Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP187594.RAtVO5DU5pwDuxc66FbHmSbpIDQAK7BE7A-YIEm53asyU130_assertion description "[These data indicate that growth factors in an autocrine or paracrine manner play a major role in regulating VEGF levels in neuroblastoma cells and that targeted therapies to phosphatidylinositol 3-kinase, mammalian target of rapamycin, and/or HIF-1alpha have the potential to inhibit VEGF expression and limit neuroblastoma tumor growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187594.RAtVO5DU5pwDuxc66FbHmSbpIDQAK7BE7A-YIEm53asyU130_provenance.
- NP187597.RAjV6_4zTFqOlFFMoRW2muN0cJ9B8AI9_UlQfJYQHmzN4130_assertion description "[Additionally, overexpression of Separase transcript strongly correlates with high incidence of relapse, metastasis, and lower 5-year overall survival rate in breast and prostate cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187597.RAjV6_4zTFqOlFFMoRW2muN0cJ9B8AI9_UlQfJYQHmzN4130_provenance.
- NP187608.RAk-RnlaVww5WrGbgJ2qUdeELeEcHKJH5YrvfR4sFPbOU130_assertion description "[Human acute myeloid leukaemia (AML) involving a core-binding factor (CBF) transcription factor is called CBF leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187608.RAk-RnlaVww5WrGbgJ2qUdeELeEcHKJH5YrvfR4sFPbOU130_provenance.
- NP187609.RArjxHQKuYYguHgAy8fschL4VeAJxIN-DXh6eIKMvJhBo130_assertion description "[To identify genetic factors that may influence the plasma levels of the 3 C4BP existing isoforms, alpha(7)beta(1), alpha(6)beta(1), and alpha(7)beta(0), we conducted a genome-wide association study by analyzing 283 437 single nucleotide polymorphisms (SNPs) in the Genetic Analysis of Idiopathic Thrombophilia (GAIT) study composed of 352 persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187609.RArjxHQKuYYguHgAy8fschL4VeAJxIN-DXh6eIKMvJhBo130_provenance.
- NP187611.RApCGQ6b3F-wHthybsGdDSev00AZFMZfvv6Ud-PMVDRMI130_assertion description "[In the placebo group, subjects possessing both the 482Ser allele of the PPAR-gamma coactivator-1alpha gene (PGC-1A) and the rare allele of two SNPs of PPARD (rs6902123 and rs3734254) had up to 2.5-fold increased risk for diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187611.RApCGQ6b3F-wHthybsGdDSev00AZFMZfvv6Ud-PMVDRMI130_provenance.
- NP187620.RAh2JLptlFVKRtv4a8w2sehjW4d9j_dejrwvkr2ABRunw130_assertion description "[There was a significant association between the MME genotypes and the SCL-90 scores for phobic anxiety, obsessive-compulsive and anxiety at a Bonferroni corrected alpha value of 0.0125.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187620.RAh2JLptlFVKRtv4a8w2sehjW4d9j_dejrwvkr2ABRunw130_provenance.
- NP187622.RAhPgsk1rqRzbRB4Ih13DDnjO108RUcV-pVJsF2xuqcsg130_assertion description "[INNO-406 was found to inhibit proliferation in HMC-1.1 cells (IC(50): 30-40 nM), but not in HMC-1.2 cells or primary neoplastic cells in patients with KIT D816V-positive SM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187622.RAhPgsk1rqRzbRB4Ih13DDnjO108RUcV-pVJsF2xuqcsg130_provenance.
- NP187626.RAkiGGBm0UQ5thpz-M5ME8XirfqClHoQmqk31Gc4L3Qlw130_assertion description "[Associations have been reported between single nucleotide polymorphisms (SNPs) of IL-10 and the Ile50Val polymorphism of the IL-4 receptor gene (IL-4R) gene and atopy and autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187626.RAkiGGBm0UQ5thpz-M5ME8XirfqClHoQmqk31Gc4L3Qlw130_provenance.
- NP187628.RAhHvmuyL8O146Y-O2L4-VxxNj8Dg0Xtx1GBjtqWh1qD4130_assertion description "[Further, corresponding to the morphological changes of nucleolus in number and size, these highly proliferating SSEA1 cells demonstrated coexpression of either D2-40 or the mesodermal marker Scl (stem cell leukemia), brachyury, and Flk-1 (vascular endothelial growth factor-2), respectively, indicative of the neoplasmtic transformation into the stromal or vascular cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187628.RAhHvmuyL8O146Y-O2L4-VxxNj8Dg0Xtx1GBjtqWh1qD4130_provenance.
- NP187629.RAqhbLHOmmBfPWC525wCbtEiFu7BzSdKRxw6lTHAmP6q4130_assertion description "[Insulin resistance in a young man with cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187629.RAqhbLHOmmBfPWC525wCbtEiFu7BzSdKRxw6lTHAmP6q4130_provenance.
- NP187632.RAvp_uts1y_-s-NYlYDq5-yPqbm5SkUEe19eVbx1XxNYc130_assertion description "[FAS and FASL were not differentially expressed, but FAST kinase was over-expressed in AN and AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187632.RAvp_uts1y_-s-NYlYDq5-yPqbm5SkUEe19eVbx1XxNYc130_provenance.
- NP187633.RAsMN7iLRRAl5mNGcuFwfy2HnCytOWoXB6d2FZigb-zvQ130_assertion description "[Since the activity of genotypes carrying the ADA*2 allele is lower than that of the more common genotype ADA*1/*1, genetic variability of the enzyme could contribute to degree of obesity in NIDDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187633.RAsMN7iLRRAl5mNGcuFwfy2HnCytOWoXB6d2FZigb-zvQ130_provenance.
- NP187635.RAuA68aXhSoUz2p_6UZq4bp_nobKxetYAeY1F6ary8q4k130_assertion description "[Enhanced binding of advanced glycation endproducts (AGE) by the ApoE4 isoform links the mechanism of plaque deposition in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187635.RAuA68aXhSoUz2p_6UZq4bp_nobKxetYAeY1F6ary8q4k130_provenance.
- NP187637.RAuOj9ss1FAxkRLGno1s5pTMuwWfK637arciItb0n1aGQ130_assertion description "[Our results show that phenotypic changes are demonstrable in peripheral blood monocytes in patients with RA, including increased expression of CR3 (CD11b/CD18) and FcRI (CD64).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187637.RAuOj9ss1FAxkRLGno1s5pTMuwWfK637arciItb0n1aGQ130_provenance.
- NP187638.RAvinhjBtFiWpDUxbxjrm0lnZFVHYoOftUyHne6hsNwJc130_assertion description "[MYC genes are deregulated in a plurality of human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187638.RAvinhjBtFiWpDUxbxjrm0lnZFVHYoOftUyHne6hsNwJc130_provenance.
- NP187639.RAhfM42rAitcXRKce07uBQr94YZwuOVyOZMtlyZRTQ_ts130_assertion description "[Reduced SHOX gene expression has been demonstrated to be associated with all skeletal abnormalities in Turner syndrome, other than scoliosis (and kyphosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187639.RAhfM42rAitcXRKce07uBQr94YZwuOVyOZMtlyZRTQ_ts130_provenance.
- NP187640.RAh8K6FWjTD1KsDLCN2n_0iUvJ2Uplzp_xZbbuVWcdu8Y130_assertion description "[Exposure of two human non-small lung cancer (NSCLC) cell lines (A549 and H1975) to curcumin could suppress MMC-induced MKK1/2-ERK1/2 signal activation and Rad51 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187640.RAh8K6FWjTD1KsDLCN2n_0iUvJ2Uplzp_xZbbuVWcdu8Y130_provenance.
- NP187644.RAtze_TFDnZxaHN-_wgE6BI5wm70yoHXRxTeevFbMtzo8130_assertion description "[The present study aims to explore the enzyme's contributions to retinal angiogenesis in oxygen-induced retinopathy (OIR) using MMP-12 knockout (KO) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187644.RAtze_TFDnZxaHN-_wgE6BI5wm70yoHXRxTeevFbMtzo8130_provenance.
- NP187659.RAvUO0IgEYwt9lU3h7CyvRqLzjQyQFMnN30gq2dWuOuxs130_assertion description "[PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187659.RAvUO0IgEYwt9lU3h7CyvRqLzjQyQFMnN30gq2dWuOuxs130_provenance.
- NP187660.RAjjH2NODoAC7vDEXGk7sh0UZk-4jXlvM3vqLYpkJyViU130_assertion description "[Microsatellite instability and BRAF mutation testing in colorectal cancer prognostication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187660.RAjjH2NODoAC7vDEXGk7sh0UZk-4jXlvM3vqLYpkJyViU130_provenance.
- NP187663.RAteEUvE-3xYgx1EKQZG8wVYSAhrz8wjFzfsF-SDZB_hU130_assertion description "[Hypertension was present in 73% of the subjects with PFD and in 78% with CFD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187663.RAteEUvE-3xYgx1EKQZG8wVYSAhrz8wjFzfsF-SDZB_hU130_provenance.
- NP187665.RAnM9rOdd4aFeigwlKjxCWUAB9fyea4Qx8mXlHRZ_p5wI130_assertion description "[The elevated MTA1 and VEGF-C expression levels were correlated with lymph node metastasis and Dukes stages (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187665.RAnM9rOdd4aFeigwlKjxCWUAB9fyea4Qx8mXlHRZ_p5wI130_provenance.
- NP187666.RAnlzsq-WJ69Yq7u8QP3z-DxgFzdAlex6bzBr1JbKW3Lc130_assertion description "[Moreover, we compare the NPM1 results with those of WT1 expression to MRD assessment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187666.RAnlzsq-WJ69Yq7u8QP3z-DxgFzdAlex6bzBr1JbKW3Lc130_provenance.
- NP187667.RAjyNi8zUoWleG4YkwhL4h526H0am_OkXL7PHwbnlq9lM130_assertion description "[Our study examined the potential of these HAI's to suppress the influence of HGF and regulate cancer metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187667.RAjyNi8zUoWleG4YkwhL4h526H0am_OkXL7PHwbnlq9lM130_provenance.
- NP187671.RAvNO-vDBPdhWiDbNZrdqundhWQRO_aVmC9QiQjlLQUHE130_assertion description "[Since the availability of molecular analysis, no studies to date have evaluated the transcriptional activation domain (exon 1) of the AR gene in this population of infertile men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187671.RAvNO-vDBPdhWiDbNZrdqundhWQRO_aVmC9QiQjlLQUHE130_provenance.
- NP187674.RApiALUBhqtmyanoaztCw83juj2UwOOx8z20uw2Ul6DoQ130_assertion description "[Sialidosis (NEU1 deficiency) and galactosialidosis (combined NEU1 and β-gal deficiency, secondary to a primary defect of PPCA) belong to the glycoprotein storage diseases, whereas GM1-gangliosidosis (β-gal deficiency) is a glycosphingolipid storage disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187674.RApiALUBhqtmyanoaztCw83juj2UwOOx8z20uw2Ul6DoQ130_provenance.
- NP187676.RArwp67SI7PYsFsgEPNMlfgSVyWI7UW61zGZT2m_4OUe0130_assertion description "[These patients have prolactin (PRL) or growth hormone (GH) oversecreting pituitary adenomas, the latter exhibiting acromegaly or gigantism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187676.RArwp67SI7PYsFsgEPNMlfgSVyWI7UW61zGZT2m_4OUe0130_provenance.
- NP187682.RAnOYmq8ms_1dLQyd52VNss4MLv1JeKV4eNlLH6eVOqMs130_assertion description "[In addition to the known association of HLA with IgAD, we identified association with a nonsynonymous variant in IFIH1 (rs1990760G>A, P = 7.3 x 10(-10)) which was previously associated with type 1 diabetes and systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187682.RAnOYmq8ms_1dLQyd52VNss4MLv1JeKV4eNlLH6eVOqMs130_provenance.
- NP187686.RAjM53O4JpT5hwICyk66EtMicPT2u7ay4m5A92TTrhP-o130_assertion description "[The single most significant SNPs from each gene associated with CIN3/cancer were PRDX3 rs7082598 (P(trend)<0.0001), and RPS19 rs2305809 (P(trend)=0.0007), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187686.RAjM53O4JpT5hwICyk66EtMicPT2u7ay4m5A92TTrhP-o130_provenance.
- NP187704.RAj9Y_2mMjtzepyGFouhfXCMDhtxd5YgJsqGbAiCAPciM130_assertion description "[CD56+CD7+ stem cell leukemia/lymphoma with D2-Jdelta1 rearrangement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187704.RAj9Y_2mMjtzepyGFouhfXCMDhtxd5YgJsqGbAiCAPciM130_provenance.
- NP187708.RAsDTk44fUJ4-U1xh9c2AtqnVZlYvvWvjfR_UFuL4r1MI130_assertion description "[Here, in an individual, we demonstrate that a homozygous novel mutation in the MMR gene MSH2 is associated with leukemia and multiple café-au-lait spots, a feature of neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187708.RAsDTk44fUJ4-U1xh9c2AtqnVZlYvvWvjfR_UFuL4r1MI130_provenance.
- NP187710.RAp9-66iv4pesTIaVhLneM9bd-XtWBcX5ziLfhX2UQoE8130_assertion description "[The presence of translocations and copy number changes involving MALT1, IGH and FOXP1 were assessed in 90 cases of gastric MALT lymphoma using interphase fluorescence in situ hybridisation (FISH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187710.RAp9-66iv4pesTIaVhLneM9bd-XtWBcX5ziLfhX2UQoE8130_provenance.
- NP187712.RAmJvSRnENe5Mq2mRUEFs3JHcvZFbEHix57jedM0Cve7s130_assertion description "[Although PTEN (phosphatase and tensin homologue deleted on chromosome 10) is one of the most commonly mutated tumour suppressors in human cancers, loss of PTEN expression in the absence of mutation appears to occur in an even greater number of tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187712.RAmJvSRnENe5Mq2mRUEFs3JHcvZFbEHix57jedM0Cve7s130_provenance.
- NP187715.RAvFWpYc704bg9aH38DCdDEfztJ0Eqc8LDx_Waj3r_vZs130_assertion description "[Increased expression of PIM2 was detected in subsets of mantle cell lymphoma, diffuse large B-cell lymphoma (DLBLC), follicular lymphoma, marginal zone lymphoma-mucosa-associated lymphoid tissue type, chronic lymphocytic leukemia, and nodal marginal zone lymphoma cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187715.RAvFWpYc704bg9aH38DCdDEfztJ0Eqc8LDx_Waj3r_vZs130_provenance.
- NP187718.RAmt3MaJ-MnlEIlw_DV-4quokWyh84uOzN5uX-mWfLNj4130_assertion description "[Interestingly, NTR-1 status did not affect tumor development in an inflammation-associated cancer model where mice were treated with AOM followed by two cycles of 5% dextran sulfate sodium (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187718.RAmt3MaJ-MnlEIlw_DV-4quokWyh84uOzN5uX-mWfLNj4130_provenance.
- NP187725.RAjeEL16gIRQf564W20lhRcizXQxhKd6_4RjAt-roBos4130_assertion description "[Most notably, four genes-COL1A2, KYNU, ACTG2 and NPPB-were differentially expressed in high and non-aggressive cell lines for all the cancer-related phenotypes investigated, suggesting that they might have important roles in the process of osteosarcoma tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187725.RAjeEL16gIRQf564W20lhRcizXQxhKd6_4RjAt-roBos4130_provenance.
- NP187729.RAl9Wp7SCHRTtQYgNVhmzqpFYg7Zd9Cy_mzIyXBzCrTrs130_assertion description "[This study showed that TS protein is highly expressed in NSCLC and that polymorphisms of TS 3'-UTR 1494del 6 bp are associated with sensitivity of lung adenocarcinoma patients to pemetrexed treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187729.RAl9Wp7SCHRTtQYgNVhmzqpFYg7Zd9Cy_mzIyXBzCrTrs130_provenance.
- NP187735.RAp0yID4m4xUNaHmrWXhoxySUhaJ5Jh7An-xrQp9iVGyk130_assertion description "[RET mutational analysis revealed a rare missense point mutation in exon 15 of RET (A891S), associated with FMTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187735.RAp0yID4m4xUNaHmrWXhoxySUhaJ5Jh7An-xrQp9iVGyk130_provenance.
- NP187743.RAmaMbddUVPhCLL-0M40iMWet_02pI5DPDNHBpOItgkmo130_assertion description "[CIP2A was an independent prognostic factor in colon cancer after controlling for other clinical confounding factors, such as stage and lymphovascular invasion, particularly in stages III and IV (hazard ratio = 2.974, P < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187743.RAmaMbddUVPhCLL-0M40iMWet_02pI5DPDNHBpOItgkmo130_provenance.
- NP187744.RArsYQQK-zVRgvs0TiJEU1fmwm0609TKTznrIWTdTOS80130_assertion description "[These include chromosomal deletions of the MEN1 locus on 11q in sporadic and MEN1 associated primary HPT, of RB1 on 13q in carcinomas, and of the FHH gene located on 3q in sporadic primary and secondary HPT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187744.RArsYQQK-zVRgvs0TiJEU1fmwm0609TKTznrIWTdTOS80130_provenance.
- NP187754.RArdckMs6MzKRvd9QC39juYfSlYdxRebHE7Ebtk2LdxcQ130_assertion description "[It is speculated that, in some patients, combination chemotherapy for childhood ALL may fail to eliminate a fetal preleukemic clone with TEL-AML1 and that a second, independent transformation event within this clone after treatment gives rise to a new leukemia masquerading as relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187754.RArdckMs6MzKRvd9QC39juYfSlYdxRebHE7Ebtk2LdxcQ130_provenance.
- NP187758.RAsXlwA4olDv_nAcIzu_PqtGY5u8MRTHZO9WMaGcB6oNc130_assertion description "[Liquid chromatography/mass spectrometry analysis of the conditioned media revealed that p21(WAF1) knockdown significantly reduced secretion of thioredoxin (Trx), a redox protein known to promote tumor angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187758.RAsXlwA4olDv_nAcIzu_PqtGY5u8MRTHZO9WMaGcB6oNc130_provenance.
- NP187775.RArGSaupLvNRKj7-JmeWcNH4n0seYRiLM286dedBpFg9g130_assertion description "[A shift from one p53 intron 2 genotype in the blood to another genotype in the tissue may be a prognostic factor in ovarian cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187775.RArGSaupLvNRKj7-JmeWcNH4n0seYRiLM286dedBpFg9g130_provenance.
- NP187782.RAlNsAvSFGpp_u23LnsTda-mVkEh8KRBKhC7zBOn_l0_Y130_assertion description "[In summary, these data underline that HSV-1 induces TTP transcription in order to reduce TNF levels generated by infected mature dendritic cell.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187782.RAlNsAvSFGpp_u23LnsTda-mVkEh8KRBKhC7zBOn_l0_Y130_provenance.
- NP187786.RApvMSNDOz_RAHWGZFzJXBGI2x_ttelOSuvqj7zospFmI130_assertion description "[MMP-11 (stromelysin-3) is a matrix metalloproteinase associated with tumor progression and poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187786.RApvMSNDOz_RAHWGZFzJXBGI2x_ttelOSuvqj7zospFmI130_provenance.
- NP187788.RAq5l6iHcKNja-ki0GoqzkZ1JZSSZSVg6vE9XKWnH9UCk130_assertion description "[Dopamine dysregulation has long been implicated in schizophrenia pathogenesis, and COMT appears to play a role in dopamine functioning, especially in prefrontal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187788.RAq5l6iHcKNja-ki0GoqzkZ1JZSSZSVg6vE9XKWnH9UCk130_provenance.
- NP187808.RAh4N7T-T80g_2Jb_2lGyf36DJbVXKVPHQj23AXs3jCao130_assertion description "[The mRNA expression of both p63 and p73 was significantly upregulated in GC-naive patients with NP versus control subjects, and a positive correlation between the p63 and p73 mRNAs was found in all nasal tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187808.RAh4N7T-T80g_2Jb_2lGyf36DJbVXKVPHQj23AXs3jCao130_provenance.
- NP187810.RAi5xJQTvrUKzOBOoESBnSLf-dCUvpd3MVJM0gYhxXYBU130_assertion description "[ATP7B mutation is well-known as a cause of Wilson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187810.RAi5xJQTvrUKzOBOoESBnSLf-dCUvpd3MVJM0gYhxXYBU130_provenance.
- NP187811.RAtbnKhkfty4waFCgeZnkeCBjeEiWBBoUio0Lkr9z5SyI130_assertion description "[Together, our data suggest that LULL1 regulates the distribution and activity of TorA within the ER and NE lumen and reveal functional defects in the mutant protein responsible for DYT1 dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187811.RAtbnKhkfty4waFCgeZnkeCBjeEiWBBoUio0Lkr9z5SyI130_provenance.
- NP187820.RArZMl031LPsQUGZo1DvpaDEjQplphYpCjYLPHmVd7jGc130_assertion description "[VHL gene mutations in renal cell carcinoma: role as a biomarker of disease outcome and drug efficacy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187820.RArZMl031LPsQUGZo1DvpaDEjQplphYpCjYLPHmVd7jGc130_provenance.
- NP187833.RAi3BOiStMM9NegBGuhLgr9AW5wbZyJJHPL1X2121miSg130_assertion description "[Tuberculin, a purified protein derivative (PPD), when diluted in adequate concentration it is utilized for an early detection and to control tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187833.RAi3BOiStMM9NegBGuhLgr9AW5wbZyJJHPL1X2121miSg130_provenance.
- NP187838.RAsB_yGwW1U76W3W8ffMiQ9YlqTjTrgDmhyQbYOg8ZcVE130_assertion description "[In rodents, heat generation and the burning of calories by the mitochondrial uncoupling protein 1 (UCP1) are important for metabolic control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187838.RAsB_yGwW1U76W3W8ffMiQ9YlqTjTrgDmhyQbYOg8ZcVE130_provenance.
- NP187849.RAsVtbruOFCPdcotnXY92qGdND9Zj9Eohu2OIRp03GkSA130_assertion description "[In contrast, hypermethylation and subsequent inactivation of the P73 gene are the most common findings in malignant lymphoproliferative disorders, especially acute lymphoblastic leukemia (ALL) and non-Hodgkin's lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187849.RAsVtbruOFCPdcotnXY92qGdND9Zj9Eohu2OIRp03GkSA130_provenance.
- NP187854.RArbmsVzhiGF8skKEnmyvQw-q26szys4mtKHOIFgkBEG4130_assertion description "[p63 and p73 in human cancer: defining the network.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187854.RArbmsVzhiGF8skKEnmyvQw-q26szys4mtKHOIFgkBEG4130_provenance.
- NP187858.RAsaqeua65vv6L7M9ch8d4TJfTpaHafk78IoR9vE2KlBk130_assertion description "[Inhibition of PC-3 human prostate cancers by analogs of growth hormone-releasing hormone (GH-RH) endowed with vasoactive intestinal peptide (VIP) antagonistic activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187858.RAsaqeua65vv6L7M9ch8d4TJfTpaHafk78IoR9vE2KlBk130_provenance.
- NP187859.RAvLDT3QnPjPOzBpjPC77bTRfFUVBzVC1faTkrmD23-qM130_assertion description "[We conclude that there is an association between higher TNF-alpha production and E. histolytica diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187859.RAvLDT3QnPjPOzBpjPC77bTRfFUVBzVC1faTkrmD23-qM130_provenance.
- NP187861.RAokyeSl-Y7JxZQvEQwZ-js-uxp1L-iRU1CoEIxQm-X8Q130_assertion description "[The neurofibromatosis type 2 gene is inactivated in schwannomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187861.RAokyeSl-Y7JxZQvEQwZ-js-uxp1L-iRU1CoEIxQm-X8Q130_provenance.
- NP187862.RAsacE3XR49_Go4fEj6mvZtZrAlw0RK6ejO6prZW_wY64130_assertion description "[These findings may indicate the important role of inflammatory cytokines such as IL-1 beta, IL-6 and TNF-alpha in the development of the clinical manifestation of GVHD and also may be indicative of the important role of IL-2 and the IL-2 receptor in allo response perhaps mainly as an autocrine effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187862.RAsacE3XR49_Go4fEj6mvZtZrAlw0RK6ejO6prZW_wY64130_provenance.
- NP187871.RAsmU06yf1LMLSUr4GvHBCb7cRxP0rpX8ydFoZbXd7oaY130_assertion description "[Also, high DROSHA expression was associated with decreased median survival in the following subgroups: adenocarcinoma (P = 0.011), grade III tumors (P = 0.038) and low-stage patients (P = 0.014).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187871.RAsmU06yf1LMLSUr4GvHBCb7cRxP0rpX8ydFoZbXd7oaY130_provenance.
- NP187878.RAgCXDxUc3FYKPACd9s_YAG5d-E-LVgbjwG92uwClo1eI130_assertion description "[By French-American-British (FAB) criteria, 27 patients had refractory anaemia (RA), 10 RA with excess blasts (RAEB), eight RAEB in transformation (RAEB-T) and 12 acute myeloid leukaemia evolving from MDS (tAML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187878.RAgCXDxUc3FYKPACd9s_YAG5d-E-LVgbjwG92uwClo1eI130_provenance.
- NP187881.RAnzLYPlqLAkY5RV_lyglmFGLmG0qn94DhwM8Pq3loKi4130_assertion description "[The h-prune-nm23-H1 protein complex and its activation of PDE-cAMP activity have been shown to correlate with breast cancer progression and metastasis formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187881.RAnzLYPlqLAkY5RV_lyglmFGLmG0qn94DhwM8Pq3loKi4130_provenance.
- NP187888.RAvnliO4kPAbVqgEQmZvtpAK-1vwUDlDfiLE35LvHXqlc130_assertion description "[In addition, the allelism at the GSTP1 locus did not increase gastric cancer and chronic gastritis risks associated with the GSTM1 or GSTT1 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187888.RAvnliO4kPAbVqgEQmZvtpAK-1vwUDlDfiLE35LvHXqlc130_provenance.
- NP187892.RAuN1FuPom0hi0evG47WpgqA9L3jId4Tta9c4IFqL2V6c130_assertion description "[One of the mutations, the deletion 96_98delAAG (p.Lys32del), had not been previously described, reinforcing the worldwide prevalence of GCK MODY and widespread existence of undetected new mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187892.RAuN1FuPom0hi0evG47WpgqA9L3jId4Tta9c4IFqL2V6c130_provenance.
- NP187894.RAlefkT4PwmiUwfLDPhScRH9muEMSpYgZFfJ8P-zQernY130_assertion description "[No pathogenic rearrangement within the DISC 1 gene in psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187894.RAlefkT4PwmiUwfLDPhScRH9muEMSpYgZFfJ8P-zQernY130_provenance.
- NP187903.RAo7gRlWriqJr0kx91vh1KZzifdQGnkwBTidkeTd1gxA8130_assertion description "[Amongst the subjects with G6PD deficiency, the OR was 159.00 (24.57-1028.94) for individuals carrying variations in both UGT1A1 and OATP2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187903.RAo7gRlWriqJr0kx91vh1KZzifdQGnkwBTidkeTd1gxA8130_provenance.
- NP187906.RAomLDuHYRdjvsxsmDXJ9zxbmE9d0A3KKRsMc-aD56jRc130_assertion description "[Clinical TPI deficiency is a rare autosomal recessive multi-system disorder characterised by non-spherocytic haemolytic anaemia, recurrent infections, cardiomyopathy, severe and fatal neuromuscular dysfunctions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187906.RAomLDuHYRdjvsxsmDXJ9zxbmE9d0A3KKRsMc-aD56jRc130_provenance.
- NP187909.RAjvAjVLGiWeYC1xr6WIlWMTotULAWGDGKQE4wBRWJJC0130_assertion description "[Hypospadias risk and polymorphism in SRD5A2 and CYP17 genes: case-control study among Indian children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187909.RAjvAjVLGiWeYC1xr6WIlWMTotULAWGDGKQE4wBRWJJC0130_provenance.
- NP187916.RArZPG6EdoTfbLqn9fi_1g4VDrXjaVw2Fw8eH6O4QOiyM130_assertion description "[Its role in the aetiology of rheumatoid arthritis (RA) however, remains unclear, as the functional studies of the B7-CTLA-4 pathway in mouse models of RA and genetic studies in humans have given contrasting results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187916.RArZPG6EdoTfbLqn9fi_1g4VDrXjaVw2Fw8eH6O4QOiyM130_provenance.
- NP187919.RAmgZ-dzTX151DFgRS6rqd-FbwVS1su-7JbS2TB5DVZMk130_assertion description "[Congenital sucrase-isomaltase (SI) deficiency is an autosomal-recessive intestinal disorder characterized by a drastic reduction or absence of sucrase and isomaltase activities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187919.RAmgZ-dzTX151DFgRS6rqd-FbwVS1su-7JbS2TB5DVZMk130_provenance.
- NP187924.RAgX52rFLeTOfbhWm6pm7TeLuK_YT6968c0DctMTwCRUk130_assertion description "[Out of the cases with a family history of any cancer, 22/53 (41.5%) EGFR mutated, 1/5 (20%) KRAS mutated and 3/19 (15.5%) ALK translocated cohorts had a family history of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187924.RAgX52rFLeTOfbhWm6pm7TeLuK_YT6968c0DctMTwCRUk130_provenance.
- NP187929.RAruoS2P1fqy0XNX9zp_MekkreN8NRUJxlhLa_KYxeLdg130_assertion description "[These data indicate that more complex mechanisms, apart from possible VCX3A gene participation, are occurring in the genesis of MR in XLI, at least in the sample of Mexican patients analysed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187929.RAruoS2P1fqy0XNX9zp_MekkreN8NRUJxlhLa_KYxeLdg130_provenance.
- NP187930.RAhqiNIXiKEmU9kGClnBSFmVSuT6onF-zGYWsXl_dt_Ys130_assertion description "[The aims of this study were to define the prevalence of the mutations 845G --> A and 187C --> G (C282Y and H63D) in the HFE gene associated with hereditary hemochromatosis in Italian patients with hepatocellular carcinoma occurring in cirrhosis and to analyze the interaction between these mutations and other established risk factors for hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187930.RAhqiNIXiKEmU9kGClnBSFmVSuT6onF-zGYWsXl_dt_Ys130_provenance.
- NP187936.RAqqwVe40NnTGqFQ93oqVg_6M7tuFRF4vTOy4APZYBQM8130_assertion description "[Indeed, adjuvant treatment with mAb 17-1A did successfully reduce the 5 years mortality among colorectal cancer patients with minimal residual disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187936.RAqqwVe40NnTGqFQ93oqVg_6M7tuFRF4vTOy4APZYBQM8130_provenance.
- NP187937.RAlmwczLPUI-ld8cVUi4ANJMWBcXhWJit_pBYZbeRICvg130_assertion description "[The proven contribution of heredity to major depression risk suggests that genetic markers may be good biomarkers for treatment outcome.The Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study and a large ancillary pharmacogenetic study in 1953 STAR*D participants constitute the largest effort to date to identify genetic predictors of antidepressant treatment outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187937.RAlmwczLPUI-ld8cVUi4ANJMWBcXhWJit_pBYZbeRICvg130_provenance.
- NP187940.RAlVT8R93ZMF5a9i4hQuXrxJLXUgXFe9AFV-kRvYvzg9g130_assertion description "[Targeting EGFR in bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187940.RAlVT8R93ZMF5a9i4hQuXrxJLXUgXFe9AFV-kRvYvzg9g130_provenance.
- NP187947.RAuZ4XtqNnXW86lDk7e9Q9IHEB4xX707ki2tbOqoSN3l0130_assertion description "[FCGR3A and FCGR2A polymorphisms may not correlate with response to alemtuzumab in chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187947.RAuZ4XtqNnXW86lDk7e9Q9IHEB4xX707ki2tbOqoSN3l0130_provenance.
- NP187952.RAiP_GEOKOZgKmNEvFLP3xpkN0vDIEKjCHBDP7cPzj-QA130_assertion description "[MeDIP analysis on 9 RCC tumours and 3 non-malignant normal kidney tissue samples was performed, and an initial shortlist of 56 candidate genes that were methylated by array analysis was further investigated; 9 genes were confirmed to show frequent promoter region methylation in primary RCC tumour samples (KLHL35 (39%), QPCT (19%), SCUBE3 (19%), ZSCAN18 (32%), CCDC8 (35%), FBN2 (34%), ATP5G2 (36%), PCDH8 (58%) and CORO6 (22%)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187952.RAiP_GEOKOZgKmNEvFLP3xpkN0vDIEKjCHBDP7cPzj-QA130_provenance.
- NP187955.RAnD5LJ8GsrDnmo7FclSfGPve_-ZmG0_SVLyVZwFfOYm0130_assertion description "[The murine and human genes for the L1 neural adhesion molecule were shown to lie on conserved regions of the X chromosome to which genes responsible for several neuromuscular diseases have been mapped and which are adjacent to the fragile site (FRAXA) associated with mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187955.RAnD5LJ8GsrDnmo7FclSfGPve_-ZmG0_SVLyVZwFfOYm0130_provenance.
- NP187958.RApQ30z_2-WvG6-frXquyW9Ar40kgcyi4aM5BnDngCFho130_assertion description "[The aim of this study was to estimate the relationship of endothelial dysfunction induced by intracellular S-adenosylhomocysteine (SAH) accumulation and DNA methylation in human umbilical vein endothelial cells (HUVEC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187958.RApQ30z_2-WvG6-frXquyW9Ar40kgcyi4aM5BnDngCFho130_provenance.
- NP187961.RAnYNtklhsb23M4Ja8-Owo54EQpmPGG0dGhBpMF-bl8Vg130_assertion description "[In our patients no effect of the MTHFR polymorphism on tHcy levels was seen This result, in addition to the limited number of patients, may partially be explained by the low prevalence of folate deficiency in our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187961.RAnYNtklhsb23M4Ja8-Owo54EQpmPGG0dGhBpMF-bl8Vg130_provenance.
- NP187963.RAvOHpSnooE49GbaeeyZYfarp3ZFGLN4WRqJXDojZJQEg130_assertion description "[RelAp43, a member of the NF-κB family involved in innate immune response against Lyssavirus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187963.RAvOHpSnooE49GbaeeyZYfarp3ZFGLN4WRqJXDojZJQEg130_provenance.
- NP187967.RAjDjnE_HBgwKUCYQASSogJla0F1DaVLiwLJ0gs2qsmqY130_assertion description "[SNP rs10757278 on chromosome 9 was genotyped in 926 patients with CAD from the CAREGENE study, in 648 patients with CVD from the Leuven Stroke Genetics Study (LSGS) and the Belgian Stroke Study (BSS) and in 828 unrelated controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187967.RAjDjnE_HBgwKUCYQASSogJla0F1DaVLiwLJ0gs2qsmqY130_provenance.
- NP187971.RAtJZLh1BUy7TEPFkhzNq50J6vmiW6QJlO5B3W3hDP2TI130_assertion description "[Association analysis of polymorphisms in IL-3, IL-4, IL-5, IL-9, and IL-13 with Graves' disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187971.RAtJZLh1BUy7TEPFkhzNq50J6vmiW6QJlO5B3W3hDP2TI130_provenance.
- NP187976.RAu40YrSdxafKOmbWpTMfNOgem8WdX5tmeqs0cVoGFwOA130_assertion description "[Thus, CD16 serves a role in NK cell-mediated spontaneous cytotoxicity through a specific association with CD2 and represents a potential mechanism underlying a human congenital immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187976.RAu40YrSdxafKOmbWpTMfNOgem8WdX5tmeqs0cVoGFwOA130_provenance.
- NP187980.RAvdJLjevJdHC4w-pPHbPnjA89h2f6YDMeSFkVvszawNc130_assertion description "[High functional levels of thrombin-activatable fibrinolysis inhibitor are associated with an increased risk of first ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187980.RAvdJLjevJdHC4w-pPHbPnjA89h2f6YDMeSFkVvszawNc130_provenance.
- NP187984.RApFjsawZDwUL4U5C9IofEs7owqzSBEsbJOySx8Zw_9S4130_assertion description "[Our preclinical study therefore supports clinical evaluation of USP7 inhibitor, alone or in combination, as a potential MM therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187984.RApFjsawZDwUL4U5C9IofEs7owqzSBEsbJOySx8Zw_9S4130_provenance.
- NP187999.RAgIPQ1S9An2BNZrT4U_hI5oWAL28XIqOckFjrKE9HEC0130_assertion description "[Some patients with glioblastoma multiform do not respond to temozolomide even though they have aberrant promoter methylation of the DNA repair enzyme O(6)-methylguanine methyltransferase (MGMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187999.RAgIPQ1S9An2BNZrT4U_hI5oWAL28XIqOckFjrKE9HEC0130_provenance.
- NP188006.RAj8evaETNiNireQGcH7rNZ_xAAt07J11-Xv1QdM_nIyg130_assertion description "[Although concomitant lesions in the ulnar nerve entrapment site at the wrist cannot be excluded, these findings indicate that CTS is not the sole distinctive feature in the majority of FAP ATTR Val30Met patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188006.RAj8evaETNiNireQGcH7rNZ_xAAt07J11-Xv1QdM_nIyg130_provenance.
- NP188011.RAt5rwLMjKqeLjY7tSezokKT89DLGvj8wGeKe30JHmY2A130_assertion description "[TRPC6 dysfunction has been associated with the onset of focal segmental glomerosclerosis; TRPP2 dysfunction is linked to autosomal-dominant polycystic kidney disease, TRPM6 mutations underlie hypomagnesemia with secondary hypocalcemia, and TRPV1 dysfunction is implicated in renal hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188011.RAt5rwLMjKqeLjY7tSezokKT89DLGvj8wGeKe30JHmY2A130_provenance.
- NP188014.RAqq3-XoFPXQpFkZ2YTvqTzi2rOTQF86RGJZBQq6RH12M130_assertion description "[Immunohistochemical analyses revealed that neither normal bone marrow (BM) plasma cells (PCs), premalignant PCs of patients with monoclonal gammopathy of unknown significance (MGUS), nor MM cells with a mature morphology showed expression of YB-1 in situ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188014.RAqq3-XoFPXQpFkZ2YTvqTzi2rOTQF86RGJZBQq6RH12M130_provenance.
- NP188018.RAhNnWNfPZbtP7Bsq_7c8VboHZXf3mjrcsp2WeYw78ozU130_assertion description "[Currently identified genetic markers of bleeding risk do not confer a risk of ICH sufficiently high to warrant routine genetic testing for patients at average risk of thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188018.RAhNnWNfPZbtP7Bsq_7c8VboHZXf3mjrcsp2WeYw78ozU130_provenance.
- NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_assertion description "[Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188022.RArfwxorav7Po1KwCCaQZxfBbz_JgVn1PlmFit33OxBnU130_provenance.
- NP188028.RAtORfM1zaUqGmUtBulqp_wGvNLCmIyHiLlysWVMPhyWk130_assertion description "[To study the role of IGF2 and H19 genes in gastric carcinogenesis, the LOI and loss of heterozygosity (LOH) status of these two genes were determined in 70 patients with gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188028.RAtORfM1zaUqGmUtBulqp_wGvNLCmIyHiLlysWVMPhyWk130_provenance.
- NP188034.RArBRXDS03lUJ18JAUf0fUQRa4tuy_HeuwwF5lHEzvifo130_assertion description "[Craniofrontonasal syndrome (CFNS, OMIM 304110) is a distinctive genetic disorder whose main clinical manifestations include coronal synostosis, widely spaced eyes, clefting of the nasal tip and various skeletal anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188034.RArBRXDS03lUJ18JAUf0fUQRa4tuy_HeuwwF5lHEzvifo130_provenance.
- NP188040.RArUZhmnbNujs0Ee6RSA_62Jvfi4J4jR2GDJDr-mm1Ohk130_assertion description "[Because combined hepatocellular-cholangiocellular carcinoma is rare and its biological features and pathogenesis have not been well established, we investigated alterations of the p53, K-ras and Rb-1 genes, as well as expression patterns of carcinoembryonic antigen and keratin, in seven combined hepatocellular-cholangiocarcinomas out of 557 hepatocellular carcinomas autopsied at Tokyo University during 30 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188040.RArUZhmnbNujs0Ee6RSA_62Jvfi4J4jR2GDJDr-mm1Ohk130_provenance.
- NP188047.RArmbHQDdU7qZmyMF04JnkpCPb98LKleWzz1fJ9E3pKOA130_assertion description "[Mutations of the CHK2 gene are found in some osteosarcomas, but are rare in breast, lung, and ovarian tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188047.RArmbHQDdU7qZmyMF04JnkpCPb98LKleWzz1fJ9E3pKOA130_provenance.
- NP188052.RAs2GZX9bYuJoRaj-f8QkfqvzA-zCJgi88l1-39l4Ta8E130_assertion description "[A primer cocktail (TR1/CA1-TR2/AF2) amplified 59 of 67 fungal species; the universal fungal primer 1 (UF1) in combination with the eukaryotic primers S3 or EU1 amplified 64 and 65 of 67 fungal species, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188052.RAs2GZX9bYuJoRaj-f8QkfqvzA-zCJgi88l1-39l4Ta8E130_provenance.
- NP188059.RAto881wSxT6ZE9gLZPYBL6f1yeYJ9g9a3VWGQFalrd9c130_assertion description "[The mucinous phenotype described in serrated polyps (MUC2+/MUC5AC+) was seen in 15 (68%) of 22 MSI-H and only 10 (14%) of 71 MSI-L/MSS cancers (P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188059.RAto881wSxT6ZE9gLZPYBL6f1yeYJ9g9a3VWGQFalrd9c130_provenance.
- NP188060.RAgsefOY7M7SV9NCkenIo8e0eA9gQ_mtoLNOl74U11D-8130_assertion description "[To describe an elderly patient with low serum alkaline phosphatase (ALP) activity detected after a pathologic fracture and to characterize hypophosphatasia in adult patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188060.RAgsefOY7M7SV9NCkenIo8e0eA9gQ_mtoLNOl74U11D-8130_provenance.
- NP188064.RAo3VQmRthV_Qs6H2CUSIfUOdiK5QgP19cAYnQPeBk3Cc130_assertion description "[We evaluated the tolerance and efficacy of interferon-alpha (IFN) monotherapy in our hemodialysis (HD) patients with chronic hepatitis C virus (HCV) infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188064.RAo3VQmRthV_Qs6H2CUSIfUOdiK5QgP19cAYnQPeBk3Cc130_provenance.