Nanopublications

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

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NP261821.RAbXjwjFqh9XG5OZHoxxId2VMc42zIj05iVDb9nSohGCw130_assertion description "[There are two known autosomal dominant genes for the hereditary ulcero-mutilating neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot-Marie-Tooth disease type 2B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261821.RAbXjwjFqh9XG5OZHoxxId2VMc42zIj05iVDb9nSohGCw130_provenance.
NP261822.RAc1sNAErPK6o998cRlY1EJNumxCxv8lLCTASU7cxbRX4130_assertion description "[Catalytically inactive lecithin: cholesterol acyltransferase (LCAT) caused by a Gly 30 to Ser mutation in a family with LCAT deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261822.RAc1sNAErPK6o998cRlY1EJNumxCxv8lLCTASU7cxbRX4130_provenance.
NP261831.RAbb2VNxex5GqvndhNjQan0v4kpJ-wR_PZkRC-ZXKGtCo130_assertion description "[To determine whether an upstream promoter mutation could account for elevated A gamma in a Black adolescent with A gamma-beta+-HPFH and sickle cell trait, we cloned the 13 kb BglII fragment containing both gamma genes into phage lambda vector EMBL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261831.RAbb2VNxex5GqvndhNjQan0v4kpJ-wR_PZkRC-ZXKGtCo130_provenance.
NP261832.RATdqJhqG9DSx9Q3bXF2w7Zp0cRV5PiaFDoWkdxTYO8cE130_assertion description "[We conducted this genetic study to test whether the ABO O1 allele is associated with low vWF plasma levels and with a reduced risk of MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261832.RATdqJhqG9DSx9Q3bXF2w7Zp0cRV5PiaFDoWkdxTYO8cE130_provenance.
NP261841.RAVvEfp4KxK_q_ndGIxpfj9xIgqpn-YBJwoOLdhLaJzYI130_assertion description "[Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261841.RAVvEfp4KxK_q_ndGIxpfj9xIgqpn-YBJwoOLdhLaJzYI130_provenance.
NP261845.RAdIEWAX05hVEsuvdzrl8tC3yvS1kwI4LUZXSgeWgFVlU130_assertion description "[This Y-sutural cataract is caused by an E233del mutation in BFSP2 which provides additional evidence supporting mutations in BFSP2 as a cause for cataract and demonstrates phenotypic variability in cataracts caused by BFSP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261845.RAdIEWAX05hVEsuvdzrl8tC3yvS1kwI4LUZXSgeWgFVlU130_provenance.
NP261847.RAVbsG3fzB0SGD2GWBlL8LZ7C3tObXnHrmgvXC3VhBLtg130_assertion description "[We have addressed this question for the putative multiple sclerosis(MS) autoantigens alphaB-crystallin, S100beta, proteolipid protein (PLP) and myelin oligodendrocyte glycoprotein (MOG)-alpha and MOG-beta isoforms, using quantitative RT-PCR on human thymus (total, cell fractions and microdissected specimen) and on a panel of peripheral tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261847.RAVbsG3fzB0SGD2GWBlL8LZ7C3tObXnHrmgvXC3VhBLtg130_provenance.
NP261849.RAflnG52tsImXMvX7R8hNUaEFC2tPAhbMIULF_u4DaDFw130_assertion description "[Knock-down of ubiquitin-specific protease 22 by micro-RNA interference inhibits colorectal cancer growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261849.RAflnG52tsImXMvX7R8hNUaEFC2tPAhbMIULF_u4DaDFw130_provenance.
NP261852.RAdHYHSlay8MPQrNQQneePoxt9IkbbqARPsBzW6Woq12c130_assertion description "[Frontotemporal dementia (FTD) with inclusion body myopathy and Paget disease of bone (IBMPFD) is a rare, autosomal-dominant disorder caused by mutations in the valosin-containing protein (VCP) gene, a member of the AAA-ATPase gene superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261852.RAdHYHSlay8MPQrNQQneePoxt9IkbbqARPsBzW6Woq12c130_provenance.
NP261857.RAdmz-DGvl0Yocu94rzp1mJz-9KbeKfMoDh93zwUT71_k130_assertion description "[These findings suggest that inhibition of COX-2 development may lead not only to inhibition of the proliferation and metastasis of prostate carcinoma but also to the inhibition of prostate carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261857.RAdmz-DGvl0Yocu94rzp1mJz-9KbeKfMoDh93zwUT71_k130_provenance.
NP261859.RAVLNj4YlbdxSU1TkiHm09U1bTGprO7l27TUXony__Je8130_assertion description "[Direct sequencing of the gamma-globin gene of the proband and her father also revealed a previously reported variant called Hb A2-Troodos [gamma116(G18)Arg-->Cys] [in cis with the IVS-II-1 (G-->A) beta0-thal mutation].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261859.RAVLNj4YlbdxSU1TkiHm09U1bTGprO7l27TUXony__Je8130_provenance.
NP261860.RAST_S-lUNkU7IIL5i63U1iJEgpe_aGriI7XAXsmjIgRc130_assertion description "[Invasive lobular carcinoma with extracellular mucin production and HER-2 overexpression: a case report and further case studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261860.RAST_S-lUNkU7IIL5i63U1iJEgpe_aGriI7XAXsmjIgRc130_provenance.
NP261862.RAc4GwCU-QHuEJptRnuOOwWrPCaxp1hFqxexI7SNqfKZg130_assertion description "[LAMB2 mutations leading to lack of laminin beta2 were identified as the molecular cause underlying Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261862.RAc4GwCU-QHuEJptRnuOOwWrPCaxp1hFqxexI7SNqfKZg130_provenance.
NP261863.RAfJHX3e5ON6WiPnAB_A8x7MaTIoj5dDvjw9xrEQPfe8I130_assertion description "[Increased expression of tumor necrosis factor-alpha, interleukin-6, platelet-derived growth factor-B and granulocyte-macrophage colony-stimulating factor mRNA in cells of bronchoalveolar lavage fluids from patients with sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261863.RAfJHX3e5ON6WiPnAB_A8x7MaTIoj5dDvjw9xrEQPfe8I130_provenance.
NP261864.RAWtd-93b4rQuBwbyRt4CL-U10VN887R0QohtdxVfJMOo130_assertion description "[Thus, inhibition of PI3K activity with concomitant administration of chemotoxic compounds may prove beneficial in preventing the development of drug resistance in patients with hormone-refractory prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261864.RAWtd-93b4rQuBwbyRt4CL-U10VN887R0QohtdxVfJMOo130_provenance.
NP261868.RAXrmTuirSXgHtXLNqcItHxeVQqyL_wZiCMcd-arIlKXc130_assertion description "[Therefore, abnormal expression and dysregulation of CTLA-4 could partly explain the mechanism of evasion of anti-tumor immune responses in breast cancer patients and therefore highlight its importance in the development and progression of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261868.RAXrmTuirSXgHtXLNqcItHxeVQqyL_wZiCMcd-arIlKXc130_provenance.
NP261879.RAWAPoHn_HnpQgsVKGqtJUkL4mbZe0_Lsl76ri-Jzvc-s130_assertion description "[The second study used freshly isolated peripheral lymphocytes from 354 cancer-free subjects to demonstrate that the ADPRT 762 A allele contributed to significantly lower adenosine diphosphate ribosyl transferase (ADPRT)/PARP-1 activities in response to H2O2 in a gene dosage-dependent manner (P < 0.0001, test for linear trend).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261879.RAWAPoHn_HnpQgsVKGqtJUkL4mbZe0_Lsl76ri-Jzvc-s130_provenance.
NP261881.RAcQi8JFunytkfc5wd9HlAtjBpk9dB56IeXBVd1kgRc48130_assertion description "[Since genetic polymorphisms affecting drug metabolizing enzymes or drug receptors are known to influence responses to drugs, exploration of these effects on treatment responses to ARBs and ACE inhibitors may provide for more targeted treatment of HF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261881.RAcQi8JFunytkfc5wd9HlAtjBpk9dB56IeXBVd1kgRc48130_provenance.
NP261891.RAdozKIohe2l9nZrR7J9HY_PnwF8Y5ffIivYhHGNepbpE130_assertion description "[Polymorphisms of IL-1beta/-1470, IL-1beta/-511, IL-1beta/-31, IL-4/-589, IL-6/-572, IL-8/-251, IL-10/-819, and TNFalpha/-308 are susceptibility loci for the development of sepsis and organ dysfunction in major trauma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261891.RAdozKIohe2l9nZrR7J9HY_PnwF8Y5ffIivYhHGNepbpE130_provenance.
NP261898.RAUPTksfm3ZfdLnMxANTHv4SbmkzzqMecDYWk3bJAGLXQ130_assertion description "[This study was designed to explore the relationship between PI3K pathway activation and the sensitivity to lapatinib in HER2--positive metastatic breast cancer patients pretreated with anthracyclins, taxanes and trastuzumab.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261898.RAUPTksfm3ZfdLnMxANTHv4SbmkzzqMecDYWk3bJAGLXQ130_provenance.
NP261903.RAbW2jmc83S4kOQUjW97fVIICnWHJjSnGoMk4Knyxpfac130_assertion description "[These results suggest that PAK1 is essential for the malignant growth of NF2-deficient cells, and that PAK1-blocking drugs could be potentially useful forthe treatment of neurofibromatosis types 2, in addition to Ras-induced cancers and neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261903.RAbW2jmc83S4kOQUjW97fVIICnWHJjSnGoMk4Knyxpfac130_provenance.
NP261905.RATAYvHdkxseI-d-j8nQAElIEPW6HHIMv0cadVemX-oyc130_assertion description "[In an analysis combining data from 2 population-based case-control studies of postmenopausal breast cancer (1,296 cases and 1,055 controls) conducted in Washington State in 1997-1999 and 2000-2004, the authors evaluated how 51 single nucleotide polymorphisms in 7 progesterone-related genes (AKR1C1, AKR1C2, AKR1C3, CYP3A4, SRD5A1, SRD5A2, and PGR) influenced breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261905.RATAYvHdkxseI-d-j8nQAElIEPW6HHIMv0cadVemX-oyc130_provenance.
NP261919.RAX_DAZpEphegD9I_LSxd1v8tTFsVpsU6iZgAqckRLQvY130_assertion description "[Drug susceptibility testing (DST) remains an important concern for implementing treatment of MDR tuberculosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261919.RAX_DAZpEphegD9I_LSxd1v8tTFsVpsU6iZgAqckRLQvY130_provenance.
NP261923.RARADA6ehUQmF8a_oqqVvavz3TE1iQSHHHK3nWedKN7I0130_assertion description "[We conclude that decreased IGF-1, IGF-1R and IGFBP-3 expression in SCAT and increased IGF-1R expression in PM of T2DM subjects might contribute to changes of fat differentiation capacity and to regulation of subclinical inflammation by PM, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261923.RARADA6ehUQmF8a_oqqVvavz3TE1iQSHHHK3nWedKN7I0130_provenance.
NP261924.RAcmLe777oZlDveF5AHXs7LdkqP9U_Br_EJ5geif6kOyg130_assertion description "[Other cDNA microarray studies have shown that hepsin is one of the highly over expressed genes in prostate cancer tissue compared with nonmalignant and benign prostatic hyperplasia tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261924.RAcmLe777oZlDveF5AHXs7LdkqP9U_Br_EJ5geif6kOyg130_provenance.
NP261927.RAWWkDwEzDkRRasYbsq7JDEKA0n5kM54bhWaSXIelxWUE130_assertion description "[Six genes (CDC42, STAT1, RALA, BCL2L1, TGFA, and EGF) were enriched in the known pancreatic cancer pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261927.RAWWkDwEzDkRRasYbsq7JDEKA0n5kM54bhWaSXIelxWUE130_provenance.
NP261929.RAUWYn9812pcWQTA3RmSWJg4rC2wavfduGFnYD5azJRXE130_assertion description "[Sialyl Lewis a and sialyl Lewis x glycotopes, which are the specific ligands for selectins, and variant forms of CD44, which are the adhesion molecules recognizing hyaluronate, are both implicated in cancer metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261929.RAUWYn9812pcWQTA3RmSWJg4rC2wavfduGFnYD5azJRXE130_provenance.
NP261933.RASwCNuOKTpHFnZcu7SzvTuxwV7ijP5jAW0YLcEy2WZTA130_assertion description "[This is the first reported association between compound heterozygous RPE65 mutations and fundus albipunctatus, indicative of a mutation-specific phenotypic effect in this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261933.RASwCNuOKTpHFnZcu7SzvTuxwV7ijP5jAW0YLcEy2WZTA130_provenance.
NP261935.RAU-rExpadYI5S0532qBA6ZglnsIBW1buMf97QwXjOBEg130_assertion description "[The proportion of carriers of ACP1*C allele (*A/ *C, *B/*C) in women with a history of repeated spontaneous abortion is lower than in normal pregnant women and other control groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261935.RAU-rExpadYI5S0532qBA6ZglnsIBW1buMf97QwXjOBEg130_provenance.
NP261940.RARvhKLK4cg5_u7nSwNei9_GMOiyk00JsXlPM2Q-37WcU130_assertion description "[Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261940.RARvhKLK4cg5_u7nSwNei9_GMOiyk00JsXlPM2Q-37WcU130_provenance.
NP261943.RAVkoLzN-PicEW1IjBsmTJ9I-gfnzqivE0oHc1VhMu07U130_assertion description "[In a sample of 2157 middle-aged men and women randomly drawn from the Potsdam cohort of the European Prospective Investigation into Cancer and Nutrition, we investigated the impact of 7 SCD1 tagging-single nucleotide polymorphisms (rs1502593, rs522951, rs11190480, rs3071, rs3793767, rs10883463 and rs508384) and 5 inferred haplotypes with frequency >5% describing 90.9% of the genotype combinations in our population, on triglycerides, body mass index (BMI), waist circumference (WC), glycated haemoglobin (HbA1c), high-sensitivity C-reactive protein (hs-CRP), gamma-glutamyltransferase (GGT), alanine aminotransferase (ALT) and fetuin-A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261943.RAVkoLzN-PicEW1IjBsmTJ9I-gfnzqivE0oHc1VhMu07U130_provenance.
NP261944.RAXKBMU2DMvo7UpVzSm2fdPbmSyxYDJ67yobO3IEJeDjA130_assertion description "[Familial hematuria (FH) is associated with at least two pathological entities: thin basement membrane nephropathy (TBMN), caused by heterozygous COL4A3/COL4A4 mutations, and C3 nephropathy caused by CFHR5 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261944.RAXKBMU2DMvo7UpVzSm2fdPbmSyxYDJ67yobO3IEJeDjA130_provenance.
NP261946.RAZ9AEqcd4ELLJ6N0yY76SOxj3T6XaqVOKxKuX5P8QyA8130_assertion description "[Data were used to build a valid partial least squares discriminate analysis (PLS-DA) model where HNF1A-MODY subjects could be separated from the other diabetes subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261946.RAZ9AEqcd4ELLJ6N0yY76SOxj3T6XaqVOKxKuX5P8QyA8130_provenance.
NP261947.RATWoiQUEWUWVplRMRmX5kC9lmUHh_34rPZVM7hNRQySc130_assertion description "[The results showed that PRDX1 and GPX1 were up-regulated by periodontitis (p<0.05), independently of the glycaemic status, whilst PRDX2 and SOD2 genes were slightly influenced by periodontitis, but significantly induced when periodontitis was associated with DM, especially under a poor glycaemic control (p<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261947.RATWoiQUEWUWVplRMRmX5kC9lmUHh_34rPZVM7hNRQySc130_provenance.
NP261953.RAcj_6nMkF1-sUqAwG7fRL9xa-xOpKk1tYUuqeW9-2HT0130_assertion description "[Accumulating genetic evidence indicates that the primate-specific gene locus G72/G30 is related to schizophrenia: it encodes for the protein pLG72, whose function is still the subject of controversy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261953.RAcj_6nMkF1-sUqAwG7fRL9xa-xOpKk1tYUuqeW9-2HT0130_provenance.
NP261956.RAUiwQjxJPy1TuFrV5soEEcc6ThDrWXPLj9x2yMGp5DJc130_assertion description "[A novel combination therapy consisting of a left ventricular assist device (LVAD) combined with pharmacologic therapy including the selective beta(2)-agonist, clenbuterol, has shown promise in restoring ventricular function in patients with heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261956.RAUiwQjxJPy1TuFrV5soEEcc6ThDrWXPLj9x2yMGp5DJc130_provenance.
NP261958.RAQG0wXCZ4XpzEH5yGrM9HBca_lbxC4i_tfKuoyDyZ_08130_assertion description "[The role of NDRG1 in cancer pathogenesis and its possible usefulness as a prognostic factor for patients with cancer is also discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261958.RAQG0wXCZ4XpzEH5yGrM9HBca_lbxC4i_tfKuoyDyZ_08130_provenance.
NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_assertion description "[There was a clear-cut clinical difference between the 28 patients having a balanced 11q23 anomaly/MLL rearrangement and the 17 patients having an unbalanced chromosomal anomaly: AML with unbalanced 11q23 anomalies occurred in older patients (P = 0.07) tended to be less frequently associated with previous exposure to topoisomerase II-active drugs and with M4/M5 FAB cytological subtypes, were always associated with other chromosomal anomalies (P < 0.0001), expressed more frequently the CD34 antigen (P = 0.05) and were of considerably poorer prognosis for achievement of CR (P = 0.005) and survival (P = 0.0005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_provenance.
NP261971.RAbFCBI5AYh-7s7Ajz2a3q-LFcCfTEirVVO6ubwMNiYUI130_assertion description "[Mutations of the NPHS2 gene are responsible for autosomal-recessive steroid-resistant nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261971.RAbFCBI5AYh-7s7Ajz2a3q-LFcCfTEirVVO6ubwMNiYUI130_provenance.
NP261973.RAdKLz04MmoeqS71_P9ejM09yQu6iqI2Ep-KyGGdwPM3M130_assertion description "[To investigate these subtype-specific changes in detail we determined the expression levels of seven splicing factors (DUSP11, HNRPAB, HNRPH3, SLU7, SFR2IP, SFPQ, SF3B14) and three intron retention events (PARC, IER3, FGD2) in a cohort of 165 patients with inflammatory diseases of the colon (120 with IBD) and 30 healthy controls by real time PCR (TaqMan).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261973.RAdKLz04MmoeqS71_P9ejM09yQu6iqI2Ep-KyGGdwPM3M130_provenance.
NP261974.RAcNqOvb9Qe5nBV6KRAQ3YLZ5QfmwbsOYAap7cqYvSBlc130_assertion description "[Here, we demonstrate that erlotinib-induced cell growth inhibition in EGFR high-expressing human H322 NSCLC cells was accompanied by G1/S phase arrest, which was largely caused by a decrease in expression of G1/S-related cyclins, suppression of activities of cyclin-dependent kinase (CDK) 2 and CDK4, induction of CDK inhibitor p27(KIP1), and retinoblastoma hypophosphorylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261974.RAcNqOvb9Qe5nBV6KRAQ3YLZ5QfmwbsOYAap7cqYvSBlc130_provenance.
NP261975.RAbIWhg98irM-l2vFIsamOO_UeCbVrNlIh7UNm-P0EkaA130_assertion description "[There was no evidence of an association between the clinical variables and schizophrenia across the genotypes among the three HSP70 gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261975.RAbIWhg98irM-l2vFIsamOO_UeCbVrNlIh7UNm-P0EkaA130_provenance.
NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion description "[We have analyzed EGFR and HER2 mutations and the expression of the two products of the CDKN2A gene (p14(arf) and p16(INK4a)) in 116 NSCLC that have been previously analyzed for TP53 and KRAS mutations in relation to smoking history of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance.
NP261990.RAZixvHflacrasQZml_B0Ddmmq720yHOCoWRgw8rPViPQ130_assertion description "[The results showed that: 1) in one case of squamous cell carcinoma with invasion, the number of chromosomal abnormalities was much greater in the invasive than in non-invasive parts, with marked topographical heterogeneities; 2) the DNA-ploidies were largely shifted to the higher side with aneuploid stem-lines and polyploid cells in the invasive parts of all malignant tumors; 3) the expression of HLA-DR was induced at the invasive fronts of malignant melanomas; 4) the GS-I specific sugar residue(D-galactose) appeared in all extra-mammary Paget's cells; and 5) expression of `oncogenes` was found in about 60% of all malignant tumors examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261990.RAZixvHflacrasQZml_B0Ddmmq720yHOCoWRgw8rPViPQ130_provenance.
NP261993.RAb8wPByZMxFxLBjpQFMLCrO_7lO7Pu763Htie5t7XaQE130_assertion description "[In the present study, the inhibitory mechanism of rhapontigenin isolated from Vitis coignetiae was investigated on HIF-1α stability and angiogenesis in human prostate cancer PC-3 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261993.RAb8wPByZMxFxLBjpQFMLCrO_7lO7Pu763Htie5t7XaQE130_provenance.
NP261994.RAapGv6RTaXbkHViTXAkrTBTlL8kerx0p9Uppzx8XnJPk130_assertion description "[No associations were found between the polymorphisms OGG1 Ser326Cys, XRCC1 Arg280His, and XRCCI Arg399Gln and risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261994.RAapGv6RTaXbkHViTXAkrTBTlL8kerx0p9Uppzx8XnJPk130_provenance.
NP262009.RAezoh6iFS8Cc-vMs51V3vHmd4E2is5c9I6Jw8tkUTWWE130_assertion description "[Triplet repeat polymorphism within the NOTCH4 gene located near the junction of the HLA class II and class III regions in narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262009.RAezoh6iFS8Cc-vMs51V3vHmd4E2is5c9I6Jw8tkUTWWE130_provenance.
NP262015.RAU6PLz9D840fKYFRnZ5HTMq1RKzEoQsAehJvOebQ9ZV0130_assertion description "[The DNA mismatch repair gene mutations underlying hereditary non-polyposis colorectal cancer syndrome (HNPCC) also predispose, besides colorectal and endometrial cancer, to gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262015.RAU6PLz9D840fKYFRnZ5HTMq1RKzEoQsAehJvOebQ9ZV0130_provenance.
NP262025.RAZ4yvFk-jPrS9VfQKRVg8LAxdvTtFsOe7imLGq2EwbLo130_assertion description "[These presentations are consistent with atypical severe combined immunodeficiency (SCID)/Omenn Syndrome and the diagnosis was confirmed by demonstration of homozygosity for the R841W mutation in the catalytic core of RAG1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262025.RAZ4yvFk-jPrS9VfQKRVg8LAxdvTtFsOe7imLGq2EwbLo130_provenance.
NP262030.RAexCR3ueSW3IeIxzZjI6OYDtpHDLXo5lKy4gZFOlCVKE130_assertion description "[Mucin glycosylating enzyme GALNT2 regulates the malignant character of hepatocellular carcinoma by modifying the EGF receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262030.RAexCR3ueSW3IeIxzZjI6OYDtpHDLXo5lKy4gZFOlCVKE130_provenance.
NP262040.RATW3YSTymJxcIK1a_oMYg-O4qb8CjCB4lR0PwJqi2Jg4130_assertion description "[Recent studies have revealed that the TWEAK-Fn14 ligand-receptor pair likely plays an important role in a variety of cellular processes and in the pathogenesis of several human diseases, including atherosclerosis, stroke, rheumatoid arthritis and cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262040.RATW3YSTymJxcIK1a_oMYg-O4qb8CjCB4lR0PwJqi2Jg4130_provenance.
NP262046.RAW_3FMtluMSFb5kRXI-8R4dcrjvwsqUCkWc3agVmldF8130_assertion description "[We retrospectively evaluated the cases of 183 patients with primary breast cancer who underwent surgery after NAC (anthracycline and taxane) at the National Cancer Center Hospital (NCCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262046.RAW_3FMtluMSFb5kRXI-8R4dcrjvwsqUCkWc3agVmldF8130_provenance.
NP262052.RAWm1B5adBFxAGsghEJmR2Gy1d8SPkIQWF1ZzxU8kGUtA130_assertion description "[Novel loci have been identified for monogenic hypercholesterolemia, such as low-density lipoprotein (LDL) receptor (LDLR)-associated protein, proprotein convertase subtilisin-like kexin type 9, and ATP-binding cassette transporters ABCG5 and ABCG8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262052.RAWm1B5adBFxAGsghEJmR2Gy1d8SPkIQWF1ZzxU8kGUtA130_provenance.
NP262053.RARZz_0SFwu3t9TNMXlV4vdgKEDqo6aq-bllchUgjwXVo130_assertion description "[Several significant associations were found after correcting for multiple testing: (1) the DDC gene was strongly associated with both adulthood (P=0.00053; odds ratio (OR)=2.17) and childhood ADHD (P=0.0017; OR=1.90); (2) the MAOB gene was found specifically associated in the adult ADHD sample (P=0.0029; OR=1.90) and (3) the 5HT2A gene showed evidence of association only with the combined ADHD subtype both in adults (P=0.0036; OR=1.63) and children (P=0.0084; OR=1.49).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262053.RARZz_0SFwu3t9TNMXlV4vdgKEDqo6aq-bllchUgjwXVo130_provenance.
NP262054.RAfFT05QbRmJr-71rOxpHUghnMlP52h-Wg4I9JQWYFLlM130_assertion description "[The association of GATA5 hypermethylation with metastasis and progression-free survival of patients indicates that epigenetic alterations of GATA5 participate in renal cell carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262054.RAfFT05QbRmJr-71rOxpHUghnMlP52h-Wg4I9JQWYFLlM130_provenance.
NP262062.RAZ-VfAV616TYirnr0E1M2ZkLN_ZNE19EiML5t0zi65R8130_assertion description "[Stem cell transplantation (SCT) is increasingly being recognised as the treatment of choice in eligible patients with Ph(+)ALL, but disease-relapse remains a problem in a proportion of patients prior to and after SCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262062.RAZ-VfAV616TYirnr0E1M2ZkLN_ZNE19EiML5t0zi65R8130_provenance.
NP262063.RAYvpAnz6LFelBKJ0ZZKPjb8BjCQUlUmIMVfar2Xcsd4U130_assertion description "[We found that the CD163 expression rate in breast cancer tissues varied significantly and correlated with estrogen receptor status (p<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262063.RAYvpAnz6LFelBKJ0ZZKPjb8BjCQUlUmIMVfar2Xcsd4U130_provenance.
NP262065.RAYTBwf73_XNXbBGxTOgooFmea6ahEl7LBEDj98JRgvQw130_assertion description "[CD14 gene polymorphism is not associated with asthma but rather with bronchial obstruction and hyperreactivity in Slovenian children with non-atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262065.RAYTBwf73_XNXbBGxTOgooFmea6ahEl7LBEDj98JRgvQw130_provenance.
NP262069.RATh7a_hx-gELdCD-PGhTkxjHb9W7bZEliRHVVOf2NCls130_assertion description "[Lymphomatoid papulosis (LyP) is defined as a recurrent self-healing papulonodular eruption with the histological features of a (CD30+) cutaneous T-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262069.RATh7a_hx-gELdCD-PGhTkxjHb9W7bZEliRHVVOf2NCls130_provenance.
NP262072.RAT29gb03glvttlNOBMDzUZF-mEyLMZzgNOSc5A8kGsc8130_assertion description "[A higher expression of CCR1, CCR3, CCR4, CCR5, and CCR8 was seen in AVH-B than in CHB-infected patients and HCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262072.RAT29gb03glvttlNOBMDzUZF-mEyLMZzgNOSc5A8kGsc8130_provenance.
NP262082.RAS-j--95wlnt_zi915qqWxbvx85V7wyEyXtNeiwjMHxo130_assertion description "[Patients with LPHD and NLRCHD clearly differed from patients with CHD with nodular sclerosis or mixed cellularity, as they presented with an earlier disease stage and infrequent mediastinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262082.RAS-j--95wlnt_zi915qqWxbvx85V7wyEyXtNeiwjMHxo130_provenance.
NP262084.RAZK67cuIHSJ4f1B8VTT9pntjWwc8jNFzbXFoFTudA90M130_assertion description "[LOX-1-mediated uptake of RLPs may thus play important roles in atherogenesis by inducing LOX-1 expression and VSMC migration especially in the settings of postprandial hyperlipidemia, diabetes and metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262084.RAZK67cuIHSJ4f1B8VTT9pntjWwc8jNFzbXFoFTudA90M130_provenance.
NP262097.RAXxMrhGNBzIcsH5LMeXFtsf3bws1XNSws0yYb1RZIv0A130_assertion description "[Deficiency of GPIb or GPIX results in Bernard-Soulier syndrome (BSS), a bleeding disorder in which platelets are giant and have multiple functional defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262097.RAXxMrhGNBzIcsH5LMeXFtsf3bws1XNSws0yYb1RZIv0A130_provenance.
NP262102.RAXkpaWiWriZVaesoGefpVPvoBQhQw56BvNSKDNcNymTw130_assertion description "[The disregulated in vivo expression of CD28 was related to the RA patients' disease activity and suggests that modulation of CD28 surface levels may be an additional mechanism to finely tune the delicate responsiveness/tolerance balance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262102.RAXkpaWiWriZVaesoGefpVPvoBQhQw56BvNSKDNcNymTw130_provenance.
NP262105.RAQe-KDEzx36SRBjKE0WJ5kgXuVZTg4AcAngaaZ1AwXcs130_assertion description "[Relative quantitative RT-PCR protocol for TrkB expression in neuroblastoma using GAPD as an internal control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262105.RAQe-KDEzx36SRBjKE0WJ5kgXuVZTg4AcAngaaZ1AwXcs130_provenance.
NP262116.RAfPvRzWOUljaYzxH5918ABA3lSVd9Vg0Kn2OlSsgQjRA130_assertion description "[The identification of mutations in the transglutaminase-1 gene as a cause of lamellar ichthyosis implicates transglutaminases in other congenital recessive ichthyoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262116.RAfPvRzWOUljaYzxH5918ABA3lSVd9Vg0Kn2OlSsgQjRA130_provenance.
NP262117.RAbkNypm7Gi45IR4BS5LiQoAp6IFobNd2Dg4erj3-FDuQ130_assertion description "[GRN was analysed in 502 probands with frontal variant FTD (fvFTD), FTD with motoneuron disease (FTD-MND), primary progressive aphasia (PPA) and corticobasal degeneration syndrome (CBDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262117.RAbkNypm7Gi45IR4BS5LiQoAp6IFobNd2Dg4erj3-FDuQ130_provenance.
NP262128.RAXdPcTx1a28-Ut2ujoafpnOOoq0Z7cVFZP0m2GUzVOwY130_assertion description "[Here, we searched for TFB1M and TFB2M nucleotide variants in a cohort of PD-patients (n=300) and healthy controls (n=200) from Spain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262128.RAXdPcTx1a28-Ut2ujoafpnOOoq0Z7cVFZP0m2GUzVOwY130_provenance.
NP262130.RAeAPkkMFaDDJ746gnRmtigCYzi532vbT6Gqv-OJkRV-M130_assertion description "[To investigate whether genetic polymorphism of alcohol dehydrogenase (ADH) 2 and aldehyde dehydrogenase (ALDH) 2 was related to alcoholic testicular atrophy, we determined restriction fragment-length polymorphisms of the ADH2 and ALDH2 genes in 43 Japanese male alcoholics and 50 healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262130.RAeAPkkMFaDDJ746gnRmtigCYzi532vbT6Gqv-OJkRV-M130_provenance.
NP262132.RAfWG8Z5FMRHX4A3XqDXwJFCAixlE-3RLBUXY63mLNjlU130_assertion description "[FGFR2 and MAP3K1 are members of the RAS/RAF/MEK/ERK-signaling pathway and have been identified from genome-wide association studies to be breast cancer susceptibility genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262132.RAfWG8Z5FMRHX4A3XqDXwJFCAixlE-3RLBUXY63mLNjlU130_provenance.
NP262141.RAQkZafdU-_TZcPh-9Edpalknh4lgCBt9DDfgKaPQWa9o130_assertion description "[Maspin expression is transactivated by p63 and is critical for the modulation of lung cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262141.RAQkZafdU-_TZcPh-9Edpalknh4lgCBt9DDfgKaPQWa9o130_provenance.
NP262145.RATAxjiRPeKK3BUrHHU01krhtWGjQaajuRXbsSamor73w130_assertion description "[Anaplastic large T-cell lymphoma (ALCL) is frequently associated with the t(2;5)(p23;q35).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262145.RATAxjiRPeKK3BUrHHU01krhtWGjQaajuRXbsSamor73w130_provenance.
NP262147.RAbTveE49egtVZ2xv3pu2xbdNSqB2Dk3mhfTcrdvcC_8w130_assertion description "[A homozygous R769Q mutation in the calpain-3 gene and absence of muscle calpain-3 protein confirmed a calpainopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262147.RAbTveE49egtVZ2xv3pu2xbdNSqB2Dk3mhfTcrdvcC_8w130_provenance.
NP262150.RATxU1ioLIiGhoH0ezKEk4X96qIiNNSHELsVjbxOj0iOU130_assertion description "[GASDERMIN, suppressed frequently in gastric cancer, is a target of LMO1 in TGF-beta-dependent apoptotic signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262150.RATxU1ioLIiGhoH0ezKEk4X96qIiNNSHELsVjbxOj0iOU130_provenance.
NP262155.RASmg5G8Lrm22w-2z4OTvqZGrGCuPwX423BdnHkTWS8YE130_assertion description "[Because a single nucleotide polymorphism (SNP) within the FoxP3 gene (rs3761548 in the promoter region) is associated with susceptibility to Graves' disease, this study detected rs3761548 in a hospital-based case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262155.RASmg5G8Lrm22w-2z4OTvqZGrGCuPwX423BdnHkTWS8YE130_provenance.
NP262157.RAdWvVWUz1-qiRj32bwLH0U67owJjvb3c_kVjeNQVk-LU130_assertion description "[Importantly, fascin up-regulates other proteins that are known to be critical for the execution of metastasis such as urokinase-type plasminogen activator (uPA) and the matrix metalloproteases (MMP)-2 and MMP-9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262157.RAdWvVWUz1-qiRj32bwLH0U67owJjvb3c_kVjeNQVk-LU130_provenance.
NP262158.RATwsvFHFAjdes-WFa5cO9LcehMFezAICZgsnCpNSuerU130_assertion description "[mRNA and protein levels of TNFalpha, IL-12(p35), IL-12(p40), IL-15, IL-18 and IL-23(p19) were quantified in biopsies from active CD patients, CD patients on a gluten-free diet (GFD), healthy controls, and patients with non-CD inflammation and mild histological changes in the intestine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262158.RATwsvFHFAjdes-WFa5cO9LcehMFezAICZgsnCpNSuerU130_provenance.
NP262164.RAcU2WOOYlOOR1YQOVvKjgYSFXcK9RMp1lo4-mFd9nWM0130_assertion description "[Evidence for a locus (IDDM16) in the immunoglobulin heavy chain region on chromosome 14q32.3 producing susceptibility to type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262164.RAcU2WOOYlOOR1YQOVvKjgYSFXcK9RMp1lo4-mFd9nWM0130_provenance.
NP262165.RAeTrFV5Y8ejLZfYuJosnFXo2bN1WBCWV75EEpjw55fUs130_assertion description "[We tested the hypothesis that the (-1072)G > A and (-444)A > C promoter polymorphisms of leukotriene C4 synthase confer risk of transient ischemic attack (TIA), ischemic stroke, ischemic heart disease (IHD), asthma, and chronic obstructive pulmonary disease (COPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262165.RAeTrFV5Y8ejLZfYuJosnFXo2bN1WBCWV75EEpjw55fUs130_provenance.
NP262166.RAUqCt3sFk7PRnetudL0m1vtizdnyU91Ic2w1imBvVius130_assertion description "[p53 Integrates host defense and cell fate during bacterial pneumonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262166.RAUqCt3sFk7PRnetudL0m1vtizdnyU91Ic2w1imBvVius130_provenance.
NP262167.RASi_a9rpBF-9pSESh4lOAM6RtsS0O7zUDaFUw5R7fQP4130_assertion description "[We conclude that DMBT1 is likely to play a differential role in the genesis of digestive tract carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262167.RASi_a9rpBF-9pSESh4lOAM6RtsS0O7zUDaFUw5R7fQP4130_provenance.
NP262171.RARybaAsKySxynzBEiZLwzH-2wQrfR3tImez3RsqAlZdw130_assertion description "[Classic galactosemia is a potentially lethal metabolic disorder that results from profound impairment of the enzyme galactose-1-phosphate uridylyltransferase (GALT); despite decades of research, the underlying mechanism of pathophysiology remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262171.RARybaAsKySxynzBEiZLwzH-2wQrfR3tImez3RsqAlZdw130_provenance.
NP262175.RAanExIqU1xJU3OMIut-r4xADn4ltCnRece4LYjRnT8xE130_assertion description "[Piebaldism is an autosomal dominant disorder characterized by congenital hypopigmented patches of skin and hair and has been found to be associated with mutations in the KIT or SLUG genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262175.RAanExIqU1xJU3OMIut-r4xADn4ltCnRece4LYjRnT8xE130_provenance.
NP262178.RAdfwyqIKTXhF5LRPBzVKnOhsNdL8tb1AU5FhowpFMhKw130_assertion description "[In addition, 125Tg B cells remain competent to increase CD86 expression in response to both T cell-dependent (anti-CD40) and T cell-independent (anti-IgM or LPS) signals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262178.RAdfwyqIKTXhF5LRPBzVKnOhsNdL8tb1AU5FhowpFMhKw130_provenance.
NP262180.RAdCLIYTA1I_gcaLOhv6G18eZYWKtMjN298UICojqUt_s130_assertion description "[A total of 125 long-standing type 1 diabetic patients were ranked by renal mesangial expansion score (MES) based on renal biopsy findings and diabetes duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262180.RAdCLIYTA1I_gcaLOhv6G18eZYWKtMjN298UICojqUt_s130_provenance.
NP262181.RAR8mrPI088WC59Tecydlzpal7tbxNaXahmAJjKJb5hpM130_assertion description "[The aim of this study was to evaluate critically the recently modified activated-partial-thromboplastin-time (APTT)-based activated protein C (APC)-resistance tests, which are more specific for the factor V Leiden mutation than the first generation APC-resistance tests.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262181.RAR8mrPI088WC59Tecydlzpal7tbxNaXahmAJjKJb5hpM130_provenance.
NP262187.RAUb3brpfRUDciQZYtv-C4HEfnkiiHGXD2p6ZzvltHcck130_assertion description "[Results from tissue microarray in this study and our previous reports revealed that stomatin-like protein 2 (SLP-2) is notably associated with tumorigenesis and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262187.RAUb3brpfRUDciQZYtv-C4HEfnkiiHGXD2p6ZzvltHcck130_provenance.
NP262191.RATX6bgQY5cOFGZNJnNj2T9gHMwxN6C6eqPbMkqbJPVGc130_assertion description "[Fluorescently labeled probes specific for ERG-related rearrangements involving the TMPRSS2-ERG fusion as well as TMPRSS2-ETV1 and TMPRSS2-ETV4 were used to assess samples for gene rearrangements indicative of malignancy under a design of sequential trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262191.RATX6bgQY5cOFGZNJnNj2T9gHMwxN6C6eqPbMkqbJPVGc130_provenance.
NP262192.RAYwUH9yM6wRL8ViADigy8z3RxUcI5lFVQkhqTnFSRNWQ130_assertion description "[In this review, we describe current evidence and controversies regarding the relationship between UPS and neurodegenerative disorders such as PD, and discuss several scientific discrepancies that await further clarification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262192.RAYwUH9yM6wRL8ViADigy8z3RxUcI5lFVQkhqTnFSRNWQ130_provenance.
NP262197.RAe2V7eUPRXQLLNtf-2GFNry12GYvRIsP29EijIgEtojQ130_assertion description "[C(-260)-->T polymorphism in the promoter of the CD14 monocyte receptor gene as a risk factor for myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262197.RAe2V7eUPRXQLLNtf-2GFNry12GYvRIsP29EijIgEtojQ130_provenance.
NP262202.RAT1RqiibwKGjBb4E88cbDk3JOQQqmFtOC7e1iiOK0NHI130_assertion description "[Furthermore, a distinct phosphorylated form of Cx43, as well as the autophagosome-targeted form of LC3 (microtubule-associated protein light chain 3) targeted to lipid rafts in cardiac tissue, and both were increased in heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262202.RAT1RqiibwKGjBb4E88cbDk3JOQQqmFtOC7e1iiOK0NHI130_provenance.
NP262205.RAftntEoNMQ1Xj6CxAB5BQEAPp6I79360qd2NynK7aQvs130_assertion description "[No significant difference was found in IL1RN and IL1B (-511 and +3953) genotype distributions between CAD and control subjects or MVD and control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262205.RAftntEoNMQ1Xj6CxAB5BQEAPp6I79360qd2NynK7aQvs130_provenance.
NP262209.RATwhwxD7_-5u_Fps1a62ER6VXBh5cDZE8MkLv00LJKZ0130_assertion description "[In addition, the specific alterations in MAL and/or MAL2 expression observed in specific types of carcinoma provides a basis to understand the loss of the polarized phenotype that frequently accompanies the neoplastic transformation process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262209.RATwhwxD7_-5u_Fps1a62ER6VXBh5cDZE8MkLv00LJKZ0130_provenance.
NP262216.RAYGIC7_YroOZuO3xZrD9ZmZNg3mq1syEP0UKs2UyPWF0130_assertion description "[SUZ12 mutations were identified in 1 of 2 patients with myelodysplastic syndrome/myeloproliferative neoplasms with 17q acquired uniparental disomy and in 2 of 2 myelofibrosis cases with focal 17q11 deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262216.RAYGIC7_YroOZuO3xZrD9ZmZNg3mq1syEP0UKs2UyPWF0130_provenance.
NP262218.RAal02Rw0KYTTnMPW5an__-uy3o0hM1fu4xZ2UB5Sww6o130_assertion description "[These data suggest that in human GBM overexpression of delta EGFR is associated with differential genotoxic stress-provoked p53 mRNA induction whereas MDM2 mRNA expression is apparently not directly affected by EGFR status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262218.RAal02Rw0KYTTnMPW5an__-uy3o0hM1fu4xZ2UB5Sww6o130_provenance.
NP262220.RAUsEhCpi47brF3jIE5UNf48BhCPe1w_Wiu1G1ATNN1IE130_assertion description "[Haplotype-based analysis revealed the CAD and control groups differed significantly in the frequencies of haplotype ACC at positions -238, -857 and -863 (OR = 1.77; 95% CI = 1.05-2.98; P = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262220.RAUsEhCpi47brF3jIE5UNf48BhCPe1w_Wiu1G1ATNN1IE130_provenance.
NP262223.RAYE6R5LWZIx8BqYBXUAfFwjYuzlp9uZJA8UiCT3BFQbo130_assertion description "[Measuring sCD14 in tuberculosis may help monitor anti-tuberculosis treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262223.RAYE6R5LWZIx8BqYBXUAfFwjYuzlp9uZJA8UiCT3BFQbo130_provenance.
NP262224.RAf41POt-sh4oF-hpK3GisFHdMB4UfowMXe0gT_VZJrXk130_assertion description "[In 45/112 patients without the established risk factors for RVO (hyper-tension, hypercholesterolemia and diabetes) or characteristics known to be associated to increased PAI-1 activity (overweight, hypertriglyceridemia, and smoking habit) the contemporary presence of ACE DD and PAI-1 4G4G genotype was significantly associated with a risk for RVO (OR = 8.26, 95% CI 1.18-57.92; p = 0.034).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262224.RAf41POt-sh4oF-hpK3GisFHdMB4UfowMXe0gT_VZJrXk130_provenance.
NP262228.RAbucf3fsg0qu6VOw42mGttd7LCGVXfus_73Aiw1Sat6I130_assertion description "[As a result of the t(11;22)(q24;q12) chromosomal translocation characterizing the Ewing family of tumors (ET), the amino terminal portion of EWS, an RNA binding protein of unknown function, is fused to the DNA-binding domain of the ets transcription factor Fli1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262228.RAbucf3fsg0qu6VOw42mGttd7LCGVXfus_73Aiw1Sat6I130_provenance.
NP262230.RAeJ46PazVDF5mD0VFPoMhdALdWSXxIrDVsvugMLb1YaM130_assertion description "[Higher plasma vascular endothelial growth factor levels correlate with menopause, overexpression of p53, and recurrence of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262230.RAeJ46PazVDF5mD0VFPoMhdALdWSXxIrDVsvugMLb1YaM130_provenance.

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