9fdoFXGajeRSsYKRYE-2lKk5z4qv3PAZQM4130_provenance.
- NP146211.RAiXwFWwfgBaQiNoaQG08nQfRfnhkQBcwjIVBpRZ0tNGQ130_assertion description "[Ischaemic stroke patients with heterozygous factor V Leiden present with multiple brain infarctions and widespread atherothrombotic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146211.RAiXwFWwfgBaQiNoaQG08nQfRfnhkQBcwjIVBpRZ0tNGQ130_provenance.
- NP146214.RAhSoeB3iXJSftJibYXySA3WmlXvV9A9zgNQzHAsNNxJw130_assertion description "[In this hypertensive population, the association of ACE inhibitor use with risk of nonfatal stroke varied by AGT genotype/is a protective association between ACE inhibitor use and nonfatal stroke risk among individuals with ThrThr genotype of AGT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146214.RAhSoeB3iXJSftJibYXySA3WmlXvV9A9zgNQzHAsNNxJw130_provenance.
- NP146216.RAiE9xirtIGXSCWL7Xq8-Ueeg2AInfFSU7e7ZfhdaQymU130_assertion description "[Maternal and neonatal thrombophilia, especially presence of FVL or antiphospholipid antibodies, may be important in the pathogenesis of perinatal arterial ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146216.RAiE9xirtIGXSCWL7Xq8-Ueeg2AInfFSU7e7ZfhdaQymU130_provenance.
- NP146229.RAkpvunaIM60owvOxKH2pu5eoV3EJyc-VztUmyAyiWWUA130_assertion description "[Our results suggest that IL-1Ra and TNF-alpha gene polymorphism is associated with the susceptibility to ischemic stroke in a Korean population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146229.RAkpvunaIM60owvOxKH2pu5eoV3EJyc-VztUmyAyiWWUA130_provenance.
- NP146234.RAqx6olcKJaqiZ3tCp3BYI4vaXkbVNRQnMxMCxkvFgHQk130_assertion description "[levels of soluble and platelet P-selectin are increased in acute ischemic stroke, indicating a possible role of P-selectin ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146234.RAqx6olcKJaqiZ3tCp3BYI4vaXkbVNRQnMxMCxkvFgHQk130_provenance.
- NP146236.RAoK8Ua6Jxxk52M_LD7edE3WpN-fWg0qztNvWOFLf_Fqs130_assertion description "[Carriers of the IL-1-RA appeared to have an increased risk of stroke in association with a febrile episode prior to strokes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146236.RAoK8Ua6Jxxk52M_LD7edE3WpN-fWg0qztNvWOFLf_Fqs130_provenance.
- NP146238.RAi7yuU4wIkwyEAej4WkgZKxWLM86eCILHhRjnVunp4DU130_assertion description "[Allele 2 of IL1RN, present in nearly one-quarter of stroke patients, may contribute to genetic risk for ischemic stroke and confirm the previously identified association with cerebrovascular disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146238.RAi7yuU4wIkwyEAej4WkgZKxWLM86eCILHhRjnVunp4DU130_provenance.
- NP146244.RAkMd1k6pzTpqaLBFLPw4uzpAx946cHbnCSenb8RrDFIY130_assertion description "[There is an association between ICAM-1 gene K469E polymorphism and ischemic stroke, and E allele may be a genetic risk factor of IS among Guangxi Zhuangs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146244.RAkMd1k6pzTpqaLBFLPw4uzpAx946cHbnCSenb8RrDFIY130_provenance.
- NP146246.RAuuPrtOoGfbPcNki4re8RXNHE-38plthawHf3Ek8ma-c130_assertion description "[HSP70-1+190G/C may affect susceptibility to ischemic stroke (IS) and smoking along with HSP70-1+190G/C may increase the risk of IS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146246.RAuuPrtOoGfbPcNki4re8RXNHE-38plthawHf3Ek8ma-c130_provenance.
- NP146250.RAtkLkBcSB5LWviVunErgufyD7GZm-cnvqevJ36dv4Ru0130_assertion description "[Of the 10 candidate SNPs analyzed in this pilot study, the variant allele of the nonsynonymous SNP, VCAM1 G1238C, may be associated with protection from stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146250.RAtkLkBcSB5LWviVunErgufyD7GZm-cnvqevJ36dv4Ru0130_provenance.
- NP146251.RAlNUwaVOQFwOSfKypDUwpldYgSxE3JguLU0BJ8gBoqq0130_assertion description "[2 missense polymorphisms in exon 4 (Ala140Asp & Glu155DeltaGlu) were detected/allele genotype affected CSF cholesterol, serum homocysteine.risk of vascular dementia, stroke, and early-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146251.RAlNUwaVOQFwOSfKypDUwpldYgSxE3JguLU0BJ8gBoqq0130_provenance.
- NP146255.RAkle463_71QwoC4SOZ3qzJoamWws9XcQwi1heGn0RM-M130_assertion description "[The 4G/4G polymorphism of PAI-1 is likely to be associated with ischemic stroke, although the direction of the effect is not consistent from study to study, possibly due to LD with a causative allele and/or stroke heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146255.RAkle463_71QwoC4SOZ3qzJoamWws9XcQwi1heGn0RM-M130_provenance.
- NP146256.RAqHaGAoMPP5usJsO7GJ3ikLxnQKHUVgmygJagH9glM4I130_assertion description "[the insertion/deletion (4G/5G) polymorphism of the plasminogen activator inhibitor type-1 gene affects the risk for ischemic stroke/failed to demonstrate a significant association between the 4G/5G polymorphism and ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146256.RAqHaGAoMPP5usJsO7GJ3ikLxnQKHUVgmygJagH9glM4I130_provenance.
- NP146257.RAlhwgczKBMFQqG6BWkoTVkUVGmIOYbyYUktA6ilsD5mo130_assertion description "[The levels of P-selectin, tPA antigen, and PAI-1 activity were all significantly higher in stroke patients compared with controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146257.RAlhwgczKBMFQqG6BWkoTVkUVGmIOYbyYUktA6ilsD5mo130_provenance.
- NP146262.RAomXCagkUVEI4eQXi2SPIawfSFgtNp7-P0F8DZxEp8D0130_assertion description "[In a relatively small population of elderly subjects, the association of high lipoprotein (a) and fibrinogen levels appears to carry an increased risk of pooled coronary heart disease and stroke mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146262.RAomXCagkUVEI4eQXi2SPIawfSFgtNp7-P0F8DZxEp8D0130_provenance.
- NP146263.RAmq7PZSnhvkygZXlBn5sfVP6_l3z0gyAKEfjBBbAkfp8130_assertion description "[Aspirin lowers the increased Lp (a) levels in patients with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146263.RAmq7PZSnhvkygZXlBn5sfVP6_l3z0gyAKEfjBBbAkfp8130_provenance.
- NP146266.RAlarB1hswLU8fZGam2RnNKPj5C9wpY9yaZq5V2x_foE4130_assertion description "[Regulation of NADPH oxidase by NF-kB may represent a possible mechanism whereby pro-inflammatory factors induce oxidative stress in atherosclerosis, hypertension, diabetes, stroke or heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146266.RAlarB1hswLU8fZGam2RnNKPj5C9wpY9yaZq5V2x_foE4130_provenance.
- NP146277.RAtF-JvJ_22fqR8Kx5Ea7FsZbqPM8B6NavUC037Kwk8Xk130_assertion description "[early onset stroke without peripheral neuropathy caused by mutation in MFN2 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146277.RAtF-JvJ_22fqR8Kx5Ea7FsZbqPM8B6NavUC037Kwk8Xk130_provenance.
- NP146279.RAveQXoSVgZspRlUSEWDGh4yyAOWTeQKGRovMjaB_P85s130_assertion description "[The p22phox C242T polymorphism may have a protective effect against cardioembolic infarction in ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146279.RAveQXoSVgZspRlUSEWDGh4yyAOWTeQKGRovMjaB_P85s130_provenance.
- NP146285.RAnhtrwsVJnlEgAKH2xa7upxIAgtckvXDAYH-YBPzIr0U130_assertion description "[APOA1 to APOB ratio is related to myocardial infarction and stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146285.RAnhtrwsVJnlEgAKH2xa7upxIAgtckvXDAYH-YBPzIr0U130_provenance.
- NP146288.RAjZepLbU96tnEvdoA5gP19DAqP89PewusWmfHc_ztI2w130_assertion description "[Comparison of the prevalence of high FVIIIc levels in pediatric stroke patients and healthy subjects with and without FVL/PT 20210 indicated that high FVIII levels are an independent risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146288.RAjZepLbU96tnEvdoA5gP19DAqP89PewusWmfHc_ztI2w130_provenance.
- NP146293.RAozQzmibnpFbkyFhSjwSNCLwzNL7gBSXveFGNIWBeAM8130_assertion description "[Polymorphisms in DNA repair genes may be important in the aetiology of stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146293.RAozQzmibnpFbkyFhSjwSNCLwzNL7gBSXveFGNIWBeAM8130_provenance.
- NP146295.RAoY9m0aHxLF-vgKOZf7cTmzcwl9uQCuyS9mlOSue7Q0I130_assertion description "[NT-proBNP, cTnT, or cTnI do not have roles in acute ischemic stroke when other risk factors are considered ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146295.RAoY9m0aHxLF-vgKOZf7cTmzcwl9uQCuyS9mlOSue7Q0I130_provenance.
- NP146297.RAkzNraMXHfZvztQOcTeUZzQQ33Wjt0D8XA4Vgv7dG8d4130_assertion description "[Polymorphisms of coagulation factor XIII subunit A and risk of hemorrhagic stroke in young white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146297.RAkzNraMXHfZvztQOcTeUZzQQ33Wjt0D8XA4Vgv7dG8d4130_provenance.
- NP146302.RAkkCShF0Q88n_86lS-zoW8-51qmRYXgsEZ5h59lJfQ40130_assertion description "[The prevalence of E3/E3 was lower & that of E4-containing phenotypes was higher in stroke patients/prevalence of E4-containing phenotypes was significantly higher in ischemic vs hemorrhagic & in small-vessel vs large-vessel stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146302.RAkkCShF0Q88n_86lS-zoW8-51qmRYXgsEZ5h59lJfQ40130_provenance.
- NP146304.RAlOnk3cbEHFm2LTMaKJ8ABOU3H8qoqfiGbLNsok15DL0130_assertion description "[This report describe 2 female cousins with neonatal stroke/was heterozygous for the plasminogen activator inhibitor-1 4G variant and compound heterozygous for the A1298C and C677T methylenetetrahydrofolate reductase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146304.RAlOnk3cbEHFm2LTMaKJ8ABOU3H8qoqfiGbLNsok15DL0130_provenance.
- NP146308.RAgeWT8FI0TKqwGc4amo-bUTUfEJuSP07ACYDB6t96WHA130_assertion description "[A significant increase of S-100B protein blood plasma concentrations was seen in patients with severe stroke; S-100 protein blood plasma concentration assessed on the 1st day after the stroke has highest diagnostic utility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146308.RAgeWT8FI0TKqwGc4amo-bUTUfEJuSP07ACYDB6t96WHA130_provenance.
- NP146310.RAl2YmD48YUAnilD6Q10_4ic7lSitth-x9RaFNnXz9HZY130_assertion description "[NT-proBNP, cTnT, or cTnI do not have roles in acute ischemic stroke when other risk factors are considered ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146310.RAl2YmD48YUAnilD6Q10_4ic7lSitth-x9RaFNnXz9HZY130_provenance.
- NP146311.RAoxwCvmEk3ff9WuqqMNF7duJVq60I2kYXjt38MrszdSs130_assertion description "[ALOX5AP (encoding 5-lipoxygenase-activating protein) associated with myocardial infarction and stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146311.RAoxwCvmEk3ff9WuqqMNF7duJVq60I2kYXjt38MrszdSs130_provenance.
- NP146318.RArXQneZXZFfzE4rUESAlZtE5kS47cvL9sPv_7yi6hQNQ130_assertion description "[Genetic variation in the promoter region of the beta-fibrinogen gene is associated with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146318.RArXQneZXZFfzE4rUESAlZtE5kS47cvL9sPv_7yi6hQNQ130_provenance.
- NP146329.RAt8Sl0q6uh7PRzD7P-7s5WWZn4337-Z6gBsQORFNEQGk130_assertion description "[Sleep apnea is independently associated with raised levels of CRP and fibrinogen in patients with acute ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146329.RAt8Sl0q6uh7PRzD7P-7s5WWZn4337-Z6gBsQORFNEQGk130_provenance.
- NP146330.RAoc3fBzQeCf79Ub_V6nRRB5IsUQostWfB0CRTal2fMrg130_assertion description "[Association between polymorphisms in the beta2-adrenergic receptor gene with myocardial infarction and ischaemic stroke in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146330.RAoc3fBzQeCf79Ub_V6nRRB5IsUQostWfB0CRTal2fMrg130_provenance.
- NP146331.RAvi5zSYJ_Nb-Wq8QFE6NIM-fPixqxQtheH4boJk3ReRw130_assertion description "[Glu27 allelic variant of the beta2-AR gene may be a determinant of ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146331.RAvi5zSYJ_Nb-Wq8QFE6NIM-fPixqxQtheH4boJk3ReRw130_provenance.
- NP146338.RAvekcX3viPecUiHJsi6DMPlM6_3vzviaroHlyKuf19_w130_assertion description "[whole blood tissue factor procoagulant activity and plasma FVIIa in ten patients with type 2 diabetes mellitus and 11 non-diabetic patients at baseline and 6, 12, 24, and 48 hours (h) after presentation for acute stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146338.RAvekcX3viPecUiHJsi6DMPlM6_3vzviaroHlyKuf19_w130_provenance.
- NP146342.RAmekDZT6hphLTM780S3j1HLXZWdJyQh3FgDlFhWGD0qc130_assertion description "[a synergistic association of CST3 and APOE4 alleles was observed in predicting vascular dementia patients so CST3 might interact with APOE4 on conferring vascular pathologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146342.RAmekDZT6hphLTM780S3j1HLXZWdJyQh3FgDlFhWGD0qc130_provenance.
- NP146348.RAsUNtqJrA9AZaK4VrWspMjgqtqQBPfLrAfUpfrA4WV7Y130_assertion description "[Variants of SREBF2 might be genetic factors involved in the pathogenesis of vascular dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146348.RAsUNtqJrA9AZaK4VrWspMjgqtqQBPfLrAfUpfrA4WV7Y130_provenance.
- NP146351.RAhJ9qh05Wvg_WXikw65p4CGtw5mRpZb9YmIe53VW6fl4130_assertion description "[The frequency of ApoE epsilon4 allele carriers was significantly overrepresented in Alzheimer disease group compared with Vascular Dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146351.RAhJ9qh05Wvg_WXikw65p4CGtw5mRpZb9YmIe53VW6fl4130_provenance.
- NP146354.RAjnY3jpxyfVql74VfdGJ_U81eHjU5dYU-VeWA8_OGvs4130_assertion description "[the allele T of C-770T and the haplotype TTGA of the promoter SNPs in LIGHT gene might decrease the expression of LIGHT and subsequently increase the susceptibility to vascular dementia in females ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146354.RAjnY3jpxyfVql74VfdGJ_U81eHjU5dYU-VeWA8_OGvs4130_provenance.
- NP146355.RAkPyN3yzjVw1XDDblr6o17Hks-Hf5yrSKnE3S_Lm46S8130_assertion description "[In the present study we found decreased vasopressin in several hypothalamic nuclei in vascular dementia indicating diminished production of certain hormones and neurotransmitters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146355.RAkPyN3yzjVw1XDDblr6o17Hks-Hf5yrSKnE3S_Lm46S8130_provenance.
- NP146357.RArgF283HZ1qZQJOxsW7lpmm-QDUdx3uGJJ8cdu0iXk_Q130_assertion description "[there is no significant difference in the genotype, allele and haplotype frequencies of PRNP codon 129 and 219 polymorphisms between Korean vascular dementia patients and normal controls ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146357.RArgF283HZ1qZQJOxsW7lpmm-QDUdx3uGJJ8cdu0iXk_Q130_provenance.
- NP146366.RArMDY2HUIUYNxwvKSayZtoqZDSemwJLnR6dcRlKOyNl0130_assertion description "[Microdeletion of chromosome 7q in patients with Williams syndrome have loss of medial elastin that affects the discharge of baroreceptors and consequently the baroreflex sensitivity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146366.RArMDY2HUIUYNxwvKSayZtoqZDSemwJLnR6dcRlKOyNl0130_provenance.
- NP146369.RAl1G2bMtKDjVeKRt1tZIcmSPxHV7qiyeG9eYnnzKNd08130_assertion description "[Maps within the critical region of Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146369.RAl1G2bMtKDjVeKRt1tZIcmSPxHV7qiyeG9eYnnzKNd08130_provenance.
- NP146370.RAgzQnC7WU1JedkQidmfKNnGdP4PkgyRkvhJQSP6ZW_L0130_assertion description "[Encodes an E3 ubiquitin ligase; putatively involved in phenotype determination of Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146370.RAgzQnC7WU1JedkQidmfKNnGdP4PkgyRkvhJQSP6ZW_L0130_provenance.
- NP146375.RAmXRa3A1y29ui-R0rq8rNHqJnG_Eb_eJaOb-R1neIpTc130_assertion description "[Williams syndrome transcription factor (WSTF) is targeted to replication foci through direct interaction with the DNA clamp PCNA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146375.RAmXRa3A1y29ui-R0rq8rNHqJnG_Eb_eJaOb-R1neIpTc130_provenance.
- NP146376.RAtWzPIbwLkvkriop_x-AJr5badmuBXxHroaB8hYI8EnQ130_assertion description "[Cutaneous T-cell lymphoma (CTCL) cell lines revealed pronounced resistance to death ligands (TRAIL and TNF-alpha) as compared to cell lines of T-cell acute lymphoblastic leukemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146376.RAtWzPIbwLkvkriop_x-AJr5badmuBXxHroaB8hYI8EnQ130_provenance.
- NP146381.RAsSdqr7aosWmwDEeWckXH8t04J-CK0ZcoslNF9TF8KY0130_assertion description "[Short isoforms of Aiolos were detected at low levels in bone marrow of normal volunters, but were not overexpressed in a patient with acute T-cell leukemia/for unaltered Aiolos indicates tumor suppressor function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146381.RAsSdqr7aosWmwDEeWckXH8t04J-CK0ZcoslNF9TF8KY0130_provenance.
- NP146382.RAp5VJhXolxrK1Dy-lCtUcJ3Wtda_C3Mf6OvZHZyCVzlc130_assertion description "[HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146382.RAp5VJhXolxrK1Dy-lCtUcJ3Wtda_C3Mf6OvZHZyCVzlc130_provenance.
- NP146384.RAtPYTq57lzkZfr4qEY3tSsb0YRg_fpgQ5cG_ZiRhr2Q4130_assertion description "[CALM-AF10+ T-ALL associatd with elevated expression of subset of HOXA genes and some of there transcriptional and functional regulators, as well as specific overexpression of oncogene BMI1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146384.RAtPYTq57lzkZfr4qEY3tSsb0YRg_fpgQ5cG_ZiRhr2Q4130_provenance.
- NP146388.RArc1hXwioGCxtKLZGg4jfJGsA7g7uyVxrs9w_ktW0c94130_assertion description "[Cutaneous T-cell lymphoma (CTCL) cell lines revealed pronounced resistance to death ligands (TRAIL and TNF-alpha) as compared to cell lines of T-cell acute lymphoblastic leukemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146388.RArc1hXwioGCxtKLZGg4jfJGsA7g7uyVxrs9w_ktW0c94130_provenance.
- NP146390.RAiu-9PxALoChDoQa_hNVioYhX1vjblSEweBxf9cuouNA130_assertion description "[Cutaneous T-cell lymphoma (CTCL) cell lines revealed pronounced resistance to death ligands (TRAIL and TNF-alpha) as compared to cell lines of T-cell acute lymphoblastic leukemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146390.RAiu-9PxALoChDoQa_hNVioYhX1vjblSEweBxf9cuouNA130_provenance.
- NP146394.RAo_Sgg8IDhFA4m6QAn0f6Y45q653oZs0-7o2rdMOXKyU130_assertion description "[Alu-mediated, large deletion-spanning introns 19-26 in PHKA2 is associated with X-linked liver glycogenosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146394.RAo_Sgg8IDhFA4m6QAn0f6Y45q653oZs0-7o2rdMOXKyU130_provenance.
- NP146409.RAtpn-a0PlxBRx9dNdAbXB3WFFxwygNLx00mUVN_6vF8g130_assertion description "[The present study identified 2 novel VEGFR3 mutations in Japanese families with Milroy's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146409.RAtpn-a0PlxBRx9dNdAbXB3WFFxwygNLx00mUVN_6vF8g130_provenance.
- NP146413.RAptoPmYj9D4fJcjdlGMm3nqlisWP0Haniz-fjEmi4dBs130_assertion description "[HMGA2 plays a central role in the pathogenesis of Lymphangiomyomatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146413.RAptoPmYj9D4fJcjdlGMm3nqlisWP0Haniz-fjEmi4dBs130_provenance.
- NP146414.RAs-yFm9JRtfcl8ABsyfrbCP_kgNDhfFXd-eCs_VgLf5Y130_assertion description "[CD44v6-positive sorted lymphangioleiomyomatosis cells showed loss of heterozygosity at the TSC2 locus; binding of CD44v6 antibody resulted in loss of cell viability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146414.RAs-yFm9JRtfcl8ABsyfrbCP_kgNDhfFXd-eCs_VgLf5Y130_provenance.
- NP146418.RAnskNtoYTSsBz49ED5Pn8oBx2wMuowW2WAzFpVeWkZmI130_assertion description "[Data showed podoplanin (D2-40 monoclonal antibody) was positive in thin-wall branching vessels and confirmed the current concept of lymphangiogenic origin of the tumor vessels in lymphangioleiomyoma/lymphangioleiomyomatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146418.RAnskNtoYTSsBz49ED5Pn8oBx2wMuowW2WAzFpVeWkZmI130_provenance.
- NP146430.RAo_XgxEqUPYLMJVGhXZ_g6q_KBTj8hkuyVeYVwQe2h4w130_assertion description "[TSLC1 inhibits nasopharyngeal carcinoma cell growth by arresting cells in G (0) -G (1) phase in normal culture conditions/serum, TSLC1 induced apoptosis/is a tumor suppressor gene in NPC; its loss is seen in lymphatic metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146430.RAo_XgxEqUPYLMJVGhXZ_g6q_KBTj8hkuyVeYVwQe2h4w130_provenance.
- NP146431.RArkev1Snd7mp-hhffi3t_C5tgn6uLbbzkKOURw_f1uf8130_assertion description "[MT1-MMP is primarily secreted in the oral squamous cell carcinoma (OSCC) cells and is involved in the invasiveness of the OSCC and lymphatic metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146431.RArkev1Snd7mp-hhffi3t_C5tgn6uLbbzkKOURw_f1uf8130_provenance.
- NP146432.RAvG7Q3J7oFnrRe1i1GsP4MJQqJf5MiMbfSkD7igyGYl8130_assertion description "[Single Nucleotide Polymorphism in matrix metalloproteinase-3 promoter is associated with lymphatic metastasis in esophageal squamous cell carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146432.RAvG7Q3J7oFnrRe1i1GsP4MJQqJf5MiMbfSkD7igyGYl8130_provenance.
- NP146446.RAihcMA1yis3eRNTvnci8-fMb6HlcuZTVGT3_dsDXRMSQ130_assertion description "[Increased circulating levels of interleukin 1 receptor, type II is associated with Hepatitis C virus positive patients and with those affected also by non-Hodgkin's lymphoma and cryoglobulinemia syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146446.RAihcMA1yis3eRNTvnci8-fMb6HlcuZTVGT3_dsDXRMSQ130_provenance.
- NP146448.RAs9F1ivgRy2qvJHiTYdeioM8ruPPNK8Hm1AOGXre-VmQ130_assertion description "[Data demonstrate high serum levels of CXCL10 in mixed cryoglobulinemia (MC) and that CXCL10 in MC+autoimmune thyroiditis patients are significantly higher compared to MC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146448.RAs9F1ivgRy2qvJHiTYdeioM8ruPPNK8Hm1AOGXre-VmQ130_provenance.
- NP146449.RAoGxtc2Ereen6VJWDgF9Dw299aUjQJFNUv8F6C7JNVUc130_assertion description "[up-regulation of CXCL13 gene expression is a feature of HCV-infected patients/levels of this chemokine in liver as well as skin of patients with active mixed cryoglobulinemia vasculitis suggest a possible interrelation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146449.RAoGxtc2Ereen6VJWDgF9Dw299aUjQJFNUv8F6C7JNVUc130_provenance.
- NP146451.RAqSW2POYq-Wv69nIZc-xIO_12RzmDtt4q3DBHe3HDLyk130_assertion description "[VCAM-1 is mainly involved in the pathogenesis of hepatitis C-mixed cryoglobulinemia associated severe vasculitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146451.RAqSW2POYq-Wv69nIZc-xIO_12RzmDtt4q3DBHe3HDLyk130_provenance.
- NP146454.RAnyRta0eqaSGyf1GpslNvzg4pp2neNLdYShgRXMJZwbs130_assertion description "[persistent production of CXCL13 and IgG within infected tissue, two characteristics of ectopic germinal centers, are definitive features of Lyme neuroborreliosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146454.RAnyRta0eqaSGyf1GpslNvzg4pp2neNLdYShgRXMJZwbs130_provenance.
- NP146464.RAoO8zHBbKPjEIdB3KAJC7nxAi-oK1WpG00qfShH4-774130_assertion description "[Polymorphism of the endothelial nitric oxide synthase predicts risk for severe diabetic retinopathy/enos4) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146464.RAoO8zHBbKPjEIdB3KAJC7nxAi-oK1WpG00qfShH4-774130_provenance.
- NP146472.RAo8qBYCagH72P11s8fr-Cq3H7BsQYh1tL5gopXfTpglg130_assertion description "[Direct implication of adhesion molecules in the pathogenesis or progression of type 2 diabetic retinopathy cannot be supported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146472.RAo8qBYCagH72P11s8fr-Cq3H7BsQYh1tL5gopXfTpglg130_provenance.
- NP146476.RAlaX1FjXMNU1Sf4ahcuc0w4hPssmeDNozv0-jafPwOc8130_assertion description "[Strong relationship between soluble L-selectin and diabetic retinopathy.strong correlation between sL-selectin and HbA1c/L-selectin is increased with poor glycemic control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146476.RAlaX1FjXMNU1Sf4ahcuc0w4hPssmeDNozv0-jafPwOc8130_provenance.
- NP146484.RAi0BjkTtdjDn0XNfKtcbb5HvlOjhaXwD0UgW8elOhPDQ130_assertion description "[There is a relationship between VEGF, TNF-alpha, IL-6 and the development of the diabetic retinopathy in children with diabetes mellitus type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146484.RAi0BjkTtdjDn0XNfKtcbb5HvlOjhaXwD0UgW8elOhPDQ130_provenance.
- NP146489.RAsB0rcrfNWtrmG4T4di_c3yc1MmzKnaWtIy7W-ceFtcc130_assertion description "[VEGF, Ets-1, and ERK1 act synergistically in the development of diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146489.RAsB0rcrfNWtrmG4T4di_c3yc1MmzKnaWtIy7W-ceFtcc130_provenance.
- NP146495.RAoIKVBrtwgbBxLyeLbNasJ6NpzRzgfjuLw3cxlvxfZi4130_assertion description "[C (-634) G genotype was found to increase the risk for diabetic retinopathy in patients with microalbuminuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146495.RAoIKVBrtwgbBxLyeLbNasJ6NpzRzgfjuLw3cxlvxfZi4130_provenance.
- NP146498.RAiPDkAq545u55zu7DEVKv-C3qmddkBUzXpUO7J6qCDVI130_assertion description "[IL-6 and tumor necrosis factor-alpha levels were higher in type 2 diabetes mellitus patients with proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146498.RAiPDkAq545u55zu7DEVKv-C3qmddkBUzXpUO7J6qCDVI130_provenance.
- NP146506.RArUkU_-YJBjfnq6GHzd4VI6Xeqe5p0mEeh2BmmwCUn7w130_assertion description "[Direct implication of adhesion molecules in the pathogenesis or progression of type 2 diabetic retinopathy cannot be supported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146506.RArUkU_-YJBjfnq6GHzd4VI6Xeqe5p0mEeh2BmmwCUn7w130_provenance.
- NP146508.RAkY8UesZ-QxybQnTehfpj_styOehhnsTn4ZvSGcmyEmc130_assertion description "[we observed, in a cohort of Caucasians with C-peptide-negative type 1 diabetes, a novel association between the functional FokI VDR polymorphism and severe diabetic retinopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146508.RAkY8UesZ-QxybQnTehfpj_styOehhnsTn4ZvSGcmyEmc130_provenance.
- NP146515.RAoEk_NBBdeGQrjxP4sc5Iw6qS7VmPWHiAsx7RsAK0tMY130_assertion description "[data indicate that the M55V polymorphism in the small ubiquitin-like protein 4 (SUMO4) gene is associated with a reduced risk of diabetic retinopathy in type 1 diabetes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146515.RAoEk_NBBdeGQrjxP4sc5Iw6qS7VmPWHiAsx7RsAK0tMY130_provenance.
- NP146517.RAmZsVh7OCcd6K0WQbeAiZOm2ccxlDWGsK3afujx9cpnQ130_assertion description "[Elevated in vitreous fluid of patients with proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146517.RAmZsVh7OCcd6K0WQbeAiZOm2ccxlDWGsK3afujx9cpnQ130_provenance.
- NP146519.RAoL47rtHdq4V5SB9QCJmVxM6PuOmwMiQXDC2gOu20oEk130_assertion description "[Significance of core 2 GlcNAc-T in the pathogenesis of capillary occlusion in diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146519.RAoL47rtHdq4V5SB9QCJmVxM6PuOmwMiQXDC2gOu20oEk130_provenance.
- NP146522.RAt_vuxrs9Pj6spxY7XS_Y6yH1ytBBUweGqAKfn9TvVjA130_assertion description "[role of TNF-alpha in the development of diabetic retinopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146522.RAt_vuxrs9Pj6spxY7XS_Y6yH1ytBBUweGqAKfn9TvVjA130_provenance.
- NP146523.RArHwRmSvTDFIKeTcMtvp5Fg_uUzjtdoyhetyesaYdwuQ130_assertion description "[The association between TNF-alpha and proliferative retinopathy in type 1 diabetic patients suggests that inflammation might play a role in the pathogenesis of proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146523.RArHwRmSvTDFIKeTcMtvp5Fg_uUzjtdoyhetyesaYdwuQ130_provenance.
- NP146525.RAg99b8UWiTXqKVVeB7jRSZmariE200dUQDshwc5AgR9w130_assertion description "[NF-kappaB is involved in the formation of epiretinal membranes after proliferative diabetic retinopathy, especially for the development of vascular endothelial cell component.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146525.RAg99b8UWiTXqKVVeB7jRSZmariE200dUQDshwc5AgR9w130_provenance.
- NP146532.RAsYKkoEA6Zy16kW5WQqj9i-eoyLXMO2_QvpZrHA2r8w0130_assertion description "[Increased plasma level of the bFGF confirmed the importance of this candidate gene in the formation of proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146532.RAsYKkoEA6Zy16kW5WQqj9i-eoyLXMO2_QvpZrHA2r8w0130_provenance.
- NP146537.RAqYMEVSsl99ADMutOewZpjMhzv1EIQGcFCeULUJQ3r9s130_assertion description "[DRB1*04 may be a protective factor in paucibacillary leprosy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146537.RAqYMEVSsl99ADMutOewZpjMhzv1EIQGcFCeULUJQ3r9s130_provenance.
- NP146546.RAs0o8RWhx08Rm4yBv1L9RokIq-nR1C5wfXClP8Qj9I9E130_assertion description "[Results use data from multidimensional NMR spectroscopy to elucidate the molecular interactions between Abeta peptide and alpha-synuclein which may lead to onset of Lewy body dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146546.RAs0o8RWhx08Rm4yBv1L9RokIq-nR1C5wfXClP8Qj9I9E130_provenance.
- NP146552.RAnoOb5-1Yb7tp41qOC7Y3meVptIcIqMMRWyuc2o4FVzU130_assertion description "[Significant reductions in dopamine transporter occur in the caudate and anterior and posterior putamens in subjects with Lewy body dementia compared with subjects with Alzheimer disease and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146552.RAnoOb5-1Yb7tp41qOC7Y3meVptIcIqMMRWyuc2o4FVzU130_provenance.
- NP146555.RAjzoGvAA6B2w_qXTApcMCMz6Hg4_EdI4Q81CJbzQ6TzA130_assertion description "[Beta-amyloid may contribute selectively to cognitive impairment of Lewy body disease and may contribute to timing of dementia relative to motor signs of parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146555.RAjzoGvAA6B2w_qXTApcMCMz6Hg4_EdI4Q81CJbzQ6TzA130_provenance.
- NP146559.RAgWJESBe8R-Cyin2QeOPQXX9qNv724ktSObLPfGReVFU130_assertion description "[Reduced striatal tyrosine hydroxylase in incidental Lewy body disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146559.RAgWJESBe8R-Cyin2QeOPQXX9qNv724ktSObLPfGReVFU130_provenance.
- NP146562.RAtfcdpzWw_4GUCkmivXxL58NiJbjtQZK8qie2BKBwxp4130_assertion description "[Mutations are found in Hirschsprung's disease in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146562.RAtfcdpzWw_4GUCkmivXxL58NiJbjtQZK8qie2BKBwxp4130_provenance.
- NP146564.RAo65IU5sbS31nEBCkLuQiIYEpolFR51E-wO85srLUTM0130_assertion description "[Decreased expression of SK3 channels in the aganglionic bowel may contribute to motility dysfunction in Hirschsprung's disease bowel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146564.RAo65IU5sbS31nEBCkLuQiIYEpolFR51E-wO85srLUTM0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion description "[May be a modifier of a gene associated with Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_assertion description "[ZFHX1B may be an important gene for normal embryonic neural crest development/indicate that Hirschsprung's disease can be regarded as a congenital malformation/were located at exon 8 of ZFHX1B in 3 of 4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146567.RAvR-JCImNAI8UjGiB5-bynPKwpNxE6rj8aGo21B6R0fQ130_provenance.
- NP146571.RAsROw4rVcBCOea32Xh2FcIAaFXSgt1VTgrur9k9KJ-Uw130_assertion description "[Mutations are found in Hirschsprung's disease in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146571.RAsROw4rVcBCOea32Xh2FcIAaFXSgt1VTgrur9k9KJ-Uw130_provenance.
- NP146572.RAtFZghafimIV65hO1QEEYCZ407G9FM9XLa0BZJ3ctPdk130_assertion description "[In conclusion, Multiplex Ligation-dependent Probe Amplification assessment of rearrangements in the RET proto-oncogene and in 3 other associated genes, ZEB2, EDN3 and GDNF did not show any variants in 80 sporadic Hirschsprung disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146572.RAtFZghafimIV65hO1QEEYCZ407G9FM9XLa0BZJ3ctPdk130_provenance.
- NP146573.RAkQn9RK20574eNsdCQuE25ELG2H9bfRVsGN8A6V0g-3s130_assertion description "[RET gene mutations in 2 of 15 patients with Hirschsprung's disease in Taiwan/Y146N mutation we identified was novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146573.RAkQn9RK20574eNsdCQuE25ELG2H9bfRVsGN8A6V0g-3s130_provenance.
- NP146577.RAunK4rw5y1oAZwYo-fIuRn4FztL4DMfHBqKV6iFhC8-k130_assertion description "[A variant located in the 3'untranslated region of the RET gene, which slows down mRNA decay in patients with Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146577.RAunK4rw5y1oAZwYo-fIuRn4FztL4DMfHBqKV6iFhC8-k130_provenance.
- NP146580.RAomdt5hHYxOh5az0bMK1K63B603VxZ2HqbmaHATvzO1c130_assertion description "[a common non-coding RET variant within a conserved enhancer-like sequence in intron 1 is significantly associated with Hirschsprung disease susceptibility ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146580.RAomdt5hHYxOh5az0bMK1K63B603VxZ2HqbmaHATvzO1c130_provenance.
- NP146590.RAqjGptXDiKff5p-ReKbakbfzjDb_Zqd5R4Lanxk0HYFM130_assertion description "[Two GDNF mutations identified in Hirschsprung disease patients have reduced binding affinity for the receptor ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146590.RAqjGptXDiKff5p-ReKbakbfzjDb_Zqd5R4Lanxk0HYFM130_provenance.
- NP146591.RAk4yXL0oDr7VeZESanVNTtHBpcrroYykJDujWMJR8uqg130_assertion description "[RET enhancer modulates expression in the enteric nervous system consistent with its proposed role in Hirschsprung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146591.RAk4yXL0oDr7VeZESanVNTtHBpcrroYykJDujWMJR8uqg130_provenance.