Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP148763.RAXupkJMUO-wxZlMvBzOHngHvAXU7LX3AO9_S-TEWA0Uo130_assertion description "[Citrullinemia is a metabolic disorder characterized by elevated plasma concentrations of citrulline and ammonia/citrullinemia (type II, CTLN2) has been attributed to citrin deficiency caused by mutations in the SLC25A13 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148763.RAXupkJMUO-wxZlMvBzOHngHvAXU7LX3AO9_S-TEWA0Uo130_provenance.
- NP148774.RAYHlRei2_VyKFhwlWGAjI6vMz0-po6SordXJXH-GSh3E130_assertion description "[Traumatic brain injury was not associated with higher rates of amnestic mild cognitive impairment or dementia, and APOE-epsilon4 was not associated with cognition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148774.RAYHlRei2_VyKFhwlWGAjI6vMz0-po6SordXJXH-GSh3E130_provenance.
- NP148784.RAVSpAF6t9sT86v4yst_vLPeyZlUmgPok47iROuetKnxM130_assertion description "[These associations did not differ between strata of APOEepsilon4 genotype/observations do not suggest that variation in the MMP3 gene is causally involved in dementia or AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148784.RAVSpAF6t9sT86v4yst_vLPeyZlUmgPok47iROuetKnxM130_provenance.
- NP148787.RAVx0CguAqglGXmFo7R8B0gPIsiiCVofWL-bLCZ6Wqo6g130_assertion description "[In this population of elderly women, although having at least one epsilon4 allele increased the chances of an earlier death, having dementia increased the risk of death regardless of APOE genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148787.RAVx0CguAqglGXmFo7R8B0gPIsiiCVofWL-bLCZ6Wqo6g130_provenance.
- NP148791.RARLVC16naUQpxyp4S-xZJxhPvuAiM92m4hUZoPqoPp_w130_assertion description "[The results partially support studies of older adults that suggest that increased cognitive asymmetries reflect risk for dementia and are associated with the APOE-epsilon 4 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148791.RARLVC16naUQpxyp4S-xZJxhPvuAiM92m4hUZoPqoPp_w130_provenance.
- NP148793.RAa0pf3DjTNZN3IG8xg6t04q-2UcsHFCSM-jvmVhKWKYs130_assertion description "[Individuals with a family history of AD and the APOE epsilon4 allele, additional genetic or environmental factors may accelerate the onset of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148793.RAa0pf3DjTNZN3IG8xg6t04q-2UcsHFCSM-jvmVhKWKYs130_provenance.
- NP148796.RAepCjETXfjh0hz52wJnO_NplSFhFdtWuWpL0QBp4W65U130_assertion description "[Data evaluate and compare the bcl2, bax, and nestin patterns in the frontal cortices of Alzheimer and multiple-infarct dementia patients, and in normal aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148796.RAepCjETXfjh0hz52wJnO_NplSFhFdtWuWpL0QBp4W65U130_provenance.
- NP148798.RAeNFbc-Vmy1KUOiUpLMYkU661-adUjkOB7808QS4hri0130_assertion description "[In diseased brain the ability of astrocytes to counteract the destructive effects of MMP through expression of TIMP-1 is diminished by chronic activation/studies reveal new opportunities for therapeutics in HIV-associated dementia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148798.RAeNFbc-Vmy1KUOiUpLMYkU661-adUjkOB7808QS4hri0130_provenance.
- NP148801.RAeksLV27yP6dJCtPbWva_uYeS4_tSjEKw8OmhMYqFiOw130_assertion description "[report describes a tau S305S family where mutation carriers have frontotemporal dementia and parkinsonism; findings support previous studies demonstrating that the S305S mutation influences splicing of tau exon 10 & results in an overproduction of 4R tau ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148801.RAeksLV27yP6dJCtPbWva_uYeS4_tSjEKw8OmhMYqFiOw130_provenance.
- NP148810.RAQMSoxkoxehmYq09INamAotiPbLP8UpjJvMifCMxK9tA130_assertion description "[Genetic variant in S100beta increases the risk of low cognitive performance and dementia, possibly by favouring a splicing event increasing S100beta2 isoform expression in the brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148810.RAQMSoxkoxehmYq09INamAotiPbLP8UpjJvMifCMxK9tA130_provenance.
- NP148812.RAZFJpAdoq8VksET7ZqyMTcpRI8osD6lfqpgLGmX75HV8130_assertion description "[The PSEN1 mutation (P264L causes disease that begins with spastic paraparesis and is associated with dementia that is not of the Alzheimer type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148812.RAZFJpAdoq8VksET7ZqyMTcpRI8osD6lfqpgLGmX75HV8130_provenance.
- NP148815.RARlMGo8zHj6dL0_BZbtUC1J0a_PfC6S4wUIY9PNoGq24130_assertion description "[We describe a case of a young patient suffering from a rapidly progressive cognitive decline, associated with delusions, myoclonus and seizures and with no family history for dementia anddemonstrated a de novo presenilin 1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148815.RARlMGo8zHj6dL0_BZbtUC1J0a_PfC6S4wUIY9PNoGq24130_provenance.
- NP148833.RAT7Fuacrym-D-Axl5xh9Tr9FIBkwNatUe6-ebxGIyT-c130_assertion description "[This report on a South African family that presented with progressive dementia and a movement disorder affecting numerous family members/of the JPH3 CTG repeat revealed pathogenic expansions in three affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148833.RAT7Fuacrym-D-Axl5xh9Tr9FIBkwNatUe6-ebxGIyT-c130_provenance.
- NP148835.RAc9x0ByOyPQxIhrGF4pBQ_5Ib_ZcRKcFIrs1uyqj0bmc130_assertion description "[An asymmetric degenerative process is associated with mutations in the progranulin (PGRN) gene and is seen in 3 PGRN cases presenting with either corticobasal syndrome or frontotemporal dementia and language deterioration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148835.RAc9x0ByOyPQxIhrGF4pBQ_5Ib_ZcRKcFIrs1uyqj0bmc130_provenance.
- NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_assertion description "[PGRN mutations at 17q21 may occur in apparently sporadic frontotemporal lobar dementia with ubiquitinated inclusions cases and in cases presenting with either primary progressive aphasia or the behavioral variant of frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_provenance.
- NP148841.RAURsXrmyxkbMKzyfnWQiduLdoic1vC3JLZX6HOV5aKdE130_assertion description "[A single GRN mutation in the two families studied was associated with variable clinical presentations consistent with the frontotemporal dementia syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148841.RAURsXrmyxkbMKzyfnWQiduLdoic1vC3JLZX6HOV5aKdE130_provenance.
- NP148842.RAa31ZpbEU25gcmgtUDzila0KTWSAbVyfNXlzgSGsrC9A130_assertion description "[Progranulin null mutations in both sporadic and familial frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148842.RAa31ZpbEU25gcmgtUDzila0KTWSAbVyfNXlzgSGsrC9A130_provenance.
- NP148851.RARiPa-Kes5KQvfTGcPeX_Smx_rZyikvIBFxRP0gBOCnM130_assertion description "[Decreased BDNF may be a pathogenetic factor involved not only in dementia and depression, but also in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148851.RARiPa-Kes5KQvfTGcPeX_Smx_rZyikvIBFxRP0gBOCnM130_provenance.
- NP148865.RAULVoGWLX5DyYjvNSBm9XobaeSV7_tngGhyhja7q6gg4130_assertion description "[role of aggregation by tissue transglutaminase in Lewy body formation in Parkinson's disease and dementia with Lewy bodies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148865.RAULVoGWLX5DyYjvNSBm9XobaeSV7_tngGhyhja7q6gg4130_provenance.
- NP148869.RAdryhEu38p4eOUc-Za_WWzTmGyWarut8vXPI8r3RZf8w130_assertion description "[A 55-year-old German patient with inclusion body myopathy and frontotemporal dementia who harbors a heterozygous R155C missense mutation residing in the N-terminal CDC48 domain of VCP, which is involved in ubiquitin binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148869.RAdryhEu38p4eOUc-Za_WWzTmGyWarut8vXPI8r3RZf8w130_provenance.
- NP148870.RAUfiOkLglNwiL9EY_82vsUjrmVzNMX8Fd_vKBwkVZOP8130_assertion description "[A patient with Inclusion body myopathy with Paget disease of bone and frontotemporal dementia carried a novel heterozygous base pair change, 47832C > T, in the VCP gene that resulted in substitution of an arginine residue by cysteine at position 93 (R93C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148870.RAUfiOkLglNwiL9EY_82vsUjrmVzNMX8Fd_vKBwkVZOP8130_provenance.
- NP148872.RAWpcgSCIZkWyDXPfi0Ct9fV7g2sHolazlqMsrqsmixRQ130_assertion description "[early-onset dementia is linked to specific mutations in the BRI2 { REVIEW } ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148872.RAWpcgSCIZkWyDXPfi0Ct9fV7g2sHolazlqMsrqsmixRQ130_provenance.
- NP148873.RAU5mdWxarIibuZfx_nHT1tNjqzd5jP8XFXyntieCSwZE130_assertion description "[in familial British dementia the mutated precursor BRi2 protein may undergo furin cleavage within neurones to produce the amyloid peptide ABri ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148873.RAU5mdWxarIibuZfx_nHT1tNjqzd5jP8XFXyntieCSwZE130_provenance.
- NP148874.RAW_HtNlZkggQEudH4UuyOeR9UVR4lQpepYeCoUWohGk4130_assertion description "[alpha1-antitrypsin deficiency and dementia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148874.RAW_HtNlZkggQEudH4UuyOeR9UVR4lQpepYeCoUWohGk4130_provenance.
- NP148881.RAeSP05PphxQR79uixl0Z92Y3IVLkH5KH60hBWRU8GEk8130_assertion description "[KIBRA T-- > C polymorphism contributes to modulate episodic memory amongst community-dwelling older adults free of dementia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148881.RAeSP05PphxQR79uixl0Z92Y3IVLkH5KH60hBWRU8GEk8130_provenance.
- NP148883.RAc6tQ4uPnOip6x5itjUvwgHfJsRc-W-YAPci953NcAWk130_assertion description "[Levels of E2F1 protein were greater in the nucleus of neurons in brains of HIV-infected patients exhibiting dementia when compared to HIV-negative subjects or HIV-positive neurologically normal patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148883.RAc6tQ4uPnOip6x5itjUvwgHfJsRc-W-YAPci953NcAWk130_provenance.
- NP148884.RARmKpj0gzMsWO8Wn1cXJ63357UoCz3_qHd_1bbIxaXuI130_assertion description "[Correlation between IGF-I and Mini Mental State Examination in Alzheimer's disease suggests a mechanism involving immuno-somatopause in progression of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148884.RARmKpj0gzMsWO8Wn1cXJ63357UoCz3_qHd_1bbIxaXuI130_provenance.
- NP148890.RAepruBoliL6JK-NYV_gHUErbvSUwXG9piuQkRG7uxRoA130_assertion description "[Data evaluate and compare the bcl2, bax, and nestin patterns in the frontal cortices of Alzheimer and multiple-infarct dementia patients, and in normal aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148890.RAepruBoliL6JK-NYV_gHUErbvSUwXG9piuQkRG7uxRoA130_provenance.
- NP148891.RAVSvHxQ1uAdgwSIMr4s8pBTnNO8ekK78Wq-VwOREwcI8130_assertion description "[our data nevertheless argue against a major genetic role of MAO-A polymorphism in frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148891.RAVSvHxQ1uAdgwSIMr4s8pBTnNO8ekK78Wq-VwOREwcI8130_provenance.
- NP148893.RAeHDEkHCNa_cjI7wB7wWu8pePfOyt44t7jn_9fpsXaFs130_assertion description "[overexpression of alpha-synuclein apparently recapitulates several important features of brains with PD and dementia with Lewy bodies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148893.RAeHDEkHCNa_cjI7wB7wWu8pePfOyt44t7jn_9fpsXaFs130_provenance.
- NP148900.RAWO3tGB5yciQQothrhr4n6cSrOq6BMRApG5yGLYhOXWU130_assertion description "[A novel amyloid protein precursor mutation (Glu693Delta) -producing variant in Japanese pedigrees has been suggested as a cause of Alzheimer's-type dementia because of enhanced formation of synaptotoxic amyloid beta oligomers rather than amyloid fibrils.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148900.RAWO3tGB5yciQQothrhr4n6cSrOq6BMRApG5yGLYhOXWU130_provenance.
- NP148904.RAaPQCTTeEJMte4EhsGGljd_fmtwGkq4QNRmTGvI3iIqE130_assertion description "[The constant and abundant amyloid beta x-42 deposition in sporadic dementia with Lewy bodies suggests that alpha-synucleinopathy is also promoted by amyloid precursor protein dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148904.RAaPQCTTeEJMte4EhsGGljd_fmtwGkq4QNRmTGvI3iIqE130_provenance.
- NP148909.RAZ5uhNpFXS3lh62tMaHF85G7dzmPz1DQ9e27G3LrVeRI130_assertion description "[Ours is the first case of a woman with premutation alleles in the FMR1 gene who also had dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148909.RAZ5uhNpFXS3lh62tMaHF85G7dzmPz1DQ9e27G3LrVeRI130_provenance.
- NP148910.RAc4Yd4_uXnBZGnyJcn9Hdde_TjJyOuEu9LbFD1RGk2Kc130_assertion description "[The apoE epsilon4 carriers may be more vulnerable to environmental factors, and thus, lifestyle interventions may greatly modify dementia risk particularly among the genetically susceptible individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148910.RAc4Yd4_uXnBZGnyJcn9Hdde_TjJyOuEu9LbFD1RGk2Kc130_provenance.
- NP148918.RAVqzorkz3u_QJslBVi8K5rgO_xgv4Y9BagCaInyYH6o8130_assertion description "[These preliminary data suggest that the TGF genetic variability may be important in the risk of vascular related dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148918.RAVqzorkz3u_QJslBVi8K5rgO_xgv4Y9BagCaInyYH6o8130_provenance.
- NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_assertion description "[PON2*S and apoE4 alleles have interactive effect on the development of the two most common forms of dementias AD and VD, and further support the hypothesis that cardiovascular factors contribute to the development of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_provenance.
- NP148926.RAYekNtLQxoHM0ftsqgk0QQxeXLbvZ_mQ0uDRPSpFRaXQ130_assertion description "[Overexpression of uPAR in the central nervous system of patients with AIDS dementia suggests that the uPA/uPAR system may contribute to the tissue injury and neuronal damage in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148926.RAYekNtLQxoHM0ftsqgk0QQxeXLbvZ_mQ0uDRPSpFRaXQ130_provenance.
- NP148939.RAa478tpvzivjQ9MPoL7XuR5dIv4IsH1o3A0htshGydio130_assertion description "[Enhanced activation of Rho kinase contributes to augmented contraction of the basilar artery to serotonin after subarachnoid hemorrhage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148939.RAa478tpvzivjQ9MPoL7XuR5dIv4IsH1o3A0htshGydio130_provenance.
- NP148941.RARsElyO_hkjSI6NSorjMbWwqS7_wrd6I0nxvf6KfkzYg130_assertion description "[Augmented release of ET-1 is correlated with the rupture of the abnormal vessel confirming its role in vasospasm after subarachnoid hemorrhage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148941.RARsElyO_hkjSI6NSorjMbWwqS7_wrd6I0nxvf6KfkzYg130_provenance.
- NP148942.RAczBbmA0HTepcB8DgftkhR3LdzPNAKGCTR1dAw-TjSHU130_assertion description "[genetic variation of ENOS influencing nitric oxide regulation contributes to the risk of angiographic vasospasm in patients with aneurysmal subarachnoid hemorrhage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148942.RAczBbmA0HTepcB8DgftkhR3LdzPNAKGCTR1dAw-TjSHU130_provenance.
- NP148943.RAfWV82fC7mBjzzQ6dD5OU2lq5RnqH1zO4HK4dUmM6UxE130_assertion description "[the eNOS T-786C mutation was not associated with either a susceptibility to subarachnoid hemorrhage (SAH) or vasospasm after SAH, or with aneurysm size in Korean population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148943.RAfWV82fC7mBjzzQ6dD5OU2lq5RnqH1zO4HK4dUmM6UxE130_provenance.
- NP148944.RAVlS9gk5yRlPsAY0RQHl5BzkUK3OYVyPpeNpo5z_bOH8130_assertion description "[This study suggests a role of the APOE gene in the etiology of aneurysmal subarachnoid hemorrhage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148944.RAVlS9gk5yRlPsAY0RQHl5BzkUK3OYVyPpeNpo5z_bOH8130_provenance.
- NP148968.RAWKWj5rZX7yqs6svw_SfqWLazqU_yTQdKpVq6UtfNsbU130_assertion description "[A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148968.RAWKWj5rZX7yqs6svw_SfqWLazqU_yTQdKpVq6UtfNsbU130_provenance.
- NP148977.RAeFcQ2QcQN5I0XHBfiu4KISVN56C9WuzbdJDtNJRFpYY130_assertion description "[the transcriptional regulation of the Gb3S gene by Sp1 might affect the verotoxin sensitivity of endothelial cell and Hemolytic uremic syndrome progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148977.RAeFcQ2QcQN5I0XHBfiu4KISVN56C9WuzbdJDtNJRFpYY130_provenance.
- NP148978.RAXe2avF9-TpwMAgez8UY2aYqe0JsyH0ENywhWevhqbHE130_assertion description "[Mutations in the complement regulators factor H, membrane cofactor protein (MCP), and factor I are associated with atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148978.RAXe2avF9-TpwMAgez8UY2aYqe0JsyH0ENywhWevhqbHE130_provenance.
- NP148980.RAbF-7N8k9HM4p974d2xhxWlZgmJH6ekQnPgP-LfnxF-8130_assertion description "[ADAMTS13 is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome; its activity level cannot be used to distingush between TTP and HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148980.RAbF-7N8k9HM4p974d2xhxWlZgmJH6ekQnPgP-LfnxF-8130_provenance.
- NP148981.RAVXLEGJZimDkK1ZohD1d61Na9po3OBu84m0mlJqI_BTk130_assertion description "[Age < 3 mo at onset seems to be characteristic of CFH and IF mutation-associated atypical hemolytic uremic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148981.RAVXLEGJZimDkK1ZohD1d61Na9po3OBu84m0mlJqI_BTk130_provenance.
- NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_assertion description "[Deletion of two closely related genes, complement factor H-related 1 (CFHR1) and complement factor H-related 3 (CFHR3), increases the risk of atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148983.RATWpdrktlO93dwOAPvhMn3Iav-vHdlpuQGLMLoWi7eck130_provenance.
- NP148984.RAYCg5cYgZgNdMCgQ5QYgfuGHLNx7H-eyHIikCF5fzSqE130_assertion description "[interaction of CX (3) CR1 (+) cells with fractalkine present on activated endothelial cells may contribute to renal injury in hemolytic uremic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148984.RAYCg5cYgZgNdMCgQ5QYgfuGHLNx7H-eyHIikCF5fzSqE130_provenance.
- NP148987.RAVHb7iv2GqcHG0E9e7hNReUw5uhbH2s8r-Hz_o3oaEoM130_assertion description "[regulation of interferon-gamma secretion, and not interleukin-4 in vitro, as well as inhibition of Th1 cell-induced isotype switching and attenuation of experimental allergic encephalomyelitis identifies NTB-A as a regulator of T cell response ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148987.RAVHb7iv2GqcHG0E9e7hNReUw5uhbH2s8r-Hz_o3oaEoM130_provenance.
- NP148988.RARxXDRPhm4KByStsEIXKDBMXvpSlP5PDGFHIQlP4ecRE130_assertion description "[FADD dominant-negative transgenic mice are resistant to experimental autoimmune encephalomyelitis; FADD therefore serves as an enhancer of autoimmune encephalomyelitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148988.RARxXDRPhm4KByStsEIXKDBMXvpSlP5PDGFHIQlP4ecRE130_provenance.
- NP148990.RAfORGWkG-uZ8uDfaDFo0HVyEme9ywb9tYOiCatK2T5Uo130_assertion description "[Human MOG is immunogenic and induces experimental autoimmune encephalomyelitis in C57BL/6 mice via an encephalitogenic B cell response to epitopes on human MOG protein that most likely cross-react with mouse determinants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148990.RAfORGWkG-uZ8uDfaDFo0HVyEme9ywb9tYOiCatK2T5Uo130_provenance.
- NP148996.RASPYpoEvu83yhZEqCOVp3wngub-9I-o5FRgMcyX9XHWY130_assertion description "[infertile women with endometriosis or unexplained infertility had significantly weakened trophinin expression in the endometrium in the mid-luteal phase ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148996.RASPYpoEvu83yhZEqCOVp3wngub-9I-o5FRgMcyX9XHWY130_provenance.
- NP148997.RAZpS_A2leGeLxrETFb59zfyYxlXcLD9-DdcROfeQC2R8130_assertion description "[characterization of the MATER gene and its protein; this provides a basis for investigating their clinical implications in autoimmune premature ovarian failure and infertility in women ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148997.RAZpS_A2leGeLxrETFb59zfyYxlXcLD9-DdcROfeQC2R8130_provenance.
- NP148998.RAUoQbMf33umJuCdUfme-PPplxfHRM1qgUzf47fTcp0ug130_assertion description "[Hyperleptinemia and high follicular fluid leptin are important pathologies of polycystic ovarian syndrome with infertility ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148998.RAUoQbMf33umJuCdUfme-PPplxfHRM1qgUzf47fTcp0ug130_provenance.
- NP149003.RAcvylJhneYrv7iK2fNyAiDxVCVjVn8xMz1o4sF-GRgDk130_assertion description "[Impairment of the mechanisms involved in the regulation of activation of complement system factor iC3b may be important in the pathogenesis of endometriosis and endometriosis-associated infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149003.RAcvylJhneYrv7iK2fNyAiDxVCVjVn8xMz1o4sF-GRgDk130_provenance.
- NP149009.RAQEXCn8b9WwV8suYKVEOf9waMC-8qQUmk-8N4TGWsvk4130_assertion description "[investigation of the immediate effect of ovulation induction with hCG on peripheral VEGF levels in 6 women with primary infertility enrolled in the IVF/ET program ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149009.RAQEXCn8b9WwV8suYKVEOf9waMC-8qQUmk-8N4TGWsvk4130_provenance.
- NP149010.RAZY4hPlr7NDKnuU6NgXLk-cRX_NWvwdO5yEXSkvlVK9g130_assertion description "[description of familial occurrence of combined partial 17, 20-desmolase and 17alpha-hydroxylase deficiency in phenotypically normal normotensive women who presented with primary infertility, anovulation and persistent cervical dysmucorrhea ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149010.RAZY4hPlr7NDKnuU6NgXLk-cRX_NWvwdO5yEXSkvlVK9g130_provenance.
- NP149011.RARVlGjJcKncaLFl_SIgzJXI7Van9w3BSrq_9R0DdaTeI130_assertion description "[In patients with idiopathic infertility, GSTM1 polymorphism might be an important source of variation in susceptibility of spermatozoa to oxidative damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149011.RARVlGjJcKncaLFl_SIgzJXI7Van9w3BSrq_9R0DdaTeI130_provenance.
- NP149018.RASOVy-ZMN1d-Xo7H_2bY3btWzAWTKsM0GD6sN0Dt2YLg130_assertion description "[constitutive expression of IL-10 by lung inflammatory cells is associated with the risk for bronchopulmonary dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149018.RASOVy-ZMN1d-Xo7H_2bY3btWzAWTKsM0GD6sN0Dt2YLg130_provenance.
- NP149021.RAQc3CxaYKJfm5phW0oZfPzo5JrnG6W4L-CkZDnhbyV9M130_assertion description "[tenascin-C is highly expressed in the walls of alveoli and bronchioli in respiratory distress syndrome and bronchopulmonary dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149021.RAQc3CxaYKJfm5phW0oZfPzo5JrnG6W4L-CkZDnhbyV9M130_provenance.
- NP149026.RAQlsjHHYB_ksi6hK2JJsKSWIi7oYm-_63DaYo2oERhtU130_assertion description "[The polymorphism of DSTAP1 are associated with the development of bronchopulmonary dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149026.RAQlsjHHYB_ksi6hK2JJsKSWIi7oYm-_63DaYo2oERhtU130_provenance.
- NP149034.RAf_AfaPtcXZ6z2dEb1l4oSMvEWRxGQlDKA95Aj5RCDJQ130_assertion description "[An 8.94-fold and 6.73-fold increase in expression of caspase-3mRNA in intracranial aneurysm and AAA, respectively, were obtained relative to the normal vessels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149034.RAf_AfaPtcXZ6z2dEb1l4oSMvEWRxGQlDKA95Aj5RCDJQ130_provenance.
- NP149042.RAQV3LLbEyBgU_LSh0XX4oL2usZJjRtMLuT6_CyBM2_y0130_assertion description "[( Single nucleotide polymorphisms) SNPs in strong linkage disequilibrium and haplotypes constituting these SNPs in versican gene are associated with intracranial aneurysms (IAs)/in or near versican gene may play role in susceptibility to IAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149042.RAQV3LLbEyBgU_LSh0XX4oL2usZJjRtMLuT6_CyBM2_y0130_provenance.
- NP149052.RAfx8uFFTsctBHujHMWpe5Cf76M7moZaIs8JkEH0wACdE130_assertion description "[the single-nucleotide polymorphism at CD14/-159 is associated with the development of biliary atresia and idiopathic neonatal cholestasis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149052.RAfx8uFFTsctBHujHMWpe5Cf76M7moZaIs8JkEH0wACdE130_provenance.
- NP149053.RATD7SvkkvC6nJ-G8exZKQss_aoE0zOLmeSClyciYd67M130_assertion description "[results suggest that heterozygous cryptic family 1 (CFC1) mutation may represent a genetic predisposition to biliary atresia splenic malformation syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149053.RATD7SvkkvC6nJ-G8exZKQss_aoE0zOLmeSClyciYd67M130_provenance.
- NP149056.RAdTXjC_vYTLtm1jMGWGUYSJW_pfuGRasYmEeUEaV4btc130_assertion description "[MxA mRNA expression was also significantly higher in early stage of biliary atresia (BA) and in choledochal cyst than in late stage of BA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149056.RAdTXjC_vYTLtm1jMGWGUYSJW_pfuGRasYmEeUEaV4btc130_provenance.
- NP149063.RAdWyLas65FKL6vsNgzFZ6hM4dyI4HtUO043467w1Bkp0130_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." NP149063.RAdWyLas65FKL6vsNgzFZ6hM4dyI4HtUO043467w1Bkp0130_provenance.
- NP149065.RAclqTpdbk16Mv2-qdBZfUh7xRA8xypVacBzAVNaCH00I130_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." NP149065.RAclqTpdbk16Mv2-qdBZfUh7xRA8xypVacBzAVNaCH00I130_provenance.
- NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_assertion description "[Based on the constitutive signaling and cellular expression pattern of EBI2, it is suggested that it may function in conjunction with BILF1 in the reprogramming of the cell during EBV infection ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_provenance.
- NP149073.RAarzXRRKMwvw663gWRBb2I-pshzUs2saXKkwCWkvURE8130_assertion description "[Redox control of EBV infection: prevention by thiol-dependent modulation of functional CD21/EBV receptor expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149073.RAarzXRRKMwvw663gWRBb2I-pshzUs2saXKkwCWkvURE8130_provenance.
- NP149079.RAfRNlyVZ5lJEg8fYqKGYMxFqxuKLzyRsglQB-MOnG-GU130_assertion description "[The median maternal plasma protein Z concentration was significantly lower in patients with pyelonephritis during pregnancy than in patients with normal pregnancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149079.RAfRNlyVZ5lJEg8fYqKGYMxFqxuKLzyRsglQB-MOnG-GU130_provenance.
- NP149083.RAZms8Wk-Wr4ZyGulNcWNhgQ6TONMewcd_kMFfhiw1sEw130_assertion description "[The present study demonstrates the differential up-regulation of Egr-1 in the thrombus-covered wall of human Abdominal Aortic Aneurysm (AAA) and also suggests its possible contribution to the thrombogenic and inflammatory pathogenesis in human AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149083.RAZms8Wk-Wr4ZyGulNcWNhgQ6TONMewcd_kMFfhiw1sEw130_provenance.
- NP149088.RAVXO4u9sLLZzNXRgyuYKWyPrfDRxHiD1zjDvVcBvWMUs130_assertion description "[The genetic mutation of plasma PAF-AH gene appear to be an independent risk factor for AAA (abdominal aortic aneurysm) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149088.RAVXO4u9sLLZzNXRgyuYKWyPrfDRxHiD1zjDvVcBvWMUs130_provenance.
- NP149091.RAcTbl0DQxvQZmyU0a_XmQa9Z0iTelktARYZoBizql2wI130_assertion description "[genetic variation in TIMP3 may contribute to the pathogenesis of abdominal aortic aneurysm ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149091.RAcTbl0DQxvQZmyU0a_XmQa9Z0iTelktARYZoBizql2wI130_provenance.
- NP149092.RAS_Sz7mRYxA8aJXxYa9vWOkImsZ4gTWeXUD7yIjp2aAY130_assertion description "[The secretory levels of PGE (2), TXB (2) and IL-6 were highest in ruptured abdominal aortic aneurysms and statistically higher than those in intact abdominal aortic aneurysms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149092.RAS_Sz7mRYxA8aJXxYa9vWOkImsZ4gTWeXUD7yIjp2aAY130_provenance.
- NP149098.RAfrNm_7hk-pYWOhP8fs7v5Qe-fz9WmTEs2XiZx5t3Dx4130_assertion description "[Differentially expressed Ig kappa-C gene only in abdominal aortic aneurysm (AAA) is candidate gene that may play pivotal role in pathogenesis of AAA formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149098.RAfrNm_7hk-pYWOhP8fs7v5Qe-fz9WmTEs2XiZx5t3Dx4130_provenance.
- NP149102.RAR2yLlAZN_wJGfGyCfH8xbPexGCsOIdyjtnYcKgim7jg130_assertion description "[MIF and matrix metalloproteinases may have roles in development of human abdominal aortic aneurysms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149102.RAR2yLlAZN_wJGfGyCfH8xbPexGCsOIdyjtnYcKgim7jg130_provenance.
- NP149111.RAWtUYeDcd9H6uKVkflAAxd0g5WxM26bTr_2_Ud8SpRwg130_assertion description "[results show that XT-I polymorphisms potentially confer to the genetic susceptibility of abdominal aortic aneurysm ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149111.RAWtUYeDcd9H6uKVkflAAxd0g5WxM26bTr_2_Ud8SpRwg130_provenance.
- NP149114.RAdKBD4mN3S1h4J4PFzVVQH2BYZv86aLAD0s4PwUuzj5c130_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." NP149114.RAdKBD4mN3S1h4J4PFzVVQH2BYZv86aLAD0s4PwUuzj5c130_provenance.
- NP149115.RAWHcthWmFApEeV_PQ39MHcuaw487sHhsumdpwQv2qVBA130_assertion description "[Patients with viral meningitis showed high concentrations of inosine, guanosine, xanthine, urate and neuron-specific enolase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149115.RAWHcthWmFApEeV_PQ39MHcuaw487sHhsumdpwQv2qVBA130_provenance.
- NP149118.RAZWIuQ68iyxMw3oC6efk_MXPGurZsYStSHUW06ASRH5k130_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." NP149118.RAZWIuQ68iyxMw3oC6efk_MXPGurZsYStSHUW06ASRH5k130_provenance.
- NP149119.RAash3GPr_xUYJIh19EwN8F4JaGjBSxICA_ctS6Q98Qvo130_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." NP149119.RAash3GPr_xUYJIh19EwN8F4JaGjBSxICA_ctS6Q98Qvo130_provenance.
- NP149120.RAZRfdHhI3DPu33iidwBajxUG2MSKUNmyWEUWFT6gmNxg130_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." NP149120.RAZRfdHhI3DPu33iidwBajxUG2MSKUNmyWEUWFT6gmNxg130_provenance.
- NP149122.RASnKizneBbb0VKJ-2psT1UTr_G6EDFaxlY2rSBNbgjlg130_assertion description "[NOS-1 mRNA and protein levels hint that not only NOS-3, but also NOS-1 may be involved in the regulation of systemic hyperdynamic circulation and portal hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149122.RASnKizneBbb0VKJ-2psT1UTr_G6EDFaxlY2rSBNbgjlg130_provenance.
- NP149123.RAT41ZwxtgNDal7b54L89CUPEK0A02s7hWlrWkAxMtuZM130_assertion description "[Elevated serum urotensin II is associated with chronic liver disease and portal hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149123.RAT41ZwxtgNDal7b54L89CUPEK0A02s7hWlrWkAxMtuZM130_provenance.
- NP149127.RAYCctuIo9D7yAPJmtu9XtoSeEwIwd-qsVE_PJPhlNjqM130_assertion description "[Overexpression of CTGF is one of the most important features of idiopathic portal hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149127.RAYCctuIo9D7yAPJmtu9XtoSeEwIwd-qsVE_PJPhlNjqM130_provenance.
- NP149134.RAVTyaBoks-wqCxNzI1EZc8ZyVte6qFsYgPsmRToEnFSY130_assertion description "[During bacterial meningitis, CXCL5 is elevated in cerebrospinal fluid, where it is involved in the recruitment of neutrophils to the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149134.RAVTyaBoks-wqCxNzI1EZc8ZyVte6qFsYgPsmRToEnFSY130_provenance.
- NP149136.RAVBA5bo9uuDCs_hIq2vi902thU7w49wJonX6GpWOXSFA130_assertion description "[Reduced levels of gamma-interferon secretion in response to chlamydial 60 kDa heat shock protein amongst women with pelvic inflammatory disease and a history of repeated Chlamydia trachomatis infections ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149136.RAVBA5bo9uuDCs_hIq2vi902thU7w49wJonX6GpWOXSFA130_provenance.
- NP149137.RAcvPoM3VOaQYJ53NWL3u0vTuAwK9lFPA3fm6WXgPRxZo130_assertion description "[Increased activity of alpha-mannosidase in the peritoneal fluid is associated with gynecologic cancers and pelvic inflammatory disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149137.RAcvPoM3VOaQYJ53NWL3u0vTuAwK9lFPA3fm6WXgPRxZo130_provenance.
- NP149148.RAfD86-2R2lIdf5tcKrTR_Cgteo4oAj6zqIHvROoQpcJM130_assertion description "[Muscle fibers of patients with inclusion body myositis show increased frequencies of Atg8/LC3 (+) autophagosomes and that intracellular amyloid beta-protein colocalized with Atg8/LC3 in degenerating muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149148.RAfD86-2R2lIdf5tcKrTR_Cgteo4oAj6zqIHvROoQpcJM130_provenance.
- NP149167.RAZa2PlJpII0-EhvInjFnXhKZPRzHnQQyDoPKAMcWRh78130_assertion description "[Role of genes TPH2, 5-HTT, and MAOA regulating the serotonin metabolic pathway in the brain stain in the etiopathogenesis of the sudden infant death syndrome was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149167.RAZa2PlJpII0-EhvInjFnXhKZPRzHnQQyDoPKAMcWRh78130_provenance.
- NP149171.RAQd4cn-nOgfk8BTV0RTDDHoT7P02M8TcvhqTE5lhjeZw130_assertion description "[data show that mutant SCN5A channels operate normally under baseline conditions in vitro but abnormally under reduced pH conditions; findings suggest that infants with 2 copies of S1103Y have a 24-fold increased risk for sudden infant death syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149171.RAQd4cn-nOgfk8BTV0RTDDHoT7P02M8TcvhqTE5lhjeZw130_provenance.
- NP149173.RAWTyVrmvb8b6_i7QEhWNXW1amTyKi6h-yOJJlR6et_IY130_assertion description "[Report cardiac SCN5A gene mutations in sudden infant death syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149173.RAWTyVrmvb8b6_i7QEhWNXW1amTyKi6h-yOJJlR6et_IY130_provenance.
- NP149174.RAS1wDS5EfeIGIfHQTHZptDcIdARe4RrR3ialFWu-daos130_assertion description "[The second of 220 SIDs cases was a compound heterozygous for the prevalent MTP G1528C mutation and a novel 1 bp deletion in exon 18 of the MTPalpha-subunit gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149174.RAS1wDS5EfeIGIfHQTHZptDcIdARe4RrR3ialFWu-daos130_provenance.
- NP149179.RAaDnsoKCgHDIyigfIP9tLcE9S504vvPiWoRU7NGLFXTk130_assertion description "[Report cardiac KCNQ1 gene mutations in sudden infant death syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149179.RAaDnsoKCgHDIyigfIP9tLcE9S504vvPiWoRU7NGLFXTk130_provenance.
- NP149181.RAStoiGIQEfLJ1nM87YlNedVAe_Cid5vm3dE-XCNEEVr8130_assertion description "[Finds a link between RyR2 mutations and the alterations of ion channels that may trigger cardiac arrhythmias associated with SIDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149181.RAStoiGIQEfLJ1nM87YlNedVAe_Cid5vm3dE-XCNEEVr8130_provenance.
- NP149185.RAdbjfDnA6OVyR0U4o1zgx8EOZy1L9ddPoojv9zU20sGQ130_assertion description "[Distinct roles for CD39 and P2-purinergic signaling in both tissue remodeling and fibrogenesis with respect to human pancreatic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149185.RAdbjfDnA6OVyR0U4o1zgx8EOZy1L9ddPoojv9zU20sGQ130_provenance.
- NP149188.RAXSzFDVPb62UZJNaqE8W5DpBNpmO_JmfcB-25AORd0DY130_assertion description "[Distinct roles for CD39 and P2-purinergic signaling in both tissue remodeling and fibrogenesis with respect to human pancreatic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149188.RAXSzFDVPb62UZJNaqE8W5DpBNpmO_JmfcB-25AORd0DY130_provenance.
- NP149190.RAbha1ZuDZh9Iq7E65TmMIgyxELoSv5EhUPiq52Xj3QRk130_assertion description "[The prevalence of Foxp3-positive Tregs and dendritic cells was significantly higher in squamous cell carcinoma and Bowen's disease than in actinic keratosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149190.RAbha1ZuDZh9Iq7E65TmMIgyxELoSv5EhUPiq52Xj3QRk130_provenance.