Nanopublications LDF server

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

• NP147473.RAq4CEPx8L-geUhP6bfM3kLsL5dHEEXvDLynyYWCsnnis130_assertion description "[GFAP was strong expression in both reactive astrocytes and astrocytomas/of both GFAP is more focal in oligodendrogliomas, with staining of mainly intervening astrocytic processes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147473.RAq4CEPx8L-geUhP6bfM3kLsL5dHEEXvDLynyYWCsnnis130_provenance.
• NP147474.RAp78M0Mjvh6L4BsrrUJ3dj9LOyBBncXfAFIYQhkNmC6k130_assertion description "[Data show that the very high frequency of IDH1 mutations occurrs in diffuse astrocytomas, oligodendrogliomas, oligoastrocytomas and secondary glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147474.RAp78M0Mjvh6L4BsrrUJ3dj9LOyBBncXfAFIYQhkNmC6k130_provenance.
• NP147475.RAnMChLKrFh3tyNonw4s0NjC28UlBykeYS6qn66ASlCLg130_assertion description "[DFFB haploinsufficiency from 1p allelic loss is a contributing factor in oligodendroglioma development ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147475.RAnMChLKrFh3tyNonw4s0NjC28UlBykeYS6qn66ASlCLg130_provenance.
• NP147476.RAilGBhTmezckKz-ZyeeZ0WpOQ0Q75ojdEmtPnI9l3A58130_assertion description "[results from the immunohistochemical analyses of rPTPbeta/zeta expression should prompt further evaluation of this protein as a novel oligodendroglioma marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147476.RAilGBhTmezckKz-ZyeeZ0WpOQ0Q75ojdEmtPnI9l3A58130_provenance.
• NP147478.RApB2boT7VHzbeeofLeo5sZkW3ObAkyVj1CPG1G2aNjps130_assertion description "[Expression of Bcl-x was strongly expression in both reactive astrocytes and astrocytomas/of Bcl-x is more focal in oligodendrogliomas, with staining of mainly intervening astrocytic processes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147478.RApB2boT7VHzbeeofLeo5sZkW3ObAkyVj1CPG1G2aNjps130_provenance.
• NP147480.RAlBmMtBhjAd2nBOUD_J3qCpz3kBTZG80nS4hTicLQqyU130_assertion description "[Underexpression of rho GDP dissociation inhibitor alpha is associated with oligodendroglioma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147480.RAlBmMtBhjAd2nBOUD_J3qCpz3kBTZG80nS4hTicLQqyU130_provenance.
• NP147483.RAuDopCMrFY0SkXRHZWEepK6VKmpXRsSoaRdp8UfmGdAI130_assertion description "[expressed by cells of the oligodendrocyte lineage in vitro and by oligodendrogliomas in vivo; could play a role in migration of tumor cells in oligodendrocytic tumors ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147483.RAuDopCMrFY0SkXRHZWEepK6VKmpXRsSoaRdp8UfmGdAI130_provenance.
• NP147486.RAoN6e-pkUMKvpD0ZE8t69JL9IHSEOUT385f3gD0nNzcM130_assertion description "[GSTP1 and GSTM1 polymorphisms have a role in survival from anaplastic astrocytoma, anaplastic oligodendroglioma, and anaplastic oligoastrocytoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147486.RAoN6e-pkUMKvpD0ZE8t69JL9IHSEOUT385f3gD0nNzcM130_provenance.
• NP147489.RAjMtepc0gSOwbl56e0EhVqnn3ryYjMHTZadD05Eu-LrU130_assertion description "[Comparative genomic hybridization and immunohistochemical assessment of EGFR, PTEN, p53, and MIB-1 expression in 13 oligodendrogliomas, one oligoastrocytoma and 23 high-grade astrocytomas is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147489.RAjMtepc0gSOwbl56e0EhVqnn3ryYjMHTZadD05Eu-LrU130_provenance.
• NP147490.RAmw5_C3KQ9ODCtfvZP37AjOZEJYGv_-3xOy5EC5GL_qM130_assertion description "[overexpression of peroxiredoxin 6 is associated with oligodendroglioma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147490.RAmw5_C3KQ9ODCtfvZP37AjOZEJYGv_-3xOy5EC5GL_qM130_provenance.
• NP147495.RAmAdH6EAqbJIrJ8-6iC9Awuc2mSYGtyAgCdGiPv62Hp4130_assertion description "[study identified two novel ABCA12 mutations in two unrelated non-bullous congenital ichthyosiform erythroderma patients; both patients presented with multiple skin malignancies including malignant melanoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147495.RAmAdH6EAqbJIrJ8-6iC9Awuc2mSYGtyAgCdGiPv62Hp4130_provenance.
• NP147507.RAutWp2dMyM965QIgCoHnuwKs-K2gT3s_yPXP8IsEFXXA130_assertion description "[Polymorphism of the angiotensin-converting enzyme gene is associated with metabolic syndrome X [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147507.RAutWp2dMyM965QIgCoHnuwKs-K2gT3s_yPXP8IsEFXXA130_provenance.
• NP147508.RAvxbHcVDxVywVC_qnKwEPowhtOUIua2XWpoqMkUx34WM130_assertion description "[adipose tissue can be recognized as a source of CT-1, which could account for the high circulating levels of CT-1 in patients with metabolic syndrome X ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147508.RAvxbHcVDxVywVC_qnKwEPowhtOUIua2XWpoqMkUx34WM130_provenance.
• NP147510.RAuvygmO5dpOIBAes2mwqzvc0Ss8ycs_3w0ZzXpuWOMvI130_assertion description "[A total of 45% of participants (80 of 177) in the highest quartile of fetuin-A had metabolic syndrome X compared with 24% of participants (42 of 177) in the lowest quartile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147510.RAuvygmO5dpOIBAes2mwqzvc0Ss8ycs_3w0ZzXpuWOMvI130_provenance.
• NP147514.RAuQrYO0u2bAvSbVSgo4s5uCGNBANncwwUkwlXFgx8vo0130_assertion description "[Apolipoprotein C-III and E polymorphisms and cardiovascular syndrome, hyperlipidemia, and insulin resistance in renal transplantation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147514.RAuQrYO0u2bAvSbVSgo4s5uCGNBANncwwUkwlXFgx8vo0130_provenance.
• NP147523.RAjhJNIminu7lca_F0WPEL7iZPdrNjpnN3GqLrO884vjc130_assertion description "[Plays an essential role for development of hyperlipidemia and atherosclerosis as a result of degradation of apolipoprotein E.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147523.RAjhJNIminu7lca_F0WPEL7iZPdrNjpnN3GqLrO884vjc130_provenance.
• NP147528.RAjYmtyPGjpVKAQhVnqcj4J-hS5D3FxBCBdQWitcaSIjY130_assertion description "[results imply that systemic elevation of lipoprotein lipase expression may be potentially useful for the treatment of hyperlipidemias, obesity, and insulin resistance ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147528.RAjYmtyPGjpVKAQhVnqcj4J-hS5D3FxBCBdQWitcaSIjY130_provenance.
• NP147531.RArWZzLCaCJjrK_ZalDpT39x3id4RmAq5w_1d4DMgiFg8130_assertion description "[Oncostatin M directly lowers the plasma triglycerides in hyperlipidemia by stimulating the transcription of ACSL3/5 in the liver.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147531.RArWZzLCaCJjrK_ZalDpT39x3id4RmAq5w_1d4DMgiFg8130_provenance.
• NP147532.RAoV0EUyWbYZUhvkzU-eJhjhwWBPqNfkScWN3AzqeSvvs130_assertion description "[Hyperlipidemia, exhibited as a high free fatty acid level, modulates GLUT4 gene expression in cardiac muscle via a complex mechanism including GLUT4 and the PPARgamma genes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147532.RAoV0EUyWbYZUhvkzU-eJhjhwWBPqNfkScWN3AzqeSvvs130_provenance.
• NP147536.RAlcyzuVjYPZvW09RaIMHWVqh5G9C2BdR5_7PfNdIBA8A130_assertion description "[Report the anticoagulant effect of dietary fish oil in hyperlipidemia: a study of hepatic gene expression in apolipoprotein E2 (APOE2) knock-in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147536.RAlcyzuVjYPZvW09RaIMHWVqh5G9C2BdR5_7PfNdIBA8A130_provenance.
• NP147542.RAoxeCSz5UM1R_Nu_KQ7IrCi7waJhIWoKs0EyGNj2j66A130_assertion description "[Carboxypeptidase E degradation contributes to palmitate-induced beta-cell ER stress and apoptosis; CPE is a major link between hyperlipidemia and beta-cell death pathways in diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147542.RAoxeCSz5UM1R_Nu_KQ7IrCi7waJhIWoKs0EyGNj2j66A130_provenance.
• NP147547.RAq2fMJQ8kfgTrGbWEj_xHstUKpKtQkbF9VR-fBs1cpGE130_assertion description "[study demonstrates that the Ret Gly691Ser mutation is associated with primary vesicoureteral reflux and may be one of the genetic causes of this condition in the French-Canadian population in Quebec ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147547.RAq2fMJQ8kfgTrGbWEj_xHstUKpKtQkbF9VR-fBs1cpGE130_provenance.
• NP147549.RArt6SSztsx3Ps_XvRTh4__RqK6Gp-uJs1zKOb1ZeLWJQ130_assertion description "[VEGF-A/TGF-beta1 polymorphisms could be genetic markers of the process of urinary tract infection and vesicoureteral reflux.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147549.RArt6SSztsx3Ps_XvRTh4__RqK6Gp-uJs1zKOb1ZeLWJQ130_provenance.
• NP147551.RApDutpLBU3YeBmJm3VECGfXNk6xCNsUZ-G2ohwdoDvNg130_assertion description "[43 novel mutations in COL1A1 and COL1A2 are found in patients with type II osteogenesis imperfecta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147551.RApDutpLBU3YeBmJm3VECGfXNk6xCNsUZ-G2ohwdoDvNg130_provenance.
• NP147562.RAnmrQw9kFvl-HjOoOteVLcjS7M1YDQQEGOBn64h1RW2I130_assertion description "[Mutations were identified in nine COL1A1/COL1A2 associated with osteogenesis imperfecta type I-IV genes by scanning with DHPLC ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147562.RAnmrQw9kFvl-HjOoOteVLcjS7M1YDQQEGOBn64h1RW2I130_provenance.
• NP147563.RAiaDaYWGPY-ohHcelIHrX0O5KSiLxmwhg-M4dm_OoBeQ130_assertion description "[This study is the first report that osteogenesis imperfecta is associated with the mutation Q644X of COL1A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147563.RAiaDaYWGPY-ohHcelIHrX0O5KSiLxmwhg-M4dm_OoBeQ130_provenance.
• NP147569.RAhBQRgJ8P1JMjfJQSx3DqiF7nwZcuEaJOkBAR3PLx9t0130_assertion description "[Screening of 78 subjects diagnosed with osteogenesis imperfecta type II or III, identified three probands with mutations in CRTAP and 16 with mutations in LEPRE1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147569.RAhBQRgJ8P1JMjfJQSx3DqiF7nwZcuEaJOkBAR3PLx9t0130_provenance.
• NP147575.RAo1BlLBHCuua3C7UCmbklFCbwLs9VjEd6GyXj-m3CfsU130_assertion description "[An R27Q missense mutation in the CAV3 gene can lead to various clinical phenotypes including hyper-CK-emia, rippling muscle disease, distal myopathy, and limb-girdle musclar dystrophy 1C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147575.RAo1BlLBHCuua3C7UCmbklFCbwLs9VjEd6GyXj-m3CfsU130_provenance.
• NP147576.RApPB5VgIYmRQ20_GrX8j-GQw4t1KxETWDM9Tljv8L0DU130_assertion description "[A heterozygous 80 G-- > A substitution in the caveolin-3 gene is associated with sporadic distal myopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147576.RApPB5VgIYmRQ20_GrX8j-GQw4t1KxETWDM9Tljv8L0DU130_provenance.
• NP147578.RAojmG8n3eKwkB3E6FbQtdnTK4K-xaz_RexsiYDnLkRDQ130_assertion description "[GNE mutation develops distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147578.RAojmG8n3eKwkB3E6FbQtdnTK4K-xaz_RexsiYDnLkRDQ130_provenance.
• NP147583.RAtCTUmE0u67_RCHihwzEQ0LPj7wYIyPRtAjWeKSy8OT4130_assertion description "[The dysferlin gene, a strong candidate gene responsible for two other distal myopathies in the same region, is located centromeric to PAC3-H52 and can thereby formally be excluded as cause for Welander distal myopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147583.RAtCTUmE0u67_RCHihwzEQ0LPj7wYIyPRtAjWeKSy8OT4130_provenance.
• NP147586.RAo_rFozYwyi3V9bjh1YtfJd9zmG4gjeZEAljY34-FHnQ130_assertion description "[Tibial muscular dystrophy patients with truncating mutations in C-terminal titin show a more severe phenotype with earlier onset implying a genotype-phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147586.RAo_rFozYwyi3V9bjh1YtfJd9zmG4gjeZEAljY34-FHnQ130_provenance.
• NP147587.RAovtMiqRXtbqhV3GHqf_DWuw2wuW2t8GIwAF95pCiLi8130_assertion description "[Shows a higher methylation in all six patients with familial partial lipodystrophy when compared with progeria patients with other LMNA mutations as well as the healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147587.RAovtMiqRXtbqhV3GHqf_DWuw2wuW2t8GIwAF95pCiLi8130_provenance.
• NP147590.RAvCvuIsfg1Deq3YDGZFjVH5_s0c7r9gY7rA6EeoCgHMY130_assertion description "[LMNA p.G608G mutation results in a uniform phenotype through early to mid-childhood, in keeping with that described in classical Hutchinson-Gilford progeria syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147590.RAvCvuIsfg1Deq3YDGZFjVH5_s0c7r9gY7rA6EeoCgHMY130_provenance.
• NP147594.RArppjrqGW2MZAtrj34sgGyyMeXK1t0Snkx6EpQlLwBjc130_assertion description "[Unusual LMNA mutations associated with severe progeria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147594.RArppjrqGW2MZAtrj34sgGyyMeXK1t0Snkx6EpQlLwBjc130_provenance.
• NP147597.RAskxJYenFMBGg9cFVxojDAgVbfJkLvmbmPcl-1xrcJ98130_assertion description "[Expression of progerin leads to alterations in nuclear morphology, which may underlie pathology in Hutchinson-Gilford progeria syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147597.RAskxJYenFMBGg9cFVxojDAgVbfJkLvmbmPcl-1xrcJ98130_provenance.
• NP147598.RAi-XWm4rE7cqBACUSG1s920TD4FyUvctAJ-FCAvmL9Og130_assertion description "[partial splice site selection in Hutchinson-Gilford progeria syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147598.RAi-XWm4rE7cqBACUSG1s920TD4FyUvctAJ-FCAvmL9Og130_provenance.
• NP147604.RAsK_oiQawmLPE2H68_39YPHxbgyFnhZ_Wy_7WZl04gEE130_assertion description "[Secretion levels of sIL-2R, IL-6, IL-8, IL-10, and TNF-alpha, but not IL-4 and IL-12, are elevated in activated T-cells in large granular lymphocytic leukemia associated with autoimmune disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147604.RAsK_oiQawmLPE2H68_39YPHxbgyFnhZ_Wy_7WZl04gEE130_provenance.
• NP147606.RAmJwhDEJ4iXIN0dN_IJNV5H3vlkKqxWpZYGmp9y-AJ6U130_assertion description "[analysis of expression on leukocytes, hematopoietic cell lines, and a variety of myeloid and lymphoid leukemias ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147606.RAmJwhDEJ4iXIN0dN_IJNV5H3vlkKqxWpZYGmp9y-AJ6U130_provenance.
• NP147609.RAnNKCxQg16f6a2ElQ8SDMaLBsAEIOGf2Nbzj5tNa1zEM130_assertion description "[E2a-Pbx1 and Bmi-1 are likely to play a role in the pathogenesis of human lymphoid leukemias through downregulation of the INK4A-ARF gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147609.RAnNKCxQg16f6a2ElQ8SDMaLBsAEIOGf2Nbzj5tNa1zEM130_provenance.
• NP147611.RAsMM5wD7w6FS9CfY4yC-EEa9Nqm6wi-6eTpw-imDmgs8130_assertion description "[The interplay between Syk and ZAP-70 in thymocytes, certain T cells, and B-chronic lymphocytic leukemia cells will modulate the amplitude of antigen-mediated receptor signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147611.RAsMM5wD7w6FS9CfY4yC-EEa9Nqm6wi-6eTpw-imDmgs8130_provenance.
• NP147615.RAgzRbjJQmKOzDhydXPZAdFK7iiPbLl2IVldxDM_lD3E8130_assertion description "[IRTA4/FcRH2 expression as detected by flow cytometry was significantly lower in the poor prognosis subgroup as compared to ZAP-70-CD38- B-chronic lymphocytic leukemia cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147615.RAgzRbjJQmKOzDhydXPZAdFK7iiPbLl2IVldxDM_lD3E8130_provenance.
• NP147617.RAhuikQvVkNdezOa0Phs2D5xfMW4pfhbUSf5YGFzTFjeU130_assertion description "[Hypermethylation of the p15INK4b gene promoter in B-chronic lymphocytic leukemia was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147617.RAhuikQvVkNdezOa0Phs2D5xfMW4pfhbUSf5YGFzTFjeU130_provenance.
• NP147623.RApt4QSmlsP6TN5Vqpn1uErsqilF3KRZVcgDRDEIHhzH4130_assertion description "[COX-2 overexpression likely represents an additional mechanism of resistance to apoptosis in B chronic lymphoid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147623.RApt4QSmlsP6TN5Vqpn1uErsqilF3KRZVcgDRDEIHhzH4130_provenance.
• NP147624.RAgg7Tx9A76XQpeXsXusoJqRfmflSTcCNIy3aWSGJo2UQ130_assertion description "[In lymphocytes obtained from healthy persons more t-PA and PAI-1 was detected than in lymphocytes from patients with chronic lymphoid leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147624.RAgg7Tx9A76XQpeXsXusoJqRfmflSTcCNIy3aWSGJo2UQ130_provenance.
• NP147628.RAqG7FY96Yu_TdL_81OKP7H57A3hIh6treRS70FwOvG9k130_assertion description "[Secretion levels of sIL-2R, IL-6, IL-8, IL-10, and TNF-alpha, but not IL-4 and IL-12, are elevated in activated T-cells in large granular lymphocytic leukemia associated with autoimmune disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147628.RAqG7FY96Yu_TdL_81OKP7H57A3hIh6treRS70FwOvG9k130_provenance.
• NP147629.RAkRBA-L65kkYeyKQpFkxS1SMlwiHWaZLv7-MSgTyY6MU130_assertion description "[prognostic significance of soluble CD23 in advanced stages of B-chronic lymphocytic leukemia and its role as an indicator for aggressive or indolent courses of disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147629.RAkRBA-L65kkYeyKQpFkxS1SMlwiHWaZLv7-MSgTyY6MU130_provenance.
• NP147630.RAon8PcqUkbt5QALhOgLWqyr7XTcKO4FEueAbQi431Rps130_assertion description "[IRTA4/FcRH2 expression as detected by flow cytometry was significantly lower in the poor prognosis subgroup as compared to ZAP-70-CD38- B-chronic lymphocytic leukemia cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147630.RAon8PcqUkbt5QALhOgLWqyr7XTcKO4FEueAbQi431Rps130_provenance.
• NP147639.RAvbmQOzFls4DRXegil9GZ4PcBJZA3dZoajUxon_-qrHQ130_assertion description "[This review examines new concepts underlying fractalkine-mediated leukocyte migration and tissue damage, focusing primarily on the pathophysiological roles of fractalkine in rheumatic diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147639.RAvbmQOzFls4DRXegil9GZ4PcBJZA3dZoajUxon_-qrHQ130_provenance.
• NP147643.RAnOkOyWWpKBPwlt0vZC9PIfCZvSRrZMcvn6cQOk1k9u8130_assertion description "[Sequencing of the entire coding region and splice junctions of AKT2 and the relationship of genetic variations in the gene with multiple metabolic diseases is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147643.RAnOkOyWWpKBPwlt0vZC9PIfCZvSRrZMcvn6cQOk1k9u8130_provenance.
• NP147644.RAoe-izCZufIW7KZDpcW1NG8nO0I-6NzZ158yvgQbUFjQ130_assertion description "[Improvement and restoration of mitochondrial function and oxidative capacity through activation of PGC-1 alpha could provide new treatments for metabolic diseases, as suggested by the evidence in this review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147644.RAoe-izCZufIW7KZDpcW1NG8nO0I-6NzZ158yvgQbUFjQ130_provenance.
• NP147646.RAkNLLdts8Kl3tDPGatV7aDRqZGd6yJMWrIEo8u1i1gXk130_assertion description "[direct regulation of hypoxia-inducible factor 1 alpha subunit stability by GSK-3 may influence physiological processes or pathophysiological situations such as metabolic diseases or tumors ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147646.RAkNLLdts8Kl3tDPGatV7aDRqZGd6yJMWrIEo8u1i1gXk130_provenance.
• NP147659.RAjG4uAO0XkIKAEcRV-Sbm8-JvlG65H67Zxz3yZHQyEmc130_assertion description "[the PPARG Pro12Ala polymorphism might represent a genetic susceptibility factor for preterm birth and constitute a link between preterm birth and metabolic diseases later in life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147659.RAjG4uAO0XkIKAEcRV-Sbm8-JvlG65H67Zxz3yZHQyEmc130_provenance.
• NP147662.RAufXhGC3bp38hdlu6m8WSIW2ooVnWGcdWDgTPKQwRd3M130_assertion description "[This report of two novel WFS1 mutations expands the molecular spectrum of Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147662.RAufXhGC3bp38hdlu6m8WSIW2ooVnWGcdWDgTPKQwRd3M130_provenance.
• NP147664.RAsWsH3dLh-Lbc27qgiPb0o3sunBv7VX-r9lDEWg1hxKU130_assertion description "[Results reported eight novel WFS1 mutations in Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147664.RAsWsH3dLh-Lbc27qgiPb0o3sunBv7VX-r9lDEWg1hxKU130_provenance.
• NP147665.RAr8_-ZAXBAlDmWDz4xfGB92X7Jh5OboT-qD_YB4eZHVM130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147665.RAr8_-ZAXBAlDmWDz4xfGB92X7Jh5OboT-qD_YB4eZHVM130_provenance.
• NP147666.RAlAcnv1m1TRWUVJ1DEbaXv3Ule1czlHwYNJf6rtl_Bjc130_assertion description "[Mutations in one single gene, Wolfram syndrome 1 (WFS1), have been reported to account for most familial cases with low-frequency hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147666.RAlAcnv1m1TRWUVJ1DEbaXv3Ule1czlHwYNJf6rtl_Bjc130_provenance.
• NP147668.RAuT3oD88cQNZfHC-mYu8JKda2hZit5aJ_tYGbIcXeJZk130_assertion description "[most causative changes identified in the WFS1 gene occurred in exon 8, and only one was identified outside this region in exon 4 in patients with Wolfram syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147668.RAuT3oD88cQNZfHC-mYu8JKda2hZit5aJ_tYGbIcXeJZk130_provenance.
• NP147672.RApScd0UpJs5yvcIkVjAHvKS5FthRdTGDUmc76q8fsA_g130_assertion description "[The WFS1 gene is located on the short arm of chromosome 4 in Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147672.RApScd0UpJs5yvcIkVjAHvKS5FthRdTGDUmc76q8fsA_g130_provenance.
• NP147676.RAjMGGgRk7L64c9LSddJdKe1TMBkdzVNvP17-AWqTOnOk130_assertion description "[This study does not support the involvement of tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147676.RAjMGGgRk7L64c9LSddJdKe1TMBkdzVNvP17-AWqTOnOk130_provenance.
• NP147677.RAtRDeT80mEjH-yfcR1zAncwMEuh_R83nQM3Ei2wEkno8130_assertion description "[CRMP1 and EVC genes are located near WFS1, the Wolfram syndrome type 1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147677.RAtRDeT80mEjH-yfcR1zAncwMEuh_R83nQM3Ei2wEkno8130_provenance.
• NP147684.RAv0_2LfpWixCPM_94oU_tQZRiYkGvODldnPBbDksGM3o130_assertion description "[COX-2 is overexpressed in ependymomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147684.RAv0_2LfpWixCPM_94oU_tQZRiYkGvODldnPBbDksGM3o130_provenance.
• NP147686.RAh0frgp0YPM7tbYpvz881v8JP5ZEwzKSDBamqylG3MPc130_assertion description "[4.1B gene deletion was statistically more common in ependymomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147686.RAh0frgp0YPM7tbYpvz881v8JP5ZEwzKSDBamqylG3MPc130_provenance.
• NP147687.RAkLVAhdUu1cRmw9lVVSXRNKlsWIbn9XXKcPt4PFemW2E130_assertion description "[4.1R loss of expression was statistically more common in ependymomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147687.RAkLVAhdUu1cRmw9lVVSXRNKlsWIbn9XXKcPt4PFemW2E130_provenance.
• NP147691.RArUwoXusPK6ZpphzmyvpNiPs-7D_NGbWJ_44n8goImgM130_assertion description "[Disruption of the STK9 gene causes severe X-linked infantile spasms and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147691.RArUwoXusPK6ZpphzmyvpNiPs-7D_NGbWJ_44n8goImgM130_provenance.
• NP147694.RAgJhfkjQoRdcCOSmqf0Bnrln-6_NndNuw3ietKXRROqc130_assertion description "[people with TSC2 mutations were significantly more likely than those with TSC1 mutations to have autistic disorder, a low IQ, and a history of infantile spasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147694.RAgJhfkjQoRdcCOSmqf0Bnrln-6_NndNuw3ietKXRROqc130_provenance.
• NP147701.RAqENIl9tKB0ih9WQpC_A9_AzwPvAmGowC1u5w9TJm04c130_assertion description "[Considering genotype-phenotype correlation, we suggest screening of the most common mutation, the c.428 _ 451 dup mutation by PCR, in patients with infantile spasm syndrome, Partington syndrome and non-syndromic X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147701.RAqENIl9tKB0ih9WQpC_A9_AzwPvAmGowC1u5w9TJm04c130_provenance.
• NP147706.RAgSXERTGCGERuLaM9pI-IFc9RFSE3eqLDEDSQU5yb8tE130_assertion description "[A novel missense mutation at position c.134T > A resulting in amino acid change at codon V45E in Norrie disease with neurological disorder and infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147706.RAgSXERTGCGERuLaM9pI-IFc9RFSE3eqLDEDSQU5yb8tE130_provenance.
• NP147711.RAvh-CBPhRezPNrh20Z40cd1IPtV2ib19rAIfFuDbofJY130_assertion description "[prothrombin G20210A mutation is a risk factor in patients with persistent foramen ovale and otherwise unexplained cerebral ischemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147711.RAvh-CBPhRezPNrh20Z40cd1IPtV2ib19rAIfFuDbofJY130_provenance.
• NP147712.RAmQaREACZa0Q-3x-x1908kyP255LRMU5O3GeRlr_qf3A130_assertion description "[study suggests that PrPC has physiological relevance to cerebral ischemic injury and could be useful as a therapeutic target for the treatment of cerebral ischemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147712.RAmQaREACZa0Q-3x-x1908kyP255LRMU5O3GeRlr_qf3A130_provenance.
• NP147718.RArG1AZ2Vch7dRA8c1oW45a3uYqwOkB0FsvuLe5A6SsO8130_assertion description "[Elevated serum MMP-9 in systemic lupus erythematosus may reflect neuropsychiatric involvement, particularly cognitive dysfunction/MMP-9 concentration may be associated with small-vessel cerebral vasculopathy and risk of cerebral ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147718.RArG1AZ2Vch7dRA8c1oW45a3uYqwOkB0FsvuLe5A6SsO8130_provenance.
• NP147720.RAp7GY0TvQMFUwsXUQW9XPWMuYctbMuSzI4I0s_DwOwHs130_assertion description "[Midkine is expressed in astrocytes during the early period of human brain ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147720.RAp7GY0TvQMFUwsXUQW9XPWMuYctbMuSzI4I0s_DwOwHs130_provenance.
• NP147721.RAlGUCDH5cOZNjwz6ZB_pYCp1UfH5YqOnUuGDfMRYyDZ4130_assertion description "[Results point out that brain-specific angiogenesis inhibitor 2 controls VEGF transcription through GA-binding protein under normal conditions and cerebral ischemia [GA-binding protein gamma].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147721.RAlGUCDH5cOZNjwz6ZB_pYCp1UfH5YqOnUuGDfMRYyDZ4130_provenance.
• NP147723.RAtKODmiHvYfCZt-uQDKZ_eQHnCwjJ1JdfI80TGk85s3g130_assertion description "[Overexpression of transgenic SOD1 in hyperglycemic rats reduces blood-brain barrier permeability and matrix metalloproteinase-9 activation after transient focal cerebral ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147723.RAtKODmiHvYfCZt-uQDKZ_eQHnCwjJ1JdfI80TGk85s3g130_provenance.
• NP147730.RAuMM9E_mOZ0t6qV8GsUbA-pgM8IjCSDsPkFNivCaz5vs130_assertion description "[EPO contributes to regulation of hypothalamo-pituitary-adrenal (HPA) axis activation; in pathological conditions such as brain ischemia, this growth factor may control HPA axis function, preventing possible detrimental effects of HPA overactivation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147730.RAuMM9E_mOZ0t6qV8GsUbA-pgM8IjCSDsPkFNivCaz5vs130_provenance.
• NP147731.RAppwiOf3FtdjA0I3sLg9rskoUAsljTZlX1yBHr3KV-vk130_assertion description "[Direct AT (1) inhibition and indirect AT (2) receptor stimulation are associated factors normalizing cerebrovascular compliance, reducing cerebrovascular inflammation and decreasing the vulnerability to brain ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147731.RAppwiOf3FtdjA0I3sLg9rskoUAsljTZlX1yBHr3KV-vk130_provenance.
• NP147743.RAluAI3Z3082a7ZeDXjhipPe8xHnpEoFAc4CQSzCgQAjA130_assertion description "[A Bence Jones V kappa l light chain monoclonal antibody fragment is reported that is responsible for myeloma-associated proximal tubulopathy with increased phosphaturia manifested as tubular acidosis and phosphate loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147743.RAluAI3Z3082a7ZeDXjhipPe8xHnpEoFAc4CQSzCgQAjA130_provenance.
• NP147747.RArqbfQ96LlHmNV2TarDr9qIhamru_WgpXo9XRxEdmaqc130_assertion description "[Acidosis increases the CA IX expression via a hypoxia-independent mechanism that operates through modulation of the basic CA9 transcriptional machinery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147747.RArqbfQ96LlHmNV2TarDr9qIhamru_WgpXo9XRxEdmaqc130_provenance.
• NP147750.RArVSQUlF5UMlO2Y7pWjr5DHV3l8nCT9M2vCEC6cCQsuM130_assertion description "[Defects in laforin may lead to increased levels of misfolded and/or target proteins, which may eventually affect the physiological processes of the neuron, and likely to be the primary trigger in the physiopathology of lafora disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147750.RArVSQUlF5UMlO2Y7pWjr5DHV3l8nCT9M2vCEC6cCQsuM130_provenance.
• NP147751.RAoPKyU2Nrt_iHmj6VXWXubaT8z_gQwBpnawnzAuF-8rA130_assertion description "[Results suggest that the altered subcellular localization of mutant proteins of the EPM2A and NHLRC1 genes could be one of the molecular bases of the Lafora disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147751.RAoPKyU2Nrt_iHmj6VXWXubaT8z_gQwBpnawnzAuF-8rA130_provenance.
• NP147759.RAuIYi-7Q_DNH_pF4HZl0tipGAgOHdI4GIc9HWKguG3BQ130_assertion description "[The glycine59serine missense mutation in p150 (glued) knock-in mice abrogates the normal function of the protein and accelerates motor neuron degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147759.RAuIYi-7Q_DNH_pF4HZl0tipGAgOHdI4GIc9HWKguG3BQ130_provenance.
• NP147762.RAh2hfsTA3u2TMc6kGW-AbUrKTK2piYm6MgHuBgKN9r78130_assertion description "[In this review we critically analyze the data supporting the notion that VEGF is a factor involved in motor neuron degeneration and review the studies linking VEGF to other diseases of the peripheral and central nervous systems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147762.RAh2hfsTA3u2TMc6kGW-AbUrKTK2piYm6MgHuBgKN9r78130_provenance.
• NP147764.RAjwbFfDaYEMNLUKqWPp4sUXlgc7dXxpXvJXybPkT3zJs130_assertion description "[Misfolding of amyotrophic lateral sclerosis-related mutant SOD1 induces endoplasmic reticulum stress, which may contribute to the motor neuron degeneration in amyotrophic lateral sclerosis pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147764.RAjwbFfDaYEMNLUKqWPp4sUXlgc7dXxpXvJXybPkT3zJs130_provenance.
• NP147765.RAjoEzsaMIYzU1dOiTrObd7KTJCbQDyE5C-CVGk4b-aYk130_assertion description "[cathepsin B is involved in the motor neuron degeneration in ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147765.RAjoEzsaMIYzU1dOiTrObd7KTJCbQDyE5C-CVGk4b-aYk130_provenance.
• NP147781.RAkYPG3Dohrc9gq_8XANfr8o83-B2K8BwVpoSnKWBl6pU130_assertion description "[Novel mutations in the tumor necrosis factor receptor associated factor (TRAF) domain alter the subcellular localization of TRIM37, and are associated with Wilm's tumor in a patient with mulibrey nanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147781.RAkYPG3Dohrc9gq_8XANfr8o83-B2K8BwVpoSnKWBl6pU130_provenance.
• NP147782.RAjcVzp7JDCHIKb7_DGALisgvq9lcVZXeEPzlc6R-45ZI130_assertion description "[A genetic variation in the WISP1 gene locus is associated with spinal osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147782.RAjcVzp7JDCHIKb7_DGALisgvq9lcVZXeEPzlc6R-45ZI130_provenance.
• NP147785.RArcI9XNL5KSoeaE1TnXbu-e8XAvjH0Adp5xj9HJZQ87c130_assertion description "[mutational analysis of the GNAS1 gene is a strong supportive tool for the diagnosis of pseudohypoparathyroidism type 1a ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147785.RArcI9XNL5KSoeaE1TnXbu-e8XAvjH0Adp5xj9HJZQ87c130_provenance.
• NP147791.RAozaW10T8VeI_Sa0qIlYlVXe2WEbqMoJWwTqGJeZqWmI130_assertion description "[allelic expression and methylation of CpG islands within exon 1A of GNAS1 in patients with sporadic pseudohypoparathyroidism type 1b, consistent with a maternal imprinting defect ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147791.RAozaW10T8VeI_Sa0qIlYlVXe2WEbqMoJWwTqGJeZqWmI130_provenance.
• NP147803.RAhZZR5lR2W_qt3qJILuBvRBQWODYmgxjUrGY97nC3s8g130_assertion description "[Polymorphisms of genes encoding the AT1 receptor as risk factors for orthostatic hypotension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147803.RAhZZR5lR2W_qt3qJILuBvRBQWODYmgxjUrGY97nC3s8g130_provenance.
• NP147808.RAnF0rVsJpUoRcaEkzxyS1RcqJ2O6kJzqgpKwdPIOMYsw130_assertion description "[Data suggested suggested Arg548 may play an important role in ESR1 function in precocious puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147808.RAnF0rVsJpUoRcaEkzxyS1RcqJ2O6kJzqgpKwdPIOMYsw130_provenance.
• NP147813.RAr849vdIO6rVtWdGKKJlP4DBFk9iG5Bhelv_Ete04-7w130_assertion description "[gnas1 gene mutations were identified in subjects with fibrous dysplasia of bone ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147813.RAr849vdIO6rVtWdGKKJlP4DBFk9iG5Bhelv_Ete04-7w130_provenance.
• NP147817.RAhjPKBlUYnfjl1fHOZ3R1iPDhmA2-TAr-Gj_tHULLD9c130_assertion description "[The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3, 5, 3'-triiodothyronine toxicosis of McCune-Albright syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147817.RAhjPKBlUYnfjl1fHOZ3R1iPDhmA2-TAr-Gj_tHULLD9c130_provenance.
• NP147820.RAlIJRj5fcKhAqmBdKleyL2L2esI-yx_SG-V8EgV_ADB0130_assertion description "[Intratumoral IL-6, which is differently regulated by various factors, might contribute to excessive grwoth hormone production in the majority of somatotroph adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147820.RAlIJRj5fcKhAqmBdKleyL2L2esI-yx_SG-V8EgV_ADB0130_provenance.
• NP147822.RAo5yp1a0twOzS_WiAaOXJmnYNwiia0LI-0s5K8VhlPcc130_assertion description "[T393C SNP could be considered as a genetic marker to predict the clinical course of patients suffering from oropharyngeal and hypopharyngeal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147822.RAo5yp1a0twOzS_WiAaOXJmnYNwiia0LI-0s5K8VhlPcc130_provenance.
• NP147824.RAjO1Jt0b8UcfzDUOR2fkNrm3BtANyv4cTjT5b9AZVxgY130_assertion description "[This study demonstrated that p53 codon 72 Pro homozygosity is associated with a higher risk of developing hypopharyngeal cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147824.RAjO1Jt0b8UcfzDUOR2fkNrm3BtANyv4cTjT5b9AZVxgY130_provenance.
• NP147841.RArevRxWnNHuUeUk6G4w3OxEsa-gkWynvFmX7w9deJRwY130_assertion description "[Point mutations of AE1 resulting in nonselective cation conductance were associated with hemolytic anemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147841.RArevRxWnNHuUeUk6G4w3OxEsa-gkWynvFmX7w9deJRwY130_provenance.
• NP147844.RApymTXkeNfhNLefRsQLPzzAiqFriJ2t-vvK3XiPyVfrY130_assertion description "[Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147844.RApymTXkeNfhNLefRsQLPzzAiqFriJ2t-vvK3XiPyVfrY130_provenance.
• NP147848.RAsWBbTWjZ4a4ZLXoKsvRqtmU8HQZnrTI90xhdoF-XvCA130_assertion description "[MMP-2 expression was increased in posterior wall of thoracic aortic aneurysms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147848.RAsWBbTWjZ4a4ZLXoKsvRqtmU8HQZnrTI90xhdoF-XvCA130_provenance.
• NP147850.RAl2MaN4IkLlxv2db_fgbQ7__zmpVhzGMJJx-utbt-lZM130_assertion description "[targeted analysis involving NOTCH1 exons previously implicated in familial and sporadic bicuspid aortic valve demonstrates overrepresentation of NOTCH1 missense variants among patients with bicuspid aortic valves and thoracic aortic aneurysms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147850.RAl2MaN4IkLlxv2db_fgbQ7__zmpVhzGMJJx-utbt-lZM130_provenance.
• NP147852.RAtzFcVQXCqkajeB6dkYdcp-QytirB__ednH7Dnj2hEjg130_assertion description "[MYH11 mutations are likely to be specific to the phenotype of thoracic aortic aneurysms and dissections associated with patent ductus arteriosus and result in a distinct aortic and occlusive vascular pathology potentially driven by IGF-1 and Ang II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147852.RAtzFcVQXCqkajeB6dkYdcp-QytirB__ednH7Dnj2hEjg130_provenance.

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