Nanopublications LDF server

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

• NP147077.RAo-reroZCkqQ6J64xb7Y-J98EtXVAhi0QhJ9Mbxknrd0130_assertion description "[These data provide new insights into the role of CC-10 in lung diseases and the possibility that the CC-10 concentration in serum could be a new marker indicating the severity of bronchial asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147077.RAo-reroZCkqQ6J64xb7Y-J98EtXVAhi0QhJ9Mbxknrd0130_provenance.
• NP147078.RAoDP1cRwxjTzwJU-dXrfogF6KsDh2lB2aDV4FprOUXrI130_assertion description "[Inhibition of PTEN expression in fibroblasts may contribute to the pathogenesis of fibrotic lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147078.RAoDP1cRwxjTzwJU-dXrfogF6KsDh2lB2aDV4FprOUXrI130_provenance.
• NP147079.RAtSuJtWtiVxFNhQFM5my4aGNx2utaHHStldjAqD_GtUg130_assertion description "[the mechanisms of pulmonary hypertension and vascular loss in chronic lung disease and identifies gremlin 1 as a potentially important mediator of vascular changes in hypoxic pulmonary hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147079.RAtSuJtWtiVxFNhQFM5my4aGNx2utaHHStldjAqD_GtUg130_provenance.
• NP147082.RAkiChTvvAjfyOprcT9kISafsGDOkzM0dMzfBRH96ebh8130_assertion description "[Co-activation of hKvLQT1 improves CaCC-mediated Cl- secretion in native CF airway epithelia, and may have a therapeutic effect in the treatment of CF lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147082.RAkiChTvvAjfyOprcT9kISafsGDOkzM0dMzfBRH96ebh8130_provenance.
• NP147083.RAmm7UGJucj731ZIi6VTBCaaNeT4rf-RjpkP6R8nHY3JE130_assertion description "[infiltrated neutrophils from patients with chronic inflammatory lung diseases and rheumatoid arthritis highly express CCR1, CCR2, CCR3, CCR5, CXCR3, and CXCR4 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147083.RAmm7UGJucj731ZIi6VTBCaaNeT4rf-RjpkP6R8nHY3JE130_provenance.
• NP147084.RAqznSVfdgJGWRdSsJ8Yc7Fl3f483IhuzVqoQ-VLKmWnE130_assertion description "[evidence of gene-gene interaction in the pathogenesis of CF lung disease, whereby high TGF-beta1 production enhances the modulatory effect of MBL2 on the age of first bacterial infection and the rate of decline of pulmonary function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147084.RAqznSVfdgJGWRdSsJ8Yc7Fl3f483IhuzVqoQ-VLKmWnE130_provenance.
• NP147087.RAuBIqzXLg7WAP-x8Fp50-DgZ5kK-kp79r0RqA99DR1nw130_assertion description "[Differences in amounts of SP-B resulting from the promoter single nucleotide polymorphism could affect the clinical presentation of pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147087.RAuBIqzXLg7WAP-x8Fp50-DgZ5kK-kp79r0RqA99DR1nw130_provenance.
• NP147088.RAjMpDyfkaxGBAAKfyEcyMA6f4iEsqBAkIz_x3JrBPTak130_assertion description "[Current state of knowledge concerning the lung diseases associated with mutations in the SP-B and SP-C genes, and the potential roles of abnormal SP-B and SP-C expression and genetic variation in these genes in other lung diseases/. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147088.RAjMpDyfkaxGBAAKfyEcyMA6f4iEsqBAkIz_x3JrBPTak130_provenance.
• NP147095.RAlscrwodIzHa6MVlRrIGLffj6n3jRFeQz3uisNWMQpQU130_assertion description "[the SNP-607/AA genotype that had lower IL-18 levels might be a genetically protective factor against renal involvement in Chinese patients with SLE and against development of severe nephritis in patients with LN ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147095.RAlscrwodIzHa6MVlRrIGLffj6n3jRFeQz3uisNWMQpQU130_provenance.
• NP147098.RAn1ybxT75Bva5AUg55qQ69LjtKRVN1UULw0do3z47iQ0130_assertion description "[Overexpression of caveolin-1 in mesangial cells suppresses MAP kinase activation and cell proliferation induced by bFGF and PDGF, two major cytokines in mesangioproliferative nephritis (MN)/expression vector is potential therapy for MN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147098.RAn1ybxT75Bva5AUg55qQ69LjtKRVN1UULw0do3z47iQ0130_provenance.
• NP147103.RAlwr3ezoclF877OtHq_TpO6sXVHP0Gd6KQjny1aUJ1P4130_assertion description "[Report renal expression of alpha-smooth muscle actin and c-Met in children with Henoch-Schonlein purpura nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147103.RAlwr3ezoclF877OtHq_TpO6sXVHP0Gd6KQjny1aUJ1P4130_provenance.
• NP147108.RAi8RKV-cSm94PIW6Va1yiB4L2tSGWahy7SAVhLulvsis130_assertion description "[TNF-alpha can play a crucial role in the immunopathogenesis of nephritis by the induction of CCL2, ICAM-1 and VCAM-1 expression via the activation of the intracellular MAPK signaling pathway, which may contribute to macrophage and lymphocyte infiltration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147108.RAi8RKV-cSm94PIW6Va1yiB4L2tSGWahy7SAVhLulvsis130_provenance.
• NP147118.RAtVuhZqqRCB5BJNH_eYlfAe7l8rE20YciVdK8oc9zXWI130_assertion description "[angiotensin converting enzyme (ACE) activity was significantly reduced in patients with pulmonary arterial hypertension related to connective tissue disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147118.RAtVuhZqqRCB5BJNH_eYlfAe7l8rE20YciVdK8oc9zXWI130_provenance.
• NP147122.RAlByMoMufoM7GLSDK1DKjWLbE4I8zhNvAJsVEIhv9D54130_assertion description "[Serum IL-2 levels were significantly decreased in patients with burning mouth syndrome compared with controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147122.RAlByMoMufoM7GLSDK1DKjWLbE4I8zhNvAJsVEIhv9D54130_provenance.
• NP147125.RAlny93DgtN3j6wd99GZurab3pR0tMbLjBSNliD2Qs7sY130_assertion description "[the levels of sCD14 and sTLR-2 in saliva were upregulated in oral lichen planus and burning mouth syndrome/epithelial cells in the saliva of patients exhibited elevated levels of CD14 mRNA and decreased levels of TLR-2 mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147125.RAlny93DgtN3j6wd99GZurab3pR0tMbLjBSNliD2Qs7sY130_provenance.
• NP147131.RApWTqpKuq2CVyOUWWdwahl8jEy17Z16DbeaeboF0M5C4130_assertion description "[CYP1A1 4887A may be a risk factor for the development of reactive arthritis, especially in the presence of Mn SOD 1183T/T ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147131.RApWTqpKuq2CVyOUWWdwahl8jEy17Z16DbeaeboF0M5C4130_provenance.
• NP147132.RAghHMkYHeU8TfxjPEpmxCSSzTUjkyj9B5C2410rXmc8g130_assertion description "[The SLC 11A1 274T 823C 1703G 1729+55 del 4 TGTG+ haplotype is associated with the development of reactive arthritis in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147132.RAghHMkYHeU8TfxjPEpmxCSSzTUjkyj9B5C2410rXmc8g130_provenance.
• NP147133.RAl2NJKIHSBrgCsHkXlCDbx4DvIeRcJdmqlKQb0e6EQRc130_assertion description "[CYP1A1 4887A may be a risk factor for the development of reactive arthritis, especially in the presence of Mn SOD 1183T/T ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147133.RAl2NJKIHSBrgCsHkXlCDbx4DvIeRcJdmqlKQb0e6EQRc130_provenance.
• NP147135.RAsHmPE0Q-13ktu0plQr4aJLlsHF7mmKdrui8DcDyvHWE130_assertion description "[could have a significant role in the progression of gingivitis to periodontitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147135.RAsHmPE0Q-13ktu0plQr4aJLlsHF7mmKdrui8DcDyvHWE130_provenance.
• NP147136.RAhundP9Yuqv_uTGo9obik6iX4BuXOJaGCR6MZ_Ol2_5k130_assertion description "[Cystatin C was higher in saliva and gingival crevicular fluid in periodontally healthy children than in children with chronic gingivitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147136.RAhundP9Yuqv_uTGo9obik6iX4BuXOJaGCR6MZ_Ol2_5k130_provenance.
• NP147142.RAravgTMLLW7IzS0KlOAO6s7D6LckQ6JzB1wLoTDzcnq0130_assertion description "[The TLR2- and TLR4-stimulating activity of supragingival plaque is associated with clinical parameters for gingivitis and periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147142.RAravgTMLLW7IzS0KlOAO6s7D6LckQ6JzB1wLoTDzcnq0130_provenance.
• NP147145.RAgxwz8QYWEzz2YYuW_eBT52cinJIaCvgBQd11xHkImjs130_assertion description "[Immunolocalization of inducible nitric oxide synthase in gingiva in localized juvenile periodontitis patients/in gingivitis/expressed high levels of iNOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147145.RAgxwz8QYWEzz2YYuW_eBT52cinJIaCvgBQd11xHkImjs130_provenance.
• NP147146.RAqPJ3UDSJGsUIomFr21UKVE122B7ABXV-2QNayA7SOG4130_assertion description "[An inverse relationship is shown for the first time in the ratio between ICAM1-expressing lymphocytes and transforming growth factor (TGF) -beta 1 serum concentrations during the clinical stages of acute rheumatic fever.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147146.RAqPJ3UDSJGsUIomFr21UKVE122B7ABXV-2QNayA7SOG4130_provenance.
• NP147151.RApWkteK2nZ8Or5wppNBAPEwejYv3k6QEIaeb7SM8rCu0130_assertion description "[HLA DQA1*03 allele may be a protecting factor in Turkish children with rheumatic fever/combination of the DRB1*04 and DQA1*03 alleles may be a stronger protective factor than the DQA1*03 allele alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147151.RApWkteK2nZ8Or5wppNBAPEwejYv3k6QEIaeb7SM8rCu0130_provenance.
• NP147160.RAtnTMTZMA_r8AmqURb7UJO9eI_JXT8AJtfDYUoYvhE0Q130_assertion description "[Study on TLR-2 as a risk factor for coronary restenosis.a functional TLR-2 is protective and potentially involved in a reaction pattern preventing restenosis/for the TLR-2 Arg753Gln SNP may be of importance for stratifying a patient's risk ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147160.RAtnTMTZMA_r8AmqURb7UJO9eI_JXT8AJtfDYUoYvhE0Q130_provenance.
• NP147165.RAkVWgcqw5ynur4Z0aHw6oScGRhTDB2HQuhdihR06DDiA130_assertion description "[innate immune response of monocytes against M.lepraeis is mediated by TLR2, the mutation in the intracellular domain of TLR2 gene is associated with IL-12 production in lepromatous leprosy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147165.RAkVWgcqw5ynur4Z0aHw6oScGRhTDB2HQuhdihR06DDiA130_provenance.
• NP147166.RAnIZJml8OyCKaZl3xYgJ9rZDhqcVCEKTXPKByaAGMCSY130_assertion description "[The impaired apoptosis response to DNA damage in NBS1 deficient cells might be one of the important mechanisms of cancer predisposition in hereditary disease Nijmegen breakage syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147166.RAnIZJml8OyCKaZl3xYgJ9rZDhqcVCEKTXPKByaAGMCSY130_provenance.
• NP147167.RAgmk2MQND1xhiqP-BfIgi7mXJNenRtG89XNj9IDmbUa4130_assertion description "[TRPM6 mutants are found in patients with a rare but severe hereditary disease called hypomagnesaemia with secondary hypocalcaemia -- { REVIEW } ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147167.RAgmk2MQND1xhiqP-BfIgi7mXJNenRtG89XNj9IDmbUa4130_provenance.
• NP147172.RAklX1vO3Afx3LYH0Oyt_1hxmCVF_FWuxQD7y_faHQwXU130_assertion description "[Homozygosity for the 643C > T (R215W) mutation will also lead to a, possibly very, severe disease phenotype and Nijmegen breakage syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147172.RAklX1vO3Afx3LYH0Oyt_1hxmCVF_FWuxQD7y_faHQwXU130_provenance.
• NP147173.RAn8WbeEal9yFnPhHHswWWMLhpLnAep7KHmdtA3DuFWjE130_assertion description "[expression at normal levels in Nijmegen breakage syndrome cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147173.RAn8WbeEal9yFnPhHHswWWMLhpLnAep7KHmdtA3DuFWjE130_provenance.
• NP147174.RAhIRpx7U4Vg8RjyrfsqBzX4LQCdUV8DKCWaFeChOw9q8130_assertion description "[Data suggest that Nijmegen breakage syndrome 1 (Nbs1) functions in both ATR- (ataxia-telangiectasia and Rad3-related protein) and ataxia telangiectasia mutated protein-dependent signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147174.RAhIRpx7U4Vg8RjyrfsqBzX4LQCdUV8DKCWaFeChOw9q8130_provenance.
• NP147175.RArLM8APTgL3qR6wVA4A2o6ih1H4SHXfNlQNWVifE7vH8130_assertion description "[Data reveal a role for the Rad50 complex in V (D) J recombination, and demonstrate that the protein product of the disease-causing allele responsible for Nijmegen breakage syndrome encodes a protein with residual DNA double-strand break repair activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147175.RArLM8APTgL3qR6wVA4A2o6ih1H4SHXfNlQNWVifE7vH8130_provenance.
• NP147185.RAgCXt7FAvZ9VBHnqfuA7Jhs-i52CBSpz8hei2f-KOsbU130_assertion description "[Werner protein (WRN), which is defective in Werner syndrome (WS) patients, belongs to the RecQ family helicases and interacts with several DNA metabolic proteins, including DNA repair factors and telomere associated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147185.RAgCXt7FAvZ9VBHnqfuA7Jhs-i52CBSpz8hei2f-KOsbU130_provenance.
• NP147188.RAqSKn6-w6DafP6mBQWrtKj5D25lwQiEUEJNjxsfXaCtc130_assertion description "[a functional interaction between Werner syndrome protein and two factors that bind to DNA breaks, Ku and poly (ADP-ribose) polymerase 1--REVIEW ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147188.RAqSKn6-w6DafP6mBQWrtKj5D25lwQiEUEJNjxsfXaCtc130_provenance.
• NP147190.RAv9LegG4pE1oEem226F_dBaW23SCks50zO_zBsvhT990130_assertion description "[Results suggest that nuclear DNA helicase II plays a role in promoting the DNA processing function of Werner syndrome helicase, which in turn might be necessary for maintaining genomic stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147190.RAv9LegG4pE1oEem226F_dBaW23SCks50zO_zBsvhT990130_provenance.
• NP147195.RAuB4lbJqMTKrwGjacWts5Le0B-lv9ku85De5DW06k9fU130_assertion description "[Poly (ADP-ribose) polymerase 1 inactivates the catalytic activities of the Werner syndrome protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147195.RAuB4lbJqMTKrwGjacWts5Le0B-lv9ku85De5DW06k9fU130_provenance.
• NP147198.RAloUKA0dHaPuYEggLnqW3rivi1txqAcTGa0u3dIgWoBk130_assertion description "[An association between the TGF-beta1 genetic profile and the development of PVR (proliferative vitreoretinopathy) was detected in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147198.RAloUKA0dHaPuYEggLnqW3rivi1txqAcTGa0u3dIgWoBk130_provenance.
• NP147203.RApfedYQ7uZr-Tob7UBcXBy48UroUByIA9t8V7r6JAOR8130_assertion description "[sequence variation in diaphragmatic hernia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147203.RApfedYQ7uZr-Tob7UBcXBy48UroUByIA9t8V7r6JAOR8130_provenance.
• NP147204.RAqB8ZRPe_I92fpDHSLLZGfCjmvomXY-Wc4g7N6Dcpcyw130_assertion description "[There was a clear increase in the number of MMP-1-reactive capillaries and fibroblasts in congenital diaphragmatic hernia lungs compared with controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147204.RAqB8ZRPe_I92fpDHSLLZGfCjmvomXY-Wc4g7N6Dcpcyw130_provenance.
• NP147206.RAu1pbtSSMwUqdjGwrRcYfmjY7K6PKFBNvgpSul55rvHA130_assertion description "[Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147206.RAu1pbtSSMwUqdjGwrRcYfmjY7K6PKFBNvgpSul55rvHA130_provenance.
• NP147217.RAhmvtvUwlR2VaFDLWhFbWDCFHYGiqfbiPQyVKPVFHuf8130_assertion description "[These findings suggest that tubular TLR-9 activation has a pathogenetic role in tubulointerstitial inflammation and damage in experimental and human lupus nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147217.RAhmvtvUwlR2VaFDLWhFbWDCFHYGiqfbiPQyVKPVFHuf8130_provenance.
• NP147218.RAhcdykYaP-KoA2hC6SvzbOFnofwg5s8krsQl_uSRON4Y130_assertion description "[in lupus nephritis RANTES may participate in interstitial lesions via CCR5+ cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147218.RAhcdykYaP-KoA2hC6SvzbOFnofwg5s8krsQl_uSRON4Y130_provenance.
• NP147221.RAnEITzxjGbi0t335QpCBETNWShgSZuLq_GJupycgllP0130_assertion description "[an A/G or G/G genotype may predispose to the development of systemic lupus erythematosus and further indicate that the patients with these genotypes may be at higher risk of developing lupus nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147221.RAnEITzxjGbi0t335QpCBETNWShgSZuLq_GJupycgllP0130_provenance.
• NP147233.RAta9PVIgxF0--lv00_8dw2IGuJmrX_UFTNbVGyaIQ534130_assertion description "[the low expressing A allele is a significant risk factor for developing lupus nephritis that is gene dosage-dependent in African Americans ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147233.RAta9PVIgxF0--lv00_8dw2IGuJmrX_UFTNbVGyaIQ534130_provenance.
• NP147234.RAsLlmTZ3lMWeB0RMPdEM2Ut5vCs1GAZns4OhXD8XvD0E130_assertion description "[our data suggest that deletion of the hv3005 and the 3-30.3 genes may predispose individual SLE patients to the development of lupus nephritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147234.RAsLlmTZ3lMWeB0RMPdEM2Ut5vCs1GAZns4OhXD8XvD0E130_provenance.
• NP147238.RAtdlXEd-ysQtzhIYQTd3qpNC8ecgj5cJO7ZCvR4wFYgg130_assertion description "[in lupus nephritis COX-2 and monocytes/macrophages but not COX-1 isoform are involved in the inflammatory process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147238.RAtdlXEd-ysQtzhIYQTd3qpNC8ecgj5cJO7ZCvR4wFYgg130_provenance.
• NP147240.RAl2mwHNJk40S18-kGB-f98ap0455T5CTwgGSmwBz3qjQ130_assertion description "[retinoic acid-inducible gene-I is expressed in lupus nephritis [letter]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147240.RAl2mwHNJk40S18-kGB-f98ap0455T5CTwgGSmwBz3qjQ130_provenance.
• NP147246.RArYY7Wm5BGQIi0wwSClLuHtvHwS4ZEl9h2k9YerXQFQI130_assertion description "[Autoantibodies against mCRP are prevalent in patients with lupus nephritis and are associated with disease activity and renal tubulointerstitial lesions ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147246.RArYY7Wm5BGQIi0wwSClLuHtvHwS4ZEl9h2k9YerXQFQI130_provenance.
• NP147250.RAqfuKXV6_rqRgiMsPzhN6gA5rxBZtCTHx9_0gDX5SQzA130_assertion description "[in bone fracture patients, 12 proteins were related to bone/cartilage metabolism, including: TGF-beta induced protein IG-H (3), cartilage acidic protein 1, procollagen C proteinase enhancer protein and TGF-beta receptor III.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147250.RAqfuKXV6_rqRgiMsPzhN6gA5rxBZtCTHx9_0gDX5SQzA130_provenance.
• NP147251.RAnl95mV1Zpoi5IuFLNnl_K2BciaLeAF16XFBK43xaIgQ130_assertion description "[Reduced fecal elastase 1 connected with lowered serum levels of vitamin D3 is associated with osteoporotic bone fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147251.RAnl95mV1Zpoi5IuFLNnl_K2BciaLeAF16XFBK43xaIgQ130_provenance.
• NP147252.RAtOARVUJX1H6NaKxKfDW9qMcxfNN75VPLbLTQMpqy4cM130_assertion description "[in bone fracture patients, 12 proteins were related to bone/cartilage metabolism, including: TGF-beta induced protein IG-H (3), cartilage acidic protein 1, procollagen C proteinase enhancer protein and TGF-beta receptor III.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147252.RAtOARVUJX1H6NaKxKfDW9qMcxfNN75VPLbLTQMpqy4cM130_provenance.
• NP147257.RAsjWbSiCwxyMzy1eIRheujzkBv_x5rVMEzB-esku05aU130_assertion description "[pituitary hormone deficiency due to novel mutation R99Q in hot spot region of PROP-1 causing growth disorder; mutant PROP-1 displays a decrease in DNA binding on a paired box response element and trans-activation of a luciferase reporter gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147257.RAsjWbSiCwxyMzy1eIRheujzkBv_x5rVMEzB-esku05aU130_provenance.
• NP147260.RAhxaZ5l42P3pxBmfWTHb4UdRs80gGU7MFkT43Xn26FGM130_assertion description "[Physiological regulator of phosphate homeostasis/FGF23 with normal renal function results in hypophosphatemia, low 1, 25-dihydroxyvitamin D levels, and rickets/osteomalacia/to development of hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147260.RAhxaZ5l42P3pxBmfWTHb4UdRs80gGU7MFkT43Xn26FGM130_provenance.
• NP147261.RAmKb8rC_C91Ve9rLr5MUSK74OBgntFbCaELKxQ3c_pMw130_assertion description "[Comparison of ApaI and Taq1 genotypes finds no relationship between vitamin D receptor gene allelic polymorphisms and osteomalacia/. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147261.RAmKb8rC_C91Ve9rLr5MUSK74OBgntFbCaELKxQ3c_pMw130_provenance.
• NP147263.RAjiUCeLEK4A4qSNII39U7j_8fJkN0Gt7gT9fCCXqBojE130_assertion description "[An " in vitro " high-speed screening method followed by QSAR analysis was developped to investigate ABCB11-drugs interactions and predict compounds with a risk of drug-induced intrahepatic cholestasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147263.RAjiUCeLEK4A4qSNII39U7j_8fJkN0Gt7gT9fCCXqBojE130_provenance.
• NP147266.RAsvW_o-OY9z7GZe4vVIQiWkXi3Kh9d4veGFjmOv2DkJY130_assertion description "[This study demonstrates that splicing mutations in the MDR3 gene can cause intrahepatic cholestasis of pregnancy with normal gamma-GT and may be associated with stillbirths and gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147266.RAsvW_o-OY9z7GZe4vVIQiWkXi3Kh9d4veGFjmOv2DkJY130_provenance.
• NP147268.RAqssmcXx4xpiKvFQf7tBYcIqmXwRwLd4uOc4p4q145w8130_assertion description "[The molecular characterization of 68 Progressive familial intrahepatic cholestasis type 3 (PFIC3) screened for ABCB4 mutations to date, is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147268.RAqssmcXx4xpiKvFQf7tBYcIqmXwRwLd4uOc4p4q145w8130_provenance.
• NP147269.RAjl3Yy6ZA6HwkWrsyIuniMhf7yJDnMNpS3-O-W0WGcq8130_assertion description "[sequence variation in women with intrahepatic cholestasis of pregnancy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147269.RAjl3Yy6ZA6HwkWrsyIuniMhf7yJDnMNpS3-O-W0WGcq8130_provenance.
• NP147272.RAvCSOTA6psgAX68qN8DmZirl-CHJgJqMgXdeu7aqHK3E130_assertion description "[Hepatic down-regulation of Farnesoid X receptor contributes to severety of familial intrahepatic cholestasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147272.RAvCSOTA6psgAX68qN8DmZirl-CHJgJqMgXdeu7aqHK3E130_provenance.
• NP147273.RAl4T_FAIonbJavvbolJFv6xMlK6I1pPODjH9Rvt_hBxM130_assertion description "[investigation of the association of polymorphisms of HLA class II DRB1 & DQB1 alleles & risk for intrahepatic cholestasis of pregnancy (ICP); results indicate that HLA-DR11 allele is associated with the susceptibility of ICP in the Chinese Changsha area ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147273.RAl4T_FAIonbJavvbolJFv6xMlK6I1pPODjH9Rvt_hBxM130_provenance.
• NP147274.RAvz-SgHPOu6KiOyPFcnuui57erhjHc3fnsgpiUJ_Aryg130_assertion description "[investigation of the association of polymorphisms of HLA class II DRB1 & DQB1 alleles & risk for intrahepatic cholestasis of pregnancy (ICP); results indicate that HLA-DR11 allele is associated with the susceptibility of ICP in the Chinese Changsha area ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147274.RAvz-SgHPOu6KiOyPFcnuui57erhjHc3fnsgpiUJ_Aryg130_provenance.
• NP147276.RApGxAMDF1aYBnwL1LBzf6weKAGSapA37q8QahlB_S9Ac130_assertion description "[The purpose of this study was to evaluate the role of coding variation in hPXR (NR1I2) in intrahepatic cholestasis of pregnancy (ICP) and to functionally asses the response of PXR variants to ligands of interest in ICP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147276.RApGxAMDF1aYBnwL1LBzf6weKAGSapA37q8QahlB_S9Ac130_provenance.
• NP147282.RAv4nfPTSDg4xIDVBgM8Bw8HGPNzCrVCNS76pY28eWQ3A130_assertion description "[the induction of claudin7 expression by ELF3 appears critical to the formation of the epithelial structures in biphasic synovial sarcoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147282.RAv4nfPTSDg4xIDVBgM8Bw8HGPNzCrVCNS76pY28eWQ3A130_provenance.
• NP147283.RAkOzQsR7HtI1rBO4LGOH9Uc6QC3h_a6ngughjd31XFSs130_assertion description "[The researchers investigated the expression of epidermal growth factor receptors in synovial sarcomas and found no associated mutations in EGFR genomic sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147283.RAkOzQsR7HtI1rBO4LGOH9Uc6QC3h_a6ngughjd31XFSs130_provenance.
• NP147287.RAresqnx0IPiHdX2SFiTRsD00nBKYpOQqw7tg3u6Q_grw130_assertion description "[These results demonstrate that C-erb-B2 (HER2/neu) may play a role in the tumorigenesis of synovial sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147287.RAresqnx0IPiHdX2SFiTRsD00nBKYpOQqw7tg3u6Q_grw130_provenance.
• NP147288.RAr26Kt2D3TFxXh-ya8nTfcOyRtDYOVwH2Z3iK6VUiZnc130_assertion description "[High levels of MYCN expression was useful for distinguishing synovial sarcoma from other childhood-spindled cell sarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147288.RAr26Kt2D3TFxXh-ya8nTfcOyRtDYOVwH2Z3iK6VUiZnc130_provenance.
• NP147289.RAhzcOkQtvI70wZoUEa1L9kKINuXlBvD4tfV9tcmAN-3k130_assertion description "[E-cadherin downregulation is associated with the loss or absence of glandular epithelial differentiation in certain synovial sarcoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147289.RAhzcOkQtvI70wZoUEa1L9kKINuXlBvD4tfV9tcmAN-3k130_provenance.
• NP147293.RAqA5VfRPm-eW9X1YtIgFH7-qFoLLK0RmVt9T_PgMLOh0130_assertion description "[ligand-activated KIT and platelet-derived growth factor receptor beta tyrosine kinase receptors are expressed in synovial sarcoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147293.RAqA5VfRPm-eW9X1YtIgFH7-qFoLLK0RmVt9T_PgMLOh0130_provenance.
• NP147295.RAuFNsaYKlIBjajkdRfrBRTXuhk0n-y6Al5mHxQXV7v3o130_assertion description "[Weak to absent protein expression suggests RASSF1 and MLH1 post-transcription deregulation in monophasic synovial sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147295.RAuFNsaYKlIBjajkdRfrBRTXuhk0n-y6Al5mHxQXV7v3o130_provenance.
• NP147298.RAo4XSbhWRJCLZOiGELCAd93ls9dNzuIppF1Dy-193r2k130_assertion description "[RT-PCR detection of SSX2 in paraffin-embedded tissue allowed for molecular diagnosis of synovial sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147298.RAo4XSbhWRJCLZOiGELCAd93ls9dNzuIppF1Dy-193r2k130_provenance.
• NP147301.RAnYNI7SX3o1x8cPMw8W6utlXnk2g2lrH8o1WTKZ1MD5g130_assertion description "[A synovial sarcoma of classic morphology contained a novel t (20; X) SS18L1 (strong homology to SS18 on Ch20)/SSX1 fusion transcript in which nucleotide 1216 (exon 10) of SS18L1 was fused in-frame with nucleotide 422 (exon 6) of SSX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147301.RAnYNI7SX3o1x8cPMw8W6utlXnk2g2lrH8o1WTKZ1MD5g130_provenance.
• NP147302.RAq5xcBM9rEET45_cuyxczuNDKVuq-zBl4YYCCG-NXNQY130_assertion description "[siRNA targeting of SS18-SSX1 may have therapeutic potential in the treatment of synovial sarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147302.RAq5xcBM9rEET45_cuyxczuNDKVuq-zBl4YYCCG-NXNQY130_provenance.
• NP147307.RAreS8yDqDrHlgqyuzJxCSrEiGoE0AVokX7VWWQdYxYjs130_assertion description "[MMP-2 expression seemed to have an important role to play in the epithelial differentiation of tumour cells in synovial sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147307.RAreS8yDqDrHlgqyuzJxCSrEiGoE0AVokX7VWWQdYxYjs130_provenance.
• NP147314.RAidFHIJ5s0jU_FhKlv3iLgQ8SkGfZowTggefJq9uDTiQ130_assertion description "[PTEN mutations were detected in 7 cases (14.3%) of synovial sarcoma, and all of these were monophasic tumors ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147314.RAidFHIJ5s0jU_FhKlv3iLgQ8SkGfZowTggefJq9uDTiQ130_provenance.
• NP147323.RAimrm0L7eriTJobFVw-bftmf6nFrqfRLk7_TOsQLuP4A130_assertion description "[Ksp-cad is a useful tumor type associated marker for distinguishing chromophobe renal cell carcinoma and renal oncocytoma from the wide range of nonintercalated cell-related adult renal epithelial neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147323.RAimrm0L7eriTJobFVw-bftmf6nFrqfRLk7_TOsQLuP4A130_provenance.
• NP147344.RAi1fa3HptfKeDi-7RRbuA7qpR_mDcbmNWJWSFzohETko130_assertion description "[in testicular cancer two nonredundant SNPs in CYP1A1 (cytochrome P450 family 1 subfamily A polypeptide) were inversely associated with nonseminoma: CYP1A1 promoter SNP rs4886605 and rs2606345 intron 1 SNP ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147344.RAi1fa3HptfKeDi-7RRbuA7qpR_mDcbmNWJWSFzohETko130_provenance.
• NP147347.RAuc1ZeRuodncZ-ICcbShp_QSoxZBUGva2wMoAex-tHWE130_assertion description "[XPA, ERCC1 and XPF DNA repair protein expression is reduced in testis neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147347.RAuc1ZeRuodncZ-ICcbShp_QSoxZBUGva2wMoAex-tHWE130_provenance.
• NP147350.RAtZRZqEy4QXh-ThQ6ro4nREkFO3TclLPBIa_T-ZJBLDk130_assertion description "[XPA, ERCC1 and XPF DNA repair protein expression is reduced in testis neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147350.RAtZRZqEy4QXh-ThQ6ro4nREkFO3TclLPBIa_T-ZJBLDk130_provenance.
• NP147366.RAhu6rRRMVILjdFONts_3ffts7JL-XGzTWomq21W1ZfSM130_assertion description "[Of 36 novel pathogenic USH2A mutations, 31 were located in exons 22-73 in Scandinavian patients with Usher syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147366.RAhu6rRRMVILjdFONts_3ffts7JL-XGzTWomq21W1ZfSM130_provenance.
• NP147368.RAvbPmx9D6LGltM5WHgu8BgpBt1ZQ2U6rBV9QHh3sI8VE130_assertion description "[Three novel mutations were found in USH2A in Usher syndrome type II Dutch patients, one point mutation and two missense mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147368.RAvbPmx9D6LGltM5WHgu8BgpBt1ZQ2U6rBV9QHh3sI8VE130_provenance.
• NP147379.RAr44idN4HhsLEXE3tnxzaPtb-AhicdqluS5WVC7mgKcE130_assertion description "[A family of autosomal dominant hypocalcemia with a positive correlation between serum calcium and magnesium: a novel gain of function mutation (Ser (820) Phe) in the calcium-sensing receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147379.RAr44idN4HhsLEXE3tnxzaPtb-AhicdqluS5WVC7mgKcE130_provenance.
• NP147382.RAgaSEaUC5nFcddZYjfPtPkPFiZp3GOD7dkCPczVljdlk130_assertion description "[Deficiency/mutations of TRPM6 causes hypomagnesemia with secondary hypocalcemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147382.RAgaSEaUC5nFcddZYjfPtPkPFiZp3GOD7dkCPczVljdlk130_provenance.
• NP147383.RAnFa-pqPl0keapt1m5aH0EiLvl5iAazfv1SRoth0gXI0130_assertion description "[Fibroblast growth factor-23 in patients with transient hypoparathyroidism: its important role in serum phosphate regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147383.RAnFa-pqPl0keapt1m5aH0EiLvl5iAazfv1SRoth0gXI0130_provenance.
• NP147389.RAu7FjakNVL9ZKVUsSsCaMLC-N-4LCCNBEauG3OZI9Elk130_assertion description "[GATA3 mutations may have a role in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147389.RAu7FjakNVL9ZKVUsSsCaMLC-N-4LCCNBEauG3OZI9Elk130_provenance.
• NP147391.RAlLim4wCwPRFHIB7Pm3sZdZAGqhC43Vo33JGhMf9JLkM130_assertion description "[Three novel mutations in the GATA3 gene responsible for familial hypoparathyroidism and deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147391.RAlLim4wCwPRFHIB7Pm3sZdZAGqhC43Vo33JGhMf9JLkM130_provenance.
• NP147406.RAra0BTfkVPGHJcLj-kNHcjlfS8XepRhhO9yUpDBRYfDQ130_assertion description "[The roles of BAFF protein and interferon gamma in IgA production of tonsillar mononuclear leukocytes in patients with IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147406.RAra0BTfkVPGHJcLj-kNHcjlfS8XepRhhO9yUpDBRYfDQ130_provenance.
• NP147408.RAmzw1jb7nca3-g5RMkXEsllIRPAk--ReqC1Mkkar--ZU130_assertion description "[lymphotactin, as well as MCP-1, may contribute to leukocyte infiltration and disease progression in IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147408.RAmzw1jb7nca3-g5RMkXEsllIRPAk--ReqC1Mkkar--ZU130_provenance.
• NP147416.RAimMOtJXCwAGpLuxyioGeLVB7FPc8jDPglOSswFLna3s130_assertion description "[In this Chinese population, the 2093C-2180T haplotype at the 3'UTR of MEGSIN gene is associated with more severe forms of IgA nephropathy, and more rapid disease progression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147416.RAimMOtJXCwAGpLuxyioGeLVB7FPc8jDPglOSswFLna3s130_provenance.
• NP147417.RAm9ti4eC9qLXKp-ETxBrz86iSt9bh_FjoRWCVfmniGmA130_assertion description "[Fcgr3b genotype influences the disease susceptibility and severity of IgA nephropathy in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147417.RAm9ti4eC9qLXKp-ETxBrz86iSt9bh_FjoRWCVfmniGmA130_provenance.
• NP147418.RAsO5iZouFP_Vhj6hZOvU22G3-_LqbZECDDi207HmnbKM130_assertion description "[no significant difference in the genotypic and allelic frequencies of the identified 954T > C and 1038A > G polymorphisms between the sporadic IgA nephropathy patients and normal controls was found ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147418.RAsO5iZouFP_Vhj6hZOvU22G3-_LqbZECDDi207HmnbKM130_provenance.
• NP147422.RAkYnBuJH3bR601lscVNAl1b0_igKRLIdcAbAZTAuBQgU130_assertion description "[The expression of MMP-9 was significantly increased in mesangial proliferative glomeruli and interstitial vascular walls of IgA nephropathy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147422.RAkYnBuJH3bR601lscVNAl1b0_igKRLIdcAbAZTAuBQgU130_provenance.
• NP147429.RAlVpJ3FDxSdtWhPGrFAmM5ULo2_zai4b_nahj2-eD2OY130_assertion description "[IFN-gamma gene polymorphisms are associated with disease susceptibility and disease progression in IgA nephropathy in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147429.RAlVpJ3FDxSdtWhPGrFAmM5ULo2_zai4b_nahj2-eD2OY130_provenance.
• NP147446.RApvTLjm608alhzvSgvsslFTxxuoihv85ciNVbbSAaLoI130_assertion description "[The AA genotype at MCP-1 -2518 was an independent risk factor for the progression of renal disease in Japanese patients with IgA nephropathy, and was closely associated with renal survival ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147446.RApvTLjm608alhzvSgvsslFTxxuoihv85ciNVbbSAaLoI130_provenance.
• NP147460.RAuFlBoJDfT47b8A19NoddvuXia94CEsOEIo5kT1B893k130_assertion description "[filamin A is the first gene known to cause isolated nonsyndromic valvular heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147460.RAuFlBoJDfT47b8A19NoddvuXia94CEsOEIo5kT1B893k130_provenance.
• NP147461.RAtU53skMQYOXy9e3Bf93SV4rNhx4Vo3Gb4wGLhhuwmCM130_assertion description "[Mutations of PIK3CA is associated with anaplastic oligodendrogliomas, high-grade astrocytomas, and medulloblastomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147461.RAtU53skMQYOXy9e3Bf93SV4rNhx4Vo3Gb4wGLhhuwmCM130_provenance.
• NP147464.RAlW6WIlnBdbj5qVf8o7LMh03DQ_1wR4S4Wu9gfUhnnIg130_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." NP147464.RAlW6WIlnBdbj5qVf8o7LMh03DQ_1wR4S4Wu9gfUhnnIg130_provenance.
• NP147468.RAoarsvNY5zCYRFiEOQdzIAoYJomfJ-IrzjwRXiy48OV0130_assertion description "[Nogo-a expression in glial CNS tumors may be a marker to differentiate between oligodendrogliomas and other gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147468.RAoarsvNY5zCYRFiEOQdzIAoYJomfJ-IrzjwRXiy48OV0130_provenance.
• NP147469.RAoQNe0G2J5rtav9lobHuyJQT-a6ANu-mUpfhlLx-I26g130_assertion description "[Overexpression of OLIG2 was not only found in oligodendroglioma samples and normal neural tissue but also in a wide spectrum of malignant cell lines including leukemia, non-small cell lung carcinoma, melanoma, and breast cancer cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147469.RAoQNe0G2J5rtav9lobHuyJQT-a6ANu-mUpfhlLx-I26g130_provenance.
• NP147471.RAtOqO8LqsOFSmyxxln2PXQrayoWhClqNUO6YiS8v47MI130_assertion description "[We also have shown that the loss of ATAD 3A/3B may be involved in the transformation pathway and the chemosensitivity of oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147471.RAtOqO8LqsOFSmyxxln2PXQrayoWhClqNUO6YiS8v47MI130_provenance.
• NP147472.RAo3Y916uFEAbQ8PzejWOThElExoASFH1YG9f2SHF-f-I130_assertion description "[INI1hSNF5 and PARVG do not seem to be the tumor suppressor genes involved in oligodendroglioma development and progression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147472.RAo3Y916uFEAbQ8PzejWOThElExoASFH1YG9f2SHF-f-I130_provenance.

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