Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP148785.RAvTQn0Cv8T2w6JIaZ2FHSmZnf-L0Z5jb8vfVoHXAUeGE130_assertion description "[We found that subjects APOE epsilon4 non-carriers and 6A/6A homozygous for the MMP-3 polymorphism were at increased risk of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148785.RAvTQn0Cv8T2w6JIaZ2FHSmZnf-L0Z5jb8vfVoHXAUeGE130_provenance.
- NP148788.RAsCn6ie7TkbVhAL2uj4gAnUo59LKPE-Z1ZQoqQYt3Oqw130_assertion description "[Our study suggests that LRPAP1-D and APOE E4 alleles significantly increase the susceptibility to degenerative dementias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148788.RAsCn6ie7TkbVhAL2uj4gAnUo59LKPE-Z1ZQoqQYt3Oqw130_provenance.
- NP148789.RAqsWBk3NjtuVjAzLMZA_ZD2kKzSf6O8-ea3RXmmXWr-Y130_assertion description "[Data show that the ApoE epsilon4 allele frequency is significantly higher in the Alzheimer's disease patients than in the non-Alzheimer dementia patients or in the control groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148789.RAqsWBk3NjtuVjAzLMZA_ZD2kKzSf6O8-ea3RXmmXWr-Y130_provenance.
- NP148792.RArfJnwAgLcbcii14H4BZFDILF2db9MYfjAmgXeuthsXs130_assertion description "[AD patients who carry the ApoE epsilon4 allele are at greater risk than noncarriers for developing psychotic symptoms, particularly as the severity of their dementia progresses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148792.RArfJnwAgLcbcii14H4BZFDILF2db9MYfjAmgXeuthsXs130_provenance.
- NP148794.RAjPqBbzwNjnlzJGkEJ5DTuut_-TriD2q3fRDI_Hgjg0c130_assertion description "[Involvemenet of this allele is still unknown, but increased genetic risk for developing Alzheimer disease is associated with changes in microscopic white matter integrity well before the onset of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148794.RAjPqBbzwNjnlzJGkEJ5DTuut_-TriD2q3fRDI_Hgjg0c130_provenance.
- NP148800.RAsFOKN4w3GziXCsKNQuTqppoUsFpmggydw8SGvN3jE3c130_assertion description "[although PSEN1 mutations are the most frequent cause, the MAPT R406W mutation is an important cause of early-onset familial dementia clinically diagnosed as Alzheimer's disease in Japanese ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148800.RAsFOKN4w3GziXCsKNQuTqppoUsFpmggydw8SGvN3jE3c130_provenance.
- NP148802.RAvPaDWEkal4xGNT4r3GAD2ukSDEVQ7WQhkHL37fpweS8130_assertion description "[novel MAPT mutation (P301T) is associated with familial frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148802.RAvPaDWEkal4xGNT4r3GAD2ukSDEVQ7WQhkHL37fpweS8130_provenance.
- NP148805.RAswVrRwklFVx_vj0LWpz5zKwMWwtpNX2ryRDl-sQKN3U130_assertion description "[Familial frontotemporal dementia associated with the novel MAPT mutation T427M.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148805.RAswVrRwklFVx_vj0LWpz5zKwMWwtpNX2ryRDl-sQKN3U130_provenance.
- NP148806.RArFFtpGBtRwvvzhdLjJjvco1ovhpPLBSROAz-wTWFs-0130_assertion description "[novel missense mutation in exon 12 of the tau gene, G335V, in a German family with frontotemporal dementia of early age at onset, in the third decade of life ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148806.RArFFtpGBtRwvvzhdLjJjvco1ovhpPLBSROAz-wTWFs-0130_provenance.
- NP148813.RAncp5ikoAjLV0bOs9ucat-RVKkoi7Zk9wgJ72SPlkAhg130_assertion description "[New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148813.RAncp5ikoAjLV0bOs9ucat-RVKkoi7Zk9wgJ72SPlkAhg130_provenance.
- NP148814.RAgfIHTsetXyGEBGySdn0zYwEEfh-Rb8hn5kDsbLhjQTE130_assertion description "[present study demonstrates that PSEN1 linked autosomal dominant early onset Alzheimer's disease has to be considered, even when ataxia precedes dementia, the Pro117Ala mutation being responsible for a predominant precocious ataxia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148814.RAgfIHTsetXyGEBGySdn0zYwEEfh-Rb8hn5kDsbLhjQTE130_provenance.
- NP148819.RAnfxeRmJFpr2nrQtB46Arn52FrOyZsm29FhRrnv4Pyfo130_assertion description "[Alternative transcripts of presenilin 1 are associated with sporadic frontotemporal dementia, deletions having been identified within the exon 4-8 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148819.RAnfxeRmJFpr2nrQtB46Arn52FrOyZsm29FhRrnv4Pyfo130_provenance.
- NP148820.RAoZLkHR9R8jS8DZ6s4k0CjN5iq-S9upBWETlb4chywGM130_assertion description "[To our knowledge, this is the first evidence that a gene known to be involved in tau phosphorylation, GSK3B, is associated with risk for primary neurodegenerative dementias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148820.RAoZLkHR9R8jS8DZ6s4k0CjN5iq-S9upBWETlb4chywGM130_provenance.
- NP148824.RAo3_GlPt2UXj3lcFW9nyenqpMwtTddOahX3Yx5CFHwVo130_assertion description "[CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148824.RAo3_GlPt2UXj3lcFW9nyenqpMwtTddOahX3Yx5CFHwVo130_provenance.
- NP148826.RAv7-zu5qbDsLuSbzmr6ADBReEKVoBO8HSv57LaiFMeRs130_assertion description "[We report a case of Gerstmann-Straussler-Scheinker disease with the PRPc Q217R mutation mimicking frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148826.RAv7-zu5qbDsLuSbzmr6ADBReEKVoBO8HSv57LaiFMeRs130_provenance.
- NP148827.RAvIMZkfPHiTSXobKUuf-OkQ_5jMCsWG7StJfemGMDEUw130_assertion description "[analysis of a novel PRNP mutation in a patient with a slow progressive dementia syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148827.RAvIMZkfPHiTSXobKUuf-OkQ_5jMCsWG7StJfemGMDEUw130_provenance.
- NP148828.RAltkBlXpgeUbNUnkgcUB_SwouNU8Y_ZeaWUwOShcwNpg130_assertion description "[A South African family had a progressive dementia and atypical pathology associated with kuru-like prion protein plaques/original mutation in this family occurred on a PRNP allele encoding a 1-octapeptide repeat deletion polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148828.RAltkBlXpgeUbNUnkgcUB_SwouNU8Y_ZeaWUwOShcwNpg130_provenance.
- NP148831.RAhbKeOTCT_yHpf0CB38jUKZSnB8_1AewoCx9LuxTh_N4130_assertion description "[No relationship between pattern of cholinergic deficits and distribution pattern of lesions in amygdala of patients with Alzheimer's disease or dementia with Lewy bodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148831.RAhbKeOTCT_yHpf0CB38jUKZSnB8_1AewoCx9LuxTh_N4130_provenance.
- NP148832.RApvSyuQSWmhglHX7nxK80yUDdvX4kPH9yMVpDTwlzQug130_assertion description "[These findings show that significant thalamic presynaptic cholinergic deficits occur only in cases of combined cortical and subcortical neurodegeneration in which dementia developed after prolonged parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148832.RApvSyuQSWmhglHX7nxK80yUDdvX4kPH9yMVpDTwlzQug130_provenance.
- NP148837.RAm9zYkbE_B4zhbfGuvDAdj1oh35F4wcoM3u4VNZYyOmM130_assertion description "[We describe a new mutation in the PGRN gene (A303AfsX57) associated with late-onset frontotemporal dementia and with " cat's eye " shaped intranuclear and cytoplasmatic ubiquitin immunoreactive inclusions in the neuropathological exam.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148837.RAm9zYkbE_B4zhbfGuvDAdj1oh35F4wcoM3u4VNZYyOmM130_provenance.
- NP148843.RAkWSYjYcOk1zESmcPpFnKxdmC0fEfXGWWars_uHf2RpE130_assertion description "[the mutation spectrum in PGRN leading to loss of functional PGRN as the basis for frontotemporal dementia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148843.RAkWSYjYcOk1zESmcPpFnKxdmC0fEfXGWWars_uHf2RpE130_provenance.
- NP148844.RAgCfuQ1h9lXPzWEIVXN5k3QjeR3E8otVwGLDzBSGY3SU130_assertion description "[Data show progranulin immunoreactivity throughout the medial temporal lobe in all dementia with Lewy bodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148844.RAgCfuQ1h9lXPzWEIVXN5k3QjeR3E8otVwGLDzBSGY3SU130_provenance.
- NP148847.RAr1imhtP9p2YAzf8Zthxk3JCOTVkTeUkvfJc399SekHQ130_assertion description "[PGRN haploinsufficiency leads to neurodegeneration because of reduced PGRN-mediated neuronal survival; and involvement of PGRN in frontotemporal dementia pathogenesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148847.RAr1imhtP9p2YAzf8Zthxk3JCOTVkTeUkvfJc399SekHQ130_provenance.
- NP148852.RAuXywr3KZ-LsTKwnoJLe9YuZHPxgNUYK2-kp1BGBL_HI130_assertion description "[Our results suggest that VGLUT1 expression in the prefrontal cortex could be used as a valuable neurochemical marker of dementia in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148852.RAuXywr3KZ-LsTKwnoJLe9YuZHPxgNUYK2-kp1BGBL_HI130_provenance.
- NP148854.RAtmaVPlc8nIC8YAXy5USaLpHF2163FlD-iEl9v_uXd7s130_assertion description "[Whilst dementia severity is closely related to impaired cerebral glucose metabolism, CSF t-tau is less closely related and appears to be less well suited for assessment of disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148854.RAtmaVPlc8nIC8YAXy5USaLpHF2163FlD-iEl9v_uXd7s130_provenance.
- NP148859.RAgpYLoextKWpGHVnHUkT7oD_kQb7w_DgQwu36I6_0Mrk130_assertion description "[The composite Guam parkinsonism-dementia complex neuropathology profile of tau, alpha-synuclein and 8, 12-iso-iPF (2alpha) -VI isoprostane reported here more closely resembles that seen in other tauopathies including frontotemporal dementias (FTDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148859.RAgpYLoextKWpGHVnHUkT7oD_kQb7w_DgQwu36I6_0Mrk130_provenance.
- NP148860.RAkJhAd1sLm0NcwCcWpV_inYhZdzsjM8-3bDxafYhe48M130_assertion description "[This is a possible candidate gene in frontal lobe dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148860.RAkJhAd1sLm0NcwCcWpV_inYhZdzsjM8-3bDxafYhe48M130_provenance.
- NP148862.RArChsaanfRzY-t6_WurmS7Ln7ubdVtRrkB1wCSZCzGeY130_assertion description "[The composite Guam parkinsonism-dementia complex neuropathology profile of tau, alpha-synuclein and 8, 12-iso-iPF (2alpha) -VI isoprostane reported here more closely resembles that seen in other tauopathies including frontotemporal dementias (FTDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148862.RArChsaanfRzY-t6_WurmS7Ln7ubdVtRrkB1wCSZCzGeY130_provenance.
- NP148867.RAuJxcr6kdxWCy2hluvdqTAZv-YhFLvepGKTRox3oHI-8130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148867.RAuJxcr6kdxWCy2hluvdqTAZv-YhFLvepGKTRox3oHI-8130_provenance.
- NP148868.RAhlJRdkbhM8IHpW3Niwu3HpxARu-hqYXKqs1PNnBx8XE130_assertion description "[Mutations of the valosin-containing protein gene (VCP) at 9p13 cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148868.RAhlJRdkbhM8IHpW3Niwu3HpxARu-hqYXKqs1PNnBx8XE130_provenance.
- NP148882.RApdhLDPrYjeCwxmGzNx4scNHehmSrVcUtGVSGBcsSp80130_assertion description "[frameshift results in the premature termination of the encoded product, which is designated " maspardin " (Mast syndrome, spastic paraplegia, autosomal recessive with dementia) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148882.RApdhLDPrYjeCwxmGzNx4scNHehmSrVcUtGVSGBcsSp80130_provenance.
- NP148885.RAm8ia9gYnp_HSki9SGCJqY7HCiaDA4CG-ZwuQlf9l3UY130_assertion description "[This study suggests IDE may be indirectly related to dementia via its regulation of insulin levels, but it is not a major gene for Alzheimer's.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148885.RAm8ia9gYnp_HSki9SGCJqY7HCiaDA4CG-ZwuQlf9l3UY130_provenance.
- NP148886.RAvYDiYHFTMQLzN2lj2Oq4rKx0ROCvelMKoUScTKL5ZvI130_assertion description "[familial aggregation & clinical presentation of frontotemporal dementia + motor neuron disease; TDP-43 antibody stained neuronal inclusions similar in distribution & morphology to neuronal cytoplasmatic inclusions & neuronal intranuclear inclusions ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148886.RAvYDiYHFTMQLzN2lj2Oq4rKx0ROCvelMKoUScTKL5ZvI130_provenance.
- NP148897.RAsZT73MFn0YxMJREBkkLghtwOjcXUB0fa2DwPVifUzNw130_assertion description "[EAAT1 was strongly expressed in a subset of cortical pyramidal neurons in dementia cases showing Alzheimer-type pathology/addition, tau (which is a marker of neurofibrillary pathology) colocalized to those same pyramidal cells that expressed EAAT1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148897.RAsZT73MFn0YxMJREBkkLghtwOjcXUB0fa2DwPVifUzNw130_provenance.
- NP148898.RAulUX3RMxuM9GkjvzoyE5PBFw9NoXCEKsRPp2DPpYaMc130_assertion description "[EAAT1 parameters were mutually correlated (p < 0.01) and correlations were shown with dementia severity (p < 0.05 MMSE-expression, p < 0.005 MMSE-mRNA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148898.RAulUX3RMxuM9GkjvzoyE5PBFw9NoXCEKsRPp2DPpYaMc130_provenance.
- NP148903.RAhyvr8iLQ9QehjggNi6QYfnbq2T-q5LBVh-rPqhflRCg130_assertion description "[Increase in APP gene dosage is linked to a phenotype consisting of early onset dementia and CAA with frequent ICH/phenotype does not depend on the size of the duplicated region, but may vary between families and between the genders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148903.RAhyvr8iLQ9QehjggNi6QYfnbq2T-q5LBVh-rPqhflRCg130_provenance.
- NP148906.RAhT2hO5eMF7QCZ2ELa5DzjfzOzdnvcxvXfPtqGFSQc1w130_assertion description "[In patients with Alzheimer disease, low plasma levels of Abeta40 and Abeta42 are associated with a significantly more rapid cognitive decline than are high levels in patients with Alzheimer disease, using the Blessed Dementia Scale.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148906.RAhT2hO5eMF7QCZ2ELa5DzjfzOzdnvcxvXfPtqGFSQc1w130_provenance.
- NP148907.RAka-wxoCAr5vtJ3t_yp2DB4iRUD_kGU311zT22dRDIzU130_assertion description "[This exploratory study has shown altered activities of the enzyme carnosinase in patients with dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148907.RAka-wxoCAr5vtJ3t_yp2DB4iRUD_kGU311zT22dRDIzU130_provenance.
- NP148908.RAjvVkf7nyB9jL8OVbwMarC8X9SLIMRMX8j3boiRFv-HM130_assertion description "[An inhibitory deficit and its impact across the lifespan are specifically associated with the fragile X premutation status, and may be a precursor for development of a more severe form of cognitive impairment or dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148908.RAjvVkf7nyB9jL8OVbwMarC8X9SLIMRMX8j3boiRFv-HM130_provenance.
- NP148911.RAhGrdVYQVJ7En3Eivdos4w6778DKBtMPbmkNunBU1oJs130_assertion description "[The analysis of NAT2 polymorphism does not seem to be useful in predicting the risk of PD with dementia or AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148911.RAhGrdVYQVJ7En3Eivdos4w6778DKBtMPbmkNunBU1oJs130_provenance.
- NP148915.RApLsNnnZYM6YzI8B_1aGGf_UUz5o2gvIUmjkJ3Va7-YQ130_assertion description "[PAR-2 is up-regulated on neurons in conjunction with neuroinflammation in brain tissue from patients with HIV-1-associated dementia/cytokines TNF-alpha and IL-1 beta are also increased in HIV-1-associated dementia brains.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148915.RApLsNnnZYM6YzI8B_1aGGf_UUz5o2gvIUmjkJ3Va7-YQ130_provenance.
- NP148917.RAv4wLS_7hKnUsPGgVssVLh09GdahugEIyWLOvx0Vb794130_assertion description "[A possible role of the novel polymorphism as independent susceptibility factor of Alzheimer's dementia is shown ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148917.RAv4wLS_7hKnUsPGgVssVLh09GdahugEIyWLOvx0Vb794130_provenance.
- NP148919.RAl6yYGauYRPUEEGSV3RH6Qopwv7MkRTag57qBeqaowZ0130_assertion description "[Finds decreasing risk of dementia with increasing ApoA-1 concentrations and joint effect of ApoA-1 and ApoE-1 gene on risk of dementia in Japanese American men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148919.RAl6yYGauYRPUEEGSV3RH6Qopwv7MkRTag57qBeqaowZ0130_provenance.
- NP148921.RAv_nfog5x4jCbKOLbYfI5mg2NGLZWTlwKX9So912PbUU130_assertion description "[Activation of p53 mediated pathways in the glia of HIV-associated dementia patients may contribute to neuroinflammatory processes that promote neurodegeneration by inhibiting glial proliferation and/or promoting glial cell dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148921.RAv_nfog5x4jCbKOLbYfI5mg2NGLZWTlwKX9So912PbUU130_provenance.
- NP148923.RAkLR5AfWycIb3XIDULGq17bRfETPjmUW8JXMBWNcRp1U130_assertion description "[description of an Italian family with hereditary dementia associated with a novel mutation in the presenilin 2 gene (A85V mutation) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148923.RAkLR5AfWycIb3XIDULGq17bRfETPjmUW8JXMBWNcRp1U130_provenance.
- NP148927.RAm9Ay2XoUZeN7MkhBL5QRkkusKLMI6xUaR1yvbd8jFKM130_assertion description "[nicotinic modulation of thalamo-cortical circuitry as a key component in the control of conscious awareness in dementia with Lewy bodies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148927.RAm9Ay2XoUZeN7MkhBL5QRkkusKLMI6xUaR1yvbd8jFKM130_provenance.
- NP148929.RAsgfaDo5tHKG8_1vkcXXMgo4-KAA5J8dW4VLnRAtZMqk130_assertion description "[C-reactive protein plays a role in development of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148929.RAsgfaDo5tHKG8_1vkcXXMgo4-KAA5J8dW4VLnRAtZMqk130_provenance.
- NP148933.RAmlVDYLEHBLKCPNuz7PN5GHasDVVpcAoD7BUVqiwZUhA130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148933.RAmlVDYLEHBLKCPNuz7PN5GHasDVVpcAoD7BUVqiwZUhA130_provenance.
- NP148934.RAlI2XWNwY4F4aF-9PRo8m3z2GLXdSaJMt40g55xFGd9g130_assertion description "[Among all kallikreins measured, detectable levels in cerebrospinal fluid are identified for kallikrein K7/most notable difference is seen between controls and frontotemperol dementia patients and controls and Alzheimer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148934.RAlI2XWNwY4F4aF-9PRo8m3z2GLXdSaJMt40g55xFGd9g130_provenance.
- NP148945.RAoZrzEsO1sJUOfO1YS_ZqqvfBMyF2fGbAFwkg1BfuVR8130_assertion description "[the A/T polymorphism of SERPINA3 gene is associated with the risk factor for aneurysmal subarachnoid hemorrhage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148945.RAoZrzEsO1sJUOfO1YS_ZqqvfBMyF2fGbAFwkg1BfuVR8130_provenance.
- NP148949.RAhn7FifuHYMbZ9aWG4WldfYhs5uwUGz6TsUwLq4vKWCM130_assertion description "[Genetically influenced variation in BDNF function plays a role in recovery from subarachnoid hemorrhage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148949.RAhn7FifuHYMbZ9aWG4WldfYhs5uwUGz6TsUwLq4vKWCM130_provenance.
- NP148950.RAlW80dtIrY7JdqHdjKyNbe2Vs6p9vE4LqDWOxSmMDEX0130_assertion description "[Increased expression/occurred on astrocytic processes/of AQP1 and AQP4 on reactive astrocytes in subarachnoid hemorrhage/be involved in brain edema formation or resolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148950.RAlW80dtIrY7JdqHdjKyNbe2Vs6p9vE4LqDWOxSmMDEX0130_provenance.
- NP148952.RAoIH8e9N9OMTzmre9DgUuKtWlW1pOr_dThk2sAR1QJQ8130_assertion description "[apolipoprotein E genotype is not shown to increase risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage in a meta-analysis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148952.RAoIH8e9N9OMTzmre9DgUuKtWlW1pOr_dThk2sAR1QJQ8130_provenance.
- NP148953.RAvTartQ2AybhZAq7u0CWsf5n9iBg2_4Qe1dNhp65x8gU130_assertion description "[In patients with subarachnoid hemorrhage, the expression of the E4 allele is associated with a higher risk of a negative outcome and delayed ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148953.RAvTartQ2AybhZAq7u0CWsf5n9iBg2_4Qe1dNhp65x8gU130_provenance.
- NP148955.RAkp0qWC_bRk7KoJt6ZT87WIDPBuxK5HbdfpLvkybnxCU130_assertion description "[Homozygousbeta1AR Arg389Gly predicts cardiac troponin release in subarachnoid hemorrhage/homozygous B1AR Arg389Gly & homozygous deletion of B2AR increases the odds of reduced left ventricular ejection fraction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148955.RAkp0qWC_bRk7KoJt6ZT87WIDPBuxK5HbdfpLvkybnxCU130_provenance.
- NP148957.RAo4PnufKB6MvzsVs8vejZPCzkkqtAMF1atkwLwtiNsL0130_assertion description "[structural and functional characterization of three different factor H proteins purified from the plasma of patients with atypical hemolytic uremic syndrome who carry the factor H mutations W1183L, V1197A, or R1210C ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148957.RAo4PnufKB6MvzsVs8vejZPCzkkqtAMF1atkwLwtiNsL0130_provenance.
- NP148958.RAngg950VFc21C34slrCzFsuA_97teuWOQJprSEXKOKJ0130_assertion description "[mutated FH enables complement activation on the surface of platelets and their activation, which may contribute to the development of thrombocytopenia in Atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148958.RAngg950VFc21C34slrCzFsuA_97teuWOQJprSEXKOKJ0130_provenance.
- NP148962.RAtUoicfDMxuRFL2TEKdsYUoFnyIE5Zh8G8u_4cDfTBnU130_assertion description "[Heterozygous CFH/CFHL1 hybrid gene in which exons 1-21 are derived from CFH and exons 22/23 from CFHL1 causing Hemolytic Uremic Syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148962.RAtUoicfDMxuRFL2TEKdsYUoFnyIE5Zh8G8u_4cDfTBnU130_provenance.
- NP148964.RArSJ1ZNbAadYDEQA-giPPU9I5YJgGN0KGDoL4fMEGCXI130_assertion description "[Two different factor H mutations associated with atypical hemolytic uremic syndrome were examined: in one, factor H accumulated in cells, and in the other, membrane binding was reduced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148964.RArSJ1ZNbAadYDEQA-giPPU9I5YJgGN0KGDoL4fMEGCXI130_provenance.
- NP148969.RAhwA3PK13n6x96w6Z9oBgKl651bVZDL2hQpt7m4bNSEo130_assertion description "[study reports mutations in C3 in association with atypical hemolytic uremic syndrome (aHUS); 9 novel mutations in 14 aHUS patients with a persistently low serum C3 level are described ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148969.RAhwA3PK13n6x96w6Z9oBgKl651bVZDL2hQpt7m4bNSEo130_provenance.
- NP148971.RAtvkKYCcgb2g5GSOI4xLnFhr34PlJX_INB633Bv07YXs130_assertion description "[MCP mutation and complete paternal uniparental disomy of chromosome 1 could have an additive effect in determining the severity of the hemolytic-uremic syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148971.RAtvkKYCcgb2g5GSOI4xLnFhr34PlJX_INB633Bv07YXs130_provenance.
- NP148993.RArMkTc50HpIWXjjxgLSTeotM2cBS5NUGLtDPeudeCW2U130_assertion description "[Transgenic mice expressing C3a/glial fibrillary acidic protein (GFAP) in the brain progress to severe experimental autoimmune encephalomyelitis during the chronic phase of the disease, with significant mortality compared with nontransgenic littermates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148993.RArMkTc50HpIWXjjxgLSTeotM2cBS5NUGLtDPeudeCW2U130_provenance.
- NP149001.RAtMxmS93j0CMyZTbKypWICEiZbltNHRsmzFw8X7zJ2N8130_assertion description "[Defect in the local control of IL1 may be involved in the pathophysiology of endometriosis and related infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149001.RAtMxmS93j0CMyZTbKypWICEiZbltNHRsmzFw8X7zJ2N8130_provenance.
- NP149008.RApkPxincVw_6ipLrjkDksm0nyZNM-yAsLze8JiRGKEHM130_assertion description "[Results suggest the involvement of SRY gene in sex reversal which further supports the relationship between SRY alterations, gonadal dysgenesis and/or primary infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149008.RApkPxincVw_6ipLrjkDksm0nyZNM-yAsLze8JiRGKEHM130_provenance.
- NP149014.RArD4PLNyG7YlavyVrNoUQubgB3J43dm6o_CPUT30HFjM130_assertion description "[KGF may hold promise for the treatment of very premature neonates with bronchopulmonary dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149014.RArD4PLNyG7YlavyVrNoUQubgB3J43dm6o_CPUT30HFjM130_provenance.
- NP149019.RAm_sXjjDpyYDNHfI7La9V3UkgliIOM1PtMwNaCsGnW1Q130_assertion description "[MMP16 polymorphisms appear to influence not only the pulmonary expression and function of MMP16 but also the risk of bronchopulmonary dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149019.RAm_sXjjDpyYDNHfI7La9V3UkgliIOM1PtMwNaCsGnW1Q130_provenance.
- NP149022.RAowP_Xqqvnc---q2dQDZ7tbb04HHlKeIS6Ji_IL97D70130_assertion description "[strong and early expression of interleukin-1 receptor antagonist (IL-1Ra) proves to be non-protective due to the robust expression of airway agonist interleukin-1beta seen by day 5 in premature infants who develop bronchopulmonary dysplasia (BPD) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149022.RAowP_Xqqvnc---q2dQDZ7tbb04HHlKeIS6Ji_IL97D70130_provenance.
- NP149023.RAkd-zj9TPHcHa1lV62robWSHcRwbFQqbEMp1Gmpo6gdo130_assertion description "[The D allele of ACE is associated with an increased risk and severity of bronchopulmonary dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149023.RAkd-zj9TPHcHa1lV62robWSHcRwbFQqbEMp1Gmpo6gdo130_provenance.
- NP149024.RAn7T4f_IYHGpscVH-ayfWUfmoD6cIMILVXGRZ_UF_6P0130_assertion description "[MMP-9 level and TIMP-1 levels increased after birth but are not linked to bronchopulmonary dysplasia outcome; low MMP-2 level at birth is associated with the development of BPD ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149024.RAn7T4f_IYHGpscVH-ayfWUfmoD6cIMILVXGRZ_UF_6P0130_provenance.
- NP149027.RAoIsEqy1_T9LGam6ZZl6h4-AufcNNjKuUEJVEQl0TwQw130_assertion description "[High levels of pulmonary trypsin-2 may be associated with the development of bronchopulmonary dysplasia in preterm infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149027.RAoIsEqy1_T9LGam6ZZl6h4-AufcNNjKuUEJVEQl0TwQw130_provenance.
- NP149028.RAi2LAhR2457tCXmaM0XIzTNadiSj9Kl17FEjY56xip2A130_assertion description "[strong expression of PAR (2) was detected in myofibroblasts of thickened and fibrotic alveolar walls in prolonged respiratory distress syndrome or bronchopulmonary dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149028.RAi2LAhR2457tCXmaM0XIzTNadiSj9Kl17FEjY56xip2A130_provenance.
- NP149035.RAgoP7TnMWfkXKUf9fi-RdZCvw_InPO7DlftB02qEeo2U130_assertion description "[Our analysis of the entire coding region of TIMP-1, -2, and -3, which are the main inhibitors of metalloproteinase activity in the extracellular matrix, failed to show an association between genetic polymorphisms and an intracranial aneurysm ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149035.RAgoP7TnMWfkXKUf9fi-RdZCvw_InPO7DlftB02qEeo2U130_provenance.
- NP149036.RAs8Q79haaXBmBrfGUnxTR0bLDnpbz78XTeLDHoJSV_5g130_assertion description "[strong evidence for racial/ethnic differences in the association of SNP and specific haplotypes of the elastin gene with the intracranial aneurysm phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149036.RAs8Q79haaXBmBrfGUnxTR0bLDnpbz78XTeLDHoJSV_5g130_provenance.
- NP149039.RAgoagSr0KAXU1PeOXODKEUZJVMXXbGJkpUgm9nvRsJLg130_assertion description "[Significant genotypic association in the dominant model was noted between an exonic single nucleotide polymorphism [SNP]of COL1A2 and familial intracranial aneurysm patients; this SNP induces Ala to Pro substitution at AA 459, on a triple-helical domain ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149039.RAgoagSr0KAXU1PeOXODKEUZJVMXXbGJkpUgm9nvRsJLg130_provenance.
- NP149045.RAq5LhcuaJzB16Zz7hw-1FxkP1BuNuggeLIJmbBlEbeqQ130_assertion description "[elevated TIMP-1 levels may reflect the degree of hepatic fibrosis and development of portal hypertension with biliary atresia; TIMP-1 may play a role in the pathophysiology of post-Kasai biliary atresia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149045.RAq5LhcuaJzB16Zz7hw-1FxkP1BuNuggeLIJmbBlEbeqQ130_provenance.
- NP149049.RAscT0Pat2tRn_hSaYYhcqvKZ3jdCr3_p8IMVBR0IFIwQ130_assertion description "[The process is not associated with genetic variation of K469E ICAM-1 polymorphism in biliary atresia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149049.RAscT0Pat2tRn_hSaYYhcqvKZ3jdCr3_p8IMVBR0IFIwQ130_provenance.
- NP149055.RAlx4Qh1VutYTWOi1ssN57wRy2RGOitD-qbOrTNfDuqyM130_assertion description "[JAG1 gene abnormality may be an aggravating factor in extrahepatic biliary atresia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149055.RAlx4Qh1VutYTWOi1ssN57wRy2RGOitD-qbOrTNfDuqyM130_provenance.
- NP149057.RAnXRXKKi1waVCMbaArpC9IZf1vkYLaZP2OmhAzRIof3A130_assertion description "[Our present study suggests that serum IL-6 and IL-10 levels are related to fever, and the CSF IL-6 level, myoclonic jerks, in SSPE patients in PNG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149057.RAnXRXKKi1waVCMbaArpC9IZf1vkYLaZP2OmhAzRIof3A130_provenance.
- NP149059.RAtZtLItJPDuIhnatjJe8pPX_8uozMYBnRW0THgzEm1M0130_assertion description "[MMP-9 (matrix metalloproteinase-9)/TIMP-1 (tissue inhibitor of metalloproteinase-1) ratios of SSPE (subacute sclerosing panencephalitis) patients were significantly higher than controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149059.RAtZtLItJPDuIhnatjJe8pPX_8uozMYBnRW0THgzEm1M0130_provenance.
- NP149061.RAj4gvKMO5BetkWknsaXXM4TpJx8y19OC0bOdRH_PO5Z4130_assertion description "[Our findings suggest that the MMP-9 level in CSF is an indicator of inflammatory damage to the brain in SSPE (subacute sclerosing panence).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149061.RAj4gvKMO5BetkWknsaXXM4TpJx8y19OC0bOdRH_PO5Z4130_provenance.
- NP149062.RAmPKLdXR0A8eU5HjisgQXaSF6O5cEz8iejEbn51pMw_E130_assertion description "[Possible effects of genetic polymorphisms in the susceptibility to subacute sclerosing panencephalitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149062.RAmPKLdXR0A8eU5HjisgQXaSF6O5cEz8iejEbn51pMw_E130_provenance.
- NP149068.RAqt61aQkEJOsB09o3VSlEuJAXWvnWZr16po-KM4Z7yJs130_assertion description "[Methylation of the DAPK gene is associated with cell transformation in HPV and EBV infection in cervical cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149068.RAqt61aQkEJOsB09o3VSlEuJAXWvnWZr16po-KM4Z7yJs130_provenance.
- NP149070.RAvGSlkOB1N-qETHC_Yte-KjVgh8NTjC-Y-yUpZ4PPsfw130_assertion description "[TIMP1 functions as a differentiating and survival factor of GC B cells by modulating CD44 and SHP1 in the late centrocyte/post-GC stage, regardless of EBV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149070.RAvGSlkOB1N-qETHC_Yte-KjVgh8NTjC-Y-yUpZ4PPsfw130_provenance.
- NP149075.RAib8iQ9mHm2hcJL6ASt0mMdpKLhVzDRLc18NRVKpx2Y8130_assertion description "[Nm23-H1 and EBNA3C can modulate expression of COX-2 in the context of EBV infection and transformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149075.RAib8iQ9mHm2hcJL6ASt0mMdpKLhVzDRLc18NRVKpx2Y8130_provenance.
- NP149076.RAsLFG87mfNxBDeWIbDa1QexqHuuVcAS5i0Anz6pthTrw130_assertion description "[3 genes were upregulated in patients with chronic EBV infection: guanylate binding protein 1, tumor necrosis factor-induced protein 6, and guanylate binding protein 5; they may be associated with the inflammatory reaction or with cell proliferation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149076.RAsLFG87mfNxBDeWIbDa1QexqHuuVcAS5i0Anz6pthTrw130_provenance.
- NP149080.RArxXQeNqcANXb9ELhjHUujpifW51C47PcK5uEePVPpVQ130_assertion description "[significant increase of MMP-9 and TIMP-1 in the urine of children with acute pyelonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149080.RArxXQeNqcANXb9ELhjHUujpifW51C47PcK5uEePVPpVQ130_provenance.
- NP149081.RAk7-niUllvyanidS4P6o5otaNli9wzTIRxVTi9Mnpx-0130_assertion description "[association between TIMP-1 and the process of renal scarring in pyelonephritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149081.RAk7-niUllvyanidS4P6o5otaNli9wzTIRxVTi9Mnpx-0130_provenance.
- NP149082.RAscGODv0Ua2K4Q4oe4hPjfGnct7F-xbpvvz8tXwCBGG8130_assertion description "[blocks transmigration of granulocytes into urine; entrapped and activated granulocytes, protected from apoptosis, might destroy renal parenchyma and contribute to the pathogenesis of renal scarring following acute pyelonephritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149082.RAscGODv0Ua2K4Q4oe4hPjfGnct7F-xbpvvz8tXwCBGG8130_provenance.
- NP149084.RAtdbVhzjh1zSjXOHb2xXh_kpWhW6CBjBothlXCFeudtI130_assertion description "[study shows the IL-10-1082'A'allele is associated with abdominal aortic aneurysms (AAA), although this association is likely to be secondary to an association between IL-10-1082 genotype & other markers of cardiovascular disease rather than AAA per se ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149084.RAtdbVhzjh1zSjXOHb2xXh_kpWhW6CBjBothlXCFeudtI130_provenance.
- NP149085.RAi_FYw5BBCMYidiX8u8jm7fVI_tfbj3SQ11mXli-HlzI130_assertion description "[identified significant interactions between MMP10 (nt+180) polymorphisms and gender in abdominal aortic aneurysm ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149085.RAi_FYw5BBCMYidiX8u8jm7fVI_tfbj3SQ11mXli-HlzI130_provenance.
- NP149089.RAtKHHNNglCaF5ZQteyOQzjePlKo9_UM74Ncx6t4mwJJo130_assertion description "[CX3CL1+ and CX3CR1+ cells are present in abdominal aortic aneurysms and may contribute to the recruitment of inflammatory cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149089.RAtKHHNNglCaF5ZQteyOQzjePlKo9_UM74Ncx6t4mwJJo130_provenance.
- NP149096.RAtEMUiuaOR5VcKVnAPKuuDryN-4faGR8w_0p-gkOIdAM130_assertion description "[The IL-6 572G > C polymorphism is associated with abdominal aortic aneurysms (AAAs), however it is too rare to be an important cause of most AAAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149096.RAtEMUiuaOR5VcKVnAPKuuDryN-4faGR8w_0p-gkOIdAM130_provenance.
- NP149097.RAkvyh_Q1-Y6bnKayHcxpvvsnvzZxC7rJyIgN4seeZuLo130_assertion description "[Serum resistin concentrations were more strongly associated with aortic diameter than adipokines that are more intimately associated with adiposity in obesity and abdominal aortic aneurysm ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149097.RAkvyh_Q1-Y6bnKayHcxpvvsnvzZxC7rJyIgN4seeZuLo130_provenance.
- NP149100.RAn7lEJVRiMjVnz3rHh7yEBKeqz6W2DjvwD-K6awGqqO8130_assertion description "[A localized increase in MMP-8 and -9, mediated by native mesenchymal cells, presents a potential pathway for collagen breakdown and abdominal aortic aneurysm rupture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149100.RAn7lEJVRiMjVnz3rHh7yEBKeqz6W2DjvwD-K6awGqqO8130_provenance.
- NP149104.RAr9Op6ZQOBLZwLc1UjaVIZj_-HGfwj5sSHPM161jPOQc130_assertion description "[CX3CL1+ and CX3CR1+ cells are present in abdominal aortic aneurysms and may contribute to the recruitment of inflammatory cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149104.RAr9Op6ZQOBLZwLc1UjaVIZj_-HGfwj5sSHPM161jPOQc130_provenance.
- NP149112.RAmWmheu0oStCrkKnvfxgj3LHY_ZsJA_6uTQWoXJUV_y0130_assertion description "[C-reactive protein (CRP) elevation in patients with abdominal aortic aneurysm is independent of the most important CRP genetic polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149112.RAmWmheu0oStCrkKnvfxgj3LHY_ZsJA_6uTQWoXJUV_y0130_provenance.
- NP149116.RAgbyosDgJPuyFVdkulhxjoULSSgXYJ1-qruuyuToaenA130_assertion description "[expressed in CSF of children with bacterial or viral meningitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149116.RAgbyosDgJPuyFVdkulhxjoULSSgXYJ1-qruuyuToaenA130_provenance.
- NP149117.RArH-EeATdPr4D6eIET2i1lGciyu3VhI9TUckIbayiBaY130_assertion description "[The results revealed that mononuclear cells were highly immunoreactive for TIMP-1, TIMP-2 and MMP-9 during viral meningitis and that the expression of TIMPs in polymorphonuclear cells was even higher during bacterial meningitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149117.RArH-EeATdPr4D6eIET2i1lGciyu3VhI9TUckIbayiBaY130_provenance.
- NP149124.RAjW-B_BGsqceWedbbrVy_m2Ab0fgA_UHbLcFJEEKYtWI130_assertion description "[ischemia-reperfusion injury and excessive shear stress secondary to portal hypertension might augment HO-1 expression in the graft liver ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149124.RAjW-B_BGsqceWedbbrVy_m2Ab0fgA_UHbLcFJEEKYtWI130_provenance.
- NP149131.RAqvi3MBvXfGdoQ_aK2NS25viQHU2BqjAXJLIrSZMU5xc130_assertion description "[Human guanylate binding protein-1 may be a useful surrogate marker for diagnosis of bacterial meningitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149131.RAqvi3MBvXfGdoQ_aK2NS25viQHU2BqjAXJLIrSZMU5xc130_provenance.