Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP205925.RAWRP5oEOJDWDWPD0eN6MJwm7lEs_uzaBNI5LbZ7JDwNQ130_assertion description "[These studies demonstrate that synthetic agonists of TLR9 interfere with growth and angiogenesis also by EGFR- and ADCC-independent mechanisms affecting endothelial cell functions and provide a strong rationale to combine IMO with bevacizumab and EGFR inhibitory drugs in colon cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205925.RAWRP5oEOJDWDWPD0eN6MJwm7lEs_uzaBNI5LbZ7JDwNQ130_provenance.
- NP205926.RAekvtT59gwTdMvFyAawXMZ4R64ge2o0N4wXhr9jUSulE130_assertion description "[The further inactivation of the Pten, p53, and E2f2 tumor suppressors in MYC-induced lymphomas resulted in distinct and diagnostic CpG island methylation signatures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205926.RAekvtT59gwTdMvFyAawXMZ4R64ge2o0N4wXhr9jUSulE130_provenance.
- NP205936.RAU8wbG3lYjKy6imMgMxgOwsBmBvc-hUgmqUfF5gbzZmE130_assertion description "[We have investigated the immunohistochemical expression of thymidine phosphorylase before and after the administration of anthracycline, and/or anthracycline/taxane-based preoperative chemotherapy in a consecutive series of 55 patients with primary operable breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205936.RAU8wbG3lYjKy6imMgMxgOwsBmBvc-hUgmqUfF5gbzZmE130_provenance.
- NP205937.RAQUIP1UiV9K738oL224ysO1o3IIIh-zWr9Oci5BX_EkI130_assertion description "[The promoter region (424 bp upstream from exon 1) showed promoter activity and includes multiple transcription factor consensus binding motifs, including those for Sp1, Nkx-2, CdxA, SRY, MyoD, Ik-2, HNF-3b, Staf, Oct-1, Nkx-2, v-Myb, and AML 1a.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205937.RAQUIP1UiV9K738oL224ysO1o3IIIh-zWr9Oci5BX_EkI130_provenance.
- NP205938.RAel1gs_c6sesZT-bL-Rvr8H069CB_Ul--PLZv8qGr7Lw130_assertion description "[The authors report on a 23-year-old man with Klinefelter syndrome (47,XXY) and bipolar disorder who was treated successfully with unilateral DBS of the thalamic Vim for essential tremor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205938.RAel1gs_c6sesZT-bL-Rvr8H069CB_Ul--PLZv8qGr7Lw130_provenance.
- NP205945.RATNO8z0oCmrzDUu7eqUoe-ctSr9b9eDmQp0evZ_6HQS4130_assertion description "[Familial urticaria pigmentosa: report of a family and review of the role of KIT mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205945.RATNO8z0oCmrzDUu7eqUoe-ctSr9b9eDmQp0evZ_6HQS4130_provenance.
- NP205947.RAU8ZPv1UC-f3B88Apzd07YiST4wW49VIZog9iYi7eLOk130_assertion description "[NADPH oxidase-generated reactive oxygen species (ROS) are highly implicated in the development of angiotensin II (AngII)-dependent hypertension mediated in part through the hypothalamic paraventricular nucleus (PVN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205947.RAU8ZPv1UC-f3B88Apzd07YiST4wW49VIZog9iYi7eLOk130_provenance.
- NP205948.RAZHkw-_mX17_QdOPKeQanH-6pUe8I293rrHZnPJ_-720130_assertion description "[XLH is an important disease, it is the subject of several classic articles in the medical sciences (Scriver et al., 1991), and it has been an important stimulus to study renal hypophosphatemias and how they are involved in rickets and osteomalacia (Scriver, 1974; Scriver and Tenenhouse, 1991).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205948.RAZHkw-_mX17_QdOPKeQanH-6pUe8I293rrHZnPJ_-720130_provenance.
- NP205953.RAQz_iisNoQGalvTdDnObsASA1Rpjn7xB7j1vKXrYnf9c130_assertion description "[Our study demonstrates that the promoters for MK and VEGF are active in cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205953.RAQz_iisNoQGalvTdDnObsASA1Rpjn7xB7j1vKXrYnf9c130_provenance.
- NP205956.RAe5ktmSR8i-xzS6Ib95htZwLNM7bmSisWBrFfxJpEusk130_assertion description "[IQGAP1 and IQGAP2 are reciprocally altered in hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205956.RAe5ktmSR8i-xzS6Ib95htZwLNM7bmSisWBrFfxJpEusk130_provenance.
- NP205960.RAS_2nRtDPaHdpgFDjK0eL_RnfmdxBtPujHVAgrO7CCak130_assertion description "[This suggests that genetic variation in MYO9B is associated with CD, SLE, and RA and that MYO9B is a general risk factor for autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205960.RAS_2nRtDPaHdpgFDjK0eL_RnfmdxBtPujHVAgrO7CCak130_provenance.
- NP205973.RAY4oy08t3IREVUZmTJ5w2oqzss6f0zy41w-u_cpSdYpc130_assertion description "[The aim of this study was to evaluate the association of NOS2 polymorphisms Ser608Leu (rs2297518) in exon 16, -954G/C and -1173C/T, both in the promoter region, with gastric cancer and chronic gastritis and the association of cancer with risk factors such as smoking, alcohol intake and H. pylori infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205973.RAY4oy08t3IREVUZmTJ5w2oqzss6f0zy41w-u_cpSdYpc130_provenance.
- NP205982.RAdJQrRtJK3ANANwmWPjnPKR33CZdBSQZnZvEVp5T4HH8130_assertion description "[Tumorigenesis involves differentiation arrest; therefore, the expression of several proto-oncogenes in neuroectodermal tumors was investigated to evaluate the potential involvement of the EGF-R gene in glial differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205982.RAdJQrRtJK3ANANwmWPjnPKR33CZdBSQZnZvEVp5T4HH8130_provenance.
- NP205984.RATlOIN56np9GwZzjkaq_Wc6jbcZLOcUXmYVDrH4tgDDE130_assertion description "[These data suggest that miR-21 expression is increased in pancreatic cancer cells and that miR-21 contributes to the cell proliferation, invasion, and chemoresistance of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205984.RATlOIN56np9GwZzjkaq_Wc6jbcZLOcUXmYVDrH4tgDDE130_provenance.
- NP205992.RAfJVcELLBNBINF7HK8DQZRvkCVjP3PDnfVvph61enf9U130_assertion description "[A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205992.RAfJVcELLBNBINF7HK8DQZRvkCVjP3PDnfVvph61enf9U130_provenance.
- NP205998.RAXJ7fGDrV7i9_IoT5TCPhcoB3JPVGfHMSQCRiuM9z-w0130_assertion description "[HMGA2 gene is a promising target for ovarian cancer silencing therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205998.RAXJ7fGDrV7i9_IoT5TCPhcoB3JPVGfHMSQCRiuM9z-w0130_provenance.
- NP206014.RASR4PNvPVeiqViiw5G6dCWn63C6CLSGZzynwAuCOV9gU130_assertion description "[Identification of a novel cell death receptor mediating IGFBP-3-induced anti-tumor effects in breast and prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206014.RASR4PNvPVeiqViiw5G6dCWn63C6CLSGZzynwAuCOV9gU130_provenance.
- NP206015.RAZDDP15jHOJnleJjQZbRx7bIfZ0ef_fxCMgdlPNp0IBY130_assertion description "[Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206015.RAZDDP15jHOJnleJjQZbRx7bIfZ0ef_fxCMgdlPNp0IBY130_provenance.
- NP206016.RATDOETpCIBV0o0ElUdG2LvIo9PPU90SlqlJ9nlt_XWK4130_assertion description "[Additive effect of PTK787/ZK 222584, a potent inhibitor of VEGFR phosphorylation, with Idarubicin in the treatment of acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206016.RATDOETpCIBV0o0ElUdG2LvIo9PPU90SlqlJ9nlt_XWK4130_provenance.
- NP206018.RAfGGL5f63gOnNvnCbnWoGpijli882Kpt8t0bIuLictLE130_assertion description "[Tumour cell karyotypes from patients with Burkitt lymphoma (BL) or Burkitt's type leukemia (ALL3) were studied for correlation with survival, bone marrow and cerebral spinal fluid involvement (CSF), human immunodeficiency virus (HIV) serology, and for recurrent cytogenetic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206018.RAfGGL5f63gOnNvnCbnWoGpijli882Kpt8t0bIuLictLE130_provenance.
- NP206020.RATqQGlo4Sur9Ek2ESBGlBh0_o7msHyVwW8rML7FlAOaA130_assertion description "[Cyclin D1 was absent in four tumors; all except one tumor showed expression of TP53 protein, and three of nine MPNSTs had expression of normal-sized MDM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206020.RATqQGlo4Sur9Ek2ESBGlBh0_o7msHyVwW8rML7FlAOaA130_provenance.
- NP206025.RAfpDhx9URn7FmnkYt83JPlbpZPd2yGMf0e6JhaJGSEm4130_assertion description "[We investigated retrospectively the frequency and the discriminative value of TCR Vbeta CDR3 oligoclonality in pediatric (v)SAA and MDS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206025.RAfpDhx9URn7FmnkYt83JPlbpZPd2yGMf0e6JhaJGSEm4130_provenance.
- NP206033.RATJccn4sB2IYnrtEZjtfTaL24wCOis8H70uG1EyKbHBo130_assertion description "[This review article will summarize the available published breast cancer data on the interaction between the relevant SNPs for CYP2D6, CYP3A, CYP2B6, and CYP2C19 and the efficacy of tamoxifen, their role in individualisation of hormonal therapy and the role of the commercially available genotyping kits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206033.RATJccn4sB2IYnrtEZjtfTaL24wCOis8H70uG1EyKbHBo130_provenance.
- NP206041.RAQhuwlh-xCcm97cSU1q84GhRgWfmGe3wFNZGuDpAYHOo130_assertion description "[Rsal and Dral polymorphisms of CYP2E1 and Mspl polymorphism of CYP1A1 were studied in 260 controls and 511 alcoholic patients, without any clinical symptoms (n = 202) or with various ethanol-related diseases (n = 309), such as liver cirrhosis (n = 110), esophageal cancer (n = 62), upper aerodigestive tract cancer (n = 96), and other miscellaneous diseases (n = 41).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206041.RAQhuwlh-xCcm97cSU1q84GhRgWfmGe3wFNZGuDpAYHOo130_provenance.
- NP206044.RATcyWgsKAZLbsgvnY1AE7E9j1tKNqi5r07ZOZd2eg2XQ130_assertion description "[The homozygous carrier of the mutation Gly-188-Arg in the rhodopsin gene showed a later subjective onset of symptoms than the heterozygotes, suggesting that the photoreceptor degeneration induced by the mutation is not dramatically influenced by mutant allele dosage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206044.RATcyWgsKAZLbsgvnY1AE7E9j1tKNqi5r07ZOZd2eg2XQ130_provenance.
- NP206048.RAcR_C3AiBuKebZULYIYq5wG60FNCY871a-VlC_aGEOK8130_assertion description "[In this study, in situ hybridization techniques were used to determine the location of interstitial collagenase and tissue inhibitor of metalloproteinase (TIMP) gene expression in samples from 11 squamous cell carcinomas of the head and neck (particularly the oral cavity) and from non-neoplastic mucosa of the same region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206048.RAcR_C3AiBuKebZULYIYq5wG60FNCY871a-VlC_aGEOK8130_provenance.
- NP206050.RATB6dV-EZT74Aeo0Sj4ruMZZkf-9EF0aLhvKD2JfSnRI130_assertion description "[The finding of a greatly amplified c-myc gene in all cell lines of the SCLC-V class examined strongly suggests a role for the c-myc gene in the phenotypic conversion and malignant behaviour of human lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206050.RATB6dV-EZT74Aeo0Sj4ruMZZkf-9EF0aLhvKD2JfSnRI130_provenance.
- NP206060.RAZJWW9TKlT147Yxgv0taQ8HA_plBWuto48lg6ALGTfDo130_assertion description "[Since MMP-13 was more frequently expressed than MMP-8 in plasma cells of strongly recurring keratocysts and malignant plasmacytomas, it is concluded that plasma cell MMP-13 has a particularly important role in benign and malignant bone-destructive lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206060.RAZJWW9TKlT147Yxgv0taQ8HA_plBWuto48lg6ALGTfDo130_provenance.
- NP206070.RAWLT0w_qhtvEvmiSvGSNNAsCxg8BuQi_CRGz05BEszjo130_assertion description "[A second, de novo, missense mutation (c.293A>G [p.Asn97Ser]) was subsequently identified in an individual of Iraqi origin; this individual was diagnosed with CPVT from a screening of 61 arrhythmia samples with no identified RYR2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206070.RAWLT0w_qhtvEvmiSvGSNNAsCxg8BuQi_CRGz05BEszjo130_provenance.
- NP206086.RAeyDvNI90NFR4FAS8Z-mge_QFdm2lovaE4Rd-1CnlDOk130_assertion description "[JAK1 mutations were more prevalent among adult subjects with the T cell precursor ALL, where they accounted for 18% of cases, and were associated with advanced age at diagnosis, poor response to therapy, and overall prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206086.RAeyDvNI90NFR4FAS8Z-mge_QFdm2lovaE4Rd-1CnlDOk130_provenance.
- NP206091.RAeG05Fo6ghtOA1sLJLQwtjvSVhO8gHfcVMYIXuhSZooA130_assertion description "[Two additional pregnant women, one with a bromocriptine-treated PRL-secreting adenoma (subject C), and a normal woman (subject D) were studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206091.RAeG05Fo6ghtOA1sLJLQwtjvSVhO8gHfcVMYIXuhSZooA130_provenance.
- NP206096.RAeEdyNyvwmHyf-0JTbvFxS-OIc8KOLM_JdJI5jBH3wN0130_assertion description "[Immunoglobulin heavy chain variable genes (IGHV@) somatic mutations were analysed in five patients with PIOL, one patient with concomitant PCNSL and one patient with systemic DLBCL involving the eye.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206096.RAeEdyNyvwmHyf-0JTbvFxS-OIc8KOLM_JdJI5jBH3wN0130_provenance.
- NP206097.RAQeZMLLyup6dGdbCWx1Y9LT2tukNX8ppfJh0Jwc5D9Gg130_assertion description "[We reported previously that IL-4 induced cell cycle arrest in G1 phase through an increase in p21(WAF1/CIP1) expression in human renal cell carcinoma (RCC) cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206097.RAQeZMLLyup6dGdbCWx1Y9LT2tukNX8ppfJh0Jwc5D9Gg130_provenance.
- NP206099.RAVUbc4Pc4Hs3HNXOpRRGXqRr68pShhlLarCCcaZYQESY130_assertion description "[We examined the methylation profile of 2 CpG islands (I and IV) at the promoters of the brain-derived neurotrophic factor (BDNF) gene, which is well known to be involved in the pathophysiology of depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206099.RAVUbc4Pc4Hs3HNXOpRRGXqRr68pShhlLarCCcaZYQESY130_provenance.
- NP206100.RAU0fgTLIxICnHkE1dFhpA0HBBc9FPAxZuxBEQx9cZuQE130_assertion description "[Our study provides further evidence for an association between null genes for C4A and familial lupus, and suggests, in an unusually large kindred, that several other genetic factors are involved in the production of antinuclear antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206100.RAU0fgTLIxICnHkE1dFhpA0HBBc9FPAxZuxBEQx9cZuQE130_provenance.
- NP206106.RAejDwhLFCkiJj_SYftB_eCrhDasZGHQqB2_ZowkmDUhM130_assertion description "[Recently, mutations in five genes from the pre-replication complex (ORC1, ORC4, ORC6, CDT1, and CDC6), crucial in cell-cycle progression and growth, were identified in individuals with MGS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206106.RAejDwhLFCkiJj_SYftB_eCrhDasZGHQqB2_ZowkmDUhM130_provenance.
- NP206107.RAbhxR80rcp7xQn_NRjJuhhaqCcfCIfYOLAxIQkMLCggw130_assertion description "[In the present study, the BacMam vector, a baculovirus pseudotyped with the glycoprotein from vesicular stomatitis virus, was used as a recombinant vector to express classical swine fever virus (CSFV) E2 protein under the control of the immediate early 1 (ie1) promoter from shrimp white spot syndrome virus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206107.RAbhxR80rcp7xQn_NRjJuhhaqCcfCIfYOLAxIQkMLCggw130_provenance.
- NP206114.RAaPZ66w7JHUC9nHgCGX8_shH9Xxb4ImwUKwC81EfhKPI130_assertion description "[Eight patients with CFI mutations carried at least one additional known genetic risk factor for aHUS, such as a mutation in MCP, CFH, C3 or CFB; a compound heterozygous second mutation in CFI; or mutations in both the MCP and CFH genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206114.RAaPZ66w7JHUC9nHgCGX8_shH9Xxb4ImwUKwC81EfhKPI130_provenance.
- NP206116.RAWX0mndQgze2D7A15dcrhyUN0f7UTvokneEiNY-QAU-8130_assertion description "[p-AKT expression was significantly associated with longer colorectal cancer-specific survival in Kaplan-Meier analysis (log-rank P = .0005), univariate Cox regression (HR, 0.62; 95% CI, 0.47-0.82; P = .0006) and multivariate analysis (adjusted HR, 0.75; 95% CI, 0.56-0.99; P = .048) adjusting for clinical and molecular variables including PIK3CA, MSI, CIMP and LINE-1 hypomethylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206116.RAWX0mndQgze2D7A15dcrhyUN0f7UTvokneEiNY-QAU-8130_provenance.
- NP206117.RAVc35t34EWwbUl0gd-vtyjGaUaUrdf3gILnRE57SATMs130_assertion description "[Therefore, PON-1 (or G3C9) administration may be clinically beneficial for CD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206117.RAVc35t34EWwbUl0gd-vtyjGaUaUrdf3gILnRE57SATMs130_provenance.
- NP206118.RAUrEewqsNmDu06iVGGPlCSllFB8avids4mgGtxdBzKO8130_assertion description "[Suppression of GLUT 4 mRNA is observed in patients with impaired glucose tolerance, and therefore, may occur early in the evolution of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206118.RAUrEewqsNmDu06iVGGPlCSllFB8avids4mgGtxdBzKO8130_provenance.
- NP206121.RAda31DNW8g2B9j9ve_FV3vu-FA_hhCtULNsl4aLGrw1g130_assertion description "[Lower caspase-14 expression was associated with advanced clinical stage in ovarian cancer (P = 0.04, ANOVA) and with shorter overall survival among ovarian cancer patients with serous tumors (n = 62) in both univariate (P = 0.005) and multivariate (P = 0.03) analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206121.RAda31DNW8g2B9j9ve_FV3vu-FA_hhCtULNsl4aLGrw1g130_provenance.
- NP206125.RAQa0VIsDONR8lvOnzO-8e5-pJf_PHeVtVPB58UOhBj3g130_assertion description "[In vivo, tumor growth inhibition, (18)F-fluoro-deoxy-glucose positron emission tomography (FDG-PET), and proton nuclear magnetic resonance were carried out to evaluate the growth inhibitory and metabolic responses, respectively, in CRC xenografts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206125.RAQa0VIsDONR8lvOnzO-8e5-pJf_PHeVtVPB58UOhBj3g130_provenance.
- NP206126.RAfdPpGI2-91ZEjXIp5D0dkF5nV2cs6Ccz03hIxG9n-Ks130_assertion description "[Our previous work suggested that loss of FMRP-mediated regulation of protein expression and enzymatic function of the PI3K catalytic subunit p110β contributes to dysregulated protein synthesis in a mouse model of FXS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206126.RAfdPpGI2-91ZEjXIp5D0dkF5nV2cs6Ccz03hIxG9n-Ks130_provenance.
- NP206129.RAUTZV8Omoz7cKW4tZxVDU2HsIKmlWitLbpTGJ5Fc7m4w130_assertion description "[The present data suggest a novel mechanism in the regulation of ETAR expression in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206129.RAUTZV8Omoz7cKW4tZxVDU2HsIKmlWitLbpTGJ5Fc7m4w130_provenance.
- NP206132.RASK33hA57pGVdlgqHXWlbskYtgcrHYmM6T5m_KpxaM7k130_assertion description "[Although some investigators have shown that mutant PS1 processing is unaltered (with the exception of PS1-deltaE9, which lacks the cleavage site) in stably transfected cells and PS1-FAD transgenic mice, other investigators have reported altered FAD mutant PS1 and PS2 protein processing in transiently transfected cells and human FAD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206132.RASK33hA57pGVdlgqHXWlbskYtgcrHYmM6T5m_KpxaM7k130_provenance.
- NP206133.RAeTGXQg3QbZvJFRvv3Odj9FIqokC5OrGRV56Ts9KW6lA130_assertion description "[Expression of the chemokine receptor CXCR4 by cancers has been shown to correlate with tumor aggressiveness and poor prognosis and may also contribute to metastatic seeding of organs that express its ligand SDF-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206133.RAeTGXQg3QbZvJFRvv3Odj9FIqokC5OrGRV56Ts9KW6lA130_provenance.
- NP206134.RAZ7Map5C_2BIcGXoOs6SjVhAnZwA8eGaVQ_gWcY_P41s130_assertion description "[KIR1D/KIR1D was found in association with susceptibility to syphilis in the Chinese Han population that belongs to KIR gene haplotype A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206134.RAZ7Map5C_2BIcGXoOs6SjVhAnZwA8eGaVQ_gWcY_P41s130_provenance.
- NP206138.RAUk2cFi4qgO91bRkIGhuSIfE-ZuwHFR8nRErVoW59r9Q130_assertion description "[Whereas all normal tissues and benign lesions were positive for beta2-m and HLA-A, -B, and -C antigens, total loss of HLA class I antigens was found in 37% (11 of 30) of in situ carcinomas, in 43% (56 of 131) of the primary tumors, and in 70% (31 of 45) of the lymph node metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206138.RAUk2cFi4qgO91bRkIGhuSIfE-ZuwHFR8nRErVoW59r9Q130_provenance.
- NP206141.RAWpFPoLHbeiyYEeSusHLHsskMAzc_PEnLgsymVUTTCp8130_assertion description "[Congenital hypertrichosis terminalis and AFA have been previously reported as independent autosomal dominant traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206141.RAWpFPoLHbeiyYEeSusHLHsskMAzc_PEnLgsymVUTTCp8130_provenance.
- NP206146.RAdnXpJEnZ7wFMy4P-dJ80k3Q-s1cpVzl40CSV-KXqig8130_assertion description "[Breast cancer treatment outcome with adjuvant tamoxifen relative to patient Cyp2D6 and Cyp2c19 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206146.RAdnXpJEnZ7wFMy4P-dJ80k3Q-s1cpVzl40CSV-KXqig8130_provenance.
- NP206148.RAZjdOp8kxLbZHOwkPePouSYlBlOKyTcnm91y3Bnk3rRA130_assertion description "[Mutations in four members of the connexin gene family have been shown to underlie distinct genetic forms of deafness, including GJB2 [connexin 26 (Cx26)], GJB3 (Cx31), GJB6 (Cx30) and GJB1 (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206148.RAZjdOp8kxLbZHOwkPePouSYlBlOKyTcnm91y3Bnk3rRA130_provenance.
- NP206152.RAa-ZFuB-fpnnjXmjRDlZKs0YNkPzXBJSjAfC2G5Zbqzg130_assertion description "[An elevated frequency of CAs was observed in individuals with the XPD exon 23 A allele (AA and AC) genotypes (F = 3.6, P = 0.028, ANOVA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206152.RAa-ZFuB-fpnnjXmjRDlZKs0YNkPzXBJSjAfC2G5Zbqzg130_provenance.
- NP206159.RAYKUH0TaghIDzMlU6tf9sQEqxREgZ4gyROIwrSsHgn8o130_assertion description "[We investigated p43-placental isoferritin expression at the maternal fetal tissue interface and in fetal kidneys in Down's syndrome (DS) compared with normal control samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206159.RAYKUH0TaghIDzMlU6tf9sQEqxREgZ4gyROIwrSsHgn8o130_provenance.
- NP206161.RAQhwpnUgNpLcsGXkYnA2SbSz_g-D4ULimBs8bF47X83Q130_assertion description "[C35 was reported to be a new biomarker and therapeutic target for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206161.RAQhwpnUgNpLcsGXkYnA2SbSz_g-D4ULimBs8bF47X83Q130_provenance.
- NP206163.RAZyXkr1tmdha9IItlcOthCePClTVZW7_gzUWMNDt3HHI130_assertion description "[Expression of dynamin 1 and Synapsin 1, key pre-synaptic proteins associated with synaptic transmission, which are typically decreased in brains of AD patients, were considerably enhanced in the brains of AD mice treated with BM-MSCs and this response was sustained beyond 2 months.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206163.RAZyXkr1tmdha9IItlcOthCePClTVZW7_gzUWMNDt3HHI130_provenance.
- NP206171.RAXPhHIUKlvfe08HK3QUZS1qKaBzsLvwIU3_FQF3QrDnI130_assertion description "[In the present study, a series of ten homotypic (consisting of blastemal, epithelial, and stromal elements) and ten heterotypic (consisting of triphasic histology and a muscle component) Wilms' tumour cases were examined for expression of HGF and met, using in situ hybridization, immunohistochemistry, and western blot analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206171.RAXPhHIUKlvfe08HK3QUZS1qKaBzsLvwIU3_FQF3QrDnI130_provenance.
- NP206175.RAbYWPlDTDNNrjCRpaktFRveWUNo-AgxnjLTlIlVOJ84U130_assertion description "[The gene defective in X-linked agammaglobulinemia (XLA) has recently been isolated and identified as btk, a non-receptor protein tyrosine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206175.RAbYWPlDTDNNrjCRpaktFRveWUNo-AgxnjLTlIlVOJ84U130_provenance.
- NP206176.RAVH0s7EH8JyYrD00E6mKda-SnH3wVUHCpXjTA-HkfbgM130_assertion description "[Both DCM-associated mutations result in amino acid substitutions of highly conserved residues in helices contributing to the flavin-adenine dinucleotide (FAD)-binding domain of TXNRD2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206176.RAVH0s7EH8JyYrD00E6mKda-SnH3wVUHCpXjTA-HkfbgM130_provenance.
- NP206179.RAXu6etJTkiFZNtpJFI-L1htFnF3E93s7BJm9GIy49go0130_assertion description "[The C allele of -399 T/C polymorphism in the promoter regions of NPY is an independent risk factor for ischemic stroke, suggesting that NYP system may involve in the mechanisms of stroke pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206179.RAXu6etJTkiFZNtpJFI-L1htFnF3E93s7BJm9GIy49go0130_provenance.
- NP206182.RAZnlxu5tOyYUm_HJzWrEo1bNE_MwvBT64xodr4DAj6Hc130_assertion description "[Aside from its potent vasodilatory action, PGI2 contributed critically to the development of renovascular hypertension via the activation of the renin-angiotensin-aldosterone system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206182.RAZnlxu5tOyYUm_HJzWrEo1bNE_MwvBT64xodr4DAj6Hc130_provenance.
- NP206184.RAZ3U56pXEONP2kgkJNai75R3rxiiDhML6hgSxHaYOEOU130_assertion description "[The target of B19 parvovirus infection is the human erythroid progenitor cell.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206184.RAZ3U56pXEONP2kgkJNai75R3rxiiDhML6hgSxHaYOEOU130_provenance.
- NP206194.RAUHLQsit1rhvwx5FqZCWhP9nXwDo8fsGF442yD2rsmds130_assertion description "[In SCA17 patients, one patient presented ataxia, the other seven patients showed parkinsonism (three PD and four MSA-P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206194.RAUHLQsit1rhvwx5FqZCWhP9nXwDo8fsGF442yD2rsmds130_provenance.
- NP206196.RAZCTLtFmMj_w-YhR-AHUB-_Ve7OxbxG-KVVot2lCdrHo130_assertion description "[Patients with the dystonia plus syndrome DYT5 display levodopa-responsive dystonia sometimes associated with tremor or parkinsonism (DYT5a, mutations in GCH1); a more severe phenotype with psychomotor involvement can be seen in recessive forms (DYT5b with TH mutations, SPR-deficiency syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206196.RAZCTLtFmMj_w-YhR-AHUB-_Ve7OxbxG-KVVot2lCdrHo130_provenance.
- NP206198.RAQR8ENKCL9dYdlVw6pUN4NzJjXshCib1GD6DRa8sqiI4130_assertion description "[When cells were incubated with 0.1% or 1% FBS, ERK activation was significantly greater in cells from asthmatic subjects (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206198.RAQR8ENKCL9dYdlVw6pUN4NzJjXshCib1GD6DRa8sqiI4130_provenance.
- NP206205.RAfFVX1rKhLtwrPUQMfPU0U_bBqhl7Gf4D3M2UJiXHfJw130_assertion description "[The IGF-I gene was expressed at high levels in normal myometrium and in leiomyomas but appears to be repressed in leiomyosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206205.RAfFVX1rKhLtwrPUQMfPU0U_bBqhl7Gf4D3M2UJiXHfJw130_provenance.
- NP206208.RAe5tMpNUKwnzfflUC4MHLfwial5whh_1kS2JdMW4zBco130_assertion description "[Imbalanced distribution of Plasmodium falciparum MSP-1 genotypes related to sickle-cell trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206208.RAe5tMpNUKwnzfflUC4MHLfwial5whh_1kS2JdMW4zBco130_provenance.
- NP206214.RAY-rueF06fB8c2IPHmLLDF9OstV7p5NuW2sdBWSU8xhA130_assertion description "[Twenty-four normal-functioning elderly individuals participated in the study, with 16 subjects exhibiting no change in their Dementia Rating Scale (DRS) scores over an 1-year period (Stable Group), and 8 subjects exhibiting a decline in DRS scores over the 1-year period (Decline group).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206214.RAY-rueF06fB8c2IPHmLLDF9OstV7p5NuW2sdBWSU8xhA130_provenance.
- NP206219.RAQH6lMCo0M1nfFDjXxzA_EDqaXTx1QzQlcmk-PYxGkhU130_assertion description "[Mucolipidosis type IV (MLIV) is a lysosomal storage disorder caused by mutations in the MCOLN1 gene, a member of the transient receptor potential (TRP) cation channel gene family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206219.RAQH6lMCo0M1nfFDjXxzA_EDqaXTx1QzQlcmk-PYxGkhU130_provenance.
- NP206223.RARxipwAwL9OgeawT3klP8gYRqAnWi3RbWnhSbo9RR53E130_assertion description "[Molecular screening of the PPARGC1 gene in 24 morbidly obese French-Canadians revealed 13 variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206223.RARxipwAwL9OgeawT3klP8gYRqAnWi3RbWnhSbo9RR53E130_provenance.
- NP206227.RAVTOcr0qvISjFFigZdWD1lAe7lvqgGOwmVMVFTyB8MT8130_assertion description "[Multivariable logistic regression analysis with adjustment for age, body mass index, and smoking status revealed that the T-->G (3' UTR) polymorphism of the thrombospondin 2 gene (THBS2), the -603A-->G polymorphism of the coagulation factor III gene (F3), and the G-->T (intron 2) polymorphism of the adipocyte, C1Q, and collagen domain containing (adiponectin) gene (ADIPOQ) were significantly associated with the prevalence of type 2 diabetes mellitus in men, and that the A-->G (Arg160Gly) polymorphism of the paraoxonase 1 gene (PON1) was significantly associated with this condition in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206227.RAVTOcr0qvISjFFigZdWD1lAe7lvqgGOwmVMVFTyB8MT8130_provenance.
- NP206231.RARQRT8UZR2JYugX82PAia0Urja8b1j2GpFvFNhH6yo7I130_assertion description "[Thus, WWOX may be considered as a novel important genetic marker in cervical cancer and the association between the altered expression of FHIT and WWOX may be a critical event in the progression of this neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206231.RARQRT8UZR2JYugX82PAia0Urja8b1j2GpFvFNhH6yo7I130_provenance.
- NP206234.RAaa2Idg91RlrK_FCKqMrdRpkl94urypUtoLcPW7VkaH4130_assertion description "[Giant axonal neuropathy (GAN) is a disorder characterized pathologically by distal neurofilament-filled bulbous swellings in axons, and widespread collection of intermediate filaments, including masses of vimentin filaments in cultured skin fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206234.RAaa2Idg91RlrK_FCKqMrdRpkl94urypUtoLcPW7VkaH4130_provenance.
- NP206240.RAQprbIh63sA07pZ0K9pcsPiHEjadCy3EhVDL8PHZnZb4130_assertion description "[Heterozygous germ line mutations in the Breast CAncer1 (BRCA1) and BRCA2 genes can lead to a high risk of breast and ovarian cancer, in addition to a significantly increased susceptibility of pancreatic, prostate and male breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206240.RAQprbIh63sA07pZ0K9pcsPiHEjadCy3EhVDL8PHZnZb4130_provenance.
- NP206248.RAbN39bVnUnokcTqPE85_WbOaxd2DoY_hOt2TWUeKtn4Y130_assertion description "[Genetic variation in the tumor necrosis factor-alpha promoter region and in the stress protein hsp70-2: susceptibility and prognostic implications in breast carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206248.RAbN39bVnUnokcTqPE85_WbOaxd2DoY_hOt2TWUeKtn4Y130_provenance.
- NP206255.RAepNfLPR9cgwdFBmOCUd4a8_wdjh-9-vwB9JdqW3Ep6Y130_assertion description "[Here, we describe a previously unreported MDS family carrying a missense GATA2 mutation (p.Thr354Met), one patient with MDS/AML carrying a frameshift GATA2 mutation (p.Leu332Thrfs*53), another with MDS harboring a GATA2 splice site mutation, and 3 patients exhibiting MDS or MDS/AML who have large deletions encompassing the GATA2 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206255.RAepNfLPR9cgwdFBmOCUd4a8_wdjh-9-vwB9JdqW3Ep6Y130_provenance.
- NP206257.RAcK2nWj-nzoL9jpqsApNL_6uJQNsxfNdSfEp98p53Jug130_assertion description "[The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the accumulation of autofluorescent lipopigments in the neurons and other cell types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206257.RAcK2nWj-nzoL9jpqsApNL_6uJQNsxfNdSfEp98p53Jug130_provenance.
- NP206263.RAeTIb0b6ibNED3KrPThdI5P34RNfDVS3NE8VHuQltOTg130_assertion description "[The gene expression of cytokines/chemokines in skin biopsies from the CL group showed higher transcript levels of modulatory (IL10 and TGFB1), anti-inflammatory (IL4), and pro-inflammatory (TNF, IFNG, IL12B, CCL2, CCL3, CCL5, CXCL10) biomarkers in recent lesions than in late lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206263.RAeTIb0b6ibNED3KrPThdI5P34RNfDVS3NE8VHuQltOTg130_provenance.
- NP206265.RAcV_Cq7rPu4Ui83oI29yAUQdgEKqgxtAKjX_kmBFSikA130_assertion description "[No significant differences in the allele frequencies and genotype distributions of VEGF -460 C/T (p = 0.54, 0.90), +405 G/C (p = 0.31, 0.17), and +936 C/T polymorphisms (p = 0.46, 0.24) were observed between endometrial carcinoma patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206265.RAcV_Cq7rPu4Ui83oI29yAUQdgEKqgxtAKjX_kmBFSikA130_provenance.
- NP206273.RASWJ1RJcW8Wp5-q2sxb_JK5b2PWwx7wQmqBiwnOZkzy0130_assertion description "[Given as a prophylactic treatment, a single muscle electrogene transfer of plasmid coding canstatin fused to human serum albumin (CanHSA), slowed down the development of two xenografted human carcinomas from mammary (MDA-MB-231) and prostate origin (PC-3) in nude mice and delayed lung metastatic spreading of B16F10 melanoma cells in syngenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206273.RASWJ1RJcW8Wp5-q2sxb_JK5b2PWwx7wQmqBiwnOZkzy0130_provenance.
- NP206291.RAaIcYPNMMnRKz9Pz3yDqE5iFnv66OCpUgYmWeXdYNifk130_assertion description "[We found no association between IL1B -511C/T genotypes and geriatric depression susceptibility (P = 0.213), depression severity (HAM-D scores; P = 0.766) or cognitive function (MMSE scores; P = 0.827); however, compared with depressed subjects carrying the -511C allele, depressed subjects who were -511T homozygotes showed a significantly later depression age of onset of 7 years (P = 0.021).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206291.RAaIcYPNMMnRKz9Pz3yDqE5iFnv66OCpUgYmWeXdYNifk130_provenance.
- NP206293.RAVy9DwPRwXiI0E3F_cUfBdWDDOlSsaJ0NLbjGOF434Po130_assertion description "[Real-time reverse transcription-PCR analysis of pathology-negative ALN (n = 72) confirm that of all the markers tested, mam and TFF1 have the highest apparent sensitivity for detection of micrometastatic breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206293.RAVy9DwPRwXiI0E3F_cUfBdWDDOlSsaJ0NLbjGOF434Po130_provenance.
- NP206299.RATgOUI6tgJPEDueJiD9HM_lH3eqh2L_y1I_xXkIT0rg4130_assertion description "[The VDR FokI polymorphism was not significantly associated with colorectal adenoma and did not modify the effect of vitamin D or calcium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206299.RATgOUI6tgJPEDueJiD9HM_lH3eqh2L_y1I_xXkIT0rg4130_provenance.
- NP206300.RAYQ_fzvNV5pTnxItWUSdv5XSseT-NDje3wMI_nIPqr54130_assertion description "[BCL2L12 is a recently identified gene belonging to the BCL2 family, members of which are implicated in hematologic malignancies, including chronic lymphocytic leukemia (CLL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206300.RAYQ_fzvNV5pTnxItWUSdv5XSseT-NDje3wMI_nIPqr54130_provenance.
- NP206303.RAcH_EJfUkfVpy42S8jRqEz3SZknJfFiM0xEetS8lxRbk130_assertion description "[In this paper, we examine the expression profiles of two new putative pluripotent stem cell genes, the embryo/cancer sequence A gene (ECSA) and the cancer/testis gene Brother Of the Regulator of Imprinted Sites (BORIS), in human oocytes, preimplantation embryos, primordial germ cells (PGCs) and embryo stem (ES) cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206303.RAcH_EJfUkfVpy42S8jRqEz3SZknJfFiM0xEetS8lxRbk130_provenance.
- NP206305.RAaKnw02wl-AOPUykMdIvDsVT70YckjfLpD35ibWY5m1M130_assertion description "[This study revealed the following characteristics of these disorders: 1) subjects with CLCNKB mutations showed one or more biochemical features of Gitelman syndrome (including hypomagnesemia, hypocalciuria, and fractional chloride excretion insensitivity to thiazide administration); and 2) subjects with KCNJ1 mutations appeared to show normal fractional chloride excretion sensitivity to furosemide and thiazide administration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206305.RAaKnw02wl-AOPUykMdIvDsVT70YckjfLpD35ibWY5m1M130_provenance.
- NP206307.RAb0ykViOVOCqeQbxoyCgjOI1E79pWBsMHejBe3JnrN8g130_assertion description "[4-Aminobiphenyl (4-ABP), a potent carcinogen in rodents (liver cancer) and human (bladder cancer), is found as an environmental contaminant and in tobacco smoke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206307.RAb0ykViOVOCqeQbxoyCgjOI1E79pWBsMHejBe3JnrN8g130_provenance.
- NP206308.RAQnmgX5yUxW8wRMeueDFUFaP3jatZfMo5vQRNndHL7zo130_assertion description "[A patient is reported with del11p13, low catalase level, nephroblastoma, chordee and cryptorchidism, no evident mental retardation, and with normal irides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206308.RAQnmgX5yUxW8wRMeueDFUFaP3jatZfMo5vQRNndHL7zo130_provenance.
- NP206309.RAVn7HrSXPGuyhVa5dpF3cVG11pKbbBOqRstb6KYAWwSs130_assertion description "[We conclude that there is no evidence for the TOPBP1*Arg309Cys variant to confer an increased risk for breast cancer in the German population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206309.RAVn7HrSXPGuyhVa5dpF3cVG11pKbbBOqRstb6KYAWwSs130_provenance.
- NP206311.RAbe_NmMgLLVmvR2Cx7Jn7_3ndBK-IBUE3N098nokSV3o130_assertion description "[We describe the role of allelism at the glutathione S-transferase GSTM1, GSTM3, GSTT1 and cytochrome P450 CYP1A1, CYP2E1, CYP2D6 loci in determining individual susceptibility to laryngeal SCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206311.RAbe_NmMgLLVmvR2Cx7Jn7_3ndBK-IBUE3N098nokSV3o130_provenance.
- NP206317.RAQqzFeDTW7zxbv_AhPfhXJVynlYA7mUmWqMjcOGutxjY130_assertion description "[If our observations can be confirmed in larger studies, the findings will provide further evidence to support the role of IGF-I in breast cancer and the link between genetic polymorphism and cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206317.RAQqzFeDTW7zxbv_AhPfhXJVynlYA7mUmWqMjcOGutxjY130_provenance.
- NP206322.RAZ-R-l32pqXSWDFu-Aib-TZoPyrocvKQefNv3twKJxkk130_assertion description "[We took advantage of a cohort of 91 patients with resected NSCLC, for which we had matched frozen and paraffin-embedded samples to explore the comparative molecular portraits of ERCC1-positive and ERCC1-negative tumors of NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206322.RAZ-R-l32pqXSWDFu-Aib-TZoPyrocvKQefNv3twKJxkk130_provenance.
- NP206323.RAaW7Ysjvz_IJaSZ7ad2ipv9uYSLibGQjNSTUa2ep3dlg130_assertion description "[Myxoma virus protein M029 is a dual function immunomodulator that inhibits PKR and also conscripts RHA/DHX9 to promote expanded host tropism and viral replication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206323.RAaW7Ysjvz_IJaSZ7ad2ipv9uYSLibGQjNSTUa2ep3dlg130_provenance.
- NP206333.RAUjijVBN5L1_nf0hIcIFc9z4nSnw5wOrssMJEIHOhL1k130_assertion description "[Two meta-analyses are presented here concerning the association of Plasminogen Activator Inhibitor 1 (PAI-1) 4G/5G polymorphism and the methylene-tetrahydrofolate reductase (MTHFR) C677T polymorphism with the risk of developing PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206333.RAUjijVBN5L1_nf0hIcIFc9z4nSnw5wOrssMJEIHOhL1k130_provenance.
- NP206337.RAQeV-J85R5Q7SSMnH6YqO6JhzuLZ0FjOyME8_w-rMJEA130_assertion description "[Using the approach we have isolated and characterized several non-alpha globin clones from a Kurdish Jew with homozygous beta thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206337.RAQeV-J85R5Q7SSMnH6YqO6JhzuLZ0FjOyME8_w-rMJEA130_provenance.
- NP206341.RAblMBL0OpdKlfoC-Alq7rDQyiLFlg3pp7BXQiFYHYpg0130_assertion description "[Mutations have been described in the genes encoding Fc gamma RI, interleukin-2 and natural resistance associated macrophage protein, which are all candidate genes for susceptibility loci associated with autoimmune diabetes in non-obese diabetic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206341.RAblMBL0OpdKlfoC-Alq7rDQyiLFlg3pp7BXQiFYHYpg0130_provenance.
- NP206342.RAa8We57u2Vwv0cfW4MQUVaRiHJGTCul-wF5H4fSu_hvo130_assertion description "[The sensitivity, specificity, PPV and NPV of DNA hybrid capture HPV testing for detecting high-grade cervical intraepithelial neoplasia (CIN) were 86%, 44%, 26% and 93%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206342.RAa8We57u2Vwv0cfW4MQUVaRiHJGTCul-wF5H4fSu_hvo130_provenance.
- NP206344.RAZNmnjr9Roq4uVi-6wR81OSlKpSIhm6LjP9PgPqcAIAY130_assertion description "[We evaluated 36 tag SNPs across CD36 in the HyperGen population sample of 2020 African-Americans for impact on the MetS and its quantitative traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206344.RAZNmnjr9Roq4uVi-6wR81OSlKpSIhm6LjP9PgPqcAIAY130_provenance.
- NP206352.RASOrLZjU5DJT9r2Ru8Ohy1ut5Al03I1sGijA-v6ycUsE130_assertion description "[Sequence variation in the putative large surface glycoprotein (E2/NS1) of hepatitis C virus (HCV) was analyzed over 18 months in 4 patients with chronic relapsing non-A, non-B liver disease, of whom 2 were treated with lymphoblastoid interferon-alpha.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206352.RASOrLZjU5DJT9r2Ru8Ohy1ut5Al03I1sGijA-v6ycUsE130_provenance.
- NP206353.RAdkYxbRSQUGs4e5IeIl2vccKYVDkGARsqs8grkHE0Vt8130_assertion description "[Lack of GPI anchor expression due to mutations can cause an acquired clonal hematologic disorder called paroxysmal nocturnal hemoglobinuria (PNH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206353.RAdkYxbRSQUGs4e5IeIl2vccKYVDkGARsqs8grkHE0Vt8130_provenance.