Nanopublications

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

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NP281454.RATjSkk9N0-WuVAAh-8fiWVzv4RaEu7ZWCKKdtCxmO490130_assertion description "[Described here are two tumors belonging to the rare category of CIC-DUX4-positive primitive sarcomas, with detailed cytogenetic and genomic information regarding this novel subclass of pediatric malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281454.RATjSkk9N0-WuVAAh-8fiWVzv4RaEu7ZWCKKdtCxmO490130_provenance.
NP281455.RARjXARx68BD1drNIG4WXh9PoQV-X7105foCD_B2-WjuI130_assertion description "[Ten months after the combination therapy thrombocytopenia developed and cytogenetic analysis showed 45,XX,-7, indicating an evolution to myelodysplastic syndrome (MDS) associated with monosomy 7.G-CSF and EPO treatment together with immunosuppression may be an effective therapy in SAA patients, but such a therapy may increase the risk of evolution to MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281455.RARjXARx68BD1drNIG4WXh9PoQV-X7105foCD_B2-WjuI130_provenance.
NP281457.RAZDbx1_IcBeDufRYkKFfvP8kP3AOOpIKn_QFrYoz6DWk130_assertion description "[A novel mechanism for TNF-alpha regulation by p38 MAPK: involvement of NF-kappa B with implications for therapy in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281457.RAZDbx1_IcBeDufRYkKFfvP8kP3AOOpIKn_QFrYoz6DWk130_provenance.
NP281460.RASV6JbmVfz-dNFCv0wSxX3VmvOso_06-MzuhX5eAsMEI130_assertion description "[We aimed to test whether there exist common or inverse associations between polymorphisms in the pattern recognition receptors TLR2, TLR4 and CD14 and T1D and allergic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281460.RASV6JbmVfz-dNFCv0wSxX3VmvOso_06-MzuhX5eAsMEI130_provenance.
NP281464.RATE3amzCciHXRQIu-H9RjfDcJlf-QqKOOUwCjVnJnuYg130_assertion description "[Our ability to detect low levels of mtDNA mutations in blood samples of carriers will allow us to reassess the prevalence of the MTTL1 3243A>G mutation in patients with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281464.RATE3amzCciHXRQIu-H9RjfDcJlf-QqKOOUwCjVnJnuYg130_provenance.
NP281469.RAW-tEOBBCecxqk8MqCoZR3QC3jaFKmlCE2a0TrPh37UE130_assertion description "[Important roles of glycosylphosphatidylinositol (GPI)-specific phospholipase D and some GPI-anchored proteins in the pathogenesis of hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281469.RAW-tEOBBCecxqk8MqCoZR3QC3jaFKmlCE2a0TrPh37UE130_provenance.
NP281470.RAbDdF1Ax-taxOR8QX0XBqYszK7U2f6WsRXHhJhUyKy00130_assertion description "[In MMR gene mutation carriers, MMR and methylation defects appeared up to 12 years before endometrial carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281470.RAbDdF1Ax-taxOR8QX0XBqYszK7U2f6WsRXHhJhUyKy00130_provenance.
NP281472.RAcQvh9RXxpYqfhasLyRdYgCPCdrPLb4PFsS9tuWCJJV8130_assertion description "[X-linked hydrocephalus, HSAS (hydrocephalus due to stenosis of aqueduct of Sylvius), MASA (mental retardation, aphasia, shuffling gait, and adducted thumbs), and CRASH (corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus) syndromes are allelic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281472.RAcQvh9RXxpYqfhasLyRdYgCPCdrPLb4PFsS9tuWCJJV8130_provenance.
NP281474.RAQgwTDzg2bo7SnhkVX4kjCxFhlXm_oMvvARQNRsHDZwo130_assertion description "[We identified individual SNPs/haplotypes in TNFA/TNFRSF1B and IL12B genes that appear to modulate immunity to rubella vaccination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281474.RAQgwTDzg2bo7SnhkVX4kjCxFhlXm_oMvvARQNRsHDZwo130_provenance.
NP281476.RAf7K8KTzZerfbdMfdte7k9gWFGpvr6Ld06T1LD3Cg3MI130_assertion description "[In our study, we analysed two MBL2 and MASP2 functional polymorphisms (MBL2 allele A/0 and MASP2 D120G) as well as MASP2 polymorphism (Y371D) responsible for an amino acidic change in the protein in 215 HCC patients (HBV-infected, HCV-infected, HBV/HCV co-infected and patients with HCC with no viral infection) and 164 healthy controls to give new insights regarding the role of these two molecules in HCC and viral infection pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281476.RAf7K8KTzZerfbdMfdte7k9gWFGpvr6Ld06T1LD3Cg3MI130_provenance.
NP281477.RAXf3YATUl1mCGh21MIECRBYva7UgeTbGo_pHkgksEvEk130_assertion description "[We investigated the interplay between the activation of human telomerase reverse transcriptase (hTERT), the catalytic rate-limiting component of the telomerase complex, and the expression of latent/lytic EBV genes during the establishment of a stably latent EBV infection of normal B lymphocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281477.RAXf3YATUl1mCGh21MIECRBYva7UgeTbGo_pHkgksEvEk130_provenance.
NP281479.RAZJA7m5VijYx2Z4h2dPMdIfZUKxSP72ZnMHy44m0Ut7w130_assertion description "[c-Met receptor tyrosine kinase (RTK) has not been extensively studied in malignant pleural mesothelioma (MPM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281479.RAZJA7m5VijYx2Z4h2dPMdIfZUKxSP72ZnMHy44m0Ut7w130_provenance.
NP281483.RAbcO7q75RQS3oTsq7PSxghFaTFiQPMKfTlego8t71KVg130_assertion description "[To our knowledge, this is the first description of TBX3 haploinsufficiency caused by a genomic deletion in a patient with UMS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281483.RAbcO7q75RQS3oTsq7PSxghFaTFiQPMKfTlego8t71KVg130_provenance.
NP281492.RAWSdehsNx9qqYEHasS33zoc_OZPD9Vfe4BdXtbSnuB90130_assertion description "[TRB3, a mammalian tribbles homolog, whose chromosomal region 20p13-p12 has been linked to human type 2 diabetes, impairs insulin signaling through the inhibition of Akt phosphorylation and is overexpressed in murine models of insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281492.RAWSdehsNx9qqYEHasS33zoc_OZPD9Vfe4BdXtbSnuB90130_provenance.
NP281493.RAaSIyMWt8J5f2iHhD-h6QIES0VacHEfE-ywCRkmbNxDw130_assertion description "[To investigate if human tumours display altered CD44 expression we performed reverse transcriptase a polymerase chain reaction (PCR) analysis of CD44 in 49 specimens from normal colonic mucosa, primary colon and rectal tumours, normal liver, and metastases of 20 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281493.RAaSIyMWt8J5f2iHhD-h6QIES0VacHEfE-ywCRkmbNxDw130_provenance.
NP281497.RAd4zwAH2TNHxUU7S_KfmXsCDa2AAx4VttNFDV7s9uvHA130_assertion description "[Studies in transgenic mice harboring X-RARalpha and RARalpha-X fusion genes and In mice lacking X genes have helped unravel the molecular mechanisms underlying APL leukemogenesis, which lead to the development of novel therapeutic strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281497.RAd4zwAH2TNHxUU7S_KfmXsCDa2AAx4VttNFDV7s9uvHA130_provenance.
NP281504.RAcqH755r7TcGnUK9doKm6rgtgO2nLCP_ShB1xoNqBUPA130_assertion description "[Although TCF7L2 encodes TCF4, which cooperates with β-catenin in colorectal carcinogenesis, the fusion lacks the TCF4 β-catenin-binding domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281504.RAcqH755r7TcGnUK9doKm6rgtgO2nLCP_ShB1xoNqBUPA130_provenance.
NP281505.RAZve-W58ff31-5lmHnwXGYRRa6srlQlLJKCLWG8-mH1g130_assertion description "[Patients with moderately advanced HD are at risk for SDH after transplantation surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281505.RAZve-W58ff31-5lmHnwXGYRRa6srlQlLJKCLWG8-mH1g130_provenance.
NP281507.RAXFyPPRKTVqaQwmYTasua8NR9aIpd-Tj3hMsMcwCe05A130_assertion description "[The assembly of very low density lipoproteins in rat hepatoma McA-RH7777 cells is inhibited by phospholipase A2 antagonists.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281507.RAXFyPPRKTVqaQwmYTasua8NR9aIpd-Tj3hMsMcwCe05A130_provenance.
NP281508.RAeH4Mm_31cV1qBGPyOG3PIfFXyn8Wr6Ah_DmArqz7oJg130_assertion description "[In addition, PTEN mutations have been described in a few patients with autism spectrum disorders (ASDs) and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281508.RAeH4Mm_31cV1qBGPyOG3PIfFXyn8Wr6Ah_DmArqz7oJg130_provenance.
NP281513.RAT1vdk8j6OUk4cnFASAaw311lVvBDgKlPD31x1Em6iTM130_assertion description "[A glutamine (Gln)/arginine (Arg) polymorphism at amino acid residue 192 in PON1 was significantly associated with stroke (P=0.003 in multivariate analysis, including age, sex, LDL, hypertension, diabetes, smoking, and pravastatin treatment as covariates).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281513.RAT1vdk8j6OUk4cnFASAaw311lVvBDgKlPD31x1Em6iTM130_provenance.
NP281516.RAV1hzinaPX-HzdhQp76FxDe9mtUtJ82sVI4hVY6epZGU130_assertion description "[Dysregulated cytokine/cytokine receptor expression may occur in B-cell lymphoproliferative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281516.RAV1hzinaPX-HzdhQp76FxDe9mtUtJ82sVI4hVY6epZGU130_provenance.
NP281518.RAd8A5dDHi0J1Qvt04ylpudBfKjO2fqahzd4NyvnJxy3w130_assertion description "[None of the nodules were diagnosed as malignant based on the US criteria, but all except one patient had a cytology of their thyroid nodules that was read as malignant, without revealing the subtype of their PTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281518.RAd8A5dDHi0J1Qvt04ylpudBfKjO2fqahzd4NyvnJxy3w130_provenance.
NP281521.RAUTX4fDfuBivha4eLIGCIeatcHLCj8ujC6TxeqWc0Du4130_assertion description "[Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281521.RAUTX4fDfuBivha4eLIGCIeatcHLCj8ujC6TxeqWc0Du4130_provenance.
NP281522.RAapeQ6SgOFL5p5TQlsvyMmu46xv4tN9_qDyXPDcYdciQ130_assertion description "[A non-imprinted gene from 15q11-q13, GABRB3, encoding the beta3 subunit of the GABAA receptor, also showed significantly reduced expression in multiple Rett, Angelman and autism brain samples, and Mecp2 deficient mice by quantitative immunoblot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281522.RAapeQ6SgOFL5p5TQlsvyMmu46xv4tN9_qDyXPDcYdciQ130_provenance.
NP281523.RAXbk5JTNVGXEpcVkJwtCoRnolOs74bLfLnog1YXhNa2E130_assertion description "[MUC1 as a discriminator between endometrium from fertile and infertile patients with PCOS and endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281523.RAXbk5JTNVGXEpcVkJwtCoRnolOs74bLfLnog1YXhNa2E130_provenance.
NP281532.RASW4CxhLLdz1fLaNUFi5HEzf0-hNL6fhrM0svvx0L97E130_assertion description "[In an attempt to determine a possible relationship between MDR and poor outcome in this population, histologic samples obtained from 45 non-Hodgkin's lymphoma HIV-infected patients without previous cytotoxic therapy were submitted to immunohistochemical analysis using monoclonal antibody C494 specific for the MDR-1 isoform of P-gp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281532.RASW4CxhLLdz1fLaNUFi5HEzf0-hNL6fhrM0svvx0L97E130_provenance.
NP281538.RAdvXtDAHRoX-0Y4Q5Pcfz4R0IDoCGdW1misfvFgIOafE130_assertion description "[Identification of homologous regions in human immunodeficiency virus I gp41 and human MHC class II beta 1 domain. I. Monoclonal antibodies against the gp41-derived peptide and patients' sera react with native HLA class II antigens, suggesting a role for autoimmunity in the pathogenesis of acquired immune deficiency syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281538.RAdvXtDAHRoX-0Y4Q5Pcfz4R0IDoCGdW1misfvFgIOafE130_provenance.
NP281543.RAT207dRzNLcPcEW9EUfO9XKa6X0SAWoxLniRSbY0mPP8130_assertion description "[In the sarcoidosis group IL-4R alpha(+1902)AA and IL-10(-1082)G allele correlated with higher BALF ENA-78 levels (p=0.0258, p=0.0230).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281543.RAT207dRzNLcPcEW9EUfO9XKa6X0SAWoxLniRSbY0mPP8130_provenance.
NP281546.RAaPMJA42nCnHZXvvzq-P6iWjU0Md0misoaXcK84THCzU130_assertion description "[Cytokine-induced phosphorylation of ERK1/2 was diminished in RA HPC whereas phosphorylated STAT3 and STAT5 molecules accumulated to a similar extent as in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281546.RAaPMJA42nCnHZXvvzq-P6iWjU0Md0misoaXcK84THCzU130_provenance.
NP281550.RAfjSjmgVmaGpPOJNsdRl7ED8UIWSRXkBCc9j3lGXQ5gs130_assertion description "[The allel-specific abnormal transcript of the HSP70 gene on chromosome 6 thus may underlie the altered stress and/or immune response in major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281550.RAfjSjmgVmaGpPOJNsdRl7ED8UIWSRXkBCc9j3lGXQ5gs130_provenance.
NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_assertion description "[Acute myelomonocytic leukemia with eosinophilia is commonly associated with pericentric inversions of chromosome 16, involving the core binding factor beta gene (CBFB) on 16q22 and the myosin heavy chain gene (MYH11) on 16p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_provenance.
NP281556.RAVBDQaFUtx0eZUXC0cBIJJMMnv_6m3UtukgRUGQ-LD6c130_assertion description "[Moreover, GPR43 regulates plasma lipid profile and inflammatory processes, which further indicates that GPR43 could have the ability to modulate the etiology and pathogenesis of metabolic diseases such as obesity, type 2 diabetes mellitus, and cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281556.RAVBDQaFUtx0eZUXC0cBIJJMMnv_6m3UtukgRUGQ-LD6c130_provenance.
NP281559.RAcLWxrcLjCLHMs-zhU6PXsqJSd_tKoAJCE2oDl0quu2s130_assertion description "[CD133, but not CD146, mRNA expression is increased in cancer patients with metastatic disease, specifically with bone metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281559.RAcLWxrcLjCLHMs-zhU6PXsqJSd_tKoAJCE2oDl0quu2s130_provenance.
NP281564.RAc0o2PhporqhZWqdOMV6x9l0OUMvfnWJkHvOBYUZzLUQ130_assertion description "[Apolipoprotein A-I(Zavalla) (Leu159-->Pro): HDL cholesterol deficiency in a kindred associated with premature coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281564.RAc0o2PhporqhZWqdOMV6x9l0OUMvfnWJkHvOBYUZzLUQ130_provenance.
NP281566.RAb_4ytbcJYiZxKTXN-Kogj_wDsO7kgHLNmYSXsyRmc1c130_assertion description "[These data indicated that R-CHOP chemotherapy resistance in diffuse large B-cell lymphoma may involve interactions between the BCL2 and IL10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281566.RAb_4ytbcJYiZxKTXN-Kogj_wDsO7kgHLNmYSXsyRmc1c130_provenance.
NP281575.RAb8Iue7A7ji4g7yCF2gGNgluQyJLxgdaNdT9XkLZNY1k130_assertion description "[Presence of p63 in invasive breast carcinomas of luminal type, as seen at molecular level, suggests caution to include p63 as a marker of basal-like carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281575.RAb8Iue7A7ji4g7yCF2gGNgluQyJLxgdaNdT9XkLZNY1k130_provenance.
NP281580.RAWS7dTYxuBnNldpQiRL-53Ihk26k9l3QxqXFfq7AVNfs130_assertion description "[We analyzed the ability of CD4(+) T cells to recognize an HLA-DR-restricted AFP-derived epitope in 41 hepatocellular carcinoma patients and 24 non-hepatocellular carcinoma control patients using intracellular cytokine assays for IFN-gamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281580.RAWS7dTYxuBnNldpQiRL-53Ihk26k9l3QxqXFfq7AVNfs130_provenance.
NP281581.RAahsaG9OMY2p2h4w6djFRNeYcY_R2YhAmJeZckklr7Zc130_assertion description "[These findings support the hypothesis of IL-1 cluster variability as a shared genetic risk factor contributing to GM deficits both in bipolar disorder and in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281581.RAahsaG9OMY2p2h4w6djFRNeYcY_R2YhAmJeZckklr7Zc130_provenance.
NP281585.RAbOEKsEQIp36u0LPpu6KwG_UjEQYF8NED26I27Z0YWSo130_assertion description "[We suggest that 3p- syndrome associated features are primarily caused by loss of CNTN4 and CRBN, with loss of CHL1 probably having an additional detrimental effect on the cognitive functioning of the present patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281585.RAbOEKsEQIp36u0LPpu6KwG_UjEQYF8NED26I27Z0YWSo130_provenance.
NP281586.RAXU3jX3S4gRnQwUW5nXHMcWs3R66yhOs5ktILsdyw-oU130_assertion description "[Both YAC128 and R6/2 HD mutant mice showed a reduced expression of TGF-β(1) in the cerebral cortex, localized in neurons, but not in astrocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281586.RAXU3jX3S4gRnQwUW5nXHMcWs3R66yhOs5ktILsdyw-oU130_provenance.
NP281587.RAZZf-wC_WsCqAsuRJKhQnak-pAW-xiu_SN0NxZ1zm_S4130_assertion description "[The balanced translocation t(11;22)(q24;q12) is specific for the Ewing's sarcoma/peripheral primitive neuroectodermal tumors (ES/PNETs) and results in the EWS/FLI-1 fusion transcript, which can be detected by reverse transcription polymerase chain reaction (RT-PCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281587.RAZZf-wC_WsCqAsuRJKhQnak-pAW-xiu_SN0NxZ1zm_S4130_provenance.
NP281599.RAVDOaulXlR7ga8yr2s_XnxTF93MrKiMu0UYltUmrBMhE130_assertion description "[Our study suggests how skin-homing CD8+ T-lymphocytes from patients with early stage CTCL can suppress the in vitro growth of skin-homing CD4+ T-lymphocytes, indicating immune surveillance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281599.RAVDOaulXlR7ga8yr2s_XnxTF93MrKiMu0UYltUmrBMhE130_provenance.
NP281606.RAfCQhyvQcL2JfCConqklb7lJU8KaVFrqhCpdP-UyseMU130_assertion description "[In this study, we performed mutational analysis on genomic DNA from a child with H-JEB and identified a nonsense mutation in the alpha 3 chain gene (LAMA3) consisting of a homozygous C-to-T transition resulting in a premature termination codon (CGA-->TGA) on both alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281606.RAfCQhyvQcL2JfCConqklb7lJU8KaVFrqhCpdP-UyseMU130_provenance.
NP281608.RAV6jlZnx6CSw2VCaIKDURkd3WfB1ogVQGfiWyhNfg_Cc130_assertion description "[Composite MMP-9 genotypes but not other SNPs were associated with MI, whereas MMP-1/MMP-3 genotypes were CAD-associated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281608.RAV6jlZnx6CSw2VCaIKDURkd3WfB1ogVQGfiWyhNfg_Cc130_provenance.
NP281609.RAT-JIWxmD73LHQYPkEiq7TMyKn6K84u9MLR3Flb8CB1s130_assertion description "[The HLA haplotype DRB1*15-DPB1*05 can be a susceptibility gene marker for the development of TDI-induced asthma among the exposed workers in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281609.RAT-JIWxmD73LHQYPkEiq7TMyKn6K84u9MLR3Flb8CB1s130_provenance.
NP281611.RAdrakfLKz0O5QUeT4kMp632YUALrFXMT_UQaUs5Lo3uQ130_assertion description "[Genetic analysis of families with Milroy's disease identified mutations in VEGFR3 as a cause of congenital lymphedema, confirming the importance of VEGFC/VEGFR3 signaling in lymphatic development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281611.RAdrakfLKz0O5QUeT4kMp632YUALrFXMT_UQaUs5Lo3uQ130_provenance.
NP281614.RAWPwxkoD2JFfCLl_cxUOFGERYnBNxQ4s4WEA2Rm-6x30130_assertion description "[Three of the 20 cases with SIM exhibited novel microsatellite alleles, 2 with Barrett's oesophagus and 1 with short segment SIM and an associated adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281614.RAWPwxkoD2JFfCLl_cxUOFGERYnBNxQ4s4WEA2Rm-6x30130_provenance.
NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_assertion description "[Moreover, when XPD mutations prevent interaction with the p44 subunit of TFIIH, transactivation directed by certain nuclear receptors is inhibited, regardless of TTD versus XP phenotype, thus explaining the overlapping symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281616.RAeXRRTqUkFIcZhXW1eT1Ox9AgW7c5nwTfjJdypLxcbUw130_provenance.
NP281619.RAaX5b6WxiezxS3fhP7izOveGMxpGMsGgShZo0T1Vpj8g130_assertion description "[The purpose of this study was to elucidate the clonality of fibrous dysplasia based on X-chromosome inactivation mosaicism and polymorphism in female somatic cells at the phosphoglycerate kinase (PGK) and androgen receptor (AR) loci using microdissection technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281619.RAaX5b6WxiezxS3fhP7izOveGMxpGMsGgShZo0T1Vpj8g130_provenance.
NP281622.RATTVUDTLGGjP6yfY9uWm8YITEG8peZTaxG0dCn04MaZk130_assertion description "[To determine whether mutation analysis could replace enzymatic analysis for the diagnosis of PH1, DNA samples from 127 consecutive unrelated patients in whom there was a high clinical suspicion of primary hyperoxaluria were analyzed for the presence of the G630A and T853C mutations, which together account for approximately 34% of the mutant alleles in our patient cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281622.RATTVUDTLGGjP6yfY9uWm8YITEG8peZTaxG0dCn04MaZk130_provenance.
NP281624.RAVYNvqj4ZPhYgprsaO1SxUp6MIMvRAClBW_31Lt1FGzE130_assertion description "[Moreover, although recombinant tumor necrosis factor-related apoptosis inducing ligand (TRAIL)/Apo2L showed little cytotoxic effect in most B-CLL samples examined, pretreatment with NS-398 sensitized 8 of 16 B-CLL samples to TRAIL-induced apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281624.RAVYNvqj4ZPhYgprsaO1SxUp6MIMvRAClBW_31Lt1FGzE130_provenance.
NP281629.RAfGV0jgVyI8m9lwO5ieB9wvklm5ZdK1bJkbE0XPqjvu8130_assertion description "[More therapy-resistant forms and axial arthropathy can be treated with anti-TNF drugs, predominantly infliximab and adalimumab.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281629.RAfGV0jgVyI8m9lwO5ieB9wvklm5ZdK1bJkbE0XPqjvu8130_provenance.
NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_assertion description "[The recognition of the clinical phenotype associated with more than 50 different mutations in GRN has expanded the clinical knowledge of FTD to include presentations that resemble Alzheimer's disease, Lewy body disease, and corticobasal syndrome, with a variable age at onset (35-89 years) within families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_provenance.
NP281633.RAe8eNaDhLeGZ1ej-Ddk36fWrCOTZqUuu5JMf0hU4ngEo130_assertion description "[The NCLs include eight forms that result from genetic deficiency on genes CLN(1) to CLN(8), respectively: four classic forms with clinical onset at varying ages-infantile (INCL), late-infantile (LINCL), juvenile (JNCL), and adult (ANCL)-and four variants of late-infantile onset-the Finnish variant LINCL (fLINCL), Portuguese variant LINCL (pLINCL), Turkish variant LINCL (tLINCL), and progressive epilepsy with mental retardation (EPMR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281633.RAe8eNaDhLeGZ1ej-Ddk36fWrCOTZqUuu5JMf0hU4ngEo130_provenance.
NP281634.RATkx5_usEYfPpy7WnYJVj32t7SqRZqRbIF16Dl8gWn4g130_assertion description "[Our results suggested that mutations of the DCC gene may be involved in the pathogenesis of neuroblastomas but failed to account for the relatively high frequency of the altered expression, implying that other mechanisms are responsible for the inactivation of the DCC gene in neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281634.RATkx5_usEYfPpy7WnYJVj32t7SqRZqRbIF16Dl8gWn4g130_provenance.
NP281641.RAejjbaHsrtWHyh2Gx7rHRbQkOXAgNnpSWFXRY9knij0U130_assertion description "[Thus, we set out to identify novel single nucleotide polymorphisms (SNPs) within SRC-1 (NCoA1), SRC-3 (NCoA3, AIB1), NCoR (NCoR1), and SMRT (NCoR2), and test the most promising SNPs for associations with breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281641.RAejjbaHsrtWHyh2Gx7rHRbQkOXAgNnpSWFXRY9knij0U130_provenance.
NP281645.RAQ05iRwjbb5VedURAd6bHo1wQ9SkpdGB7H7Q4fb-Vnto130_assertion description "[Focal PPK is one of the hallmarks of pachyonychia congenita, a rare autosomal dominant disorder resulting from mutations in the keratin genes KRT6A, KRT6B, KRT16 or KRT17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281645.RAQ05iRwjbb5VedURAd6bHo1wQ9SkpdGB7H7Q4fb-Vnto130_provenance.
NP281647.RARnmGE2SIPhQpOwJ5MAtmkkowK8EJNTlOpnbYB5CQwnk130_assertion description "[Results with PGD indicate a significant decrease in spontaneous abortions, from 81% before PGD to 13% after PGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281647.RARnmGE2SIPhQpOwJ5MAtmkkowK8EJNTlOpnbYB5CQwnk130_provenance.
NP281649.RAZcLRf_iB_741FfIQan7O-gpZQ0tWBbl6mNaqrhgk080130_assertion description "[In this study, we report that C1orf61 expression is associated with the progression of liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281649.RAZcLRf_iB_741FfIQan7O-gpZQ0tWBbl6mNaqrhgk080130_provenance.
NP281672.RAQjzcAwRBwEMO0hxVV3kkVFQJ46PdOF6p5y3fGMED4tU130_assertion description "[In hCRPtg/BW mice, CRP protects against SLE by increasing blood and mesangial clearance of immune complexes and by preventing their accumulation in the renal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281672.RAQjzcAwRBwEMO0hxVV3kkVFQJ46PdOF6p5y3fGMED4tU130_provenance.
NP281684.RAcYkbeaBBekkvzUloAApD__KV1Bef_ujKvcExVzbJTD8130_assertion description "[These results demonstrate a Na(V)1.7 mutant with biophysical characteristics common to PEPD (impaired fast inactivation) and IEM (hyperpolarized activation, slow deactivation, and enhanced ramp currents) associated with a clinical phenotype with characteristics of both IEM and PEPD and show that this mutation renders DRG and trigeminal ganglion neurons hyperexcitable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281684.RAcYkbeaBBekkvzUloAApD__KV1Bef_ujKvcExVzbJTD8130_provenance.
NP281688.RAfEzGClrUeqtDl_YZBDgbn4f9rhMoa_6mbQ_dbaKTfYA130_assertion description "[ABCB1 gene polymorphisms and expression of P-glycoprotein and long-term prognosis in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281688.RAfEzGClrUeqtDl_YZBDgbn4f9rhMoa_6mbQ_dbaKTfYA130_provenance.
NP281689.RAftGyIlgmGFh8kM4cz2DMeVt41LASGvCGMiI59ncnf10130_assertion description "[Having confirmed expression of Wld(S) protein, we found that Wld(S) delayed ON axonal degeneration in experimental rat glaucoma for at least 2 weeks, especially in proximal ON where wild-type axons are most severely affected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281689.RAftGyIlgmGFh8kM4cz2DMeVt41LASGvCGMiI59ncnf10130_provenance.
NP281690.RAfswG0z3-x1WC5NB_5EkmbUaS4j_L_5UwBEoplG3KrS8130_assertion description "[A3AR and NF-kappaB levels were also analyzed in phytohemagglutinin (PHA) and lipopolysaccharide (LPS)-stimulated PBMC in the presence and absence of antibodies against interleukin 2 (IL-2) and tumor necrosis factor-alpha (TNF-alpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281690.RAfswG0z3-x1WC5NB_5EkmbUaS4j_L_5UwBEoplG3KrS8130_provenance.
NP281692.RAbOKg340iYfwjzaP2qvZGdEOZYPfLKRixIIcgp5S4ABo130_assertion description "[We investigated the (TA)n polymorphism in exon 18 of the LDLR gene on chromosome 19p13.2 performing an association analysis in 244 typical migraine-affected patients, 151 suffering from migraine with aura (MA), 96 with migraine without aura (MO) and 244 unaffected controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281692.RAbOKg340iYfwjzaP2qvZGdEOZYPfLKRixIIcgp5S4ABo130_provenance.
NP281694.RAQfnV4wwNgMGuzUq6bBKsdlWT40Rl7f5Rs3vfjcod5kY130_assertion description "[Thirty additional cases were CD5 negative suggestive of leukemic marginal zone lymphoma in most cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281694.RAQfnV4wwNgMGuzUq6bBKsdlWT40Rl7f5Rs3vfjcod5kY130_provenance.
NP281696.RARmtNTxArwvVUYM6NBfkcrB8xumpchnW66bvBR0boJJc130_assertion description "[Heterozygous nonsense and missense mutations of the human TGIF gene have been associated with holoprosencephaly, the most common congenital malformation of the forebrain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281696.RARmtNTxArwvVUYM6NBfkcrB8xumpchnW66bvBR0boJJc130_provenance.
NP281700.RATc7mVH0H7SOsU7IWe2TXT6s-DKcvAHaNreqVsFpDF2E130_assertion description "[To determine the association between expression of TRAIL-R2 and p53 mutation status in lung cancers, we compared the two events in 20 small-cell lung cancer (SCLC) cell lines, 20 NSCLC cell lines, and 30 primary NSCLC tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281700.RATc7mVH0H7SOsU7IWe2TXT6s-DKcvAHaNreqVsFpDF2E130_provenance.
NP281701.RAfJRuCAwQsRtuSy_eKI6NiL8DRfR4qG4wdIUwxeOtkLk130_assertion description "[Duane's syndrome is an unusual congenital form of strabismus where there is paradoxical anomalous lateral rectus innervation of the affected eye due to misdirection of axons destined for the medial rectus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281701.RAfJRuCAwQsRtuSy_eKI6NiL8DRfR4qG4wdIUwxeOtkLk130_provenance.
NP281704.RARCt-TF3p7siJh_8-M-JSg_mb-qF9q__N3TdeCtukEX0130_assertion description "[Patients with essential hypertension and echocardiographically diagnosed LVH were included in a double-blind study to receive treatment with either the angiotensin II type 1 receptor (AT1-receptor) antagonist irbesartan (n = 41), or the beta-1 adrenergic receptor blocker atenolol (n = 43) as monotherapy for 3 months.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281704.RARCt-TF3p7siJh_8-M-JSg_mb-qF9q__N3TdeCtukEX0130_provenance.
NP281712.RAfq25iU0YwYKLD_Qk6cCrEkzL5r9eu0hbV1CQ4Eotbfw130_assertion description "[Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281712.RAfq25iU0YwYKLD_Qk6cCrEkzL5r9eu0hbV1CQ4Eotbfw130_provenance.
NP281715.RAepiZ5Lkkciw1bEaly7WFVZ5tjg_nquc_eJZNDemi_Fs130_assertion description "[Using a 15% cut-off for methylation, we observed significantly higher methylation in genes MGMT, PAX5, CDH13, WT1, THBS1, GATA5 in the ovarian cancer group, while in the ESR1 gene we observed significantly higher methylation in the control group compared with the ovarian cancer group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281715.RAepiZ5Lkkciw1bEaly7WFVZ5tjg_nquc_eJZNDemi_Fs130_provenance.
NP281716.RAZGNgtazqUtuNAwxNNNXI8LoRN7VgsqWa8elf1U_jdEk130_assertion description "[Epigenetic screen of human DNA repair genes identifies aberrant promoter methylation of NEIL1 in head and neck squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281716.RAZGNgtazqUtuNAwxNNNXI8LoRN7VgsqWa8elf1U_jdEk130_provenance.
NP281727.RAerV9m_eacRqca6za5BQEF0o-BSGyTbhbiDos9DnNuwc130_assertion description "[Monocyte chemoattractant protein-1 (MCP-1) is a potent chemokine and plays an important role in cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281727.RAerV9m_eacRqca6za5BQEF0o-BSGyTbhbiDos9DnNuwc130_provenance.
NP281731.RAdK8tDIF_YOPsYIXPOVNAOg-YMvZCznRU34-76gE8a80130_assertion description "[Mutational analysis of the cystathionine beta-synthase gene: a splicing mutation, two missense mutations and an insertion in patients with homocystinuria. Mutations in brief no. 120. Online.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281731.RAdK8tDIF_YOPsYIXPOVNAOg-YMvZCznRU34-76gE8a80130_provenance.
NP281734.RAe7YVBILuqH-JjCccuEijYQJ2Qicr764nq0JQJQJM6fs130_assertion description "[Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281734.RAe7YVBILuqH-JjCccuEijYQJ2Qicr764nq0JQJQJM6fs130_provenance.
NP281738.RAV8CIEBuCTyGvepWce6OGh0LzzcOE24Y8oFR5NzNYsvI130_assertion description "[To study quantitatively the promoter methylation of hMLH1, p16INK, TIMP3 and TPEF genes in patients with colorectal cancer and synchronous polyps, and correlate it with some clinicomorphological features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281738.RAV8CIEBuCTyGvepWce6OGh0LzzcOE24Y8oFR5NzNYsvI130_provenance.
NP281740.RAVBtmWmIZhFlK9sPMyu-bXQCtXPQV3NoMEfeZ-gAGlcg130_assertion description "[The immunohistochemical DHS defined a large subset of DLBCLs with double-hit biology and was strongly associated with poor outcome in patients treated with R-CHOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281740.RAVBtmWmIZhFlK9sPMyu-bXQCtXPQV3NoMEfeZ-gAGlcg130_provenance.
NP281742.RAUB_1mXK4YbYxDEKyO2HqQabEuHdcdVGYWuJp2kUaGQ4130_assertion description "[High-level SCCRO expression was identified in 94% of normal (32/34) and adenomatous (29/31) adrenocortical specimens but in only 63% (45/72) of adrenocortical carcinoma (ACC) specimens ( P = .001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281742.RAUB_1mXK4YbYxDEKyO2HqQabEuHdcdVGYWuJp2kUaGQ4130_provenance.
NP281746.RAa9nJYdX_0ZLwEFHHpiyNx_pciN9Cej84_uu_8489ABA130_assertion description "[The viral load in maternal plasma samples was determined by a quantitative reverse transcriptase-PCR assay; co-receptor usage of maternal isolates was determined by viral infection in cells stably expressing CCR5 or CXC chemokine receptor 4 (CXCR4) co-receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281746.RAa9nJYdX_0ZLwEFHHpiyNx_pciN9Cej84_uu_8489ABA130_provenance.
NP281756.RAVDO3Owed1uJjkxGzDv80orGB1MXWTcQXRkKF1cPO8IY130_assertion description "[CYP1A1 is largely involved in carcinogenesis through the bioactivation of numerous procarcinogens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281756.RAVDO3Owed1uJjkxGzDv80orGB1MXWTcQXRkKF1cPO8IY130_provenance.
NP281763.RAb_ekIo9EH21hOghV8wXX5vY4qbgUEVmAhPUFoDsfy-k130_assertion description "[Frasier syndrome is characterized by a 46 XY disorder of sex development, nephropathy, and increased risk for gonadoblastoma due to Wilms tumor 1(WT1) mutation in the donor splice site of intron-9, resulting in the splice form +KTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281763.RAb_ekIo9EH21hOghV8wXX5vY4qbgUEVmAhPUFoDsfy-k130_provenance.
NP281764.RARSYfKZvWHfUrBdGi1cUvIhCRU4-QXwfM4cqnNNazIv0130_assertion description "[It is concluded that LPS fever is accompanied by up-regulation of four PGE2-synthesizing enzymes [secretory (s) PLA2-IIA, cytosolic (c) PLA2-alpha, COX-2, and microsomal (m) PGES-1] and down-regulation of all PGE2 carriers and dehydrogenases studied (PGT, MOAT, 15PGDH, and CR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281764.RARSYfKZvWHfUrBdGi1cUvIhCRU4-QXwfM4cqnNNazIv0130_provenance.
NP281766.RAUUeermwrgtBnt8NT_u5QbZxKoEM9b0tOI0WyaNXVLeA130_assertion description "[beta ARK mRNA levels were increased almost threefold in both forms of heart failure, and beta ARK activity was enhanced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281766.RAUUeermwrgtBnt8NT_u5QbZxKoEM9b0tOI0WyaNXVLeA130_provenance.
NP281767.RAdqT6hP7cVW9XaEhFEqvd3eqbWKmlZvtrJVmEkuIEpIw130_assertion description "[Clinical features and molecular/biologic factors such as ZAP-70, immunoglobulin heavy chain (IGHV) gene mutation status, and cytogenetic abnormalities on fluorescent in situ hybridization (FISH) have been found to be robust predictors of treatment-free survival and overall survival among newly diagnosed patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281767.RAdqT6hP7cVW9XaEhFEqvd3eqbWKmlZvtrJVmEkuIEpIw130_provenance.
NP281779.RAZYiZo_pER2dSx7xoJufTvpFCrG599lztxdvaQUH7m5E130_assertion description "[Evaluation of DAZ microdeletions in 34 infertile men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281779.RAZYiZo_pER2dSx7xoJufTvpFCrG599lztxdvaQUH7m5E130_provenance.
NP281782.RAaRuN9ljzZ1LxI3XjmFmYVxRUTwSuwDdDPs9xY19Z0SY130_assertion description "[We speculate that the CSB-transposase fusion protein has been conserved for host antitransposon defense, or to modulate gene regulation by MER85 elements, but may cause CS in the absence of functional CSB protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281782.RAaRuN9ljzZ1LxI3XjmFmYVxRUTwSuwDdDPs9xY19Z0SY130_provenance.
NP281785.RAat-2ErOy-VxBohQIiXOTstkMxRwPINY6N6oMu6s1VT0130_assertion description "[Mutations were found predominantly at codon 12 with transversions from GGT to GTT (57%), from GGT to GAT (36%), and from GGT to TTT (one patient).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281785.RAat-2ErOy-VxBohQIiXOTstkMxRwPINY6N6oMu6s1VT0130_provenance.
NP281794.RATrLI5OJFTLcyAW-C_XaLdvtUocYMS7AMEQaE0wBmztU130_assertion description "[Evidence for an intensity-dependent interaction of NAT2 acetylation genotype and cigarette smoking in the Spanish Bladder Cancer Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281794.RATrLI5OJFTLcyAW-C_XaLdvtUocYMS7AMEQaE0wBmztU130_provenance.
NP281795.RAXQ8nEXdsL6O3O4yedGfmCPQ5J6dNzIw4vz91kAoBxlA130_assertion description "[FLU MIC values for respiratory-deficient clones were ≥64 μg/ml, and efflux pump gene expression was greatly increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281795.RAXQ8nEXdsL6O3O4yedGfmCPQ5J6dNzIw4vz91kAoBxlA130_provenance.
NP281802.RAUuT3vK_M-5zk_w2XFrNTKtMUFPWTrSf7FZ9Q0bTJMWM130_assertion description "[Of the 29 SNPs conferring high genetic susceptibility to CD, 28 were not associated with UC, thus indicating that for this SNP set there is a low level of overlap between the two major forms of IBD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281802.RAUuT3vK_M-5zk_w2XFrNTKtMUFPWTrSf7FZ9Q0bTJMWM130_provenance.
NP281805.RAfSF2QYLtgay7lJr0BbFoGFk099yvbBYcWFk1LwAVFyU130_assertion description "[Our findings suggest a link between the SMN complex and FMRP in neuronal cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281805.RAfSF2QYLtgay7lJr0BbFoGFk099yvbBYcWFk1LwAVFyU130_provenance.
NP281811.RAf7axXHlkuLCvtx2nJMSB74XO3VNUgHNwMRHU-8-WUcA130_assertion description "[To clarify the genetic role of MPO in HN, we examined the function and distribution of the -463G/A polymorphism located in the promoter region of the MPO gene with ex vivo flow cytometry analysis and a study in end-stage renal disease patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281811.RAf7axXHlkuLCvtx2nJMSB74XO3VNUgHNwMRHU-8-WUcA130_provenance.
NP281816.RAZhyeK2tEY_hYXNWmDF6WqW8EYwbWqAUT2kibiiT8fEg130_assertion description "[Somatically mutated immunoglobulin IGHV@ genes without intraclonal heterogeneity indicate a postgerminal centre origin of primary intraocular diffuse large B-cell lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281816.RAZhyeK2tEY_hYXNWmDF6WqW8EYwbWqAUT2kibiiT8fEg130_provenance.
NP281818.RAdnrHd1ozbtPS665uz8ofeBWDbyeBVJ3uQZc1P80wkVU130_assertion description "[Despite lower IL-17 production, the IL-23R gene polymorphism did not influence the development of chronic Lyme disease in a cohort of patients with Lyme disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281818.RAdnrHd1ozbtPS665uz8ofeBWDbyeBVJ3uQZc1P80wkVU130_provenance.
NP281820.RAZ_iIlpv5BTaPf8FUgUmPTU8lY__1bfQnAxcIj9SucM4130_assertion description "[However, several genes involved in SOA have been recently identified, namely N-MYC, SOX2, and CHD7 involved in Feingold (MIM 164280), anophthalmia-oesophageal-genital (MIM 600992) and CHARGE syndromes respectively (MIM 214800), suggesting that OA/TOF, at least in their syndromic forms, may be a highly genetically heterogeneous group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281820.RAZ_iIlpv5BTaPf8FUgUmPTU8lY__1bfQnAxcIj9SucM4130_provenance.
NP281828.RAfntU6ofLSAnl27cqucRH_pb6UTMP7nM47cRSW_SyOqo130_assertion description "[CAG repeat expansions cause spinocerebellar ataxia type 1 (SCA1), SCA2, SCA3, SCA6 and dentatorubral-pallidoluysian atrophy (DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281828.RAfntU6ofLSAnl27cqucRH_pb6UTMP7nM47cRSW_SyOqo130_provenance.
NP281832.RAWRHKbJykhZ5_z_93CgZSxw5tItgqrfuzZ42CtBlQWsQ130_assertion description "[Low thymidylate synthase, thymidine phosphorylase, and dihydropyrimidine dehydrogenase mRNA expression correlate with prolonged survival in resected non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281832.RAWRHKbJykhZ5_z_93CgZSxw5tItgqrfuzZ42CtBlQWsQ130_provenance.
NP281835.RAQQ53TH2UNhDNA2HWEwCVojog3T_uvILl5gLqvpsipLY130_assertion description "[Interleukin 1 beta (IL-1 beta) is a potent proinflammatory factor during viral infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281835.RAQQ53TH2UNhDNA2HWEwCVojog3T_uvILl5gLqvpsipLY130_provenance.

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