Nanopublications LDF server

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

• NP147987.RAetOR8GmoIKPOnVNPRUWtgia0E_YVXH8hNZa67ledVtg130_assertion description "[Significantly higher levels were found in soluble egg antigen-stimulated PBMC from schistosomiasis mansoni patients with degree III hepatic fibrosis compared to patients with degree I or II fibrosis, and in patients untreated for 1 year.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147987.RAetOR8GmoIKPOnVNPRUWtgia0E_YVXH8hNZa67ledVtg130_provenance.
• NP148029.RAZOl1gFsRZHMJFTvU__GWrLQDa6yytNsKMqLEMqYPM1I130_assertion description "[diabetic microangiopathy is genetically heterogeneous; PON1 Leu/Leu increases the risk for retinopathy and PON2 Ser/Ser increases the risk for microalbuminuria ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148029.RAZOl1gFsRZHMJFTvU__GWrLQDa6yytNsKMqLEMqYPM1I130_provenance.
• NP148031.RATxFoNca09fmAeiQe16gkmFcpPWcsvnIv99DRf2clrFI130_assertion description "[AGEs, a hallmark of diabetes, induce chymase via the RAGE-ERK1/2 MAP kinase pathway/initiates an important alternative angiotensin II-generating pathway in diabetes and may play a critical role in diabetic vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148031.RATxFoNca09fmAeiQe16gkmFcpPWcsvnIv99DRf2clrFI130_provenance.
• NP148035.RAWWjbAreAk4HG0QxDyBxJ8Xb_cnMAlrTSdE9EhesmhUg130_assertion description "[May represent an important pathway in diabetes complications and a new mechanism in phagocyte- and systemic infection-induced exacerbation of diabetic vascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148035.RAWWjbAreAk4HG0QxDyBxJ8Xb_cnMAlrTSdE9EhesmhUg130_provenance.
• NP148036.RAShdb-NQBMI7rs_H81acrko81CX052nQlwOjZeIVU9Kg130_assertion description "[Suggest that higher circulating Cu/Zn SOD could protect type 1 diabetes mellitus children/adolescents against endothelial dysfunction/Cu/Zn SOD is a potential early marker of susceptibility to diabetic vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148036.RAShdb-NQBMI7rs_H81acrko81CX052nQlwOjZeIVU9Kg130_provenance.
• NP148037.RATiKkqVOOsNrZTLIuEv7-Y52-5O2bYCqtcAzjLpyx1AM130_assertion description "[LA's ability to inhibit apoptosis and proliferation of ECs could beneficially affect endothelial dysfunction, which precedes manifestation of late diabetic vascular complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148037.RATiKkqVOOsNrZTLIuEv7-Y52-5O2bYCqtcAzjLpyx1AM130_provenance.
• NP148038.RAUvXk944oRNRfYowb1wsl-39RSUAvant0X7i1W65Wd_Y130_assertion description "[LA's ability to inhibit apoptosis and proliferation of ECs could beneficially affect endothelial dysfunction, which precedes manifestation of late diabetic vascular complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148038.RAUvXk944oRNRfYowb1wsl-39RSUAvant0X7i1W65Wd_Y130_provenance.
• NP148042.RAXDk-6x8Ryh07zb5Yb4JTsfqruQ0B1dHIUjWcC5BFJ6w130_assertion description "[In this pilot study, common variants of the apolipoprotein E (APOE) and HFE genes resulting in the iron overload disorder of hereditary hemochromatosis (C282Y, H63D and S65C) were evaluated as factors in sporadic AD in an Ontario sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148042.RAXDk-6x8Ryh07zb5Yb4JTsfqruQ0B1dHIUjWcC5BFJ6w130_provenance.
• NP148043.RAaRhXPnCV6b5Wj9vvfhTGStKwlUsiOOxWWujMLhP8rtM130_assertion description "[MPO genotype GG is associated with cirrhosis in patients with hereditary hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148043.RAaRhXPnCV6b5Wj9vvfhTGStKwlUsiOOxWWujMLhP8rtM130_provenance.
• NP148048.RAZ5mHwGbtIelyIJMPWrfbzdlEUZprMzWYvFcct89AryY130_assertion description "[Although the most prevalent genotype in HH is homozygosity for C282Y mutation of the HFE gene, two additional mutations, H63D and S65C, appear to be associated with a milder form of hereditary hemochromatosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148048.RAZ5mHwGbtIelyIJMPWrfbzdlEUZprMzWYvFcct89AryY130_provenance.
• NP148050.RAahYVRQqoEGST_lsHnfZLk2CYHUsZBzjJoO2vSRAEKbc130_assertion description "[Hemochromatosis is caused by a disruption of iron hemostasis due to mutations in the HFE gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148050.RAahYVRQqoEGST_lsHnfZLk2CYHUsZBzjJoO2vSRAEKbc130_provenance.
• NP148066.RAZPL1tKekZMzn3qBoBFVLCBpjPe8X_9_eNZz5jPXnOxw130_assertion description "[Transferrin receptor (TfR) and hemochromatosis factor, as well as TfR and DMT1 interact in placental trophoblast cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148066.RAZPL1tKekZMzn3qBoBFVLCBpjPe8X_9_eNZz5jPXnOxw130_provenance.
• NP148071.RAfJG-esf_u_-Z7tEXtHSMPaNVH_nLIQ_twvLeInVQYtI130_assertion description "[Mutation in the ferroportin 1 may be related to hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148071.RAfJG-esf_u_-Z7tEXtHSMPaNVH_nLIQ_twvLeInVQYtI130_provenance.
• NP148072.RAfZE3xUnwWI3fvcjovS82ReYyyTjBpNhD0du8JmH_AmY130_assertion description "[A 3-base pair deletion in exon 5 of the ferroportin 1 gene predicting Val162 deletion was found in a family with autosomal dominant inheritance of increased body iron stores without hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148072.RAfZE3xUnwWI3fvcjovS82ReYyyTjBpNhD0du8JmH_AmY130_provenance.
• NP148076.RAcecQepvRGoIB1d4TNyXVQctNLKDRXHOUYP3YGvO1OwI130_assertion description "[metacarpophalangeal arthropathy was independently associated with older age, higher ferritin, the presence of the C282Y +/+ and C282Y/H63D hemochromatosis protein (HFE) genotypes and higher percentage of transferrin saturation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148076.RAcecQepvRGoIB1d4TNyXVQctNLKDRXHOUYP3YGvO1OwI130_provenance.
• NP148078.RAQZ8XMlIu-oTRmhqSvqUnzeZlrDmgl2boodspoL-yLFU130_assertion description "[gene coding and flanking regions were sequenced and examined for mutations that might modulate the iron burden of individuals harboring the common mutant hemochromatosis HFE genotype or cause hemochromatosis independent of mutations in the HFE gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148078.RAQZ8XMlIu-oTRmhqSvqUnzeZlrDmgl2boodspoL-yLFU130_provenance.
• NP148079.RAdZisWBLPFSop2DOhMypgtY7taOyKAqdGYORZxFu22q0130_assertion description "[hemojuvelin may have a role in juvenile hemochromatosis [letter, case report]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148079.RAdZisWBLPFSop2DOhMypgtY7taOyKAqdGYORZxFu22q0130_provenance.
• NP148086.RAaUK5y0jXzod_6QGU-CQLHXBZ9iR5HdC0jO5EQFRfCIw130_assertion description "[Here we report the positional cloning of the locus associated with juvenile hemochromatosis and the identification of a new gene crucial to iron metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148086.RAaUK5y0jXzod_6QGU-CQLHXBZ9iR5HdC0jO5EQFRfCIw130_provenance.
• NP148088.RAYI0KQGg7ZP7OYZBc3u-6jc1Xn99HZSa1_a21-jZp6WE130_assertion description "[Hemojuvelin missense mutation is associated with hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148088.RAYI0KQGg7ZP7OYZBc3u-6jc1Xn99HZSa1_a21-jZp6WE130_provenance.
• NP148091.RAUas4yGU6Z62orM1aarGM-OzRn89rNUMmLMV_nie1smU130_assertion description "[a mutation in HAMP may play a role in familial hemochromatosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148091.RAUas4yGU6Z62orM1aarGM-OzRn89rNUMmLMV_nie1smU130_provenance.
• NP148093.RATnJbNp5aSpPSNfC4u67JEVuNZQf_hZLamLr99ROjgZk130_assertion description "[Mutations in hepcidin results in hemochromatosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148093.RATnJbNp5aSpPSNfC4u67JEVuNZQf_hZLamLr99ROjgZk130_provenance.
• NP148100.RAQQp61VCuqG0MYLxYCvpQPSWWRrSIWGlW4j_0SuBeEJk130_assertion description "[Additional risk of hereditary hemochromatosis given by class I HLA antigens may be secondary to the HFE gene linkage disequilibrium with certain class I alleles or to the existence of other neighboring genetic pathogenetic factors in our Spanish sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148100.RAQQp61VCuqG0MYLxYCvpQPSWWRrSIWGlW4j_0SuBeEJk130_provenance.
• NP148105.RATJNp_Z1Pi2t28X2qsC8GmYpBwoKD6Kk_cSHr6fzCcqU130_assertion description "[ALAS2 mutations might contribute to more severe iron loading in persons with primary hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148105.RATJNp_Z1Pi2t28X2qsC8GmYpBwoKD6Kk_cSHr6fzCcqU130_provenance.
• NP148111.RAaygqeItON-DgynBk6OAvz6jwvrrOqAbG2qv_5PajNoA130_assertion description "[Our results strongly confirm that ITPR1 is the causative gene for SCA15 and suggest that we need to investigate the point mutation in ITPR1 in the patients with autosomal dominant cerebellar ataxia and tremor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148111.RAaygqeItON-DgynBk6OAvz6jwvrrOqAbG2qv_5PajNoA130_provenance.
• NP148121.RAb9RD-C1WAmsXnUKPRXqO74gcILIHJJs2GgYxS2tT4YQ130_assertion description "[missense mutations of ALK-1 cause pulmonary hypertension in patients with hereditary haemorrhagic telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148121.RAb9RD-C1WAmsXnUKPRXqO74gcILIHJJs2GgYxS2tT4YQ130_provenance.
• NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_assertion description "[Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148122.RAerur00cavLPgmw9l4HzDi-TvDsEqqfwTtBarYlQo0m8130_provenance.
• NP148123.RAavdvmAohVP_jwFvMcPa2WhVr0dhsNQD0RVCX9m1BqE8130_assertion description "[At least 26% and up to 57% of patients with idiopathic perofoveal telangiectasia carry disease-associated variations in the ATM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148123.RAavdvmAohVP_jwFvMcPa2WhVr0dhsNQD0RVCX9m1BqE8130_provenance.
• NP148127.RAZzM5kGmLy7ab9Kf-XmLaFdgPNkWv8dU1KTXO55Ga3go130_assertion description "[ENG and ALK-1 genes may have roles in hereditary haemorrhagic telangiectasia in the Italian population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148127.RAZzM5kGmLy7ab9Kf-XmLaFdgPNkWv8dU1KTXO55Ga3go130_provenance.
• NP148128.RAZhx3oi9xR45tCzGHgXLKHkn5qs-p1vHXVDMvbI25q7c130_assertion description "[ENG and ALK-1 genes may have roles in hereditary haemorrhagic telangiectasia in the Italian population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148128.RAZhx3oi9xR45tCzGHgXLKHkn5qs-p1vHXVDMvbI25q7c130_provenance.
• NP148130.RAXDFwKUL4GIjGOQpTLUQsvLb1z0JR6u7dNvLFdRLbVKY130_assertion description "[nine of 80 prescreened hemophilia A patients showed large duplications of one or more exons ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148130.RAXDFwKUL4GIjGOQpTLUQsvLb1z0JR6u7dNvLFdRLbVKY130_provenance.
• NP148132.RATknSbhH2C3McdiMbCyafGw7VjDDRJVKJmuK8ba72Tcc130_assertion description "[Unreported mutations are distributed throughout the F8 gene and they affected all F8 exons but exon 20 in Italian hemophilia a patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148132.RATknSbhH2C3McdiMbCyafGw7VjDDRJVKJmuK8ba72Tcc130_provenance.
• NP148133.RATAaayyqKdLywsCtfitj8lpCw1prQLgRuQo1CIA3L0_I130_assertion description "[Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites.(]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148133.RATAaayyqKdLywsCtfitj8lpCw1prQLgRuQo1CIA3L0_I130_provenance.
• NP148142.RASlhOcyvXqioTlfNG5Nd11aagkU3w6iR_W7ssxNqxu9k130_assertion description "[analysis of epitope repertoire of coagulation factor VIII in hemophilia A patients and healthy subjects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148142.RASlhOcyvXqioTlfNG5Nd11aagkU3w6iR_W7ssxNqxu9k130_provenance.
• NP148149.RAXKdYgyA3gBON3pOFCfa0Id_yNvVFSy5YKPGvRCymNeo130_assertion description "[Patients with elevated levels of FVIII should be screened for blood group, as the non-O group confers a particularly high risk for arterial occlusive diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148149.RAXKdYgyA3gBON3pOFCfa0Id_yNvVFSy5YKPGvRCymNeo130_provenance.
• NP148154.RAYN5TmJIZ3bjT6fGPCmoFgi6Y5IQfW3ZU7elFL7h8zvg130_assertion description "[Maternal and neonatal thrombophilia, especially presence of FVL or antiphospholipid antibodies, may be important in the pathogenesis of perinatal arterial ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148154.RAYN5TmJIZ3bjT6fGPCmoFgi6Y5IQfW3ZU7elFL7h8zvg130_provenance.
• NP148155.RAdxeIzd_-affss_dbsIXDeVXokXiTHqTdTeZaUhV5R9Q130_assertion description "[There is limited evidence of the association of fetal thrombophilias and the risk of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148155.RAdxeIzd_-affss_dbsIXDeVXokXiTHqTdTeZaUhV5R9Q130_provenance.
• NP148158.RAdVfSB2kH94yJGDqAsrb_rT4ASaqdkAgCXkzHh1uCKLo130_assertion description "[Multifocal and unifocal osteonecrosis are similarly associated with thrombophilia, hypofibrinolysis, and the eNOS T-786C polymorphism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148158.RAdVfSB2kH94yJGDqAsrb_rT4ASaqdkAgCXkzHh1uCKLo130_provenance.
• NP148161.RAfQQbUaPAuI7iirVMMTDu3LHEyN2KhTE5ztsVScc5QS4130_assertion description "[Single nucleotide polymophism in thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148161.RAfQQbUaPAuI7iirVMMTDu3LHEyN2KhTE5ztsVScc5QS4130_provenance.
• NP148165.RAeGL4YWvLSV31etwNFCcISaZ7m6IfJlY0n1yvp_Kq8yo130_assertion description "[Arfaptin 1 inhibits ADP-ribosylation factor-dependent secretion of this enzyme induced by phorbol ester in fibrosarcoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148165.RAeGL4YWvLSV31etwNFCcISaZ7m6IfJlY0n1yvp_Kq8yo130_provenance.
• NP148168.RAcO8WNt3LMryJBHQnIXUnI73lc8IibANfT7PVCklk6oI130_assertion description "[Presence of FUS/CREB3L2 and FUS/CREB3L1 in low-grade fibromyxoid sarcoma and sclerosing epithelioid fibrosarcoma suggests these neoplasms may be related.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148168.RAcO8WNt3LMryJBHQnIXUnI73lc8IibANfT7PVCklk6oI130_provenance.
• NP148171.RAYjMEB1RWr08kD12Z6OTfjRdC4pVQBmbcKHSf0LT3d7o130_assertion description "[Comparison and modulation of angiogenic responses by FGFs, VEGF and SCF in murine and human fibrosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148171.RAYjMEB1RWr08kD12Z6OTfjRdC4pVQBmbcKHSf0LT3d7o130_provenance.
• NP148177.RAYmcghOaFIxrbjitsovS9eQRCycpcAf3M3q7QRF3dVDM130_assertion description "[Collectively, our results demonstrate that treatment of HT-1080 fibrosarcoma cells exogenously with either TFPI-2 or its first Kunitz domain mutant R24K activates caspase-mediated, pro-apoptotic signaling pathways resulting in apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148177.RAYmcghOaFIxrbjitsovS9eQRCycpcAf3M3q7QRF3dVDM130_provenance.
• NP148181.RAaFS1ZHbHTWz2AVunXVja6WoHLojwlTm9urP5J6rXiaA130_assertion description "[Alterations of the TP53 gene occur not only as somatic mutations in human malignancies, but also as germline mutations in some cancer-prone families with Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148181.RAaFS1ZHbHTWz2AVunXVja6WoHLojwlTm9urP5J6rXiaA130_provenance.
• NP148182.RAYgZIgFqHEn-onjLWKn25BRU6pIfGHL7jZ_5kFjihngc130_assertion description "[A novel germline mutation in p53 gene was found in a patient with Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148182.RAYgZIgFqHEn-onjLWKn25BRU6pIfGHL7jZ_5kFjihngc130_provenance.
• NP148187.RAT1mtJryjj0xCNpbGGHIUsG8M5GWlPupTuuti17pUCTI130_assertion description "[R248W may predispose to composite tumors and to neuroblastoma in individuals with Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148187.RAT1mtJryjj0xCNpbGGHIUsG8M5GWlPupTuuti17pUCTI130_provenance.
• NP148190.RAU_qXxqfHht_8YVF8_C4EfN14XmpSt-QyyPynEoqUhRI130_assertion description "[Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148190.RAU_qXxqfHht_8YVF8_C4EfN14XmpSt-QyyPynEoqUhRI130_provenance.
• NP148191.RAS9DHXgjcVGL2eAqatFMtiFCB4jtYNJLyqFGF6tYrU30130_assertion description "[TP53 germline mutation carriers with SNP309 G allele have earlier onset of tumours; higher prevalence of MDM2 SNP309 homozygous carriers in TP53-negative group suggests allele contributes to cancer susceptibility in Li-Fraumeni syndrome & related families ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148191.RAS9DHXgjcVGL2eAqatFMtiFCB4jtYNJLyqFGF6tYrU30130_provenance.
• NP148197.RARmJiZ8XjAoH0DP5Km-TTLarBYYqYAF2XOp1Z_eXQHqU130_assertion description "[increased risk of fetal alcohol syndrome for the maternal and possibly fetal ADH1B/ADH1B genotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148197.RARmJiZ8XjAoH0DP5Km-TTLarBYYqYAF2XOp1Z_eXQHqU130_provenance.
• NP148198.RAdfVA_OR2NMdre6AJtGnR4nL9-CIVEV1a1MfnohpqkuU130_assertion description "[Data show that genotypes for the G-- > A (Asp2213Asn) polymorphism (rs529038) of ROS1 was associated (P < 0.05) with the prevalence of atherothrombotic cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148198.RAdfVA_OR2NMdre6AJtGnR4nL9-CIVEV1a1MfnohpqkuU130_provenance.
• NP148202.RAeW51fTCJ_wJRfhkcwJR2ZPXdftUet45JTY8a-KbqlX0130_assertion description "[Data show that genotypes for the 3279C-- > T polymorphism (rs7291467) of LGALS2 was associated (P < 0.05) with the prevalence of atherothrombotic cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148202.RAeW51fTCJ_wJRfhkcwJR2ZPXdftUet45JTY8a-KbqlX0130_provenance.
• NP148204.RAbm-FyZ-Q5j86EORlniNEFBU6cJgYiB1DO8tecycMjLw130_assertion description "[HGF has pivotal role for functional recovery after cerebral infarction through neuritogenesis, improved microcirculation, and prevention of gliosis/for feasibility of gene therapy in chronic stage of cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148204.RAbm-FyZ-Q5j86EORlniNEFBU6cJgYiB1DO8tecycMjLw130_provenance.
• NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_assertion description "[single nucleotide polymorphism (SNP) haplotypes may play an important role in pathogenesis of primary hypertension and be the genetic risk factors for the onset of primary hypertension with cerebral infarction in the Li nationality of Hainan, China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_provenance.
• NP148208.RAX7FRzya4fY3oWfo6pZWmHz9NBY8Y1Bzy1cVNS9qY9QA130_assertion description "[the 4G/4G-PAI-1 genotype might be a protective factor against atherothrombotic cerebral infarction (ACI), whereas the factor V point mutation (1691G-A) and the factor VII Arg/Gln353 gene polymorphism have not proved to be risk factors for ACI ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148208.RAX7FRzya4fY3oWfo6pZWmHz9NBY8Y1Bzy1cVNS9qY9QA130_provenance.
• NP148212.RAXczv3ZfitNfFiWcMTH0glbgeWU4-o4qTUizeNpHOLAY130_assertion description "[the 4G/4G-PAI-1 genotype might be a protective factor against atherothrombotic cerebral infarction (ACI), whereas the factor V point mutation (1691G-A) and the factor VII Arg/Gln353 gene polymorphism have not proved to be risk factors for ACI ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148212.RAXczv3ZfitNfFiWcMTH0glbgeWU4-o4qTUizeNpHOLAY130_provenance.
• NP148217.RAZ1wVYEJA0YGbAYcCw1PkTJiQEk4DBL6KW3EzMjdBXdQ130_assertion description "[The detection of serum sICAM-1 will be helpful in estimating the clinical severity of cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148217.RAZ1wVYEJA0YGbAYcCw1PkTJiQEk4DBL6KW3EzMjdBXdQ130_provenance.
• NP148218.RAbIyuqpt_GgCM1aLykVkG7UuxPeNqTB1d66YKEzg3PDk130_assertion description "[Midkine was expressed in choroid plexus of normal brain and released there; CSF MK levels were not high in patients with cerebral infarction but were increased in patients with meningitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148218.RAbIyuqpt_GgCM1aLykVkG7UuxPeNqTB1d66YKEzg3PDk130_provenance.
• NP148220.RAdfROzQZQqQfn6JQTMwxXKRkIKNmRtgbF46QxfavyWDg130_assertion description "[The Ser447Terls polymorphism of LPL gene is significantly associated with plasma lipids and CI/allele genotype may lead to decrease of plasma TG and increase of plasma HDL-C/allele may be a protective genotype of cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148220.RAdfROzQZQqQfn6JQTMwxXKRkIKNmRtgbF46QxfavyWDg130_provenance.
• NP148221.RASMiyqDdwrqfDRWTKjawX4usZlg2OWGtQJ6usHjhyDx8130_assertion description "[We investigated two genetic polymorphisms in the TNF locus (TNF-alpha -308 G-- > A and TNF-beta +252 A-- > G) as risk factors for cerebral infarction (CI) by determining its prevalence in 294 survivors of CI, and in 581 age, gender, and race-matched controls ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148221.RASMiyqDdwrqfDRWTKjawX4usZlg2OWGtQJ6usHjhyDx8130_provenance.
• NP148227.RAfao4ySJGd85qmpFOcklnDNF85uyfIRQ99yQzJ_EgPjQ130_assertion description "[the 4G/4G-PAI-1 genotype might be a protective factor against atherothrombotic cerebral infarction (ACI), whereas the factor V point mutation (1691G-A) and the factor VII Arg/Gln353 gene polymorphism have not proved to be risk factors for ACI ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148227.RAfao4ySJGd85qmpFOcklnDNF85uyfIRQ99yQzJ_EgPjQ130_provenance.
• NP148233.RAYcRWjLPGBsF9WHVP34NGWcOnjAHskDUgoGXnBu9QfoM130_assertion description "[Folic acid deficiency could result in reduction of TGF-beta1 protein levels and might contribute to formation of defects in the skull bone as observed in mengingocele patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148233.RAYcRWjLPGBsF9WHVP34NGWcOnjAHskDUgoGXnBu9QfoM130_provenance.
• NP148235.RAaAOxcettN9j4WZ5bt6amQRrBMVjWMYle6OlSU3W1LfQ130_assertion description "[PDGFRA P1 promoter region haplotypes do not have a major role in the development of spina bifida meningomyelocele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148235.RAaAOxcettN9j4WZ5bt6amQRrBMVjWMYle6OlSU3W1LfQ130_provenance.
• NP148239.RASsXAJyZq86fancfSX-6Vkthx5gU50hswf92Hd2uPRWM130_assertion description "[The MTRR polymorphism is a maternal risk factor for spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148239.RASsXAJyZq86fancfSX-6Vkthx5gU50hswf92Hd2uPRWM130_provenance.
• NP148243.RAfuGPHyODFpJ-n_W7Qvx_njhkQmRXpZw0vG0TZU8qH94130_assertion description "[NAT1 variants that reduce or abolish enzyme activity appear to protect against spina bifida, and to exert their influence via both the maternal and the offspring genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148243.RAfuGPHyODFpJ-n_W7Qvx_njhkQmRXpZw0vG0TZU8qH94130_provenance.
• NP148249.RAV-2-ZY6wiZCqt3Iuut-OJo2nfy8YZZNrb9WQbB42mPM130_assertion description "[These data are the first to suggest that polymorphisms in the UCP2 gene may be genetic risk factors of spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148249.RAV-2-ZY6wiZCqt3Iuut-OJo2nfy8YZZNrb9WQbB42mPM130_provenance.
• NP148253.RARcGALw6Rg9PuM3o6Rtz3DypcQ0fXQrE0VOH8QIDqPZ8130_assertion description "[single nucleotide polymorphisms on gene involved with glucose metabolism and obesity may be associated with increased susceptibility to spina bifida ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148253.RARcGALw6Rg9PuM3o6Rtz3DypcQ0fXQrE0VOH8QIDqPZ8130_provenance.
• NP148254.RAeEd9ZBAlDV5B3-NDifjkk9ms2TZam2jEfXnYuZiPsYc130_assertion description "[The data do not support a strong association between single nucleotide polymorphism of PRKCB and spina bifida risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148254.RAeEd9ZBAlDV5B3-NDifjkk9ms2TZam2jEfXnYuZiPsYc130_provenance.
• NP148257.RAS1vbUeKpw0eLYTMOB0IlILn07HMndC5wO2W5aB4m6JA130_assertion description "[Variants influence the risk of spina bifida via the maternal rather than the embryonic genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148257.RAS1vbUeKpw0eLYTMOB0IlILn07HMndC5wO2W5aB4m6JA130_provenance.
• NP148258.RAdS7PUaV-uiAMglC4GnUPRc8Q_-ZiEIO9uCWgGqbBwvY130_assertion description "[ABCC2 promoter polymorphism is not a determinant of the risk of spinal dysraphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148258.RAdS7PUaV-uiAMglC4GnUPRc8Q_-ZiEIO9uCWgGqbBwvY130_provenance.
• NP148264.RARjRYvtgowbyD0e-tMkbBV_ksueIbf3zyiKOBAzRW1AE130_assertion description "[MMP-9 plays a role in the pathophysiology of gestational hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148264.RARjRYvtgowbyD0e-tMkbBV_ksueIbf3zyiKOBAzRW1AE130_provenance.
• NP148269.RAQrC-729QrLefgjQ-R-BHMkje1TU95bXAOTG5ZPKvpEE130_assertion description "[eNOS haplotypes associated with gestational hypertension or pre-eclampsia are reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148269.RAQrC-729QrLefgjQ-R-BHMkje1TU95bXAOTG5ZPKvpEE130_provenance.
• NP148275.RASYjhW_aI_MvKM4AAzqKQr09eMr1Nxgr9yIX7IBeq2Wo130_assertion description "[The S810L missense mutation of the mineralocorticoid receptor does not play a major role in the etiology of pregnancy-induced hypertension in a German/Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148275.RASYjhW_aI_MvKM4AAzqKQr09eMr1Nxgr9yIX7IBeq2Wo130_provenance.
• NP148278.RAfZ9njQxq4nyI6XeJyuh2vbCwYKGlt1Z7-xScq-jLIBQ130_assertion description "[Higher plasma pro-MMP-9 levels, and higher pro-MMP-9/TIMP-1 ratios in women with gestational hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148278.RAfZ9njQxq4nyI6XeJyuh2vbCwYKGlt1Z7-xScq-jLIBQ130_provenance.
• NP148280.RAVxKpcpECily149qJQ2zBgmwDnkKvhgt3iClUiHf4wz4130_assertion description "[Comparison of TIMP2 levels in preeclampsia and gestational hypertension with those found in normotensive pregnancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148280.RAVxKpcpECily149qJQ2zBgmwDnkKvhgt3iClUiHf4wz4130_provenance.
• NP148281.RAa1FjrWUpPAiEeWQoaeaOkjP30dwN6xzi4uU4p65trQY130_assertion description "[altered MMP/TIMP ratios in maternal blood during gestational hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148281.RAa1FjrWUpPAiEeWQoaeaOkjP30dwN6xzi4uU4p65trQY130_provenance.
• NP148290.RAbVs_MLave1PvYILOKhmhLkE-m4Cgt9v5mnu0Oia-pQI130_assertion description "[study identified the first FIX mutations (two novel) in Albanian hemophilia B patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148290.RAbVs_MLave1PvYILOKhmhLkE-m4Cgt9v5mnu0Oia-pQI130_provenance.
• NP148291.RASZJ1RUN0HY16344sDEaQElnz6-2dNoBiS_1ze6A7-no130_assertion description "[analysis of missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val) [letter]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148291.RASZJ1RUN0HY16344sDEaQElnz6-2dNoBiS_1ze6A7-no130_provenance.
• NP148293.RATAJfDVEhd3hbGzF5e-h-xT0VrQSuOHKxfs1g1Gbp9Qg130_assertion description "[2 new point mutations and a new deletion were found in hemophilia B families from northern India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148293.RATAJfDVEhd3hbGzF5e-h-xT0VrQSuOHKxfs1g1Gbp9Qg130_provenance.
• NP148295.RAYdVnV44fCdD0cSdV9WRWupqqmGkncmRaQLjn9_AxDDA130_assertion description "[Therapeutic levels of human FIX were achieved in nonhuman primates using an adeno-associated virus as a vector for gene therapy of hemophilia B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148295.RAYdVnV44fCdD0cSdV9WRWupqqmGkncmRaQLjn9_AxDDA130_provenance.
• NP148298.RAQkitSbY1wMg-qBaFEX-Ieb5Z08bBgwU6fzLAWsEy3NQ130_assertion description "[Six novel missense mutations were identified in factor XI deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148298.RAQkitSbY1wMg-qBaFEX-Ieb5Z08bBgwU6fzLAWsEy3NQ130_provenance.
• NP148304.RAYz5GFgbhiuqZO3XEfS1-ZyO55bIspaFK51jdjXRJduQ130_assertion description "[analysis of missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val) [letter]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148304.RAYz5GFgbhiuqZO3XEfS1-ZyO55bIspaFK51jdjXRJduQ130_provenance.
• NP148308.RAXI6EVoM3YnXdQvt9MnU5XwVIHhxd3ryv1u3hxpNrQN0130_assertion description "[Substitution of a nucleotide G-- > A at position -248 in the bax gene was more frequent in patients with osteomyelitis and was associated with a longer lifespan of their peripheral blood neutrophils and lower Bax protein expression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148308.RAXI6EVoM3YnXdQvt9MnU5XwVIHhxd3ryv1u3hxpNrQN0130_provenance.
• NP148312.RAVWP0r5uZWGHWCgOhV2GTCC7ILPqeP9Md_1o2PhVRNHI130_assertion description "[The measurement of adenosine deaminase activity in ascites represents a diagnostic advance in tuberculous peritonitis among end-stage renal failure patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148312.RAVWP0r5uZWGHWCgOhV2GTCC7ILPqeP9Md_1o2PhVRNHI130_provenance.
• NP148322.RAfg6vhHHmWeyJBMcv_0ff0Oneh2jaaTF2s321Zwp_Vs8130_assertion description "[Elevated N-terminal prohormone brain nutriuretic peptide levels are associated with higher risk of cardiovascular disease among blacks with hypertensive kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148322.RAfg6vhHHmWeyJBMcv_0ff0Oneh2jaaTF2s321Zwp_Vs8130_provenance.
• NP148324.RAUS0fePJV7UDRk0GZqDZWG7WNxXKnP3xbZHyr_bvvWRs130_assertion description "[Report BNP/NT-proBNP levels in chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148324.RAUS0fePJV7UDRk0GZqDZWG7WNxXKnP3xbZHyr_bvvWRs130_provenance.
• NP148327.RAZWUrVA22NcqzN2Rdb9N7_4vukIGRLZWphzG0-pWydkg130_assertion description "[Serum fetuin-A levels are not related to all-cause or cardiovascular mortality among persons with predominantly non-diabetic stage 3 or 4 chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148327.RAZWUrVA22NcqzN2Rdb9N7_4vukIGRLZWphzG0-pWydkg130_provenance.
• NP148334.RAbkakNQJ3QYNoxjOayhnBhnmUnJdd6cRTzPTLdBk2vnU130_assertion description "[Circulating levels of visfatin and adiponectin are associated with endothelial dysfunction in all stages of chronic kidney disease, independently of inflammation and insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148334.RAbkakNQJ3QYNoxjOayhnBhnmUnJdd6cRTzPTLdBk2vnU130_provenance.
• NP148336.RAcQGjjbN7et_lZGW0qIMScZgrZIB8Ho8XJcvxw7wkkR8130_assertion description "[Inhibition of MMP-2 in transgenic mice may offer an additional approach for treatment of chronic kidney diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148336.RAcQGjjbN7et_lZGW0qIMScZgrZIB8Ho8XJcvxw7wkkR8130_provenance.
• NP148339.RAS9zLTPttDBOx8AMKnm6TOA6wLeCzjX9FsgjPy4zGukQ130_assertion description "[This study suggests that there is an interaction between leptin, IGF-1, IGFBP-3 and insulin resistance in patients with chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148339.RAS9zLTPttDBOx8AMKnm6TOA6wLeCzjX9FsgjPy4zGukQ130_provenance.
• NP148341.RAUHgV3oSd63FiQUrcuRxFs9URXiFHX40oayyweuMAZa4130_assertion description "[circulating levels of adhesion molecules in correlated positively with the stage of kidney disease and with C-reactive protein ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148341.RAUHgV3oSd63FiQUrcuRxFs9URXiFHX40oayyweuMAZa4130_provenance.
• NP148344.RAfWpU2wYv6fzeDXLwAC-oqfzbk8MPFGVIKBcTn-sdTJo130_assertion description "[Although CETP activity correlated with HDL-C levels, neither high CETP activity nor low HDL-C was associated with cardiovascular events in chronic kidney disease stage V patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148344.RAfWpU2wYv6fzeDXLwAC-oqfzbk8MPFGVIKBcTn-sdTJo130_provenance.
• NP148346.RAZrUlgE_knUI1Pu3KrXwkqHlGskpxBjMmwuT8qEWMdW8130_assertion description "[the anemia of chronic kidney disease was associated with up regulation of TNF-alpha, and possibly IL-6 and IL-8 along with increased levels of these proinflammatory cytokines in patients treated with epoetin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148346.RAZrUlgE_knUI1Pu3KrXwkqHlGskpxBjMmwuT8qEWMdW8130_provenance.
• NP148348.RAWqgXYJOzzNIDDIgK5B2Bf1YODQ5HM--HI9QCZOjiug0130_assertion description "[These data point to an interesting relationship between low IGF-1 levels and increased cardiovascular risk factors among chronic kidney disease patients as compared to age-matched healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148348.RAWqgXYJOzzNIDDIgK5B2Bf1YODQ5HM--HI9QCZOjiug0130_provenance.
• NP148355.RAen1li16uGuuiIOLYMVXN3JQ1QHE0iusx_FIl1l-24s4130_assertion description "[We identified a new candidate uromodulin-associated kidney disease locus on chromosome 1q41 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148355.RAen1li16uGuuiIOLYMVXN3JQ1QHE0iusx_FIl1l-24s4130_provenance.
• NP148358.RAT0hctj6RI3LJTcrJYWXofVK8aJ3q6iNH9vYND14xhhc130_assertion description "[concentrations in nondialyzed chronic kidney disease patients, and the relationship with acidosis, zinc, anemia, and iron supplementation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148358.RAT0hctj6RI3LJTcrJYWXofVK8aJ3q6iNH9vYND14xhhc130_provenance.
• NP148367.RAbk_rmVFZnqRWApiCf698IrJA_3QLVwGlTud3H4nX1iU130_assertion description "[elevation of serum and urine levels in patients with kidney diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148367.RAbk_rmVFZnqRWApiCf698IrJA_3QLVwGlTud3H4nX1iU130_provenance.
• NP148371.RAbxveKnTBTQgOaZ0MlPYRjQYhDWjz-PmIChqU2V-aHGE130_assertion description "[High C reactive protein and high serum fibrinogen provide prognostic information in chronic kidney disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148371.RAbxveKnTBTQgOaZ0MlPYRjQYhDWjz-PmIChqU2V-aHGE130_provenance.
• NP148376.RARf4hvgOWizTlYTkKYfhzFmZCKcjD9kurKSsD1M45cqg130_assertion description "[Genetic variation at the MYH9 locus is associated with nondiabetic end-stage kidney diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148376.RARf4hvgOWizTlYTkKYfhzFmZCKcjD9kurKSsD1M45cqg130_provenance.
• NP148377.RAXB7bri5cXB-3hoxMDMiOo2WCVa0M8KepuLOeqsWiS34130_assertion description "[Circulating FGF-23 was significantly elevated in patients with chronic kidney disease and its concentration correlated with renal creatinine clearance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148377.RAXB7bri5cXB-3hoxMDMiOo2WCVa0M8KepuLOeqsWiS34130_provenance.
• NP148379.RAdddeNt_t9DV39KFJyJokXHT7HMHPIMTCHj7gCHV7QTk130_assertion description "[This study suggests that there is an interaction between leptin, IGF-1, IGFBP-3 and insulin resistance in patients with chronic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148379.RAdddeNt_t9DV39KFJyJokXHT7HMHPIMTCHj7gCHV7QTk130_provenance.
• NP148380.RAaokdhE_JjDbZoGhRiyY_4L-cLn08bCeqTy8wTSzouFM130_assertion description "[Our study demonstrates that the novel BALP B1x isoform is occasionally found to be present in children with kidney disease but to a lesser degree in comparison with adults with chronic kidney disease on dialysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148380.RAaokdhE_JjDbZoGhRiyY_4L-cLn08bCeqTy8wTSzouFM130_provenance.

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