Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP226174.RAsnS5ZdzKAhv7bpYdorQ96fkNSIJC55wp7x2_OcW0vfQ130_assertion description "[Local secretion of IL-2 gene-transduced tumor cells abrogates their tumorigenicity and induces protective immunity and may inhibit the growth of neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226174.RAsnS5ZdzKAhv7bpYdorQ96fkNSIJC55wp7x2_OcW0vfQ130_provenance.
- NP226177.RAn7JVMXImM8pUZzxqBsHf2pdXub37oD8NsaY1J-I7WY0130_assertion description "[Prognostic value of kallikrein-related peptidase 6 protein expression levels in advanced ovarian cancer evaluated by automated quantitative analysis (AQUA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226177.RAn7JVMXImM8pUZzxqBsHf2pdXub37oD8NsaY1J-I7WY0130_provenance.
- NP226185.RAip_IMFwcUov4RJhi-XuKA29YJtkJINQoirJgONnGjY8130_assertion description "[We report a novel germline 5369delATTT mutation in BRCA2 gene, detected in a 45-year-old woman with bilateral breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226185.RAip_IMFwcUov4RJhi-XuKA29YJtkJINQoirJgONnGjY8130_provenance.
- NP226186.RAgjM5oWFEKELt6_jyla-iNLBfMuEm9-TOlUEEgeYLcyo130_assertion description "[The waiting period from notification regarding positive NBS results to diagnostic test results can be psychologically distressing to parents, causing depressive symptoms that vary depending on their perceptions about the likelihood that their infant has CF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226186.RAgjM5oWFEKELt6_jyla-iNLBfMuEm9-TOlUEEgeYLcyo130_provenance.
- NP226187.RAgsRC8K6pTOJX-vAiLJ1OSiusvj9L2KZbVR9sqcmbsz0130_assertion description "[For MMP2 -1306 C>T, MMP3 -1171 5A>6A, and MMP9 -1562 C>T, there was no association between these polymorphisms and the risk of colorectal cancer under the dominant and recessive models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226187.RAgsRC8K6pTOJX-vAiLJ1OSiusvj9L2KZbVR9sqcmbsz0130_provenance.
- NP226199.RAiA6Z6a-ceCFC1dh7CNe3ffz4_GGblp-zABPCtZoCVSg130_assertion description "[The EGFR mutation rate in pleural metastatic tissues of lung adenocarcinoma acquired through video-assisted thoracoscopic surgery was higher compared to that in surgical resection specimens, plasma specimens and pleural effusion specimens compared to previously reported results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226199.RAiA6Z6a-ceCFC1dh7CNe3ffz4_GGblp-zABPCtZoCVSg130_provenance.
- NP226208.RAoKwuNRsabfWVi_IN4zL5lvKJZaQWc5S1mwBKATEW4CM130_assertion description "[In 25 kindred members at direct risk for familial medullary thyroid carcinoma (MTC), basal peripheral plasma calcitonin (CT) levels were less than 240 pg/ml.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226208.RAoKwuNRsabfWVi_IN4zL5lvKJZaQWc5S1mwBKATEW4CM130_provenance.
- NP226209.RAkkqc0-6WfIYIgJyXBsplSA3OaB2k0fpVqgEmlBi-LQA130_assertion description "[Increased MIF concentrations were detected in the sera of patients with acute myocardial infarction (AMI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226209.RAkkqc0-6WfIYIgJyXBsplSA3OaB2k0fpVqgEmlBi-LQA130_provenance.
- NP226210.RArVHxrB1K8974eXzKMfKJsigD2TSy12W13aWaaakkOBo130_assertion description "[Thus, Hakai can affect the oncogenic phenotype both by altering E-cadherin-based intercellular adhesions and by increasing PSF's ability to bind RNAs that promote cancer-related gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226210.RArVHxrB1K8974eXzKMfKJsigD2TSy12W13aWaaakkOBo130_provenance.
- NP226216.RAvigA5NVwRdnTOXLTMJxDPz460xcJ2Eqad7dnz81KN0Y130_assertion description "[However, several dominant heterozygous mutations in the peripheral myelin protein 22 (PMP22) gene and dominant mutations in the peripheral myelin protein zero (MPZ) gene, both in the heterozygous and homozygous state, have been reported in patients with DSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226216.RAvigA5NVwRdnTOXLTMJxDPz460xcJ2Eqad7dnz81KN0Y130_provenance.
- NP226217.RArlTFN6xwlQ69PszVx36uE-fcxro_HZEE_uJnj8Rw5JM130_assertion description "[In conclusion, the results confirmed involvement of the PPARgamma pathway in NASH and the therapeutic utility of a PPARgamma ligand.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226217.RArlTFN6xwlQ69PszVx36uE-fcxro_HZEE_uJnj8Rw5JM130_provenance.
- NP226218.RAs5SGJojnIm0M6OiCBtV0jz73bd7Qua6Ja-GyQ2ddMyQ130_assertion description "[Bronchial lesions (n=88) were morphologically classified as hyperplasia (HP, n=5), squamous metaplasia (SM, n=23), low-grade dysplasia (LGD, n=14), high-grade dysplasia (HGD, n=11), intraepithelial carcinoma including 'carcinoma in situ' (CIS) (IEC, n=15), and microinvasive carcinoma (MIC, n=20).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226218.RAs5SGJojnIm0M6OiCBtV0jz73bd7Qua6Ja-GyQ2ddMyQ130_provenance.
- NP226221.RAgvH3JK7COp62-4RIkkk9d9Ee1obmDzKC9Ae3vqXhfxU130_assertion description "[In situ hybridization localized Pit-1 mRNA in all pituitary adenomas, although the mRNA levels in GH and prolactin adenomas were significantly higher than those in ACTH, null cell and gonadotroph tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226221.RAgvH3JK7COp62-4RIkkk9d9Ee1obmDzKC9Ae3vqXhfxU130_provenance.
- NP226224.RAilT_A3wbsmoDrzTaEveLxtPLQo8A0B-uOTf9Vh8cazg130_assertion description "[This study showed for the first time that polymorphisms of CD40 are associated with susceptibility to KD and CAL formation, in the Taiwanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226224.RAilT_A3wbsmoDrzTaEveLxtPLQo8A0B-uOTf9Vh8cazg130_provenance.
- NP226227.RAnyKKmGIwie7SZYAVNIYKoFAO1b8sY85bPOYtyUhnwOQ130_assertion description "[Malignant GISTs are more likely to be associated with a positive E2F1 and p53 phenotype and a negative p16 and p27(KIP1) phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226227.RAnyKKmGIwie7SZYAVNIYKoFAO1b8sY85bPOYtyUhnwOQ130_provenance.
- NP226231.RAhiAf-YzbM9oQcGNLqLfqGUJdbnsL4huFyIuII6k5B64130_assertion description "[NOD2 mutations affect muramyl dipeptide stimulation of human B lymphocytes and interact with other IBD-associated genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226231.RAhiAf-YzbM9oQcGNLqLfqGUJdbnsL4huFyIuII6k5B64130_provenance.
- NP226242.RAlZGjIT1cM6aLfDuppZFfF09e3m1kqFywL3DQrhTJQ4M130_assertion description "[If mutation of SRA1 or SRVX can reverse the sex of the XY fetus, this would explain why mutation within SRY is found only sporadically in women with XY gonadal dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226242.RAlZGjIT1cM6aLfDuppZFfF09e3m1kqFywL3DQrhTJQ4M130_provenance.
- NP226250.RAntQs2xKu2_ZM9T3nelaEKTx0QwPdlO_CHNdoiiu1Tp8130_assertion description "[In the authors' previous study, IGFBP5 was found to be significantly up-regulated in lymph node metastases compared with their paired primary breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226250.RAntQs2xKu2_ZM9T3nelaEKTx0QwPdlO_CHNdoiiu1Tp8130_provenance.
- NP226255.RAt7odTXk5QvgTdvw6RY2-fDMJYXjSZwGeUd4OaigAjiY130_assertion description "[Peptides produced by the renin-angiotensin system play a major role in the development and progression of various cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226255.RAt7odTXk5QvgTdvw6RY2-fDMJYXjSZwGeUd4OaigAjiY130_provenance.
- NP226260.RAuFq_KFgthN69BJ7lvdMMb0O7Ug_5lEv_019naPFUucw130_assertion description "[Our results demonstrate a strong genetic heterogeneity among the ethnic group and suggest that the Gly40Ser mutation of the glucagon receptor gene plays little role, if any, in the pathogenesis of type 2 diabetes and essential hypertension in the Taiwanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226260.RAuFq_KFgthN69BJ7lvdMMb0O7Ug_5lEv_019naPFUucw130_provenance.
- NP226262.RAsxB1ZM36NYUDQEtgXWxoR0sd5LPvEYlnfg3STXJ8a9s130_assertion description "[The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226262.RAsxB1ZM36NYUDQEtgXWxoR0sd5LPvEYlnfg3STXJ8a9s130_provenance.
- NP226263.RAjt4H-IvA1gpEpWW5onI0YsGN0ElRIqBgzHp51gwpicY130_assertion description "[All four PCa specimens with nuclear accumulation of p53 were stage III disease and showed DNA methylation of RIZ1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226263.RAjt4H-IvA1gpEpWW5onI0YsGN0ElRIqBgzHp51gwpicY130_provenance.
- NP226267.RAreCr1q-PNNpgVpTFaj_YXpbxOiA_kiURCxehHR6Ciyk130_assertion description "[Several neuroblastoma (NB) susceptibility loci have been identified within LINC00340, BARD1, LMO1, DUSP12, HSD17B12, DDX4, IL31RA, HACE1 and LIN28B by genome-wide association (GWA) studies including European American individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226267.RAreCr1q-PNNpgVpTFaj_YXpbxOiA_kiURCxehHR6Ciyk130_provenance.
- NP226268.RAh47pFT1zCUDa9Q-UssM-Kctq_x6W_oMZgduD1TYhPQc130_assertion description "[The results showed that the number of cells attached to FN-matrix increases upon treatment of the cells with staurosporine, indicating that the change of N-glycosylation of the FN-receptor promotes cell adhesion to the extracellular matrix, which may lead to the suppression of metastasis of cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226268.RAh47pFT1zCUDa9Q-UssM-Kctq_x6W_oMZgduD1TYhPQc130_provenance.
- NP226270.RAg5pXiqQN68xBiWi5ncF-0bIyZ-nx4Un79-ImdnXCHRA130_assertion description "[Germline VHL mutations may be detected in 5-11% of all phaeochromocytoma cases and mutation analysis of VHL and other phaeochromocytoma susceptibility genes (SDHB, SDHD and RET) should be performed in all cases of familial, multiple or early onset phaeochromocytomas, and considered in other cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226270.RAg5pXiqQN68xBiWi5ncF-0bIyZ-nx4Un79-ImdnXCHRA130_provenance.
- NP226273.RAqyMgGaGwegH2OeYF1ALRwkjPKVL7GMBnYQ1G8yhth1Q130_assertion description "[Among 144 patients with bladder transitional cell carcinoma CK-20 was positive in 131.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226273.RAqyMgGaGwegH2OeYF1ALRwkjPKVL7GMBnYQ1G8yhth1Q130_provenance.
- NP226277.RAq0Aup_twTWTl_c5REy_8zJL7n1yT-w2YKZPGJ-Qi-zA130_assertion description "[The RB-1 gene is a tumour suppressor gene, but other loci including D13S319 and D13S25 telomeric to this within 13q14.3 are deleted in B-cell chronic lymphocytic leukaemia (B-CLL), multiple myeloma and non-Hodgkin's lymphoma, with varying clinical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226277.RAq0Aup_twTWTl_c5REy_8zJL7n1yT-w2YKZPGJ-Qi-zA130_provenance.
- NP226281.RAnC1571RMY9XAKA4ZH3CazfIPWjv5C0xDV8ERxX4x7VE130_assertion description "[Human telomerase RNA component (hTR) expression, which increases in the majority of cancer cells with an acquisition of telomerase activity, was concomitantly evaluated with methylation status and human telomerase reverse transcriptase (hTERT) expression in colorectal cancers and precursor lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226281.RAnC1571RMY9XAKA4ZH3CazfIPWjv5C0xDV8ERxX4x7VE130_provenance.
- NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_assertion description "[This meta-analysis suggested that the alleles with shorter VNTR length significantly increased the risk of IDD, while the VDR (TaqI, FokI, ApaI) gene polymorphisms were not significantly associated with the risk of IDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_provenance.
- NP226287.RAvqypGLWYzmxfhzkzcq7toqB8wP4feK_0RF-Fz7W4gBE130_assertion description "[Danon disease is caused by mutations of the lysosome-associated membrane protein-2 (LAMP2) gene at Xq24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226287.RAvqypGLWYzmxfhzkzcq7toqB8wP4feK_0RF-Fz7W4gBE130_provenance.
- NP226295.RAhs8vPln47r0NA59QC3iPaOoR1LcqgfnqFlkzVMmVX38130_assertion description "[On the other hand, others are more disease specific (HLA-DRB1*11 for systemic sclerosis and HLA-DRB1 alleles encoding the `shared epitope` in RA) as well as non MHC genes, such as FcyRIIa and IIIa in SLE, the beta2 glycoprotein I gene in the aPL syndrome, and the TSHR gene in Graves' disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226295.RAhs8vPln47r0NA59QC3iPaOoR1LcqgfnqFlkzVMmVX38130_provenance.
- NP226303.RAnEilUJQUrhL200boJR5UJc1SUnmyx8DRfVYXa8bEWRU130_assertion description "[Clinical significance of runt-related transcription factor 1 polymorphism in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226303.RAnEilUJQUrhL200boJR5UJc1SUnmyx8DRfVYXa8bEWRU130_provenance.
- NP226306.RAs-z7fH6Z3adYQ3VKry8q7Fj2HvOUmLNsSxhPM-9TqX0130_assertion description "[Strong nuclear ERG overexpression was found in 36.7% of prostate carcinomas as well as in various vascular tumours, including Kaposi sarcomas (91.7%), angiosarcomas (100%) and haemangiomas (90.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226306.RAs-z7fH6Z3adYQ3VKry8q7Fj2HvOUmLNsSxhPM-9TqX0130_provenance.
- NP226311.RApKDjiq2LX0GLblSAqBM4xBA6CFEC9M2EGj2gWdhyX_Y130_assertion description "[Cancer stem cells or cancer-initiating cells (CIC) represent a theorized population of cells that give rise to tumors and are responsible for treatment resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226311.RApKDjiq2LX0GLblSAqBM4xBA6CFEC9M2EGj2gWdhyX_Y130_provenance.
- NP226315.RAhwgUt5l_p6JzjJ1CWsQqwr_crwyafMoLa9Q_Wvyx5Ok130_assertion description "[Similar analysis showed that the apoA-I[Delta(62-78)] deletion mutant in apoA-I-deficient mice caused combined hyperlipidemia characterized by increased triglycerides, cholesterol, and phospholipids in the VLDL/IDL region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226315.RAhwgUt5l_p6JzjJ1CWsQqwr_crwyafMoLa9Q_Wvyx5Ok130_provenance.
- NP226316.RAjBKp-RtFXXeMB01e1-dXNdBQOTik1BuuERDU8AmRyn0130_assertion description "[The results demonstrate high penetrance of hypokalemic alkalosis, hypomagnesemia, and hypocalciuria in patients inheriting 2 mutant NCCT alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226316.RAjBKp-RtFXXeMB01e1-dXNdBQOTik1BuuERDU8AmRyn0130_provenance.
- NP226318.RAg8KaRdr0tIkT4ZSgOBUFSc0LB5NTpprR9JucTLJ1Hdw130_assertion description "[Disrupted in Schizophrenia 1 (DISC1) is a key susceptibility gene implicated in major mental illnesses, such as schizophrenia, depression, bipolar disorder and autism, but the link between this protein and the pathology of these diseases remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226318.RAg8KaRdr0tIkT4ZSgOBUFSc0LB5NTpprR9JucTLJ1Hdw130_provenance.
- NP226323.RAhH_6VfchiKg9XpNstVNqbqUpji7yEpaua625o26nykA130_assertion description "[The low cytotoxicity of the DEFB114 peptide toward human erythrocytes is indicative of its potential therapeutic use in the treatment of LPS-induced inflammation, LPS contamination, and potentially septic shock.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226323.RAhH_6VfchiKg9XpNstVNqbqUpji7yEpaua625o26nykA130_provenance.
- NP226326.RAoQ8LN0un9jv8FXatK4LrEhrnEYwakazhzkFm1Lmopd8130_assertion description "[Assays for the detection of factor-V Leiden mutation and the plasma concentrations of protein C, protein S, antithrombin III, and lipoprotein (a) were performed on plasma samples from children with Legg-Perthes disease, and the results were compared with those for pooled plasma from normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226326.RAoQ8LN0un9jv8FXatK4LrEhrnEYwakazhzkFm1Lmopd8130_provenance.
- NP226327.RAiSSa5BpGwBlF3uVvY6hidBSPL5j0ye2U9f0zRK9fJfM130_assertion description "[All family members with maculopathy consistent with Best disease (n = 10) had an amino acid-changing mutation in the VMD2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226327.RAiSSa5BpGwBlF3uVvY6hidBSPL5j0ye2U9f0zRK9fJfM130_provenance.
- NP226338.RAsnDKp7uTQso1diQQyvSsK-d_urNV_vF94xCAEcD0RIs130_assertion description "[These results suggest that hypoxia induce the expression of HIF-1α and MDR1/P-gp in colon carcinoma and HIF-1α expression may be associated with the gene MDR1 (P-gp) and interactively involved in the occurrence of tumor multidrug resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226338.RAsnDKp7uTQso1diQQyvSsK-d_urNV_vF94xCAEcD0RIs130_provenance.
- NP226342.RAvLQTuXt1hX0eDDt-laT_33H1vewb0gl_dbdQFygoimA130_assertion description "[After more than 20 years of research, there is still uncertainty with regard to the role of CLU in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226342.RAvLQTuXt1hX0eDDt-laT_33H1vewb0gl_dbdQFygoimA130_provenance.
- NP226347.RAtFLh6iNUNcTmwLwGzPdrBHfYTSCXSj_JYb7Ep2k9gtk130_assertion description "[MTHFR 677C>T also increased the risk of leukopenia and gastrointestinal toxicity, whilst thymidylate synthase 28 bp repeat polymorphism increased the risk of anemia (odds ratio 8.48, 95% confidence interval 2.00-36.09).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226347.RAtFLh6iNUNcTmwLwGzPdrBHfYTSCXSj_JYb7Ep2k9gtk130_provenance.
- NP226351.RAn8NDPcRoLmPe-X_PxWsGvwqLyjRb4qjC-QeX1b6rTzc130_assertion description "[In this study, we investigated the molecular mechanisms associated with the MUC4-induced invasion and metastasis in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226351.RAn8NDPcRoLmPe-X_PxWsGvwqLyjRb4qjC-QeX1b6rTzc130_provenance.
- NP226355.RAkiLOXBv6RpASaMLnD0N8GDN2HQKbaEMdTMqySVjUMTA130_assertion description "[A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226355.RAkiLOXBv6RpASaMLnD0N8GDN2HQKbaEMdTMqySVjUMTA130_provenance.
- NP226359.RAtqB9qO2TvIq46y3szdDPNM4whxwbzI-1qsLYXLVNKpE130_assertion description "[A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226359.RAtqB9qO2TvIq46y3szdDPNM4whxwbzI-1qsLYXLVNKpE130_provenance.
- NP226361.RAk2qADi0VqFaSqL_lcwegQpbR11u3VbKyrvLJRfEt-as130_assertion description "[Growth hormone administration improves weight gain and reduces disease activity in interleukin 10-null mice with colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226361.RAk2qADi0VqFaSqL_lcwegQpbR11u3VbKyrvLJRfEt-as130_provenance.
- NP226362.RAhJ3PT0WjHSGq9lE7NOvk79dLMf4lb1wrnEg4le9OPEU130_assertion description "[Although these lesions are efficiently repaired in the skin, this CPD formation results in various acute effects (erythema, inflammatory responses), transient effects (suppression of immune function), and chronic effects (mutation induction and skin cancer).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226362.RAhJ3PT0WjHSGq9lE7NOvk79dLMf4lb1wrnEg4le9OPEU130_provenance.
- NP226370.RAulkqUOeG_6nE9kIjiJFm9fDV2CF6r92PWU8crQ0J3G4130_assertion description "[Frequent genetic abnormalities include mutation of the familial adenomatous polyposis (APC) and/or the mutated in colorectal cancer (MCC) genes on chromosome 5q21, activation of K-ras and loss of the tumour suppressor genes p53 and DCC (deleted in colorectal cancer).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226370.RAulkqUOeG_6nE9kIjiJFm9fDV2CF6r92PWU8crQ0J3G4130_provenance.
- NP226372.RAtEvOkrDqZM-vBVs_Hp7634rDurf233r_DyinLYLvpgI130_assertion description "[A total of 1,175 patients with RA and 3,404 controls were genotyped for the PD-1.3 A/G polymorphism, which previously was identified as being involved in susceptibility to systemic lupus erythematosus (SLE) in patients of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226372.RAtEvOkrDqZM-vBVs_Hp7634rDurf233r_DyinLYLvpgI130_provenance.
- NP226379.RAr25I3uE6QbYVYgFGN8yAmq71tOVKboDoatud9WhGeFE130_assertion description "[Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226379.RAr25I3uE6QbYVYgFGN8yAmq71tOVKboDoatud9WhGeFE130_provenance.
- NP226381.RAmj2Zx0GSUbx3L3aNe8OW1aKbM33BsTe37-YzEFNdKR0130_assertion description "[In situ hybridization with 35S-labelled riboprobes showed a pronounced expression of VEGF mRNA in acutely hypoxic proximal and distal tubules of both the cortex and medulla; VEGF protein was demonstrated in the epithelia of these tubules by immunohistochemistry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226381.RAmj2Zx0GSUbx3L3aNe8OW1aKbM33BsTe37-YzEFNdKR0130_provenance.
- NP226398.RArYd6-mAFmSAVKRQoLwZLwxn-m2x10jTrh8iKJhSijCM130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226398.RArYd6-mAFmSAVKRQoLwZLwxn-m2x10jTrh8iKJhSijCM130_provenance.
- NP226400.RAu46JOnGUuTvLkguW1q-KRZsimX3PgpeLD1phdhS0b64130_assertion description "[Latent membrane protein 1 suppresses RASSF1A expression, disrupts microtubule structures and induces chromosomal aberrations in human epithelial cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226400.RAu46JOnGUuTvLkguW1q-KRZsimX3PgpeLD1phdhS0b64130_provenance.
- NP226402.RArL-3BJpZEHiotAUCSZyX1tXPrY2vLOqZjz5Y3vI9IKs130_assertion description "[Mutations in human T-box genes TBX3, TBX5, and TBX1 cause severe genetic disorders known as Ulnar-Mammary syndrome (UMS), Holt-Oram syndrome (HOS), and DiGeorge syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226402.RArL-3BJpZEHiotAUCSZyX1tXPrY2vLOqZjz5Y3vI9IKs130_provenance.
- NP226407.RAihNOGg-s42FW_DRrX1Ie5d2UZdHbd-xzlc02zGLq-Ak130_assertion description "[Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226407.RAihNOGg-s42FW_DRrX1Ie5d2UZdHbd-xzlc02zGLq-Ak130_provenance.
- NP226409.RAmbNS3odwM4r6-mGAwcsJbEu-PVf7SU3PSE7qihZ9Nqo130_assertion description "[We also found that drusen in the eyes of AMD patients were strongly immunolabeled with HTRA1 antibody.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226409.RAmbNS3odwM4r6-mGAwcsJbEu-PVf7SU3PSE7qihZ9Nqo130_provenance.
- NP226411.RAqZtdIuZtY1clyqiCRY3j1EueNwYHnJJshd4A-u8f8MA130_assertion description "[In contrast, the lymphocyte-specific chemokine Mig (monokine induced by interferon-gamma) was strongly expressed by mononuclear cells (mainly macrophages) infiltrating the tumour margin in primary MM lesions, whereas expression was less intense in MM metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226411.RAqZtdIuZtY1clyqiCRY3j1EueNwYHnJJshd4A-u8f8MA130_provenance.
- NP226412.RAiEZ6JjUHElxPjbf9VTsMQYaRm4b186WgU0oX3qHOcik130_assertion description "[A significant association between increased expression of HLM with metastatic disease was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226412.RAiEZ6JjUHElxPjbf9VTsMQYaRm4b186WgU0oX3qHOcik130_provenance.
- NP226417.RAq00N9fYs43jpeU-pEMBVL5H2FmeZj7jMZ8L9g96bwQM130_assertion description "[Human leukemias with mutated FLT3 kinase are synergistically sensitive to FLT3 and Hsp90 inhibitors: the key role of the STAT5 signal transduction pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226417.RAq00N9fYs43jpeU-pEMBVL5H2FmeZj7jMZ8L9g96bwQM130_provenance.
- NP226425.RAtcInGqb109-oL8cQjPPOWypBUGsgW53Er4RcUGSw71o130_assertion description "[We identified five families with autosomal dominant focal segmental glomerulosclerosis in which disease segregated with mutations in the gene TRPC6 on chromosome 11q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226425.RAtcInGqb109-oL8cQjPPOWypBUGsgW53Er4RcUGSw71o130_provenance.
- NP226426.RApCpvjrwTDeOrc03pZO7n25bkiCQ4hzqq7MlJK6wG7k4130_assertion description "[Recently, BRAF has been identified as a common site of activating mutations, and, although many reports focus on its growth-promoting effects, this pathway has also been implicated in progression toward metastatic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226426.RApCpvjrwTDeOrc03pZO7n25bkiCQ4hzqq7MlJK6wG7k4130_provenance.
- NP226427.RAjtc3tUj9UBmctK8I2PUuf3oTxeiGM-dpFPUSKjcDedA130_assertion description "[These data represent the first identification of an important function of DJ-1, which is to regulate the invasion and metastasis properties of PDAC through the ERK/uPA cascade.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226427.RAjtc3tUj9UBmctK8I2PUuf3oTxeiGM-dpFPUSKjcDedA130_provenance.
- NP226432.RAmDT3a3u_ZgsG8BGJfcOIAGqwMMxqd9-yIJFNoUQTVyc130_assertion description "[In a population-based case-control study of non-Hodgkin lymphoma (NHL) (n = 518 cases, 597 controls) among women in Connecticut, we analyzed one or more single nucleotide polymorphisms (SNPs) in ten candidate genes (AKR1A1, AKR1C1, AKR1C3, CYBA, GPX1, MPO, NOS2A, NOS3, OGG1, and SOD2) that mediate oxidative stress directly or indirectly in the NADPH oxidase-dependent respiratory burst.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226432.RAmDT3a3u_ZgsG8BGJfcOIAGqwMMxqd9-yIJFNoUQTVyc130_provenance.
- NP226434.RAjlVh9Ywz6QBP6zCbwo1aUdnm76u5MNXr6DG43lFbkww130_assertion description "[The present study explores the efficacy of this purified protein as an anti-inflammatory agent, using the animal model of MS - experimental autoimmune encephalomyelitis (EAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226434.RAjlVh9Ywz6QBP6zCbwo1aUdnm76u5MNXr6DG43lFbkww130_provenance.
- NP226442.RAnfgD9e57PN4FqaD1sQ6U5m0oWB_cKkfzHrgiokI979A130_assertion description "[However, the Irish study did find an increased risk of DS associated with the MTRR polymorphism and an interactive effect of MTRR and MTHFR polymorphisms with increased risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226442.RAnfgD9e57PN4FqaD1sQ6U5m0oWB_cKkfzHrgiokI979A130_provenance.
- NP226448.RAv6yOExw2kMrwpbIJNLETMTs-DmZqs2y7DylS4v9ryHQ130_assertion description "[While many tumor cell lines no longer respond to the inhibitory effects of TGFB due to a reduction or absence of the type II receptor (TGFBR2), the role of TGFBR2 in tumors from patients with breast cancer is less clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226448.RAv6yOExw2kMrwpbIJNLETMTs-DmZqs2y7DylS4v9ryHQ130_provenance.
- NP226453.RAuL9RZRAIuMnyLNKL8moR9lOsgwr1gA8fm0XaUO7ClC4130_assertion description "[An AHC critical region of 200-500 kilobases has been defined by physical mapping and partially overlaps with a 160-kilobase dosage-sensitive sex (DSS) reversal critical region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226453.RAuL9RZRAIuMnyLNKL8moR9lOsgwr1gA8fm0XaUO7ClC4130_provenance.
- NP226454.RAkGJbFizXoyiBJP1NQIwHpKMyaHy3TTZQ13_P-IX_PzQ130_assertion description "[It is suggested that CDK6 could be potentially a therapeutic target for the treatment of the FTLD-TDP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226454.RAkGJbFizXoyiBJP1NQIwHpKMyaHy3TTZQ13_P-IX_PzQ130_provenance.
- NP226458.RAvW8Gmnu4FDxKiCVgPdafHPncwTvEnLNsTfnbgWBS6H0130_assertion description "[This review will discuss the current knowledge of the association of the HFE gene variants with neurodegenerative diseases: amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, and ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226458.RAvW8Gmnu4FDxKiCVgPdafHPncwTvEnLNsTfnbgWBS6H0130_provenance.
- NP226461.RAsw8M50i0UZwszOWy9dN0XVSUET26u0B2DEzxs8zUhrU130_assertion description "[The LAMP assay is a rapid, highly specific and sensitive method for the diagnosis of retinitis caused by HSV-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226461.RAsw8M50i0UZwszOWy9dN0XVSUET26u0B2DEzxs8zUhrU130_provenance.
- NP226463.RApNMaLcqfwxV0N_tW36iLT79PNn-fUW3sZTIRZCD_6L0130_assertion description "[models of mycobacterial infection and observed MIF-deficient mice to succumb more quickly with higher organism burden, increased lung pathology, and decreased innate cytokine production (TNF-α, IL-12, IL-10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226463.RApNMaLcqfwxV0N_tW36iLT79PNn-fUW3sZTIRZCD_6L0130_provenance.
- NP226464.RAiJyZDs6PXJ7o6lTQw1rxdKZe_j1tDIG5_Nb2Tp9fb20130_assertion description "[We investigated the in vitro effects produced by cadmium exposure in normal or tumor cells derived from human prostate epithelium, including RWPE-1 and its cadmium-transformed derivative CTPE, the primary adenocarcinoma 22Rv1 and CWR-R1 cells and LNCaP, PC-3 and DU145 metastatic cancer cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226464.RAiJyZDs6PXJ7o6lTQw1rxdKZe_j1tDIG5_Nb2Tp9fb20130_provenance.
- NP226483.RAmEM16sTh4-M524ibNO7dsGwhKyE1MOoJNs0rj4orr08130_assertion description "[Compared with double noncarriers (angiotensinogen -20aa and ACE II), double heterozygotes (ac-I/D genotype), and double homozygotes (cc-DD) had hazard ratios for atrial fibrillation of 1.2(0.9-1.6; P=0.06) and 2.4(1.4-4.1; P=0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226483.RAmEM16sTh4-M524ibNO7dsGwhKyE1MOoJNs0rj4orr08130_provenance.
- NP226489.RAtobKCqG6f1pLbERc2QQYcKBYQCajIPWNfXzfFBorxE0130_assertion description "[Nine genes have been thus far identified as the cause of different types of NCL, with ages at onset ranging from around birth to adult, although the underlying etiology of the disease still remains elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226489.RAtobKCqG6f1pLbERc2QQYcKBYQCajIPWNfXzfFBorxE0130_provenance.
- NP226495.RAoTOpw3sJDxYJOCAiqrf0Bn7_HORxKZqzDcUgouEDXgw130_assertion description "[The association with human leukocyte antigen (HLA) and non-HLA haplotypes and the presence of autoantibodies in sera of PSC patients support a crucial role for immune-mediated mechanisms in the initiation and progression of PSC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226495.RAoTOpw3sJDxYJOCAiqrf0Bn7_HORxKZqzDcUgouEDXgw130_provenance.
- NP226497.RAgDkzdwLYJU-vjjDWygSs-F1dNjwoOYE89IBdG1FYHDk130_assertion description "[This finding in conjunction with the expression of CD54 in all 17 patients with `bright SIg` CLL investigated (characterized by marked organomegaly and poor prognosis) suggest that the differential expression of CD54 in lymphoproliferative disorders may also relate to their degree of malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226497.RAgDkzdwLYJU-vjjDWygSs-F1dNjwoOYE89IBdG1FYHDk130_provenance.
- NP226498.RAtI98lzYxyi3nueNTXI50dQp_Y9s0XOsrNqL1BaZxsHQ130_assertion description "[Correlation of the SNPs of FGFR1, FGF10, FGF18 with nonsyndromic cleft lip with or without palate in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226498.RAtI98lzYxyi3nueNTXI50dQp_Y9s0XOsrNqL1BaZxsHQ130_provenance.
- NP226499.RAhfgJ-TlPmSaesOuFsSzzu17-ErFpKrqTpVMowehZ6ho130_assertion description "[The finding of two promoter mutations (-39 and -53) among 19 FCHL patients with diminished LPL, but not among the other groups of subjects, suggests a potential role of regulatory mutations of the LPL gene in the development of dyslipidemia in FCHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226499.RAhfgJ-TlPmSaesOuFsSzzu17-ErFpKrqTpVMowehZ6ho130_provenance.
- NP226501.RAlIe4upuIrKmCbuwROgcNJL-ec1C-1iwaYAhEvYfY6oE130_assertion description "[To test this hypothesis, we investigated the relationship of IL-8 gene polymorphisms and NPC in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226501.RAlIe4upuIrKmCbuwROgcNJL-ec1C-1iwaYAhEvYfY6oE130_provenance.
- NP226503.RAraa4M2z2iTK4cCAQeLUTsvSDNxyyyEbzstG-vtZw70Q130_assertion description "[We tested whether argininosuccinate lyase deficiency (ASL), a genetic disorder of the urea cycle with hepatomegaly and biochemical hepatitis, causes increased CDT results and whether this depends on the analytical method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226503.RAraa4M2z2iTK4cCAQeLUTsvSDNxyyyEbzstG-vtZw70Q130_provenance.
- NP226504.RAlFzmwqtKU1SUV_po730aTqW8ulOYcEKagEm43cPCnyg130_assertion description "[All probands met modified DSM-IV criteria for AN; all affected first, second, and third degree relatives met DSM-IV criteria for AN, bulimia nervosa (BN), or eating disorder not otherwise specified (NOS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226504.RAlFzmwqtKU1SUV_po730aTqW8ulOYcEKagEm43cPCnyg130_provenance.
- NP226508.RAvfemZ5kBH8aFtwRsGTotC5IJlSp6uvQNueB9EQZhNmY130_assertion description "[Enhanced CXCR4 expression was detected in liver metastases resected from patients with colon cancer treated by the standard FOLFOX regimen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226508.RAvfemZ5kBH8aFtwRsGTotC5IJlSp6uvQNueB9EQZhNmY130_provenance.
- NP226509.RAqr_VHbcZ3vjU7BioO6jAtq0nQpvTuQeJ3teoOCO6yfI130_assertion description "[Proteins of the ET axis were frequently expressed in bladder cancer (ET-1 in 62% of tumours, ET(A)R in 93% of tumours, and ET(B)R in 84% of tumours).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226509.RAqr_VHbcZ3vjU7BioO6jAtq0nQpvTuQeJ3teoOCO6yfI130_provenance.
- NP226510.RAlVmZL2i4NqQS35LLJlqOuf-7luQN1u72SFW7-CGv8mw130_assertion description "[In our population of MTX-treated RA patients the 2756GG genotype of the MTR gene was more common than expected and was associated with MIARN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226510.RAlVmZL2i4NqQS35LLJlqOuf-7luQN1u72SFW7-CGv8mw130_provenance.
- NP226512.RAgNH73uJRLcXZitRhtjnMnnNe5hvYaG-TvPEy-qHTVQY130_assertion description "[Transduction of MSUD lymphoblasts from the Mennonite patient with LSN-E1 alpha viruses restored the decarboxylation of alpha-oxo[1-14C]isovalerate to the normal level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226512.RAgNH73uJRLcXZitRhtjnMnnNe5hvYaG-TvPEy-qHTVQY130_provenance.
- NP226521.RAmDWOg0OTq2UCDKrV95zYXa3SasNSLcwcqlpBTRyZfVE130_assertion description "[Dose-dependent enhancements by interferon-gamma on functional responses of neutrophils from chronic granulomatous disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226521.RAmDWOg0OTq2UCDKrV95zYXa3SasNSLcwcqlpBTRyZfVE130_provenance.
- NP226524.RAkuy-yqLcbSAGJivrbv60jwdYQKtEgn52YGRVO2Di_sM130_assertion description "[Four tyrosine kinase inhibitors that have activity against KIT are currently being used in clinical trials, and one, STI571, has recently been approved by the United States Food and Drug Administration for treating patients with chronic myelogenous leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226524.RAkuy-yqLcbSAGJivrbv60jwdYQKtEgn52YGRVO2Di_sM130_provenance.
- NP226528.RAl5RZCAbphsuQcV63U5hKx2b3OmK6I_2QdcKJTOC9VdY130_assertion description "[The aim of our work is to study the possible role of clinical variables, neuropsychological performance, and the 5HTTLPR, rs25531, and val108/58Met COMT polymorphisms in the prediction of the response to fluoxetine after 4weeks of treatment in a sample of patient with MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226528.RAl5RZCAbphsuQcV63U5hKx2b3OmK6I_2QdcKJTOC9VdY130_provenance.
- NP226531.RAmm_iA_9xCR8X-7O6lNoYo09L8JZ_FcuRIwoS_J5dk9I130_assertion description "[Hepatocyte growth factor (HGF) and its receptor c-MET are commonly expressed in malignant gliomas and embryonic neuroectodermal tumors including medulloblastoma and appear to play an important role in the growth and dissemination of these malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226531.RAmm_iA_9xCR8X-7O6lNoYo09L8JZ_FcuRIwoS_J5dk9I130_provenance.
- NP226539.RAvDHmNBDIzvLCMXCokISPfLHSkqg8uKM88nK1WZN1qns130_assertion description "[Using nested RT-PCR, we compared the specificity and sensitivity of human mammaglobin (hMAM), epidermal-growth-factor receptor (EGF-R), and cytokeratin 19 (CK-19) expression as markers for circulating carcinoma cells in the peripheral blood of patients with breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226539.RAvDHmNBDIzvLCMXCokISPfLHSkqg8uKM88nK1WZN1qns130_provenance.
- NP226541.RAjgowHeyDYcPsQXdUBJSLHlCf5ttqZu-HOZ1SlgdYTM4130_assertion description "[We have identified POU1F1 as the NUP98 fusion partner in therapy-related AML with a t(3;11)(p11;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226541.RAjgowHeyDYcPsQXdUBJSLHlCf5ttqZu-HOZ1SlgdYTM4130_provenance.
- NP226542.RAs4ptDO6qk44RerPc4X2o4w0ZjqH9nbalaYpr7K7pfko130_assertion description "[In conclusion, (i) the WHO classification was associated with a more homogeneous cytogenetic pattern than the FAB classification, (ii) WHO classification and standard/revised IPSS cytogenetic categories were much more effective than IPSS for predicting MDS clinical outcome, (iii) revised cytogenetic subgroups predicted PFI more effectively than standard categories.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226542.RAs4ptDO6qk44RerPc4X2o4w0ZjqH9nbalaYpr7K7pfko130_provenance.
- NP226554.RAoJlcWGxo6mgdxn7bfmCu_BDlBATKgusattJRw9i_Oes130_assertion description "[Together, our data indicate that cfB acts as a downstream effector of TLR signaling and plays a critical role in the pathogenesis of severe bacterial sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226554.RAoJlcWGxo6mgdxn7bfmCu_BDlBATKgusattJRw9i_Oes130_provenance.
- NP226559.RAs5xJh3zRgyEPfNIndBQy1Z6hE8QoTjhAILFOjJcou0A130_assertion description "[Recently, p16 and p15 have been identified as commonly inactivated tumour suppressor genes in haematological malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226559.RAs5xJh3zRgyEPfNIndBQy1Z6hE8QoTjhAILFOjJcou0A130_provenance.
- NP226561.RAlap98gl3xxfSx1nz03lQ-uXhUuSlukkcyW8GC7P-s2E130_assertion description "[In T-cell acute lymphoblastic leukemia (T-ALL) the cardiac homeobox gene NKX2-5 (at 5q35) is variously deregulated by regulatory elements coordinating with BCL11B (at 14q32.2), or the T-cell receptor gene TRD (at 14q11.2), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226561.RAlap98gl3xxfSx1nz03lQ-uXhUuSlukkcyW8GC7P-s2E130_provenance.
- NP226564.RAis6vrZDwFzwUk_dHYu7ZLsuvUBYkgJJHyezM4QT8Ju8130_assertion description "[Overexpression of osteonectin is present in malignant tumors and correlates with disease progression and poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226564.RAis6vrZDwFzwUk_dHYu7ZLsuvUBYkgJJHyezM4QT8Ju8130_provenance.
- NP226567.RApvHbtqEdPc7lHdciRT5roDJ3LkrnqbKrgrOK_fJSVo4130_assertion description "[Muscle weakness in patients with thyrotoxicosis during hypokalemic episodes (thyrotoxic periodic paralysis [TPP]) occurs sporadically and mostly in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226567.RApvHbtqEdPc7lHdciRT5roDJ3LkrnqbKrgrOK_fJSVo4130_provenance.
- NP226568.RAl3gQkf6Vo1Ex-ftAmmBf0EzMoDQ8IkD1slKX6oejUbU130_assertion description "[Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226568.RAl3gQkf6Vo1Ex-ftAmmBf0EzMoDQ8IkD1slKX6oejUbU130_provenance.
- NP226575.RAuQgCQ9PVbCpjEc9OvEu5m8D6PPuM9HKYeLEiB_BS33k130_assertion description "[While >20% of adult ALL Ph1 chromosome-negative undergo methylation of p73, p57, and p15, only 3% of childhood ALL carried such anomalies, which is very significant when a higher fraction of pediatric patients has non-Ph1 ALL than do the adult patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226575.RAuQgCQ9PVbCpjEc9OvEu5m8D6PPuM9HKYeLEiB_BS33k130_provenance.