Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP316706.RAe1vNflyH-cnpXKz6NdcqWuY25wD58B49M_wmdPuVD9Q130_assertion description "[IL-1beta+3954_T/C (OR 2.1, 1.0-4.3), IL-1RN*2/L (OR 3.5, 1.7-7.3) and IL-10-592_C/A (OR 3.2, 1.5-6.8) were individually associated with GC, and a combination of these cytokine polymorphisms with H pylori vacA s1b and m1 further increased the risk (OR 7.2, 1.4-36.4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316706.RAe1vNflyH-cnpXKz6NdcqWuY25wD58B49M_wmdPuVD9Q130_provenance.
- NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_assertion description "[Notably, the human ABCG1 gene maps to chromosome 21q22.3, and individuals with Down syndrome (DS) typically manifest with Alzheimer's disease (AD) neuropathology in their 30s.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316711.RAc91ONkrimiFZ-Ico9CCtxhVYFLB1n6e77d9LtZt9JXw130_provenance.
- NP316713.RAdYeGBxFM-Z6DBMGJGkMQDR5GVB6cwcigXzVEsOhb7EY130_assertion description "[Several of the MEF2 targets are mutated in human neurological disorders including epilepsy and autism spectrum disorders, suggesting that these disorders may be caused by disruption of an activity-dependent gene program that controls synapse development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316713.RAdYeGBxFM-Z6DBMGJGkMQDR5GVB6cwcigXzVEsOhb7EY130_provenance.
- NP316714.RAYrua4M8Q1z3Y9WmdBnD9TzQz0-WnokU8OeY1DPj80jk130_assertion description "[We have determined the presence and kinetics of granulocyte macrophage colony stimulating factor (GM-CSF) antibodies induced after repeated administration of a yeast expressed GM-CSF product in prostate cancer patients with minimal recurrent disease using a panel of assays for detection and characterization of antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316714.RAYrua4M8Q1z3Y9WmdBnD9TzQz0-WnokU8OeY1DPj80jk130_provenance.
- NP316716.RAcn7R_DymkuTqUvBLObHLYMY1ByCl2NmU66Vd0oNpd2A130_assertion description "[Targeted inhibition of AEG1 might lead to the shutdown of key elemental characteristics of HCC and could lead to an effective therapeutic strategy for HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316716.RAcn7R_DymkuTqUvBLObHLYMY1ByCl2NmU66Vd0oNpd2A130_provenance.
- NP316717.RAY2XSCFc4-8WgJjNtpKrZghSnDVb10O-LwzLNfqB__Z0130_assertion description "[Two receptor chains, IL-10RA and IL-10RB, are known to mediate the functions of interleukin-10 (IL-10), which has been shown to be involved in the progression of persistent hepatitis C virus (HCV) infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316717.RAY2XSCFc4-8WgJjNtpKrZghSnDVb10O-LwzLNfqB__Z0130_provenance.
- NP316724.RAS7775eysDiXTk4u-_-ewpuZVJuXTW1hV7spHR4aiHdo130_assertion description "[Suppressor of cytokine signalling (SOCS)1 and SOCS3 epigenetic silencing were occasionally detected, whereas SOCS1 was frequently mutated in diffuse large B-cell lymphoma and polymorphic post-transplant lymphoproliferative disorders, possibly as a cause of aberrant somatic hypermutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316724.RAS7775eysDiXTk4u-_-ewpuZVJuXTW1hV7spHR4aiHdo130_provenance.
- NP316732.RAezrsEp4Nq04yurbnqAFOOCRBg1i0_3irW6t7F7QesuI130_assertion description "[Wheat SPT resulted positive in 29 bakers and was associated with work-related asthma (p<0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316732.RAezrsEp4Nq04yurbnqAFOOCRBg1i0_3irW6t7F7QesuI130_provenance.
- NP316737.RAWjBcjc9TkcSPInpvZxn0PHwHhZHW5NkPl8jvlO1C2G0130_assertion description "[Intranasal administration of GSI during influenza infection also led to higher mortality, and higher virus load with excessive inflammation and an impaired production of IFN-γ in lungs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316737.RAWjBcjc9TkcSPInpvZxn0PHwHhZHW5NkPl8jvlO1C2G0130_provenance.
- NP316741.RAXECp3NGamXZI5KMUW-TOAi6eRWh5K6zpwAvopbZIfkU130_assertion description "[Biallelic mutations in the base-excision repair gene MYH have recently been associated with recessive inheritance of multiple colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316741.RAXECp3NGamXZI5KMUW-TOAi6eRWh5K6zpwAvopbZIfkU130_provenance.
- NP316746.RATOra8aDjc8Q0Pk_N58U2EmjUzF2781JDCJnFiYZ-MpE130_assertion description "[However, since high HbA2 levels are diagnostic for beta-thalassemia trait and a lowered level for an alpha- or delta-mutation, co-inheritance of delta- and beta-gene defects may lead to misinterpretation of diagnostic results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316746.RATOra8aDjc8Q0Pk_N58U2EmjUzF2781JDCJnFiYZ-MpE130_provenance.
- NP316747.RAfJCLMD2bCr8psjHdmLWGeczisZIWCXdFdGqhu2sxUDo130_assertion description "[ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316747.RAfJCLMD2bCr8psjHdmLWGeczisZIWCXdFdGqhu2sxUDo130_provenance.
- NP316750.RAZvnCubWi7wNlkcspm465qpQowjpzBdce-11fVO3nYBI130_assertion description "[The approach was a family based association study involving a total of 512 Italian patients and their parents, 401 having cleft lip with or without cleft palate (CL/P) and 111 with cleft palate only (CPO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316750.RAZvnCubWi7wNlkcspm465qpQowjpzBdce-11fVO3nYBI130_provenance.
- NP316756.RAeEM5LYeX0cGehlSH84ZX_fMZUjo-7YwC2SvXa63GnWc130_assertion description "[Bioimplant-generated TSP-2 potently inhibited tumor growth and angiogenesis of human squamous cell carcinomas, malignant melanomas, and Lewis lung carcinomas that were implanted at a distant site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316756.RAeEM5LYeX0cGehlSH84ZX_fMZUjo-7YwC2SvXa63GnWc130_provenance.
- NP316763.RAXV3XZBBzDj5DXTRwH8MA6QCsIaOQE6DpKcKk6Fd7ES0130_assertion description "[Mutations in myotubularin cause myotubular myopathy, a devastating congenital myopathy with unclear pathogenesis and no current therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316763.RAXV3XZBBzDj5DXTRwH8MA6QCsIaOQE6DpKcKk6Fd7ES0130_provenance.
- NP316768.RAbvyZE2ZoGGuiHqccTpJmz7NS_Tj7mLIU0K3MqaF7fkc130_assertion description "[This study aims to investigate the activation of mTOR pathway in cervical carcinomas and whether inhibition of mTOR with rapamycin, as well as specific siRNA, could lead to decreased proliferation, induced cell cycle arrest and apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316768.RAbvyZE2ZoGGuiHqccTpJmz7NS_Tj7mLIU0K3MqaF7fkc130_provenance.
- NP316772.RAQg4FO4GeIxQl2NO8_lTlpa5Mqhasagu60H0JvMhx6Jc130_assertion description "[The current point prevalence of MDD was nearly identical according to the two measures (DIS, 2.8%; IDD, 2.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316772.RAQg4FO4GeIxQl2NO8_lTlpa5Mqhasagu60H0JvMhx6Jc130_provenance.
- NP316775.RAdvlb6sghPL6SlP5ro_k_DNabZhPazFEDILEoKdOWhg4130_assertion description "[The observations demonstrate that (1) human ASM tissue expresses messenger RNA and surface protein for FcepsilonRII, as well as for all the Fcgamma receptor subtypes, (2) in contrast to unaltered Fcgamma subtype expression, however, relative to control human ASM, FcepsilonRII is significantly up-regulated in inherently asthmatic ASM tissue, (3) up-regulated expression of FcepsilonRII represents, at least in part, an inducible phenomenon that is largely attributed to IgE immune complex-coupled activation of the receptor, and (4) the latter action is associated with FcepsilonRII-induced autologous elaboration of the proinflammatory cytokine, IL-1beta, by the atopic sensitized ASM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316775.RAdvlb6sghPL6SlP5ro_k_DNabZhPazFEDILEoKdOWhg4130_provenance.
- NP316776.RAZebq2WCbLyLD-CkxmBgWZ-UjZ-IJPnGKFwPUdQWw00Q130_assertion description "[Fifty-five percent of families ascertained through an ASP have at least one parent with a lifetime diagnosis of ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316776.RAZebq2WCbLyLD-CkxmBgWZ-UjZ-IJPnGKFwPUdQWw00Q130_provenance.
- NP316780.RAbJgeqoNuIalvNn1AUzrlzcpqMCvSd2dNmtMo0SxOXYU130_assertion description "[The enhanced AP-1 activity resulting from the interaction of these hormones may increase expression of many target genes that are critical for oncogenesis and may contribute to neoplastic progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316780.RAbJgeqoNuIalvNn1AUzrlzcpqMCvSd2dNmtMo0SxOXYU130_provenance.
- NP316787.RAbULDM6rca3Pfi2bQs5HXO5RbXGNCTP1q6KX9QY8TMJE130_assertion description "[An elevated homocysteine concentration might identify patients with SLE who are likely to have premature atherosclerosis and who would benefit from evaluation of CAC by EBCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316787.RAbULDM6rca3Pfi2bQs5HXO5RbXGNCTP1q6KX9QY8TMJE130_provenance.
- NP316794.RAX0QH6oUtDcy5PkcSdNfQ1bVyTb5IAHqEUG04BM6GKFE130_assertion description "[Microphthalmia (Mi) is a basic helix-loop-helix-leucine zipper (b-HLH-ZIP) transcription factor implicated in pigmentation, mast cells, and bone development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316794.RAX0QH6oUtDcy5PkcSdNfQ1bVyTb5IAHqEUG04BM6GKFE130_provenance.
- NP316800.RAbX-5GV9fhp84pymR2zqnMoZbB6_PCgl6_HNbaD6TW6A130_assertion description "[The DFNB27 locus extends over a 17 cM region between D2S2157 and D2S2273, and may overlap the DFNA16 locus for dominantly inherited, fluctuating, progressive non-syndromal hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316800.RAbX-5GV9fhp84pymR2zqnMoZbB6_PCgl6_HNbaD6TW6A130_provenance.
- NP316803.RAVCArjwj-N-1AsTKgKQGmv4lXgU_BJq9B5JwMvUL9XgU130_assertion description "[Success rate was 73-74.4% in ALL, MPD, and NHL + LPD, versus 87-94% in ANLL, MDS, CML, and benign disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316803.RAVCArjwj-N-1AsTKgKQGmv4lXgU_BJq9B5JwMvUL9XgU130_provenance.
- NP316806.RAW0gMAon5h09be6YJ8_H-9K2-vvx8C6ZoKL0KxNM83bg130_assertion description "[We have characterized T- and B-cell responses associated with experimental autoimmune encephalomyelitis (EAE) induced in Lewis rats with recombinant beta-Synuclein (betaSync), a neuronal component.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316806.RAW0gMAon5h09be6YJ8_H-9K2-vvx8C6ZoKL0KxNM83bg130_provenance.
- NP316810.RAdFJgiISYR5Ks8GiUPgXLuNxzU8XuPlO0lDgFN2imJuQ130_assertion description "[We describe a recombinant vesicular stomatitis virus lacking its glycoprotein gene and expressing instead the HIV-1 receptor CD4 and a coreceptor, CXCR4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316810.RAdFJgiISYR5Ks8GiUPgXLuNxzU8XuPlO0lDgFN2imJuQ130_provenance.
- NP316813.RAdY93Hr1lbZwje0JRy29cKjbkc9C2q_nlaa9AqITfpEE130_assertion description "[TTR gene analysis has useful applications in genetic counselling, including prenatal diagnosis, in identifying the cause of seemingly sporadic cases of amyloid neuropathy, and in epidemiological studies of FAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316813.RAdY93Hr1lbZwje0JRy29cKjbkc9C2q_nlaa9AqITfpEE130_provenance.
- NP316815.RAT8XBp_Dpd1_riatgLUgIJwCuxw_7PfbplB_CFJPo_Bs130_assertion description "[In addition, GATA4 is supposed to be the responsible gene for the CHDs in the chromosomal 8p23 deletion syndrome, which is recognized as a malformation syndrome with clinical symptoms of facial anomalies, microcephaly, mental retardation, and congenital heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316815.RAT8XBp_Dpd1_riatgLUgIJwCuxw_7PfbplB_CFJPo_Bs130_provenance.
- NP316816.RAaucg_5yIH-QaYOhLwWYXpxjpf9dbFU3vCW8QIQ-qnPk130_assertion description "[Ten prognostic and diagnostic epigenetic breast cancer biomarkers (PITX2, RASSF1A, PLAU, LHX3, PITX3, LIMK1, SLITRK1, SLIT2, HS3ST2, and TFF1) were analyzed in tissue samples obtained from two patients with invasive ductal carcinoma of the breast.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316816.RAaucg_5yIH-QaYOhLwWYXpxjpf9dbFU3vCW8QIQ-qnPk130_provenance.
- NP316826.RAdYvGXkH1EggOUf6AQTMXEhMZpcanIuavy6eMBzA0o9s130_assertion description "[One family carries the South East Asia (SEA) deletion in alpha-thalassemia-1 determinant and the nondeletion mutation in alpha-thalassemia-2 determinant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316826.RAdYvGXkH1EggOUf6AQTMXEhMZpcanIuavy6eMBzA0o9s130_provenance.
- NP316838.RASQiQAICgCT5EIeloSc1TAAtbBDqKeOLmlaZ21U-c8rk130_assertion description "[Single intravitreal administration of Jun siRNA reduces neovascularisation in a murine model of proliferative retinopathy, and suppresses endothelial JUN and matrix metalloproteinase-2 (MMP-2) immunoreactivity in retinal vessels, data supported by its repression of MMP-2 expression and gelatinolytic activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316838.RASQiQAICgCT5EIeloSc1TAAtbBDqKeOLmlaZ21U-c8rk130_provenance.
- NP316846.RAQ-RRqXNNmKhKQAtmBaxfIRQ-xczKb6wNwEb4gj3bbAc130_assertion description "[Expression of novel molecules, MICAL2-PV (MICAL2 prostate cancer variants), increases with high Gleason score and prostate cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316846.RAQ-RRqXNNmKhKQAtmBaxfIRQ-xczKb6wNwEb4gj3bbAc130_provenance.
- NP316848.RAaWxw8O-zBjf791xImcEzY-MC4CO0tpovot49e2MrjGo130_assertion description "[Recently, we observed the upregulation of parathyroid hormone (PTH)-related protein (PTHrP) in experimental DN, associated with renal hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316848.RAaWxw8O-zBjf791xImcEzY-MC4CO0tpovot49e2MrjGo130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion description "[We then screened 200 T2D siblings/families for PSMD9 +nt460A/G, +nt437C/T and exon E197G A/G single nucleotide polymorphisms (SNPs) and performed a non-parametric linkage study to test for linkage for coronary artery disease, stroke/TIA, macro-vasculopathy and macrovascular pathology of T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316852.RAbSK9lVJqU4l8b4HWrucGJ64ZRUhWxwLq_VOyDP0QVvw130_assertion description "[Recently, the instance of beta-lactamase-negative ampicillin (AMP)-resistant (BLNAR) strains of Haemophilus influenzae has exhibited a marked increase in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316852.RAbSK9lVJqU4l8b4HWrucGJ64ZRUhWxwLq_VOyDP0QVvw130_provenance.
- NP316859.RAdL219FlvL_GbLyar-gV9qw8_cSYtJ4VQnH7OT5ZVdAM130_assertion description "[These findings identify p50 as having a negative effect on MnSOD induction upon repeated applications of TPA and provide an insight into a cause for the reduction of MnSOD expression during early stages of skin carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316859.RAdL219FlvL_GbLyar-gV9qw8_cSYtJ4VQnH7OT5ZVdAM130_provenance.
- NP316866.RAZINDf8XdBFoIIiWa9QS7V8YeUFYvNO0I-rSpTTTZJp0130_assertion description "[Thus, time- and tissue-specific impairments of transcription might explain the developmental and neurological symptoms of TTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316866.RAZINDf8XdBFoIIiWa9QS7V8YeUFYvNO0I-rSpTTTZJp0130_provenance.
- NP316868.RAX5gGQD4d3BzyWiYSjomaeVhOI9SEhYoQFbAtPZdzTho130_assertion description "[Polymorphisms in the IRF5 gene have been associated with susceptibility to autoimmune diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316868.RAX5gGQD4d3BzyWiYSjomaeVhOI9SEhYoQFbAtPZdzTho130_provenance.
- NP316874.RAVoGIA4STI-tjDSZvin6H9iX_yrxMt-9anpllFZElq6g130_assertion description "[There is good evidence that central (visceral) adiposity is important in the development of the insulin resistance or metabolic syndrome (obesity, hyperinsulinemia, dyslipidemia, glucose intolerance, hypertension, and coronary heart disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316874.RAVoGIA4STI-tjDSZvin6H9iX_yrxMt-9anpllFZElq6g130_provenance.
- NP316880.RAY5Oa6xnyG-p0Ba1RbGP4Azg_77JOiFOEhU8K-78aFpc130_assertion description "[Positive PCR-hly of the CSF was also obtained for five additional, clinically confirmed cases of CNS listeriosis for which bacterial cultures were negative presumably due to previous treatment with antibiotics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316880.RAY5Oa6xnyG-p0Ba1RbGP4Azg_77JOiFOEhU8K-78aFpc130_provenance.
- NP316882.RASVjiMTH0XX6Se3YoGSBUzGuSXEYaM2Tz5IpZ1k9VCGc130_assertion description "[ARH is rare except in Sardinia where three alleles (ARH1, ARH2 and ARH3) explain most of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316882.RASVjiMTH0XX6Se3YoGSBUzGuSXEYaM2Tz5IpZ1k9VCGc130_provenance.
- NP316883.RAZw1iXAnGz7VuIHQjd3igQLC1-rURmYD3Ol17AIr7o-g130_assertion description "[These results suggest that engagement of beta1 integrins on SLE T cells could induce FAK-mediated signaling and subsequent CD40L expression and proliferation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316883.RAZw1iXAnGz7VuIHQjd3igQLC1-rURmYD3Ol17AIr7o-g130_provenance.
- NP316885.RAa35jpzCzb3hNKvHX_MPG8b77kIJtEeipEd8LM24Qrtk130_assertion description "[In contrast, EVI1 protein isoform levels were undetectable in normal ovarian tissues, and highest in serous ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316885.RAa35jpzCzb3hNKvHX_MPG8b77kIJtEeipEd8LM24Qrtk130_provenance.
- NP316892.RAadSfI7pIrZYYvdTUA-MU73spVnMygdjYiZbJLd1AzGY130_assertion description "[Here, we show that in asbestos-related malignant pleural mesothelioma (MPM), Semaphorin-6D (Sema6D) and its receptor plexin-A1 are frequently expressed and trigger a prosurvival program that promotes anchorage-independent growth of MPM cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316892.RAadSfI7pIrZYYvdTUA-MU73spVnMygdjYiZbJLd1AzGY130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion description "[Loss of function of paraplegin (encoded by the SPG7 gene) causes hereditary spastic paraplegia, a disease characterized by retrograde degeneration of cortical motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316895.RAd-iATDe6UrAtySts75qod6HluJMl0qyFmry9sVpqSdg130_assertion description "[Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316895.RAd-iATDe6UrAtySts75qod6HluJMl0qyFmry9sVpqSdg130_provenance.
- NP316904.RAdC1AvXxVq0wgn0G5Q7uupD83f4MTW5Xm_4yMX0mxTIo130_assertion description "[The aim of this study was to test whether the interleukin (IL)-6 gene promoter region, or tumour necrosis factor (TNF)-alpha or IL-8 gene 3'-untranslated region (3'-UTR) polymorphisms could provide useful genetic markers for an individual's susceptibility to GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316904.RAdC1AvXxVq0wgn0G5Q7uupD83f4MTW5Xm_4yMX0mxTIo130_provenance.
- NP316908.RAYExRXCxc0ulSx8stxVYOS55o60fT37x1bakQpBzj17I130_assertion description "[Immunohistochemically, aside from TFEB and cathepsin K, kidney-specific cadherin was another sensitive and relatively specific marker for TFEB RCCs, supporting a distal nephron origin for these renal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316908.RAYExRXCxc0ulSx8stxVYOS55o60fT37x1bakQpBzj17I130_provenance.
- NP316910.RAUyItgaT2MexMnrA_lPUaGERlfX67ohmK7zT33nuM6IQ130_assertion description "[This study suggests that both HH and the homozygous C677T mutation in the MTHFR gene are important risk factors of BCS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316910.RAUyItgaT2MexMnrA_lPUaGERlfX67ohmK7zT33nuM6IQ130_provenance.
- NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion description "[These results show the power of combined array CGH and SAGE analysis for the identification of candidate amplicon targets and identify H2AFJ and EPS8 as novel putative oncogenes in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance.
- NP316919.RAaWd0XVU5V3P1-Xw7rL3QO1AJNZu9Mv8p24Ho4r1qk2M130_assertion description "[Our study increases the catalog of known CYLD mutations in patients with BSS/MFT to 86 and documents the variability of somatic mutations that may occur in them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316919.RAaWd0XVU5V3P1-Xw7rL3QO1AJNZu9Mv8p24Ho4r1qk2M130_provenance.
- NP316921.RAd9dM2ikt9bHJW_clemk7jCg2_hFFEKC13WSii4_o6MQ130_assertion description "[In a canine acute myocardial infarction (MI) model, a naked plasmid encoding 500 μg human hepatocyte growth factor (HGF) was delivered transendocardially to the myocardium via US/MB (HGF-US/MB), insonation (HGFUS), or alone (HGF alone).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316921.RAd9dM2ikt9bHJW_clemk7jCg2_hFFEKC13WSii4_o6MQ130_provenance.
- NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_assertion description "[In addition to the juxtacentromeric heterochromatic instability, the disease is characterized by variable reduction in serum immunoglobulin levels which cause most ICF patients to succumb to infectious diseases before adulthood as well as exhibit facial dysmorphism including hypertelorism, epicanthal folds, and low-set ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316922.RAYhQ8RAAT7Yn_bsWx48DRzDiXdKDNN1MJMoA2R82E8XM130_provenance.
- NP316925.RAQwAUn8rxAYf-btFUT-sSQwMGwcNUUNcsFTHe8T55Sdc130_assertion description "[Recent investigations indicate that excess actions of FGF23 cause several hypophosphatemic diseases whereas deficient FGF23 activity results in hyperphosphatemic tumoral calcinosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316925.RAQwAUn8rxAYf-btFUT-sSQwMGwcNUUNcsFTHe8T55Sdc130_provenance.
- NP316926.RAZlAm2bm-PS4VY1WXxyXITceHv35FwilaiZQNcZBno4w130_assertion description "[After adjusting for known prognostic features such as presence of the TEL-AML1 rearrangement, National Cancer Institute (NCI) risk status, ploidy, and race, the G allele of a common polymorphism in chemokine receptor 5 (CCR5) was associated with more favorable MRD status than the A allele (P = .009, logistic regression), when comparing `best` and `worst` risk groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316926.RAZlAm2bm-PS4VY1WXxyXITceHv35FwilaiZQNcZBno4w130_provenance.
- NP316927.RAZ33yZ30QSBblGTpKVFQZ8xxSaDDa29gtM31IKVCMQ6Q130_assertion description "[Subjects who were free of current Axis I disorders other than simple or social phobia and who had a first-degree relative with panic disorder (high risk) and subjects who had no first-degree relatives with panic disorder or major depressive disorder (low-risk) underwent two challenge procedures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316927.RAZ33yZ30QSBblGTpKVFQZ8xxSaDDa29gtM31IKVCMQ6Q130_provenance.
- NP316930.RAaCMUaaLlR7XGvRYt2Kasgj-MTfNcjHTb_fszRxoM77o130_assertion description "[A 7-year-old girl with neurofibromatosis type I (NF1) was diagnosed to have monosomy 7 myeloproliferative disease (Mo 7-MPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316930.RAaCMUaaLlR7XGvRYt2Kasgj-MTfNcjHTb_fszRxoM77o130_provenance.
- NP316934.RAbzf8n-nV0yVMH0TNPkfl-4LvBVaee-Qfbu810B_cH_g130_assertion description "[We also evaluated potential interaction effects (departure from a multiplicative interaction model) between the IL4RA SNPs and four SNPs in the IL-9 receptor (IL9R) gene previously associated with childhood wheezing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316934.RAbzf8n-nV0yVMH0TNPkfl-4LvBVaee-Qfbu810B_cH_g130_provenance.
- NP316936.RAQttUwxuolpBf2DD1oFyq45bwNbQuoiPDB1VuPfDqL4o130_assertion description "[Mutations in TSH receptor (TSHR) are notoriously associated with congenital hypothyroidism as well as with non-autoimmune subclinical hypothyroidism, a mild form of TSH resistance that is not as well characterized by diagnostic procedures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316936.RAQttUwxuolpBf2DD1oFyq45bwNbQuoiPDB1VuPfDqL4o130_provenance.
- NP316937.RAYlyO28Ufh6GiwiIKvdh4fndxCx2ohWJaLCHD8OkpoXg130_assertion description "[The involvement of the cartilage specific type II collagen gene (COL2A1) was studied in nine patients with diastrophic dysplasia in the Finnish population, where the prevalence of this chondrodystrophy clearly exceeds that reported for other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316937.RAYlyO28Ufh6GiwiIKvdh4fndxCx2ohWJaLCHD8OkpoXg130_provenance.
- NP316944.RAVktl3ZkeWu3pxNxJHsTn52oQ7TpaCq-YM0ZgJ9Y_VIM130_assertion description "[FHIT (fragile histidine triad) gene analysis in cervical intraepithelial neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316944.RAVktl3ZkeWu3pxNxJHsTn52oQ7TpaCq-YM0ZgJ9Y_VIM130_provenance.
- NP316945.RAdG-PmGywJc_5FN1ayCCukvyVBiYF_bcdUDOg8AMQJ4E130_assertion description "[The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316945.RAdG-PmGywJc_5FN1ayCCukvyVBiYF_bcdUDOg8AMQJ4E130_provenance.
- NP316946.RATph6tPrltieZgiDWKPVZ4-s-JetFhoB4PvJ84Lp25uE130_assertion description "[The aim of this study is to stress on age-related neuropsychological and electrophysiological (P(300)) changes in normal Egyptian subjects, to throw light on the value of genetic (Apo-E(4) genotype) and immunological markers [interleukin-6 (IL-6) and intercellular adhesion molecules (ICAM-1) in the serum] as tools used in early detection of cognitive decline in cerebral aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316946.RATph6tPrltieZgiDWKPVZ4-s-JetFhoB4PvJ84Lp25uE130_provenance.
- NP316948.RAZXdPu5Ksi-KpkbtBsiaS8OE4WDmyHH7GajLnYpRPZ_g130_assertion description "[The CMT1A-REPs are two large directly repeating DNA sequences located on chromosome 17p11.2-p12 flanking the region duplicated in patients with Charcot-Marie-Tooth disease type 1A (CMT1A) and deleted in patients with hereditary neuropathy with liability to pressure palsies (HNPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316948.RAZXdPu5Ksi-KpkbtBsiaS8OE4WDmyHH7GajLnYpRPZ_g130_provenance.
- NP316949.RAbpLox0NjvNUpxf4dQzY6lllKPTpRbeZeZ-cDae4F06c130_assertion description "[In another family member, LGI1 (leucine-rich, glioma inactivated 1) mutations are responsible for autosomal dominant lateral temporal epilepsy (ADLTE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316949.RAbpLox0NjvNUpxf4dQzY6lllKPTpRbeZeZ-cDae4F06c130_provenance.
- NP316960.RAbK1caqLcPPCKU2_FEGBq1LHcHLSwjTfDtQ3p99YChgw130_assertion description "[When these two genotypes, GSTM1 null and NQO1 C/C, were combined, the hazard rate for childhood leukaemia was significantly increased (P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316960.RAbK1caqLcPPCKU2_FEGBq1LHcHLSwjTfDtQ3p99YChgw130_provenance.
- NP316961.RARFmBCozCN9oeUNzgVlYqhc_VN_PAi8KQAbWX7pLDgX0130_assertion description "[Molecular detection of CEA mRNA in both pre- and postoperative blood samples is an independent, negative prognostic factor in patients with node-negative breast cancer undergoing curative surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316961.RARFmBCozCN9oeUNzgVlYqhc_VN_PAi8KQAbWX7pLDgX0130_provenance.
- NP316962.RAQrburEiOgfFkMBZGP9VTCIl8nHDG1Twn9NwrPgQuOyo130_assertion description "[We conclude that carriers of the prothrombin mutation who use oral contraceptives have a markedly increased risk of deep vein thrombosis, much higher than the risk conferred by either factor alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316962.RAQrburEiOgfFkMBZGP9VTCIl8nHDG1Twn9NwrPgQuOyo130_provenance.
- NP316966.RAWcMbj6GGaQklmaLHbWP_yyiiyt8taANLI80tFqn19QQ130_assertion description "[Autoimmune polyglandular syndrome type 1 [APS-1] comprises multiple organ-specific autoimmunities such as acquired hypoparathyroidism and autoimmune Addison's disease, and a predisposition to certain infections such as chronic mucocutaneous candidiasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316966.RAWcMbj6GGaQklmaLHbWP_yyiiyt8taANLI80tFqn19QQ130_provenance.
- NP316973.RAR49yFAsahy3EToan5ct0owtjoNokSxgZcGoeO-JbfgI130_assertion description "[Among them, the expression levels of eight genes, namely BF, FTL, IGFBP7, RARRES1, RARRES2, RBP1, SAT, and TXN according to HUGO nomenclature, were increased, whereas six: ALOX5AP, CLNS1A, EIF4A2, ELK3, REQ and SYPL, were found to be underexpressed in mesothelioma microdissected cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316973.RAR49yFAsahy3EToan5ct0owtjoNokSxgZcGoeO-JbfgI130_provenance.
- NP316980.RAZ9YH3nbjkmJi5rjaik9KIsVltFUpFkpsF7Ni7DPcAmk130_assertion description "[The apolipoprotein E (APOE) polymorphism is an established risk factor for intracerebral hemorrhage (ICH) that is related to cerebral amyloid angiopathy in the white population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316980.RAZ9YH3nbjkmJi5rjaik9KIsVltFUpFkpsF7Ni7DPcAmk130_provenance.
- NP316983.RAdiwrO8LmNPhq-Z8h6JDB8n2U0-71NVoeXxnRSgdAas4130_assertion description "[These data provide the basis for future studies evaluating the diagnostic potential of D-GPCR and its utility as a novel target in immunotherapy of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316983.RAdiwrO8LmNPhq-Z8h6JDB8n2U0-71NVoeXxnRSgdAas4130_provenance.
- NP316984.RAS9PcRPLk3pqV8aafjp1BpeZ6KgpoEfMSE6jh1Hr8qlk130_assertion description "[Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that controls genes involved in glycolysis, angiogenesis, migration, and invasion, all of which are important for tumor progression and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316984.RAS9PcRPLk3pqV8aafjp1BpeZ6KgpoEfMSE6jh1Hr8qlk130_provenance.
- NP316985.RAdWTmC-mCiFdqPKOkvkYSBeASsF3jVMJ4cHhEmyTY100130_assertion description "[No germline mutations were detected in the VHL or MET genes, suggesting that FCRC is not allelic with VHL disease or HPRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316985.RAdWTmC-mCiFdqPKOkvkYSBeASsF3jVMJ4cHhEmyTY100130_provenance.
- NP316988.RAQXCcp8xHbxRSfkKHuPQ47xAElQRDZCYyHpgCSyUaROg130_assertion description "[To determine whether inflammatory caspases are critical for the increased epithelial cell death before SjS-like disease, we investigated molecular events involving caspase-11/caspase-1 axis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316988.RAQXCcp8xHbxRSfkKHuPQ47xAElQRDZCYyHpgCSyUaROg130_provenance.
- NP316989.RAeuD-lcm0xjPmEcyM7C16-8BKUKjX1UDToMGv9RUSzFM130_assertion description "[Cloning of the calcium-sensing receptor (CaSR) along with the recognition that mutations in the CaSR gene are responsible for two familial syndromes characterized by abnormalities in the regulation of PTH secretion and Ca(2+) metabolism (Familial Hypocalciuric Hypercalcemia, FHH, and Autosomal Dominant Hypocalcemia, ADH) made it clear that extracellular Ca(2+) (Ca(2+)o) participates in its own regulation via a specific, receptor-mediated mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316989.RAeuD-lcm0xjPmEcyM7C16-8BKUKjX1UDToMGv9RUSzFM130_provenance.
- NP316997.RAUxGx9MABBwtpoVef2H9bQD85BQsiXYvjHbKuVqUrcgM130_assertion description "[Patients with complete Sertoli cell-only syndrome (SCOS) did not exhibit RBMY1, DAZ and TSPY gene expression, however, we detected very low expression of DDX3Y transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316997.RAUxGx9MABBwtpoVef2H9bQD85BQsiXYvjHbKuVqUrcgM130_provenance.
- NP316998.RAVFQSa3xb_SbIaqjB9ldcQt4l1hZIyVxKIpjlAKK0xrc130_assertion description "[We observed that NECs from smokers, as well as mono-DCs co-cultured with NECs from smokers, exhibited suppressed influenza-induced, interferon-related proteins interferon regulatory factor-7, Toll-like receptor-3, and retinoic acid inducible gene-1, likely because of the suppressed production of IFNα from the NECs of smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316998.RAVFQSa3xb_SbIaqjB9ldcQt4l1hZIyVxKIpjlAKK0xrc130_provenance.
- NP316999.RAeQLh0bzd8kC6PUcRHtNe_6lljMHOU_gDsp0bmA0SJI8130_assertion description "[The altered isoform expression in DCM hearts entails changes in the kinetic properties of total ANT protein restricting ANT function and contributing to disturbed energy metabolism in DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316999.RAeQLh0bzd8kC6PUcRHtNe_6lljMHOU_gDsp0bmA0SJI8130_provenance.
- NP317000.RAf-j4oI3OgZ0MmxSW7iMiUrIGHttVLtgcYP6GlUD_Bs8130_assertion description "[GEP NETs occur either sporadically or as part of endocrine tumor susceptibility syndromes such as multiple endocrine neoplasia type 1 (MEN1), von Hippel Lindau (VHL) syndrome, neurofibromatosis (NF-1), and possibly tuberous sclerosis (TSC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317000.RAf-j4oI3OgZ0MmxSW7iMiUrIGHttVLtgcYP6GlUD_Bs8130_provenance.
- NP317001.RATlBOcCuy-8kcdPj5gyJ4BhdH43VlG30dif2u2SiNraE130_assertion description "[Detection of viral DNA in dried blood spots using the Guthrie card (DBS test) is a reliable and practical method of diagnosing congenital cytomegalovirus (CMV) infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317001.RATlBOcCuy-8kcdPj5gyJ4BhdH43VlG30dif2u2SiNraE130_provenance.
- NP317003.RATNBWgs74T1OKbFUg908BrtgMelDsaGZIo72j1DHVWis130_assertion description "[PRL-3 protein expression was detected on ovarian cancer tissue microarrays using immunohistochemistry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317003.RATNBWgs74T1OKbFUg908BrtgMelDsaGZIo72j1DHVWis130_provenance.
- NP317009.RAUMQvImAcgCCTk2Jvr3euak-JbsSnHG6o3NKjzmwDtQw130_assertion description "[TOPK/PBK promotes cell migration via modulation of the PI3K/PTEN/AKT pathway and is associated with poor prognosis in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317009.RAUMQvImAcgCCTk2Jvr3euak-JbsSnHG6o3NKjzmwDtQw130_provenance.
- NP317010.RAQpS6BKB-C_yjwuFJ2BcRnPnrupvI6sgBO0V70XCl4RE130_assertion description "[Copy number gain and amplification of MET positively enhance tumour growth, invasiveness and metastasis in different cancer types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317010.RAQpS6BKB-C_yjwuFJ2BcRnPnrupvI6sgBO0V70XCl4RE130_provenance.
- NP317012.RAdmCld3A640nXDW0N4Gv4BZ83Ug7_eTAIL8-_B_lkPS8130_assertion description "[In transient transfection assays, transcription from both HSAL2 P1 and P2 was strikingly repressed by the WT-1 tumor suppressor protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317012.RAdmCld3A640nXDW0N4Gv4BZ83Ug7_eTAIL8-_B_lkPS8130_provenance.
- NP317014.RAdmWGTl1KSkERX04rYSqUwqvWucY9yYIzwUt8x_UYVwU130_assertion description "[The analyses were based on 375 Caucasian children screened at the Monster childhood thrombophilia centre with complete data for all prothrombotic risk factors (factor V G1691A, prothrombin G20210A, elevated lipoprotein (a), protein C-, protein S-, antithrombin-deficiency).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317014.RAdmWGTl1KSkERX04rYSqUwqvWucY9yYIzwUt8x_UYVwU130_provenance.
- NP317018.RAa5n2s0muk6BkB2ay3fIKxHcVQIDGp-OAuKGfbK6Try8130_assertion description "[These findings indicate that CD/5-FC gene therapy for prostate cancer may function with enhanced antitumor effect when combined with external beam radiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317018.RAa5n2s0muk6BkB2ay3fIKxHcVQIDGp-OAuKGfbK6Try8130_provenance.
- NP317021.RAWXlFmlJeWlNU-7mXxeGJ6KGCNPLqScXS3aPYMSSSqEg130_assertion description "[MRD-low-risk patients (MRD level <10(-4) at both TP2 and TP3) constituted 44% of patients and showed a relapse-rate of only 13%, whereas remaining patients (MRD-medium-risk patients; 30% of patients) had a relapse rate of 31%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317021.RAWXlFmlJeWlNU-7mXxeGJ6KGCNPLqScXS3aPYMSSSqEg130_provenance.
- NP317023.RAaHZKfXEiJz7pRZ566xF87ac7WYI5rYUpkWqfSyuaTEU130_assertion description "[RBM15-MKL1 (OTT-MAL) fusion transcript in an adult acute myeloid leukemia patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317023.RAaHZKfXEiJz7pRZ566xF87ac7WYI5rYUpkWqfSyuaTEU130_provenance.
- NP317028.RAYJM4HjpS3bIA8pAhGwaO7G1D0fcHFGyYiSGSwzUplcw130_assertion description "[After adjustment for multiple testing, we found a strong association between CLL risk and six genetic variants: CCNH (rs2266690, V270A), APAF1 (rs17028658, 3'region), IL16 (rs4505265, first intron), CASP8 (rs1045485, D302H), NOS2A (rs2779251, promoter), and CCR7 (rs3136687, intron 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317028.RAYJM4HjpS3bIA8pAhGwaO7G1D0fcHFGyYiSGSwzUplcw130_provenance.
- NP317029.RAekcL0oA5cN6A8C-4uaMONmQxJz3Aby4GUAeERD9DJeU130_assertion description "[Through identification of potential HtrA1 targets, studies presented herein propose that within the context of arthritis pathology HtrA1 contributes to cartilage degradation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317029.RAekcL0oA5cN6A8C-4uaMONmQxJz3Aby4GUAeERD9DJeU130_provenance.
- NP317030.RAfuYxT-4RcdzzNq1Zo83a0DL0DXXYnQZtowaiZQsyPGA130_assertion description "[For HBV genotyping, the INNO-LIPA and TRUGENE™ HBV genotyping kits were evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317030.RAfuYxT-4RcdzzNq1Zo83a0DL0DXXYnQZtowaiZQsyPGA130_provenance.
- NP317032.RAbDjhDoUVxnVv44iioeYVf32ptF5WYuLvf4l7dB3V88A130_assertion description "[Tumour necrosis factor beta alleles and hyperinsulinaemia in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317032.RAbDjhDoUVxnVv44iioeYVf32ptF5WYuLvf4l7dB3V88A130_provenance.
- NP317038.RAcyG8RJjsrpUG3RtiJ99SWmC-sdj5aGXmK-9Qd5beYHM130_assertion description "[The effects of GSTM1 and GSTT1 polymorphism on susceptibility to RCC depend on exposure to specific chemicals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317038.RAcyG8RJjsrpUG3RtiJ99SWmC-sdj5aGXmK-9Qd5beYHM130_provenance.
- NP317039.RATJVYgAC8wMHR4S45hvNGM5mv7u4QeVkn5KedwJ1Epjk130_assertion description "[Effect of estrogen on the expression of matrix metalloproteinase (MMP)-1, MMP-3, and MMP-13 and tissue inhibitor of metalloproternase-1 in osteoarthritis chondrocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317039.RATJVYgAC8wMHR4S45hvNGM5mv7u4QeVkn5KedwJ1Epjk130_provenance.
- NP317040.RAZA01AwjZCMKZH0vzoa-hTUCbzHSGuz7dVCeE5jg9oo8130_assertion description "[MTHFR A1298C polymorphism and idiopathic male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317040.RAZA01AwjZCMKZH0vzoa-hTUCbzHSGuz7dVCeE5jg9oo8130_provenance.
- NP317044.RAWgh7KZs0taRrESH8BsaH2CTpFSdHGV3QR610wun4by0130_assertion description "[Gene silencing of the mitochondrial adaptor p66(Shc) suppresses vascular hyperglycemic memory in diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317044.RAWgh7KZs0taRrESH8BsaH2CTpFSdHGV3QR610wun4by0130_provenance.
- NP317045.RAYOfGYjQ4mfAkRPOKo9gQTZ7S1knhoG3tvzU2IEq8jIA130_assertion description "[Protein S, protein C or antithrombin deficiencies confer high absolute risk of VTE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317045.RAYOfGYjQ4mfAkRPOKo9gQTZ7S1knhoG3tvzU2IEq8jIA130_provenance.
- NP317053.RAeO214aL4QzWSMkUxSce0D6UC02ZMS3zSo1bmer9C0VM130_assertion description "[Using a human TSH receptor (TSH-R) cDNA probe, we investigated TSH-R transcript levels in 13 human thyroid fragments by Northern blot analysis; 7 Graves' disease, 2 Hashimoto's disease, 3 endemic goiter, and 1 healthy thyroid gland were studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317053.RAeO214aL4QzWSMkUxSce0D6UC02ZMS3zSo1bmer9C0VM130_provenance.
- NP317055.RAaWlG6LocFZzNumeSPeTJRMe3f262oznDsaxx4dXFj5E130_assertion description "[Recent studies of the Trp53 mouse mutant showed that exencephaly susceptibility depends on the presence of two X chromosomes, not the absence of the Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317055.RAaWlG6LocFZzNumeSPeTJRMe3f262oznDsaxx4dXFj5E130_provenance.