Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP484389.RAVGePqvLPasS3tfLSzDli2YcFrAtD-9toyDzfQ0u3LdQ130_assertion description "[Large population-based studies are needed to investigate the role of IL-1 polymorphisms in the pathogenesis of developing chronic hepatitis B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484389.RAVGePqvLPasS3tfLSzDli2YcFrAtD-9toyDzfQ0u3LdQ130_provenance.
- NP484394.RAYVQipxlCZuYuMS2ZdFYqEGj9fDcTxuCL9Y1dKK9Wesg130_assertion description "[To evaluate the receptor protein which can specifically bind to beta(2)GP I on the membrane of hepatocellular carcinoma (HCC) cell line SMMC-7721, and to study the biological function of the receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484394.RAYVQipxlCZuYuMS2ZdFYqEGj9fDcTxuCL9Y1dKK9Wesg130_provenance.
- NP484408.RAdwqwjOfkePdUKNnLQGYjYbeDZeQ0z905dcP5bi9hCUM130_assertion description "[n-Chimaerin mRNA (2.2 x 10(3) base-pairs) is specifically expressed in the brain, with the highest amounts being in the hippocampus and cerebral cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484408.RAdwqwjOfkePdUKNnLQGYjYbeDZeQ0z905dcP5bi9hCUM130_provenance.
- NP484412.RASNOmg60VcfRCwe6H-MHAooETHacGiF3flZobn_bcJJg130_assertion description "[Because hyper-response of plasma cortisol to vasopressin is documented in some patients with Cushing's syndrome due to adrenal adenoma (CS) or ACTH-independent macronodular adrenocortical hyperplasia (AIMAH), we analyzed the expression of V(1a), V(2), V(3) receptor and AVP mRNA in human adrenal tissues by quantitative competitive RT-PCR or real-time PCRs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484412.RASNOmg60VcfRCwe6H-MHAooETHacGiF3flZobn_bcJJg130_provenance.
- NP484414.RARJshQ_EFnXiRIbZO3o5myxUncqKDuR1Xb21Evi15JMs130_assertion description "[Immunohistochemical overexpression of p53 protein was found in 21% of NHL patients, with the highest incidence of p53 immunoreactivity in cases of Burkitt's lymphoma, follicle center lymphoma grade III, and diffuse large B-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484414.RARJshQ_EFnXiRIbZO3o5myxUncqKDuR1Xb21Evi15JMs130_provenance.
- NP484416.RAV40yvx1nZBBqlugvBnoLKGtTPEpDZrt1LDvRv13F3Hc130_assertion description "[We investigated the role of four thrombosis genes: coagulation factor V (F5), intercellular adhesion molecule 1 (ICAM1), protein C (PROC), and thrombomodulin (THBD) in cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484416.RAV40yvx1nZBBqlugvBnoLKGtTPEpDZrt1LDvRv13F3Hc130_provenance.
- NP484420.RAZB8g6CwV2c_DQGwgPwLZj-uu0V706v_eWGOhkcxFk5M130_assertion description "[The methylation status of the RASSF1A promoter was analyzed in 38 primary thyroid tumors, including 1 poorly differentiated thyroid carcinoma, 5 medullary thyroid carcinoma (MTC), 10 follicular thyroid carcinoma (FTC), 9 undifferentiated thyroid carcinoma (UTC), and 13 papillary thyroid carcinoma (PTC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484420.RAZB8g6CwV2c_DQGwgPwLZj-uu0V706v_eWGOhkcxFk5M130_provenance.
- NP484422.RAZ1N0TCMQBCU3SNsjPOZjlH7N6SmMEa5mITANPzAd40g130_assertion description "[Sustained reduction of Ang II tone by AT1-receptor antagonism could be considered as a preventive and therapeutic approach for brain ischemia and stress-related and mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484422.RAZ1N0TCMQBCU3SNsjPOZjlH7N6SmMEa5mITANPzAd40g130_provenance.
- NP484426.RAX_vaSHwjX-8DxnweMcPRfbgHeX8RJ7vc01GHT-yh06c130_assertion description "[Mice deficient in CD18, which lack all four CD11 integrins, have leukocytosis and increased susceptibility to bacterial infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484426.RAX_vaSHwjX-8DxnweMcPRfbgHeX8RJ7vc01GHT-yh06c130_provenance.
- NP484428.RAbjyZ_IVEsUZcDbDEtCCR7PgTLMNvfI1I8PYXCjM7ZEo130_assertion description "[The CYP3A5 polymorphism is associated with increased levels of the mutagenic AFB1-exo-8,9-epoxide, particularly in individuals with low CYP3A4, and this may modulate individual risk of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484428.RAbjyZ_IVEsUZcDbDEtCCR7PgTLMNvfI1I8PYXCjM7ZEo130_provenance.
- NP484433.RAdKW5pR_VfdoDAm3DIuhs8oMhdT4n5G_fhzDZwmO2LWY130_assertion description "[Intermediate layer cells were also positive for p53 in the majority of the cases of both juvenile (69%) and adult (75%) laryngeal papillomatosis and in a minority of the cases of inverted papilloma (18%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484433.RAdKW5pR_VfdoDAm3DIuhs8oMhdT4n5G_fhzDZwmO2LWY130_provenance.
- NP484441.RAdJoDyAW2-4wKl5_ZyGsk7rT0hnUHa1pcsPzbT3hMq0s130_assertion description "[Correlation between visual acuity and OCT-measured retinal nerve fiber layer thickness in a family with ADOA and an OPA1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484441.RAdJoDyAW2-4wKl5_ZyGsk7rT0hnUHa1pcsPzbT3hMq0s130_provenance.
- NP484445.RAcYDtX6YZRPzOcC4jlaGAdOSUthQb6506b8IvzSRPz7E130_assertion description "[Here we report the identification of two non-homologous brain disease-related genes, with one coding for a serine protease inhibitor (SERPINI1) and the other for a programmed cell death-related gene (PDCD10), being tightly linked together by an asymmetric bidirectional promoter in an evolutionarily conserved fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484445.RAcYDtX6YZRPzOcC4jlaGAdOSUthQb6506b8IvzSRPz7E130_provenance.
- NP484447.RARwoj-cisNSEfAfGBoomdNoryonJVgxhArnTl-d1Jtk8130_assertion description "[Disruption of a novel ectodermal neural cortex 1 antisense gene, ENC-1AS and identification of ENC-1 overexpression in hairy cell leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484447.RARwoj-cisNSEfAfGBoomdNoryonJVgxhArnTl-d1Jtk8130_provenance.
- NP484449.RAYBmZVCfOW1zbbtEgkKTyWpPGArtu_cF2EQC9QXuJzeo130_assertion description "[Insulin autoantibodies and high titre islet cell antibodies are preferentially associated with the HLA DQA1*0301-DQB1*0302 haplotype at clinical type 1 (insulin-dependent) diabetes mellitus before age 10 years, but not at onset between age 10 and 40 years. The Belgian Diabetes Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484449.RAYBmZVCfOW1zbbtEgkKTyWpPGArtu_cF2EQC9QXuJzeo130_provenance.
- NP484450.RASekbiSPOkKNLWjFt0mVFfwlySeQyq-GCXw1vusDHPtk130_assertion description "[In conclusion, our study enhances our understanding of how cardiomyopathy-linked cTnC mutations affect the response of reconstituted thin filaments to calcium upon cTnI phosphorylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484450.RASekbiSPOkKNLWjFt0mVFfwlySeQyq-GCXw1vusDHPtk130_provenance.
- NP484451.RAa4mfJ3XVrZlF4omC9sQofzJPhnxSO5uhF2pRb7HEybU130_assertion description "[Protein and mRNA expression of TGF-beta isoforms, TGF-beta 1, -beta 2 and -beta 3, and deposition of fibronectin containing extra domain A (fibronectin EDA+) and plasminogen activator inhibitor-1 (PAI-1) were studied in human chronic glomerulonephritis and diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484451.RAa4mfJ3XVrZlF4omC9sQofzJPhnxSO5uhF2pRb7HEybU130_provenance.
- NP484460.RAYeeaA7OwQus2eG26RtDTIe-IJzDcizb-1d1w8UoHSm8130_assertion description "[In the fruitfly Drosophila melanogaster, a human DAGK ortholog, DGK2, was shown to underlie the phenotype of the visual mutant retinal degeneration A (rdgA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484460.RAYeeaA7OwQus2eG26RtDTIe-IJzDcizb-1d1w8UoHSm8130_provenance.
- NP484461.RARftWcFJV1_h1GTYPhAamTTc1X0nbCpn7dj-3wsovt4c130_assertion description "[Pulsed field gel electrophoresis (PFGE) revealed a 220 kb SacII fragment in one CMT1A patient with duplication instead of a 500 kb SacII fragment as previously reported (1, 3, 4, 6-9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484461.RARftWcFJV1_h1GTYPhAamTTc1X0nbCpn7dj-3wsovt4c130_provenance.
- NP484468.RAV5B4C6YZkNJe6Hbdq2xjzK4YLvxAN4fF4D8H4fJJuCs130_assertion description "[DRD2 and NCAM1 are functional candidate genes for substance dependence; the TTC12 and ANKK1 loci are not well characterized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484468.RAV5B4C6YZkNJe6Hbdq2xjzK4YLvxAN4fF4D8H4fJJuCs130_provenance.
- NP484470.RAaa590AROttnIH8V0pNGbXPhSKPLPWAhWVMWeb3t76aA130_assertion description "[Mutations in the gene encoding epsilon-sarcoglycan (SGCE) have been found in some patients with MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484470.RAaa590AROttnIH8V0pNGbXPhSKPLPWAhWVMWeb3t76aA130_provenance.
- NP484472.RAb9AjvafJpqPI1AYVi8q-DuLXX-QcHlntScH5ERHqYVw130_assertion description "[These results in obese monkeys (with mimAb1) and in FGFR1 knockout mice (with FGF21) demonstrated the essential role of FGFR1c in FGF21 function and suggest fat as a critical target tissue for the cytokine and antibody.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484472.RAb9AjvafJpqPI1AYVi8q-DuLXX-QcHlntScH5ERHqYVw130_provenance.
- NP484475.RAX_KYexbIYAdUVrvtRmHOtpfQHtdhw0hd51yCdX8iLr8130_assertion description "[Because the disease is usually caused by heterozygous mutations of ELA2, a gene encoding for neutrophil elastase (NE), we have investigated in G-CSF-responder and nonresponder patients affected by SCN the expression of polypeptides that constitute the antimicrobial machinery of these cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484475.RAX_KYexbIYAdUVrvtRmHOtpfQHtdhw0hd51yCdX8iLr8130_provenance.
- NP484484.RAQaie6oNnVyJKdds6qoNIx9Q719zy5JPLz-A3iPfBaIE130_assertion description "[Paroxysmal dyskinesias (PDs), a clinically and genetically heterogeneous group of episodic movement disorders, include kinesigenic PD (PKD), exercise-induced PD (PED) and non-kinesigenic PD (PNKD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484484.RAQaie6oNnVyJKdds6qoNIx9Q719zy5JPLz-A3iPfBaIE130_provenance.
- NP484491.RAfeYjWmxTwm2_44bjntZl6A99uHXTzNF3EmNA5-C9Hik130_assertion description "[The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484491.RAfeYjWmxTwm2_44bjntZl6A99uHXTzNF3EmNA5-C9Hik130_provenance.
- NP484494.RAXcGAFNRwDrc2tRyzL0N9EYbdZSmzjxHwp6zcOZ2QFoI130_assertion description "[CD8+ but not CD4+ T cells require cognate interactions with target tissues to mediate GVHD across only minor H antigens, whereas both CD4+ and CD8+ T cells require direct leukemic contact to mediate GVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484494.RAXcGAFNRwDrc2tRyzL0N9EYbdZSmzjxHwp6zcOZ2QFoI130_provenance.
- NP484495.RAQUdyhVYUwZB42KjjBgOJVm0M3by5DqBLBDtLKWXdPeU130_assertion description "[This is the first study to definitively show that point mutations in the HSD11B2 gene abolish 11 beta HSD2 enzymatic activity in the syndrome of AME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484495.RAQUdyhVYUwZB42KjjBgOJVm0M3by5DqBLBDtLKWXdPeU130_provenance.
- NP484497.RAfkskAnby8TrcHaGXxua-5qPPBQYQ_hHwy3RnUgC9s-A130_assertion description "[Matrix metalloproteinase 3 is a mediator of pulmonary fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484497.RAfkskAnby8TrcHaGXxua-5qPPBQYQ_hHwy3RnUgC9s-A130_provenance.
- NP484500.RASWoA7jYU8ciFtk_ZXyFdQhBkkI84lh-APhLY9WWVcZI130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an adult-onset, dominantly inherited neurodegenerative disease caused by expansion of a glutamine repeat tract in ataxin-1 (ATXN1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484500.RASWoA7jYU8ciFtk_ZXyFdQhBkkI84lh-APhLY9WWVcZI130_provenance.
- NP484501.RAekNwEedcSa6_XQlJQFFPgTyEqOr2SSKK1sm6dXu0Smw130_assertion description "[The emergence of partially demethylated epigenotypes and re-establishment of normal p15 protein expression following the initial decitabine courses implicate pharmacologic demethylation as a possible mechanism resulting in hematologic response in MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484501.RAekNwEedcSa6_XQlJQFFPgTyEqOr2SSKK1sm6dXu0Smw130_provenance.
- NP484506.RAe5KHJjt5LMvvxIzydRTub7SgHXzusLVY4G6FCNJZbj0130_assertion description "[In summary, this study found that many different human cancers express ROR1 and that ROR1 may play a functional role in promoting tumor cell growth, suggesting that this orphan-receptor tyrosine-kinase-like protein may be a potential target for therapy directed against a variety of human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484506.RAe5KHJjt5LMvvxIzydRTub7SgHXzusLVY4G6FCNJZbj0130_provenance.
- NP484513.RAQVVRoTrVh81iaKy5_TYrzBDGz7ZeE2GsZzovq4sskvA130_assertion description "[Human endogenous retroviral family W (HERV-W) RNA present in circulating viral particles (Multiple Sclerosis associated RetroViral element, MSRV) has been associated with the evolution and prognosis of Multiple Sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484513.RAQVVRoTrVh81iaKy5_TYrzBDGz7ZeE2GsZzovq4sskvA130_provenance.
- NP484520.RAa_8ufKas_jf33ZRd69rp5Mjde-X0oaZfgxPEXpOLPcw130_assertion description "[Using an allele-specific PCR assay, four polymorphisms each were genotyped for Cx40 and Cx50 in 190 Caucasian patients with schizophrenia and 190 controls matched for sex, age and ethnicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484520.RAa_8ufKas_jf33ZRd69rp5Mjde-X0oaZfgxPEXpOLPcw130_provenance.
- NP484523.RAcUKcrYzKuKvmXeYcUi21PSzgOKGRNaMwkiqCrREreGA130_assertion description "[LOH at the APC/MCC gene (5Q21) in gastric cancer and preneoplastic lesions. Prognostic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484523.RAcUKcrYzKuKvmXeYcUi21PSzgOKGRNaMwkiqCrREreGA130_provenance.
- NP484526.RAXKGqvoKu_DGI1YSh5mSSuvanrGMc1rCY_4G-aSaWaFo130_assertion description "[The polarized localization of the BPA1 and alpha(6)beta(4) proteins to the basal aspect of the peripheral tumor cells was largely retained in invasive but nonmetastatic lesions, but was lost upon progression to metastatic growth of head and neck squamous cell carcinomas (SCC), in which pericellular staining extended into many tumor cell layers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484526.RAXKGqvoKu_DGI1YSh5mSSuvanrGMc1rCY_4G-aSaWaFo130_provenance.
- NP484527.RARsOOcwmJULKnbhu22nON966paSs21YWIl_XiRO4BkKw130_assertion description "[Restoration of the PTEN gene to highly invasive prostate cancer PC-3 cells or expression of a dominant negative version of the PI3K target, Akt also significantly inhibited invasion and downregulated protein expression of urokinase-type plasminogen activator (uPA) and matrix metalloproteinase (MMP)-9, markers for cell invasion, indicating a central role of the PI3K-Akt pathway in this process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484527.RARsOOcwmJULKnbhu22nON966paSs21YWIl_XiRO4BkKw130_provenance.
- NP484533.RAYPkSq6RrwAmDr51Ond4EcZ4mN4tCZnIQd5jtRIKYB78130_assertion description "[In adult rats, when obstructive cholestasis was maintained for 8 weeks, a significant up-regulation of Slc23a2 accompanied by a down-regulation of Slc23a1 was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484533.RAYPkSq6RrwAmDr51Ond4EcZ4mN4tCZnIQd5jtRIKYB78130_provenance.
- NP484536.RAXPy--dgjbUdRexyb6c6EGDXW6axCp0mL1hDuzsBE9_c130_assertion description "[Haplotype combinations at the calpain-10 gene (CAPN10) within this region were shown to increase diabetes risk in several populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484536.RAXPy--dgjbUdRexyb6c6EGDXW6axCp0mL1hDuzsBE9_c130_provenance.
- NP484537.RATC1fncCBrI7kos7c0RjYiLFQ4LJBOqV4Qbzf8Zrn5T0130_assertion description "[The gene for secreted frizzled-related protein 1 (SFRP1) encodes a soluble Wnt antagonist and is located in a chromosomal region (8p22-p12) that is often deleted in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484537.RATC1fncCBrI7kos7c0RjYiLFQ4LJBOqV4Qbzf8Zrn5T0130_provenance.
- NP484538.RAWpetiRwhLAmqm5sAKyoWvpsUImN_tFzA4YFmGyzNhFc130_assertion description "[The frequency of IgG and/or IgM anti-FKBP12 autoantibodies detected by ELISA was as follows; SLE (15/39), SSc (11/27), CREST (4/7), RA (2/8), MCTD (0/5), Graves' disease (4/12), IDDM (2/6), PM/DM (0/3), MG (1/4), AIH (2/6), PBC (4/9), and healthy subjects (5/118).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484538.RAWpetiRwhLAmqm5sAKyoWvpsUImN_tFzA4YFmGyzNhFc130_provenance.
- NP484541.RAeqTPFL2KHnDapTL1T-drnkGIc5VdjD2XCpPSKy0qroI130_assertion description "[Six of the previously identified SNPs showed a statistically significant association with breast cancer risk: rs2981582 (FGFR2), rs3803662 (TNRC9), rs12443621 (TNRC9), rs889312 (MAP3K1), rs3817198 (LSP1) and rs2107425 (H19).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484541.RAeqTPFL2KHnDapTL1T-drnkGIc5VdjD2XCpPSKy0qroI130_provenance.
- NP484542.RATQqnDq7G6NOiWpOAHCeydO0ymkG20OJRUrq9DCKAckA130_assertion description "[Methylation of the glutathione-S-transferase M3 gene promoter is associated with oxidative stress in acute-on-chronic hepatitis B liver failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484542.RATQqnDq7G6NOiWpOAHCeydO0ymkG20OJRUrq9DCKAckA130_provenance.
- NP484547.RAavktEwPL_Xxgr0LjeMsAcXtTsuQ54YrukQKlcj1HQbo130_assertion description "[The concentration of HGF in bronchoalveolar lavage fluid (BALF) was significantly higher than in normal controls (0.23 +/- 0.09 pg/microg) in patients with IPF (0.77 +/- 0.88 pg of HGF/microg of albumin, P < 0.001), lung fibrosis associated with rheumatoid arthritis (0.50 +/- 0.64 pg/microg, P < 0.01), and sarcoidosis (0.41 +/- 0.61 pg/microg, P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484547.RAavktEwPL_Xxgr0LjeMsAcXtTsuQ54YrukQKlcj1HQbo130_provenance.
- NP484548.RAa-AgOlienOn7iIlmVIIq6YZpFNVxaUUg-51llA8Oi1g130_assertion description "[A third region, at 11p13-15 between WT1 and RRM1, was also affected by LOH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484548.RAa-AgOlienOn7iIlmVIIq6YZpFNVxaUUg-51llA8Oi1g130_provenance.
- NP484552.RAZqHaZ2ZzG9UMGLVX-C2YC0TV0XYBUNF0i47C3QMjxEE130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484552.RAZqHaZ2ZzG9UMGLVX-C2YC0TV0XYBUNF0i47C3QMjxEE130_provenance.
- NP484553.RAVcCj2bxFW_4aUOVlXfRfVmysFDqYGyCf5grVdJNT3Ro130_assertion description "[Clinical risk classification is inaccurate in predicting relapse in adult patients with acute lymphoblastic leukemia, sometimes resulting in patients receiving inappropriate chemotherapy or stem cell transplantation (SCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484553.RAVcCj2bxFW_4aUOVlXfRfVmysFDqYGyCf5grVdJNT3Ro130_provenance.
- NP484555.RAXDB01KWZo4AP6LlSDAFUlwFPELK7QH0jTkuiAmc56r8130_assertion description "[Thalassemia intermedia due to co-inheritance of beta0/beta(+)-thalassemia and (- -SEA) alpha-thalassemia/Hb Westmead [alpha122(H5)His > Gln (alpha2)] in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484555.RAXDB01KWZo4AP6LlSDAFUlwFPELK7QH0jTkuiAmc56r8130_provenance.
- NP484559.RAQvREYmPWbIkm05fJq-l7IgH07MoOQBIFxlQtLhQ-1h0130_assertion description "[The fact that SHP controls a complex set of genes in multiple metabolic pathways suggests the intriguing possibility of developing new therapeutics for metabolic diseases, including fatty liver, dyslipidemia and obesity, by regulating SHP with small molecules.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484559.RAQvREYmPWbIkm05fJq-l7IgH07MoOQBIFxlQtLhQ-1h0130_provenance.
- NP484561.RAQ-GJeea56Ysmx0zVpJ__FLv1LhakIvMFsIoSMq95dLo130_assertion description "[This data suggests that BMI1 gene is aberrant at the chromosomal level in a subset of gliomas, and possibly contributes to brain tumour pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484561.RAQ-GJeea56Ysmx0zVpJ__FLv1LhakIvMFsIoSMq95dLo130_provenance.
- NP484564.RAZ5HRMeXDSVc8T4pDmiK_G5XqN-8UQ8Zi7x-gkB2RZEs130_assertion description "[CCND1-IGH@ translocation is considered pathognomonic of mantle cell lymphoma (MCL), as this distinct chromosomal abnormality has not been reported in any other subtypes of mature B-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484564.RAZ5HRMeXDSVc8T4pDmiK_G5XqN-8UQ8Zi7x-gkB2RZEs130_provenance.
- NP484573.RAa7l930t-oCN639LwQevvKre_XLXYJ5P_QQ1OzxhBGnU130_assertion description "[Nelfinavir efficiently induced cell death in carboplatin-sensitive (SKOV3, OV-GH-5) and carboplatin-resistant (OVCAR3, OV-GH-1) ovarian cancer cell lines as well as in cancer biopsies and ascites samples from patients with recurrent ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484573.RAa7l930t-oCN639LwQevvKre_XLXYJ5P_QQ1OzxhBGnU130_provenance.
- NP484578.RATN9_Qjr07_XFbl3alsrPpKvKY6FGhkof6KJLwH7mzAk130_assertion description "[The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484578.RATN9_Qjr07_XFbl3alsrPpKvKY6FGhkof6KJLwH7mzAk130_provenance.
- NP485071.RAarTMI9p1tBtUZ1i_6Z59AirKgPjc28ttn0PYh_33abU130_assertion description "[An internal tandem duplication (ITD) of the juxtamembrane domain-coding sequence of the FLT3 gene (FLT3-ITD) is found in 20-25% of adult acute myeloid leukemia (AML) and at a lower frequency in childhood AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485071.RAarTMI9p1tBtUZ1i_6Z59AirKgPjc28ttn0PYh_33abU130_provenance.
- NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_assertion description "[In this study we examined the expression of menin in parathyroid tumors from primary hyperparathyroidism (PHP), secondary hyperparathyroidism (SHP), and MEN1 and thyroid tumors including Basedow's disease, thyroid cancer, and adrenocortical tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_provenance.
- NP485081.RAfyl1zDNX0VehplcOmcIX8R4XmvEYCGnt4vTG_6lllYo130_assertion description "[High lipoprotein(a) [Lp(a)] levels and small-sized apolipoprotein(a) [apo(a)] phenotypes have been linked to acute coronary syndromes (ACS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485081.RAfyl1zDNX0VehplcOmcIX8R4XmvEYCGnt4vTG_6lllYo130_provenance.
- NP485093.RASwoQnLUSpPodnbkbnJcUEkamuiPAPcbdbkWrZRDB0lw130_assertion description "[This minireview gets an insight into recent findings on the implication of IL-1ra and its gene polymorphism in diabetes and obesity, discusses the potential dual effects of IL-1ra observed in different models, and comments on future directions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485093.RASwoQnLUSpPodnbkbnJcUEkamuiPAPcbdbkWrZRDB0lw130_provenance.
- NP485098.RAYolfDuqNgz8lm5fWwy1sKIfeYMEEE44XgD23yzN3s-4130_assertion description "[Here, we establish an important role for histone H4 lysine 16 acetylation (H4K16Ac) and the histone acetyltransferase hMOF in the regulation of TMS1/ASC, a proapoptotic gene that undergoes epigenetic silencing in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485098.RAYolfDuqNgz8lm5fWwy1sKIfeYMEEE44XgD23yzN3s-4130_provenance.
- NP485099.RAeUuQFsO03fXc2JjTMrGBnGh0z_rKwR59tiBXMZNs-OY130_assertion description "[Prostasin silencing in BPH-1 was associated with up-regulation of iNOS, ICAM-1, IL-6, and IL-8, and down-regulation of cyclin D1; as well as reduced proliferation and invasion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485099.RAeUuQFsO03fXc2JjTMrGBnGh0z_rKwR59tiBXMZNs-OY130_provenance.
- NP485104.RAaNq5LbLhpljW9dGmm18Au3T8ZzJCe2pNHwThG6BIajM130_assertion description "[Associations of IL10 haplotypes with prostate cancer were explained by high linkage disequilibrium between two tagSNPs (rs1800890 and rs3024496) and -1082G>A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485104.RAaNq5LbLhpljW9dGmm18Au3T8ZzJCe2pNHwThG6BIajM130_provenance.
- NP485109.RARLemxX7-8jpXgOpr1vfmeq59aU3rAhutacr7mKjeSkQ130_assertion description "[Mutational activation of the RAS-RAF-MAPK and the Wnt pathway in small intestinal adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485109.RARLemxX7-8jpXgOpr1vfmeq59aU3rAhutacr7mKjeSkQ130_provenance.
- NP485111.RATej00HpRcR7HF9fyM9J6X_fp2lFjMpyZrEzHSqXvHRU130_assertion description "[To test whether the genetic variants of CAK genes modify the risk of lung cancer, we compared the manifestation of 25 single nucleotide polymorphisms (SNPs) and the haplotypes of Cdk7, MAT1 and cyclin H between 500 patients with lung cancer and 517 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485111.RATej00HpRcR7HF9fyM9J6X_fp2lFjMpyZrEzHSqXvHRU130_provenance.
- NP485118.RAfOMLnw19ZQaizcmEaTuJ-xmH9VkJUTJpDk2kWZbATVA130_assertion description "[We hypothesized that activation of NHE mediates hyperglycaemia-induced endothelial dysfunction via calcium-dependent calpain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485118.RAfOMLnw19ZQaizcmEaTuJ-xmH9VkJUTJpDk2kWZbATVA130_provenance.
- NP485120.RAZ4BRciU1wQjaH0BpxcxQk-bpKZQAitPagU_dXNtUDNc130_assertion description "[Recent studies have highlighted the role of specific oncogenes such as TCL1, MTCP-1, and ATM in the case of T-cell and p53 mutations in the case of B-cell PLLs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485120.RAZ4BRciU1wQjaH0BpxcxQk-bpKZQAitPagU_dXNtUDNc130_provenance.
- NP485121.RASxpMqTbW9IQsLOBNqqiOuCnKLzxikLje_RdG_W6oPjg130_assertion description "[Furthermore, a maternal-only history vs a paternal-only history of hypertension or diabetes was associated with strong odds of being an RFC case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485121.RASxpMqTbW9IQsLOBNqqiOuCnKLzxikLje_RdG_W6oPjg130_provenance.
- NP485122.RARAMbVJb2LIYGMcBpH90TA20VhQ41HsV7n-gmthYtcCg130_assertion description "[In this paper, we employ a mixed integer programming based classification algorithm named hyper-box enclosure method (HBE) for the classification of some cancer types with a minimal set of predictor genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485122.RARAMbVJb2LIYGMcBpH90TA20VhQ41HsV7n-gmthYtcCg130_provenance.
- NP485125.RAYC08RHA55o_WGROQ-pEsbj5IqwxkGGNQGEVioovGpsY130_assertion description "[A further case of a t(11;20)(p15;q11.2) translocation in an acute myeloid leukemia (FAB M2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485125.RAYC08RHA55o_WGROQ-pEsbj5IqwxkGGNQGEVioovGpsY130_provenance.
- NP485128.RATyoLoMF0mvDu-X6OgLk7bL4rO6VgZREd_GAOqjEVxM0130_assertion description "[The intronic GAA repeat expansion in the frataxin (FXN) gene causes the hereditary neurodegenerative disorder Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485128.RATyoLoMF0mvDu-X6OgLk7bL4rO6VgZREd_GAOqjEVxM0130_provenance.
- NP485135.RAXFapvJ29H3MTnM48r1rlpn8R4Z2IjKDDKDvsDIdwDGE130_assertion description "[Polymorphisms of DBP gene were significantly association with human PFM, especially in female, suggesting the importance of DBP gene in the pathogenesis of human obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485135.RAXFapvJ29H3MTnM48r1rlpn8R4Z2IjKDDKDvsDIdwDGE130_provenance.
- NP485139.RAUqX3IYW9eJS7mv3uTTA7O-jRpEFA1pL55bCoLUzNgPY130_assertion description "[From 33 (33 %) mixed subtype infections, ST1, 3 (14 %) was significantly related to GI symptoms (p = 0.045), and eight mixed infections with three different STs, which are under reported, were also identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485139.RAUqX3IYW9eJS7mv3uTTA7O-jRpEFA1pL55bCoLUzNgPY130_provenance.
- NP485140.RAbh9PdoNl7fheP4g83hhuscPPpWfLM4TEdJwNXYzDmFA130_assertion description "[No associations between the GSTM1 alleles, including the null allele, and cataracts were detected in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485140.RAbh9PdoNl7fheP4g83hhuscPPpWfLM4TEdJwNXYzDmFA130_provenance.
- NP485143.RAd0YEOJv2pWvcs06Uk8KQl_4_0ZNwzCUzpNNVS57XMkI130_assertion description "[Myelofibrosis (MF) is a BCR-ABL1-negative myeloproliferative neoplasm diagnosed de novo or developed from essential thrombocythemia (ET) or polycythemia vera (PV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485143.RAd0YEOJv2pWvcs06Uk8KQl_4_0ZNwzCUzpNNVS57XMkI130_provenance.
- NP485144.RAVWNmm8m-zVBnScab3xn6dna0bsKLCN2RWB46EgBJves130_assertion description "[Stroke-like lesions (SLL) are common radiological findings in patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (SLE; MELAS) harboring the m.3243A>G MTTL1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485144.RAVWNmm8m-zVBnScab3xn6dna0bsKLCN2RWB46EgBJves130_provenance.
- NP485155.RAaqI4steWEUSVkBpGNk0kMhv1kg_Ppwm4IMw8lcEKOUg130_assertion description "[Acute monocytic leukemia with (8;22)(p11;q13) translocation. Involvement of 8p11 as in classical t(8;16)(p11;p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485155.RAaqI4steWEUSVkBpGNk0kMhv1kg_Ppwm4IMw8lcEKOUg130_provenance.
- NP485159.RAV7MDJ-PW6RpzI2b3t-PtfwFtOmdqO6TsPYh3KPLSXtQ130_assertion description "[The role of poly(ADP-ribose) polymerase-1 in CNS disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485159.RAV7MDJ-PW6RpzI2b3t-PtfwFtOmdqO6TsPYh3KPLSXtQ130_provenance.
- NP485160.RARIEBoHbsQYyF-WroguKyx2pfCT4_9iSY-3qCtWuZRxE130_assertion description "[The antiproliferative effect of XRT/RSV treatment correlated with increased expression of p15, p21, and mutant p53 and decreased expression of cyclin B, cyclin D, and cdk2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485160.RARIEBoHbsQYyF-WroguKyx2pfCT4_9iSY-3qCtWuZRxE130_provenance.
- NP485166.RAdAl3B994EgGTn1ju3akr0oIkiEDv8s2wkCeLDi6Bkfs130_assertion description "[These results indicate that overexpression of Angptl4 may promote invasion and metastasis in CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485166.RAdAl3B994EgGTn1ju3akr0oIkiEDv8s2wkCeLDi6Bkfs130_provenance.
- NP485184.RAcPycSeTvj-irH_6UAVi3CD0k2AzkLxxKk-Ldy0TG7vw130_assertion description "[The murine SLC19A3 gene maps to central chromosome 1 in the region defined as a seizure susceptibility locus in the DBA/2J mouse strain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485184.RAcPycSeTvj-irH_6UAVi3CD0k2AzkLxxKk-Ldy0TG7vw130_provenance.
- NP485202.RAUlnP8bQd1M2xcIf1pxUdGvl7D8n4LUvcQsHO2QETd6w130_assertion description "[The prevalences of thyroid disease, insulin-dependent and non-insulin-dependent diabetes were compared in first degree relatives of diabetics with and without coexisting autoimmune thyroid disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485202.RAUlnP8bQd1M2xcIf1pxUdGvl7D8n4LUvcQsHO2QETd6w130_provenance.
- NP485203.RAQTF2ZZofGdYrQh1UZLJJTAtz6BwQ30wQAmxeyQ7jKWs130_assertion description "[We find that wild-type PIP5K2A but not the schizophrenia-associated mutant (N251S)-PIP5K2A activates heteromeric KCNQ2/KCNQ3 and KCNQ3/KCNQ5, the molecular correlate of neuronal M channels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485203.RAQTF2ZZofGdYrQh1UZLJJTAtz6BwQ30wQAmxeyQ7jKWs130_provenance.
- NP485208.RAfg13HqWZpCXWoSoGB2mTgk5lKekztjlPT26QWKOq0JI130_assertion description "[In this study we assessed the growth responsiveness to TGF-beta 1 in pancreatic cancer cell lines and characterized the levels of expression of TGF-beta receptors in these cell lines and in human pancreatic cancer tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485208.RAfg13HqWZpCXWoSoGB2mTgk5lKekztjlPT26QWKOq0JI130_provenance.
- NP485209.RAeNqioi8kjPy3XmuLjFXMiYR0PDrPKCM5cIgZTO1njP4130_assertion description "[Glycyl-tRNA synthetase (GARS), which encodes the enzyme responsible for charging tRNA(Gly) with glycine in both the cytoplasm and mitochondria, is implicated to Charcot-Marie-Tooth disease 2D (CMT2D) and distal hereditary motor neuropathy type V (dHMN-V).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485209.RAeNqioi8kjPy3XmuLjFXMiYR0PDrPKCM5cIgZTO1njP4130_provenance.
- NP485210.RAWr80nKvlERojV8Ff4jCSBvfXl6oroJ54GLnBJeQA3Og130_assertion description "[The most common histological variety was motor neurone disease type inclusion (MNDI) (n = 18), followed by corticobasal degeneration (CBD) (n = 12), then Pick's disease (n = 6), dementia lacking distinctive histology (DLDH) (n = 6) and PSP (n = 3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485210.RAWr80nKvlERojV8Ff4jCSBvfXl6oroJ54GLnBJeQA3Og130_provenance.
- NP485211.RAUcthWKzb5Yb6j2iHWVthK65SFOjWfIor-sHqWwVjEU0130_assertion description "[Already, mutations in KATP and ZAC/HYMAI have been shown to be associated with type 1 and type 2 diabetes mellitus in later life; some mutations in KATP are amenable to treatment with sulfonylureas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485211.RAUcthWKzb5Yb6j2iHWVthK65SFOjWfIor-sHqWwVjEU0130_provenance.
- NP485212.RASgTzsKtUIqfSpbdH5wEagsmszoeezrehgvTCfB5UKbI130_assertion description "[KRAS mutations were found in 31 of 69 (45%) CC examined and in two cases of tumour surrounding non-neoplastic liver tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485212.RASgTzsKtUIqfSpbdH5wEagsmszoeezrehgvTCfB5UKbI130_provenance.
- NP485218.RAUN1ADhR5pqcMvVNOc97pBI2OIiD4sBSISSi3RLNyVBY130_assertion description "[Our results thus suggest that GSTP1 and GSTT1 gene polymorphisms modulate susceptibility to smoking-related cancers of the oral cavity and pharynx.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485218.RAUN1ADhR5pqcMvVNOc97pBI2OIiD4sBSISSi3RLNyVBY130_provenance.
- NP485219.RAZk7rc_cqGjBsl_bZvXNuqwINaxWBsM7oadfzeWkPnVY130_assertion description "[The frequencies of HLA-DRB3 * 0202 (100%), HLA-DRB1 * 1302 (67%), HLA-DRB3 * 0301 (67%), and HLA-DQB1 * 0301 (67%) were significantly increased in children with multiple sclerosis and the frequencies of HLA-DRB1 * 1501 (40%) and HLA-DRB5 * 0101 (40%) were significantly increased in children with ADEM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485219.RAZk7rc_cqGjBsl_bZvXNuqwINaxWBsM7oadfzeWkPnVY130_provenance.
- NP485225.RAc15SowgrA-uF0ODgavBbFoDfu9m6kpkL8f5o_qfxWEA130_assertion description "[We have assessed the impact of these mutations in a cohort of 494 patients treated within the randomized phase 3 United Kingdom Leukaemia Research Fund Chronic Lymphocytic Leukemia 4 (UK LRF CCL4) trial that compared chlorambucil and fludarabine with and without cyclophosphamide in previously untreated patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485225.RAc15SowgrA-uF0ODgavBbFoDfu9m6kpkL8f5o_qfxWEA130_provenance.
- NP485227.RAVsq8u2dxY2bCZOAPZXilxC3Jek3XllVLF7J0YdB-SYU130_assertion description "[A significant association of the rs729302 A allele with RA susceptibility was found in both sets (odds ratio (OR) 1.22, 95% CI 1.09 to 1.35, p<0.001 in the combined analysis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485227.RAVsq8u2dxY2bCZOAPZXilxC3Jek3XllVLF7J0YdB-SYU130_provenance.
- NP485229.RAc7RXsgqsEYm3_DTTh8emPKUasv00d10NUNYHbvPbOkE130_assertion description "[Heregulin-induced activation of HER2 and HER3 increases androgen receptor transactivation and CWR-R1 human recurrent prostate cancer cell growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485229.RAc7RXsgqsEYm3_DTTh8emPKUasv00d10NUNYHbvPbOkE130_provenance.
- NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_assertion description "[Subgroup analysis by ethnicity showed significantly stronger effects for the BST1 (rs11724635) in Asian vs Caucasian populations and similar effects for SNCA, LRRK2, LAMP3, HIP1R, and STK39 in Asian and Caucasian populations, while MAPT rs2942168 and SYT11 rs34372695 were monomorphic in the Asian population, highlighting the role of population-specific heterogeneity in PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_provenance.
- NP485236.RAaGrNcJT0s16IzMDOHCiWSB_BMP9AbmxG2bGou5YWT1w130_assertion description "[We conclude, that HLA DQA1*0501 and DQA1*0501-DQB1*0201 (DQ2) are strongly associated with Graves' disease in both populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485236.RAaGrNcJT0s16IzMDOHCiWSB_BMP9AbmxG2bGou5YWT1w130_provenance.
- NP485241.RAcm5tY9E4RV-E1sUGpfiaT4fx0Dtav6s2jsBQe0f5vb8130_assertion description "[This p53 polymorphism modulates risk to smoking-induced lung cancer independently of other genetic risk factors such as germ line polymorphism of CYP1A1 or GST1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485241.RAcm5tY9E4RV-E1sUGpfiaT4fx0Dtav6s2jsBQe0f5vb8130_provenance.
- NP485243.RAZPKwy2AeqWcz30ljv8_h__tzHT-xIFgVn6P4CXeY0eM130_assertion description "[The CYP2D6 metaboliser status of patients prescribed risperidone for the treatment of psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485243.RAZPKwy2AeqWcz30ljv8_h__tzHT-xIFgVn6P4CXeY0eM130_provenance.
- NP485250.RAXPYjA2b6U-e7EFqGjyeogbzjakIn6f4VNpi2_Jyb0BI130_assertion description "[The basic residues of placenta growth factor type 2 retrieve sequestered angiogenic factors into a soluble form: implications for tumor angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485250.RAXPYjA2b6U-e7EFqGjyeogbzjakIn6f4VNpi2_Jyb0BI130_provenance.
- NP485253.RAX0YggCmUazUVqqvaP6TstvdAe6j45v8aCzSxTWiqi0c130_assertion description "[Animal studies suggest that impaired mitochondrial biogenesis attributable to downregulation of the peroxisome proliferator-activated receptor gamma coactivator (PGC)-1 transcriptional pathway is integral of mitochondrial dysfunction in heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485253.RAX0YggCmUazUVqqvaP6TstvdAe6j45v8aCzSxTWiqi0c130_provenance.
- NP485254.RAefSQawHOvryKnjVAJPKSXYSenvQxxRWm59kAKGIWT5E130_assertion description "[Usefulness of HGAL and LMO2 immunohistochemistry in the identification of follicular lymphomas of the non-gastric gastrointestinal tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485254.RAefSQawHOvryKnjVAJPKSXYSenvQxxRWm59kAKGIWT5E130_provenance.
- NP485255.RAV_Oefe7c5xIObXAwstKbmYk0ywb0fuoBZmwioqRj30w130_assertion description "[Promoter methylation analyses of PLCD1 and PLCE1 performed in cell lines and tumor biopsies revealed that methylation of PLCD1 can contribute to reduced expression in 40% of the microsatellite instable carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485255.RAV_Oefe7c5xIObXAwstKbmYk0ywb0fuoBZmwioqRj30w130_provenance.
- NP485257.RAdH1HK1JME1JpI0rRU5cDydUN5ftI73dXO6kyWz85Kys130_assertion description "[Our results are compatible with a role for UII in glucose homeostasis and diabetes although we cannot rule out the possibility that PER3 gene may underlie the reported associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485257.RAdH1HK1JME1JpI0rRU5cDydUN5ftI73dXO6kyWz85Kys130_provenance.
- NP485258.RATe5FJR55iFMRmq5u1m8IpHrU7M_-_VUhnjpmGUF4GDw130_assertion description "[Of the 12 heterotransplant Wilms' tumors, PAX2, PAX8, and WT1 were concomitantly expressed in seven tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485258.RATe5FJR55iFMRmq5u1m8IpHrU7M_-_VUhnjpmGUF4GDw130_provenance.
- NP485261.RAegCOLoZbK-m5PhFqXZOcVNYFUbkQhCqMbs1xLDg3FBo130_assertion description "[The Niemann-Pick type C (NPC) disease is characterized by accumulation of lipids within the late endosome/lysosome (LE/LY) compartment as a result of dysfunctions of the NPC1 or NPC2 proteins and an altered distribution and/or functioning of proteins involved in the regulation of membrane dynamics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485261.RAegCOLoZbK-m5PhFqXZOcVNYFUbkQhCqMbs1xLDg3FBo130_provenance.