Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP185977.RAuP3kZKl6dRggkTi4IXXsc5KF3vp5l6Isrp72Nsepqec130_assertion description "[These Nef functions could contribute to impaired CD4(+)-T-helper-cell responses found in HIV-1-infected patients with progressive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185977.RAuP3kZKl6dRggkTi4IXXsc5KF3vp5l6Isrp72Nsepqec130_provenance.
- NP185978.RAjcRhewXS5z3MBwITej7uHIddwLljU3Y1xoQSpqpfbOQ130_assertion description "[Chromosome 17 contains at least four genes implicated in breast cancer (TP53, ERBB2 (Her2/neu), BRCA1, and NM23), as well as other putative tumor suppressor genes and oncogenes implicated in loss of heterozygosity or allelic imbalance studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185978.RAjcRhewXS5z3MBwITej7uHIddwLljU3Y1xoQSpqpfbOQ130_provenance.
- NP185982.RAlv6CwDa38FMFs5XLfmC_LEm4OPJ2vZgw2ZOYGLKiqKM130_assertion description "[Only two of these 35 genes (PTGS2/COX2 and CXCL1/GRO1)were also upregulated in breast cancer metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185982.RAlv6CwDa38FMFs5XLfmC_LEm4OPJ2vZgw2ZOYGLKiqKM130_provenance.
- NP185989.RAjxyg4wE9m3lFY3-OO9DvbtDfn1j3l5AJjYp7pZJswKo130_assertion description "[DUSP6 (alias PYST1), one of the dual-specificity tyrosine phosphatases, is localized on 12q21, one of the regions of frequent allelic loss in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185989.RAjxyg4wE9m3lFY3-OO9DvbtDfn1j3l5AJjYp7pZJswKo130_provenance.
- NP185994.RAtV3DZxSClAwQfW0P04B-YuYgmVXUed0Sh5HDlAgUKzY130_assertion description "[Using a severe combined immunodeficient (SCID) mouse model, we demonstrate that enhanced expression of heparanase by myeloma cells dramatically up-regulates their spontaneous metastasis to bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185994.RAtV3DZxSClAwQfW0P04B-YuYgmVXUed0Sh5HDlAgUKzY130_provenance.
- NP185995.RAmBEU4u57dicvQBfCF91MISBvM3ptx_W9jkOGIFsl2EQ130_assertion description "[Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185995.RAmBEU4u57dicvQBfCF91MISBvM3ptx_W9jkOGIFsl2EQ130_provenance.
- NP185998.RAm41SgG1oMiTpQikHbfC76UtvPcovp_PTP8JdRKeTBwg130_assertion description "[Furthermore, the innate immune system has been shown to be activated in psoriasis, and many of the genes associated with the disease are concerned with the signalling pathways of the innate immune system, notably interleukin-23 and nuclear factor κB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185998.RAm41SgG1oMiTpQikHbfC76UtvPcovp_PTP8JdRKeTBwg130_provenance.
- NP186004.RAoJwOZLcrQK-VSoA37jKCAobXDCLn7fRNir8H0KysnSw130_assertion description "[Subjects with MCI who had abnormal results on both FDG-PET and episodic memory were 11.7 times more likely to convert to AD than subjects who had normal results on both measures (p <or= 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186004.RAoJwOZLcrQK-VSoA37jKCAobXDCLn7fRNir8H0KysnSw130_provenance.
- NP186005.RAkW2cb5UFjUtIxc1VwWsRnrFbgafvj_LtZpFaSa1WoFk130_assertion description "[The inverse correlation between miR-100 and Plk1 expression was also detected in nude mice SPC-A1/DTX tumor xenografts and clinical lung adenocarcinoma tissues and was proved to be related with the in vivo response to docetaxel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186005.RAkW2cb5UFjUtIxc1VwWsRnrFbgafvj_LtZpFaSa1WoFk130_provenance.
- NP186008.RAhSi5h6I7mf7kDXinbwON9IndVQnYZ7t42S7nK2i-SCw130_assertion description "[Although mutations in the metabolic enzyme IDH1 were rare in the other common gastrointestinal malignancies in this series (2%), they were found in three tumors (25%) of an initial series of 12 biliary tract carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186008.RAhSi5h6I7mf7kDXinbwON9IndVQnYZ7t42S7nK2i-SCw130_provenance.
- NP186017.RAt3S4t0QY06MrxXnBMb880xxDKKw2HHcKjETP4VkRUoQ130_assertion description "[Germline mutations in the STK11/LKB1 gene cause Peutz-Jeghers syndrome, an autosomal-dominantly inherited condition characterized by mucocutaneous pigmentation, hamartomatous gastrointestinal polyposis, and an increased risk for various malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186017.RAt3S4t0QY06MrxXnBMb880xxDKKw2HHcKjETP4VkRUoQ130_provenance.
- NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_assertion description "[The complete lack of novel driver point mutations in the examined series highlights the unique role of MED12 mutations in genesis of uterine leiomyomas, and suggests that these mutations alone may be sufficient for tumor development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_provenance.
- NP186021.RAmxqbriGa3rB4Xn0_K1rLPoXz7Sp5g_gJXCLybDfVDVc130_assertion description "[For 1-week-old patient with congenital lactic acidemia and hypotonia (confirmed mutations in DLD gene), the rate was 1.5 μM O(2) per min per 10(7) cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186021.RAmxqbriGa3rB4Xn0_K1rLPoXz7Sp5g_gJXCLybDfVDVc130_provenance.
- NP186022.RAjClnveGNXoNsULEdF9bwWbKbdNe8CdTV6HvcCiOzTtw130_assertion description "[NOTCH and phosphatidylinositide 3-kinase/phosphatase and tensin homolog deleted on chromosome ten/AKT/mammalian target of rapamycin (mTOR) signaling in T-cell development and T-cell acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186022.RAjClnveGNXoNsULEdF9bwWbKbdNe8CdTV6HvcCiOzTtw130_provenance.
- NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_assertion description "[Multiallelic DNA probes from within the alpha globin cluster were used to determine the number of copies of this locus in three cell lines containing trisomies of the short arm of chromosome 16 and one with a familial inversion, inv(16).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_provenance.
- NP186043.RAkcxjXj2eKR4av8FRwGoLwel8dILh3lc2sQGX86EEpdc130_assertion description "[The authors suggest the need for a screening program for patients with HBL of the CNS which is designed to confirm or exclude ocular or visceral lesions associated with von Hippel-Lindau syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186043.RAkcxjXj2eKR4av8FRwGoLwel8dILh3lc2sQGX86EEpdc130_provenance.
- NP186046.RAu-JboP6FCDQ7B_2kxkO6BG6G13z1bBGPB1bS-vyLnPo130_assertion description "[A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186046.RAu-JboP6FCDQ7B_2kxkO6BG6G13z1bBGPB1bS-vyLnPo130_provenance.
- NP186048.RAkot0K6hmelRw_fG_KgYu4VQ_GbNfAfDy3mFZQPUBljo130_assertion description "[Similar results have been found analyzing Gale-3 expression: 97.8% of PTC and 55% of FAs were positive for this marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186048.RAkot0K6hmelRw_fG_KgYu4VQ_GbNfAfDy3mFZQPUBljo130_provenance.
- NP186056.RAgf15yhNWK7OgYOzD8Co6T3FqRgml_lT3Jey-tCl3xvA130_assertion description "[A 140 kb homozygous deletion from 22q12 in one meningioma directed us towards the cloning and characterization of a new member of the human beta-adaptin gene family (named BAM22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186056.RAgf15yhNWK7OgYOzD8Co6T3FqRgml_lT3Jey-tCl3xvA130_provenance.
- NP186057.RAlOy-vhqeHsor53WmLS8sp5W-sQxDo_NIitRw-9JRCNU130_assertion description "[The ALDH2 deficiency in Chinese has been implicated in alcohol flush reaction and reported to be a negative risk factor for development of alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186057.RAlOy-vhqeHsor53WmLS8sp5W-sQxDo_NIitRw-9JRCNU130_provenance.
- NP186059.RAtLuv-m0_nf2jG6hXDjeJGNWz2ZVzMs9-6gFoKCbM8Ts130_assertion description "[Moreover, when mice deficient in low-density lipoprotein receptor (LDLR) were bone-marrow transplanted with NLRP3-deficient, ASC (also known as PYCARD)-deficient or IL-1alpha/beta-deficient bone marrow and fed on a high-cholesterol diet, they had markedly decreased early atherosclerosis and inflammasome-dependent IL-18 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186059.RAtLuv-m0_nf2jG6hXDjeJGNWz2ZVzMs9-6gFoKCbM8Ts130_provenance.
- NP186064.RAgxLiEufHqr6mPdZG0_b1Z2nLW5_MwIhg8xsHDnl7ujs130_assertion description "[Common variants in the transcription factor 7-like 2 (TCF7L2) gene have been identified as the strongest genetic risk factors for type 2 diabetes (T2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186064.RAgxLiEufHqr6mPdZG0_b1Z2nLW5_MwIhg8xsHDnl7ujs130_provenance.
- NP186065.RApmAZVZbvB26LaUyK7WgVky8a9NEfJ8Y1JYZnQA4yrCY130_assertion description "[Reverse transcription polymerase chain reaction of the PML-RAR alpha rearrangement is useful for the monitoring of minimal residual disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186065.RApmAZVZbvB26LaUyK7WgVky8a9NEfJ8Y1JYZnQA4yrCY130_provenance.
- NP186067.RAitm4tAlUmPZO7Gq1z-9BMsHFN80gyK7OoCwsyAGJTOk130_assertion description "[Except for a mutation in one of seven (14%) meningeal hemangiopericytomas (codon 238; TGT-->TTT, Cys-->Phe), no mutations were observed in exons 5-8 of the p53 gene in any of the following tumors of the nervous system and its coverings: 13 schwannomas, 12 central neurocytomas, 22 meningiomas, 10 choroid plexus papillomas and carcinomas, and 30 neuroblastomas of the sympathetic nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186067.RAitm4tAlUmPZO7Gq1z-9BMsHFN80gyK7OoCwsyAGJTOk130_provenance.
- NP186074.RArZ4D4MQ0RkUs-pVOn0OJieDvBpRL0LLlxeIEBzTFpw8130_assertion description "[After adjusting for confounding risk factors (such as hypertension, diabetes, tobacco smoking, and alcohol consumption), the ApoM gene TC genotype, C allele of T-778C, and A allele of C-1065A were associated with a risk of ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186074.RArZ4D4MQ0RkUs-pVOn0OJieDvBpRL0LLlxeIEBzTFpw8130_provenance.
- NP186081.RAtwEmleabgABOVlp6W_ARScjlZ8sKx4hWjmWSivzpS8M130_assertion description "[Somatic mutations of the X-linked transcription factor gene, GATA1, have been detected uniformly and exclusively in DS AMkL cases, which may lead to altered expression of GATA1 target genes and alter the metabolism of drugs including ara-C. Hyperdiploid acute lymphoblastic leukemia (ALL) cells with extra copies of chromosome 21, generate higher levels of the active methotrexate (MTX) metabolite, MTX polyglutamates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186081.RAtwEmleabgABOVlp6W_ARScjlZ8sKx4hWjmWSivzpS8M130_provenance.
- NP186085.RAvioFCejWxM8_d4Rp0ExzKIZXncU5QuH5mYbWSJkRU9w130_assertion description "[On the basis of an endogenous source of EPO in the brain, we have focused on a potential role of EPOR in brain tumour growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186085.RAvioFCejWxM8_d4Rp0ExzKIZXncU5QuH5mYbWSJkRU9w130_provenance.
- NP186090.RAnz6o_UMbz7RVhii4Vjl0VhY2D2NTq1Y45yuBJBDawG4130_assertion description "[Familial amyloidotic polyneuropathy type 1 (FAP-1) is a type of systemic amyloidosis caused by mutant transthyretin (mTTR) that is mainly produced in the liver.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186090.RAnz6o_UMbz7RVhii4Vjl0VhY2D2NTq1Y45yuBJBDawG4130_provenance.
- NP186093.RAsApkEqeFY3VDAFLrzH3z8YhJ_gt8jM02LYhi0CurnBU130_assertion description "[ST2 has been reported as the most dominant genotype in the survey of Blastocystis infection among the various monkey species, sequence comparison of the 150bp variable region of the small subunit rRNA (SSU rRNA) gene was conducted among ST2 isolates of humans and monkeys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186093.RAsApkEqeFY3VDAFLrzH3z8YhJ_gt8jM02LYhi0CurnBU130_provenance.
- NP186095.RAmYHtmH-AfNQVb0ME4-hgqC1dGO-dpkHaplPY1qEL1D4130_assertion description "[The expression of NR1 and NR2C subunit transcripts is decreased in the thalamus in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186095.RAmYHtmH-AfNQVb0ME4-hgqC1dGO-dpkHaplPY1qEL1D4130_provenance.
- NP186097.RAmiIyqHxAitBcQUTYz6NhF3MyAWq3yqtl1nqqICzuIJc130_assertion description "[Characterization of human lymphocyte antigen class I antigen-processing machinery defects in renal cell carcinoma lesions with special emphasis on transporter-associated with antigen-processing down-regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186097.RAmiIyqHxAitBcQUTYz6NhF3MyAWq3yqtl1nqqICzuIJc130_provenance.
- NP186102.RAjsIsLeKXUa_diXIE9w0R7KZuc9dh06B5z_OwMGe4WH0130_assertion description "[CAC was measured three times in six years among 436 subjects with type 1 diabetes and 526 control subjects participating in the Coronary Artery Calcification in Type 1 Diabetes (CACTI) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186102.RAjsIsLeKXUa_diXIE9w0R7KZuc9dh06B5z_OwMGe4WH0130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion description "[The authors present here the clinical, anatomic, and endocrine-metabolic studies of three patients, with a view toward careful delineation of the syndrome and further characterization of the metabolic defect.The most striking and consistent metabolic derangements present in all of these patients were fasting hypoglycemia (less than 20 mg/dL), postprandial hyperglycemia (more than 250 mg/dL), marked hyperinsulinemia (more than 2000 μU/mL), and severe insulin resistance (less than a 20 percent decrease in blood sugar with 0.3 to 1.0 U/kg of regular insulin IV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186110.RAgH3JT05lF8bsgLOzSuo6WspjVfa2HfkG1OcgfFEkAJM130_assertion description "[Moreover, miR-199a/b-3p can target tumor-promoting PAK4 to suppress HCC growth through inhibiting PAK4/Raf/MEK/ERK pathway both in vitro and in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186110.RAgH3JT05lF8bsgLOzSuo6WspjVfa2HfkG1OcgfFEkAJM130_provenance.
- NP186116.RAgPIobicApWp4Wprg992c_Tp1f--BLengUBac6OLQt4o130_assertion description "[In this study, we found CPVL/CHN2 rs39059 was associated with diabetic retinopathy in the Chinese type 2 diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186116.RAgPIobicApWp4Wprg992c_Tp1f--BLengUBac6OLQt4o130_provenance.
- NP186124.RAipwW19cE2BVP7Vim9pflaqcTc4ghcpNEwNbJLRnurBc130_assertion description "[The 577X allele of the ACTN3 gene is associated with improved exercise capacity in women with McArdle's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186124.RAipwW19cE2BVP7Vim9pflaqcTc4ghcpNEwNbJLRnurBc130_provenance.
- NP186126.RAkCKqoWsIW_-wGV0kaGQ0vzkznr-mutgH7BAppDlGxx4130_assertion description "[Intrahepatic mRNA levels of type-I interferon (IFN) receptor genes have been shown to correlate with the clinical efficacy of IFN therapy in patients with chronic hepatitis C. Recently, co-infection by serologically-silent hepatitis B virus (HBV) has been assumed to be associated with the poor IFN response in patients with chronic hepatitis C. The aim of this study was to investigate the relationship between the co-infection of serologically-silent HBV and type-I IFN receptor gene expression in the liver of patients with chronic hepatitis C. The intrahepatic mRNA levels of IFNAR2, one of the two subunits of the type-I IFN receptor, were quantified and compared with both the prevalence of HBV DNA and the hepatitis C virus (HCV) genotype in 45 patients with chronic hepatitis C, who were negative for hepatitis B surface antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186126.RAkCKqoWsIW_-wGV0kaGQ0vzkznr-mutgH7BAppDlGxx4130_provenance.
- NP186138.RAvoOVJMVgsWnOsGfIy8HDkiY59BE3vw4mGX0EBG1EEOU130_assertion description "[We resequenced SF3B1, U2AF35, and SRSF2 in 371 children with MDS or juvenile myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186138.RAvoOVJMVgsWnOsGfIy8HDkiY59BE3vw4mGX0EBG1EEOU130_provenance.
- NP186140.RAkRgCQBHWhnCbJPIqWavuBtMevofTWo8vuxxn6IafERU130_assertion description "[Tyrosine hydroxylase (TH) is a theoretical candidate gene determining susceptibility to Parkinson's disease (PD), and an association between one allele of a polymorphism at the TH locus and sporadic PD has been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186140.RAkRgCQBHWhnCbJPIqWavuBtMevofTWo8vuxxn6IafERU130_provenance.
- NP186144.RAn6PBYfv4YPG6Z-D7RFXTACqPnfb3GzmkadEC3p0IchE130_assertion description "[While only minor differences were observed between the blood samples of the diseased and the healthy subjects regarding the TCR genes, CD5, HLA-DR and CD5+CD19 positive cells occurred in higher proportions in the blood samples of the subjects susceptible to periodontal disease than in healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186144.RAn6PBYfv4YPG6Z-D7RFXTACqPnfb3GzmkadEC3p0IchE130_provenance.
- NP186148.RAnWE5hRkuoC6gbdLI7TWL4b9NtrUm370DjWnJz0dDu5c130_assertion description "[Using a newly developed nonradioisotopic method of polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP) analysis combined with the direct sequencing using the fluorescence-labeled terminator, we identified seven missense mutations, 527 A-->G, 1003 G-->A, 1159 C-->T, 1160 G-->A, 1229 G-->A, 1246 G-->A, and 1361 G-->A, in eight Japanese patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186148.RAnWE5hRkuoC6gbdLI7TWL4b9NtrUm370DjWnJz0dDu5c130_provenance.
- NP186152.RAp6GBmPRn1yX9KjfydR4VRvfPlEWssqE5QepKgiSSVi0130_assertion description "[HLA-DRB1*15 was found to be associated with multiple sclerosis in the Lithuanian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186152.RAp6GBmPRn1yX9KjfydR4VRvfPlEWssqE5QepKgiSSVi0130_provenance.
- NP186154.RAju5krAV7Sjj6Muc4CdkwMK8gq7AqoBEHoS0yyrHYSKA130_assertion description "[The effects of the deoxycytidine analogue decitabine (5-aza-2'-deoxycytidine), which depletes DNA methyl transferase 1 (DNMT1), on melanoma differentiation were examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186154.RAju5krAV7Sjj6Muc4CdkwMK8gq7AqoBEHoS0yyrHYSKA130_provenance.
- NP186158.RAj4fW6kcr9uFGh_fwNZiuIHiQMCJyxgvwbo43V0NCEQU130_assertion description "[The inactivation mechanisms and functional role of p16INK4a in three Asian esophageal squamous cell carcinoma (ESCC) cell lines were investigated by polymerase chain reaction (PCR) amplification, DNA sequencing, methylation-specific PCR analysis, reverse transcription-PCR, Western blotting, and colony formation assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186158.RAj4fW6kcr9uFGh_fwNZiuIHiQMCJyxgvwbo43V0NCEQU130_provenance.
- NP186160.RAmYuEhWZIIDSQXiiNvlX2ONOO4k7cXpJWrA06osiUhxk130_assertion description "[Identification of OTX2 as a medulloblastoma oncogene whose product can be targeted by all-trans retinoic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186160.RAmYuEhWZIIDSQXiiNvlX2ONOO4k7cXpJWrA06osiUhxk130_provenance.
- NP186162.RAvljKwSPKeTjtJtaAHq2uISC-6NClFXH_-st9YHZnoSU130_assertion description "[The incidence of overexpression of HER2/neu in bladder cancer is one of the highest among all human malignancies tested; such overexpression is thought to play a role in the aberrant proliferation of cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186162.RAvljKwSPKeTjtJtaAHq2uISC-6NClFXH_-st9YHZnoSU130_provenance.
- NP186165.RAni1MBJw5i2MMgm42XeUGPaFl6tRROP3bROTZ6eoUkSg130_assertion description "[Further studies should be devoted to elucidate the functional roles of NK systems in (a) the neuropathogenesis and neuroprotection during the course of PD, (b) the efficacy of NK receptor drugs towards PD, and (c) potential therapeutic intervention that targets at the prevention or treatment of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186165.RAni1MBJw5i2MMgm42XeUGPaFl6tRROP3bROTZ6eoUkSg130_provenance.
- NP186169.RApqHtHtPB7w7txgJuF1V0DD5GW-y9DuBoTVm0fb0ldiI130_assertion description "[The steroid receptor coactivator AIB1 (amplified in breast cancer-1) is a transcriptional coactivator which has been found to be amplified in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186169.RApqHtHtPB7w7txgJuF1V0DD5GW-y9DuBoTVm0fb0ldiI130_provenance.
- NP186174.RAmMEDF5LMVXHfror3IZzk8bvvMsa_I6SU04IGq7PFMdI130_assertion description "[Here we show that missense mutations in PTPN11 (MIM 176876)-a gene encoding the nonreceptor protein tyrosine phosphatase SHP-2, which contains two Src homology 2 (SH2) domains-cause Noonan syndrome and account for more than 50% of the cases that we examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186174.RAmMEDF5LMVXHfror3IZzk8bvvMsa_I6SU04IGq7PFMdI130_provenance.
- NP186176.RAkBsMv5THg8FcHvaf8U-xzrGMumJ74FXPXEjSlMF89yY130_assertion description "[SIP1 overexpression could not be linked to down-regulated E-cadherin in diffuse-type tumors, but was found to be involved in the pathogenesis of intestinal-type gastric carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186176.RAkBsMv5THg8FcHvaf8U-xzrGMumJ74FXPXEjSlMF89yY130_provenance.
- NP186177.RAqChYGxSaenZJFOnOV5ZJ4q56c3YXHgLQtiKfd2Ng-IQ130_assertion description "[This effect seems mediated at least partially by its ability to physically interact with p63, thus affecting a cell invasion pathway, and accordingly, p63 is deregulated in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186177.RAqChYGxSaenZJFOnOV5ZJ4q56c3YXHgLQtiKfd2Ng-IQ130_provenance.
- NP186179.RAphKM4ljaBg0nclOp8bTw5ODJ5IlILOa32AsmJupIhPk130_assertion description "[Surviving SENP2-Tg mice showed growth retardation, and developed cardiomyopathy with impaired cardiac function with aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186179.RAphKM4ljaBg0nclOp8bTw5ODJ5IlILOa32AsmJupIhPk130_provenance.
- NP186186.RAm067zxqIRB5tGkX0ed_Fj31xMFIe-PIz5eJuZDspWxA130_assertion description "[Quantitative analysis of senile plaques in Alzheimer disease: observation of log-normal size distribution and molecular epidemiology of differences associated with apolipoprotein E genotype and trisomy 21 (Down syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186186.RAm067zxqIRB5tGkX0ed_Fj31xMFIe-PIz5eJuZDspWxA130_provenance.
- NP186190.RAuQO6n7up3eqxY0cgfOXAbLC4d07WgkvnmFB5JZPL1jM130_assertion description "[Further, oncogene analyses showed that RAS mutations are not evenly distributed among different molecular subclasses of MM, with the prevalence being increased in MM-expressing cyclin D1 (P = .015) and decreased in MM with t(4;14) (P = .055).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186190.RAuQO6n7up3eqxY0cgfOXAbLC4d07WgkvnmFB5JZPL1jM130_provenance.
- NP186192.RAqLlUfyigiEQzPjoDvOXfuBSSLADGk5JWCUQAS8pcOYY130_assertion description "[In conclusion, RACK1 is an independent prognosis-related factor and promotes breast carcinoma proliferation and invasion/metastasis in vitro and in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186192.RAqLlUfyigiEQzPjoDvOXfuBSSLADGk5JWCUQAS8pcOYY130_provenance.
- NP186202.RAus6jePLio1h-i-JIst6iojlwTgmArTZqVNr7pNmuew0130_assertion description "[No significant differences in MIF gene polymorphism were observed in patients with biopsy-proven GCA compared to controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186202.RAus6jePLio1h-i-JIst6iojlwTgmArTZqVNr7pNmuew0130_provenance.
- NP186205.RAkO0Ll9B2822CNPBHrLjpK7JbdGBuj4V3K5HZJYQWLIE130_assertion description "[We also found a significant increase in the expression of CXCR4 and CCR7 in B-CLL cells from patients with stage IV compared with stage 0 disease (P = .001 and P = .02, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186205.RAkO0Ll9B2822CNPBHrLjpK7JbdGBuj4V3K5HZJYQWLIE130_provenance.
- NP186218.RAt3grbvxsmM87l6wGsPrAdw_WPA1cxj9-TCVN1Nya3f4130_assertion description "[Altogether, our results reveal an additional regulatory mechanism for ETS2, which plays key roles in cancer and development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186218.RAt3grbvxsmM87l6wGsPrAdw_WPA1cxj9-TCVN1Nya3f4130_provenance.
- NP186220.RAs9k97lYoYUTmRGQV-g4VgIZTLsIQhS2S-Tut_vlIXp0130_assertion description "[Taken together, these data suggest that T. cruzi infection stimulates smooth muscle cell proliferation and is likely a result of the upregulation of the ERK-cyclin D1-endothelin-1 pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186220.RAs9k97lYoYUTmRGQV-g4VgIZTLsIQhS2S-Tut_vlIXp0130_provenance.
- NP186221.RAomsMYE3sBgh-1W8tWK4YxJkdeKz190Rt6R9nRHRmOHQ130_assertion description "[STAT3 and MMP-1 may be involved in the development and metastasis of GC, and treatment targeting TIMP-1 may be a promising strategy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186221.RAomsMYE3sBgh-1W8tWK4YxJkdeKz190Rt6R9nRHRmOHQ130_provenance.
- NP186223.RAqOrio7lGiI_valWefOkixGX--ss8-F7apNSkUKAUHxU130_assertion description "[Mice lacking p35, and thus p35/cdk5 kinase activity, display severe cortical lamination defects and suffer from sporadic adult lethality and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186223.RAqOrio7lGiI_valWefOkixGX--ss8-F7apNSkUKAUHxU130_provenance.
- NP186226.RApsJWd_8_G9nrzKnJAKusIZPGeYV4T5QSyD3fWhIZY38130_assertion description "[In order to clarify the role of Beclin 1 in gastric carcinogenesis and subsequent progression, its expression was examined by immunohistochemistry and in situ hybridization (ISH) on tissue microarrays containing gastric carcinomas, adjacent non-neoplastic mucosa, and metastatic lymph node.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186226.RApsJWd_8_G9nrzKnJAKusIZPGeYV4T5QSyD3fWhIZY38130_provenance.
- NP186230.RAi8wOHGjLAwVU7SuwgEAqoM9cP9dwonZUFsOdHa62Z-0130_assertion description "[The ligand-less receptor HER2/neu (erbB-2) has been proposed as a prognostic marker of gastric cancer that correlates with poor clinical outcome, indicating that HER2 signals play an important role in gastric cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186230.RAi8wOHGjLAwVU7SuwgEAqoM9cP9dwonZUFsOdHa62Z-0130_provenance.
- NP186235.RAhBCvlgpC6HJ16ODqrAX2LzdvSChy59dv52iWehxVa5E130_assertion description "[Functional defects and the influence of age on the frequency of CD4+ CD25+ T-cells in type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186235.RAhBCvlgpC6HJ16ODqrAX2LzdvSChy59dv52iWehxVa5E130_provenance.
- NP186239.RAiLeyy7PNysco_9N0JRlrN1z0_tYTOoTMPrpCkYM-qgc130_assertion description "[In the present study, the risk of CAD associated with abdominal obesity, as estimated by the waist circumference, was largely dependent on the concomitant variation in plasma lipoprotein and insulin concentrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186239.RAiLeyy7PNysco_9N0JRlrN1z0_tYTOoTMPrpCkYM-qgc130_provenance.
- NP186241.RAnsZHaPhDKtBJEKZCSBHElU5jAiOmQ9yFgtSKIyLB2-k130_assertion description "[MTA1/GAPDH mRNA level in NSCLC with lymph node metastasis (4.242+/-3.758) was significantly higher in NSCLC without lymph node metastasis (P=0.0169).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186241.RAnsZHaPhDKtBJEKZCSBHElU5jAiOmQ9yFgtSKIyLB2-k130_provenance.
- NP186246.RAuftZXZqR6m5U_n2KRhImMHRzC8gN-nA2IHatrHFZsFc130_assertion description "[Our data confirm involvement in the CDC4-cyclin E pathway of the development of the CIN phenotype in human CRC, and find that amplification of the Aurora-A is a common target for disruption of this pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186246.RAuftZXZqR6m5U_n2KRhImMHRzC8gN-nA2IHatrHFZsFc130_provenance.
- NP186248.RAszhdLu8WUFFUqXIGF4tk3UpovEpomYZ3BC3l9BgCESw130_assertion description "[In this chapter we present the MENX syndrome and its phenotype, and we compare it to the human MEN syndromes; we discuss the current state of knowledge regarding the genes associated to inherited MEN, with a particular focus on CDKN1B; we present recent clinical and basic findings about the MEN4 syndrome and the functional characterization of the CDKN1B mutations identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186248.RAszhdLu8WUFFUqXIGF4tk3UpovEpomYZ3BC3l9BgCESw130_provenance.
- NP186256.RAjzxshzyG0gqGjrwiBRgt86jRGmNk6uQ5t0bhIQdKAXs130_assertion description "[These results showed that MSH2/MLH1 rearrangements in Spanish patients at risk for HNPCC seem to be a less frequent mutational event than in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186256.RAjzxshzyG0gqGjrwiBRgt86jRGmNk6uQ5t0bhIQdKAXs130_provenance.
- NP186262.RAuxYp-um6IfakrcqjWXdfY0ELrXOXK8MLY_pyF33xpfo130_assertion description "[The t(2;5)(p23;q35) translocation creates a fusion gene NPM-ALK (p80) that encodes a product with tyrosine kinase activity believed to play an important role in development of anaplastic large cell lymphoma (ALCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186262.RAuxYp-um6IfakrcqjWXdfY0ELrXOXK8MLY_pyF33xpfo130_provenance.
- NP186267.RAn7wyAFegOomtlVtKK9DLPOG4DJ_iOSAanDO2VE2lEdw130_assertion description "[DNA repair gene ERCC2, XPC, XRCC1, XRCC3 polymorphisms and associations with bladder cancer risk in a French cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186267.RAn7wyAFegOomtlVtKK9DLPOG4DJ_iOSAanDO2VE2lEdw130_provenance.
- NP186269.RApzIwUI6U0TBULmi1_eabXvRtqSF_yZtG_WYlP58EsZA130_assertion description "[WIF1 and DKK3 promoter methylation were detected in 63.3% (95/150) and 61.3% (92/150) of breast carcinoma samples, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186269.RApzIwUI6U0TBULmi1_eabXvRtqSF_yZtG_WYlP58EsZA130_provenance.
- NP186271.RAjdK28Qm77L2so_Rn9fgHM6XJ3janJrhUgKiZ3lYNWaU130_assertion description "[DNA methylation defects affecting ICR1 or ICR2 account for approximately 60% of SRS and BWS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186271.RAjdK28Qm77L2so_Rn9fgHM6XJ3janJrhUgKiZ3lYNWaU130_provenance.
- NP186272.RAhrO9T2-8ibQLOMbtgkgh7f7K6APq_JQDxj0Pwx4mt-k130_assertion description "[Six different genes causing autosomal dominant SCA are mapped: SCA1, SCA2, Machado-Joseph disease (MJD)/SCA3, SCA4, SCA5, and dentatorubropallidoluysian atrophy (DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186272.RAhrO9T2-8ibQLOMbtgkgh7f7K6APq_JQDxj0Pwx4mt-k130_provenance.
- NP186274.RAtqbbNXugZ-LeGnZWKJmQ4ipvR0NZg1gGMVCBXtPvVYo130_assertion description "[Our data suggest that IL-10 SNP, including -2849, which is associated with differential production, do not play a major role in the susceptibility of DIP OA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186274.RAtqbbNXugZ-LeGnZWKJmQ4ipvR0NZg1gGMVCBXtPvVYo130_provenance.
- NP186276.RAsZmBF8wCNIgiTh1rOZQsFQZL1bZGhXR19uS5TjK0Ol4130_assertion description "[The GSTT1 null genotype was associated with asthma risk in non-smoker adults (OR = 2.06, 95% CI: 1.21-3.71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186276.RAsZmBF8wCNIgiTh1rOZQsFQZL1bZGhXR19uS5TjK0Ol4130_provenance.
- NP186280.RAnH2ARr0Bigmoc6EOSwK5RsteyP_U0vcAU_aH7QKaWIY130_assertion description "[Moreover, macrophage PPAR-γ was required for accelerating pioglitazone-mediated recovery from dextran sodium sulfate (DSS) colitis, providing a cellular target for the anti-inflammatory effects of PPAR-γ agonists in IBD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186280.RAnH2ARr0Bigmoc6EOSwK5RsteyP_U0vcAU_aH7QKaWIY130_provenance.
- NP186286.RAm0jRg1MjlVgPbyBmvG3OXQOjHjcXEgPFaUd5E547uP4130_assertion description "[Sorsby's fundus dystrophy (SFD) and age related macular degeneration (ARMD) are retinal diseases associated with a high level of accumulation of mutant and wild type TIMP-3, respectively, in Bruch's membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186286.RAm0jRg1MjlVgPbyBmvG3OXQOjHjcXEgPFaUd5E547uP4130_provenance.
- NP186289.RAgHqp6WX8HmBYSQ_HLOhCE3L_buplzee4zH1V2_ocoSc130_assertion description "[ARLTS1 is a tumor suppressor gene initially described as a low-penetrance cancer gene: a truncated Trp149Stop (MUT) polymorphism is associated with general familial cancer aggregation and, particularly, high-risk familial breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186289.RAgHqp6WX8HmBYSQ_HLOhCE3L_buplzee4zH1V2_ocoSc130_provenance.
- NP186294.RAiadmvr9obufPCEAcaFrgDbqN2c64EG3v4Wq2agUCWfo130_assertion description "[Human studies and knockout mice demonstrated a role for the guanosine triphosphatase RAC1 in the development of ulcerative colitis; increased expression of RAC1 was associated with susceptibility to colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186294.RAiadmvr9obufPCEAcaFrgDbqN2c64EG3v4Wq2agUCWfo130_provenance.
- NP186297.RAn-o4WJJNkWQbRbJ_fiAOzLcvJcr5UO9e561rAg-iTi8130_assertion description "[All SCCs and the BCC with additional Cyclin D1 gene copies showed positivity for Cyclin D1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186297.RAn-o4WJJNkWQbRbJ_fiAOzLcvJcr5UO9e561rAg-iTi8130_provenance.
- NP186302.RAjVoxf50maY_Boo6gYsStBUGjmFsvf3pmRCcW6uENjQA130_assertion description "[The 936CC-1451CC genotype in the 3' UTR showed not only susceptibility for ESRD but also higher plasma VEGF levels and mRNA stability, indicating the contribution of VEGF to chronic kidney disease progression, especially in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186302.RAjVoxf50maY_Boo6gYsStBUGjmFsvf3pmRCcW6uENjQA130_provenance.
- NP186305.RAl2q-4YvxPXd-tgl21rrTQa8vVbqzpnsCHHsimxWIF_E130_assertion description "[Vascular endothelial growth factor synthesis by human omental mesothelial cells is augmented by fibroblast growth factor-2: possible role of mesothelial cell on the development of peritoneal metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186305.RAl2q-4YvxPXd-tgl21rrTQa8vVbqzpnsCHHsimxWIF_E130_provenance.
- NP186308.RAiHfFJPV5HZpjPR5L9ezPYiQeqdeC5np7ckAIsNKJIlc130_assertion description "[These results suggest that the EGFR +2073 A/T and HER2 +655 A/G polymorphisms are not associated with endometrial cancer in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186308.RAiHfFJPV5HZpjPR5L9ezPYiQeqdeC5np7ckAIsNKJIlc130_provenance.
- NP186310.RAokbmrBeR17jPmHhl3JoEuSOe6dAcaH-b55sWuyuramA130_assertion description "[Presenilin (PS1) and (PS2) are the centers of gamma-secretase that release Abeta from APP in Alzheimer's disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186310.RAokbmrBeR17jPmHhl3JoEuSOe6dAcaH-b55sWuyuramA130_provenance.
- NP186317.RApZ6POZX4a0TKiFf-CtCXZMPB5Onb_05kq4BJdcW6ILQ130_assertion description "[Recently, mutations in myosin heavy chain (MYH7), cardiac actin (ACTC), and troponin T (TNNT2) were associated with left ventricular noncompaction, a form of cardiomyopathy characterized with hypertrabeculation that may also include reduced function of the left ventricle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186317.RApZ6POZX4a0TKiFf-CtCXZMPB5Onb_05kq4BJdcW6ILQ130_provenance.
- NP186321.RAjO6cQXj5pZ4huIhEfZftkrlL9-dlxU7Z6C95oElF0Gk130_assertion description "[The frequencies of aberration in the TOP1 gene copy number, the CEN-20 copy number and the TOP1/CEN-20 ratio were analyzed and associated with overall survival (OS), time to recurrence (TTR) and in a subgroup analysis of rectal cancer patients only with time to local recurrence (LR in RC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186321.RAjO6cQXj5pZ4huIhEfZftkrlL9-dlxU7Z6C95oElF0Gk130_provenance.
- NP186322.RAoN2wuLR7sEjsiyKHPaxlF6md1tTn1gfJLLUE6AtU4dU130_assertion description "[Candidate polymorphisms within interleukin-1 beta (IL-1beta), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-alpha), cellular differentiation marker 14 (CD14) and toll-like receptor 4 (TLR4) were evaluated by logistic regression analysis for association with increased risk for severe sepsis (sepsis plus organ dysfunction or shock).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186322.RAoN2wuLR7sEjsiyKHPaxlF6md1tTn1gfJLLUE6AtU4dU130_provenance.
- NP186332.RAgCaPs_f2zKRtyLVLxNNOqplFuZvJXle5evlowLezdLc130_assertion description "[Spinal muscular atrophy (SMA), an inherited disease of motor neuron dysfunction, results from insufficient levels of the survival motor neuron (SMN) protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186332.RAgCaPs_f2zKRtyLVLxNNOqplFuZvJXle5evlowLezdLc130_provenance.
- NP186335.RAs27vlgXKDTPjpwmnzJvfR2W1jIbXEbc_rubXetDb-HE130_assertion description "[Morning ACTH and 17-hydroxyprogesterone levels correlated positively with adrenal dimensions and frequency of TART.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186335.RAs27vlgXKDTPjpwmnzJvfR2W1jIbXEbc_rubXetDb-HE130_provenance.
- NP186344.RAkhZuqZzXXDPdL66m4KaqmT1A3XTE3p7R9y-CnqLZYNc130_assertion description "[Recently, we reported that depletion of RRM2 by systemic delivery of a nanoparticle carrying RRM2-specific siRNA suppresses head and neck tumor growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186344.RAkhZuqZzXXDPdL66m4KaqmT1A3XTE3p7R9y-CnqLZYNc130_provenance.
- NP186345.RAkKNxn5EkKoX8XxBC33OhujY0mwgcwazwoennRoZUEIY130_assertion description "[Gene polymorphisms of angiotensin-converting enzyme and angiotensin II type 1 receptor among chronic kidney disease patients in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186345.RAkKNxn5EkKoX8XxBC33OhujY0mwgcwazwoennRoZUEIY130_provenance.
- NP186348.RAkKZDFrVHv6ISMiLj5UEYp4IEWcL43ucU0zZisYgzYAw130_assertion description "[Comparative study of p63 and p53 expression in tissue microarrays of malignant melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186348.RAkKZDFrVHv6ISMiLj5UEYp4IEWcL43ucU0zZisYgzYAw130_provenance.
- NP186364.RAiZ5yHqu3aPpUcFTndeR78jJ1-aydjNvTtAxbaY1TZ-M130_assertion description "[A novel mutation in RASA1 causes capillary malformation and limb enlargement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186364.RAiZ5yHqu3aPpUcFTndeR78jJ1-aydjNvTtAxbaY1TZ-M130_provenance.
- NP186367.RAp9OyXnDnezvP4RVkZsiwllUo6Xhbyw28JhWoka3ba-U130_assertion description "[The results affirm the utility of systematic characterization of the cancer genome in clinically annotated specimens and suggest the particular importance of the PI3K pathway in patients who have aggressive endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186367.RAp9OyXnDnezvP4RVkZsiwllUo6Xhbyw28JhWoka3ba-U130_provenance.
- NP186371.RAvx8sggxmzxoOSygs3Y7haQOrJugmhM_2LMyxm2NBVMQ130_assertion description "[Lower serum concentrations of the copper-dependent ferroxidase ceruloplasmin (21.7 +/- 4.1 vs 30.4 +/- 6.4 mg/dL; P < .001) and decreased liver ferroportin (FP-1; P = .009) messenger RNA expression were found in these patients compared with NAFLD patients with high liver or serum copper concentrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186371.RAvx8sggxmzxoOSygs3Y7haQOrJugmhM_2LMyxm2NBVMQ130_provenance.
- NP186382.RAlIF4s-hXS6HljB1xF6rfNs4FZJxz5xa-Lc1JEWX6pZM130_assertion description "[We conclude that variants in TTC12 exon 3, NCAM1 exon 12, and the two 3'-ends of ANKK1 and DRD2 co-regulate risk for comorbid AD and DD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186382.RAlIF4s-hXS6HljB1xF6rfNs4FZJxz5xa-Lc1JEWX6pZM130_provenance.
- NP186386.RAvEYAmnvJhLxNJDGVVI2n6SQzp6nyZOgvgUwDfDGZ3yg130_assertion description "[The results suggest that lower birth weight and maternal smoking during pregnancy may interact with DRD5 and DAT1 (birth weight only) in influencing associated antisocial behavior symptoms (ODD and conduct disorder).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186386.RAvEYAmnvJhLxNJDGVVI2n6SQzp6nyZOgvgUwDfDGZ3yg130_provenance.
- NP186388.RApZdn32dWJXg-Pj63n4NwFpBt3rQIuk230ak63sHvgdo130_assertion description "[BCT and TNF-alpha can reverse HCC MDR in nude mouse MDR1 model of liver neoplasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186388.RApZdn32dWJXg-Pj63n4NwFpBt3rQIuk230ak63sHvgdo130_provenance.
- NP186389.RAoLxX2IR3uj0kLbKy3oUAHocZp_yEIADFR3UWlRvepys130_assertion description "[Here we discuss the role of GITR and 4-1BB on T cells during viral infections and in cancer immunotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186389.RAoLxX2IR3uj0kLbKy3oUAHocZp_yEIADFR3UWlRvepys130_provenance.