Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP185574.RAr2s7Nwm3UXqWIhIaf2CiOukuhxb9QIBdtCh0yPyzXF0130_assertion description "[However, retrospective analyses of all 76 cases revealed that the survival profile and therapeutic responses were very similar in NHL patients bearing lymphomas with a mutant p53 or with the wild-type p53 even within the subclasses characterized by frequent p53 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185574.RAr2s7Nwm3UXqWIhIaf2CiOukuhxb9QIBdtCh0yPyzXF0130_provenance.
- NP185577.RAvdJCil5eji4o3OdBYSjs5GCPrmL1yehIL3RavZYkrm8130_assertion description "[The clinical implications for CAD and a better understanding of the functional basis for the association of CFH and MPO variants with circulating MPO levels require further study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185577.RAvdJCil5eji4o3OdBYSjs5GCPrmL1yehIL3RavZYkrm8130_provenance.
- NP185579.RAiDtYL7pwkfE4Ue6sZYprVw3ec-2C2Wn3nc-4gqX97VY130_assertion description "[We have demonstrated that the factor(s) responsible for the suppression of HIV-1 LTR-mediated gene expression are not the CC chemokines RANTES, MIP-1alpha, and MIP-1beta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185579.RAiDtYL7pwkfE4Ue6sZYprVw3ec-2C2Wn3nc-4gqX97VY130_provenance.
- NP185580.RAuiTSw8vVSVxVdf9hKYGXFYClPxZMWjxhDfSv8TB9hE4130_assertion description "[Collectively, these data reveal differential consequences of p19(Arf) inactivation in prostate cancer and MEFs upon Pten loss that are independent of the p53 pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185580.RAuiTSw8vVSVxVdf9hKYGXFYClPxZMWjxhDfSv8TB9hE4130_provenance.
- NP185582.RAh5UZtU7v1ulupf1jHHKv5mlUIPdhohEO1rDlMa4xj3I130_assertion description "[Our data did not show that CYP3A5, MDR-1 or MAPT polymorphisms are linked to impaired motor performance in children after treatment for ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185582.RAh5UZtU7v1ulupf1jHHKv5mlUIPdhohEO1rDlMa4xj3I130_provenance.
- NP185590.RAoH_dPDDOPlM7iNeJxp-gjVWdlskJAMGjOijctp3z89U130_assertion description "[To investigate whether there is evidence of linkage in affected Japanese sib-pairs we performed nonparametric and parametric linkage analysis of a total of 253 familial aneurysm cases including 111 affected sib-pairs (ASP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185590.RAoH_dPDDOPlM7iNeJxp-gjVWdlskJAMGjOijctp3z89U130_provenance.
- NP185594.RAqOdK2-T7Lcg80N9RjtLagoxR87kvkawIKYC7MemKi00130_assertion description "[In multivariate analysis, independent predictors of greater BMD (at the hip or spine) were: age (younger for the hip, older for the spine), greater body weight, greater height (hip only), higher level of physical activity now and during adolescence, no family history of osteoporosis, and VDR genotype (hip only).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185594.RAqOdK2-T7Lcg80N9RjtLagoxR87kvkawIKYC7MemKi00130_provenance.
- NP185598.RAiPgQUs9VmUAiLBMRdwXIH_ctU68PkLz_E6HhFU2OfG8130_assertion description "[(1) A cosmid containing NAT2 has been used in fluorescence in-situ hybridization on human exfoliated bladder cells collected from unselected bladder cancer outpatients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185598.RAiPgQUs9VmUAiLBMRdwXIH_ctU68PkLz_E6HhFU2OfG8130_provenance.
- NP185604.RAs1d59N-NG_YRp8kbw76gnlAB7p021aZilA47roWf5E4130_assertion description "[Loss of the wild-type BRCA1 allele was observed in 3/3 breast tissues (2 breast carcinomas and 1 ductal carcinoma in situ) but in 0/6 colorectal tissues (5 carcinomas and 1 adenoma), suggesting that BRCA1 loss is not critical for colorectal tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185604.RAs1d59N-NG_YRp8kbw76gnlAB7p021aZilA47roWf5E4130_provenance.
- NP185609.RAijclxbYcHik6ifCd9huKGIZgSTzVWP8JdIFORQmlrqw130_assertion description "[We compared the frequency of low-affinity alleles of two FcgammaR polymorphisms (FcgammaRIIA and FcgammaRIIIA) among 235 patients with systemic lupus erythematosus (SLE) and proven nephritis (nephritis patients) and among 352 SLE patients with no evidence of renal disease (non-nephritis control subjects).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185609.RAijclxbYcHik6ifCd9huKGIZgSTzVWP8JdIFORQmlrqw130_provenance.
- NP185611.RArPo4t-cXY3maEiTIbJ1NimZLtymEuas9Q05DI0mfaHA130_assertion description "[The Menkes protein (MNK or ATP7A) is an important component of the mammalian copper transport pathway and is defective in Menkes disease, a fatal X-linked disorder of copper transport.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185611.RArPo4t-cXY3maEiTIbJ1NimZLtymEuas9Q05DI0mfaHA130_provenance.
- NP185618.RAr1iL2cxOXVI_tqEKwQoJDfQKdAOLY18RXUPY4k550d8130_assertion description "[Craniofrontonasal syndrome (CFNS) is characterized by craniosynostosis, hypertelorism, a broad nasal tip and occasionally cleft lip and palate, and is caused by a mutation in the ephrin-B1 gene (EFNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185618.RAr1iL2cxOXVI_tqEKwQoJDfQKdAOLY18RXUPY4k550d8130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion description "[This paper summarizes recent findings concerning sodium (SCN1A) and potassium channel (KCNQ2 and KCNQ3) dysfunctions in the pathogenesis of rare and common idiopathic epilepsies (IE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185626.RAuR0PKdtF8WGrnkMDQo8LhHHeNWT1qKofKdAX5SFndl0130_assertion description "[This study investigated whether the level of breast cancer risk associated with BMD in women with a positive family history of breast cancer is different from that in women without a family history of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185626.RAuR0PKdtF8WGrnkMDQo8LhHHeNWT1qKofKdAX5SFndl0130_provenance.
- NP185629.RAsE5Fk5sZDe-J2sk16IwD7hIN31eQkRN2vnRZQjtOYjo130_assertion description "[Niemann-Pick disease (NPD) types A/B are both caused by a deficiency of lysosomal acid sphingomyelinase and display autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185629.RAsE5Fk5sZDe-J2sk16IwD7hIN31eQkRN2vnRZQjtOYjo130_provenance.
- NP185634.RApDtJGXMm2r_Lz3RAwyXYWrI5YixMfpz6nQq9LkY_2wo130_assertion description "[In addition, characterization of the UGT1A locus and genetic studies directed at understanding the role of bilirubin glucuronidation and the biochemical basis of the clinical symptoms found in unconjugated hyperbilirubinemia have uncovered the structural gene polymorphisms associated with Crigler-Najjar's and Gilbert's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185634.RApDtJGXMm2r_Lz3RAwyXYWrI5YixMfpz6nQq9LkY_2wo130_provenance.
- NP185646.RAiubBZtMQjvIRg1_D4NJfTQGOWHMfvex-g5ZHGVrbibU130_assertion description "[The association between IL-1B C-31T genotypes and various indices of obesity was then investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185646.RAiubBZtMQjvIRg1_D4NJfTQGOWHMfvex-g5ZHGVrbibU130_provenance.
- NP185647.RAjQy8slxa9bcG9kJkHFfQWRcd5QD_pqaXqwyorsAoaSk130_assertion description "[Outcome modeling with CRLF2, IKZF1, JAK, and minimal residual disease in pediatric acute lymphoblastic leukemia: a Children's Oncology Group study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185647.RAjQy8slxa9bcG9kJkHFfQWRcd5QD_pqaXqwyorsAoaSk130_provenance.
- NP185649.RAsFdIb6WhyVcmTwaUWg9TE83YwbzGiuyUti60e1znu2I130_assertion description "[The thrombotic risk factors decreased levels of activated protein C resistance ratios and protein C, elevated homocysteine and the MTHFR 677 C-->T mutation are likely risk factors for placental vasculopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185649.RAsFdIb6WhyVcmTwaUWg9TE83YwbzGiuyUti60e1znu2I130_provenance.
- NP185653.RAtdtNvYT0aEa7cfqqEDLxMkU7ZuusPTjCOw2K-cVKtc8130_assertion description "[The total MRI score and MRI erosion score increased significantly from baseline to one year despite falls in clinical measures of inflammation including erythrocyte sedimentation rate (ESR), C reactive protein (CRP), and swollen joint count (p < 0.01 for all).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185653.RAtdtNvYT0aEa7cfqqEDLxMkU7ZuusPTjCOw2K-cVKtc8130_provenance.
- NP185655.RApu6kS97oYlgHKCVUv3KWAR4tVb18643bWyDbrdyTgjk130_assertion description "[These findings indicate that MET, which encodes a receptor involved in growth and motility signaling, is a downstream target of PAX3-FKHR in alveolar rhabdomyosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185655.RApu6kS97oYlgHKCVUv3KWAR4tVb18643bWyDbrdyTgjk130_provenance.
- NP185660.RApdooV8HQhPqlUccxNLJypSpbXn4R7PfII2VPVHY-8ik130_assertion description "[We investigated the prevalence and clinico-biological correlations of FLT3 ITDs and D835 mutations in 90 patients with acute promyelocytic leukemia (APL) receiving the AIDA protocol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185660.RApdooV8HQhPqlUccxNLJypSpbXn4R7PfII2VPVHY-8ik130_provenance.
- NP185664.RAkYZlv2Ej3dyReBM8mSqwpDezl3ZHv79MoiHFvE1bv1U130_assertion description "[Shigella flexneri type III secreted effector OspF harbors a phosphothreonine lyase activity that irreversibly dephosphorylates MAP kinases (MAPKs) p38 and ERK in infected epithelial cells and thereby, dampens innate immunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185664.RAkYZlv2Ej3dyReBM8mSqwpDezl3ZHv79MoiHFvE1bv1U130_provenance.
- NP185670.RAj9xy5WfuFmS2qnKsEOXiCIw950FvPsqi5t_Yy7XRudA130_assertion description "[Superoxide release and CYBB gene expression by EDA-ID cells were significantly decreased compared with healthy cells and similar to cells from patients with X-linked chronic granulomatous disease (X91(0) CGD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185670.RAj9xy5WfuFmS2qnKsEOXiCIw950FvPsqi5t_Yy7XRudA130_provenance.
- NP185673.RAq_1LS1qwYE6fx48h93KKp--T1sCUv2KI_2giAlp8rF0130_assertion description "[Expression of vasopressin receptors in ACTH-independent macronodular bilateral adrenal hyperplasia causing Cushing's syndrome: molecular, immunohistochemical and pharmacological correlates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185673.RAq_1LS1qwYE6fx48h93KKp--T1sCUv2KI_2giAlp8rF0130_provenance.
- NP185674.RAqaTAVUEEhGDwOTt-EuP9lXdH_ZzkRPGzmJbY7uodoSE130_assertion description "[Type I procollagen was examined in cultured skin fibroblasts from a patient with a lethal variant of osteogenesis imperfecta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185674.RAqaTAVUEEhGDwOTt-EuP9lXdH_ZzkRPGzmJbY7uodoSE130_provenance.
- NP185681.RAr5LiTQO1rOIo15Ab5xsGlk0sTxeiGrOhPGu4pGU3C_o130_assertion description "[Since polymorphic variants in the glutathione S-transferase (GST) and N-acetyl transferase (NAT) genes have been associated with cancer risk, we explored the possible links between GSTM1, GSTP1, GSTT1 and NAT2 variants and the frequency of micronuclei (MN) in human lymphocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185681.RAr5LiTQO1rOIo15Ab5xsGlk0sTxeiGrOhPGu4pGU3C_o130_provenance.
- NP185687.RAjHv1Mm022i-Gqzf64FE2Bl2dvgNDsYN2Osa_VAB9o_k130_assertion description "[Some families exhibited concordance of ABCR alleles with macular degeneration phenotype, but others did not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185687.RAjHv1Mm022i-Gqzf64FE2Bl2dvgNDsYN2Osa_VAB9o_k130_provenance.
- NP185688.RAqMdHpR1Fbru5I6LWnr0kjRYGE_QqZrU3F1TYkpS3j4k130_assertion description "[Amplification of the EGFR gene has been implicated in the pathogenesis of primary GBM, in particular the small cell phenotype, and this finding may contribute to its aggressive clinical behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185688.RAqMdHpR1Fbru5I6LWnr0kjRYGE_QqZrU3F1TYkpS3j4k130_provenance.
- NP185692.RAq-06i3mdo962D91L-_Pzvy7aNsXa8geqlBGQMtOVc60130_assertion description "[The hGPX1 CT genotype (Pro-Leu) had decreased recurrence time (p=0.03) after BCG therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185692.RAq-06i3mdo962D91L-_Pzvy7aNsXa8geqlBGQMtOVc60130_provenance.
- NP185698.RApLB3ad_ubAXcNAVneidZeIe6dQefhJScttGL3-hl904130_assertion description "[Negative ERG responses also were found in his father, who had macular degeneration, and one of the proband's three children who showed no fundus changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185698.RApLB3ad_ubAXcNAVneidZeIe6dQefhJScttGL3-hl904130_provenance.
- NP185699.RAoc5xx_7aDb1icIwgciApftmR9bnntZUNWqEs45ekvjw130_assertion description "[We report the findings of relative hyperperfusion by Tc-99m HMPAO SPECT in the medial orbitofrontal cortex and anterior temporal lobe in four affected family members carrying a presenilin 1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185699.RAoc5xx_7aDb1icIwgciApftmR9bnntZUNWqEs45ekvjw130_provenance.
- NP185701.RAvnv5tGDm-tMTpMifHZqswAyMklzv0iBpnhBHm61eyT4130_assertion description "[This study suggests the lack of association of SDF-1 3'A, MCP-1 (-2518), CCR5-Delta32 polymorphisms with death and HCC occurrence in cirrhotic HCV-infected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185701.RAvnv5tGDm-tMTpMifHZqswAyMklzv0iBpnhBHm61eyT4130_provenance.
- NP185704.RAuF3N0PJ_4ZU3CY_7jvBORpaJLSCMOc89Hwmesp18m-o130_assertion description "[In an attempt to identify such mutations, the region encompassing the delta-globin gene from three Greek Cypriot families suspected of having delta-thalassemia was amplified by polymerase chain reaction (PCR), and DNA sequence determined using an automated fluorescence-based sequencer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185704.RAuF3N0PJ_4ZU3CY_7jvBORpaJLSCMOc89Hwmesp18m-o130_provenance.
- NP185707.RAjOh-sS5gNKPniSxGeKF98zZBh8_Jg03rbTcZAjGmriM130_assertion description "[PKM2 expression might be an adverse prognostic factor for signet-ring cell carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185707.RAjOh-sS5gNKPniSxGeKF98zZBh8_Jg03rbTcZAjGmriM130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion description "[Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185710.RAtr2O6lbowJYYNrik0xHnWqvl4fP62FEYq-llZ-rmAkg130_assertion description "[Our data point to the direct involvement of APC, CDH1, and CTNNB1 promoter methylation in the early stages of breast cancer progression and suggest that they may represent a useful tool for the detection of tumor cells in clinical specimens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185710.RAtr2O6lbowJYYNrik0xHnWqvl4fP62FEYq-llZ-rmAkg130_provenance.
- NP185712.RAmMoWIlg50qdSMqJnpjrKMbLF3W07TMKqIUTw5sqi62U130_assertion description "[We found that besides to the well-established aforementioned sequence variations of FV and Prothrombin, the FSAP Marburg I (FSAP-MI) polymorphism was significantly associated with the development of DVTs (1.65 (1.16-2.34) OR (95% CI)) and recurrent thromboembolic events (DVT and PE) (2.13 (1.35-3.36) OR (95% CI)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185712.RAmMoWIlg50qdSMqJnpjrKMbLF3W07TMKqIUTw5sqi62U130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion description "[The combined results based on all studies showed that there was a statistically significant link between CCND1 G870A polymorphism and DTC risk (GG vs. AA: OR=0.83, 95%CI=0.71-0.96).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185719.RAuYTJVDW0vHEG0mS8NGxk4XSBOPolwUjIyQ0GUuuS_gY130_assertion description "[Together, these results indicated that the HTPAP tagSNP +357 GG+GC genotypes may influence HCC metastatic potential and clinical prognosis by down-regulating HTPAP expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185719.RAuYTJVDW0vHEG0mS8NGxk4XSBOPolwUjIyQ0GUuuS_gY130_provenance.
- NP185721.RAvYSm6qagCT8NL6ZFDtfs36BlsTsX81OcSoxnLBSvSAk130_assertion description "[Evidence for a role of Langerhans cell-derived IL-16 in atopic dermatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185721.RAvYSm6qagCT8NL6ZFDtfs36BlsTsX81OcSoxnLBSvSAk130_provenance.
- NP185726.RAoe-Xtqb6pAu6IDyIuBhc6EYgxI8N5MYDtkPL0z4rd-M130_assertion description "[Behavioral effects were measured with the Hamilton Depression Rating Scale (HDRS) both 24 h before and 24 h after TRP depletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185726.RAoe-Xtqb6pAu6IDyIuBhc6EYgxI8N5MYDtkPL0z4rd-M130_provenance.
- NP185729.RAgurNEcPkXAz4DCiL33rHnfvqAgTIwtb5IlfevweCDsw130_assertion description "[The purpose of this study is to evaluate the role of the cell survival gene clusterin in radiation-induced cell death in human LNCaP and PC-3 prostate cancer models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185729.RAgurNEcPkXAz4DCiL33rHnfvqAgTIwtb5IlfevweCDsw130_provenance.
- NP185731.RAiUXL8d4cA_qSEJqgS5RTFgjVJ0Gh5IXlU10OReW69iU130_assertion description "[In endometrial adenocarcinomas COX-2 and F-series prostanoid (FP) receptor expression and prostanoid biosynthesis (PGE(2) and PGF(2alpha)) are elevated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185731.RAiUXL8d4cA_qSEJqgS5RTFgjVJ0Gh5IXlU10OReW69iU130_provenance.
- NP185735.RAkmZa7Psuva6RZzs7YUcA2R-xG6jw75HNrybKbUbgaaU130_assertion description "[STMN1 is overexpressed across a broad range of human malignancies (leukemia, lymphoma, neuroblastoma; ovarian, prostatic, breast and lung cancers and mesothelioma).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185735.RAkmZa7Psuva6RZzs7YUcA2R-xG6jw75HNrybKbUbgaaU130_provenance.
- NP185738.RAifpUoj29TlrEiZjkTodYBUP_wc8w1b8ulmWSZvVDsxU130_assertion description "[CoxBoost revealed a three-biomarker (CHK1pS345, Caveolin1, and RAB25) and a two-biomarker (CD31 and Cyclin E1) model that correlated with recurrence-free survival (RFS) in all residual breast cancers and in HR-positive disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185738.RAifpUoj29TlrEiZjkTodYBUP_wc8w1b8ulmWSZvVDsxU130_provenance.
- NP185741.RAg0Si5LDQPYSzd5QZE4pnBZ3yIicIu8VlHDqw4hHtwFI130_assertion description "[In cells from 86% of probands with nonlethal OI we identified biochemical alterations compatible with heterozygosity for a mutation that affected expression or structure of alpha chains of type I procollagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185741.RAg0Si5LDQPYSzd5QZE4pnBZ3yIicIu8VlHDqw4hHtwFI130_provenance.
- NP185742.RAutgV79ol2SgBr7V62wTjhNz0bke_r7Wzjh9D14yJSSU130_assertion description "[In contrast, other activating mutations like FLT3 and NRAS mutations were very rarely detected in AML1-rearranged leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185742.RAutgV79ol2SgBr7V62wTjhNz0bke_r7Wzjh9D14yJSSU130_provenance.
- NP185744.RAhqTREiqw6JRhU6uDCi3WSELXz1KFAQtKBhmShPirNdo130_assertion description "[Several genes whose expression is thought to be related to tumor progression such as c-Met, urokinase-type plasminogen activator receptor, ezrin, HMG-1, oncomodulin, cathepsin, and caveolin were thereby isolated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185744.RAhqTREiqw6JRhU6uDCi3WSELXz1KFAQtKBhmShPirNdo130_provenance.
- NP185747.RAva2ZanfbjORIoMblwBQ0HJF1Xof_N6yWxdEFMABXLO0130_assertion description "[Toward a pharmacogenetic approach to male infertility: polymorphism of follicle-stimulating hormone beta-subunit promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185747.RAva2ZanfbjORIoMblwBQ0HJF1Xof_N6yWxdEFMABXLO0130_provenance.
- NP185749.RAmRAUqi8VaU8cWzn-teRpfGPW0dMcG54s42rkRw5-Xns130_assertion description "[We genotyped selected single nucleotide polymorphisms (SNPs) in or near diabetes-associated loci, including EXT2, CDKAL1, CDKN2A/B, IGF2BP2, HHEX, LOC387761, and SLC30A8 in DPP participants and performed Cox regression analyses using genotype, intervention, and their interactions as predictors of diabetes incidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185749.RAmRAUqi8VaU8cWzn-teRpfGPW0dMcG54s42rkRw5-Xns130_provenance.
- NP185760.RAs4MJ46bMNw5u_fUrvfSqqmSbYXNAtKsqsMjge0oz6XQ130_assertion description "[The GSTT1 null genotype conferred a 1.06-fold increased risk of gastric cancer, which was not significant (95% confidence interval [CI]: 0.94-1.19).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185760.RAs4MJ46bMNw5u_fUrvfSqqmSbYXNAtKsqsMjge0oz6XQ130_provenance.
- NP185767.RApQHuYpuSnxhLWmJsE0eU3EJFWTw1heDb6yRzotULvR0130_assertion description "[Increased intestinal expression of heme oxygenase-1 and its localization in patients with ulcerative colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185767.RApQHuYpuSnxhLWmJsE0eU3EJFWTw1heDb6yRzotULvR0130_provenance.
- NP185771.RAl5viZ-IRM8SV5DpMpAllZDinpxSg2gCNfDuf8tjpjaQ130_assertion description "[Among our consensus findings we are confident that: 1) crystalline silica exposure can contribute to the development of several AID; 2) solvent exposure can contribute to the development of systemic sclerosis; 3) smoking can contribute to the development of seropositive rheumatoid arthritis; and 4) an inverse association exists between ultraviolet radiation exposure and the risk of development of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185771.RAl5viZ-IRM8SV5DpMpAllZDinpxSg2gCNfDuf8tjpjaQ130_provenance.
- NP185776.RAuEdLxaPbj5yiRhbTo5Awb8FTv8Epmipf9VhhTTSTjtI130_assertion description "[The proinflammatory interleukin (IL)-1B polymorphisms increase the risk of hypochlorhydria and gastric atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185776.RAuEdLxaPbj5yiRhbTo5Awb8FTv8Epmipf9VhhTTSTjtI130_provenance.
- NP185781.RAgXJKbs366dqbHDDjrUssluexf94vLP4x7eUvcagpxvs130_assertion description "[Methods to identify the plasma T4-binding abnormalities that can cause euthyroid hyperthyroxinemia were evaluated in patients with excess T4-binding globulin, familial dysalbuminemic hyperthyroxinemia, prealbumin-associated hyperthyroxinemia, and autoantibody binding of T4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185781.RAgXJKbs366dqbHDDjrUssluexf94vLP4x7eUvcagpxvs130_provenance.
- NP185783.RAmwJx-VexbGJIMEChFhmW0C4w8GGNjPOwtNNtmkvkZhU130_assertion description "[In a naturalistic prospective cohort study with a total of 190 fully assessed patients, improvement of depression symptoms during the 3 weeks following initiation of antidepressant therapy was recorded using the 21-item Hamilton Depression Rating Scale (HDRS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185783.RAmwJx-VexbGJIMEChFhmW0C4w8GGNjPOwtNNtmkvkZhU130_provenance.
- NP185785.RAji9cxCJzOXulc33N_bNNHPoNSoD9Ftlg_f7UTaJu5w0130_assertion description "[In addition, recent observations based on positional cloning strategies in the mk/mk mouse and the Belgrade (b/b) rat rodent models of hypochromic, microcytic anemia have shown that the phenotypic abnormality in iron metabolism is associated with a mutation in the Nramp2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185785.RAji9cxCJzOXulc33N_bNNHPoNSoD9Ftlg_f7UTaJu5w0130_provenance.
- NP185790.RAiULwK-ATOOqxvuOmPyThkJtAyLe2JRaoAdlnjN6MuTo130_assertion description "[In 180 HCC patients who were admitted to Asahikawa Medical College Hospital from 1987 to 1995, 10 patients (6%) had HCC associated with pure alcoholic liver disease (Al-HCC), whereas the HCC in 165 patients was associated with chronic viral liver diseases, in 2 with primary biliary cirrhosis, in 1 each with coexistence of the hepatitis C virus infection and hemochromatosis, and in 2 with cirrhosis of unknown origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185790.RAiULwK-ATOOqxvuOmPyThkJtAyLe2JRaoAdlnjN6MuTo130_provenance.
- NP185791.RAtzWr1XHTYgDp7MjX51aITCT1fBE_csFkoLpA01YaBg0130_assertion description "[We report herein the pathway that connects SP along with other modulators of neuroimmunoregulation to the induction of HO-1 and the inflammatory mediator macrophage inflammatory protein (MIP)-3alpha/CCL20 in IPDL cells, which play an important role in the development of periodontitis or inflammation during orthodontic tooth movement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185791.RAtzWr1XHTYgDp7MjX51aITCT1fBE_csFkoLpA01YaBg0130_provenance.
- NP185800.RAmWHtQhA2Grp8U_zy73UHbIeEpNoPoZBGRVW9wXuK4b8130_assertion description "[The expression of claudin-1, activity of matrix metalloproteinase (MMP)-2, and cleavage of laminin-5 gamma2 chains were assessed by Western blot analysis, immunohistochemistry, and zymography in OSC cell lines (OSC-4 and NOS-2, highly invasive; OSC-7, weakly invasive) and their xenografts in severe combined immunodeficient (SCID) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185800.RAmWHtQhA2Grp8U_zy73UHbIeEpNoPoZBGRVW9wXuK4b8130_provenance.
- NP185802.RAksroIY-htwT_vUgBMmshbeSm2doAsqqv4QW9gHSsvBM130_assertion description "[The association of T-LGL was analysed with a number of immunogenetic factors in 66 patients, including human leucocyte antigen (HLA) and killer-cell immunoglobulin-like receptor (KIR) genotype, KIR/KIR-L mismatch, CTLA-4 (+49 A/G),CD16-158V/F, CD45 polymorphisms, cytokine single nucleotide polymorphisms including: TNF-alpha (-308G/A), TGF-beta1 (codons 10 C/T, 25 G/C), IL-10 (-1082 G/A), IL-6 (-174 C/G), and IFN-gamma(+874 T/A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185802.RAksroIY-htwT_vUgBMmshbeSm2doAsqqv4QW9gHSsvBM130_provenance.
- NP185807.RAnCDeHt0qUQ7diGlo-xlZ_-_I6103lTFW6VZcTFcQ8vM130_assertion description "[Our result indicates that p53 alterations are infrequent in CCSK and do not seem to be primary genetic events in the pathogenesis of CCSK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185807.RAnCDeHt0qUQ7diGlo-xlZ_-_I6103lTFW6VZcTFcQ8vM130_provenance.
- NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_assertion description "[In the absence of evidence of linkage disequilibrium between A2 and B27 in the general population, the data suggest that the presence of A2 in B27 positive AS patients enhances the risk of AAU above that associated with B27 alone, and that other MHC-linked genetic factors, in addition to B27, are associated with susceptibility to AAU in AS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185815.RAuyKTpg-UIwO3mJliYdKzFArbCcD4LwrVz8jRFzXLTMY130_provenance.
- NP185821.RAt8qtmqildADqMebeY4OsKrKu-EtyulMz02zGPihIyzQ130_assertion description "[GH secretagogues (GHS) have been used for the differential diagnosis of ACTH-dependent Cushing's syndrome (CS) since 1997 due to their ability to increase ACTH and cortisol levels in Cushing's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185821.RAt8qtmqildADqMebeY4OsKrKu-EtyulMz02zGPihIyzQ130_provenance.
- NP185822.RAnn-nz0jUorbBI3NYFjOtIr_W0DCdQMPaLKKHZmBBOL0130_assertion description "[In addition to families with a strong history of early-onset DGC, CDH1 mutation screening should be offered to isolated cases of DGC in individuals ages <35 years and for families with multiple cases of LBC, with any history of DGC or unspecified GI malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185822.RAnn-nz0jUorbBI3NYFjOtIr_W0DCdQMPaLKKHZmBBOL0130_provenance.
- NP185823.RAtirs7UGmxCnXfSKGZO1mC3kHR7AF0jvl-plr9wTs7qQ130_assertion description "[Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185823.RAtirs7UGmxCnXfSKGZO1mC3kHR7AF0jvl-plr9wTs7qQ130_provenance.
- NP185824.RAlQMmq7QoCFyn2DIjP7dCcKgTN9uiR9y_F8cHXqy8sBM130_assertion description "[Cytoplasmic bcl-2 expression increased from BPE to SEH, whereas it decreased in CEH and EC with emergence of only nuclear expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185824.RAlQMmq7QoCFyn2DIjP7dCcKgTN9uiR9y_F8cHXqy8sBM130_provenance.
- NP185826.RAiLtPm0pG3qawlDDgR8ow7Lhd8MbK_U0_FOYTHnKre7Y130_assertion description "[Viral K-cyclin derived from Kaposi's sarcoma-associated herpesvirus is homologous with mammalian D-type cyclins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185826.RAiLtPm0pG3qawlDDgR8ow7Lhd8MbK_U0_FOYTHnKre7Y130_provenance.
- NP185838.RAvW0Lqp0xSZ_5KXwy1zczQc7RrOEcWutIy78OCMuVOVY130_assertion description "[Consensus regions of chromosome gains were identified on both histologic subtypes, on swine chromosomes 3p13-p17 (75% of the SSMs and 71% of the NMs), 12q (100% of the SSMs and 57% of the NMs) and 14q11-q21 (75% of the SSMs and 42% of NMs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185838.RAvW0Lqp0xSZ_5KXwy1zczQc7RrOEcWutIy78OCMuVOVY130_provenance.
- NP185845.RAp7h1Ki9H3pFmWg31xgORgZIrGFt54BgbKX2mFi_Yd7s130_assertion description "[The retinoblastoma tumor suppressor protein (Rb) is mutated or expressed at very low levels in several tumor types, including retinoblastoma and osteosarcoma, as well as small cell lung, colon, prostate, bladder, and breast carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185845.RAp7h1Ki9H3pFmWg31xgORgZIrGFt54BgbKX2mFi_Yd7s130_provenance.
- NP185850.RAuCGIqJy4ntV3QhoYo4cHnc0xrGQsmXS6HU-FGxjA0ck130_assertion description "[The PTPN22 C1858T polymorphism is associated with skewing of cytokine profiles toward high interferon-alpha activity and low tumor necrosis factor alpha levels in patients with lupus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185850.RAuCGIqJy4ntV3QhoYo4cHnc0xrGQsmXS6HU-FGxjA0ck130_provenance.
- NP185854.RAiClkcXWlAfj5tKjRrsTq9pZoMJa9ylMEFLZ0a5p63xQ130_assertion description "[These data indicate that detection of TAL-1 gene abnormality is important for diagnosis and monitoring of MRD in a subset of T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185854.RAiClkcXWlAfj5tKjRrsTq9pZoMJa9ylMEFLZ0a5p63xQ130_provenance.
- NP185856.RAgARYEog3g0JvlkY62S0FFkdPkISNerkNhYp0F4HPiTc130_assertion description "[These data support the notion that the disruption of eEF-2K expression in breast cancer cells results in the down-regulation of signaling pathways affecting growth, survival and resistance and has potential as a therapeutic approach for the treatment of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185856.RAgARYEog3g0JvlkY62S0FFkdPkISNerkNhYp0F4HPiTc130_provenance.
- NP185857.RAohgtBkThw5hEbRAfCqTEFXQ2d9aqwZQrDcnR5rJUy44130_assertion description "[Accordingly, we have examined the effect of IFN beta 2/IL-6 on expression of the IL-1- and tumor necrosis factor-unresponsive acute phase protein alpha 1-antitrypsin (alpha 1 AT) in human hepatoma-derived hepatocytes and in human mononuclear phagocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185857.RAohgtBkThw5hEbRAfCqTEFXQ2d9aqwZQrDcnR5rJUy44130_provenance.
- NP185865.RAq4nBbYTBfNG39WtwqRlVJuCO6YII7pY0FqDs2c_Op2U130_assertion description "[p53 mutations were observed in 3 of 8 grade II astrocytomas and 4 of 14 grade II astrocytomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185865.RAq4nBbYTBfNG39WtwqRlVJuCO6YII7pY0FqDs2c_Op2U130_provenance.
- NP185866.RAsgRw4IeP7vAHujp9fcLWScQ5nq1L9UCfxPznlwfjYX8130_assertion description "[We used a subset of autosomal SNPs from the Affymetrix 500K+50K SNP GeneChip marker set to examine genetic linkage with multiple highly heritable osteoporosis-related traits, including BMD of the hip and spine, heel ultrasound (attenuation and speed of sound), and geometric indices of the hip, in two generations from the Framingham Osteoporosis Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185866.RAsgRw4IeP7vAHujp9fcLWScQ5nq1L9UCfxPznlwfjYX8130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion description "[We report the first case of leukodystrophy with systemic cytochrome oxidase deficiency caused by a loss of function mutation in the SURF1 gene in a 2-year-old girl presenting with failure to thrive, global neurodevelopmental regression, and lactic acidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185875.RAqktOp9zkP7RGf5AVGaysMlmWrit8C07m-BrtQ0Ccqtg130_assertion description "[Here, we identified Calpain5 as a target of HOXA10 transcriptional regulation in endometrial cells as well as its aberrant regulation in endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185875.RAqktOp9zkP7RGf5AVGaysMlmWrit8C07m-BrtQ0Ccqtg130_provenance.
- NP185885.RAjf66t69W7HFXMX_XTDG97fR74QFnfLvxfIh4syya5xw130_assertion description "[The CCR5 deletion mutation fails to protect against multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185885.RAjf66t69W7HFXMX_XTDG97fR74QFnfLvxfIh4syya5xw130_provenance.
- NP185887.RAoVAM3vhNj8MsfvATi1UXYNRcYbhv6ag52dA4pHzKFm8130_assertion description "[In the case of the CASP3 77G>A, subjects with the GG genotype were at a 1.19-fold increased risk of lung cancer compared with those with at least one variant allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185887.RAoVAM3vhNj8MsfvATi1UXYNRcYbhv6ag52dA4pHzKFm8130_provenance.
- NP185890.RAngjr-NFoKS8fTuvvRJc3HaiJqhJkugNrWbIP9zERoho130_assertion description "[We started to screen patients with primary breast and ovarian cancer and a strong family history of both cancers by sequencing the full-length coding regions of BRCA1 and BRCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185890.RAngjr-NFoKS8fTuvvRJc3HaiJqhJkugNrWbIP9zERoho130_provenance.
- NP185892.RAqeC6JeVaxMGYfSYTphOo65BWqkmwfXomz6LXzOsxz08130_assertion description "[PARK6 appears to be an important locus for early-onset parkinsonism in European Parkin-negative patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185892.RAqeC6JeVaxMGYfSYTphOo65BWqkmwfXomz6LXzOsxz08130_provenance.
- NP185893.RAkuTHIrZwb14pPdNk4ziO4DrulH7Sn5tKnSEw_-kmw0Q130_assertion description "[Recent discovery of mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene in lung adenocarcinoma greatly stimulated biomarker research on predictive factors for EGFR tyrosine kinase inhibitors (TKI), such as gefitinib and erlotinib.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185893.RAkuTHIrZwb14pPdNk4ziO4DrulH7Sn5tKnSEw_-kmw0Q130_provenance.
- NP185894.RAum8plxo6cibKvDNI_7pkgYX7e2X8CacQYnbMM43DtcY130_assertion description "[The aim of this study was to evaluate the ability of HBcAg- and HBeAg-specific genetic immunogens to induce HBc/HBeAg-specific CD4(+)/CD8(+) T-cell immune responses and the potential to induce liver injury in HBV-transgenic (Tg) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185894.RAum8plxo6cibKvDNI_7pkgYX7e2X8CacQYnbMM43DtcY130_provenance.
- NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_assertion description "[The purpose of this study was to examine the prognostic and oxaliplatin predictive value of mismatch repair (MMR) status and common hot spot mutations, which we previously identified in stage II and III colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_provenance.
- NP185900.RAvXvqKimNahNJxO7Yhjh4ZVKymDshqY_CWnPvMlBeVlc130_assertion description "[There was a nonsignificant tendency toward better antiviral efficacy with ETV+ADV combination therapy compared to LAM+ADV combination therapy and ETV monotherapy for MDR CHB in Korea, where tenofovir is not yet available.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185900.RAvXvqKimNahNJxO7Yhjh4ZVKymDshqY_CWnPvMlBeVlc130_provenance.
- NP185912.RAj7lnnxY6bsPcEbO16M-ZSQgvHuakx9X7PN9Syfono4k130_assertion description "[TMC6 and TMC8 are identical to the EVER1 and EVER2 genes implicated in epidermodysplasia verruciformis, a recessive disorder comprising susceptibility to cutaneous human papilloma virus infections and associated nonmelanoma skin cancers, providing additional genetic and tissue systems in which to study the TMC gene family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185912.RAj7lnnxY6bsPcEbO16M-ZSQgvHuakx9X7PN9Syfono4k130_provenance.
- NP185913.RAilwxFKjWiJ7dgufKrR_idIHM1DdmnuABYE36mAq2sVA130_assertion description "[Mutations in APTX , SETX and MRE11 are common in patients with autosomal recessive ataxia and oculomotor apraxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185913.RAilwxFKjWiJ7dgufKrR_idIHM1DdmnuABYE36mAq2sVA130_provenance.
- NP185924.RAk6lqQUQpg3b0-_OBcInUXt3Z9BhlSAmaZQsFKUx3lrc130_assertion description "[Regulation of parathyroid hormone type 1 receptor dynamics, traffic, and signaling by the Na+/H+ exchanger regulatory factor-1 in rat osteosarcoma ROS 17/2.8 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185924.RAk6lqQUQpg3b0-_OBcInUXt3Z9BhlSAmaZQsFKUx3lrc130_provenance.
- NP185928.RAi4yL2x8Gu0eqM6U5fHNliPtbwv7UrNBVUXCbm9Y17_k130_assertion description "[The regulatory role of vitamin D receptor (VDR) gene variants of Bsm I, Apa I, Taq I, and Fok I polymorphisms on vitamin D(3)-modulated macrophage phagocytosis with live Mycobacterium tuberculosis and lymphoproliferative response to M. tuberculosis culture filtrate antigen (CFA) was studied in patients with pulmonary tuberculosis (n = 46) and in normal healthy subjects (NHS) (n = 64).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185928.RAi4yL2x8Gu0eqM6U5fHNliPtbwv7UrNBVUXCbm9Y17_k130_provenance.
- NP185931.RAsk0qV_YdLqZRwhjPImMGUDqF660XWga1N6GmeXe11rs130_assertion description "[In this study p53 alteration frequencies were evaluated in 13 BRCA1, 11 BRCA2 and 55 BRCAx breast tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185931.RAsk0qV_YdLqZRwhjPImMGUDqF660XWga1N6GmeXe11rs130_provenance.
- NP185932.RAjWwHdHEd_f9cTsHRilvqq9nlbIUiDLLuHwlxOs4Vus0130_assertion description "[The relationships between diarrhoea and polymorphisms in UGT1A8 (2; 518C>G, 3; 830G>A), UGT1A7 (622C>T), UGT1A9 (-275T>A), UGT2B7 (-840G>A) and ABCC2 (-24C>T, 3972C>T) or the co-administered immunosuppressant were investigated using the Cox proportional hazard model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185932.RAjWwHdHEd_f9cTsHRilvqq9nlbIUiDLLuHwlxOs4Vus0130_provenance.
- NP185933.RAkdsB-QO_0W-in2UjUCh2oQPsPIyRFjutV5jOzWMjcI4130_assertion description "[The comparison of gene expression profiles between HBx-expressing primary hepatocytes and HBV-infected liver samples shows a consistent alteration of many cellular genes including a subset of oncogenes (such as c-myc and c-myb) and tumor suppressor genes (such as APC, p53, WAF1 and WT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185933.RAkdsB-QO_0W-in2UjUCh2oQPsPIyRFjutV5jOzWMjcI4130_provenance.
- NP185946.RArwNZaiID-_WivvJLnomMk9sVMR-I8KccgjPHIv1rKHU130_assertion description "[In this work, we modified this system by incorporating a cancer-specific promoter, the human telomerase reverse transcriptase (hTERT) promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185946.RArwNZaiID-_WivvJLnomMk9sVMR-I8KccgjPHIv1rKHU130_provenance.
- NP185948.RAivBJragasb0jGFi2aGExdBNZsTaxfsymP1S3EwoLI9Q130_assertion description "[The aim of this study was to determine whether the interaction between chemokine receptor 6 (CCR6) and its ligand, macrophage inflammatory protein-3 alpha (MIP-3alpha), correlates with metastasis of hepatocellular carcinoma (HCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185948.RAivBJragasb0jGFi2aGExdBNZsTaxfsymP1S3EwoLI9Q130_provenance.
- NP185953.RAhCrZo0tmGgh6EtQyM9iUz35jRu5-oLvbvQdaTIMilho130_assertion description "[Using BAC recombination and transgenesis, we characterized the expression of human sclerostin (SOST) from normal (SOST(wt)) or Van Buchem (SOST(vbDelta) alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185953.RAhCrZo0tmGgh6EtQyM9iUz35jRu5-oLvbvQdaTIMilho130_provenance.
- NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_assertion description "[The -93G>A (rs1800734) polymorphism located in the promoter of mismatch repair gene, MLH1, has been identified as a low-penetrance variant for cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185958.RAtqZf4a-mbJF3l9cFW3NdOdNjleGCHyh_707ZhP60aPU130_provenance.
- NP185967.RAhZYDKQMDvuJ7uVXSvHzqE8P4Uzg98jpmqqqqL6JAXVc130_assertion description "[To confirm this finding we used PCR from genomic DNA and direct sequencing to analyze exons 2 through 10 of the menin gene in eight patients from four pedigrees with MEN-1 syndrome or an affected relative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185967.RAhZYDKQMDvuJ7uVXSvHzqE8P4Uzg98jpmqqqqL6JAXVc130_provenance.
- NP185976.RAhH_I6-lMwWHV_IZDkzHm9glju7s5oZ9nioQ3fbXFP2E130_assertion description "[These results suggest that NF90 inhibits influenza virus replication during the early phase of infection through direct interaction with viral NP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185976.RAhH_I6-lMwWHV_IZDkzHm9glju7s5oZ9nioQ3fbXFP2E130_provenance.