Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP186390.RAnV5-uFOEzEjbBjGQKueGIKp0NXJYBlMDVM8i_TrY9qI130_assertion description "[Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186390.RAnV5-uFOEzEjbBjGQKueGIKp0NXJYBlMDVM8i_TrY9qI130_provenance.
- NP186394.RAlzQ092Uik_7QIGD1QU_hXSPoRFgxbhL18rSjkGQ2Oo8130_assertion description "[To investigate the expression of the implantation factors leukemia inhibitory factor (LIF), interleukin-11 (IL-11), and IL-6ST/gp130 in the endometrium to examine the relationship between loss of implantation and abnormal uterine cavity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186394.RAlzQ092Uik_7QIGD1QU_hXSPoRFgxbhL18rSjkGQ2Oo8130_provenance.
- NP186396.RAiuq_YszFIWdLUCXevylvUNqpIFdsT3hU44zivbaj7ik130_assertion description "[Incorporating the AdIL-1Ra transfected TTNT cells in the BAL device and testing in the GalN-induced FHF rat model resulted in significantly reduced plasma IL-6 levels, and a trend toward improved survival was seen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186396.RAiuq_YszFIWdLUCXevylvUNqpIFdsT3hU44zivbaj7ik130_provenance.
- NP186409.RAtYP9TCnETX9XwOX-naD_zWAQbb340djcINgwmhCijDc130_assertion description "[Ions that affect tip-link integrity and a mutation in PCDH15 that causes a recessive form of deafness disrupt interactions between CDH23 and PCDH15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186409.RAtYP9TCnETX9XwOX-naD_zWAQbb340djcINgwmhCijDc130_provenance.
- NP186412.RAsRIoMYEjZxGbHcnNxPwW0kYiDkX8nnXUhrl4KxUyOnA130_assertion description "[A novel mutation in the calcium-sensing receptor gene in a Chinese subject with persistent hypercalcemia and hypocalciuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186412.RAsRIoMYEjZxGbHcnNxPwW0kYiDkX8nnXUhrl4KxUyOnA130_provenance.
- NP186419.RAikjWFwPIX_o_vurbi9LE7dUtDtG3z2JgkIbrB3bwVP4130_assertion description "[In the longitudinal study, the EGF rs4444903 A > G polymorphism was found to be an independent predictor of cirrhosis development (O.R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186419.RAikjWFwPIX_o_vurbi9LE7dUtDtG3z2JgkIbrB3bwVP4130_provenance.
- NP186424.RAoXLqH8LCyWiltsGG-yl3B6WZIlSjVOZrJKUGj8sf-sc130_assertion description "[All AML samples expressed matrix metalloproteinase (MMP)-2 and/or MMP-9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186424.RAoXLqH8LCyWiltsGG-yl3B6WZIlSjVOZrJKUGj8sf-sc130_provenance.
- NP186429.RAkEpzI8xXxxF8rC9nsD2Q3bV45dIL-y7eRun4AShZy0o130_assertion description "[Therefore, we concluded that MRTF-A/B are potent repressors of cancer progression and metastasis and may be good targets for cancer therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186429.RAkEpzI8xXxxF8rC9nsD2Q3bV45dIL-y7eRun4AShZy0o130_provenance.
- NP186433.RAqR0BanJNPhHG7XZ-L9a_i_e5CY7A-nlW2M5deRDAd-0130_assertion description "[Walker-Warburg Syndrome (WWS) and muscle-eye-brain disease (MEB) are caused by mutations in two genes involved in O-mannosylation, POMT1 and POMGnT1, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186433.RAqR0BanJNPhHG7XZ-L9a_i_e5CY7A-nlW2M5deRDAd-0130_provenance.
- NP186441.RAvrc9ZGraeQOBT2FvXXv2EVZNwlt6ReUu5Jfe2uyzLtc130_assertion description "[Multiple ADH genes modulate risk for drug dependence in both African- and European-Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186441.RAvrc9ZGraeQOBT2FvXXv2EVZNwlt6ReUu5Jfe2uyzLtc130_provenance.
- NP186449.RAo5i5iLy_IeOBAg_5K8BpLKbPeuFwxh5vt_cjCneUOvA130_assertion description "[In this study, we showed that IL-32γ inhibited tumor growth in IL-32γ-overexpressing transgenic mice inoculated with melanoma as well as colon tumor growth in xenograft nude mice inoculated with IL-32γ-transfected colon cancer cells (SW620).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186449.RAo5i5iLy_IeOBAg_5K8BpLKbPeuFwxh5vt_cjCneUOvA130_provenance.
- NP186454.RAgX_zDYqXvPH1FPuhvwqmzmtplpcn8_GeHD3rbxA-jjU130_assertion description "[These results show that the GH1 T1663A A/A genotype can decrease the risk for colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186454.RAgX_zDYqXvPH1FPuhvwqmzmtplpcn8_GeHD3rbxA-jjU130_provenance.
- NP186458.RAnxbrljAcJ_8o8A1Tu54-d376xMDZifQ2c_whCOE0PfQ130_assertion description "[In 90% of the renal transplants performed in patients with MCP-HUS, there has been no recurrence of the primary disease, whilst >50% of factor I or factor H deficient patients have had a prompt recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186458.RAnxbrljAcJ_8o8A1Tu54-d376xMDZifQ2c_whCOE0PfQ130_provenance.
- NP186461.RAqMDhfIVJzzdPonnyQQpFk8dJwMZNqpEGkHRtDLVX_Ag130_assertion description "[Since these SNPs are known to be associated with PSA levels in men without PCa diagnoses, these latter associations may reflect the enrichment of low grade, low stage cases diagnosed by contemporary disease screening with PSA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186461.RAqMDhfIVJzzdPonnyQQpFk8dJwMZNqpEGkHRtDLVX_Ag130_provenance.
- NP186466.RAg4mwIz4qbymYI-it0ZD80YO3q1kZZmpwCV1-2HTfIJo130_assertion description "[This study showed consistent expression and common mutational activation of PDGFRA in small intestinal inflammatory fibroid polyps as in their gastric counterparts, and these lesions should be considered PDGFRA-driven benign neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186466.RAg4mwIz4qbymYI-it0ZD80YO3q1kZZmpwCV1-2HTfIJo130_provenance.
- NP186467.RAm6fwOjstM_XdIWihk00jg1tTtT0t0EHB1UxvEk1hu94130_assertion description "[Although 2 common mechanisms of multiple drug resistance, P-gp and GST-pi, might be responsible for drug resistance in neuroblastoma, this complex mechanism has no direct significant impact on prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186467.RAm6fwOjstM_XdIWihk00jg1tTtT0t0EHB1UxvEk1hu94130_provenance.
- NP186468.RAgcD4u3etS_pRX49cA9uRQOoKBzf5OQ1YlmBB6ktBBnw130_assertion description "[Members of the PEA3 subfamily of ETS-domain transcription factors fulfil such a role and have been associated with tumour metastasis in several different cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186468.RAgcD4u3etS_pRX49cA9uRQOoKBzf5OQ1YlmBB6ktBBnw130_provenance.
- NP186471.RAj_uZ-NoKbpPtc6zMk0Fg7MaBETRCEphz1EDSt6LAVuk130_assertion description "[The relation between islet cell specific antibodies, other autoantibodies and antibodies to cow's milk proteins was studied in IDDM and pre-IDDM by analysing islet cell antibodies (ICA), insulin autoantibodies (IAA), anti-nuclear (ANA), anti-reticulin class IgA [ARA(IgA)], smooth muscle, anti-mitochondria, parietal cell (PCA), adrenal and thyroid antibodies and antibodies to cow's milk formula (CMF), beta-lactoglobulin (BLG) and bovine serum albumin (BSA) in a population based study with more than 650 children with newly diagnosed IDDM and more than 550 initially non-diabetic siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186471.RAj_uZ-NoKbpPtc6zMk0Fg7MaBETRCEphz1EDSt6LAVuk130_provenance.
- NP186473.RAoB6vMj-0rKbjoY6V51KA5olwcaBypSpjF8cvknAK3Yk130_assertion description "[Monocytes from patients with IgA nephropathy expressed a higher level of MMP-9 mRNA than those from patients with other forms of glomerulonephritis or from healthy controls (MMP-9 to glyceraldehyde-3-phosphate dehydrogenase ratio: IgA nephropathy, 1.68 +/- 0.24; membranous nephropathy, 0.22 +/- 0.08; minimal-change nephrotic syndrome, 0.24 +/- 0.06; focal glomerulosclerosis, 0.32 +/- 0.08; non-IgA proliferative glomerulonephritis, 0.30 +/- 0.12; and healthy controls, 0.16 +/- 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186473.RAoB6vMj-0rKbjoY6V51KA5olwcaBypSpjF8cvknAK3Yk130_provenance.
- NP186474.RAqj8Vc6TxTnow8c7bBLm9JIzY5WPncfjM8tl4XIhagV8130_assertion description "[In conclusion, MTHFR, MTR, DNMT3b, and EHMT2 polymorphisms are associated with colorectal cancer, and rare variants of MTR and MTRR may reduce promoter hypermethylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186474.RAqj8Vc6TxTnow8c7bBLm9JIzY5WPncfjM8tl4XIhagV8130_provenance.
- NP186476.RAlx2j4fAjgoj9eSOPEVeqrB9UcWoP8g6OmRRw1QFDnK4130_assertion description "[Targeting survivin and p53 in pediatric acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186476.RAlx2j4fAjgoj9eSOPEVeqrB9UcWoP8g6OmRRw1QFDnK4130_provenance.
- NP186481.RAm3eyILwAcP96j7fsnC05pYU64hDPxKtqzDHR_nlwJso130_assertion description "[Significant associations were found between carriers of the minor alleles of APOE-epsilon2, FABP2-A54T, UCP1-L229M, LPL-HindIII, LPL-S447X and LPL-T1973C, patients bearing a combination of LPL-D9N, LPL-N291S and LPL-P207L and obesity-related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186481.RAm3eyILwAcP96j7fsnC05pYU64hDPxKtqzDHR_nlwJso130_provenance.
- NP186485.RArWE1hs53-aoYUDaMah9DboFfGJBR4n1HWQ2c8ATWmPE130_assertion description "[We performed p53 (exons 4-8) gene mutation analysis on 24 surgically resected human esophageal cancer specimens by PCR, single-strand conformation polymorphism, and DNA sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186485.RArWE1hs53-aoYUDaMah9DboFfGJBR4n1HWQ2c8ATWmPE130_provenance.
- NP186491.RAjpb5J_8NBIvjxviGCKCjesz8cs3GfXyQYjcJRMUuJck130_assertion description "[We have used a heterogeneous stock of mice to identify Hectd2, an E3 ubiquitin ligase, as a quantitative trait gene for prion disease incubation time in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186491.RAjpb5J_8NBIvjxviGCKCjesz8cs3GfXyQYjcJRMUuJck130_provenance.
- NP186492.RAg7iXo6ZCWiw2_759XzlyMqYss6oa4T5lZg43SX0obpQ130_assertion description "[Relationship between ERCC1 polymorphisms, disease progression, and survival in the Gynecologic Oncology Group Phase III Trial of intraperitoneal versus intravenous cisplatin and paclitaxel for stage III epithelial ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186492.RAg7iXo6ZCWiw2_759XzlyMqYss6oa4T5lZg43SX0obpQ130_provenance.
- NP186495.RAiEZlEHU5am-K01_v6voX1IG2s5LVkjvCk8vtdl7PJwg130_assertion description "[Here, we report that CB1 and CB2 cannabinoid receptors are expressed in human colorectal adenoma and carcinoma cells, and show for the first time that THC induces apoptosis in colorectal cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186495.RAiEZlEHU5am-K01_v6voX1IG2s5LVkjvCk8vtdl7PJwg130_provenance.
- NP186500.RAkn9WVKm2KUIucWheNtgdvyPlojmPK0eL2MWxinQiOcM130_assertion description "[Using a tissue microarray, this enhanced AGR2 expression was seen as early as premalignant PIN lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186500.RAkn9WVKm2KUIucWheNtgdvyPlojmPK0eL2MWxinQiOcM130_provenance.
- NP186506.RAqb9J9TUvPzAq_L_jH9CJFN2AtANt2Ec_fGJJ69S3pUY130_assertion description "[Overexpression of phosphatase of regenerating liver (PRL)-3 is associated with the progression of diverse human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186506.RAqb9J9TUvPzAq_L_jH9CJFN2AtANt2Ec_fGJJ69S3pUY130_provenance.
- NP186510.RAlnVpLaT8nOKQhF1ou3ZbN8UAP8IUAjrPQSetn1xbtLg130_assertion description "[Cardiovascular disease is prevalent in first-degree relatives of young adults with premature-onset peripheral arterial occlusive disease (premature PAD), but it is not known whether the genetic influence is independent of other risk factors, the most prevalent of which is smoking.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186510.RAlnVpLaT8nOKQhF1ou3ZbN8UAP8IUAjrPQSetn1xbtLg130_provenance.
- NP186518.RAka6V2Bs5ji3cpSlQKRr5SZxPG3ZkSl4HGwHKHMveb1M130_assertion description "[Strong cMET[pY1003] membrane immunoreactivity was expressed in 6% of 149 tumors analyzed and was significantly associated with progressive disease (P = 0.019) and shorter TTP (P = 0.041).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186518.RAka6V2Bs5ji3cpSlQKRr5SZxPG3ZkSl4HGwHKHMveb1M130_provenance.
- NP186519.RAraQYK5IWI8SXpFgRbkvrEgFsGXPhxSFKSRLHvLYBaM4130_assertion description "[The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locus: implications for multiple nonhemolytic familial hyperbilirubinemia phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186519.RAraQYK5IWI8SXpFgRbkvrEgFsGXPhxSFKSRLHvLYBaM4130_provenance.
- NP186524.RAkhFwaN4H7X4iLNNnub8Kf_COKmjiADLYeMQBm3hNyd4130_assertion description "[X-linked chronic granulomatous disease (X-CGD) is a primary immunodeficiency caused by mutations in the CYBB gene encoding the phagocyte nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase catalytic subunit gp91(phox).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186524.RAkhFwaN4H7X4iLNNnub8Kf_COKmjiADLYeMQBm3hNyd4130_provenance.
- NP186541.RAiUDydrUiTAANXEyTEg1vyupnLPwbdsK3n7wZHqY95UQ130_assertion description "[Although the link between the BRCA1 tumour-suppressor gene and hereditary breast and ovarian cancer is established, the role, if any, of BRCA1 in non-familial cancers is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186541.RAiUDydrUiTAANXEyTEg1vyupnLPwbdsK3n7wZHqY95UQ130_provenance.
- NP186546.RAs5JGRff4l6dwgENm74E5j8YtUYhD03sPguiaIzE2QvY130_assertion description "[A retrospective study of surgically resected breast cancers from 73 patients revealed significant clinical differences associated with u-PA and PAI-2 expression in cancer cells, associated with a poor and a good prognosis, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186546.RAs5JGRff4l6dwgENm74E5j8YtUYhD03sPguiaIzE2QvY130_provenance.
- NP186551.RAs5VW4J8zD8PaiHsn8rLYql39myfP7sx2lEsBdMDLrvE130_assertion description "[Peripheral blood mononuclear cells from healthy donors and patients with advanced non-small cell lung cancer, bone metastatic breast or prostate cancer, or lung metastatic colorectal cancer, were stimulated with zoledronate (5 microM) and interleukin (IL)-2 (1000 IU/mL) for 14 days.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186551.RAs5VW4J8zD8PaiHsn8rLYql39myfP7sx2lEsBdMDLrvE130_provenance.
- NP186554.RAgNMeUZjVY0Oq77O8sqwX1wrNZhAIsaHh0R8dwmeRUn8130_assertion description "[The association of family history of premature CHD with CAC was assessed in 5347 asymptomatic individuals (47% men; mean age 62+/-10 years) in the Multi-Ethnic Study of Atherosclerosis (MESA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186554.RAgNMeUZjVY0Oq77O8sqwX1wrNZhAIsaHh0R8dwmeRUn8130_provenance.
- NP186556.RAprNbDbW5PFeEC98UPq6KF9R7bfn89PBv9JYmgXKKwPk130_assertion description "[TGFbeta regulated gene expression by Smads and Sp1/KLF-like transcription factors in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186556.RAprNbDbW5PFeEC98UPq6KF9R7bfn89PBv9JYmgXKKwPk130_provenance.
- NP186561.RAkdT_HVAYR7BsJdrPb4TF4KZ_7fLzwqzH7NkZMtcGCrE130_assertion description "[Fabry disease (FD) is an X-linked recessive disorder caused by the deficient activity of the lysosomal enzyme alpha-galactosidase A (alpha-Gal A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186561.RAkdT_HVAYR7BsJdrPb4TF4KZ_7fLzwqzH7NkZMtcGCrE130_provenance.
- NP186563.RAn-_rqqbWgTqqCEaQ3oDGI5SJKR8kwu4WPyPJHa0S7mo130_assertion description "[Exogenous administration of insulin-like growth factor (IGF)-I has anti-depressant properties in rodent models of depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186563.RAn-_rqqbWgTqqCEaQ3oDGI5SJKR8kwu4WPyPJHa0S7mo130_provenance.
- NP186568.RAsjt2u9A-e36rzkjjJ8k3x_-VEtxuc_qFwrqEsbO-ELQ130_assertion description "[miR-124 is a brain-enriched microRNA that plays a crucial role in neural development and has been shown to be down-regulated in glioma and medulloblastoma, suggesting its possible involvement in brain tumor progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186568.RAsjt2u9A-e36rzkjjJ8k3x_-VEtxuc_qFwrqEsbO-ELQ130_provenance.
- NP186574.RAuuFnisz8u5-pAMeAacv1yeKh65vcRnESqBbWhdiJYGc130_assertion description "[We argue that TRPV1 antagonists alone or in conjunction with other analgesics will improve the quality of life of people with migraine, chronic intractable pain secondary to cancer, AIDS or diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186574.RAuuFnisz8u5-pAMeAacv1yeKh65vcRnESqBbWhdiJYGc130_provenance.
- NP186577.RAmQOG-ACKwwaOtepb5WLIvCtINwRljABfTHzQisy7zDY130_assertion description "[We report the isolation and characterization of genomic sequences coding for the 5' end of human retinoic acid receptor beta 1, a fetal RAR isoform which is also expressed in small cell lung cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186577.RAmQOG-ACKwwaOtepb5WLIvCtINwRljABfTHzQisy7zDY130_provenance.
- NP186581.RAn7rj_JScE8yKJXykiaKxqOo2D5BmQRkAsmYhik1RFs8130_assertion description "[The purpose of our study was to characterize the expression of CCL27 and CCL17 in the inflammatory skin diseases: psoriasis, atopic dermatitis (AD) and acute allergic contact dermatitis (ACD) induced in nickel-sensitive individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186581.RAn7rj_JScE8yKJXykiaKxqOo2D5BmQRkAsmYhik1RFs8130_provenance.
- NP186587.RArJfxUvEkeiCUh1bRpk1FMGlW2SyLbTNobG8WZ_TQgkg130_assertion description "[We report a case of osteoma cutis associated with a GNAS mutation in a 7-month-old boy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186587.RArJfxUvEkeiCUh1bRpk1FMGlW2SyLbTNobG8WZ_TQgkg130_provenance.
- NP186588.RAsrdDeXcxtanMmIpibdaI1NTD0kG8DfRamSSx3nKiGNY130_assertion description "[The rarity of these mutants in human cancer and their multiple occurrence in BRCA-associated breast tumours suggests that these novel p53 mutants are selected during malignant progression in the unique genetic background of BRCA1- and BRCA2-associated tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186588.RAsrdDeXcxtanMmIpibdaI1NTD0kG8DfRamSSx3nKiGNY130_provenance.
- NP186594.RAgx8-7mx_-n-ZqjUqGoof35o6YfX91YLxZorJrXwgwAg130_assertion description "[The translocation t(8;21)(q22;q22) affecting AML1 and ETO genes is known to be one of the frequent chromosome translocations in acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186594.RAgx8-7mx_-n-ZqjUqGoof35o6YfX91YLxZorJrXwgwAg130_provenance.
- NP186601.RAu2tMHm49ko_kpwnUdEHtWEPWCnYabQXeYcI8yw1lcos130_assertion description "[Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186601.RAu2tMHm49ko_kpwnUdEHtWEPWCnYabQXeYcI8yw1lcos130_provenance.
- NP186606.RAjDUIEg_hd7FPST76Fl1lJrhyozK8n8ugeE-XQ2dlGj0130_assertion description "[Thus, tumor derived cathepsin D assists breast cancer progression by reducing cystatin C activity, which, in turn, enhances cysteine cathepsin proteolytic activity, revealing a new link between protease classes in the protease web.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186606.RAjDUIEg_hd7FPST76Fl1lJrhyozK8n8ugeE-XQ2dlGj0130_provenance.
- NP186621.RApgrUOU4TO3fVnGEAcfbFk3LmnNsgiXU6H72g7zSXwu0130_assertion description "[In ACs, high miR-155 expression tended to a significant negative prognostic effect on survival in univariate analysis (P = 0.086) and was an independent prognostic factor in multivariate analysis (HR 1.87, CI 95% 1.01 - 3.48, P = 0.047).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186621.RApgrUOU4TO3fVnGEAcfbFk3LmnNsgiXU6H72g7zSXwu0130_provenance.
- NP186622.RAjT_2Gq36wGhXYGTWoPy-rCmgPRixpEobMoNKi1BkOPM130_assertion description "[After lentiviral-mediated gene transfer of INPP5D into CD34(+) cells derived from AML patients (n=12) the granulocyte macrophage-colony stimulating factor (GM-CSF)-dependent proliferation was reduced in all samples analyzed (average 86%; range 72-93%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186622.RAjT_2Gq36wGhXYGTWoPy-rCmgPRixpEobMoNKi1BkOPM130_provenance.
- NP186625.RApakedxJ18OxRqWCISw7U8suC0skWgoDXKP0oLuDwVZI130_assertion description "[The results showed that; (i) genotypes with the +54C allele (C/C or C/T) significantly increased the risk of developing both ESCC and GCA compared to the +54T/T genotype (age and gender adjusted odds ratio [OR] = 1.45 and 2.28, 95% confidence interval [CI] = 1.06-1.99 and 1.58-3.30, respectively), and this association was significant only among non-smokers (OR = 1.68 and 2.64, 95% CI = 1.01-2.80 and 1.43-4.87 for ESCC and GCA, respectively), and individuals without a family history of upper gastrointestinal cancer (OR = 2.63 and 2.97, 95% CI = 1.36-5.10 and 95% CI = 1.32-6.68 for ESCC and GCA, respectively); (ii) compared with the -347G/G genotype, the -347GA and GA/GA genotypes significantly increased the risk of developing GCA (OR = 1.45, 95 % CI = 1.03-2.04); (iii) there was a significant association of CDH1-160C/-347G/+54C and -160C/-347GA/+54C haplotypes with the development of GCA, compared with the -160C/-347G/+54T haplotype (OR = 1.80 and 2.21, 95% CI = 1.33-2.44 and 1.43-3.42, respectively); and (iv) the influence of CDH1 SNP on the depth of tumor invasion and lymphatic metastasis in ESCC and GCA patients was not observed in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186625.RApakedxJ18OxRqWCISw7U8suC0skWgoDXKP0oLuDwVZI130_provenance.
- NP186626.RAsGrlcwO3_6oSF9dYd4_I6ALGGV7lSGB8vHB7H2wYVPI130_assertion description "[Single nucleotide polymorphisms (SNPs, n = 114) in nine RAAS-related genes (AGT, REN, ACE, ACE2, AGTR1, CYP11B2, NR3C2, MAS1, and CMA1) were assessed for their correlation with blood pressure and hypertension using genotype data of 8842 individuals from the Korea Association Resource subject pool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186626.RAsGrlcwO3_6oSF9dYd4_I6ALGGV7lSGB8vHB7H2wYVPI130_provenance.
- NP186633.RAvdrxvbX0MKch3ZX-yHeI8DjWek5ARhjJuBLUqRfqqT8130_assertion description "[Mycoplasma-mediated secretion of proinflammatory cytokines, such as tumor necrosis factor alpha, interleukin-1 (IL-1), and IL-6, by macrophages and of up-regulating cytokines by mitogenically stimulated lymphocytes plays a major role in mycoplasma-induced immune system modulation and inflammatory responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186633.RAvdrxvbX0MKch3ZX-yHeI8DjWek5ARhjJuBLUqRfqqT8130_provenance.
- NP186634.RAl6TRbh5YaY4rBZTc1GWZtEbOKt22ccm0y8yxqkFcdJc130_assertion description "[Translocation (1;6)(p12;p23) in ANLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186634.RAl6TRbh5YaY4rBZTc1GWZtEbOKt22ccm0y8yxqkFcdJc130_provenance.
- NP186639.RAg-ZIZkl2cllFn0Ej6yLaaqI3zxPsjdcpvZwGKvqRSFs130_assertion description "[Polymorphisms in the genes ERCC2, XRCC3 and CD3EAP influence treatment outcome in multiple myeloma patients undergoing autologous bone marrow transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186639.RAg-ZIZkl2cllFn0Ej6yLaaqI3zxPsjdcpvZwGKvqRSFs130_provenance.
- NP186644.RAkOPAWL3GmI5zoTGfW48LRU1k4hNl_R_W9LyycO6Erq8130_assertion description "[Immunohistochemistry, double in situ hybridization, PCR, PCR-SSCP, and sequencing were used to study the changes in the p16 and RB genes in 106 patients with lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186644.RAkOPAWL3GmI5zoTGfW48LRU1k4hNl_R_W9LyycO6Erq8130_provenance.
- NP186645.RAk-n9a0dv9bDeK_63r_mFl0EavhWMdUY1Jc4k0A5qNxA130_assertion description "[To investigate the association of polymorphism in the angiotensin-converting enzyme (ACE) I/D gene, angiotensinogen M235T gene, and angiotensin II type 1 receptor A1166C gene with body mass index, body fat pattern, and obesity-associated hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186645.RAk-n9a0dv9bDeK_63r_mFl0EavhWMdUY1Jc4k0A5qNxA130_provenance.
- NP186651.RAq-FkU6XNIq-8SRzbcV9-zjs3CIKrFEDWZIU0B2PF2qI130_assertion description "[Association of CD1A +622 T/C, +737 G/C and CD1E +6129 A/G genes polymorphisms with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186651.RAq-FkU6XNIq-8SRzbcV9-zjs3CIKrFEDWZIU0B2PF2qI130_provenance.
- NP186653.RAgSZoOtvmdtwQcKdh_Zd6SJjq-_WcK_egzWuUainGQpU130_assertion description "[To cast light on relations of cyclooxygenase-2 (COX-2) expression to lymphocytic thyroiditis and thyroid tumorigenesis, protein levels were immunohistochemically assessed and compared with inducible nitric oxide synthase (iNOS) in a total of 181 cases: follicular adenoma, 23; well-differentiated papillary carcinoma, 85; poorly differentiated papillary carcinoma, 25; anaplastic carcinoma, 7; and follicular carcinoma, 41.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186653.RAgSZoOtvmdtwQcKdh_Zd6SJjq-_WcK_egzWuUainGQpU130_provenance.
- NP186661.RAni8zn5_Cw4cLOcrOtOXwtf6c_ghInoDs2O50sgNS5uc130_assertion description "[Predictive value of TP53 fluorescence in situ hybridization in cytogenetic subgroups of acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186661.RAni8zn5_Cw4cLOcrOtOXwtf6c_ghInoDs2O50sgNS5uc130_provenance.
- NP186665.RAkvkJ8Xp_ZrIO4i_F51MI1JSmprjcGJiOT_48r3TWGuo130_assertion description "[Aberrant DNA methylation is a hallmark of carcinogenesis and GSTP1 hypermethylation is the most common molecular alteration in human prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186665.RAkvkJ8Xp_ZrIO4i_F51MI1JSmprjcGJiOT_48r3TWGuo130_provenance.
- NP186667.RApd93poDwn1xCfCHPLktlvHZbXP3hhnqtsslax5FSeVg130_assertion description "[Using sequencing and/or immunohistochemical analyses, we investigated ATRX alterations (mutation/loss of expression) and their association with TP53 and IDH1 or IDH2 mutations in 140 adult WHO grade II, III and IV gliomas, 17 pediatric WHO grade II and III astrocytomas and 34 pilocytic astrocytomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186667.RApd93poDwn1xCfCHPLktlvHZbXP3hhnqtsslax5FSeVg130_provenance.
- NP186668.RAhhJn17ixlhkF0K7a1AvkTXivTiyc4I2aawNXglC6WDY130_assertion description "[The association of a base substitution with the hyperexpression of the prolactin gene in eutopic prolactinomas suggests that different mechanisms may mediate the formation of eutopic and ectopic prolactin-secreting tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186668.RAhhJn17ixlhkF0K7a1AvkTXivTiyc4I2aawNXglC6WDY130_provenance.
- NP186676.RAt4Knr_5I_pMOXsUDDCzFZ49pTTVrgCVfgjCSlMDzuJ8130_assertion description "[ADMA, 5-HT, 8-isoPGF2α, ET-1 levels, and PAC were significantly higher (p<0.0001, each), whereas SOD activity and NO level were significantly lower in HAPE-p than HAPE-f (p ≤ 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186676.RAt4Knr_5I_pMOXsUDDCzFZ49pTTVrgCVfgjCSlMDzuJ8130_provenance.
- NP186677.RAhGT66AvaX8MENVRd0VEbRlhjc3NQckWb1z1FJm-ahUo130_assertion description "[Furthermore, RUNX3 restoration inhibited tumor growth and metastasis in animal models, which was consistent with inhibition of angiogenesis as determined by evaluating VEGF expression and tumor microvessel formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186677.RAhGT66AvaX8MENVRd0VEbRlhjc3NQckWb1z1FJm-ahUo130_provenance.
- NP186678.RAr0aXDTEbShfOq-A9hAbUPywk911H8JvNcFrG51MBd6I130_assertion description "[MYC locus alterations were observed in 21 cases: MYC/IG (mainly IGH@) fusions in 11 cell lines and three patients (2 MM and 1 PCL), and extra signals and/or abnormal MYC localizations in seven patients (5 MM and 2 PCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186678.RAr0aXDTEbShfOq-A9hAbUPywk911H8JvNcFrG51MBd6I130_provenance.
- NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_assertion description "[The study revealed that 4 genotypes (- -(SEA)/ -alpha(3.7), - -(SA)/-alpha(3.7), - -(SEA)/-alpha(3.7 Sallanches), - -alpha(3.7)/-alpha(3.7 Sallanches)) were responsible for Hb H disease, the alpha+ thalassemia mutation (-alpha(3.7) deletion) being the most common defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186681.RAojOQL5-zPjrg4TYFCnxNKh47PikU9UynugF0cNdZ7AA130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP186686.RAvUGFT2gvotVv6bygaBieXRJhnRatgOFhxEc4mZt1mrc130_assertion description "[We investigated whether genetic variations in the leptin (LEP) and LEPR genes are associated with risk of breast cancer, or once diagnosed, with survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186686.RAvUGFT2gvotVv6bygaBieXRJhnRatgOFhxEc4mZt1mrc130_provenance.
- NP186693.RAtJkCj5zxrG_v1zn56KAZXin6qKWMc3SjJo79PNiNQ94130_assertion description "[These efforts have revealed several acquired resistance mechanisms and candidates, including EGFR secondary mutations (T790M and other rare mutations), MET amplification, PTEN downregulation, CRKL amplification, high-level HGF expression, FAS-NFκB pathway activation, epithelial-mesenchymal transition, and conversion to small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186693.RAtJkCj5zxrG_v1zn56KAZXin6qKWMc3SjJo79PNiNQ94130_provenance.
- NP186698.RAsQbT_F7jkNAOYSMj6Vpt_67o8Q5BKQTaY_94I5X2p5k130_assertion description "[As a part of the MED-PED (make early diagnosis-prevent early death) project we are currently investigating children, adolescents and their relatives who are suspected to be affected with FH in our out-patient clinic for metabolic diseases using MED-PED inclusion criteria and confirming the diagnosis by means of DNA analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186698.RAsQbT_F7jkNAOYSMj6Vpt_67o8Q5BKQTaY_94I5X2p5k130_provenance.
- NP186702.RAskuPZhg88PUl1C1NnL8xElT2JzwI31XVK-XiLu9Ug84130_assertion description "[To investigate the presence of various isoforms of the estrogen receptor (ER) in SLE we isolated RNA from mononuclear cells of lupus patients and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186702.RAskuPZhg88PUl1C1NnL8xElT2JzwI31XVK-XiLu9Ug84130_provenance.
- NP186704.RAh9vISdm71T-BZ0CF5346YLEn0YXTsMrayAbeiZpA7-0130_assertion description "[The subjects with 1 copy of the minor allele of these 7 single-nucleotide polymorphisms had higher Beck Depression Inventory scores and IL-6 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186704.RAh9vISdm71T-BZ0CF5346YLEn0YXTsMrayAbeiZpA7-0130_provenance.
- NP186712.RAgp_bK0r77LAgMRvjLmMGmHfn2R88DnL8QlVYC10YseQ130_assertion description "[Investigation of the effect of MDM2 SNP309 and TP53 Arg72Pro polymorphisms on the age of onset of cutaneous melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186712.RAgp_bK0r77LAgMRvjLmMGmHfn2R88DnL8QlVYC10YseQ130_provenance.
- NP186716.RAlEKJOHj3a3tpIcL0X0pitPACUxcco90aax9Sdsu8fxs130_assertion description "[Interface tissue fibroblasts are able to produce RANKL, OPG, and cathepsin K and may contribute indirectly and directly to pathologic periprosthetic collagenolysis and bone destruction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186716.RAlEKJOHj3a3tpIcL0X0pitPACUxcco90aax9Sdsu8fxs130_provenance.
- NP186717.RAj6fVZQD0gLKQvCHdO14-t5NOG5smh-6lIm9td-K860E130_assertion description "[AP-1 and colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186717.RAj6fVZQD0gLKQvCHdO14-t5NOG5smh-6lIm9td-K860E130_provenance.
- NP186721.RAhaaopGS_WQ7ML1RkqBVLUU16girZfYd4s_L1I5QN4fU130_assertion description "[Results showed that IFN-γ and high glucose synergistically stimulated matrix metalloproteinase 1 (MMP-1), a proteinase essential for vascular tissue remodelling and atherosclerosis, in U937 mononuclear cells, but Rs-LPS inhibited the MMP-1 stimulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186721.RAhaaopGS_WQ7ML1RkqBVLUU16girZfYd4s_L1I5QN4fU130_provenance.
- NP186722.RAm_M2UZaEQyQLpV6yNGns22L01c7brcaEen4Eb-9Vzqo130_assertion description "[Since all patients were not obese, we might hypothesize that in Rett syndrome leptin and adiponectin might participate to clinical manifestations other than weight balance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186722.RAm_M2UZaEQyQLpV6yNGns22L01c7brcaEen4Eb-9Vzqo130_provenance.
- NP186727.RApHR5UOcCwQo4ZPRlbP2mjOk58s_H9_cpCoHNLfcwKbc130_assertion description "[Thrombospondin-4 is a putative tumour-suppressor gene in colorectal cancer that exhibits age-related methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186727.RApHR5UOcCwQo4ZPRlbP2mjOk58s_H9_cpCoHNLfcwKbc130_provenance.
- NP186732.RArDhtVv_hNVFa1DpjNZMRi8z3WFQqQKWO_v7nXPkIBBs130_assertion description "[Problems with the regulation of PCD have been implicated in a number of diseases including myocardial infarction, cancer and autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186732.RArDhtVv_hNVFa1DpjNZMRi8z3WFQqQKWO_v7nXPkIBBs130_provenance.
- NP186748.RAgMiTkT87mpZg8ghpi2hz2ASnREFzJd0ALBeJLR6kFBw130_assertion description "[Although hyperhomocysteinaemia and methylenetetrahydrofolate reductase gene polymorphism are accepted risk factors for cardiovascular disease, their association with micro angiopathy or blood pressure in diabetic patients is still being debated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186748.RAgMiTkT87mpZg8ghpi2hz2ASnREFzJd0ALBeJLR6kFBw130_provenance.
- NP186749.RAuTuMA2j8oj4OV-BBL_hDRCivtmXPdm9JEr6vFQ0Qtb4130_assertion description "[DUSP4 is involved in negative feedback control of EGFR signaling, and we provide functional validation for its role as a growth suppressor in EGFR-mutant lung adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186749.RAuTuMA2j8oj4OV-BBL_hDRCivtmXPdm9JEr6vFQ0Qtb4130_provenance.
- NP186756.RAni9tEThTWMCaehpdNMArx_RD9ikmePjFvUwC85StP-g130_assertion description "[These results of our meta-analysis suggest that there is no overall association between NAT2 polymorphism and CRC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186756.RAni9tEThTWMCaehpdNMArx_RD9ikmePjFvUwC85StP-g130_provenance.
- NP186760.RAqAtC7CM4wZ6b2zKlecFIb0fQAhiDYptd55arzCzeA1g130_assertion description "[The aim of this study is to investigate the role of single-nucleotide polymorphisms (SNPs) of the glucocorticoid receptor (GR) and of the related co-chaperone FKBP5 genes in the development of glucocorticoid (GC) resistance in Crohn's disease (CD) and ulcerative colitis (UC) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186760.RAqAtC7CM4wZ6b2zKlecFIb0fQAhiDYptd55arzCzeA1g130_provenance.
- NP186761.RAmgOueCk6fmNVBB_DMaGX-BCsz4gxeoZui0A5NEHj3us130_assertion description "[However, few data exist on the possible association of specific HLA-class II alleles or haplotypes with ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186761.RAmgOueCk6fmNVBB_DMaGX-BCsz4gxeoZui0A5NEHj3us130_provenance.
- NP186763.RAiSVZ6xupH37n0dhY639kpX1KBbUW6jM1BJtYns_ztAg130_assertion description "[The Panel concluded that: 1) the association between active smoking and breast cancer is consistent with causality and 2) the association between SHS and breast cancer among younger, primarily premenopausal women who have never smoked is consistent with causality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186763.RAiSVZ6xupH37n0dhY639kpX1KBbUW6jM1BJtYns_ztAg130_provenance.
- NP186767.RAh_IfsrcckV3TlE1OJQehBI5487e7JdAQJ0_ieB1sj4w130_assertion description "[Two genome-wide association studies (GWAS) identified the β-microseminoprotein (MSMB) promoter SNP, rs10993994:C>T, as significantly associated with prostate cancer (PC) risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186767.RAh_IfsrcckV3TlE1OJQehBI5487e7JdAQJ0_ieB1sj4w130_provenance.
- NP186771.RAs8XUPa3Uy9CvTDgXygefJaXEywXPYUdqzswxTLBUD9Y130_assertion description "[Although Sp1, USF1, and GATA1 levels are critical determinants of hRFC transcription in ALL, neither DNA methylation nor promoter polymorphisms contribute to differences in hRFC expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186771.RAs8XUPa3Uy9CvTDgXygefJaXEywXPYUdqzswxTLBUD9Y130_provenance.
- NP186773.RAkVtunixRaJmYqgbooeTgty0DBSU3RWsqkfTsQ0e3ShE130_assertion description "[Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186773.RAkVtunixRaJmYqgbooeTgty0DBSU3RWsqkfTsQ0e3ShE130_provenance.
- NP186776.RAhhPPFihvzinmofkSJCxQ-ckJj0IKPURNrcK4YHQbOy0130_assertion description "[In the gene polymorphism studies MMP-9 has been suggested to be involved in the pathogenesis of heart disease, cancer, bipolar disorder, and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186776.RAhhPPFihvzinmofkSJCxQ-ckJj0IKPURNrcK4YHQbOy0130_provenance.
- NP186777.RAq2zIBukS1vb3EkgoPztGwEXFEt8fGxTK9GB9yGi1OdE130_assertion description "[Cux1 is an effector of the transforming growth factor beta (TGFβ) pathway, PAR(2) receptor signaling, and cellular migration, mechanisms intimately related to inflammatory bowel diseases (IBD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186777.RAq2zIBukS1vb3EkgoPztGwEXFEt8fGxTK9GB9yGi1OdE130_provenance.
- NP186780.RAjjOZY7uVVUddCAdHDtRFusRgqFAk-KdM5kHjrCxe0u8130_assertion description "[The earliest observable lesions of recurrent CD are microscopic erosions at the specialized follicle-associated epithelium (FAE), which lines the Peyer's patches.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186780.RAjjOZY7uVVUddCAdHDtRFusRgqFAk-KdM5kHjrCxe0u8130_provenance.
- NP186782.RAmFbaZ3Ayf-QcZUSsuiL8IHxtep0ZwovVfrP3Px0Jj64130_assertion description "[Despite the fact that the number of patients tested is small, there is good evidence that the Bal I DRD3 polymorphism does not play a major role in the genetic component of anorexia nervosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186782.RAmFbaZ3Ayf-QcZUSsuiL8IHxtep0ZwovVfrP3Px0Jj64130_provenance.
- NP186788.RArlsYLlLUBiWafpaL4BgwVOsoHEFbxm0dTaClK0nTUAU130_assertion description "[These findings suggest that the A1166C polymorphism of the AT1 receptor gene is associated with collagen type I synthesis and myocardial stiffness in patients with hypertensive heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186788.RArlsYLlLUBiWafpaL4BgwVOsoHEFbxm0dTaClK0nTUAU130_provenance.
- NP186789.RAsui1wk426trhLCHI38V7bPLRJq-DvH3uRWSSuJhxyYU130_assertion description "[In addition, overexpression of MTDH led to increased acquisition of CD44(+) /CD24(-/low) markers that are characteristic of breast cancer stem cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186789.RAsui1wk426trhLCHI38V7bPLRJq-DvH3uRWSSuJhxyYU130_provenance.
- NP186796.RAutyN04EIZuUkRdXgCuPc2R0_AFEx9Ec60wHAUh4Plp0130_assertion description "[We investigated whether polymorphisms in the GSTM1, GSTT1 and GSTP1 genes modified the risk for chronic pancreatitis (CP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186796.RAutyN04EIZuUkRdXgCuPc2R0_AFEx9Ec60wHAUh4Plp0130_provenance.
- NP186800.RAvQIcz9ln0UteekfGraKSsi2BRriHlc-CpbNGV4tUZ4Q130_assertion description "[In vivo fluorescence videomicroscopy and radiolabel distribution studies of ELP delivery to human tumors (SKOV-3 ovarian carcinoma and D-54MG glioma) implanted in nude mice demonstrated that hyperthermic targeting of the thermally responsive ELP for 1 h provides a approximately 2-fold increase in tumor localization compared to the same polypeptide without hyperthermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186800.RAvQIcz9ln0UteekfGraKSsi2BRriHlc-CpbNGV4tUZ4Q130_provenance.
- NP186805.RAgehHUlV2fAm1vqNljq18ecLHmZwRuP6MGUM_DDG6CJs130_assertion description "[Glucose-6-phosphate dehydrogenase deficiency (G6PD) is the most common inherited enzymopathy affecting approximately 400 million people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186805.RAgehHUlV2fAm1vqNljq18ecLHmZwRuP6MGUM_DDG6CJs130_provenance.
- NP186816.RArQWYiVW8Tt-kSFcwOVA8p4etq8Wcj0HD51sL2eMB_bI130_assertion description "[However, the TS3'-UTR polymorphism increased breast cancer risk among Asian women (del6 vs. ins6; OR 1.41; 95% CI 1.01-1.98) but not Caucasian women using the homozygote comparison.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186816.RArQWYiVW8Tt-kSFcwOVA8p4etq8Wcj0HD51sL2eMB_bI130_provenance.
- NP186826.RApZTQf0kNYDc3kZ30rAdWgZjUK-PWkGduM9SrwKmtjL4130_assertion description "[This transcription pattern is in good correlation with the keratinisation and differentiation patterns of the two epithelia: perianal biopsies preferentially expressed K16 and K17 while penile warts mainly expressed K10, markers of parakeratotic and orthokeratotic epithelia, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186826.RApZTQf0kNYDc3kZ30rAdWgZjUK-PWkGduM9SrwKmtjL4130_provenance.