Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP172045.RARkf9PijRXa73twqCnGDcpVZ907XThR5SXCLH3ZglrZg130_assertion description "[Role of p53 in neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172045.RARkf9PijRXa73twqCnGDcpVZ907XThR5SXCLH3ZglrZg130_provenance.
- NP172052.RAVzPwYrgb6XmBktWEk9qJVFkrZ6AEjFKvZ-R8GrHVIFM130_assertion description "[In 44 patients with coronary artery disease or hypercholesterolemia (not on lipid-lowering treatment), lipid profile and endothelial function (brachial artery flow-mediated dilation, FMD) were measured at baseline and after treatment with statins for 8-12 weeks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172052.RAVzPwYrgb6XmBktWEk9qJVFkrZ6AEjFKvZ-R8GrHVIFM130_provenance.
- NP172054.RAZ8bFcKJd6krlfToxDC5Cm1gsT_C8JtKujh7bsvSDEdk130_assertion description "[Homozygous loss in the genomic sequence, a mechanism for inactivating tumor-suppressor genes (TSGs) in cancer, has been used as a tag for the identification of novel TSGs, and array-based comparative genomic hybridization (array-CGH) has a great potential for high-throughput identification of this change.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172054.RAZ8bFcKJd6krlfToxDC5Cm1gsT_C8JtKujh7bsvSDEdk130_provenance.
- NP172059.RAQvtjKH1JXmdM54u2jSAY8nln4mnmQbY053kzDVs4CSA130_assertion description "[Catechol-O-methyl transferase (COMT) is a candidate gene for schizophrenia with a role in dopamine metabolism, particularly in frontal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172059.RAQvtjKH1JXmdM54u2jSAY8nln4mnmQbY053kzDVs4CSA130_provenance.
- NP172060.RAQQn0cq2T-iszGKap1fFszFsCBt9RuEddOtQGttqq_J4130_assertion description "[Neuroferritinopathies are dominantly inherited movement disorders associated with nucleotide insertions in the L-ferritin gene that modify the protein's C-terminus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172060.RAQQn0cq2T-iszGKap1fFszFsCBt9RuEddOtQGttqq_J4130_provenance.
- NP172067.RAd6aCeRYCScRJd5gVjAAh8pfJV-_VCuQDBbdRLkW4MTI130_assertion description "[Genomewide linkage analyses were conducted of serum creatinine, estimated GFR (eGFR), and urine albumin-creatinine ratio (UACR) in search of genetic susceptibility loci for chronic kidney disease in 1351 black (median age 63 yr, 70% women, 79% hypertensive) and 1022 white individuals (median age 61 yr, 56% women, 75% hypertensive) from sibships in which two or more members had essential hypertension diagnosed before age 60 yr. After adjustment for gender, age, diabetes, and use of angiotensin inhibitors, the logarithm-transformed measure of serum creatinine was heritable in both ethnic groups (0.45 in black individuals [P < 0.001]; 0.39 in white individuals [P < 0.001]), as was eGFR (0.52 in black individuals [P < 0.001]; 0.39 in white individuals [P < 0.001]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172067.RAd6aCeRYCScRJd5gVjAAh8pfJV-_VCuQDBbdRLkW4MTI130_provenance.
- NP172069.RAfEKysvdUfAKyUmKFtDBSDV3N_smPqbe5UjLo7LaoHyM130_assertion description "[To investigate the role of NO and inducible NO synthase (iNOS) in the development of diabetes in EMC-D virus-infected mice, we infected iNOS-deficient DBA/2 mice with EMC-D virus (2 x 10(2) PFU/mouse).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172069.RAfEKysvdUfAKyUmKFtDBSDV3N_smPqbe5UjLo7LaoHyM130_provenance.
- NP172070.RAWPLXPUiXaICdGXWSrmrBDnrOWaW_JT7P5ZU6HO4RTxQ130_assertion description "[The TaqI A single-nucleotide polymorphism (SNP) in the DRD2 gene and the 3' variable number tandem repeat (VNTR) polymorphism in the DAT1 gene have been implicated in psychiatric disorders and drug addictions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172070.RAWPLXPUiXaICdGXWSrmrBDnrOWaW_JT7P5ZU6HO4RTxQ130_provenance.
- NP172074.RAaXTEOiE3dZApMZq-LfSlJOEud99Gh4LzAlQ19EHKpok130_assertion description "[The neurotrophin hypothesis of depression and antidepressant drug action postulates that reduced activity of neurotrophic factors, particularly brain-derived neurotrophic factor (BDNF), plays an important role in the pathogenesis of major depression, and that its restoration may represent a critical mechanism underlying antidepressant therapeutic effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172074.RAaXTEOiE3dZApMZq-LfSlJOEud99Gh4LzAlQ19EHKpok130_provenance.
- NP172077.RAVJ1dgc3ukO4gG-ITXYxeFaFYro-GihFOsS2kSRD4Rwc130_assertion description "[Analysis of blasts from single patients disclosed that LEDGF/p75 was the most consistently upregulated mRNA in resistant AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172077.RAVJ1dgc3ukO4gG-ITXYxeFaFYro-GihFOsS2kSRD4Rwc130_provenance.
- NP172079.RAYREFF9Wm6kfyUjkuQ-VdLoPSmrvqmPGIyeUEQX0xpOQ130_assertion description "[Runx1 stimulates Stat3 signalling via direct transcriptional repression of SOCS3 and SOCS4 and this is essential for cancer cell growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172079.RAYREFF9Wm6kfyUjkuQ-VdLoPSmrvqmPGIyeUEQX0xpOQ130_provenance.
- NP172080.RAS3APxfJIE8QUO3dGrSWE18tC45uGidwYr0yPf9d5ZI8130_assertion description "[Inactive heterozygous aldehyde dehydrogenase-2 (ALDH2(*)1/(*)2) and less-active alcohol dehydrogenase-1B (ADH1B(*)1/(*)1) increase the risk of esophageal cancer in East Asian drinkers, and esophageal cancer multiplicity is strongly associated with ALDH2(*)1/(*)2. p53 alterations are key molecular events in multifocal carcinogenesis in the esophagus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172080.RAS3APxfJIE8QUO3dGrSWE18tC45uGidwYr0yPf9d5ZI8130_provenance.
- NP172085.RAfwfGhFzUrZp3WsvzJLCHiIauFqttmzAjCMpaegdAeq0130_assertion description "[Compared with the normal lung tissues, PPARγ expression was much higher in the NNK-induced lung tumor tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172085.RAfwfGhFzUrZp3WsvzJLCHiIauFqttmzAjCMpaegdAeq0130_provenance.
- NP172086.RAQhzGxeQloKUl5IxJbVoYDc4whUB9L-JujoUUFXFVnUE130_assertion description "[s-VEGF-A appears be a good prognostic factor for colorectal cancer and includes VEGF165 and VEGF165b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172086.RAQhzGxeQloKUl5IxJbVoYDc4whUB9L-JujoUUFXFVnUE130_provenance.
- NP172088.RAUnzMU2OAx13iCsorVk647d0dyEaTqj-tsjzCkUwgV8M130_assertion description "[Spectrum of mutation and frequency of allelic deletion of the p53 gene in ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172088.RAUnzMU2OAx13iCsorVk647d0dyEaTqj-tsjzCkUwgV8M130_provenance.
- NP172090.RAWdjLFc0QSBtNsNScury2AN07gJE--Hp-MxIix9vQzf0130_assertion description "[We examined MC1R and ASIP genotypes in relation to phenotypic characteristics, sporadic and familial melanoma risk, and melanoma thickness as an indicator of disease progression in a Mediterranean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172090.RAWdjLFc0QSBtNsNScury2AN07gJE--Hp-MxIix9vQzf0130_provenance.
- NP172092.RAVwg3IWnMTrXxUrIqL90oVVoBfZDDvsjbTG9H1AA9K3E130_assertion description "[The present meta-analysis suggests that TLR4 gene Asp299Gly and Thr399Ile polymorphisms are not associated with the susceptibility of tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172092.RAVwg3IWnMTrXxUrIqL90oVVoBfZDDvsjbTG9H1AA9K3E130_provenance.
- NP172094.RAcoDNTnlmjZwB1OF38qsWNwUe_v5cXkHbmmXLpvpPqQc130_assertion description "[Our combined findings provide new insights into PER2 regulation and the biochemical basis of FASPS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172094.RAcoDNTnlmjZwB1OF38qsWNwUe_v5cXkHbmmXLpvpPqQc130_provenance.
- NP172106.RAf1-8JdqoIyxOhxB8p5_2L88iNc57QGJuGzFLkKa-4N4130_assertion description "[Sequencing and restriction digestion analysis demonstrated a TPM1 mutation V95A that cosegregated with HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172106.RAf1-8JdqoIyxOhxB8p5_2L88iNc57QGJuGzFLkKa-4N4130_provenance.
- NP172108.RAS-uERck9fUsszl63KKp9cteVewlQj2_fma8-XdicKOM130_assertion description "[Patients with Rubenstein-Taybi Syndrome secondary to mutation/deletion of the CBP gene on chromosome 16 are predisposed to a variety of developmental anomalies as well as cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172108.RAS-uERck9fUsszl63KKp9cteVewlQj2_fma8-XdicKOM130_provenance.
- NP172109.RAU_5_WbPYNUjX-SGVW3J0PsH4Yz06-nhXGGWFLS1Kyfg130_assertion description "[Treatment of human esophageal cancer KYSE 510 cells with 5-50 microM of EGCG for 12-144 h caused a concentration- and time-dependent reversal of hypermethylation of p16(INK4a), retinoic acid receptor beta (RARbeta), O(6)-methylguanine methyltransferase (MGMT), and human mutL homologue 1 (hMLH1) genes as determined by the appearance of the unmethylation-specific bands in PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172109.RAU_5_WbPYNUjX-SGVW3J0PsH4Yz06-nhXGGWFLS1Kyfg130_provenance.
- NP172112.RAclXpxOUMTsqqg59CKoIAokfcUkQN6P0oe9JXC8C7VZ8130_assertion description "[No HFE-HLA-A associations were found to modulate the ALL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172112.RAclXpxOUMTsqqg59CKoIAokfcUkQN6P0oe9JXC8C7VZ8130_provenance.
- NP172114.RAZQSstbbb8LkR9_-f-XFWnKysLxxgPLbcdtNAZQNMi7Q130_assertion description "[Role of phosphatidylinositol 4-phosphate (PI4P) and its binding protein GOLPH3 in hepatitis C virus secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172114.RAZQSstbbb8LkR9_-f-XFWnKysLxxgPLbcdtNAZQNMi7Q130_provenance.
- NP172121.RAfDrqoTWXHBx7zN7hRxcI2ORTTiMc56lDOkQB6GtSA7c130_assertion description "[Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive lysosomal storage disorder caused by a genetic defect in N-acetylgalactosamine-6-sulfate sulfatase (GALNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172121.RAfDrqoTWXHBx7zN7hRxcI2ORTTiMc56lDOkQB6GtSA7c130_provenance.
- NP172123.RAYqG1ww6PiOf17dfv0pvraIiyRVwfptOfIO8ZzTyL68o130_assertion description "[Consistent with these results, preclinical studies have demonstrated that rAd5 vectors expressing simian immunodeficiency virus (SIV) Gag failed to reduce peak or setpoint viral loads after SIV challenge of rhesus monkeys (Macaca mulatta) that lacked the protective MHC class I allele Mamu-A*01 (ref.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172123.RAYqG1ww6PiOf17dfv0pvraIiyRVwfptOfIO8ZzTyL68o130_provenance.
- NP172127.RAZh4UD0j-o2mY8dg8v_az_G-kT9AJX-o1nAz29fK9eGI130_assertion description "[The aim of this study was to examine the impact of parental type 2 diabetes on the autonomic nervous system and to determine whether autonomic neuropathy is present and associated with changes in 24-h ambulatory blood pressure (AMBP) and urinary albumin excretion rate (UAER) in nondiabetic subjects with parental type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172127.RAZh4UD0j-o2mY8dg8v_az_G-kT9AJX-o1nAz29fK9eGI130_provenance.
- NP172135.RAQGhFrHHORskTXnMVWajVhYlQPP9aksLbKXx9uvBRTcs130_assertion description "[The increase in CSF levels of lactate dehydrogenase (LDH), glucose-6-phosphate isomerase (G6PI), and fructose-bisphosphate aldolase A (ALDOA) were validated on a larger group of sCJD patients including three possible codon 129 polymorphism carriers and three control groups consisting of nondemented, neurological cases as well as patients suffering from Alzheimer's disease or vascular dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172135.RAQGhFrHHORskTXnMVWajVhYlQPP9aksLbKXx9uvBRTcs130_provenance.
- NP172136.RAaU4vNoIqu414G0-SygcKndfz22TtecAnTScpuU8_8oY130_assertion description "[More than 20 microscopic specimens were produced from a single AgarCyto cell block, and standard laboratory protocols have been successfully applied for H&E staining, immunohistochemistry for Ki-67 and p53, and in situ hybridization for the centromere of human chromosome 1 and human papilloma virus Type 16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172136.RAaU4vNoIqu414G0-SygcKndfz22TtecAnTScpuU8_8oY130_provenance.
- NP172142.RATtYof-vClwJwOJSXyIUWb_KNr_oOQ32qWNTa-M3yTxg130_assertion description "[This deletion (Spanish G gamma A gamma (delta beta)(0) thalassemia) is nearly identical in size and location to that of HPFH-1, but extends an additional 8.5 to 9 kb in the 3' direction, and therefore results in loss of the sequences near the 3' breakpoint of HPFH-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172142.RATtYof-vClwJwOJSXyIUWb_KNr_oOQ32qWNTa-M3yTxg130_provenance.
- NP172144.RASOcIJcG20OaK_wxsT0WY4aM-bp17yJrVHeRgqKWaTEo130_assertion description "[Additionally, we show that WIF1 inhibits in vivo bladder tumor growth in nude mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172144.RASOcIJcG20OaK_wxsT0WY4aM-bp17yJrVHeRgqKWaTEo130_provenance.
- NP172151.RARAOvzI43OA54bzg_xcuEtkVrT6A5knU74kv3i6YiA18130_assertion description "[We observed higher beta-amyloid load, beta-amyloid 1-42 and pTau concentrations in frontal cortex of PS1-E280A compared with EOSAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172151.RARAOvzI43OA54bzg_xcuEtkVrT6A5knU74kv3i6YiA18130_provenance.
- NP172155.RARxM7ui8CZ3n3A3iaKOl5tHYJryQn8CPpJaJ9LOuBNg4130_assertion description "[Modulation of cholesterol transport by insulin-treated gestational diabetes mellitus in human full-term placenta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172155.RARxM7ui8CZ3n3A3iaKOl5tHYJryQn8CPpJaJ9LOuBNg4130_provenance.
- NP172158.RAdoYoYo2S2P6N670keKh9UtUGT7rh9n3R0K8RT10ybDI130_assertion description "[In aggregate, these results suggest that S100A4 is a critical mediator of invasion in endometrial cancer and is upregulated by the TGF-beta1 signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172158.RAdoYoYo2S2P6N670keKh9UtUGT7rh9n3R0K8RT10ybDI130_provenance.
- NP172171.RAU_73mpG7ggvysHniyeplotVrgdbafKRvrC_2c8H7vxo130_assertion description "[Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172171.RAU_73mpG7ggvysHniyeplotVrgdbafKRvrC_2c8H7vxo130_provenance.
- NP172172.RAc-O1N6kbAc9XAjf6Svq_LflYM4qm3jjhSqRnuxphjy8130_assertion description "[Our results demonstrate that elevated IL-32 levels during viral infection mediate antiviral effects by stimulating the expression of IFN-λ1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172172.RAc-O1N6kbAc9XAjf6Svq_LflYM4qm3jjhSqRnuxphjy8130_provenance.
- NP172184.RAeJQp9fTH0_uapMz6dNUrruGnqFee5_sQGtojQ3Bj2PE130_assertion description "[The BRAF(V600E) mutation leading to constitutive signaling of MEK-ERK pathways causes papillary thyroid cancer (PTC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172184.RAeJQp9fTH0_uapMz6dNUrruGnqFee5_sQGtojQ3Bj2PE130_provenance.
- NP172186.RAUkl-w3N-Xe5aiPAM9rRmupfhUkdsQ_YOeaVQidekXLc130_assertion description "[To investigate DNA ploidy and expression of MMP-9, TIMP-2, and E-cadherin in gastric carcinoma and to explore the mechanism of invasion and metastasis of gastric carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172186.RAUkl-w3N-Xe5aiPAM9rRmupfhUkdsQ_YOeaVQidekXLc130_provenance.
- NP172189.RAURIuEfu7zCiYBa6tbu-HX8OqZX5ZAQlg_19zfow6PgQ130_assertion description "[gamma synuclein (SNCG), previously identified as a breast cancer-specific gene (BCSG1), is also highly associated with breast or ovarian cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172189.RAURIuEfu7zCiYBa6tbu-HX8OqZX5ZAQlg_19zfow6PgQ130_provenance.
- NP172192.RAbm0Sbhg04xs4cuqbRZUm82F8mIihqeEP631vS7Smn3A130_assertion description "[Cytochrome P450 2A6 (CYP2A6) catalyzes the metabolic activation of several procarcinogens including dietary and environmental nitrosamines, and the involvement of CYP2A6 in cancer development has been postulated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172192.RAbm0Sbhg04xs4cuqbRZUm82F8mIihqeEP631vS7Smn3A130_provenance.
- NP172194.RAe-K0ar0UTODM847t2HwD5vH3C8bPZCnqMB8AJYCHLQc130_assertion description "[Mutations in codons 12 or 13 of the first exon of the N-RAS gene have been reported in myelodysplastic syndromes (MDS) in frequencies that vary between 9% and 40% depending on the techniques used in analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172194.RAe-K0ar0UTODM847t2HwD5vH3C8bPZCnqMB8AJYCHLQc130_provenance.
- NP172197.RAZYhe6XAoaztTi1n6Qwgwm84FB1Rkh535Is-HGzJi9ZU130_assertion description "[Our findings, decreased LAMP-2 gene expression and increased LC3 gene expression, are consistent to the previous studies with dopaminergic neuronal cells in vitro and in vivo, which may contribute to the pathogenesis of sporadic PD by altering CMA and autophagy activities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172197.RAZYhe6XAoaztTi1n6Qwgwm84FB1Rkh535Is-HGzJi9ZU130_provenance.
- NP172200.RAYyokMLIFzVr-KKNYz_NEW4ZAhfNMlIbe6Uw0mSU9HAI130_assertion description "[However, COX-2 mRNA expression in nasal polyps from the AIAR group (0.38 +/- 0.10) was markedly and significantly lower than in polyps from the ATAR group (2.93 +/- 0.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172200.RAYyokMLIFzVr-KKNYz_NEW4ZAhfNMlIbe6Uw0mSU9HAI130_provenance.
- NP172201.RASrN99BHii1ICYAq9COFVCvWEhkcxQyRFGuDCnU7b6qM130_assertion description "[Recessive mutations in the FRAS1-related extracellular matrix 1 (FREM1) gene have been shown to cause bifid nose with or without anorectal and renal anomalies (BNAR) syndrome and Manitoba oculotrichoanal (MOTA) syndrome, but have not been previously implicated in the development of CDH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172201.RASrN99BHii1ICYAq9COFVCvWEhkcxQyRFGuDCnU7b6qM130_provenance.
- NP172204.RAeRtl2nJsWMinQQ-jGfaV4mbeu5eUeJmNYjyU7NIwlDk130_assertion description "[Metastasis-associated protein 1 (MTA1) high expression has been detected in a wide variety of human aggressive tumors and plays important roles in the malignant biological behaviors such as invasion, metastasis, and angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172204.RAeRtl2nJsWMinQQ-jGfaV4mbeu5eUeJmNYjyU7NIwlDk130_provenance.
- NP172208.RASAHZQidZBjVmbfplze6bDBop56ZBAJRdTLdGoXXQ2yE130_assertion description "[X-linked hypophosphatemic rickets/osteomalacia (XLH), autosomal dominant and recessive hypophosphatemic rickets/osteomalacia (ADHR and ARHR) share common clinical features including high fibroblast growth factor 23 (FGF23) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172208.RASAHZQidZBjVmbfplze6bDBop56ZBAJRdTLdGoXXQ2yE130_provenance.
- NP172209.RAfwAmBOQuZ5GmKjZLFR7ZtRwU-Q4F74h8Q-7I0QDnykA130_assertion description "[Changes in miR-143, miR-145, miR-146a, miR-146b, miR-378, miR-584, SPARC and RPS14 were examined in del(5q) (n=10) and non-del(5q) (n=18) myelodysplastic syndrome patient samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172209.RAfwAmBOQuZ5GmKjZLFR7ZtRwU-Q4F74h8Q-7I0QDnykA130_provenance.
- NP172211.RAYxKWjGNnfRCC-1BYlpR0p1ioOaMkZN_VaQ42bbTOCTY130_assertion description "[Expression of MHC class I and class II molecules within the prostate tumor microenvironment are consequential for T-cell-mediated immunotherapeutic approaches against prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172211.RAYxKWjGNnfRCC-1BYlpR0p1ioOaMkZN_VaQ42bbTOCTY130_provenance.
- NP172212.RAVaDbjL1ZbW0sDkFpBnh3_ebP9nkhQ2QnoKCofVvsyjw130_assertion description "[In the early RA group, synovial FN was found to be totally degraded to a mixture of FN fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172212.RAVaDbjL1ZbW0sDkFpBnh3_ebP9nkhQ2QnoKCofVvsyjw130_provenance.
- NP172215.RARae4SlPDbwTujaQOOkuHvZbw5aZgHLFhdaBj5YsTEW0130_assertion description "[High incidence of p53 alterations (mutation, deletion, overexpression) in head and neck primary tumors and metastases; absence of correlation with clinical outcome. Frequent protein overexpression in normal epithelium and in early non-invasive lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172215.RARae4SlPDbwTujaQOOkuHvZbw5aZgHLFhdaBj5YsTEW0130_provenance.
- NP172218.RAVuI17tQC_ivIfe36usW-KV_uGyDhT7C2RlZPrW9z52o130_assertion description "[We found no association between NAT2 and breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172218.RAVuI17tQC_ivIfe36usW-KV_uGyDhT7C2RlZPrW9z52o130_provenance.
- NP172223.RATNmsN7RgurRYBKU3XyOmfJOr2HlctDcwJrBymdL2QXU130_assertion description "[PURPOSE EWS-ETS fusion genes are the driving force in Ewing's sarcoma pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172223.RATNmsN7RgurRYBKU3XyOmfJOr2HlctDcwJrBymdL2QXU130_provenance.
- NP172227.RAWDU_M2KPq6ZHGpnxwcdDiB9XLQ-ftT4EvfXp2JL_124130_assertion description "[IL-15 and interferon-gamma levels were reduced in OHB-infected individuals when compared to those patients who resolved HBV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172227.RAWDU_M2KPq6ZHGpnxwcdDiB9XLQ-ftT4EvfXp2JL_124130_provenance.
- NP172231.RATi1-ZlCRFD3aC6BgBrOmrjQgEUL7j7A8HzONAakXc3I130_assertion description "[p53-LOH and p53 mutations were found in 62.2% and 39.4% of primary tumors, respectively, and in 57.9% and 25% of hepatic metastases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172231.RATi1-ZlCRFD3aC6BgBrOmrjQgEUL7j7A8HzONAakXc3I130_provenance.
- NP172234.RAaYgCottT5bXMQo5bQe6Jw4EA25EYh0P7mazrDPEdAGw130_assertion description "[Differential expression of MARCKS and other calmodulin-binding protein kinase C substrates in cultured neuroblastoma and glioma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172234.RAaYgCottT5bXMQo5bQe6Jw4EA25EYh0P7mazrDPEdAGw130_provenance.
- NP172236.RAZo6bXYadsLmdw56J5LnGR1rW-OQz-acf72Vcbrl4dFQ130_assertion description "[In this study, we aimed to explore the impact of DNA methylation profile in BCL2/E1B adenovirus interacting protein 3 (BNIP3), extracellular superoxide dismutase (EC-SOD) and glutathione-S-transferase P1 (GSTP1) on the oxidative stress in CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172236.RAZo6bXYadsLmdw56J5LnGR1rW-OQz-acf72Vcbrl4dFQ130_provenance.
- NP172240.RAcT4LKN8totJz7p2jyupHTmu7-uIrHGdZtcrKKaZI6rY130_assertion description "[In this study, we used MCF-7 breast cancer sublines with variable levels of the steroid receptor coactivator 1 (SRC-1) to investigate the importance of coactivator levels in basal and estrogen-inducible expression of SDF-1alpha/CXCL12, cathepsin D and cMyc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172240.RAcT4LKN8totJz7p2jyupHTmu7-uIrHGdZtcrKKaZI6rY130_provenance.
- NP172241.RAZHxWWGt5ohkxL22gdtbahDrXQ92FuyAUvVDlZ4osZsI130_assertion description "[Normal human prostate expressed BMP 4 mRNA predominantly, as did the human prostate cancers PC-3 and DU-145.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172241.RAZHxWWGt5ohkxL22gdtbahDrXQ92FuyAUvVDlZ4osZsI130_provenance.
- NP172247.RAYYZwtV5GZ2ljpySlV3DL06bCn33CF5Fec7pd_LUR_Pk130_assertion description "[These findings conflict with those in multiple system atrophy and other prion diseases such as fatal familial insomnia, which enter the differential diagnosis of GSS and are characterized by prominently disrupted sleep-wake and BcT degrees cycles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172247.RAYYZwtV5GZ2ljpySlV3DL06bCn33CF5Fec7pd_LUR_Pk130_provenance.
- NP172248.RAWgVlPlk_zuOi4d927EMi6u738VNTmuBwxKa4muKnxKk130_assertion description "[Previously, we demonstrated that follicle stimulating hormone (FSH) enhanced VEGF expression and facilitated ovarian cancer angiogenesis via the PI3K/AKT signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172248.RAWgVlPlk_zuOi4d927EMi6u738VNTmuBwxKa4muKnxKk130_provenance.
- NP172250.RAZBjYl4iAHcYhGGlBoGOvdYVT9xitdzP7gTzclP0W2vo130_assertion description "[We aimed to study whether single nucleotide polymorphisms (SNPs) of the MC1R and ASIP genes contribute to the pathogenesis of the polygenic pigment skin disorder, vitiligo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172250.RAZBjYl4iAHcYhGGlBoGOvdYVT9xitdzP7gTzclP0W2vo130_provenance.
- NP172251.RATSKK-ci4JKE1ViGAbgqQryl0xZT0iF3vlzMQmScM5FI130_assertion description "[STK15 copy number is amplified in 12% of OSCCs and nuclear STK15 protein expression increases with tumour progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172251.RATSKK-ci4JKE1ViGAbgqQryl0xZT0iF3vlzMQmScM5FI130_provenance.
- NP172256.RAWJUJxOpoLhHMadvHYF-VKTAwpIeV41ZxEUYU07mPYmY130_assertion description "[These results suggest that the polymorphism in the PTH gene would be a useful genetic marker for lower BMD and the susceptibility for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172256.RAWJUJxOpoLhHMadvHYF-VKTAwpIeV41ZxEUYU07mPYmY130_provenance.
- NP172262.RAbJL2FRTfnyr6YxZci5kc5p_DEYPApNgUFjcVDolaSsk130_assertion description "[Although IAP homologs have recently been demonstrated to suppress apoptosis in mammalian cells, their expression and role in human ovarian epithelial cancer and chemotherapy resistance are unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172262.RAbJL2FRTfnyr6YxZci5kc5p_DEYPApNgUFjcVDolaSsk130_provenance.
- NP172266.RAU5dN3__8dYZlmH_Q0k2pxKIBgb5LCvvuiB0qnDbN94A130_assertion description "[Regarding clinical outcome: (i) UM CLL from the IGHV1-2/1-3/1-18/1-46/7-4-1/IGKV1-39 cluster had poorer prognosis than UM/M cases, or UM cases using the same IGHV genes but not in clusters; (ii) M CLL from the IGHV3-21/IGLV3-21 cluster had TTT similar to UM CLL, and shorter than M CLL expressing IGHV3-21 but not in cluster.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172266.RAU5dN3__8dYZlmH_Q0k2pxKIBgb5LCvvuiB0qnDbN94A130_provenance.
- NP172273.RAQD-WGPjlQfiOGqxPpsMea9YN-0LOrBdnXa3bcB5ZxLI130_assertion description "[The risk allele in IL4 is present in nearly 90% of white Europeans, while less than a quarter are carriers in some other populations, highlighting the need to consider possible ethnic differences in allergy-related responsiveness to VDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172273.RAQD-WGPjlQfiOGqxPpsMea9YN-0LOrBdnXa3bcB5ZxLI130_provenance.
- NP172278.RAQJtx3O0a8EO1sqro0wgYNl5sOU3iModpgAbLyFUV5fQ130_assertion description "[Centromeres are critical structures in cell division, and CENP-B is the most important protein of the centromeric complex recognized by autoantibodies from patients with scleroderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172278.RAQJtx3O0a8EO1sqro0wgYNl5sOU3iModpgAbLyFUV5fQ130_provenance.
- NP172280.RAeFPWWRvpOVQH7SO3mAk7BO4sa0uBhiJdddhGKLZmhwk130_assertion description "[Both the myotonic dystrophy type 1 (DM1) and the X-linked dominant Charcot-Marie-Tooth disease (CMTX1) are well-established inherited neuromuscular disorders characterized by progressive weakness and atrophy of the distal limb muscles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172280.RAeFPWWRvpOVQH7SO3mAk7BO4sa0uBhiJdddhGKLZmhwk130_provenance.
- NP172287.RAYRj3oBQMpvgnCm_A_fXkVS3znSGX9Z9t_XcFasv2Oj8130_assertion description "[To clarify this problem, we analyzed the p53-mutational status of HCCs in Jiang-su province in China, where AFB1 contamination of the staple food significantly differs between the northern and southern parts (prominent only in the latter), while other conditions are quite similar.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172287.RAYRj3oBQMpvgnCm_A_fXkVS3znSGX9Z9t_XcFasv2Oj8130_provenance.
- NP172290.RAWqyxuReQZj0SIGLEa8H0TWWIfHBEU9y6OxcRpDUlvcQ130_assertion description "[Epigenetic silencing of DACH1 induces loss of transforming growth factor-β1 antiproliferative response in human hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172290.RAWqyxuReQZj0SIGLEa8H0TWWIfHBEU9y6OxcRpDUlvcQ130_provenance.
- NP172292.RAdh3RMpd1X0AgHg00b5Kn6PK4OmmwPCyrx5uI_jL7WDg130_assertion description "[As our knowledge expands regarding the regulation and functions of FGF23, the assessment of FGF23 will become an important diagnostic marker as well as a therapeutic target for management of disordered mineral metabolism in a variety of acquired and hereditary disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172292.RAdh3RMpd1X0AgHg00b5Kn6PK4OmmwPCyrx5uI_jL7WDg130_provenance.
- NP172293.RAdJmcTFMi6RXvKqd0CpaNtZwbbNET2KYD080c7qB0lcQ130_assertion description "[Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172293.RAdJmcTFMi6RXvKqd0CpaNtZwbbNET2KYD080c7qB0lcQ130_provenance.
- NP172297.RAYutaVpJ8I0hG0UsC0FRBW8t9jO0NaWixAovmKkuW3QI130_assertion description "[We examined the modulation of XPG gene expression by HuIFN-beta in UV-sensitive cells from Cockayne syndrome complementation B (CSB), xeroderma pigmentosum complementation A (XPA) and normal control cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172297.RAYutaVpJ8I0hG0UsC0FRBW8t9jO0NaWixAovmKkuW3QI130_provenance.
- NP172298.RAf3_jrPw8JOL2ZrcnY74YqQJhU57UpYegjmt5LXrHPfs130_assertion description "[Transient stabilization of p53 in non-small cell lung carcinoma cultures arrested for growth by retinoic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172298.RAf3_jrPw8JOL2ZrcnY74YqQJhU57UpYegjmt5LXrHPfs130_provenance.
- NP172302.RAWDcXH7slndAaUcJt6PWM9PHJF31ACYmtZ6qrbOYpAPM130_assertion description "[We then measured the allele-specific expression in hereditary nonpolyposis colorectal cancer (HNPCC) patients with MLH1 mRNAs bearing different stop-codon or frame-shift mutations, or in-frame deletions, in order to detect the effects of nonsense-mediated mRNA decay (NMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172302.RAWDcXH7slndAaUcJt6PWM9PHJF31ACYmtZ6qrbOYpAPM130_provenance.
- NP172306.RAe-2MbquiVAaQNclCpeNBUg6ZLPTjOKWpcnMTdns1cRE130_assertion description "[Genetic manipulation of stromal cell-derived factor-1 attests the pivotal role of the autocrine SDF-1-CXCR4 pathway in the aggressiveness of breast cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172306.RAe-2MbquiVAaQNclCpeNBUg6ZLPTjOKWpcnMTdns1cRE130_provenance.
- NP172307.RAdOsP7OWOUNa5-sVS2nnu_k7hxei77JGYrISTyjscyWM130_assertion description "[Identifiable risk factors for NIHF other than PV in the remaining 25 cases included cystic hygroma, seven (three 45,X; two 46,XX; two no growth); complex cardiac anomaly, six; infection, three (two CMV, one chlamydia); twin-twin transfusion, two; lymphangiectasia, two; diaphragmatic hernia, tracheal atresia, trisomy 21, congenital cystic adenomatoid malformation, one each.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172307.RAdOsP7OWOUNa5-sVS2nnu_k7hxei77JGYrISTyjscyWM130_provenance.
- NP172323.RAVSO6Fo31wB6rV468ASjXlHIVz9wnKBsWdqDLA3_YyTI130_assertion description "[Molecular genetic studies have indicated that hemizygosity at the elastin locus (ELN) may account for the cardiac abnormalities seen in WS, but that mental retardation and hypercalcemia are likely caused by other genes flanking ELN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172323.RAVSO6Fo31wB6rV468ASjXlHIVz9wnKBsWdqDLA3_YyTI130_provenance.
- NP172324.RAVj976UgwiH3XBubT8b3iGGUtFTHgtNtg8r-a2sVO5aM130_assertion description "[EBV infection was detected with in situ hybridization for EBV-encoded RNAs (EBERs) and by immunohistochemical staining for latent membrane protein 1 (LMP-1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172324.RAVj976UgwiH3XBubT8b3iGGUtFTHgtNtg8r-a2sVO5aM130_provenance.
- NP172330.RAa_qALjW1_nGiHYr67EbV_WafOx4L2Qj3WDxz8hzspHM130_assertion description "[In the present study the expressions of laminin isoforms alpha1-alpha5, beta1-beta3, gamma1, and gamma2 were examined during progression of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172330.RAa_qALjW1_nGiHYr67EbV_WafOx4L2Qj3WDxz8hzspHM130_provenance.
- NP172336.RAUH9fqLO2crHG24ZsK_n_jVoalRyTsUkhgT55pC5w26A130_assertion description "[MUC7, which is primarily associated with the submucosa, as opposed to MUC4 and MUC5AC, which are primarily expressed in the epithelium, was significantly decreased in the nasal polyp xenografts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172336.RAUH9fqLO2crHG24ZsK_n_jVoalRyTsUkhgT55pC5w26A130_provenance.
- NP172338.RAXK-V784gqlAGVEtJhG485Hctu1t0fWzMDHzBpqN9_hY130_assertion description "[Significantly, in a cohort of 159 primary breast cancers, high nuclear levels of LMO4 were an independent predictor of death from breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172338.RAXK-V784gqlAGVEtJhG485Hctu1t0fWzMDHzBpqN9_hY130_provenance.
- NP172346.RAeMmoaRX6Y9uWFPwJ3f0_A0OHzON5a23F_NMGMM4D2y0130_assertion description "[AML1 mutations were significantly associated with -7/7q-, whereas MDS/AML patients without AML1 mutations showed a high frequency of -5/5q- and a complex karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172346.RAeMmoaRX6Y9uWFPwJ3f0_A0OHzON5a23F_NMGMM4D2y0130_provenance.
- NP172349.RAZtbqVRg9D_psWVy303PoYTyHfqhjIlKwXXHpCi_vaqA130_assertion description "[Human Ago2 is required for efficient microRNA 122 regulation of hepatitis C virus RNA accumulation and translation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172349.RAZtbqVRg9D_psWVy303PoYTyHfqhjIlKwXXHpCi_vaqA130_provenance.
- NP172350.RAenc7wYSrj2W409I7DlNB82dBd9eZwfwg-HOQ0YfcyTE130_assertion description "[To study the correlation of 15-LO-1 expression with mtp53 in prostate cancer, we immunostained 48 prostatectomy specimens obtained by transurethral resection of the prostate and needle biopsy (median age 68 years, range 52-93) of different Gleason grades (n = 48), using antibodies specific for 15-LO-1, mtp53 and MIB-1 (a proliferation marker).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172350.RAenc7wYSrj2W409I7DlNB82dBd9eZwfwg-HOQ0YfcyTE130_provenance.
- NP172354.RAaPMz-Oio_opIuVqrxNPEZf5P-Jw7EAmC0R2iz5B8xeM130_assertion description "[These results demonstrate that AXII and AXIIR play important roles in MM and that targeting the AXII/AXIIR axis may be a novel therapeutic approach for MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172354.RAaPMz-Oio_opIuVqrxNPEZf5P-Jw7EAmC0R2iz5B8xeM130_provenance.
- NP172362.RAXoegECa75aUL3arXN6njAnBJ-hswoPtD7u9AqPZ7Oik130_assertion description "[The identification of de novo dominant mutations in KMT2D (MLL2) as the main cause of Kabuki syndrome (KS) has shed new light on the pathogenesis of this well-delineated condition consisting of a peculiar facial appearance, short stature, organ malformations and a varying degree of intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172362.RAXoegECa75aUL3arXN6njAnBJ-hswoPtD7u9AqPZ7Oik130_provenance.
- NP172373.RAUPDEmpAT5D58Tv0rHV3VHpLZfSUSBlr3U7UCvdNrCgU130_assertion description "[The relationship between DSM-III-R schizophreniform disorder, delusional disorder (DD) and psychotic disorder not otherwise specified (PD-NOS) and schizophrenia and affective illness (AI) remains uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172373.RAUPDEmpAT5D58Tv0rHV3VHpLZfSUSBlr3U7UCvdNrCgU130_provenance.
- NP172377.RAcneyAh5FwsLGInCtEYsNuid6ErYnjdtpQTzLnlqtFoc130_assertion description "[Circulating levels of the cytokine visfatin/PBEF-1 are influenced by renal function, but are not associated with fat mass or surrogate markers of insulin resistance in patients with CKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172377.RAcneyAh5FwsLGInCtEYsNuid6ErYnjdtpQTzLnlqtFoc130_provenance.
- NP172383.RAUFC-ih1jwzD_wlyHpzDJhSZFkm48TwGlnuZ4ikYtXhU130_assertion description "[Treatment strategies utilizing inhibition of miR-182 expression or overexpression of the PFN1 gene might benefit patients with TNBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172383.RAUFC-ih1jwzD_wlyHpzDJhSZFkm48TwGlnuZ4ikYtXhU130_provenance.
- NP172387.RAWuh6h8lccP9YQhLEksu-4qDhhzVAnEo14pwCDzuQonY130_assertion description "[Given the population frequency of C282Y and the connection between iron and cancer, clarification of the mechanism of HFE associations in leukemia and cancer will have strong implications in public health.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172387.RAWuh6h8lccP9YQhLEksu-4qDhhzVAnEo14pwCDzuQonY130_provenance.
- NP172388.RASTcPzCF8FGKizbihDkpLHJBmjYKM7JGaJWkUZYcJ3L0130_assertion description "[To determine the molecular epidemiology and prognostic importance of structural and numeric FOXP1 gene aberrations with respect to BCL-6 gene and to FOXP1 protein expression in 389 diffuse large B-cell lymphomas (DLBCL) from the pre-rituximab era on tissue microarrays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172388.RASTcPzCF8FGKizbihDkpLHJBmjYKM7JGaJWkUZYcJ3L0130_provenance.
- NP172390.RAQ3dzB_-wDOCmt-YjQ3aJTZH5TgqM6I4T9Hw0ewdDMi8130_assertion description "[The current data indicate that p53 mutations are not late events in osteosarcoma tumor progression, because they are evident before the development of metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172390.RAQ3dzB_-wDOCmt-YjQ3aJTZH5TgqM6I4T9Hw0ewdDMi8130_provenance.
- NP172392.RATXRxrVl2qkecx-kgZl-WpN8qUbedN7aVC1SSkspCBKA130_assertion description "[Genetic heterogeneity has become a major inconvenience in the genotyping and molecular epidemiology of the intestinal protozoan parasite Giardia intestinalis, in particular for the major human infecting genotype, assemblage B. Sequence-based genotyping of assemblage B Giardia from patient fecal samples, where one or several of the commonly used genotyping loci (beta-giardin, triosephosphate isomerase and glutamate dehydrogenase) are implemented, is often hampered due to the presence of sequence heterogeneity in the sequencing chromatograms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172392.RATXRxrVl2qkecx-kgZl-WpN8qUbedN7aVC1SSkspCBKA130_provenance.
- NP172393.RAe4W7_A5WUQEKCZtKxpWMfyzovvSHJ3Zf4mBrlQb4IGY130_assertion description "[Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172393.RAe4W7_A5WUQEKCZtKxpWMfyzovvSHJ3Zf4mBrlQb4IGY130_provenance.
- NP172396.RAf3bOUiE_GMUU0gGHqu-yxX5J71J1zkSPaJdY7PCBgWo130_assertion description "[Cox survival analysis demonstrated that cytoplasmic HP1γ expression was an independent prognostic marker and out-performed pathological Gleason score for predicting PSA-recurrence after radical prostatectomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172396.RAf3bOUiE_GMUU0gGHqu-yxX5J71J1zkSPaJdY7PCBgWo130_provenance.
- NP172397.RAW24Irw6O2vI1lptRAPCK98IJ2SLrrElTHc-pVYrMaUM130_assertion description "[Combined hazard ratios suggested that an abnormal p53 status had an unfavourable impact on survival: in any stage nonsmall cell lung cancer (NSCLC) the mean (95% confidence interval) was 1.44 (1.20-1.72) (number of studies included in the subgroup was 11), 1.50 (1.32-1.70) in stages I-II NSCLC (n=19), 1.68 (1.23-2.29) in stages I-IIIB NSCLC (n=5), 1.68 (1.30-2.18) in stages III-IV NSCLC (n=9), 1.48 (1.29-1.70) in surgically resected NSCLC (n=20), 1.37 (1.02-1.85) in squamous cell carcinoma (n=9), 2.24 (1.70-2.95) in adenocarcinoma (n=9), 1.57 (1.28-1.91) for a positive immunohistochemistry with antibody 1801 (n=8), 1.25 (1.09-1.43) for a positive immunohistochemistry with antibody DO-7 (n=16), and 1.65 (1.35-2.00) for an abnormal molecular biology test (n=13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172397.RAW24Irw6O2vI1lptRAPCK98IJ2SLrrElTHc-pVYrMaUM130_provenance.
- NP172403.RAbP1sDzq27hlWkzc0JBCZqkS0aI5Z8gMvDkHLP7h2JUQ130_assertion description "[We found evidence of statistically significant gene-tobacco interaction for GSTM1, NAT2, and GSTP1, the negative association between tobacco smoking and PD being significantly enhanced in subjects expressing GSTM1-1 activity, in NAT2 fast acetylators, and in those with the GSTP1*B*C haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172403.RAbP1sDzq27hlWkzc0JBCZqkS0aI5Z8gMvDkHLP7h2JUQ130_provenance.
- NP172404.RAYpQfUZOKI5CHi3HqG5KpqwEILh8xcrlG3QAaZFR1Tdg130_assertion description "[There was no association of the SLC6A3 genotype with obesity for non-Hispanic whites (N = 420).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172404.RAYpQfUZOKI5CHi3HqG5KpqwEILh8xcrlG3QAaZFR1Tdg130_provenance.
- NP172411.RAfGY7QGY20YO5GwsUI4Mc3FLOY_dO2u-cj0WAlMOnJC8130_assertion description "[Association of Chlamydia pneumoniae with coronary artery disease and its progression is dependent on the modifying effect of mannose-binding lectin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172411.RAfGY7QGY20YO5GwsUI4Mc3FLOY_dO2u-cj0WAlMOnJC8130_provenance.
- NP172417.RAZMdmOH4KLocd4vr3DLSdAINImn8F7MhnxBc5XkenyiU130_assertion description "[The data suggest that the presence of the PiZ allele for alpha1 antitrypsin deficiency, in a double dose, is associated with genetic haemochromatosis and may contribute to the earlier onset of cirrhosis in these patients, though it does not increase the risk of hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172417.RAZMdmOH4KLocd4vr3DLSdAINImn8F7MhnxBc5XkenyiU130_provenance.