Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP145206.RASNYOilpCu0yL2qHk1r-_EDy-ZC3jcB-ppvSRHyoLvdI130_assertion description "[the SAA1 alpha/alpha genotype is a risk factor for amyloidosis in BD ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145206.RASNYOilpCu0yL2qHk1r-_EDy-ZC3jcB-ppvSRHyoLvdI130_provenance.
- NP145207.RAb7ZJ46k_yzWOPvbNdu2M9Q6-wQRbKE9ngE1_NDCuan8130_assertion description "[homozygosity for an amyloidogenic transthyretin mutation may have an effect on phenotype and long term outcome in fatal neuropathic amyloidosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145207.RAb7ZJ46k_yzWOPvbNdu2M9Q6-wQRbKE9ngE1_NDCuan8130_provenance.
- NP145211.RAeo8SifNO_qMH67CI6XQalzCHKK9MVfER-MWQR7v6AVo130_assertion description "[a novel transthyretin (TTR) variant, aspartic acid-18 glutamic acid (Glu), causing TTR-related cardiac amyloidosis in a heterozygote ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145211.RAeo8SifNO_qMH67CI6XQalzCHKK9MVfER-MWQR7v6AVo130_provenance.
- NP145214.RAZfkARKY0ME6GCfYlzi3mi5inn7A1w4MQLHGEp1NODLc130_assertion description "[Lattice phenotype resulting from TGFBI A546D mutation in this family is distinct from that observed in previously described pedigree carrying the A546D mutation and exhibiting phenotype designated " polymorphic corneal amyloidosis ".]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145214.RAZfkARKY0ME6GCfYlzi3mi5inn7A1w4MQLHGEp1NODLc130_provenance.
- NP145216.RAVPeCAU8fWsP1SIyzwwj8_KjLr2EV9CVXBFPHhc7N9OE130_assertion description "[Corneal amyloidosis with an autosomal dominant mode of inheritance is characterized clinically by the presence of refractile polymorphic corneal opacities, which is caused by an A546D mutation in the TGFBI gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145216.RAVPeCAU8fWsP1SIyzwwj8_KjLr2EV9CVXBFPHhc7N9OE130_provenance.
- NP145218.RAYjthIQXpFG1U2pD5C5Z0uTW-R_0aFypFLKQj8GLqq50130_assertion description "[Senile systemic amyloidosis was associated with age, myocardial infarctions, the G/G (Val/Val) genotype of the exon 24 polymorphism in the alpha2-macroglobulin (alpha2M), and the H2 haplotype of the tau gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145218.RAYjthIQXpFG1U2pD5C5Z0uTW-R_0aFypFLKQj8GLqq50130_provenance.
- NP145222.RAZis9tXkX9SCGEFRAfb5FX6w05JeERYicUV2AvsbFAuI130_assertion description "[Though the effects of the MEFV genotypes seem clear, there are definitely other modifying factors or genes such as MICA on the development of amyloidosis and on the course of the disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145222.RAZis9tXkX9SCGEFRAfb5FX6w05JeERYicUV2AvsbFAuI130_provenance.
- NP145224.RAfgq-vRyJamnExbGvKGkt2OxYEmj8m4ZOFzfWYkR9bEE130_assertion description "[in Turkish Mediterranean Fever patients and their families, frequency of carriers was 27%, and the M694V/M694V genotype was more common in patients with amyloidosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145224.RAfgq-vRyJamnExbGvKGkt2OxYEmj8m4ZOFzfWYkR9bEE130_provenance.
- NP145227.RAb2UVc3hP7prPdwgrfxBw_af_c3ls4w72EF1mfiJT0QA130_assertion description "[To investigate the roles of hIAPP and islet amyloidosis in type 2 diabetes mellitus, transgenic mice expressing hIAPP in their islet beta cells were generated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145227.RAb2UVc3hP7prPdwgrfxBw_af_c3ls4w72EF1mfiJT0QA130_provenance.
- NP145244.RAX7M3Z-UJfETKmhKmPl92B9mBdw49KJV9I5XAyYN5uzk130_assertion description "[in 3 German amyloidosis patients, sequenced the FGA exon 5 and demonstrated heterozygosity for the p.Glu526Val mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145244.RAX7M3Z-UJfETKmhKmPl92B9mBdw49KJV9I5XAyYN5uzk130_provenance.
- NP145245.RAZiV-urfMh3fejd1pEtoFQg_EP_DZd0F7wHJzBSj4KCY130_assertion description "[Hereditary systemic amyloidosis comprises several autosomal dominant diseases caused by mutations in a number of plasma proteins, including the fibrinogen Aalpha-chain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145245.RAZiV-urfMh3fejd1pEtoFQg_EP_DZd0F7wHJzBSj4KCY130_provenance.
- NP145248.RAXW8qTVFjHpkEusE75Whic-Ww2N8Fs9ay434SNhvNC9A130_assertion description "[NFKBIA 3'UTR GG genotype associated with an increased risk for extensive colitis in Hungarian inflammatory bowel disease patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145248.RAXW8qTVFjHpkEusE75Whic-Ww2N8Fs9ay434SNhvNC9A130_provenance.
- NP145252.RASS6bnnVnASrtdGxxRuLxWoxfPxXNAJMJOvZFE3CX-KQ130_assertion description "[Possesses antiapoptotic effects in the colonic mucosa by activating Akt, which prevents apoptosis and mediates tissue recovery during colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145252.RASS6bnnVnASrtdGxxRuLxWoxfPxXNAJMJOvZFE3CX-KQ130_provenance.
- NP145255.RAT4qJa9wCD-NwfFAr-IU9lilyLy1ESaWbXy2qxuDvj-Y130_assertion description "[NFATc2 has a role in colitis by controlling mucosal T cell activation in an IL-6-dependent manner ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145255.RAT4qJa9wCD-NwfFAr-IU9lilyLy1ESaWbXy2qxuDvj-Y130_provenance.
- NP145263.RAVU4N2aShTGYApidZJzWV_v1o5GHwikGOlKlPWu4ZVB0130_assertion description "[Agt gene was associated with the susceptibility to Henoch-Schonlein purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145263.RAVU4N2aShTGYApidZJzWV_v1o5GHwikGOlKlPWu4ZVB0130_provenance.
- NP145274.RAeceKhTjc2nQSs7sSeZa1xOt1fg8CtoU1ID9s2rwWN0E130_assertion description "[Increased frequency of HLA A2, A11, and B35 alleles in unselected pediatric Henoch Schonlein purpura patient population may be a risk factor for susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145274.RAeceKhTjc2nQSs7sSeZa1xOt1fg8CtoU1ID9s2rwWN0E130_provenance.
- NP145275.RARVVUNjUNnnoSttX8dPbKahK4vMZRZr6YSPQbp0nE0qQ130_assertion description "[Henoch-Schonlein purpura and cutaneous leukocytoclastic angiitis exhibit different HLA-DRB1 genotype associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145275.RARVVUNjUNnnoSttX8dPbKahK4vMZRZr6YSPQbp0nE0qQ130_provenance.
- NP145277.RAabkgRvLdYHa02IDp4IN5QlcPCFl7AA9KMTI1NQLOhC8130_assertion description "[CTLA-4 +49 A/G polymorphism does not contribute to susceptibility to Henoch-Schonlein purpura; however, the presence of CTLA-4 AG genotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145277.RAabkgRvLdYHa02IDp4IN5QlcPCFl7AA9KMTI1NQLOhC8130_provenance.
- NP145285.RAfYOOeuCS4lVhlff0vhD6hz7qn16Wi9-4I6E2SgQKhX0130_assertion description "[in Turkish Mediterranean Fever patients and their families, frequency of carriers was 27%, and the M694V/M694V genotype was more common in patients with amyloidosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145285.RAfYOOeuCS4lVhlff0vhD6hz7qn16Wi9-4I6E2SgQKhX0130_provenance.
- NP145286.RAV4Q-8A0M3483oWDErk-HUSHO40pG5NxFaZqX0H7Lvb0130_assertion description "[persistently elevated, serum levels of ICAM-2 throughout the various phases and types of Hemorrhagic fever with renal syndrome (HFRS) may be associated with the hyperfunctioning of the cellular immune response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145286.RAV4Q-8A0M3483oWDErk-HUSHO40pG5NxFaZqX0H7Lvb0130_provenance.
- NP145289.RAVATtbHHZTIO4evonxi9Ev4olu95UsDvHYqTZOODUMYk130_assertion description "[Mutations of MVK found in hyper-IgD and periodic fever syndrome patients affect the stability and/or maturation of MVK in vitro in a temperature-sensitive manner and may explain the chain of events leading to episodic inflammation and fever.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145289.RAVATtbHHZTIO4evonxi9Ev4olu95UsDvHYqTZOODUMYk130_provenance.
- NP145294.RAb-WY2Xk4_eC2HwOWZzBDK9iq4clloA7bvqAbksxjXa8130_assertion description "[Single nucleotide polymorphisms in LMX1B gene is associated with nail dysplasia in the nail patella syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145294.RAb-WY2Xk4_eC2HwOWZzBDK9iq4clloA7bvqAbksxjXa8130_provenance.
- NP145304.RARmeNjApezvW1qyJgvrCXrcrMk0ymjadwBwZ9q3bfv2I130_assertion description "[Association of polymorphisms of the transforming growth factor-beta1 gene with the rate of progression of HCV-induced liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145304.RARmeNjApezvW1qyJgvrCXrcrMk0ymjadwBwZ9q3bfv2I130_provenance.
- NP145305.RATe717800FsptMwEaXY_4HgAUNE-bnUOuU-AbQW9slB8130_assertion description "[Established liver fibrosis patients had the homozygote G/G TGF-beta genotype, which has been associated with increased development of fibrosis/of our patients had the G/C genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145305.RATe717800FsptMwEaXY_4HgAUNE-bnUOuU-AbQW9slB8130_provenance.
- NP145307.RAc7_GFR5MGcHX4iCXTpKYKS8yMmZrFtlwbNNzobmk5k4130_assertion description "[The genetic mutation of MTHFR C667T is possibly an important mechanism of hyperhomocysteinemia in liver cirrhosis/level of plasm homocysteine may be an eary indicator for liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145307.RAc7_GFR5MGcHX4iCXTpKYKS8yMmZrFtlwbNNzobmk5k4130_provenance.
- NP145310.RAe3AEeLSajDY8bAywinQlUDtRrWPll0K2tIvjKikBpGY130_assertion description "[C282Y or H63D heterozygosity is an independent risk factor for liver fibrosis and cirrhosis in HCV infected individuals/for HFE mutations should be considered in HCV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145310.RAe3AEeLSajDY8bAywinQlUDtRrWPll0K2tIvjKikBpGY130_provenance.
- NP145319.RAZmGHPJ8pfeNyV7yFV2FbJTBBc2dnlq5jZBGkKYikLa4130_assertion description "[Reduced circulating adiponectin occurs in rat fatty liver disease, but it is elevated in a mouse cirrhosis with similar findings in humans/hepatic expression of adiponectin receptors (AdipoR2 and AdipoR1) was only found in liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145319.RAZmGHPJ8pfeNyV7yFV2FbJTBBc2dnlq5jZBGkKYikLa4130_provenance.
- NP145325.RAUzcerjLyt56OjLAv1Gqa4bhfdw88NE8MX7lyk8yxNlc130_assertion description "[In conclusion, this study shows a role for resistin as an intrahepatic cytokine exerting proinflammatory actions in HSCs, via a Ca2+/NF-kappaB-dependent pathway and suggests involvement of this adipokine in the pathophysiology of liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145325.RAUzcerjLyt56OjLAv1Gqa4bhfdw88NE8MX7lyk8yxNlc130_provenance.
- NP145326.RAYFMADExIPUETifEbwVB9L-qYEy_ciLOW_7VQaMZA9jo130_assertion description "[In patients with decompensated liver cirrhosis, intraabdominal production of leptin may contribute to the metabolic picture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145326.RAYFMADExIPUETifEbwVB9L-qYEy_ciLOW_7VQaMZA9jo130_provenance.
- NP145327.RAaHi2ZvodGIcwXFZa4R2l70mvOfv7i5ztnzmLvZcgpsA130_assertion description "[In liver cirrhosis, the effects of leptin on energy intake and expenditure seem to be altered insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145327.RAaHi2ZvodGIcwXFZa4R2l70mvOfv7i5ztnzmLvZcgpsA130_provenance.
- NP145330.RAWUFwmyFPyKaRTefY8xQjHoobYiywK-FSMnics7ncrcg130_assertion description "[The EGF gene polymorphism genotype is associated with risk for development of hepatocellular carcinoma in liver cirrhosis through modulation of EGF levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145330.RAWUFwmyFPyKaRTefY8xQjHoobYiywK-FSMnics7ncrcg130_provenance.
- NP145336.RATMrjakc72Msv1IiNI-otZgMwozyVrAsTq9l1pdh78dE130_assertion description "[Imbalance of IGF-1 and IGFBP-3 may play a role in hepatocarcinogenesis and tumor development of liver cirrhosis patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145336.RATMrjakc72Msv1IiNI-otZgMwozyVrAsTq9l1pdh78dE130_provenance.
- NP145342.RASA7gmhimzUCFmKZAYdznArFuSO1Svop7HYNON2sM8UA130_assertion description "[VEGF appeared more common as compared to CD 34 in early liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145342.RASA7gmhimzUCFmKZAYdznArFuSO1Svop7HYNON2sM8UA130_provenance.
- NP145344.RAUlNekJPx3gLrsAWBUCXgHDl4xTbWw3T2Psex2RFOrMo130_assertion description "[VEGF may play an important role in the angiogenesis and prognosis of hepatocellular carcinoma, as well as in the angiogenesis of liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145344.RAUlNekJPx3gLrsAWBUCXgHDl4xTbWw3T2Psex2RFOrMo130_provenance.
- NP145348.RAU4SEi-olb1WFJLc_680hFlw-UmsqyysBsUANLvnKGrQ130_assertion description "[Reduced circulating adiponectin occurs in rat fatty liver disease, but it is elevated in a mouse cirrhosis with similar findings in humans/hepatic expression of adiponectin receptors (AdipoR2 and AdipoR1) was only found in liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145348.RAU4SEi-olb1WFJLc_680hFlw-UmsqyysBsUANLvnKGrQ130_provenance.
- NP145351.RAaNkdi9xc3VbES-TE5SKqOn60wLsvkitikFbZabafrLQ130_assertion description "[An imbalance between the decreased ADAMTS13: AC and its increased substrate may reflect the predisposing state for platelet thrombi formation in patients with advanced liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145351.RAaNkdi9xc3VbES-TE5SKqOn60wLsvkitikFbZabafrLQ130_provenance.
- NP145354.RAX-m5z_iOZUPzcvsvTZMFzde0nEE_KSs8pptYHJbWIqU130_assertion description "[PTN was expressed in HSCs, Kupffer cells, and hepatocytes in fibrotic liver/propose that pleitrophin specifically antagonizes the TGFbeta1 activity during liver fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145354.RAX-m5z_iOZUPzcvsvTZMFzde0nEE_KSs8pptYHJbWIqU130_provenance.
- NP145356.RAUgCrLgxIIaZCHbR0aiEuRIs0EmsypFSfj3vXUgkz_8Q130_assertion description "[Established liver fibrosis patients had an improvement in necroinflammatory index after pirfenidone treatment when correlated with plasminogen activator inhibitor-1 and angiotensinogen-6 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145356.RAUgCrLgxIIaZCHbR0aiEuRIs0EmsypFSfj3vXUgkz_8Q130_provenance.
- NP145357.RAffJWIROvSaVTjUFDTyBIAFtE995dkLyP1LT8mZ2PMnY130_assertion description "[The binding site for NF-Y is critical for ZNF267 gene regulation and, herewith, the activation of this transcriptional factor plays an important role in the activation process of hepatic stellate cells and in liver fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145357.RAffJWIROvSaVTjUFDTyBIAFtE995dkLyP1LT8mZ2PMnY130_provenance.
- NP145364.RAaUOc68JZqtKeeC3ixxYKgvwgejlr-GXB163Jb3MnCZU130_assertion description "[Our findings implicate the muscular GLUT4 system in the glucose intolerance of liver cirrhosis by a mechanism different from that in diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145364.RAaUOc68JZqtKeeC3ixxYKgvwgejlr-GXB163Jb3MnCZU130_provenance.
- NP145369.RAfs7hkAcOPV5nuULONQZLmf_Prryg8qOgInhDTZ26YIo130_assertion description "[the cytokeratin 8 mutation G61C, which has been found to be associated with cryptogenic liver cirrhosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145369.RAfs7hkAcOPV5nuULONQZLmf_Prryg8qOgInhDTZ26YIo130_provenance.
- NP145372.RAQmpibEHyM8J7k7KrjKFY0ZAhy0r9wyjwOD8hL7r43LE130_assertion description "[Decreased production of platelets by megakaryocytes due to low thrombopoietin concentration could be a possible cause of thrombocytopenia in liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145372.RAQmpibEHyM8J7k7KrjKFY0ZAhy0r9wyjwOD8hL7r43LE130_provenance.
- NP145373.RART8NAijoxXN0Evuw0MqhEld51AuiJbnAdNG9YT10yPE130_assertion description "[Antagonists may prove beneficial in the treatment of proliferative liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145373.RART8NAijoxXN0Evuw0MqhEld51AuiJbnAdNG9YT10yPE130_provenance.
- NP145377.RAcSE1Eu5aIVMLyxMLcXPvS4mPR0ky3ToFplnaRP0tJJs130_assertion description "[Data show that S-adenosylmethionine blocks collagen I production and liver fibrosis by preventing transforming growth factor-beta induction of the COL1A2 promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145377.RAcSE1Eu5aIVMLyxMLcXPvS4mPR0ky3ToFplnaRP0tJJs130_provenance.
- NP145380.RAb68xIt8JoSRA_sBjVC-9m7pmy9GnNCCMuv8Lso378JQ130_assertion description "[A disturbed GLP-1 secretion does not play a role in blunting the insulin response observed in patients with diabetes and liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145380.RAb68xIt8JoSRA_sBjVC-9m7pmy9GnNCCMuv8Lso378JQ130_provenance.
- NP145381.RAXHHNkgSvyApbJuOFj_9OJ3y8pTH0XWFD__UIOb26Wac130_assertion description "[Patient with chronic hepatitis C, carrying the CPT1A minor allele are at the decreased risk of developing advanced liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145381.RAXHHNkgSvyApbJuOFj_9OJ3y8pTH0XWFD__UIOb26Wac130_provenance.
- NP145391.RAfz2BNdmDkKwmq3ru_eSQviMN7tBL4d68b4i1zqLQh24130_assertion description "[mutational analysis in Ashkenazi Jews with Hermansky-Pudlak syndrome 3 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145391.RAfz2BNdmDkKwmq3ru_eSQviMN7tBL4d68b4i1zqLQh24130_provenance.
- NP145401.RAcdRuzs5lW5ioB_b_Khf56deSDQ8kpj4oveNPdank9b0130_assertion description "[VPS33A is mutated in Hermansky-Pudlak syndrome and may have a role in melanogenesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145401.RAcdRuzs5lW5ioB_b_Khf56deSDQ8kpj4oveNPdank9b0130_provenance.
- NP145402.RAQ0bq1JUAHClUr6IOf-COtqstmzOIbkIhefAKbs2kP0k130_assertion description "[Salivary IL-1 beta levels were significantly higher in children with Langerhans cell histiocytosis than in normal children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145402.RAQ0bq1JUAHClUr6IOf-COtqstmzOIbkIhefAKbs2kP0k130_provenance.
- NP145403.RAXqZATeazkf-flstMM8dZQpG3cH2Ror2h3tge9qfBzHU130_assertion description "[Increased serum level of tumor necrosis factor-alpha is associated with children with Langerhans cell histiocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145403.RAXqZATeazkf-flstMM8dZQpG3cH2Ror2h3tge9qfBzHU130_provenance.
- NP145410.RAQEw2go2a7jpnXM_XexIxSD4FZrHht_i8orxCVc_dCO8130_assertion description "[Serum levels of early hemopoietic cytokine stem cell factor (SCF) correlate with disease activity in Langerhans cell histiocytosis and are relatively higher in patients with bone lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145410.RAQEw2go2a7jpnXM_XexIxSD4FZrHht_i8orxCVc_dCO8130_provenance.
- NP145412.RAftGaY9K5rPcNFm65TH_ckUhiHsTrNohMlfne0hCqGAc130_assertion description "[Increased serum levels of the early hemopoietic cytokine FLT3-L could explain increased numbers of circulating dendritic cells in Langerhans cell histiocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145412.RAftGaY9K5rPcNFm65TH_ckUhiHsTrNohMlfne0hCqGAc130_provenance.
- NP145414.RAU2ItiE5nvYAp7CCLyRswTKafjxHTY_k2lFCyt3A8wpI130_assertion description "[Coincident expression of CCR6 and CCR7 by pathologic Langerhans cells in Langerhans cell histiocytosis may contribute to their accumulation in nonlymphoid organs such as skin and bone ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145414.RAU2ItiE5nvYAp7CCLyRswTKafjxHTY_k2lFCyt3A8wpI130_provenance.
- NP145416.RAfrfrxUYYVPiMDX1SWaK8jnLjlJdGUj92FtrThgm8B9M130_assertion description "[Myotilin a thin filament-associated Z-disc protein.It binds to alpha-actinin and filamin c and is mutated in limb girdle muscular dystrophy 1A (LGMD1A).myotilin binds F-actin and prevents filament disassembly induced by Latrunculin A ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145416.RAfrfrxUYYVPiMDX1SWaK8jnLjlJdGUj92FtrThgm8B9M130_provenance.
- NP145442.RASZ1oy5JQvHy5gZYKen7DMPMDcDxKimBNqZG7HT3JGzY130_assertion description "[Limb-girdle muscular dystrophy (LGMD) type 2I, caused by mutations in the fukutin-related protein gene (FKRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145442.RASZ1oy5JQvHy5gZYKen7DMPMDcDxKimBNqZG7HT3JGzY130_provenance.
- NP145444.RAd_T7pudoSugm9a7duqN2o7uc-s5CwDKRwPvb4Ko7Rng130_assertion description "[We report a limb-girdle muscular dystrophy 2I family with three affected sisters and a highly variable clinical course/gene sequencing showed that all three sisters carried a nonsense paternal mutation (W225X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145444.RAd_T7pudoSugm9a7duqN2o7uc-s5CwDKRwPvb4Ko7Rng130_provenance.
- NP145446.RAYZPxq9xTVSAMgyubaTp2BvXGbKQByF05gmR5zxeQDw8130_assertion description "[Rab27A/Slp2a expression in limb girdle muscular dystrophy 2B muscle provides a compensatory vesicular trafficking pathway that is able to repair membrane damage in the absence of dysferlin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145446.RAYZPxq9xTVSAMgyubaTp2BvXGbKQByF05gmR5zxeQDw8130_provenance.
- NP145451.RAYcLMNqZUEDyOEdHdAFmGU35QCtysscLh_gR4V-wAqNU130_assertion description "[Rab27A/Slp2a expression in limb girdle muscular dystrophy 2B muscle provides a compensatory vesicular trafficking pathway that is able to repair membrane damage in the absence of dysferlin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145451.RAYcLMNqZUEDyOEdHdAFmGU35QCtysscLh_gR4V-wAqNU130_provenance.
- NP145454.RAf26rv5DY5bmbyURG14MnGddFCsNxxh3Mu-EzssbP3-I130_assertion description "[Two severely affected sisters sith limb-girdle muscular dystrophy were homozygous for a dysferlin null mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145454.RAf26rv5DY5bmbyURG14MnGddFCsNxxh3Mu-EzssbP3-I130_provenance.
- NP145460.RAbZ7TJUuY87E546yCrIBFNU_pRVBBQfdZ3zrADhsI_4w130_assertion description "[beta-sarcoglycan and SPATA18 may have a role in limb-girdle muscular dystrophy type 2E ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145460.RAbZ7TJUuY87E546yCrIBFNU_pRVBBQfdZ3zrADhsI_4w130_provenance.
- NP145463.RAYa-bxV8WPtoW-E3Z9zSo67aZeYveqPrgplMdJZjn1XI130_assertion description "[CRMP-5-IgG defines a paraneoplastic ophthalmological entity of combined optic neuritis and retinitis with vitreous inflammatory cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145463.RAYa-bxV8WPtoW-E3Z9zSo67aZeYveqPrgplMdJZjn1XI130_provenance.
- NP145474.RAWkvLTeTvKNnfrPnS607VpXaCMrprmm9t0dg5TRzX18E130_assertion description "[Defects in tapasin and HLA class I antigen expression in primary maxillary sinus SCC lesions may play a role in the clinical course of the maxillary sinus cancer, because these defects were associated with poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145474.RAWkvLTeTvKNnfrPnS607VpXaCMrprmm9t0dg5TRzX18E130_provenance.
- NP145496.RAetTb-H14x_seKd20JstzIrsay_wlNeUCXk28pheB7KE130_assertion description "[An N-terminal fragment of ProSAAS is associated with tau inclusions in Pick's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145496.RAetTb-H14x_seKd20JstzIrsay_wlNeUCXk28pheB7KE130_provenance.
- NP145497.RAd2ojnhjs-miatwPc4y212JIXbHZOLzrxHBDXnPOCbU0130_assertion description "[Saitohin interacts with peroxiredoxin 6, a unique member of that family that is bifunctional and the levels of which increase in Pick disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145497.RAd2ojnhjs-miatwPc4y212JIXbHZOLzrxHBDXnPOCbU0130_provenance.
- NP145512.RAQB8NROeGlwznh41kVzurLZIlEdj6aUmiTI28A3NUw6k130_assertion description "[falls with head injury without explicit traumatic brain injury in connection with the ApoE epsilon4 allele is associated with subsequent dementia among older adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145512.RAQB8NROeGlwznh41kVzurLZIlEdj6aUmiTI28A3NUw6k130_provenance.
- NP145515.RAcNLX3P29eHT0QK5md0aVuwvwNOhgxg0JugApdG3xVL4130_assertion description "[The relationship between APOE genotype and its influence on memory performance following traumatic brain injury have been demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145515.RAcNLX3P29eHT0QK5md0aVuwvwNOhgxg0JugApdG3xVL4130_provenance.
- NP145516.RAacHnI8N0js_jv5SpYLVJfKa4dKx6THqp6YCs4llshOU130_assertion description "[Results show that recombinant human erythropoietin reduces brain injury, especially apoptotic cell death, after neonatal hypoxia-ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145516.RAacHnI8N0js_jv5SpYLVJfKa4dKx6THqp6YCs4llshOU130_provenance.
- NP145526.RAft0g6UXAX7tYxYXv6Usq9LOJOO7EzhW1bp6g1V9sMmg130_assertion description "[Results suggest that alpha6beta4 integrin-mediated interactions of astrocytes with beta (ig) -h3 transduce intracellular signals through the focal adhesion proteins, which may regulate certain aspects of astrocyte response to brain injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145526.RAft0g6UXAX7tYxYXv6Usq9LOJOO7EzhW1bp6g1V9sMmg130_provenance.
- NP145527.RAdzRK9Q0jeXLfu2hb918xD32uexkt088IQTifAuRqUxM130_assertion description "[Results suggest that alpha6beta4 integrin-mediated interactions of astrocytes with beta (ig) -h3 transduce intracellular signals through the focal adhesion proteins, which may regulate certain aspects of astrocyte response to brain injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145527.RAdzRK9Q0jeXLfu2hb918xD32uexkt088IQTifAuRqUxM130_provenance.
- NP145529.RAToavYR4hyFq-oam-Tg-IMFstJm_eoQq5-muhVIw0ZOk130_assertion description "[Higher levels of MMP-9 in human brain tissue after ischemic and hemorrhagic stroke, suggesting a contribution of MMP-9 to ischemic brain injury and perihematoma edema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145529.RAToavYR4hyFq-oam-Tg-IMFstJm_eoQq5-muhVIw0ZOk130_provenance.
- NP145533.RAenrHeCcQcx6g1j4WFdfrMSI7MgHvKGHTQ_pKuUjihww130_assertion description "[Results show increased levels of interleukin-18 in human cerebrospinal fluid following traumatic brain injury, and that administration of the IL-18 inhibitor, IL-18-binding protein, enhances neurological recovery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145533.RAenrHeCcQcx6g1j4WFdfrMSI7MgHvKGHTQ_pKuUjihww130_provenance.
- NP145536.RAXHD28RVeTZ5_2B64ZuUyWUY9hO6kfTXNH_wXbN_m4WE130_assertion description "[variation of the gene that may increase IL-6 synthesis is associated with disabling brain injury but not cognitive development despite association with worse early critical care indices ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145536.RAXHD28RVeTZ5_2B64ZuUyWUY9hO6kfTXNH_wXbN_m4WE130_provenance.
- NP145552.RAaKKcTfT27ZyMgij2cfw2UpIeO2o6q_8ABLZvVOyHzJk130_assertion description "[TWEAK may play an important role in ischemia-induced brain injury ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145552.RAaKKcTfT27ZyMgij2cfw2UpIeO2o6q_8ABLZvVOyHzJk130_provenance.
- NP145556.RAYvePwn6whST5POAqJJthHcErK9vlXNYZeQKQnB-qIxo130_assertion description "[2 heterozygous deletion mutations (c.232delC in EP 70 and c.314 _ 316delCCT in EP 65) & a heterozygous splice site mutation (c.1118 + 1G > A in EP 69) were identified in patients with benign neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145556.RAYvePwn6whST5POAqJJthHcErK9vlXNYZeQKQnB-qIxo130_provenance.
- NP145557.RAdv59SVLU7YIUvImhhmR1xVAKy9DOhFdeB6acb-b5rqo130_assertion description "[significant association between juvenile myoclonic epilepsy and a Polymorphism, Single Nucleotide within exon 2 of CX36.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145557.RAdv59SVLU7YIUvImhhmR1xVAKy9DOhFdeB6acb-b5rqo130_provenance.
- NP145561.RAVnhk2N7BD4k_Or4juEJCG2upjiO6LZNC-l5KpFDCKeQ130_assertion description "[report presents one novel and one previously described mutation in the EFHC1 gene in Italian families, reinforcing the role of this gene in juvenile myoclonic epilepsy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145561.RAVnhk2N7BD4k_Or4juEJCG2upjiO6LZNC-l5KpFDCKeQ130_provenance.
- NP145568.RAYHbHfONaXy9XgpTVxiy0Oi1SpuL49RIgNRAU8AgZhzA130_assertion description "[Increased frequency of interleukin-1beta (-511) allele 2 in febrile seizures.polymorphism of interleukin-1beta at position -511 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145568.RAYHbHfONaXy9XgpTVxiy0Oi1SpuL49RIgNRAU8AgZhzA130_provenance.
- NP145572.RASI1r9HvXLxmKLm4-G9AExLZpIOQh7FWgAU-p2B4UHZ8130_assertion description "[Mutation of the sodium channel subunit SCN1B linked again to generalized epilepsy with febrile seizures ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145572.RASI1r9HvXLxmKLm4-G9AExLZpIOQh7FWgAU-p2B4UHZ8130_provenance.
- NP145580.RARnjNQywTb6FPMaIZU7R2TOjLscpX8olewKdrAbl4rgs130_assertion description "[Data indicate that SNPs rs740423, rs2277737, rs1059684 of CSNK1G2 gene may contribute to familial febrile convulsions in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145580.RARnjNQywTb6FPMaIZU7R2TOjLscpX8olewKdrAbl4rgs130_provenance.
- NP145582.RAcpAZi2e4Du5QXl2uCYM6ORWbEE0Wf_kEotAYNSzG9Co130_assertion description "[High levels of serum IFN-alpha are correlated with febrile seizures in influenza.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145582.RAcpAZi2e4Du5QXl2uCYM6ORWbEE0Wf_kEotAYNSzG9Co130_provenance.
- NP145584.RAWfUUn8c3Ig1r6dEVJBkeafM9YcDO69NKAnkdSACNkbk130_assertion description "[GABRG2 gene might be one of the susceptibility factors for febrile seizures ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145584.RAWfUUn8c3Ig1r6dEVJBkeafM9YcDO69NKAnkdSACNkbk130_provenance.
- NP145585.RATzDKDbZNBOaNLQO24YFr_5KPqMvXQZHlkzsQ9IOLIsA130_assertion description "[truncation of the GABA (A) -receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145585.RATzDKDbZNBOaNLQO24YFr_5KPqMvXQZHlkzsQ9IOLIsA130_provenance.
- NP145586.RAV6DZg0hYe-_EO0zP6zOuvoNjK9TyWq4wubY8m6mGaI0130_assertion description "[Novel ligand-gated gamma aminobutyric acid receptor (GABRG) 2 and sodium channel voltage-gated type I alpha subunit (SCN1A) gene mutations are found in two unrelated Chinese families with generalized epilepsy with febrile seizures plus (GEFS+).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145586.RAV6DZg0hYe-_EO0zP6zOuvoNjK9TyWq4wubY8m6mGaI0130_provenance.
- NP145596.RAdow14ilTjCfEz8xVQjMOAjdhjy0uzJsxoLHu6OkQly8130_assertion description "[Since the EGF receptor is often overexpressed in skin cancers, it might be possible to significantly reduce the proliferative potential of these cells making them good targets for laser-pulsed UV light treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145596.RAdow14ilTjCfEz8xVQjMOAjdhjy0uzJsxoLHu6OkQly8130_provenance.
- NP145598.RAUNVORakSzhscL_msTvFlkA8y78Qqc40v49JeXlVl7wk130_assertion description "[Non-melanoma skin cancers express functional purinergic receptors and that P2X7 receptor agonists significantly reduce cell numbers in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145598.RAUNVORakSzhscL_msTvFlkA8y78Qqc40v49JeXlVl7wk130_provenance.
- NP145606.RAT2NvwSI_a5k04d_fvTuuBpS6TTNscJ5wilp6wdL4B-o130_assertion description "[Desensitization and internalization of three variant MC1R forms associated with red hair and increased skin cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145606.RAT2NvwSI_a5k04d_fvTuuBpS6TTNscJ5wilp6wdL4B-o130_provenance.
- NP145611.RAY9XEOZlkKqnJwcqQGj0fqcGzRRuQveA9riwYUndMnfg130_assertion description "[Overexpression of the Axl tyrosine kinase receptor is associated with the development of squamous cell skin cancers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145611.RAY9XEOZlkKqnJwcqQGj0fqcGzRRuQveA9riwYUndMnfg130_provenance.
- NP145614.RAY0Qv_f369fRS74gEFBS60nCzLe23uebTN_tJIKtIfX8130_assertion description "[MMP-2, MMP-9, TIMP-1 and TIMP-2 play an important role in the pathogenesis of non-melanoma skin cancer/immunoexpression of these proteins may be useful indicators of cutaneous cancer invasion and progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145614.RAY0Qv_f369fRS74gEFBS60nCzLe23uebTN_tJIKtIfX8130_provenance.
- NP145620.RAQ7gF1orzL-nyV_rl1Tjmki7xFcMtOcKkiJqaNehlJzs130_assertion description "[induction and expression in different skin cancer types - review ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145620.RAQ7gF1orzL-nyV_rl1Tjmki7xFcMtOcKkiJqaNehlJzs130_provenance.
- NP145621.RAfcxeXadH65Z1c9JT0mGR0P1ydcIuXpjIPUDcGEFsII0130_assertion description "[review focuses on the functionality of HLA-G in the skin and summarizes available data obtained from studies performed in skin cancer and inflammatory dermatoses [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145621.RAfcxeXadH65Z1c9JT0mGR0P1ydcIuXpjIPUDcGEFsII0130_provenance.
- NP145622.RAS7R4Ol0PmT1J047VWKpABvEVpGO11yfHlsBjPs_AFfU130_assertion description "[alpha3B chain was scarcely detected in the vessels of malignant skin cancers, though the gamma2 and beta3 chains were highly expressed in the cancer cells [laminin alpha3B]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145622.RAS7R4Ol0PmT1J047VWKpABvEVpGO11yfHlsBjPs_AFfU130_provenance.
- NP145624.RAcw1xfaf65qfhPFP2NHoJJ61PZKkwWtKpl2vGUScdZL4130_assertion description "[The results indicate a reduced non-melanoma skin cancer risk in relation to XPD Asp312Asn and Lys751Gln variants; these polymorphisms may modify the association between non-melanoma skin cancer and arsenic exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145624.RAcw1xfaf65qfhPFP2NHoJJ61PZKkwWtKpl2vGUScdZL4130_provenance.
- NP145630.RAafYHCv0aRynaxBhnLKo5gpndTntH9jFt1VTJzPMRLR0130_assertion description "[SCCA2-like serpins mediate genetic predisposition to skin cancer in a mouse model and in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145630.RAafYHCv0aRynaxBhnLKo5gpndTntH9jFt1VTJzPMRLR0130_provenance.
- NP145634.RAQumQl-Y1F8NI1Wz_TBvGrIj2HBSS_fr70Zw1utkBKuI130_assertion description "[mutated p53 has a role in human papillomavirus type 38-positive non-melanoma skin cancers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145634.RAQumQl-Y1F8NI1Wz_TBvGrIj2HBSS_fr70Zw1utkBKuI130_provenance.
- NP145635.RAUqQsJJ7AgAzUPKSGvfRXjAZpqYG95tR5JvdC-C9FhEE130_assertion description "[p38 play a critical role in the UVA-induced expression of COX-2 in keratinocytes and may serve as a potential drug target in the chemoprevention of skin cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145635.RAUqQsJJ7AgAzUPKSGvfRXjAZpqYG95tR5JvdC-C9FhEE130_provenance.
- NP145636.RAaCzfJb0l8d7gDdxzX798CsDm3cXUcgcITbQJsnRYxEw130_assertion description "[downregulation of galectin-3 is associated with epithelial skin cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145636.RAaCzfJb0l8d7gDdxzX798CsDm3cXUcgcITbQJsnRYxEw130_provenance.
- NP145639.RAXxWmw8wSnN2DUAc7enP6GgSAL8IXlPUfI9Ymjz0QZCg130_assertion description "[The presence of CD4+CD25+ (regulatory T cells in head and neck cancer patients might be, in part, responsible for downregulation of antitumour immune responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145639.RAXxWmw8wSnN2DUAc7enP6GgSAL8IXlPUfI9Ymjz0QZCg130_provenance.
- NP145643.RAZXocrv5YzzoN8T7IyNrqAQyBPhvbv19Y5S6cPgbjcNA130_assertion description "[erythropoietin and EPOR are co-expressed in tumor cells, suggesting that erythropoietin may potentially function as an autocrine or paracrine factor in head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145643.RAZXocrv5YzzoN8T7IyNrqAQyBPhvbv19Y5S6cPgbjcNA130_provenance.
- NP145655.RAcQ7kKZoTyGbh6FL9hL0ie2qtoGGRRDTO_rgvwoececU130_assertion description "[p53 induced apoptosis is inhibited by Bcl-xL in head and neck neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145655.RAcQ7kKZoTyGbh6FL9hL0ie2qtoGGRRDTO_rgvwoececU130_provenance.
- NP145658.RAS3Hhid4pTMC04kbjdIp1Pi7RsU9sliQ4I_u5e1OEtz0130_assertion description "[Inactivation of ROBO1/DUTT1 could be used as molecular signature for early detection and prognosis of the head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145658.RAS3Hhid4pTMC04kbjdIp1Pi7RsU9sliQ4I_u5e1OEtz0130_provenance.