Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP145775.RAhXyTFHdWupCEIH9bbWsq7d-z88oE0a0Yp45eDq8ReJE130_assertion description "[CHL1 expression was uniformly positive on a cell line derived from angiomyolipoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145775.RAhXyTFHdWupCEIH9bbWsq7d-z88oE0a0Yp45eDq8ReJE130_provenance.
- NP145787.RAqW-CSYr0LLpQrOSR8l_RN_JrF4A3oPrUVxne_yFZ4vU130_assertion description "[These findings suggest that Zeb1 represses T-cadherin expression and thus increases the invasive activity of gallbladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145787.RAqW-CSYr0LLpQrOSR8l_RN_JrF4A3oPrUVxne_yFZ4vU130_provenance.
- NP145790.RAkmroSAWPKKz4OEl5xto29Erd6AFq8GWBH9M_9FmVrVk130_assertion description "[Expresssed in gallbladder cancer and is related to lymph node metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145790.RAkmroSAWPKKz4OEl5xto29Erd6AFq8GWBH9M_9FmVrVk130_provenance.
- NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_assertion description "[These results suggest that the Val allele of CYP1A1 Ile462Val polymorphism and the Pro allele of TP53 Arg72Pro polymorphism contribute to an increased risk of gallbladder cancer among Japanese women and men, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_provenance.
- NP145797.RAqXDVqA0h6ozeDVcNFz5PfKEt3eU1BfhrFk2ELvwAECo130_assertion description "[the association of A-204C variation of CYP7A1 gene promoter polymorphism in gallbladder cancer patients, gallstone patients and healthy subjects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145797.RAqXDVqA0h6ozeDVcNFz5PfKEt3eU1BfhrFk2ELvwAECo130_provenance.
- NP145798.RAqxMoQnhLHQMGs0xZqXpnljgVjRAHT_KeoXjledKR5lY130_assertion description "[There seems to be an association between APOB Xbai polymorphism and gallbladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145798.RAqxMoQnhLHQMGs0xZqXpnljgVjRAHT_KeoXjledKR5lY130_provenance.
- NP145802.RAvJRjYQNhjT9ylxPNmquNGADXqL7LQ5ceJiE-Vt5aEKg130_assertion description "[Decreased E-cadherin expression is associated with advanced gallbladder cancers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145802.RAvJRjYQNhjT9ylxPNmquNGADXqL7LQ5ceJiE-Vt5aEKg130_provenance.
- NP145806.RAmNNI86h2xktqx8Msa3MGkf3KF8mnXzyjiu2H-go2eY0130_assertion description "[Aberrant Nrf2 activation provoked by Keap1 alteration is one of the molecular mechanisms for chemotherapeutic resistance in gallbladder cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145806.RAmNNI86h2xktqx8Msa3MGkf3KF8mnXzyjiu2H-go2eY0130_provenance.
- NP145812.RAk2X5YD0shdLGOedms0zXxSSMOErg_bGltAOXyIbruRY130_assertion description "[Single nucleotide polymorphisms (SNPs) in hMTH1, hOGG1 and hMYH genes are associated with risk of chronic benzene poisoning.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145812.RAk2X5YD0shdLGOedms0zXxSSMOErg_bGltAOXyIbruRY130_provenance.
- NP145818.RAqD4qCpZXIod_X8DR5jRkPa65GD6kGwAPpkHp6kDd9Rc130_assertion description "[CD30-L/CD30 and IL-6/IL-6R systems could play a major role in the pathogenesis of Graves'disease (GD), but the expression of CD30L/CD30 and IL-6/IL-6R in Hashimoto's thyroiditis (HT) suggests that Th2 mechanisms are involved in tissue damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145818.RAqD4qCpZXIod_X8DR5jRkPa65GD6kGwAPpkHp6kDd9Rc130_provenance.
- NP145821.RAiLowBZhKDHAFdjBXapcVrjAxDs0DTO_c1tz1S6AGvSo130_assertion description "[HTLV-1 infection is not associated with CTLA-4 polymorphisms in patients with Hashimoto's thyroiditis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145821.RAiLowBZhKDHAFdjBXapcVrjAxDs0DTO_c1tz1S6AGvSo130_provenance.
- NP145825.RAj5TqOVAPQUb-fX2uQAuPDaIeQLY59sybJEwLzYWwsrE130_assertion description "[expression of RET, nuclearRAS, and ERK proteins is greatly enhanced in papillary thyroid carcinoma cells and Hashimoto's thyroiditis oxyphil cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145825.RAj5TqOVAPQUb-fX2uQAuPDaIeQLY59sybJEwLzYWwsrE130_provenance.
- NP145827.RAuvIVQ26nq_tZK15dTdPYSubw2gsqX1Sdq9cY069vhnA130_assertion description "[CD30-L/CD30 and IL-6/IL-6R systems could play a major role in the pathogenesis of Graves'disease (GD), but the expression of CD30L/CD30 and IL-6/IL-6R in Hashimoto's thyroiditis (HT) suggests that Th2 mechanisms are involved in tissue damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145827.RAuvIVQ26nq_tZK15dTdPYSubw2gsqX1Sdq9cY069vhnA130_provenance.
- NP145836.RAj2uY6VoDqGCbWpgWfl_S5MXX18LTQpBMfvVdH7wFwBA130_assertion description "[To see if variants of the FasL gene played a role in Hashimoto's thyroiditis and Graves'disease, 2 FasL polymorphisms (C -843 T in the promoter, A IVS2nt-124 G in intron 2) were studied/association was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145836.RAj2uY6VoDqGCbWpgWfl_S5MXX18LTQpBMfvVdH7wFwBA130_provenance.
- NP145848.RAvcKh5oB6aI6ldACP-lh-ETLeRYQ0vNwO0vLBadW_Dhw130_assertion description "[CD30-L/CD30 and IL-6/IL-6R systems could play a major role in the pathogenesis of Graves'disease (GD), but the expression of CD30L/CD30 and IL-6/IL-6R in Hashimoto's thyroiditis (HT) suggests that Th2 mechanisms are involved in tissue damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145848.RAvcKh5oB6aI6ldACP-lh-ETLeRYQ0vNwO0vLBadW_Dhw130_provenance.
- NP145852.RAsGTzXV1bG3UXpO9tXLHMht_sR9nmZ_Gx7yHptn-qGBo130_assertion description "[First report of Cowden syndrome presenting with ovarian dysgerminoma, which implicates PTEN in the molecular pathogenesis of dysgerminoma and adds it to the phenotypic manifestations of Cowden syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145852.RAsGTzXV1bG3UXpO9tXLHMht_sR9nmZ_Gx7yHptn-qGBo130_provenance.
- NP145853.RAmR5XovONV7w9164wycSVLKrf6N62tM0p0vC6cyTgJFY130_assertion description "[Double heterozygosity with mutations in the GJB2 gene is associated with congenital deafness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145853.RAmR5XovONV7w9164wycSVLKrf6N62tM0p0vC6cyTgJFY130_provenance.
- NP145868.RAsLieWA_bVz4GOnxMR1DhjJzCZ7jjTtobD6BiKgl8HsI130_assertion description "[study of PCDH15 mutations in nonsyndromic deafness DFNB23 and type 1 Usher syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145868.RAsLieWA_bVz4GOnxMR1DhjJzCZ7jjTtobD6BiKgl8HsI130_provenance.
- NP145870.RAt_RryVnZQzUjNpYkM8vK6-RK-Xmm-Mvhquu2G0-gxlE130_assertion description "[The heterozygous R445H mutation in OPA1 was found in five patients with optic atrophy and deafness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145870.RAt_RryVnZQzUjNpYkM8vK6-RK-Xmm-Mvhquu2G0-gxlE130_provenance.
- NP145871.RAmRYbW5ISQA_lryyNFcBw2vdpNWFUcMngNPPVMbTewKA130_assertion description "[We report a phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145871.RAmRYbW5ISQA_lryyNFcBw2vdpNWFUcMngNPPVMbTewKA130_provenance.
- NP145875.RAg6EMLHHpH6wvFbDuGvlyq-hinsfYDy4w4sQQN_gCFg0130_assertion description "[findings suggest that COCH mutations are unlikely to cause abnormalities in secretion and suggest that extracellular events might cause autosomal dominant sensorineural deafness (DFNA9) pathology ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145875.RAg6EMLHHpH6wvFbDuGvlyq-hinsfYDy4w4sQQN_gCFg0130_provenance.
- NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_assertion description "[sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145877.RAoGKB3Y5NRXgFYnUGeSVTXJgrZmYkdLzGrwOjpVftZCc130_provenance.
- NP145880.RAnKWRNp_Z1jL6wEnKYHHhZjuwu5WNs-9gz0ZDkfWXIs8130_assertion description "[Biallelic mutations in AK2 (adenylate kinase 2) in seven individuals affected with reticular dysgenesis and sensorineural deafness, were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145880.RAnKWRNp_Z1jL6wEnKYHHhZjuwu5WNs-9gz0ZDkfWXIs8130_provenance.
- NP145886.RAlL1BV67zDnNdR5k_Hztcc2SBmJ5bEa_FEoS4rUve7ok130_assertion description "[main finding of this study is that velocardiofacial syndrome subjects who suffer from either ADHD or OCD have significantly higher frequency of the low-activity COMT allele compared with those who are not affected ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145886.RAlL1BV67zDnNdR5k_Hztcc2SBmJ5bEa_FEoS4rUve7ok130_provenance.
- NP145894.RAikspnODtuJFTDa5P4tcbmBc_PGu-ZFrZvDj_rKA9O6w130_assertion description "[There are predisposing effects of the DQB1*0301 allele and protective effects for DQA1*0103-DQB1*0601 with regard to narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145894.RAikspnODtuJFTDa5P4tcbmBc_PGu-ZFrZvDj_rKA9O6w130_provenance.
- NP145896.RApR1uPG15konkhI4N-mHgfeuV9INBVfLnXKEczmmkqZg130_assertion description "[the genes (hypocretin/orexin ligand and its receptor) involved in the pathogenesis of narcolepsy have been identified--REVIEW ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145896.RApR1uPG15konkhI4N-mHgfeuV9INBVfLnXKEczmmkqZg130_provenance.
- NP145899.RAr3Abt0QA3FjHmZYBRKy5wUqVZH5Je9HfveHpCGsUi1w130_assertion description "[Sleep apnea syndrome is associated with plasma soluble leptin receptor and insulin resistance independently of body mass index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145899.RAr3Abt0QA3FjHmZYBRKy5wUqVZH5Je9HfveHpCGsUi1w130_provenance.
- NP145902.RAleZ-ceDk6z8hyIBK5hBZwUycEib6PpDgiQcJBUwyoY0130_assertion description "[the hypocretin system is intact and sleepiness is not typical in relapsing remitting multiple sclerosis and optic neuritis without hypothalamic lesions on MRI ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145902.RAleZ-ceDk6z8hyIBK5hBZwUycEib6PpDgiQcJBUwyoY0130_provenance.
- NP145907.RAs8lMCvcn8cJKgNaEmdUb5Yo0U0uk651EgIZnjoYS7fY130_assertion description "[ACE gene DD homozygosity of the I/D polymorphism in intron 16 is an independent risk factor for spontaneous intracerebral hemorrhage, and not for small vessel disease stroke, in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145907.RAs8lMCvcn8cJKgNaEmdUb5Yo0U0uk651EgIZnjoYS7fY130_provenance.
- NP145909.RAm8jbLMaygfbbVPqfh41Y-NwdErbh0Z02r_bZk1apT5s130_assertion description "[study the changes of plasma insulin-like growth factor -1 (IGF-1) and IGF binding protein 3 (IGFBP3) in patients with acute cerebral infarct (ACI) and acute cerebral hemorrhage (ACH) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145909.RAm8jbLMaygfbbVPqfh41Y-NwdErbh0Z02r_bZk1apT5s130_provenance.
- NP145916.RAvpg8PuaXdVnT1MPGep0JYL6-kzW-ou_hNqOkdLF5IEE130_assertion description "[The allele T of apoB C7673T polymorphism may be related to cerebral hemorrhage with family history and increase the susceptibility of cerebral hemorrhage by changing blood lipid levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145916.RAvpg8PuaXdVnT1MPGep0JYL6-kzW-ou_hNqOkdLF5IEE130_provenance.
- NP145918.RApW1fDNb0PhYbZl1Z7iUO2eW_6Jwkhcw6hFHbvyHLUoU130_assertion description "[SERPINA3 polymorphism does not have a role in primary intracerebral hemorrhage in a Polish population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145918.RApW1fDNb0PhYbZl1Z7iUO2eW_6Jwkhcw6hFHbvyHLUoU130_provenance.
- NP145919.RAmo3Wql2_S2m4DXY9xnu5DOoDdwOwwe3dUy7a5BdF_mQ130_assertion description "[Our study did not show an association between alpha-1 antichymotrypsin signal peptide A/T polymorphism and primary intracerebral hemorrhage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145919.RAmo3Wql2_S2m4DXY9xnu5DOoDdwOwwe3dUy7a5BdF_mQ130_provenance.
- NP145922.RAvNtuE6SVrcMU0wfTj0XXV3xiwPRLCxt7QqMa4THcz4I130_assertion description "[ApoE epsilon2 carriers have an increased risk of intracerebral hemorrhage in brain arteriovenous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145922.RAvNtuE6SVrcMU0wfTj0XXV3xiwPRLCxt7QqMa4THcz4I130_provenance.
- NP145925.RAmFdQtzWHJBmueEfbCHkqYcshVXFtGBioyTKzHgfJRuE130_assertion description "[Increased plasma S100B level is found following acute spontaneous intracerebral hemorrhage, in association with a worse early and late evolution, and closely related to initial hematoma volume.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145925.RAmFdQtzWHJBmueEfbCHkqYcshVXFtGBioyTKzHgfJRuE130_provenance.
- NP145926.RArr3ZOrVvOs1-jxrUIaWt7EswoH13vuIA81KclLAQHZ0130_assertion description "[HspB8 might play important role in regulating Abeta aggregation and, therefore, development of classic senile plaques in Alzheimer's disease and cerebral amyloid angiopathy in hereditary cerebral hemorrhage with amyloidosis of Dutch type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145926.RArr3ZOrVvOs1-jxrUIaWt7EswoH13vuIA81KclLAQHZ0130_provenance.
- NP145928.RAs805EbWKi3EzrjKtBr6h1KxfH1Qta5w8iqyCGhUWtdk130_assertion description "[In cluster headaches pain relief by triptans is significantly modulated by a common genetic GNB3 variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145928.RAs805EbWKi3EzrjKtBr6h1KxfH1Qta5w8iqyCGhUWtdk130_provenance.
- NP145929.RAkKILCXW0oJof3ZzX1ZBJnLyNFq21LeqW3PG8XqmoI-A130_assertion description "[Association analysis of five polymorphic microsatellite markers in cluster headache (CH) patients reveals that genetic variations in NOS3 do not contribute greatly to CH susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145929.RAkKILCXW0oJof3ZzX1ZBJnLyNFq21LeqW3PG8XqmoI-A130_provenance.
- NP145940.RAliriCEnCKuLsNHQdUpG5evZMXIuiBE_YYDArngyk7fo130_assertion description "[ACTN4 mutations accounts for about 3.5% of familial focal glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145940.RAliriCEnCKuLsNHQdUpG5evZMXIuiBE_YYDArngyk7fo130_provenance.
- NP145941.RAm356fCsevF2L64BG_BhU6hhlYj74hFHEPrbBaXe9bA0130_assertion description "[a family with familial focal segmental glomerulosclerosis carries a missense mutation in TRPC6; the proline-to-glutamine substitution enhances TRPC6-mediated calcium signals in response to agonists & appears to alter intracellular distribution of TRPC6 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145941.RAm356fCsevF2L64BG_BhU6hhlYj74hFHEPrbBaXe9bA0130_provenance.
- NP145946.RArKINuZ7eQ7fADBpyi7yazBWojU2TdJI9cJaSerODPOg130_assertion description "[Our results suggest that IL-10 gene G-1082A polymorphism is an important marker of progression in patients with IgA nephropathy and focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145946.RArKINuZ7eQ7fADBpyi7yazBWojU2TdJI9cJaSerODPOg130_provenance.
- NP145954.RAhmtIVXSIvHV6dzu7dHSZnSvBfKLDplHs8F41RT7j-S8130_assertion description "[Data suggest that loss of modified heparan sulphate in the GBM is mediated by an increased heparanase presence and may play a role in the pathogenesis of diabetes-induced proteinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145954.RAhmtIVXSIvHV6dzu7dHSZnSvBfKLDplHs8F41RT7j-S8130_provenance.
- NP145955.RAhFs9oSm9gR8Mv1_Z-n1EXAcWHtF6aXqZMw6g3VKi0Z4130_assertion description "[The expression of nephrin mRNA maybe closely linked to the development and progression of proteinuria in diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145955.RAhFs9oSm9gR8Mv1_Z-n1EXAcWHtF6aXqZMw6g3VKi0Z4130_provenance.
- NP145959.RAt1id5T5Y0UE0NKZkL-u1HOsCAOuiT9-WSiThIpyrKH4130_assertion description "[Increased serum adiponectin might be the reflection of a compensatory response to nephrotic state characterized by massive proteinuria, hypoalbuminemia and hyperlipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145959.RAt1id5T5Y0UE0NKZkL-u1HOsCAOuiT9-WSiThIpyrKH4130_provenance.
- NP145960.RAgyZBstf8RzuQhtmz492M3-jBIK8PY7_9tMapQ53KEP4130_assertion description "[aldosterone/MR activation is linked to renal inflammation and proteinuria ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145960.RAgyZBstf8RzuQhtmz492M3-jBIK8PY7_9tMapQ53KEP4130_provenance.
- NP145961.RAkCjcAgwxlEDYxCcSXGm390N7thOFoGcWf-H6bsHvngk130_assertion description "[FY- status was strongly associated with chronic organ damage and proteinuria in sickle cell anemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145961.RAkCjcAgwxlEDYxCcSXGm390N7thOFoGcWf-H6bsHvngk130_provenance.
- NP145962.RAit51gYgF2f9oQsN8Xk7PanIgUrOu2UYyYKLypiZ1IjE130_assertion description "[Haptoglobin polymorphism was associated with more severe hypertension and proteinuria in patients with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145962.RAit51gYgF2f9oQsN8Xk7PanIgUrOu2UYyYKLypiZ1IjE130_provenance.
- NP145964.RAvaJk4R4qrUSMRISTJNpCclt7YAmDnif8F3aipZklLE0130_assertion description "[An inadequate tissue factor pathway inhibitor (TFPI) concentration as a result of elevated tissue factor (TF): tissue factor pathway inhibitor (TFPI) ratio characterizes patients with clinical manifestations of nephrotic syndrome and mild proteinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145964.RAvaJk4R4qrUSMRISTJNpCclt7YAmDnif8F3aipZklLE0130_provenance.
- NP145966.RAvDV1lQknWyh-m2r0fZEmxp1vuON6bHfH8A_SGbXhrO4130_assertion description "[HPSE is involved in the pathogenesis of proteinuria in overt diabetic nephropathy by degradation of heparan sulfates ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145966.RAvDV1lQknWyh-m2r0fZEmxp1vuON6bHfH8A_SGbXhrO4130_provenance.
- NP145973.RAuVQpc9BFKQgdrvQHcgyD8odPmomKEdYzqWjeEc87pSo130_assertion description "[Actinin-4 contributes to the invasive growth of pancreatic ductal carcinoma, and ACTN4 is one of the candidate oncogenes in this chromosome locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145973.RAuVQpc9BFKQgdrvQHcgyD8odPmomKEdYzqWjeEc87pSo130_provenance.
- NP145976.RAmsghyDvCn7Q_2iReL4PWAxy91IknGGxRQezV5zNnTH4130_assertion description "[significant association of alopecia areata in the overall data set with the Notch4 (T+1297C) polymorphism (P < 0.001) but not with Notch4 (A+3063G) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145976.RAmsghyDvCn7Q_2iReL4PWAxy91IknGGxRQezV5zNnTH4130_provenance.
- NP145977.RAlml7By08-JUSL8JaAB7kk_Bc0MiYZ_GSzQB96G_8MWI130_assertion description "[The study results do not support the hypothesis that the p.SER278Arg polymorphism of the AIRE gene is associated with an increased risk for alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145977.RAlml7By08-JUSL8JaAB7kk_Bc0MiYZ_GSzQB96G_8MWI130_provenance.
- NP145979.RAkmECM6NBG1DikvtVp_5VMbpvvYBqcmM9EjKQ-rI3DCU130_assertion description "[Data indicates that no association exists between the -2518A/G polymorphism of the MCP-1 gene and susceptibility to alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145979.RAkmECM6NBG1DikvtVp_5VMbpvvYBqcmM9EjKQ-rI3DCU130_provenance.
- NP145987.RAq0nzEKWilbPPxMXnVOVzrYpuzTsjDldwgTcTbzfk8Ck130_assertion description "[Fcgamma receptor I Ab and Fcgamma receptor I play an important role in the regulation of alopecia areata (AA), are useful for a marker of the disease prognosis and are worth intense research for the reasonable and specific therapy of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145987.RAq0nzEKWilbPPxMXnVOVzrYpuzTsjDldwgTcTbzfk8Ck130_provenance.
- NP145988.RAgrIV4ptmBuggxdFfAgF-bJQmZmxcLK_tRIg68-9GDQE130_assertion description "[Expression of CD40, CD54 and HLA-DR were seen in the hair structure including the dermal papilla in alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145988.RAgrIV4ptmBuggxdFfAgF-bJQmZmxcLK_tRIg68-9GDQE130_provenance.
- NP145990.RAjZShnrcJYhMdaWcyOnUd9LYRhxaqozS2bRfzbMEIxa8130_assertion description "[A borderline association was observed between il-1rn and patchy alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145990.RAjZShnrcJYhMdaWcyOnUd9LYRhxaqozS2bRfzbMEIxa8130_provenance.
- NP145992.RAl4g2vWH-aZhzctBis-pEo3ZGFaBDvp9EaaL5hiRzvjc130_assertion description "[In patients with autoimmune thyroiditis the HLA-B27 frequency of was higher than control values, while in patients with polyglandular activation of autoimmunity or autoimmune polyglandular syndrome type II, the HLA-B8 frequency was found to be higher.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145992.RAl4g2vWH-aZhzctBis-pEo3ZGFaBDvp9EaaL5hiRzvjc130_provenance.
- NP146009.RAqYBT_oCZ4XdxqLShZchTMwcTmQ0MLFwXthLfJL7Cf4Q130_assertion description "[RIPK2 is a marker for resolution of peritoneal dialysis-associated peritonitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146009.RAqYBT_oCZ4XdxqLShZchTMwcTmQ0MLFwXthLfJL7Cf4Q130_provenance.
- NP146012.RAnVWMx9xctzixgEOS9QGTpo7R8Z4NRnUtRzuwiIXwFZU130_assertion description "[Novel germ cell markers BOB1 were significantly upregulated in seminoma specimens, compared to normal testes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146012.RAnVWMx9xctzixgEOS9QGTpo7R8Z4NRnUtRzuwiIXwFZU130_provenance.
- NP146028.RAinl3aARajCJn_XLqDFAI-7lUjStqLh_6tEZMqK7oLp8130_assertion description "[Novel germ cell markers PROM1 were significantly upregulated in seminoma specimens, compared to normal testes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146028.RAinl3aARajCJn_XLqDFAI-7lUjStqLh_6tEZMqK7oLp8130_provenance.
- NP146030.RAintX_VIUyDYB-bKKjttsK9YHQkn6XjUot08PYeOQ3Hw130_assertion description "[The ETV4 protein was localised to nuclei of spermatogonia and revealed an intense staining in seminoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146030.RAintX_VIUyDYB-bKKjttsK9YHQkn6XjUot08PYeOQ3Hw130_provenance.
- NP146032.RAjq9glnxL6W9pxYL8zPXpr7RwvKPLsaRaw6MrWQcRa0o130_assertion description "[Seminoma patients have elevated levels of lactate dehydrogenase 1 in blood ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146032.RAjq9glnxL6W9pxYL8zPXpr7RwvKPLsaRaw6MrWQcRa0o130_provenance.
- NP146033.RAmN0D-o904ZYYwsLB9LfwT9ef3dUmHjzVzSuRGA-7zNI130_assertion description "[As a candidate gene for the gonadoblastoma locus on the Y chromosome (GBY), it has been demonstrated to be expressed at high levels in tumor germ cells of this types of tumors and testicular seminomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146033.RAmN0D-o904ZYYwsLB9LfwT9ef3dUmHjzVzSuRGA-7zNI130_provenance.
- NP146037.RAl0DbEWsHALh-S8B_UPmJoCR0EXJ2uYEUv9GIqOa480s130_assertion description "[homozygous mutations in DEHAL1 appear to cause human iodotyrosine deiodinase deficiency, leading to hereditary hypothyroidism and goiter ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146037.RAl0DbEWsHALh-S8B_UPmJoCR0EXJ2uYEUv9GIqOa480s130_provenance.
- NP146038.RAiT51gyYQgukV12mbxIKNRRMinvWYbCwxDd_ePeQj_m4130_assertion description "[The level of expression is directly correlated with the functional status of epithelial cells, being higher in multinodular goiters, and even more pronounced in hyperthyroid tissues, such as Graves'disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146038.RAiT51gyYQgukV12mbxIKNRRMinvWYbCwxDd_ePeQj_m4130_provenance.
- NP146049.RArpeFS4Am73qZAtIZwo5pjqYC0B5yvwtMbvJGGJeiyVU130_assertion description "[SDF1 gene variant is present in patients with type 1 diabetes mellitus and autoimmune thyroid disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146049.RArpeFS4Am73qZAtIZwo5pjqYC0B5yvwtMbvJGGJeiyVU130_provenance.
- NP146050.RAiHQOW6PJ_m4X4C8Q2tkDGLeYFPoqZcsjgEkHeoXnBj4130_assertion description "[At this stage, we cannot exclude the Tg region as harboring a susceptibility locus for autoimmune thyroid disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146050.RAiHQOW6PJ_m4X4C8Q2tkDGLeYFPoqZcsjgEkHeoXnBj4130_provenance.
- NP146052.RAlA_MT8J32WqDCC2Xl30iCqqJ6jJSW5QCUCUytscRbsc130_assertion description "[human TPO has a discontinuous immunodominant region recognized by human anti-thyroperoxidase autoantibodies in autoimmune thyroid diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146052.RAlA_MT8J32WqDCC2Xl30iCqqJ6jJSW5QCUCUytscRbsc130_provenance.
- NP146055.RAnqGwhQdnCUvZLYMbmDOJdCx_gmR310zvhRhB-ikJKuE130_assertion description "[work suggests that the pendrin gene should be considered a new susceptibility gene to autoimmune thyroid diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146055.RAnqGwhQdnCUvZLYMbmDOJdCx_gmR310zvhRhB-ikJKuE130_provenance.
- NP146057.RAkTECloLBmwZ4SsLeiYvUHzXDf0-rHYW99Pr4xDjMF0A130_assertion description "[Fas ligand appear to be differentially expressed on peripheral lymphocytes in the two opposite phenotypes of autoimmune thyroid disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146057.RAkTECloLBmwZ4SsLeiYvUHzXDf0-rHYW99Pr4xDjMF0A130_provenance.
- NP146061.RAovW8s9RbY4LX5buC1ISJpiqOXjo611UuLY7VHDeQGAk130_assertion description "[levels of thyroglobulin (Tg) mRNA in the TSH-stimulated lymphocytes were noticeably increased in subjects with thyroid disease suggesting an interesting relationship between production of Tg antigen in peripheral blood and autoimmunity in thyroid disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146061.RAovW8s9RbY4LX5buC1ISJpiqOXjo611UuLY7VHDeQGAk130_provenance.
- NP146064.RAsANK3OCAtySEeBMpHxJFu6RlDUG0I_AVr2XIo62nBKw130_assertion description "[CCL5 was significantly increased in Graves'disease patients compared with Hashimoto's thyroiditis or nontoxic nodular thyroid disease subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146064.RAsANK3OCAtySEeBMpHxJFu6RlDUG0I_AVr2XIo62nBKw130_provenance.
- NP146065.RAh3XDpdtgMh3NZIu1HHN15XhyLPJ8rLGesMAJmy6-sOM130_assertion description "[data showed that TNFRI polymorphisms have an important role in auimmune thyroid disease pathogenesis in both familial and case-control samples ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146065.RAh3XDpdtgMh3NZIu1HHN15XhyLPJ8rLGesMAJmy6-sOM130_provenance.
- NP146069.RAglTEFpVcH11ICtoZxOKZ5fiZpLWemEbJrJvHIQ-qX1g130_assertion description "[results suggest that polymorphisms of the FOXP3 gene may play a role in the genetic susceptibility to autoimmune thyroid diseases in Caucasians, perhaps by altering FOXP3 function and/or expression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146069.RAglTEFpVcH11ICtoZxOKZ5fiZpLWemEbJrJvHIQ-qX1g130_provenance.
- NP146070.RAqeH1o_RiKU20tAVD9bykhpL31G9ghk4_gkfZfeVVwYo130_assertion description "[review article summarizes recent studies on the regulation of IRF-4 and its function in activated T cells, human T cell lymphoma virus (HTLV-I) -infected T cells, and HTLV-I-induced adult T cell leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146070.RAqeH1o_RiKU20tAVD9bykhpL31G9ghk4_gkfZfeVVwYo130_provenance.
- NP146071.RAlVm5CCt3QiqYS7ly77UYVs0OmvMsINR4pan8qMx4upA130_assertion description "[AKT and IL-15 may be important in extranodal NK/T-cell lymphoma tumor survival ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146071.RAlVm5CCt3QiqYS7ly77UYVs0OmvMsINR4pan8qMx4upA130_provenance.
- NP146072.RAnrQSemITxqkOqaLM2nVPl7P-2FgmP_q3Syw94z3BKk8130_assertion description "[AITL is a morphologically heterogeneous T-cell lymphoma commonly expressing CXCL13 and CD10; high level of CD10 and CXCL13 did not affect survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146072.RAnrQSemITxqkOqaLM2nVPl7P-2FgmP_q3Syw94z3BKk8130_provenance.
- NP146078.RApliSox-Yu3kbdtMeLhTR2ZjARCL_f610OKlbzW_vuzA130_assertion description "[Here we show, in four cell lines of human adult T cell lymphoma/leukemia origin, that the three IL-2R subunits are compartmented together with HLA glycoproteins and CD48 molecules in the plasma membrane ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146078.RApliSox-Yu3kbdtMeLhTR2ZjARCL_f610OKlbzW_vuzA130_provenance.
- NP146099.RAg4maa-XVglSDtR0QcTmL8V_rHuPwqxpq-CzGOKOQgOk130_assertion description "[Here we show, in four cell lines of human adult T cell lymphoma/leukemia origin, that the three IL-2R subunits are compartmented together with HLA glycoproteins and CD48 molecules in the plasma membrane ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146099.RAg4maa-XVglSDtR0QcTmL8V_rHuPwqxpq-CzGOKOQgOk130_provenance.
- NP146108.RAv5OlS1KJlpdmh_KnciNDwcdQBmUWsMMF2RfIF2t7YO8130_assertion description "[Frequent mutations of Fas gene in nasal NK/T cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146108.RAv5OlS1KJlpdmh_KnciNDwcdQBmUWsMMF2RfIF2t7YO8130_provenance.
- NP146112.RAloXgwZHbtel8MHpANquiDI0_Zn2ynBZJ9JqGyH-7JAc130_assertion description "[NPM/ALK-carrying T cell lymphoma (ALK+TCL) cells secrete IL-10 and TGF-beta and express FoxP3, indicating their T regulatory (Treg) cell phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146112.RAloXgwZHbtel8MHpANquiDI0_Zn2ynBZJ9JqGyH-7JAc130_provenance.
- NP146114.RAtwQQ1xvVRgVqFiwyqxfXwzD45PsBE21Styw_1cyV4sE130_assertion description "[From 9q34 known genes, NOTCH1 could thus be the primary target of genomic DNA amplification in enteropathy-type t-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146114.RAtwQQ1xvVRgVqFiwyqxfXwzD45PsBE21Styw_1cyV4sE130_provenance.
- NP146124.RAi8U2KY-6FKADqZgBY5_4l0NUqVPziEJeu2XQIoULRxg130_assertion description "[data suggest that the Pl (A2) polymorphism is a genetic determinant of ischemic stroke in a selected high-risk hypertensive population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146124.RAi8U2KY-6FKADqZgBY5_4l0NUqVPziEJeu2XQIoULRxg130_provenance.
- NP146134.RAhJtmaJqfahq6ZgNhaacJo32V29UnISUWKDjYGxGvqTg130_assertion description "[The BC genotype of the VNTR polymorphism of GPIb-alpha is an independent predictor of recurrent events in stroke patients treated with aspirin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146134.RAhJtmaJqfahq6ZgNhaacJo32V29UnISUWKDjYGxGvqTg130_provenance.
- NP146138.RAg71fX9rhsY7j8n9CdK5vh-dWmhgT0MFDJphvdFjkjFU130_assertion description "[systematic review of interleukin-6 174G/C polymorphism and ischemic stroke [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146138.RAg71fX9rhsY7j8n9CdK5vh-dWmhgT0MFDJphvdFjkjFU130_provenance.
- NP146143.RAhBXNjTFOncJ9AwIqY9DvPOyEWZ0QYydp5qa0AHhadws130_assertion description "[Serum concentrations of IL-6, sgp130, and sIL-6R were measured in stroke patients and controls/data demonstrate genetic variation in the expression of IL-6 in stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146143.RAhBXNjTFOncJ9AwIqY9DvPOyEWZ0QYydp5qa0AHhadws130_provenance.
- NP146145.RAr9SwnuEpTkPBniHdCifbJtZMkc8PpGVER4bYnKi2DwM130_assertion description "[The TT genotype of the IL-1beta gene may be associated with an increased risk of small vessel disease stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146145.RAr9SwnuEpTkPBniHdCifbJtZMkc8PpGVER4bYnKi2DwM130_provenance.
- NP146146.RAg0TFIQCVXRNWiH7SbBAdnAn5gIurEnLU6KGRhUNjCu8130_assertion description "[The 511C/T IL-1 [beta]gene polymorphism affects the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to inflammatory stimulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146146.RAg0TFIQCVXRNWiH7SbBAdnAn5gIurEnLU6KGRhUNjCu8130_provenance.
- NP146147.RAn5NCsIcz-pFatMhcelwZSzVI8xMsAAIZm-DkQhc3_N4130_assertion description "[serum ET-1 may have a role in severe brain edema in acute stroke patients treated with t-PA ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146147.RAn5NCsIcz-pFatMhcelwZSzVI8xMsAAIZm-DkQhc3_N4130_provenance.
- NP146149.RAh-qT461tSyUffQAcInRCFvz-niacKEzlPK7hgMtTD10130_assertion description "[A common CYP4F2 V433M polymorphism might increase the risk of incident ischemic stroke in male subjects only partially through its elevating effect on BP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146149.RAh-qT461tSyUffQAcInRCFvz-niacKEzlPK7hgMtTD10130_provenance.
- NP146151.RAnenn4NRTRbaa8utAwRkMuwzxD3FHvNET-gf_l_YRXt8130_assertion description "[Significantly different distributions were seen with respect to the AC008818-1 alleles/148 associates with an increased risk of stroke incidence, & allele 144 with a protective effect/may be involved in stroke etiology and pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146151.RAnenn4NRTRbaa8utAwRkMuwzxD3FHvNET-gf_l_YRXt8130_provenance.
- NP146157.RApFx53AN0ZRT_qgcSicP3p9diDtm5P0o426NzYb1kLdw130_assertion description "[The data of this study suggest that common variants in PDE4D may contribute to the genetic risk for ischemic stroke in multiple populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146157.RApFx53AN0ZRT_qgcSicP3p9diDtm5P0o426NzYb1kLdw130_provenance.
- NP146166.RArKHiyzz5nAjVjukWdWFGqUYUGVtiOcfdhuVeX_e0fVs130_assertion description "[study concludes that eNOS -922A/G and -786T/C may affect the susceptibility to ischemic stroke and certain haplotypes of the eNOS gene may be associated with a higher susceptibility to ischemic stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146166.RArKHiyzz5nAjVjukWdWFGqUYUGVtiOcfdhuVeX_e0fVs130_provenance.
- NP146170.RAoyHXQQotgc-9wiDFN1wkBHxsSY_ERQCFZb7kYOXtglg130_assertion description "[Methylenetetrahydrofolate reductase polymorphisms are associated with pediatric stroke ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146170.RAoyHXQQotgc-9wiDFN1wkBHxsSY_ERQCFZb7kYOXtglg130_provenance.
- NP146173.RArAGjMC-Hu3ZCKbWXAL5Aky1Grp6-L0X4A-9q870-vfs130_assertion description "[MTHFR 677C > T polymorphisms interact with elevated total homocysteine levels, leading to an increased risk of ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146173.RArAGjMC-Hu3ZCKbWXAL5Aky1Grp6-L0X4A-9q870-vfs130_provenance.
- NP146177.RAuem6XI-MK4F0ADZ4EnnFSq5PO5bZT8mws_QgAd_Quws130_assertion description "[Genetic tests showed that the Arterial ischemic stroke in a child was heterozygous for the beta (degrees) -thalassemia IVS-I-1 mutation and homozygous for the methylentetrahydrofolate reductase C677T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146177.RAuem6XI-MK4F0ADZ4EnnFSq5PO5bZT8mws_QgAd_Quws130_provenance.
- NP146185.RAseixNi_rnr8SYAGxflYEEd1N4MHN2SDZtwVZWsxHuTc130_assertion description "[Data suggest that the combination of homozygous MTHFR 677T and angiotensin II type-1 receptor 1166C variants confers the risk of small-vessel-associated ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146185.RAseixNi_rnr8SYAGxflYEEd1N4MHN2SDZtwVZWsxHuTc130_provenance.
- NP146186.RAmZZT-H4dSgCw3D3a_NpGvckU-l6Djf8ZA-1HpQXZFy8130_assertion description "[there was an association between A1166C polymorphism in the angiotensin II receptor gene and ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146186.RAmZZT-H4dSgCw3D3a_NpGvckU-l6Djf8ZA-1HpQXZFy8130_provenance.
- NP146189.RAqtbJ6JUO85uRUj-B6ij4QAbSxkvm2q6U9Zzco4kt40s130_assertion description "[Paraoxonase (PON1) 192R+ genotypes were associated with stroke and myocardial infarction, particularly in subsets of patients, in patterns suggesting a possible survivor effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146189.RAqtbJ6JUO85uRUj-B6ij4QAbSxkvm2q6U9Zzco4kt40s130_provenance.
- NP146191.RAjgXxu2wzzK82r5goEibjH7_GxwzN-Bhin7_wzfEtUws130_assertion description "[PON1 activity ratio, PON1 192RR genotype and PON1 status as important risk factors for ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146191.RAjgXxu2wzzK82r5goEibjH7_GxwzN-Bhin7_wzfEtUws130_provenance.