Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP184247.RAa00iyLsKJYbrYY9jpUyeiHhblX3hH73mqQjtb7JvF18130_assertion description "[Axl belongs to the TAM (Tyro3, Axl, and Mer) receptor tyrosine kinase family, whose members function as inhibitors of innate inflammatory responses in dendritic cells and are essential to the prevention of lupus-like autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184247.RAa00iyLsKJYbrYY9jpUyeiHhblX3hH73mqQjtb7JvF18130_provenance.
- NP184248.RAZkPg17kfI77DKr8SWILhg3HrotFXbGmSuCFzYDk6PI8130_assertion description "[Recently, two missense mutations (N88S, S90L) in the Berardinelli-Seip congenital lipodystrophy gene have been identified in autosomal dominant distal hereditary motor neuropathy and Silver syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184248.RAZkPg17kfI77DKr8SWILhg3HrotFXbGmSuCFzYDk6PI8130_provenance.
- NP184250.RASw9dhO6p1R0ViuPSVCfYJGLkiFJLm4_0A3HCXaWyJyc130_assertion description "[Deficiency of dCK is associated with resistance against this compound both in vitro in cancer cell lines and in clinical practice in acute myeloid leukemia and solid tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184250.RASw9dhO6p1R0ViuPSVCfYJGLkiFJLm4_0A3HCXaWyJyc130_provenance.
- NP184258.RARM8el15Px8_u014MID3eWr1I7hdW9bwagYm4Xg-H8FY130_assertion description "[Only in rare cases has RTSH been attributed to TSHR or PAX8 gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184258.RARM8el15Px8_u014MID3eWr1I7hdW9bwagYm4Xg-H8FY130_provenance.
- NP184261.RAV1trq5AvN2c-0nB7wLxbLSW63KNsFZeiACFbctf5Ihc130_assertion description "[High mobility group box 1 (HMGB1) is a NF released extracellularly as a late mediator of lethality in sepsis and as an early mediator of inflammation following injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184261.RAV1trq5AvN2c-0nB7wLxbLSW63KNsFZeiACFbctf5Ihc130_provenance.
- NP184262.RATbezQb_9V8a2TJrGZiqd9wkKP0qZKfs7Lx_UeBKsVcM130_assertion description "[SDF-1 engineered to be resistant to dipeptidylpeptidase IV/CD26 and matrix metalloproteinase-2 cleavage and delivered by nanofibers improves blood flow in a model of peripheral artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184262.RATbezQb_9V8a2TJrGZiqd9wkKP0qZKfs7Lx_UeBKsVcM130_provenance.
- NP184264.RAfsgunvM_ytPW2cTAHHe_t-bvQ3IGF8g0pIE0J6iT5S8130_assertion description "[Statistically significant results found for the various QTs and SNPs were: rs3774933, rs230528, rs230521, rs1005819 and rs1609798 (intronic, NFKB1) with APOB; rs5361 (Missense, R greatr than S, SELE) and rs4648004 (Intronic, NFKB1) with FBG; rs4220 (Missense, K greater than R, FGB) with HCY; and rs3025035 (Intronic, VEGFA) with CHOL-H. SNPs in SELE, VEGFA, FGB and NFKB1 genes impact significantly on levels of quantitative precursors of CAD in Marwaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184264.RAfsgunvM_ytPW2cTAHHe_t-bvQ3IGF8g0pIE0J6iT5S8130_provenance.
- NP184267.RARPKa7aeamTqt2HIITYENPAySbOl2uORVpFaxYTsT3SU130_assertion description "[miR155 and BIC, its host gene, have been reported to accumulate in human B cell lymphomas, especially in diffuse large B cell lymphomas, Hodgkin lymphomas, and certain types of Burkitt lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184267.RARPKa7aeamTqt2HIITYENPAySbOl2uORVpFaxYTsT3SU130_provenance.
- NP184268.RAek6Xz9rxPXKFvQOf70SZB_DLA8tI9ySBEJfXrLg6g58130_assertion description "[We have previously identified A20-binding inhibitor of NF-kappaB activation (ABIN)-3 as an lipopolysaccharide (LPS)-inducible protein in monocytes that negatively regulates NF-B activation in response to tumour necrosis factor (TNF) and LPS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184268.RAek6Xz9rxPXKFvQOf70SZB_DLA8tI9ySBEJfXrLg6g58130_provenance.
- NP184271.RAcpZ3Ok2r-Kuh-IL_2VnqLs0ZYOurtBcE1VFR364mR4s130_assertion description "[An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184271.RAcpZ3Ok2r-Kuh-IL_2VnqLs0ZYOurtBcE1VFR364mR4s130_provenance.
- NP184275.RAf2MxGjUxOoS-_NEAghCa5YidetHUkb2QhjJCltNWrhY130_assertion description "[To analyze the frequency of mutations associated with Parkinson's disease (PD) in a general PD population compared to patients with PD selected for deep brain stimulation (DBS) and evaluate the outcome of surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184275.RAf2MxGjUxOoS-_NEAghCa5YidetHUkb2QhjJCltNWrhY130_provenance.
- NP184283.RAaj1sDlkg-yeSdQHNdIyhcCfU7g8T2KZwDiKxVgDrSqo130_assertion description "[The proportion of Treg cells and the transcription factor forkhead box P3 (FOXP3) mRNA expression in PBMCs decreased in GD patients compared with healthy subjects, and Treg cell function was impaired in patients with GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184283.RAaj1sDlkg-yeSdQHNdIyhcCfU7g8T2KZwDiKxVgDrSqo130_provenance.
- NP184284.RAU_5UodlJWqJkl1xCc6Ng8gaQAeTyzzlWVJDoAAzvQpo130_assertion description "[Since the end of the 1980s augmentation therapy with alpha-1 antitrypsin (AAT) from human plasma has been available for specific treatment of emphysema due to AAT deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184284.RAU_5UodlJWqJkl1xCc6Ng8gaQAeTyzzlWVJDoAAzvQpo130_provenance.
- NP184292.RAatODO9seyf0dp954ypPFOd8Sb9TxG6-6Q995ANX4-rU130_assertion description "[Homozygotes of type Z have a severe reduction in the serum AT concentration and may develop pulmonary emphysema or hepatic cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184292.RAatODO9seyf0dp954ypPFOd8Sb9TxG6-6Q995ANX4-rU130_provenance.
- NP184293.RAdjvI-j6kfUO3oLE5X2Bc4w2xyZrUXQqb7EV4l4doNnE130_assertion description "[We investigated the occurrence and the prevalence of GATA4, NKX2.5, ZFPM2/FOG2, GDF1, and ISLET1 gene mutations in a large cohort of individuals with CTD, including tetralogy of Fallot with or without pulmonary atresia (TOF, 178 patients), double outlet right ventricle (DORV, 13 patients), and truncus arteriosus (11 patients).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184293.RAdjvI-j6kfUO3oLE5X2Bc4w2xyZrUXQqb7EV4l4doNnE130_provenance.
- NP184300.RAbgofGMlYbn6T1vgKWl7whJMmEhm8Ir8SI43eebxCv20130_assertion description "[Of the four genetic polymorphisms examined, NK2R G231E G>A and TBX21 H33Q C>G were significantly associated with asthma control status (P = 0.041 and P = 0.006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184300.RAbgofGMlYbn6T1vgKWl7whJMmEhm8Ir8SI43eebxCv20130_provenance.
- NP184307.RAS9LMFsFJWOuEJ6IcbQXOG3_hOBc3cz37ml7d8TpB2X8130_assertion description "[In a blinded study, we analyzed 57 thin-layer slides that had been rigorously screened and classified as normal (n = 13), atypical squamous cells (ASC, n = 5), low-grade squamous intraepithelial lesions (LSIL, n = 14), and high-grade squamous intraepithelial lesions (HSIL) grade 2 (CIN2, n = 8), and grade 3 (CIN3, n = 17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184307.RAS9LMFsFJWOuEJ6IcbQXOG3_hOBc3cz37ml7d8TpB2X8130_provenance.
- NP184309.RAY8dKrF8L7yHAQZKKJgC9FsD6NfKyvtkBKhxrTmzqeJg130_assertion description "[Polymorphism in the methylenetetrahydrofolate reductase (C677T) gene and homocysteine levels: a comparison in Brazilian patients with coronary arterial disease, ischemic stroke and peripheral arterial obstructive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184309.RAY8dKrF8L7yHAQZKKJgC9FsD6NfKyvtkBKhxrTmzqeJg130_provenance.
- NP184310.RAb6-twmU6uWcvJOj7IwqNj9-vLW2tHNalFYLeYydnAII130_assertion description "[In both these disorders, the mitochondrial abnormality is secondary to the primary nuclear mutation:CAG repeat in the huntingtin gene in HD, and GAA repeat in the frataxin gene in FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184310.RAb6-twmU6uWcvJOj7IwqNj9-vLW2tHNalFYLeYydnAII130_provenance.
- NP184319.RAd9EbommkKmdFueWA2EZ8qPgvBTtChosgx6Qr2RSoIIs130_assertion description "[Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184319.RAd9EbommkKmdFueWA2EZ8qPgvBTtChosgx6Qr2RSoIIs130_provenance.
- NP184320.RAfYVtOTBeqnvuM_M3dfv1HxIqkUHF4-eYYVO0p78QP_A130_assertion description "[The inhibin alpha subunit/GAPDH mRNA ratio, but not that of betaA subunit/GAPDH mRNA, was significantly greater (P < 0.01, ANOVA) in placental tissue from Down syndrome than in control placental tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184320.RAfYVtOTBeqnvuM_M3dfv1HxIqkUHF4-eYYVO0p78QP_A130_provenance.
- NP184323.RAbHdaA2r_qh0P68gRMY9dJ6AicJGnLVc1sbhxFNes4cw130_assertion description "[Although R5+X4 tropism was associated with advanced immunodeficiency, all 4 subjects with acquired immunodeficiency syndrome dementia complex had R5 tropism in CSF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184323.RAbHdaA2r_qh0P68gRMY9dJ6AicJGnLVc1sbhxFNes4cw130_provenance.
- NP184324.RAZWVVOqeW5v5_J-1ajeRXdng3nHEcfJKLSQzU_4h4KCM130_assertion description "[The prognosis for patients with lung cancer with low FHIT/GAPDH levels (< 0.26; n = 57) was significantly worse than in the patients with high FHIT/GAPDH levels (> 0.26; n = 40; log-rank test, P = 0.0404).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184324.RAZWVVOqeW5v5_J-1ajeRXdng3nHEcfJKLSQzU_4h4KCM130_provenance.
- NP184325.RASD6tfIFXvWLaHfRIXCYLWBUpo5ojTOfok0k_VUYbopk130_assertion description "[These findings provide important insights into the pathogenesis of colitis-associated cancer and suggest that epidermal growth factor-based therapies for IBD may reduce long-term cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184325.RASD6tfIFXvWLaHfRIXCYLWBUpo5ojTOfok0k_VUYbopk130_provenance.
- NP184329.RAfaFUupgfeQUSCdu-lABY-P3iFLzY9GDxg-N0ZZ2J9OI130_assertion description "[These studies have shown that three RHC alleles - Arg151Cys, Arg160Trp and Asp294His - were associated with increased risk in all forms of skin cancer and with penetrance and age of onset in familial melanoma in mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184329.RAfaFUupgfeQUSCdu-lABY-P3iFLzY9GDxg-N0ZZ2J9OI130_provenance.
- NP184338.RAU8kq9PO4CUo6fsFmeCYPaPnqccn33HFBKSmJJeU3d0k130_assertion description "[According to this evidence, achalasia has been significantly associated with specific alleles of the human leukocyte antigen class II, PTPN22 and IL23R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184338.RAU8kq9PO4CUo6fsFmeCYPaPnqccn33HFBKSmJJeU3d0k130_provenance.
- NP184345.RAQQpzhMp-sSGWszzAwnujgDCyEifdT5TLKl4oArM78CM130_assertion description "[Many B27-negative individuals in India have developed SSA with severe clinical and radiological findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184345.RAQQpzhMp-sSGWszzAwnujgDCyEifdT5TLKl4oArM78CM130_provenance.
- NP184353.RAYCJXl1crKTCSyI5g-tIekHTHbe5vdMrQMK6JEyJJnmg130_assertion description "[Thus, exploration of the molecular pathogenesis underlying EVI1-related leukemogenesis provides insight into how shared stemness transcriptional programs contribute to leukemia progression and therapeutic resistance in AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184353.RAYCJXl1crKTCSyI5g-tIekHTHbe5vdMrQMK6JEyJJnmg130_provenance.
- NP184360.RAQIjNC7e0KrCCb-ZsGEypxdZ1zZ9mJCXnDn7jXAOPRx8130_assertion description "[Hence, recombinant fusion protein comprising C-terminus of mHSP70 genetically fused to four tandem repeats of the ectodomain of the conserved influenza matrix protein M2 (M2e) was expressed in Escherichia coli, purified under denaturing condition, refolding, and then confirmed by SDS-PAGE, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184360.RAQIjNC7e0KrCCb-ZsGEypxdZ1zZ9mJCXnDn7jXAOPRx8130_provenance.
- NP184369.RAdedSaR6HsaSIBs0Uk-HJLULRpgmdWbmtd0BM_UqJiOI130_assertion description "[HBV-positive sera double reactive for myosin or caldesmon and their homologous HBV-pol peptides also reacted with the native proteins on immunoblot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184369.RAdedSaR6HsaSIBs0Uk-HJLULRpgmdWbmtd0BM_UqJiOI130_provenance.
- NP184370.RAcqOXME15V-ltH7rHBHsxfJZfdR7UHssGGw1qQCs4OlY130_assertion description "[PCP-induced psychosis has been a useful disease model in that both the positive as well as the negative symptomatologies seen in schizophrenia are observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184370.RAcqOXME15V-ltH7rHBHsxfJZfdR7UHssGGw1qQCs4OlY130_provenance.
- NP184379.RARvdy419FglPgJCtriebNZkmcch9mj6Z83IyGF2lhoqM130_assertion description "[We identified the underlying cause to be a hitherto unreported de novo missense mutation in the LMNA gene (S143F) encoding the nuclear envelope proteins lamins A and C. Although LMNA mutations have been known to cause Hutchinson-Gilford progeria syndrome and Emery-Dreifuss muscular dystrophy, this is the first report of a patient combining features of these two phenotypes because of a single mutation in LMNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184379.RARvdy419FglPgJCtriebNZkmcch9mj6Z83IyGF2lhoqM130_provenance.
- NP184389.RAfvyjVHcUcHKG-JsfeM0ThFsdmybJN0tShwDBKHTGEEM130_assertion description "[In this study, we examined SFRP1, SFRP2, SFRP4, and SFRP5 promoter methylation in 83 patients with AML (59 children and 24 adults) and found preferential SFRP1 methylation and mRNA down-regulation in the prognostically favorable subgroup of AML with t(8;21) translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184389.RAfvyjVHcUcHKG-JsfeM0ThFsdmybJN0tShwDBKHTGEEM130_provenance.
- NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion description "[Estimating carrier risks for female relatives of Duchenne (DMD) and Becker (BMD) dystrophy sufferers depends upon calculation of segregational risks, supplemented by enzyme tests which show considerable overlap between carrier and control data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance.
- NP184391.RATQxJNwFPculGs8qarVh7Z2Po2Z_oMEfjCwc2Mry_jsI130_assertion description "[EAM-mediated delivery of the beta subunit of cyclic GMP phosphodiesterase (PDE) cDNA to mice affected with retinal degeneration (rd) allows prolonged transgene expression and rescue of rod photoreceptor cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184391.RATQxJNwFPculGs8qarVh7Z2Po2Z_oMEfjCwc2Mry_jsI130_provenance.
- NP184393.RAZtkUMjyWKGNjQwuYWf_Z1mGmzIsV2_b018X8_BYC-YQ130_assertion description "[Two TLR10-TLR1-TLR6 variants in moderate linkage disequilibrium were significantly associated with NHL: rs10008492 [odds ratio for CT genotype (OR(CT)) 1.12, 95% confidence interval (CI) 0.97-1.30; OR(TT) 1.40, 95% CI 1.15-1.71; P(trend) = 0.001] and rs4833103 (OR(AC) 0.75, 95% CI 0.64-0.88; OR(AA) 0.74, 95% CI 0.62-0.90; P(trend) = 0.002; P(dominant) = 0.0002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184393.RAZtkUMjyWKGNjQwuYWf_Z1mGmzIsV2_b018X8_BYC-YQ130_provenance.
- NP184394.RAWdfJYxbywLZPR96WxEBHerb1PDp0MvkSDCndBhJ4N8s130_assertion description "[There were no patients with deficiency of protein C or protein S. Four had resistance to activated protein C (APC) and one had APC resistance associated with antithrombin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184394.RAWdfJYxbywLZPR96WxEBHerb1PDp0MvkSDCndBhJ4N8s130_provenance.
- NP184398.RATEE1nQYE_mUxkNDyBVv_cBEgq5VGjvWwSRxoi93tcZo130_assertion description "[The immune-dominant antigen leading to severe FNAIT is the human PLT antigen (HPA)-1, whose polymorphism constitutes an epitope for human leukocyte antigens (HLAs), usually DRB3*0101 leading to an immune response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184398.RATEE1nQYE_mUxkNDyBVv_cBEgq5VGjvWwSRxoi93tcZo130_provenance.
- NP184399.RAdnifwCmWzB-cri1Jk0r-w9KF5oWc02kEkXMQZBs9WqQ130_assertion description "[For the first time, our results indicate a role of allelic variation of the 5-HT1A receptor in motion related discomfort in migraineurs and a role of the 5-HT1B receptor polymorphism in headache intensity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184399.RAdnifwCmWzB-cri1Jk0r-w9KF5oWc02kEkXMQZBs9WqQ130_provenance.
- NP184400.RAV71AXlwt5PI3To5BgnLVu54UA0vefBeSYcbzObISvBU130_assertion description "[Therefore, dysregulated expression of IGF-IR and/or Sp1 may contribute to the growth and metastasis of gastric cancer and potentially can be a target of therapeutic intervention.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184400.RAV71AXlwt5PI3To5BgnLVu54UA0vefBeSYcbzObISvBU130_provenance.
- NP184403.RAZzzo9iYRT3-mSJLqFy7zpUn1rpK8M4x7LVQ-bZkExEA130_assertion description "[Our results suggest that gene therapy based on restoration of wild type p53 protein function in pancreatic tumor cells with high amount of mutant p53 is a feasible option in pancreatic cancer treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184403.RAZzzo9iYRT3-mSJLqFy7zpUn1rpK8M4x7LVQ-bZkExEA130_provenance.
- NP184404.RAfbaBITfheHIpWilLHLpz9lyuQgs5QIGD42TtvJMxhOc130_assertion description "[Expression of the interferon-inducible chemokine IP-10 (CXCL10), a chemokine with proposed anti-neoplastic functions, in Hodgkin lymphoma and nasopharyngeal carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184404.RAfbaBITfheHIpWilLHLpz9lyuQgs5QIGD42TtvJMxhOc130_provenance.
- NP184409.RAcdk269tcJeDcTthiHBVK47oPznZqxyT_8LmyO4tDNiA130_assertion description "[Colon carcinogenesis is associated with increased expression levels of Toll-like receptor 2 and Toll-like receptor 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184409.RAcdk269tcJeDcTthiHBVK47oPznZqxyT_8LmyO4tDNiA130_provenance.
- NP184410.RATxX5YLm_cIwvV3dKPs8ULRbchr34kOmIVZ2HGkgjZUk130_assertion description "[Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184410.RATxX5YLm_cIwvV3dKPs8ULRbchr34kOmIVZ2HGkgjZUk130_provenance.
- NP184412.RAWNpNMd0N5d_iXVmpZ1mW8z0RbH6oi1oj3vKI-TE4Nj0130_assertion description "[Murine tumors show enrichment of the TGF-β/SMAD4 network, and genetic validation studies confirmed the cooperative roles of Pten, p53, and Smad4 deficiencies in prostate cancer progression, including skeletal metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184412.RAWNpNMd0N5d_iXVmpZ1mW8z0RbH6oi1oj3vKI-TE4Nj0130_provenance.
- NP184413.RAcyvu86varTTNVJtTTRgsSvSmDt61L04X9dowGZhsYuE130_assertion description "[Hypermethylation of let-7a-3 in epithelial ovarian cancer is associated with low insulin-like growth factor-II expression and favorable prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184413.RAcyvu86varTTNVJtTTRgsSvSmDt61L04X9dowGZhsYuE130_provenance.
- NP184415.RAWzZKLnT9pe4WDGp7rxmtM3WZqVcKqwcAA0eZeMBvzH0130_assertion description "[Thirty primary tumors (42%) were positive for K-ras mutations, and in 5 of these cases the SLN were positive for metastases by Hematoxylin and Eosin staining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184415.RAWzZKLnT9pe4WDGp7rxmtM3WZqVcKqwcAA0eZeMBvzH0130_provenance.
- NP184416.RAXhfk6vHrtisK5QlXDMCa-SLq3F1cF8cYXm3RL3IRtF0130_assertion description "[Our observations indicate that expression of human MPO in macrophages promotes atherosclerosis in hypercholesterolemic mice, raising the possibility that the enzyme might be a potential therapeutic target for preventing cardiovascular disease in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184416.RAXhfk6vHrtisK5QlXDMCa-SLq3F1cF8cYXm3RL3IRtF0130_provenance.
- NP184419.RAXeqaPcdm_x4NnS_help712y2giNk4g7vb_evrJqQntM130_assertion description "[Taken together, our data suggest that RTP801 is an important RA-regulated gene involved in myeloid differentiation, which could represent a therapeutic target in leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184419.RAXeqaPcdm_x4NnS_help712y2giNk4g7vb_evrJqQntM130_provenance.
- NP184421.RATgTboCmePHYyjK1yr6kYKQ3qErO9QXfNB0mHhLDGUU4130_assertion description "[Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184421.RATgTboCmePHYyjK1yr6kYKQ3qErO9QXfNB0mHhLDGUU4130_provenance.
- NP184423.RAXViEHyzOtyGq9upuJfHl--YhngvrPvNfTDVwCuEyQLo130_assertion description "[R269H PS1 mutation was associated with early age of dementia onset, higher amounts of total A beta and A beta x-42, and increased neuronal cytoskeletal changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184423.RAXViEHyzOtyGq9upuJfHl--YhngvrPvNfTDVwCuEyQLo130_provenance.
- NP184424.RAfVis-TtzSq4CXQMwYADa9kZ-X6UV7jZWbJKx6c996KU130_assertion description "[Identification and characterization of the factor H and FHL-1 binding complement regulator-acquiring surface protein 1 of the Lyme disease spirochete Borrelia spielmanii sp. nov.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184424.RAfVis-TtzSq4CXQMwYADa9kZ-X6UV7jZWbJKx6c996KU130_provenance.
- NP184425.RAVek52c17VFbUnJQWAZqnQSz9I8iEOC3uCckSvsIhCnQ130_assertion description "[The patient presented neonatally with 46,XY DSD and was diagnosed as partial androgen insensitivity syndrome carrying a disease causing AR mutation (p.Q798E).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184425.RAVek52c17VFbUnJQWAZqnQSz9I8iEOC3uCckSvsIhCnQ130_provenance.
- NP184427.RAaRz2cA4UCHOQcLY2U0riTr5T-olCOGjKrW4TNYMWYNw130_assertion description "[However, the major downstream signaling pathways that mediate its protumor effects and the role of CD44 in the progression and chemoresponse of GBM have not been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184427.RAaRz2cA4UCHOQcLY2U0riTr5T-olCOGjKrW4TNYMWYNw130_provenance.
- NP184435.RAdXxK1yfiNnX8IgX7DyQv1flMAl7u6d37NSm0LTo0LPo130_assertion description "[The myeloproliferative neoplasms (MPNs) essential thrombocythemia (ET), polycythemia vera (PV), and primary myelofibrosis (MF) are malignancies that frequently harbor the recurrent somatic point mutation JAK2(V617F).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184435.RAdXxK1yfiNnX8IgX7DyQv1flMAl7u6d37NSm0LTo0LPo130_provenance.
- NP184438.RAXEov6iUSfrGhX2C-8S9L4nZLdHlko_D86ezHIzgzpdg130_assertion description "[Loss of the ceramide transfer protein augments EGF receptor signaling in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184438.RAXEov6iUSfrGhX2C-8S9L4nZLdHlko_D86ezHIzgzpdg130_provenance.
- NP184439.RAbnOcOAZIIoKEYvV8Y05nFwYIghez1qgxVsApX81mrmc130_assertion description "[Inactive heterozygous ALDH2, alcohol flushing, and increased MCV were positively associated with hangover susceptibility in Japanese workers, suggesting that acetaldehyde is etiologically linked to the development of hangover.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184439.RAbnOcOAZIIoKEYvV8Y05nFwYIghez1qgxVsApX81mrmc130_provenance.
- NP184440.RAY9aSx4nRZHa0W4E3qYQIrcvMWHxfdMz2rKLsfbatHos130_assertion description "[We identified CRKL amplification in an EGFR inhibitor-treated lung adenocarcinoma that was not present before treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184440.RAY9aSx4nRZHa0W4E3qYQIrcvMWHxfdMz2rKLsfbatHos130_provenance.
- NP184442.RARk1I1kCu1r9NPA57TQvVJ6X_aQwbJa1G5XkAK8klBj8130_assertion description "[A significant portion of lung cancer retains the wild-type p53 gene therefore, 2-MeOE2 may have therapeutic application.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184442.RARk1I1kCu1r9NPA57TQvVJ6X_aQwbJa1G5XkAK8klBj8130_provenance.
- NP184449.RAeHGKgekLVjBQWcyE9fKi1jSbMNUoso9o-5noS23AT3M130_assertion description "[The lysophospholipase D (LysoPLD) activity of ATX was found to be significantly elevated (by ∼1.8 fold; n=20) in AH derived from human primary open angle glaucoma patients as compared to AH derived from age-matched cataract control patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184449.RAeHGKgekLVjBQWcyE9fKi1jSbMNUoso9o-5noS23AT3M130_provenance.
- NP184451.RAeSZkqn7OzVbs9fmCaRJLHqvw6FYyDShVQwuFesfmlQs130_assertion description "[When low intake of cruciferous vegetables (less than once per month) was stratified by GST genotype, higher kidney cancer risks were observed among individuals with the GSTT1 null (OR = 1.86; 95% CI: 1.07-3.23; P-interaction = 0.05) or with both GSTM1/T1 null genotypes (OR = 2.49; 95% CI: 1.08-5.77; P-interaction = 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184451.RAeSZkqn7OzVbs9fmCaRJLHqvw6FYyDShVQwuFesfmlQs130_provenance.
- NP184455.RAXX4FrRw7HvyZfV_cA9jIPBuXFW7R3kI-ODcgS_AfDEs130_assertion description "[Malaria in humans: Plasmodium falciparum blood infection levels are linked to chromosome 5q31-q33.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184455.RAXX4FrRw7HvyZfV_cA9jIPBuXFW7R3kI-ODcgS_AfDEs130_provenance.
- NP184459.RAY4uS9Jprtu7php2cGQZfnw5PZlPcOcl7pLpPuCozx_g130_assertion description "[To examine family-based transmission of the number of 5' flanking arginine vasopressin V1a receptor (AVPR1A) microsatellites, which include [(GATA)(14)] and complex [(CT)(4)-TT-(CT)(8)-(GT)(24)] repeats, in probands with a prepubertal and early adolescent bipolar disorder phenotype (PEA-BP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184459.RAY4uS9Jprtu7php2cGQZfnw5PZlPcOcl7pLpPuCozx_g130_provenance.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion description "[These findings question p.I148T or p.R74W-p.D1270N as causing by themselves CF or CBAVD and emphazises the necessity to perform a complete scanning of CFTR genes and to assign the parental alleles when novel missense mutations are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.
- NP184465.RAVjAII7geuQPxoyp68H4VjVQvX7C_wpGWxpQ6bFOUcow130_assertion description "[Ras homolog gene family member C (RhoC) is a small G protein/guanosine triphosphatase involved in tumor mobility, invasion, and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184465.RAVjAII7geuQPxoyp68H4VjVQvX7C_wpGWxpQ6bFOUcow130_provenance.
- NP184466.RAc-1vXiFNAHKfSpTM16YSqNykNuSwUqrINJz86hlrPRg130_assertion description "[RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184466.RAc-1vXiFNAHKfSpTM16YSqNykNuSwUqrINJz86hlrPRg130_provenance.
- NP184467.RAYGce652SNxBi3jcjkAyDL07e1W-7PghHCyHIcNIr34U130_assertion description "[Statistical analysis on the immunohistochemistry data of EGFR expression from 93 matched normal and breast tumor samples showed that (a) diminished EGFR expression could be detected as early as in the preneoplastic lesion (ductal carcinoma in situ) and this culminated in invasive carcinomas; (b) EGFR expression levels could distinguish between normal tissue versus carcinoma in situ and invasive carcinoma with high statistical significance (P < 0.001, n = 81).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184467.RAYGce652SNxBi3jcjkAyDL07e1W-7PghHCyHIcNIr34U130_provenance.
- NP184468.RAX7gzBw4pGhLzIesPTdfOqxKAGa2tDfNuJ-5raj-Y3AM130_assertion description "[Screening for microsatellite instability identifies frequent 3'-untranslated region mutation of the RB1-inducible coiled-coil 1 gene in colon tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184468.RAX7gzBw4pGhLzIesPTdfOqxKAGa2tDfNuJ-5raj-Y3AM130_provenance.
- NP184470.RAcxEMgNTgx3PU-A3KDQrxgt4aUyijpzywJrEUbRFiuqY130_assertion description "[Promoter methylation of MGMT gene silencing has been shown to predict benefit from chemotherapy in glioblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184470.RAcxEMgNTgx3PU-A3KDQrxgt4aUyijpzywJrEUbRFiuqY130_provenance.
- NP184474.RARtCj7Fp8ciiaaXsOk5qZEVPmtp_bsujVZRgbbVcrzIU130_assertion description "[We typed 7 SNPs spanning the gene from the promoter to 3' UTR in unrelated cases with T2DM and controls of Northern European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184474.RARtCj7Fp8ciiaaXsOk5qZEVPmtp_bsujVZRgbbVcrzIU130_provenance.
- NP184480.RAViZo1qjz3MyA626VoEAotJwSpjBWKGVZ7Apv92kkVzk130_assertion description "[AtT20 cells transplanted into nude mice induced features of Cushing's syndrome and were used as an in vivo model of ACTH-producing tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184480.RAViZo1qjz3MyA626VoEAotJwSpjBWKGVZ7Apv92kkVzk130_provenance.
- NP184481.RAcxPNGuc5cMRGm-3YbPNQqCYa_-TSSK0DKza-9EAJNzU130_assertion description "[C4A and C4B allotypes were compared in 20 patients with Felty's syndrome (FS), 52 patients with rheumatoid arthritis (RA), and 55 control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184481.RAcxPNGuc5cMRGm-3YbPNQqCYa_-TSSK0DKza-9EAJNzU130_provenance.
- NP184482.RAT_fAUIBfNtst6eMYd0LVIct7Ax1DnT_4DTDtnyqQgRY130_assertion description "[Relationship between ganglioside expression and anti-cancer effects of the monoclonal antibody against epithelial cell adhesion molecule in colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184482.RAT_fAUIBfNtst6eMYd0LVIct7Ax1DnT_4DTDtnyqQgRY130_provenance.
- NP184483.RAc7Sdix6QvDmNVi5IzXWabnBe3PiW46Fa7yDOFseGnT4130_assertion description "[DNA repair system and prostate cancer progression: the role of NBS1 polymorphism (rs1805794).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184483.RAc7Sdix6QvDmNVi5IzXWabnBe3PiW46Fa7yDOFseGnT4130_provenance.
- NP184486.RASWdf9ju6FE8t3wblSVeBJqCIrDNOHCqRsbrJSo9NLK8130_assertion description "[To characterize the phenotype of acute leukemia cases using flow cytometry, to detect mixed lineage cases and to use DNA index determination, including S-phase fraction (SPF) and p53 detection, to find if there was any correlation of SPF and p53 expression with outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184486.RASWdf9ju6FE8t3wblSVeBJqCIrDNOHCqRsbrJSo9NLK8130_provenance.
- NP184488.RATEmzbvuDMpPol6JCkTh14HxSzXrwrjRTLX7_9wUGnY8130_assertion description "[We established a cohort of patients with myoclonus dystonia syndrome and SGCE mutations to determine the extent to which psychiatric disorders form part of the disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184488.RATEmzbvuDMpPol6JCkTh14HxSzXrwrjRTLX7_9wUGnY8130_provenance.
- NP184490.RAXSQu1daN1GXsojpQyLRrC36amNj2x5FQwWD3yoDUlMc130_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." NP184490.RAXSQu1daN1GXsojpQyLRrC36amNj2x5FQwWD3yoDUlMc130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion description "[TDP-43 positive inclusions are also a feature of amyotrophic lateral sclerosis pathology, corroborating the observation of overlapping clinical features between the two conditions and reaffirming the FTD-ALS disease spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184497.RAQf7_kx2bKm6OOgsatBeraECKlV27Ck9qzX_YITzBG9g130_assertion description "[Charcot-Marie-Tooth neuropathy (CMT) type 1 is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B), the X chromosome (CMTX), and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184497.RAQf7_kx2bKm6OOgsatBeraECKlV27Ck9qzX_YITzBG9g130_provenance.
- NP184503.RAVl7qkYgtpuyFTLo0D0huzYOVOHJqhjCjzlsIEjp8rrY130_assertion description "[They were also blocked by protein tyrosine kinase (PTK) inhibitors, herbimycin A and genistein, and PKC and protein serine/threonine kinase inhibitors, H7 and HA1004.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184503.RAVl7qkYgtpuyFTLo0D0huzYOVOHJqhjCjzlsIEjp8rrY130_provenance.
- NP184504.RAfWs8O3I_tWJRmcbE7KtMVj6XBHznSeLkwE-5lJjUNQs130_assertion description "[The D allele of ACE I/D might be associated with decreased, whereas the C variant of AT1R A1166C might be associated with an elevated risk for CP in Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184504.RAfWs8O3I_tWJRmcbE7KtMVj6XBHznSeLkwE-5lJjUNQs130_provenance.
- NP184509.RAc-RvYSO8XGtJHMT4VL96dfAUKhw9yBdg_PZNr5GM6kQ130_assertion description "[Hereditary leiomyomatosis and renal cell cancer (HLRCC; OMIM 605839) is the predisposition to develop smooth muscle tumours of the skin and uterus and/or renal cancer and is associated with mutations in the fumarate hydratase gene (FH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184509.RAc-RvYSO8XGtJHMT4VL96dfAUKhw9yBdg_PZNr5GM6kQ130_provenance.
- NP184511.RAWji91QYpuTCQseJZioW6fWV9V_J4sPNCiUAReitF1O8130_assertion description "[These experiments revealed that Cys-X-Cys receptor (CXCR)1, CXCR2 and CXCR3 mRNAs, as well as Cys-X-Cys ligand (CXCL)9 (monokine induced by IFN-gamma) and CXCL10 (IFN-gamma inducible protein 10) mRNAs, were significantly upregulated in RA as compared with OA disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184511.RAWji91QYpuTCQseJZioW6fWV9V_J4sPNCiUAReitF1O8130_provenance.
- NP184517.RAdWg2opRvEk-sKyMcOPXvBEG3D9mP9GcxhNecHhYlvx4130_assertion description "[In this study, we analysed the AR gene for mutations and CAG and GGC triplets in exon 1 in 123 patients affected by TC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184517.RAdWg2opRvEk-sKyMcOPXvBEG3D9mP9GcxhNecHhYlvx4130_provenance.
- NP184518.RAZ455G7tDvSN4xJaqmjQHrxpOwyIAWxFo0UsvfxQylWY130_assertion description "[p53 overexpression had a contributing effect on altered global H3K9 acetylation of atypical pituitary adenomas (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184518.RAZ455G7tDvSN4xJaqmjQHrxpOwyIAWxFo0UsvfxQylWY130_provenance.
- NP184522.RAV9cDopa8AIF3yox2Mtf_rfCZiLGS-AaVpcNMOjMqvds130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184522.RAV9cDopa8AIF3yox2Mtf_rfCZiLGS-AaVpcNMOjMqvds130_provenance.
- NP184525.RAWJEt6RMpumf6g5gCMyd3BZ9c-qe_zFB2Jy2VFbGWl_o130_assertion description "[Adenosine deaminase messenger RNAs in lymphoblast cell lines derived from leukemic patients and patients with hereditary adenosine deaminase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184525.RAWJEt6RMpumf6g5gCMyd3BZ9c-qe_zFB2Jy2VFbGWl_o130_provenance.
- NP184526.RATAQm0ui-6nLOIR4y4y7zgHUtVnaoyvTg5xbwlTtWvwU130_assertion description "[Interaction of C1GALT1-IL5RA on the susceptibility to IgA nephropathy in Southern Han Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184526.RATAQm0ui-6nLOIR4y4y7zgHUtVnaoyvTg5xbwlTtWvwU130_provenance.
- NP184530.RAYzUyZfpMaOOQQuq_4sOvBIl6thYpQWUnr1V8X5VBFqA130_assertion description "[Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184530.RAYzUyZfpMaOOQQuq_4sOvBIl6thYpQWUnr1V8X5VBFqA130_provenance.
- NP184531.RAcOrueFK55YiR2v6NksjZHk4sD2BvXRYyX3o2TT_9M-4130_assertion description "[The long-term benefits of a finite course of interferon α (IFN) therapy include a sustained and cumulative response, as well as a reduction in the progression of fibrosis and in the development of cirrhosis and/or HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184531.RAcOrueFK55YiR2v6NksjZHk4sD2BvXRYyX3o2TT_9M-4130_provenance.
- NP184532.RAZGCEE1KUdIN3NbH6dwmDj81NFt8dXKszedxILImpZeE130_assertion description "[Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184532.RAZGCEE1KUdIN3NbH6dwmDj81NFt8dXKszedxILImpZeE130_provenance.
- NP184537.RAUr9OGBmTvdZClG-MrAtOWjvjXeVHJZvnGC4ZAArX_ds130_assertion description "[The establishment of glial tumors in vitro may not necessarily result in loss of GFAP expression early in passage nor is expression of GFAP and fibronectin mutually exclusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184537.RAUr9OGBmTvdZClG-MrAtOWjvjXeVHJZvnGC4ZAArX_ds130_provenance.
- NP184539.RARIA2Wr0XVSKOAyxUiNlW9uBSOknxS9xOB4i0tsjgy94130_assertion description "[In breast cancer, breast CSCs (BCSCs) are identified as CD24-CD44 + cells or cells with high intracellular aldehyde dehydrogenase activity (ALDH+).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184539.RARIA2Wr0XVSKOAyxUiNlW9uBSOknxS9xOB4i0tsjgy94130_provenance.
- NP184541.RAUtRF8LdXhiaOFxYDg2RsZ1PBtyjeodctTQePaPoJ4Po130_assertion description "[Collectively, these data suggest that sGCα1 regulation of p53 activity is important in prostate cancer biology and may represent an important mechanism of p53 down-regulation in those prostate cancers that express significant levels of p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184541.RAUtRF8LdXhiaOFxYDg2RsZ1PBtyjeodctTQePaPoJ4Po130_provenance.
- NP184543.RAQuzeXqwR1ETLyv1fEmao6VrqeBZFWHvyhQu9ayWZa4I130_assertion description "[A proportion of Alzheimer's disease (AD) patients treated for several months with cholinesterase (ChE) inhibitors have shown some favorable response on cognition, but the characteristics of the responders are still unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184543.RAQuzeXqwR1ETLyv1fEmao6VrqeBZFWHvyhQu9ayWZa4I130_provenance.
- NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_assertion description "[The frequency of CYP2D6 genes containing inactivating mutations was lower among 75 liver cancer patients than 200 healthy controls, and 40 cirrhotic subjects that did not develop liver cancer (frequency for carriers of two or more functional genes was 95% vs 74% vs 78%, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_provenance.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion description "[Remarkably, two clinically distinct forms of autosomal recessive muscular dystrophy, LGMD type 2B (LGMD2B) and Miyoshi myopathy, were recently mapped to the same locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- NP184565.RAbqs3G6lHVQPxzjOxa4dZbEQnfMEfFek6CrtDaC1Eg-M130_assertion description "[KIR2DS1 genotype predicts for complete cytogenetic response and survival in newly diagnosed chronic myeloid leukemia patients treated with imatinib.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184565.RAbqs3G6lHVQPxzjOxa4dZbEQnfMEfFek6CrtDaC1Eg-M130_provenance.
- NP184568.RAfemSdTqq5paW9gfDbSjJxWwK61_uhwb6c3m6Ivq7q8Q130_assertion description "[Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184568.RAfemSdTqq5paW9gfDbSjJxWwK61_uhwb6c3m6Ivq7q8Q130_provenance.
- NP184575.RAX1rxvVxZXT29SG-RuxCHnnzNiHne2C08ezCujAdeH7U130_assertion description "[Activity of the downstream PI3K effector protein kinase B (PKB) was higher in SqCas than in AdCas and was correlated with PIK3CA copy number (r = 0.75), suggesting that these copy number increases contribute to activation of PI3K signaling in SqCas of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184575.RAX1rxvVxZXT29SG-RuxCHnnzNiHne2C08ezCujAdeH7U130_provenance.