Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP150528.RAWG-G_JVIPo1HMWnRrNltNf10ho3idkGcae-BnUwdvhs130_assertion description "[A patient with familial amyloid polyneuropathy/analysis revealed a heterozygous Glu54Gly substitution (A-to-G change) in the transthyretin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150528.RAWG-G_JVIPo1HMWnRrNltNf10ho3idkGcae-BnUwdvhs130_provenance.
- NP150531.RAfDuZGX_lb9ysxKjz_vk2HxryLL8c7oLucG3rUQIPCNY130_assertion description "[show involvement of ER stress response in familial amyloid polyneuropathy by showing activation of classical unfolded protein response pathways in tissues not specialized in TTR synthesis but presenting extracellular TTR aggregate and fibril deposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150531.RAfDuZGX_lb9ysxKjz_vk2HxryLL8c7oLucG3rUQIPCNY130_provenance.
- NP150542.RAaSoLpu9XQYcliU_t7F47nlkw8q6CfdqAwY80QpCc9Eg130_assertion description "[We report a Chinese patient with amyloidotic polyneuropathy associated with a novel transthyretin mutation (V32A)...likely to be associated with late onset and low-penetrance phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150542.RAaSoLpu9XQYcliU_t7F47nlkw8q6CfdqAwY80QpCc9Eg130_provenance.
- NP150546.RAWEV5tj0EnOn-40aOBTaMl0bwRqYDgkKkBLbm7dHDtLY130_assertion description "[In a large cohort of type 1 diabetic subjects, we found an independent association between serum HSP27 and distal symmetrical polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150546.RAWEV5tj0EnOn-40aOBTaMl0bwRqYDgkKkBLbm7dHDtLY130_provenance.
- NP150557.RAU9SSp9TMQIe6U2uLMjBjH-4xkLa5aIHsVfq8t1bDgMQ130_assertion description "[Genetic variation in RBP4 is associated with amyloid polyneuropathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150557.RAU9SSp9TMQIe6U2uLMjBjH-4xkLa5aIHsVfq8t1bDgMQ130_provenance.
- NP150563.RASnXuv8N31lnbg7A6FY-yQd8at8mLX2wJw1gAVP7sgQ0130_assertion description "[Increased level of MMP-3, MMP-9, and IL-6 may be responsible for ectasia formation in patients with coronary artery ectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150563.RASnXuv8N31lnbg7A6FY-yQd8at8mLX2wJw1gAVP7sgQ0130_provenance.
- NP150568.RAdgVM6SWCPIaTaXhJvyz_D6lppkEhRY8Z_nk8ewre8Ok130_assertion description "[Patients with isolated coronary artery ectasia (CAE) have raised levels of plasma P-selectin, beta-TG and PF4 compared with control participants with angiographically normal coronary arteries, suggesting increased platelet activation in patients with CAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150568.RAdgVM6SWCPIaTaXhJvyz_D6lppkEhRY8Z_nk8ewre8Ok130_provenance.
- NP150570.RAQ7njHPei3C-93-TqyVwgt1dWWNg9cppYw76F6u7iM-8130_assertion description "[Toxoplasma gondii infection resulted in increased activity in the iron response protein IRP1, which, in this state, stabilizes transferrin receptor mRNA from degradation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150570.RAQ7njHPei3C-93-TqyVwgt1dWWNg9cppYw76F6u7iM-8130_provenance.
- NP150585.RAX95gi7UHp1sJmex7m_Yi3kaBejd4Z7Pe0D1vE_rF76o130_assertion description "[HLA-B*27/HLA-B*07 in combination with D6S273-134 allele is associated with increased susceptibility to juvenile spondylarthropathies in Croatian children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150585.RAX95gi7UHp1sJmex7m_Yi3kaBejd4Z7Pe0D1vE_rF76o130_provenance.
- NP150592.RAUwfFbYuTw4VNzXUFA_Kyvo_njOAbC5SUR6V-uxz62m0130_assertion description "[are consistent with data from studies of other HLA-class I alleles associated with HIV control that have shown that the targeting of multiple Gag epitopes is associated with relative suppression of viremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150592.RAUwfFbYuTw4VNzXUFA_Kyvo_njOAbC5SUR6V-uxz62m0130_provenance.
- NP150594.RAes_2qPcfbTErBKLzNcjpugTTAzc-ljyCZVHmlYoRsbM130_assertion description "[Expression of CD38 on CD8+ T cells is associated with poor prognostic outcome in hiv infected individuals with detectable plasma viremia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150594.RAes_2qPcfbTErBKLzNcjpugTTAzc-ljyCZVHmlYoRsbM130_provenance.
- NP150595.RATdddYpJg_MTYWow-kCgfWG6vIBMxzk1Qh5r1U4UiniY130_assertion description "[P-selectin expression, but not activated GPIIb/IIIa, is enhanced in ADP-activated platelets in the inflammatory stage of Takayasu's arteritis/may play a significant role in the inflammatory and thrombotic responses associated with intractable TA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150595.RATdddYpJg_MTYWow-kCgfWG6vIBMxzk1Qh5r1U4UiniY130_provenance.
- NP150599.RASg-BTualCMfdn4EnXp8bTLmfGY6UuuB6P3t7mqP1-gg130_assertion description "[A higher number of activated and IFN-gamma producing gamma delta T-cells are observed in patients with active Takayasu's arteritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150599.RASg-BTualCMfdn4EnXp8bTLmfGY6UuuB6P3t7mqP1-gg130_provenance.
- NP150601.RAcZCB6cG96INYtJL2-qsuRRYBV_Ltc3LcDppYbWdEVgU130_assertion description "[The present results indicate that MMP-2 can be helpful in diagnosing Takayasu arteritis [TA]and that MMP-3 and MMP-9 can be used as activity markers for TA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150601.RAcZCB6cG96INYtJL2-qsuRRYBV_Ltc3LcDppYbWdEVgU130_provenance.
- NP150609.RAag3z9LQcb7yFt-AqJSs5Ua01Hn55LOIej5TH689dYIA130_assertion description "[P-selectin expression, but not activated GPIIb/IIIa, is enhanced in ADP-activated platelets in the inflammatory stage of Takayasu's arteritis/may play a significant role in the inflammatory and thrombotic responses associated with intractable TA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150609.RAag3z9LQcb7yFt-AqJSs5Ua01Hn55LOIej5TH689dYIA130_provenance.
- NP150611.RASkjFl9U0J6QJsVmftBSetgarVv51wGjNPS23UZTQCaM130_assertion description "[Single Nucleotide Polymorphism in interleukin 12 receptor beta 2 is associated with susceptibility to radiation dermatitis in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150611.RASkjFl9U0J6QJsVmftBSetgarVv51wGjNPS23UZTQCaM130_provenance.
- NP150613.RAeazHYW2qNlSV3LHAap6aurfwOX4v9eKvOJAEd_relQ0130_assertion description "[Loss of MMP-2, MMP-3 and FN in lichen planus may be associated with the destruction of the epidermal basal layer and these MMPs may be involved in the pathogenesis of interface dermatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150613.RAeazHYW2qNlSV3LHAap6aurfwOX4v9eKvOJAEd_relQ0130_provenance.
- NP150615.RAckG98lo3GySaTuQ74364ZBIPK8FAunel6dyTCYLRvus130_assertion description "[vanilloid type 3 (TRPV3) channel is crucially involved in pruritic dermatitis [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150615.RAckG98lo3GySaTuQ74364ZBIPK8FAunel6dyTCYLRvus130_provenance.
- NP150616.RAa23W1uaxi-emNLI-b6b73ERnd90CKTWXR9xI3hmB-nQ130_assertion description "[The allele HLA-B*1301 is strongly associated with TCE-induced hypersensitivity dermatitis among exposed workers in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150616.RAa23W1uaxi-emNLI-b6b73ERnd90CKTWXR9xI3hmB-nQ130_provenance.
- NP150618.RAQRdh8Ux7O2fz7CSq-qFnMBEgJKYnuIL0nCOUeBo8wxI130_assertion description "[Single Nucleotide Polymorphism in ABCA1 is associated with susceptibility to radiation dermatitis in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150618.RAQRdh8Ux7O2fz7CSq-qFnMBEgJKYnuIL0nCOUeBo8wxI130_provenance.
- NP150624.RASolckzr2ni0IWMpKUC4YVJEs66LwXPOnNEH01MMwT-c130_assertion description "[Four new CYP21A2 missense mutations (C169R, G178R, W302R, and R426C) in Congenital Adrenal Hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150624.RASolckzr2ni0IWMpKUC4YVJEs66LwXPOnNEH01MMwT-c130_provenance.
- NP150627.RAdJhOSncam-ty6gKw5uV2a9fY1H21Nsbgq2kMflT53zs130_assertion description "[Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150627.RAdJhOSncam-ty6gKw5uV2a9fY1H21Nsbgq2kMflT53zs130_provenance.
- NP150636.RAV0PJXtuvaeuUEXJCoT0eSkgJOHejTE4S1dJ8-Efw7Xc130_assertion description "[Mutations are associated with congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150636.RAV0PJXtuvaeuUEXJCoT0eSkgJOHejTE4S1dJ8-Efw7Xc130_provenance.
- NP150640.RAfoXRLSlzInlL2qKAzcPhc9jUBzjzzv-hLOJkm7N2bzY130_assertion description "[HLA-B18 showed a significant increase in frequency in children with Congenital adrenal hyperplasia -type 21-hydroxylase deficiency ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150640.RAfoXRLSlzInlL2qKAzcPhc9jUBzjzzv-hLOJkm7N2bzY130_provenance.
- NP150647.RASPcnSp9SFH9URqwkrYxrl4eNOqhCVwaIbaA-pbL0Fgk130_assertion description "[there is a strong association in Han Chinese between a genetic marker, the human leukocyte antigen HLA-B*1502, and Stevens-Johnson syndrome induced by carbamazepine, a drug commonly prescribed for the treatment of seizures ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150647.RASPcnSp9SFH9URqwkrYxrl4eNOqhCVwaIbaA-pbL0Fgk130_provenance.
- NP150648.RAb-IXWF8Ps3DzZUrFJPeWvFoxcE1InhDa5bMfMD12HZs130_assertion description "[Increased gelatinase in culture medium of toxic epidermal necrolysis or Stevens-Johnson syndrome skin maintained in organ culture and in blister fluid indicates that these gelatinases may be responsible for detachment of epidermis in these diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150648.RAb-IXWF8Ps3DzZUrFJPeWvFoxcE1InhDa5bMfMD12HZs130_provenance.
- NP150651.RAXmbTBMaf7tsEHaKWoYtSEcr1EyIxdqfPJCE-_kFHVYg130_assertion description "[Case Report: HLA-DQ alpha heterodimers and HLA-DR alleles in tubulointerstitial nephritis and uveitis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150651.RAXmbTBMaf7tsEHaKWoYtSEcr1EyIxdqfPJCE-_kFHVYg130_provenance.
- NP150657.RASrpJcWJnqQ0OnnwLqopquwNTZvbbpSc0t-HHj8mFfFU130_assertion description "[high frequency of HLA-DRB1*1501-DQA1*0102-DQB1*0602 haplotype in paroxysmal nocturnal hemoglobinuria (PNH), including AA-PNH syndrome, and aplastic anemia (AA) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150657.RASrpJcWJnqQ0OnnwLqopquwNTZvbbpSc0t-HHj8mFfFU130_provenance.
- NP150659.RAbnOJ4CbefcKendYntpFAN5bDiRIOYDl4VfKYjXfxYQg130_assertion description "[Paroxysmal nocturnal hemoglobinuria (PNH) is characterized by absence of CD59 from the surface of affected granulocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150659.RAbnOJ4CbefcKendYntpFAN5bDiRIOYDl4VfKYjXfxYQg130_provenance.
- NP150660.RAb6okoUmVM5ux3WUX6t6wezjn6hk-YwiMwUtM984PohY130_assertion description "[Diagnostic significance of measurement of the receptor for urokinase-type plasminogen activator on granulocytes and in plasma from patients with paroxysmal nocturnal hemoglobinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150660.RAb6okoUmVM5ux3WUX6t6wezjn6hk-YwiMwUtM984PohY130_provenance.
- NP150668.RATBnray3eLZOev4K01YfUTFBbIRMEh8PIx2wvbym9o1A130_assertion description "[12 different uromodulin missense mutations were found to lead to defective endoplasmic reticulum to Golgi protein transport, suggesting a common pathogenetic mechanism in medullary cystic kidney disease and familial juvenile hyperuricemic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150668.RATBnray3eLZOev4K01YfUTFBbIRMEh8PIx2wvbym9o1A130_provenance.
- NP150671.RAQ_VWG04C4oNYxKgeVI-3Fw6uiRZSC8bJLGXkvZSCOFs130_assertion description "[TRPP2 has been suggested to function as a mechanosensitive channel that detects fluid flow in the renal tubule lumen, supporting the proposed role of the primary cilium as the unifying pathogenic concept for cystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150671.RAQ_VWG04C4oNYxKgeVI-3Fw6uiRZSC8bJLGXkvZSCOFs130_provenance.
- NP150672.RASWSbtlAeDDhVynD1gJTi8nnVk8IymHo1Qd0EZnPnS_8130_assertion description "[implications for the development of cystic kidney disease [REVIEW]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150672.RASWSbtlAeDDhVynD1gJTi8nnVk8IymHo1Qd0EZnPnS_8130_provenance.
- NP150673.RAS2BKJ6jHFbkkzguyGwx8OPlsw_Jh1wTMbUsVieAjNg0130_assertion description "[COL4A1 may be a candidate gene in unexplained familial syndromes with autosomal dominant hematuria, cystic kidney disease, intracranial aneurysms, and muscle cramps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150673.RAS2BKJ6jHFbkkzguyGwx8OPlsw_Jh1wTMbUsVieAjNg0130_provenance.
- NP150677.RAQ-99WZmCoCfS5CFTD8f7yUBuUctFX8SnpaThlyvavTo130_assertion description "[REVIEW: genetics and roles in normal hemostasis and dysfunction in blood coagulation disorders ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150677.RAQ-99WZmCoCfS5CFTD8f7yUBuUctFX8SnpaThlyvavTo130_provenance.
- NP150680.RAbqBBa6q5AlJezs9aKC0K9D7AI-4TXzj02UUc23nXyrw130_assertion description "[molecular basis of quantitative factor V deficiency associated with haplotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150680.RAbqBBa6q5AlJezs9aKC0K9D7AI-4TXzj02UUc23nXyrw130_provenance.
- NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_assertion description "[mutated in generalized epilepsy and paroxysmal dyskinesia and have implications for the pathogenesis of human epilepsy, the neurophysiology of paroxysmal movement disorders and the role of BK channels in neurological disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_provenance.
- NP150691.RAYt9VeaAgmHkhbNAnvV5ChHitt1xHZPBPYJz-G-dX8gM130_assertion description "[X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150691.RAYt9VeaAgmHkhbNAnvV5ChHitt1xHZPBPYJz-G-dX8gM130_provenance.
- NP150692.RARD8xK9N4gS_xYsYM7ROCGpYRBGIWOppDbskCK4k89f8130_assertion description "[Presented is a pedigree with infancy-onset benign hereditary chorea (BHC) caused by a novel nonsense mutation in exon 3 (523G-- > T, E175X) of the TITF-1 (Nkx2.1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150692.RARD8xK9N4gS_xYsYM7ROCGpYRBGIWOppDbskCK4k89f8130_provenance.
- NP150696.RAab1LXiiboNvLe97ppqnPk_20OysyPsshcFaGXzSe5_E130_assertion description "[High discoidin domain receptor 1 expression is associated with pulmonary sarcoidosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150696.RAab1LXiiboNvLe97ppqnPk_20OysyPsshcFaGXzSe5_E130_provenance.
- NP150700.RAdvZeymzy2bssiP-Ag1HqWSF8qDDutrcSN_31YhpKjIQ130_assertion description "[ACE2 might be involved in the progression of pulmonary sarcoidosis which may depend on gender.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150700.RAdvZeymzy2bssiP-Ag1HqWSF8qDDutrcSN_31YhpKjIQ130_provenance.
- NP150701.RAVtGkLBh38eyqHK3uEY6GPMizCbj4aqZKAlUxTE3CRDM130_assertion description "[IP-10 may play an important role in regulating lymphocytes into the lung and ENA-78 may be associated with lung parenchymal disease in pulmonary sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150701.RAVtGkLBh38eyqHK3uEY6GPMizCbj4aqZKAlUxTE3CRDM130_provenance.
- NP150707.RAeaaY692BBy4cHuqm0rN0ghOAS_AK6TjX5N_Nm4VVANA130_assertion description "[A p.Glu2857X mutation exhibits mild pathogenic effects in COL7A1, and its uniqueness enables detailed analysis and comparison of the destabilizing effects of missense mutations in dystrophic epidermolysis bullosa patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150707.RAeaaY692BBy4cHuqm0rN0ghOAS_AK6TjX5N_Nm4VVANA130_provenance.
- NP150708.RAWQ5lUg6O1_7NKzn8rmuq1Elns1Yt3osit7hj7Vez1gY130_assertion description "[Mutations in the gene for collagen VII (COL7A1) have been documented in both types of dystrophic epidermolysis bullosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150708.RAWQ5lUg6O1_7NKzn8rmuq1Elns1Yt3osit7hj7Vez1gY130_provenance.
- NP150709.RAetiy1E03Ihwl32-T1Hnj3ZiAOya4YZg2ymt_VO2WGvg130_assertion description "[Dystrophic epidermolysis bullosa may present in generalized or localized forms and the disease may be inherited in either autosomal dominant or recessive mode/analysis shows mutations in COL 7A1 in this case ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150709.RAetiy1E03Ihwl32-T1Hnj3ZiAOya4YZg2ymt_VO2WGvg130_provenance.
- NP150714.RAXFM7zkAcwAaeLv7MK2wtD7NFGc7rALDT0sSHe5vzVgc130_assertion description "[Two boys with dystrophic epidermolysis bullosa and their fathers revealed a heterozygous nucleotide G to A transition at position 6109 and 6082 in 73 exon of COL7A1, which resulted in a glycine to arginine substitution (G2037R and G2028R), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150714.RAXFM7zkAcwAaeLv7MK2wtD7NFGc7rALDT0sSHe5vzVgc130_provenance.
- NP150738.RAZ1G4MJKwCjOrLZhhllDCmugcdjV_lfVFastxOlo_kZw130_assertion description "[Cardiovascular malformations, coloboma, and facial asymmetry are common findings in CHARGE syndrome caused by CHD7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150738.RAZ1G4MJKwCjOrLZhhllDCmugcdjV_lfVFastxOlo_kZw130_provenance.
- NP150739.RAVPFyR_JtXuUaLl3CXW6xrJ7pwBuKqJ_fN_jZmAkqad0130_assertion description "[Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma are reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150739.RAVPFyR_JtXuUaLl3CXW6xrJ7pwBuKqJ_fN_jZmAkqad0130_provenance.
- NP150741.RAeEudGEA_KeIe299ShM8-VeMET7Ngay2OuSSs9NX8F7g130_assertion description "[With the exception of iris coloboma, the clinical features (cataracts, microcornea and/or corneal opacity) in all six previously reported families with mutations in the CRYAA gene were found in this family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150741.RAeEudGEA_KeIe299ShM8-VeMET7Ngay2OuSSs9NX8F7g130_provenance.
- NP150751.RAWSbuQnLeY_5vxGNXT-Y2aRd1uoYrs2jkgmX5y_2mCV4130_assertion description "[APOE gene polymorphism as a risk factor for the severity of macular edema in Type 2 diabetes mexican patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150751.RAWSbuQnLeY_5vxGNXT-Y2aRd1uoYrs2jkgmX5y_2mCV4130_provenance.
- NP150752.RAb3ZyLpU4NsXNGSNPN-RhcpYn32ohw12LJ5gnhwHddTM130_assertion description "[VEGF is considered as an important factor in the pathogenesis of macular edema/induces the rupture of the blood retinal barrier and may also influence the retinal pigment epithelial (RPE) outer retinal barrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150752.RAb3ZyLpU4NsXNGSNPN-RhcpYn32ohw12LJ5gnhwHddTM130_provenance.
- NP150756.RAUEXDZeP82ljdHKT5JFc-DNEDVXTYmB938AjGcUT-cHc130_assertion description "[we have now investigated whether the different apolipoprotein E (APO E) genotypes, in pairwise combinations with the MTHFR 677TT or ACE D/D mutation, could lead to an increased risk of leukoaraiosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150756.RAUEXDZeP82ljdHKT5JFc-DNEDVXTYmB938AjGcUT-cHc130_provenance.
- NP150758.RAU2urBhJDJY1GiTFyJ4fi5C9QR7D6z3Oyw_5JI-IqOfw130_assertion description "[We determined the role of 3 potentially functional eNOS polymorphisms (T-786C, intron 4ab, G894T) located toward the 5'flanking end of the gene as risk factors for small vessel disease [SVD]and SVD subtypes: lacunar infarction and ischemic leukoaraiosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150758.RAU2urBhJDJY1GiTFyJ4fi5C9QR7D6z3Oyw_5JI-IqOfw130_provenance.
- NP150761.RAZG9UWLD-aWtdthDzi6EHIzQzjB-l8xTslNEPVghUJpo130_assertion description "[Protein S-100b might be a promising serum marker with prognostic significance in the event of spinal cord compression resulting from epidural empyema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150761.RAZG9UWLD-aWtdthDzi6EHIzQzjB-l8xTslNEPVghUJpo130_provenance.
- NP150764.RAZf-OwlL5lYeSyctWIXBBFT8tWTJo79wXje2oa_J13hI130_assertion description "[The existence of " exonic DNA variants " involving the fibrillin-1 gene in 1 or more exons (exon 24-28) are more pronounced in patients with tetralogy of Fallot and dilated aorta in the presence of abnormal aortic histopathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150764.RAZf-OwlL5lYeSyctWIXBBFT8tWTJo79wXje2oa_J13hI130_provenance.
- NP150765.RAfkUDSZpTuvTDKwvZTOG7s7efyrztiy4GfJu24jBnG78130_assertion description "[Disturbances in both the expression and distribution of Cx43 were found in children with tetralogy of Fallot ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150765.RAfkUDSZpTuvTDKwvZTOG7s7efyrztiy4GfJu24jBnG78130_provenance.
- NP150766.RAecRCdiGuP_PZoQ0Ew5zTOey3MHHGu9eI_CYcu0UsJfg130_assertion description "[a GATA4 mutation may have a role in Tetralogy of Fallot ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150766.RAecRCdiGuP_PZoQ0Ew5zTOey3MHHGu9eI_CYcu0UsJfg130_provenance.
- NP150767.RAXGxsLsXUN25rmpudIvW7BFecFKGoLH-Da-ofRAea4N4130_assertion description "[patients with tetralogy of Fallot having the CC genotype for the p22phox gene may be at a higher state of oxidative stress than T allele carriers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150767.RAXGxsLsXUN25rmpudIvW7BFecFKGoLH-Da-ofRAea4N4130_provenance.
- NP150773.RARqzOMMeCweAnefiTwWKzKhLL-9MPj6eHWAmYlN3uIC0130_assertion description "[Reported is a patient with a congenital myasthenic syndrome due to two compound heterozygous mutations of the CHRNE gene.T ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150773.RARqzOMMeCweAnefiTwWKzKhLL-9MPj6eHWAmYlN3uIC0130_provenance.
- NP150782.RAYj6ynn9cwZb7eD6E00B-t9bFTKzMu9-D2Pr064BLpxk130_assertion description "[findings showed that recessive inheritance of mutations in Dok-7, which result in a defective structure of the neuromuscular junction, is a cause of congenital myasthenic syndromes with proximal muscle weakness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150782.RAYj6ynn9cwZb7eD6E00B-t9bFTKzMu9-D2Pr064BLpxk130_provenance.
- NP150787.RAbgU4qSXcQPMK1PquVwsm0mujD4Aikc0TAMdwQBexeJ8130_assertion description "[Deficiency of and mutations and variations in the complement factor H (CFH) gene are associated with the development of membranoproliferative glomerulonephritis type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150787.RAbgU4qSXcQPMK1PquVwsm0mujD4Aikc0TAMdwQBexeJ8130_provenance.
- NP150814.RAekytuau-RsZaJKiDV_VDEuF_XGuYp0EOh32p6DV2ULM130_assertion description "[Recent advances in epigenetic control of the CDKN1C/KCNQ1OT1 imprinted domain in both humans and mice, causing Beckwith-Wiedemann syndrome and cancer.(review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150814.RAekytuau-RsZaJKiDV_VDEuF_XGuYp0EOh32p6DV2ULM130_provenance.
- NP150825.RASRnJ5lzIiHjcTyZOaVhXvfmIczMfFbRNx8BTI4EDJ7o130_assertion description "[Interaction effect may exist between the serotonin transporter S allele and G-protein beta3 subunit 825T allele in increasing the risk of depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150825.RASRnJ5lzIiHjcTyZOaVhXvfmIczMfFbRNx8BTI4EDJ7o130_provenance.
- NP150828.RAeQOxSQ4H9ZLqiPr4-5qmVwsq3ZLSPHRD3rr_H2yLdzY130_assertion description "[Patients with bipolar disorder and depressive disorder showed a significant variations in genotype and alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150828.RAeQOxSQ4H9ZLqiPr4-5qmVwsq3ZLSPHRD3rr_H2yLdzY130_provenance.
- NP150833.RAR2kHMbcaRdvUdwQ_3mBN6oDTNr87KAjuQohD3dDZ864130_assertion description "[Association of heterozygous mutations in the HFE and HAMP genes could lead to an adult-onset form of primary iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150833.RAR2kHMbcaRdvUdwQ_3mBN6oDTNr87KAjuQohD3dDZ864130_provenance.
- NP150842.RAR1G2BKHiPnPzzQC8g_lr3xoNBDlTJvJfO9XV1VPK0AI130_assertion description "[Intra-leukocytic hemosiderin inclusions (a complex of ferritin, denatured ferritin and other material) are associated with iron overload and acute infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150842.RAR1G2BKHiPnPzzQC8g_lr3xoNBDlTJvJfO9XV1VPK0AI130_provenance.
- NP150850.RAYxZNyZjHp_KBNJJBCJnnhNRZCvGmpFExmP5tlyYPewo130_assertion description "[We review the literature regarding the prevalence, hepatic distribution and possible therapeutic implications of iron overload in chronic hepatitis C, hepatitis B, alcoholic and non-alcoholic fatty liver diseases and porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150850.RAYxZNyZjHp_KBNJJBCJnnhNRZCvGmpFExmP5tlyYPewo130_provenance.
- NP150855.RAQnaeveA1OG2TzZTCbGt3WCGl2V7li8MDojiLqTMNBWw130_assertion description "[C677I mutation is linked to anterior ischemic optic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150855.RAQnaeveA1OG2TzZTCbGt3WCGl2V7li8MDojiLqTMNBWw130_provenance.
- NP150858.RAb36BUrZSJHUz4ewoWgGt4HgQkcKjL4YW29-EPDgE-lA130_assertion description "[Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150858.RAb36BUrZSJHUz4ewoWgGt4HgQkcKjL4YW29-EPDgE-lA130_provenance.
- NP150861.RAWoIbIJbneKWiEEqZ2xPb4oFV3Nbgu8QAFfGKJANyhu4130_assertion description "[A homozygous missense mutation (T7492C) in the SACS gene, which resulted in the substitution of arginine for tryptophan at amino acid residue 2498 (W2498R) was identified in two sibling Japanese early onset spastic ataxia patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150861.RAWoIbIJbneKWiEEqZ2xPb4oFV3Nbgu8QAFfGKJANyhu4130_provenance.
- NP150870.RARSP9Z4MrcTQQO0RiUfgQPEQxgb77p1N7Galyz5-wkFk130_assertion description "[three novel mutations causing MELAS syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150870.RARSP9Z4MrcTQQO0RiUfgQPEQxgb77p1N7Galyz5-wkFk130_provenance.
- NP150871.RAbZ_IxgWM3hM0bUMRuwW-iUGBIcowTZ21M3sHcP-2Ynw130_assertion description "[The EDNRB-30G > A polymorphism could be a determinant of airway obstruction in humans with predisposing factors such as tobacco smoke exposure or asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150871.RAbZ_IxgWM3hM0bUMRuwW-iUGBIcowTZ21M3sHcP-2Ynw130_provenance.
- NP150883.RAaZ0men7AsbnX4a8fZz7ztKGUuWIuNeTD_X1k8_sYxe4130_assertion description "[This report adds further evidence to a continuous spectrum between fatal familial insomnia and CJD thesis from a large German prion pedigree with D178N mutation in the PRNP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150883.RAaZ0men7AsbnX4a8fZz7ztKGUuWIuNeTD_X1k8_sYxe4130_provenance.
- NP150885.RAZgKJJQGw09YdQ35qIrPE_ewjXanksI1XrD6HEpYyU54130_assertion description "[data presented here argue in favor of T188K in PRNP being a pathogenic mutation causing genetic Creutzfeldt-Jakob disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150885.RAZgKJJQGw09YdQ35qIrPE_ewjXanksI1XrD6HEpYyU54130_provenance.
- NP150889.RAW8HQZzg1kqyqjaR4xlmwFOsWXM3re7PJ-afImiegXgM130_assertion description "[Polymorphic microsatellite sites within 148 kb of the human prion gene complex, including the genes PRNP, PRND and PRNT, were analysed together with the Codon129 variants regarding 50 Creutzfeldt-Jakob Disease patients and 46 non-diseased control persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150889.RAW8HQZzg1kqyqjaR4xlmwFOsWXM3re7PJ-afImiegXgM130_provenance.
- NP150895.RAXwGGSeUO6TYIr4cs63-_6coSasey-fdguCI2P0BV7I4130_assertion description "[there are multiple PrP (Sc) conformations in different Creutzfeldt-Jakob disease subtypes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150895.RAXwGGSeUO6TYIr4cs63-_6coSasey-fdguCI2P0BV7I4130_provenance.
- NP150899.RAX3tlqAjSDD7T1mfJWZXsCYkxA7yK5oTdelJ1VvvVPak130_assertion description "[Doppel expression is not modified in the brains of patients with Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150899.RAX3tlqAjSDD7T1mfJWZXsCYkxA7yK5oTdelJ1VvvVPak130_provenance.
- NP150900.RASoCbbSqbg1ATJslhccc-3NPabgu3uwgMSNIg2Ak4eT8130_assertion description "[There were dramatic changes in t-tau protein levels throughout the clinical course of Creutzfeldt-Jakob disease patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150900.RASoCbbSqbg1ATJslhccc-3NPabgu3uwgMSNIg2Ak4eT8130_provenance.
- NP150903.RAbT0Zj9WcLNHbL2IjKWX7RhBKOjUf9upWWUyIekmsdCk130_assertion description "[Immunoreactive patterns of chromogranin A and B [CgA, CgB]were investigated in Creutzfeldt-Jakob disease and Alzheimer's disease/, but not CgA was selectively associated with prion protein deposits, whereas CgA was only seen in amyloid beta plaques ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150903.RAbT0Zj9WcLNHbL2IjKWX7RhBKOjUf9upWWUyIekmsdCk130_provenance.
- NP150907.RAbjAHmFWMUin-psn5nzKwPluJB5o_OJ7QkEcJli0L6cg130_assertion description "[These proteins are important diagnostic biomarkers for CJD, especially in patients with negative 14-3-3 protein findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150907.RAbjAHmFWMUin-psn5nzKwPluJB5o_OJ7QkEcJli0L6cg130_provenance.
- NP150914.RAfsfo1eJivbslXFuisOpR3974xDUmQom2SQrcJC02-H8130_assertion description "[The identification of three novel CNGA3 missense mutations in achromatopsia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150914.RAfsfo1eJivbslXFuisOpR3974xDUmQom2SQrcJC02-H8130_provenance.
- NP150917.RAe3dJU23SQZeDbHiz1DAmczxzOMpSPf5PQxhHFlHI1zc130_assertion description "[Human umbilical cord-derived CD34 (+) cells can be used as a prophylactic agent for experimental heatstroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150917.RAe3dJU23SQZeDbHiz1DAmczxzOMpSPf5PQxhHFlHI1zc130_provenance.
- NP150918.RAcLLVmqGRUftW2aX36Wm-gpMxmBfk9AL7QZeQtgVLOVI130_assertion description "[The levels of plasma PTX3 were increased in patients with arterial inflammation, especially unstable angina pectoris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150918.RAcLLVmqGRUftW2aX36Wm-gpMxmBfk9AL7QZeQtgVLOVI130_provenance.
- NP150919.RAbjDB1MpR9c0r5OSFr2dn8lEoGp4Tpd_sV_7vS6tpXIc130_assertion description "[The elevated serum SSAO activity measured through the detection of the enzyme-generated hydrogen peroxide in HD patients might indicate its contribution to the accelerated atherosclerotic disease observed in uremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150919.RAbjDB1MpR9c0r5OSFr2dn8lEoGp4Tpd_sV_7vS6tpXIc130_provenance.
- NP150924.RAYV5wx5-vwDiUJKGzrA1lk1XBSVTtG4tC102rbDxxyQw130_assertion description "[secreted in cultured osteoblasts from uremia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150924.RAYV5wx5-vwDiUJKGzrA1lk1XBSVTtG4tC102rbDxxyQw130_provenance.
- NP150925.RAcmnA1ENPWZcX2hZ9GcDF3EcDX5lbcia5_qD2vQpon9U130_assertion description "[significant elevation of anti-protein C antibodies and anti-protein S antibodies in the thrombosis group of uremia patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150925.RAcmnA1ENPWZcX2hZ9GcDF3EcDX5lbcia5_qD2vQpon9U130_provenance.
- NP150926.RASF09J-q71ycmZCIgcB3E1i25jvljztrlFRK4F8ASMNQ130_assertion description "[The effects of PrP (106-126) on DCs were elicited through a receptor complex distinct from that used by human monocytes, suggesting an involvement of DCs in prion disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150926.RASF09J-q71ycmZCIgcB3E1i25jvljztrlFRK4F8ASMNQ130_provenance.
- NP150927.RAaa1TvOtZJ2W9z5j-mciMmdjSMBZa_AkhtVfR0Zwepso130_assertion description "[The molecular interactions between PrP and tau protein highlight a potential role of tau in the biological function of PrP and the pathogenesis of transmissible spongiform encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150927.RAaa1TvOtZJ2W9z5j-mciMmdjSMBZa_AkhtVfR0Zwepso130_provenance.
- NP150928.RAZxyX4QIrpkJ5zuekAcTd0uaahvMZ_L5fbOdiAZzPSsc130_assertion description "[study of PrPC-interacting proteins (PrPIPs) by protein microarray analysis; observations suggest a hypothesis that dysregulation of the PrPC interactome may induce neurodegeneration in prion diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150928.RAZxyX4QIrpkJ5zuekAcTd0uaahvMZ_L5fbOdiAZzPSsc130_provenance.
- NP150931.RAXeIevEchl-DXC3795KDuEwnPSv_pM__tMX6PU9vAVzM130_assertion description "[C-terminal globular domain of PrPC has an impact on membrane anchoring and indicates that misfolded secreted forms of the prion protein are linked to inherited prion diseases in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150931.RAXeIevEchl-DXC3795KDuEwnPSv_pM__tMX6PU9vAVzM130_provenance.
- NP150937.RAZD1__Y0YKyVWAc7GewsVSNpiUhGJt2sbuGlJMCUkbv4130_assertion description "[The molecular interactions between PrP and tau protein highlight a potential role of tau in the biological function of PrP and the pathogenesis of transmissible spongiform encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150937.RAZD1__Y0YKyVWAc7GewsVSNpiUhGJt2sbuGlJMCUkbv4130_provenance.
- NP150944.RATSCKuKDDFy4mTjt6mlncasBhc4bdmXnI8Vxbu5BM4-I130_assertion description "[neuropathology and the characteristics of the PrPSc associated with the H187R mutation in Gerstmann-Straussler-Scheinker disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150944.RATSCKuKDDFy4mTjt6mlncasBhc4bdmXnI8Vxbu5BM4-I130_provenance.
- NP150947.RAcNl0x_Ap-hZF2Qiu-mznnOiz_5LRA3QbRScQY99xEW8130_assertion description "[Implicate COMMD1 in the pathogenesis of Wilson's disease and indicate that COMMD1 exerts its regulatory role in copper homeostasis through the regulation of ATP7B stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150947.RAcNl0x_Ap-hZF2Qiu-mznnOiz_5LRA3QbRScQY99xEW8130_provenance.
- NP150952.RAd3lvDT4DzX2bsTSbYi2oKlc2JKWQQN6DDi7bddwF3SQ130_assertion description "[There is concordance between ATP7B mutation and Wilson's disease (WD) phenotype within each family with > 1 member affected with WD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150952.RAd3lvDT4DzX2bsTSbYi2oKlc2JKWQQN6DDi7bddwF3SQ130_provenance.
- NP150961.RAcu7JmztTmAIWR1bHshAiqaRW7XcJIAbgedCKkqF8Tz8130_assertion description "[The upregulation of Loxl2 in Wilson's disease could perhaps be utilized for diagnostic purposes since their expression is up-regulated in hepatocytes even before the onset of fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150961.RAcu7JmztTmAIWR1bHshAiqaRW7XcJIAbgedCKkqF8Tz8130_provenance.
- NP150963.RAQbJhuo9fIZE5F7cgRJtLuhiknVwvOPKwVE8Nuhr7s7c130_assertion description "[Hepatic abnormalities in Long-Evans Cinnamon rats, an animal model of Wilson disease, were restored by the expression of the human ATP7B cDNA under the control of CAG promoter ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150963.RAQbJhuo9fIZE5F7cgRJtLuhiknVwvOPKwVE8Nuhr7s7c130_provenance.
- NP150964.RAQikWaz4rNTYceGiCilVftYHQOC1y6ECwaRJHyvqA0Ak130_assertion description "[Upregulation of Lox in Wilson's disease could perhaps be utilized for diagnostic purposes since their expression is up-regulated in hepatocytes even before the onset of fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150964.RAQikWaz4rNTYceGiCilVftYHQOC1y6ECwaRJHyvqA0Ak130_provenance.
- NP150973.RAfqUHScF0D-2C5FzBlN9pn3cDNnqPsg3nEjN0453a1TQ130_assertion description "[Levels of interleukin-1beta and Il1R2in the peritoneal fluid of normal women and patients with endometriosis suffering from pelvic pain and infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150973.RAfqUHScF0D-2C5FzBlN9pn3cDNnqPsg3nEjN0453a1TQ130_provenance.
- NP150977.RAc7JGJKWZD9BVisKKGXRJRVEZTqkkzf39_yifcclMsa8130_assertion description "[These findings suggest that the G allele containing variants of ESR1 XbaI and the G allele containing variants of ESR2 2681-4A > G may decrease the risk of hypospadias, whereas the ESR1 C-A haplotype may increase its risk ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150977.RAc7JGJKWZD9BVisKKGXRJRVEZTqkkzf39_yifcclMsa8130_provenance.
- NP150978.RAVyd2KufT1U9hp8DK4_UnVxjAQ4FcWtaveKol2Mq33Gs130_assertion description "[results suggest that variations in the ESR2 might influence susceptibility to hypospadias ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150978.RAVyd2KufT1U9hp8DK4_UnVxjAQ4FcWtaveKol2Mq33Gs130_provenance.