Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP322204.RAX_1Mja8g_hANuX1Zr55cMmEbLycSohV_KoA1wQVzoaY130_assertion description "[p27-p16 fusion gene inhibits angioplasty-induced neointimal hyperplasia and coronary artery occlusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322204.RAX_1Mja8g_hANuX1Zr55cMmEbLycSohV_KoA1wQVzoaY130_provenance.
- NP322210.RAZIby1ZKtd1bu0A1iK31yS_9h0j-y-6v3C--JJhx4eZo130_assertion description "[The family of vascular endothelial growth factor (VEGF) proteins include potent and specific mitogens for vascular endothelial cells that function in the lation of angiogenesis Inhibition of VEGF-induced angiogenesis either by neutralizing antibodies or dominant-negative soluble receptor, blocks the growth of primary and metastatic experimental tumors Here we report that VEGF expression is induced in Lewis lung carcinomas (LLCs) both in vitro and vivo after exposure to ionizing radiation (IR) and in human tumor cell lines (Seg-1 esophageal adenocarcinoma, SQ20B squamous cell carcinoma, T98 and U87 glioblastomas, and U1 melanoma) in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322210.RAZIby1ZKtd1bu0A1iK31yS_9h0j-y-6v3C--JJhx4eZo130_provenance.
- NP322211.RAWN6JEjEGvvRS-v8tPCzwSti-zjNyBb8r1oxWuKnmvLg130_assertion description "[5' CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322211.RAWN6JEjEGvvRS-v8tPCzwSti-zjNyBb8r1oxWuKnmvLg130_provenance.
- NP322219.RAboe51-1XMci2PZj7gOmpMKajxWOlvN5YDbifZNzpSzo130_assertion description "[These results indicated that MSP58 might play an important role in the carcinogenesis of CRC via regulation of the cyclin D1-cyclin-dependent kinase 4-p21 pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322219.RAboe51-1XMci2PZj7gOmpMKajxWOlvN5YDbifZNzpSzo130_provenance.
- NP322224.RAaIk_LylqahFfVeVSUkfZ6XGkamnmfui3FoqeeJo_tHA130_assertion description "[Identification of novel variants in the Myosin VIIA gene of patients with nonsyndromic hearing loss from Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322224.RAaIk_LylqahFfVeVSUkfZ6XGkamnmfui3FoqeeJo_tHA130_provenance.
- NP322226.RAfRTMWYyjVCPYDNCOc7vlsBsWCNqyBrV_R6JmaiqAYaI130_assertion description "[Tumors with ret/PTC gene rearrangements tended to have lymph node metastases rather than hematogenous spread.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322226.RAfRTMWYyjVCPYDNCOc7vlsBsWCNqyBrV_R6JmaiqAYaI130_provenance.
- NP322230.RAWJb9pfgitJ7Y3QrifVV8G4qddz4ih2jmnRF3V9rlijI130_assertion description "[Polymorphism at codon 72 of the p53 gene is not associated with endometriosis in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322230.RAWJb9pfgitJ7Y3QrifVV8G4qddz4ih2jmnRF3V9rlijI130_provenance.
- NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_assertion description "[We aimed to evaluate the association of non-response to antiepileptic pharmacotherapy with the frequency of variant alleles in the drug transporter genes ABCB1 and ABCC2 or in the CYP2C locus in young patients with epilepsy and an independent cohort of adults with drug-refractory epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_provenance.
- NP322233.RAeNf-7MVEOF9ZczY1yxlGfXomqwZmA-nX4Ikq2C5pAf0130_assertion description "[The role played by resident microglia and by the infiltration of peripheral monocytes/macrophages in the innate immune response during herpes simplex virus type 1 (HSV-1) encephalitis was evaluated in mice deficient for the CCR2 and CX3CR1 receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322233.RAeNf-7MVEOF9ZczY1yxlGfXomqwZmA-nX4Ikq2C5pAf0130_provenance.
- NP322240.RATSXmqlQXVQZLlG5pY3cW2V1RkVW0Xdu5xFG7Dtwfb9E130_assertion description "[Mutations within various domains of the KIT receptor that lead to constitutive activation have been identified in patients, and those involving the activation loop of the KIT receptor are the mutations most frequently detected in patients with mastocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322240.RATSXmqlQXVQZLlG5pY3cW2V1RkVW0Xdu5xFG7Dtwfb9E130_provenance.
- NP322252.RAY3yxC4PhGjV3TlqCkZ108zeVwpDtGQLPQmHhyCBvOhQ130_assertion description "[Because of the structural and biochemical similarities between the antitumor p53 and p73 proteins, the authors hypothesized that individuals who carry high-risk genotypes of p53 codon 72 and p73 G4C14-to-A4T14 polymorphisms have a higher risk of developing second primary malignancy (SPM) after index squamous cell carcinoma of the head and neck (SCCHN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322252.RAY3yxC4PhGjV3TlqCkZ108zeVwpDtGQLPQmHhyCBvOhQ130_provenance.
- NP322260.RATtufmiZacvpWKnUXj8zmHx_zmmLhhKv7_VfjwaG4Cg4130_assertion description "[Immunotherapies directed against PSA have been suggested in patients with metastatic prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322260.RATtufmiZacvpWKnUXj8zmHx_zmmLhhKv7_VfjwaG4Cg4130_provenance.
- NP322271.RAZRJGJ8x-MmNFqe9pyH8Rb75irl7vnKf9mlZdh9TatWM130_assertion description "[Diffuse sclerosing variant of papillary thyroid carcinoma: lack of BRAF mutation but occurrence of RET/PTC rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322271.RAZRJGJ8x-MmNFqe9pyH8Rb75irl7vnKf9mlZdh9TatWM130_provenance.
- NP322272.RAcq42KPbrx0ceUcgKMveb_jHTClvDnxiKpDPSJAiX1f8130_assertion description "[GAD1 mRNA expression and DNA methylation in prefrontal cortex of subjects with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322272.RAcq42KPbrx0ceUcgKMveb_jHTClvDnxiKpDPSJAiX1f8130_provenance.
- NP322274.RAeUuOCe1XGWkSISJc8fNpvfEuLDGK48CiQfj2KcgaYIM130_assertion description "[There was a higher frequency of CHL1 mRNA decrease in lung squamous cell carcinoma compared to adenocarcinoma (81% vs. 38%, P = 0.02) without association with tumor progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322274.RAeUuOCe1XGWkSISJc8fNpvfEuLDGK48CiQfj2KcgaYIM130_provenance.
- NP322277.RASsagnSCyXDteqP_LVbPqLtidS4Mjk7SFFQKO1aEy0kM130_assertion description "[Human papillomavirus, p53 and cyclin D1 expression in oropharyngeal carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322277.RASsagnSCyXDteqP_LVbPqLtidS4Mjk7SFFQKO1aEy0kM130_provenance.
- NP322278.RAQLgZzKhStGp_h50mY3b7hoaYWu2N1PlzkZ3FdXzfqkk130_assertion description "[Quantitative RT-PCR analysis confirmed that expression levels of KDM5B are significantly higher in human bladder cancer tissues than in their corresponding non-neoplastic bladder tissues (P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322278.RAQLgZzKhStGp_h50mY3b7hoaYWu2N1PlzkZ3FdXzfqkk130_provenance.
- NP322280.RAY4ZDmK5n8x9rkoC3CscEeEp6mEMTbDu3nXjwUPzK6Wo130_assertion description "[Finally, we observe that frontal-cortex DNA methylation in the BDNF gene is correlated with genotype at a nearby nonsynonymous SNP that has been previously associated with major psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322280.RAY4ZDmK5n8x9rkoC3CscEeEp6mEMTbDu3nXjwUPzK6Wo130_provenance.
- NP322281.RAV8rhpa8ILOTx5q6Pu6JABjAAx97oLuRfoGxAZ75HPmE130_assertion description "[On the other hand, the TS 1494del6 polymorphism is associated with a significantly lower risk of breast cancer and may be a potential genetic marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322281.RAV8rhpa8ILOTx5q6Pu6JABjAAx97oLuRfoGxAZ75HPmE130_provenance.
- NP322283.RAaBjAoHiqP-mEdorNhQ1K6JrhP7bIrsNOMve1ckBb1yM130_assertion description "[The expression profile suggests MT-1 could be used clinically as a marker for tumors possessing the potential for lymph node metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322283.RAaBjAoHiqP-mEdorNhQ1K6JrhP7bIrsNOMve1ckBb1yM130_provenance.
- NP322291.RAbR9eqQJyq8FSda_uqfQUQxwx0r6e1_GotEy_TJR9JSc130_assertion description "[PINCH expression was immunohistochemically examined in normal gastric mucous (n=30) and gastric adenocarcinoma (n=73), from gastric cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322291.RAbR9eqQJyq8FSda_uqfQUQxwx0r6e1_GotEy_TJR9JSc130_provenance.
- NP322293.RAfIBCwcWyXBlwSRMfC69vvF8OB5OWY7iJ0ATg_pT3dj8130_assertion description "[Blocking SOCE either by depleting STIM1 or ectopically expressing dominant-negative Orai1 accelerated TSC-related tumor development, likely because of restored AKT1 activity and enhanced tumor angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322293.RAfIBCwcWyXBlwSRMfC69vvF8OB5OWY7iJ0ATg_pT3dj8130_provenance.
- NP322295.RARW3w69i4Vl8gJk_Wr8Y9J0Los_t2AHhNiMcs-y-fCZ4130_assertion description "[Mutations in the autoimmune regulator protein AIRE1 cause a monogenic autosomal recessively inherited disease: autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322295.RARW3w69i4Vl8gJk_Wr8Y9J0Los_t2AHhNiMcs-y-fCZ4130_provenance.
- NP322301.RAbL6I_VQU_vGw8AEe8VVZdg-FGlV2a7jZvGv1sAu8kbY130_assertion description "[This 4-year boy with trisomy 16p13.3 has the smallest duplication reported of this critical region, which could not be detected without array CGH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322301.RAbL6I_VQU_vGw8AEe8VVZdg-FGlV2a7jZvGv1sAu8kbY130_provenance.
- NP322305.RAQeXhkAwZGCoeCbTE6sal75DiomM3CmXNJpU2Y2TiGp0130_assertion description "[The ACT gene, which is found on chromosome 14, has previously been proposed as a candidate for AD due to the presence of the ACT protein in senile plaques and the reported elevation of the protein in the cerebro-spinal fluid (CSF) and serum of AD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322305.RAQeXhkAwZGCoeCbTE6sal75DiomM3CmXNJpU2Y2TiGp0130_provenance.
- NP322308.RAT5fNwJwr1zoURIEJOZlJq13iwcmVR0MuRIkVFjXdG3M130_assertion description "[Niemann-Pick type C (NPC) disease is a cholesterol lipidosis caused by mutations in NPC1 and NPC2 gene loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322308.RAT5fNwJwr1zoURIEJOZlJq13iwcmVR0MuRIkVFjXdG3M130_provenance.
- NP322312.RAZhZOmtlm75EEvogQD-lsH3zVdNwxB4eQl35qdzwM0Pw130_assertion description "[Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322312.RAZhZOmtlm75EEvogQD-lsH3zVdNwxB4eQl35qdzwM0Pw130_provenance.
- NP322316.RAYC_BD8fFRY18F80kQ7eUyc246kONJhzGhMstgWxXKd8130_assertion description "[Taken together, we extracted the GPS successfully and our findings suggest that GPS functions as a tumor suppressor through influencing the P53/PI3K/AKT pathway in the carcinogenesis of hepatocellular carcinoma and may have therapeutic implications for the clinical management of hepatocellular carcinoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322316.RAYC_BD8fFRY18F80kQ7eUyc246kONJhzGhMstgWxXKd8130_provenance.
- NP322326.RATg1Je7UV49WJ8IWJyrYRJe37rN1FO71uN9I7Bj3MggU130_assertion description "[NOTCH1 mutation increased the risk of transformation to diffuse large B-cell lymphoma independently from IGHV, with this being validated in resampling tests of replicability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322326.RATg1Je7UV49WJ8IWJyrYRJe37rN1FO71uN9I7Bj3MggU130_provenance.
- NP322332.RAUHsJKrc8aQZDf0qDZYruwx737P44X_EpEXvttbeHtXs130_assertion description "[Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disease characterized by arteriovenous malformations and resulting from mutations in two major genes: ENG and ACVRL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322332.RAUHsJKrc8aQZDf0qDZYruwx737P44X_EpEXvttbeHtXs130_provenance.
- NP322333.RAcHwOL9t5s671gC2p_vGTQysp0XEXv90i64XPJoGRQJc130_assertion description "[Because the mode of action of (-)-OSU6162 is critical in determining whether psychosis is associated with dopamine D2 receptor overactivity or deficit activity, we measured the potency of (-)-OSU6162 on the binding of [3H]domperidone and on the incorporation of [35S]-GTP-gamma-S into human cloned dopamine D2 receptor-containing cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322333.RAcHwOL9t5s671gC2p_vGTQysp0XEXv90i64XPJoGRQJc130_provenance.
- NP322340.RAQ2ED5vmotxCfaEw5CkyXyYHe3h9w2d2aS3ntjRwxluc130_assertion description "[The leptin gene polymorphism was associated with hypertension independent of obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322340.RAQ2ED5vmotxCfaEw5CkyXyYHe3h9w2d2aS3ntjRwxluc130_provenance.
- NP322342.RAdFI_fjbL4Wec-qijeV_5HBRCJggXnaYzRzI4GanxM1k130_assertion description "[The aim of this human investigation is to explore the relationship of gingivitis with salivary biomarkers, periodontal pathogens, and interleukin (IL)-1 polymorphism after a transient inflammatory burden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322342.RAdFI_fjbL4Wec-qijeV_5HBRCJggXnaYzRzI4GanxM1k130_provenance.
- NP322344.RAYROmesdd-w9-_OKDRWYe0eMpcdgbkAJoUCfKcYXvtkk130_assertion description "[By using B cells from a patient with the hyper-IgM syndrome that are incapable of immunoglobulin heavy chain class switching, it was demonstrated that HC2 expression did not require prior heavy chain switch.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322344.RAYROmesdd-w9-_OKDRWYe0eMpcdgbkAJoUCfKcYXvtkk130_provenance.
- NP322345.RAXJSRIHrenoz7S0l1CtmHAzE2oMbI_pXj_Z7NmNCHAwc130_assertion description "[Our results indicate that the TIMP-2 -418C/C homozygote may be a protective factor against the development of endometriosis in North Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322345.RAXJSRIHrenoz7S0l1CtmHAzE2oMbI_pXj_Z7NmNCHAwc130_provenance.
- NP322355.RATnoIyAwNHHyx3jYViDnUX9e2ImH9bATqOaS5uoEHkow130_assertion description "[Using the clone-specific rearrangement of the T cell receptor gene as the genetic marker of the clonotype, we analyzed the clonal origin of the interleukin 2 (IL-2)-dependent human T-lymphotrophic virus I (HTLV-I)-positive T cell lines established from various adult T cell leukemia (ATL) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322355.RATnoIyAwNHHyx3jYViDnUX9e2ImH9bATqOaS5uoEHkow130_provenance.
- NP322362.RASYakEGXVwyq1n3txflC5-YxX9bUoKt-T4DQTzcfno3U130_assertion description "[Altered expression of decorin and lumican is associated with breast tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322362.RASYakEGXVwyq1n3txflC5-YxX9bUoKt-T4DQTzcfno3U130_provenance.
- NP322365.RAc_W5y1GHDK71Tq6CtT-4BB1aYcSnNtToAhuAeEogC3Q130_assertion description "[A total of 47 intracerebral melanoma metastases and 21 primary papillary thyroid carcinomas were evaluated by direct sequencing of BRAF and by immunohistochemistry using the BRAF V600E mutation-specific antibody clone VE1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322365.RAc_W5y1GHDK71Tq6CtT-4BB1aYcSnNtToAhuAeEogC3Q130_provenance.
- NP322375.RAfGgXCLdb867vEXER-IRYIO_wCr4wew2nWV27rdwzVNI130_assertion description "[Significant induction of IFN-gamma, IL-12 p70, and IL-18 was observed from sarcoid BAL fluid cells with LPS stimulation, whereas LPS tended to induce only IL-12 p70 in BAL fluid cells from healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322375.RAfGgXCLdb867vEXER-IRYIO_wCr4wew2nWV27rdwzVNI130_provenance.
- NP322384.RAd1pRjFwWeM2A0zs8noUK-ZSoPxZj94KLMw7_S-ntSV8130_assertion description "[A strong cumulative effect of five genetic variants and family history on prostate cancer risk was recently reported in a Swedish population (CAPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322384.RAd1pRjFwWeM2A0zs8noUK-ZSoPxZj94KLMw7_S-ntSV8130_provenance.
- NP322387.RARQQ3IG4gZYTFrugGmyopxAbVEZM80fqTLJdCekZRCLU130_assertion description "[Two hundred and twenty-six patients with PsA were typed for MICA exon 5 microsatellite (TM) by heteroduplex analysis and compared with 225 normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322387.RARQQ3IG4gZYTFrugGmyopxAbVEZM80fqTLJdCekZRCLU130_provenance.
- NP322391.RAaf829jyXfqK3n8nhDY_pzzj1eBqJQRWPsA1lPTrL9UI130_assertion description "[Here, we report that GATA-2 is expressed in a substantial proportion of prostate cancers and that high expression of GATA-2 is associated with biochemical recurrence and distant metastatic progression in a validation set of 203 cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322391.RAaf829jyXfqK3n8nhDY_pzzj1eBqJQRWPsA1lPTrL9UI130_provenance.
- NP322392.RAa1h7xzrY3zrx3qaqNhD--iiFdQYQfGRSBk-lw6hJC-g130_assertion description "[Aberrant TP53 protein accumulation in the neuronal component of ganglioglioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322392.RAa1h7xzrY3zrx3qaqNhD--iiFdQYQfGRSBk-lw6hJC-g130_provenance.
- NP322396.RARLtet8XYYzTT0MOV3SIMT5LZiKQvGLZP2WBqbZtqLF0130_assertion description "[A study of 274 family trios (affected child and both unaffected parents) from Australia validated the association of ST8SIA1 in individuals with MS, showing transmission disequilibrium of the paternal alleles for three additional SNPs, namely rs704219, rs2041906, and rs1558793, with p = 0.001, p = 0.01 and p = 0.01 respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322396.RARLtet8XYYzTT0MOV3SIMT5LZiKQvGLZP2WBqbZtqLF0130_provenance.
- NP322400.RAStlafvmkdetaQ0ZSDRGPsSFKCq7WAWLalSV2bEB01fM130_assertion description "[We have identified recessive mutations in ANO5 that result in a proximal limb-girdle muscular dystrophy (LGMD2L) in three French Canadian families and in a distal non-dysferlin Miyoshi myopathy (MMD3) in Dutch and Finnish families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322400.RAStlafvmkdetaQ0ZSDRGPsSFKCq7WAWLalSV2bEB01fM130_provenance.
- NP322401.RATlHt4OpVZi19ZXlJpG4snbnBBBW3euDLCa3KBAgA45s130_assertion description "[To determine if VPA does, in fact, enhance AP-1 mediated gene expression, the effects of VPA on the expression of a luciferase reporter gene were studied in transiently transfected rat C6 glioma and human SH-SY5Y neuroblastoma cells using the pGL2-control vector.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322401.RATlHt4OpVZi19ZXlJpG4snbnBBBW3euDLCa3KBAgA45s130_provenance.
- NP322408.RATBF_lFAt4u2cQkJ2futR1Fmig_PKSrf3YJCf_Jmc7f4130_assertion description "[It is possible that bile acid reflux present in patients with BE may increase reactive oxygen species production and cell proliferation via activation of PI-PLCgamma2, ERK2 MAP kinase, and NADPH oxidase NOX5-S, thereby contributing to the development of EA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322408.RATBF_lFAt4u2cQkJ2futR1Fmig_PKSrf3YJCf_Jmc7f4130_provenance.
- NP322409.RAaX9baqyIhyRWvda_EbvEaS7uTMEehjN0jCE4YlIK8_g130_assertion description "[Structural analysis of TRβ1 UTR variants indicated that reduced TRβ1 expression may be maintained in ccRCC by posttranscriptional mechanisms involving 5'UTRs and miRNA-204.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322409.RAaX9baqyIhyRWvda_EbvEaS7uTMEehjN0jCE4YlIK8_g130_provenance.
- NP322415.RAWaCMM0fl6KJQJrTjckB_JW7wXoleCQXVG_KiYJroMiY130_assertion description "[The genomic profile of mantle cell lymphoma (MCL) has been reported to be significantly different from that of other indolent lymphoproliferative disorders, Topoisomerase IIalpha, glutathione-s-transferasepi (GSTpi) and ABCG2 (BCRP) chemoresistance genes being over-expressed in MCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322415.RAWaCMM0fl6KJQJrTjckB_JW7wXoleCQXVG_KiYJroMiY130_provenance.
- NP322425.RAXZWXDsNGXcQkYCMto5VfDSrEabUFyCtLSqdwcnUC2Z0130_assertion description "[Siah2-dependent expression and activity of HIF-1α regulate its availability to form a transcriptional complex with FoxA2, resulting in expression of specific target genes, including Hes6, Sox9 and Jmjd1a, whose co-expression is sufficient for formation of NE tumors and NE lesions in PCa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322425.RAXZWXDsNGXcQkYCMto5VfDSrEabUFyCtLSqdwcnUC2Z0130_provenance.
- NP322429.RAdRhrktH8Eszh6Yl6aHGGmcFRe7wjKSHCpACzPP9h2xk130_assertion description "[This study analyzed the correlation of aPKC-iota with clinicopathology in hepatocarcinoma and Cyclin E and investigated molecular mechanisms of invasion and metastasis of hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322429.RAdRhrktH8Eszh6Yl6aHGGmcFRe7wjKSHCpACzPP9h2xk130_provenance.
- NP322432.RASngEqKZqoqullh28WQv2frXb5MGspY3ms4NbilebA84130_assertion description "[Gilbert syndrome is caused by defects in the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322432.RASngEqKZqoqullh28WQv2frXb5MGspY3ms4NbilebA84130_provenance.
- NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_assertion description "[The aim of this study was to determine the association of polymorphisms in the CARD15, TNFA, IL1B, and IL1RN genes with risk of development of CD and with the clinicopathological profile of CD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_provenance.
- NP322438.RAXoUotEeDn8W_VsyKUPQD_Ar-P9CfOIe-xAcMZDPTZtI130_assertion description "[These results are the first reported evidence of a congenital goiter with a thyroglobulin synthesis defect due to the low expression of the thyroid-specific transcription factor TTF-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322438.RAXoUotEeDn8W_VsyKUPQD_Ar-P9CfOIe-xAcMZDPTZtI130_provenance.
- NP322440.RAcHbORqLgdnN2TXDW5LTaiP9k7QhTscXcbBEwILCYH1U130_assertion description "[One possible endophenotype of alcohol dependence may be related to the P300 waveform of the event-related brain potential (ERP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322440.RAcHbORqLgdnN2TXDW5LTaiP9k7QhTscXcbBEwILCYH1U130_provenance.
- NP322441.RAeYGI18qD4NuzVkj7ESOLUDrP_ke1Y1Cj_SbkEMEIt7w130_assertion description "[XLA patients have a decreased number of mature B cells and a lack of all immunoglobulin isotypes, resulting in susceptibility to severe bacterial infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322441.RAeYGI18qD4NuzVkj7ESOLUDrP_ke1Y1Cj_SbkEMEIt7w130_provenance.
- NP322449.RAbD35qQWYIXcOm_ghJopgJWCYYMJl7-ABoO586UJJkuc130_assertion description "[To the best of our knowledge, this is the first reported case of cataracts caused by a mutation in the second extracellular loop domain of MIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322449.RAbD35qQWYIXcOm_ghJopgJWCYYMJl7-ABoO586UJJkuc130_provenance.
- NP322454.RAdIhJiz7Fy36SbDh6brgasFUqF7oL29lQjuvEAxROP5s130_assertion description "[The matrix Gla protein (MGP) is an important inhibitor of vessel and cartilage calcification that is strongly expressed in human calcified, atherosclerotic plaques and could modulate plaque calcification and coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322454.RAdIhJiz7Fy36SbDh6brgasFUqF7oL29lQjuvEAxROP5s130_provenance.
- NP322457.RAZwkBcIwAWIbTY9nywVJX6SEuMZHI73x4drqmboPQ9FU130_assertion description "[To understand the potential role of the inflammatory cytokine interleukin 6 (IL-6) in the pathogenesis of these lesions, we analyzed the IL-6 system in TSC and FCDIIb cortical lesions and in control cortex (CTX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322457.RAZwkBcIwAWIbTY9nywVJX6SEuMZHI73x4drqmboPQ9FU130_provenance.
- NP322458.RAS_oKpFY4PGCNJXQIrzU3xPGwMHPjpmfGGLiZqoYuIfE130_assertion description "[MSD is caused by mutations in the SUMF1 gene encoding the formylglycine-generating enzyme (FGE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322458.RAS_oKpFY4PGCNJXQIrzU3xPGwMHPjpmfGGLiZqoYuIfE130_provenance.
- NP322462.RAWvcB03dYLYhq9mEhZzTq06qnAQg3M2qKLR1rwyyk9Uw130_assertion description "[Translocation t(1;6)(p35.3;p25.2): a new recurrent aberration in `unmutated` B-CLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322462.RAWvcB03dYLYhq9mEhZzTq06qnAQg3M2qKLR1rwyyk9Uw130_provenance.
- NP322466.RAemaIaaalAUFvz_X9h8GXRDyX5iZt2Mszo4sVg2JQKAA130_assertion description "[Copy number variants have increasingly been recognized in the Idiopathic/Genetic Generalized Epilepsies (IGE/GGE) including juvenile myoclonic epilepsy (JME).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322466.RAemaIaaalAUFvz_X9h8GXRDyX5iZt2Mszo4sVg2JQKAA130_provenance.
- NP322469.RAfkRl7G5sa4aaSPpwD0GHjJy70fIL7L1GJvW2qIuaZdM130_assertion description "[Problem drinking (≥2 positive answers on CAGE) and negative consequences of drinking on different aspects of life were also measured.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322469.RAfkRl7G5sa4aaSPpwD0GHjJy70fIL7L1GJvW2qIuaZdM130_provenance.
- NP322471.RATuslGnI7ccbEpHBYfYdFOfbbQZHMPh8zGjjXH3IspYo130_assertion description "[We investigated the impact of MGMT methylation and expression on survival of children with high-grade glioma (HGG) registered into the German HIT-GBM database receiving temozolomide (TMZ) as part of their treatment (n = 21 relapsed, n = 4 primary).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322471.RATuslGnI7ccbEpHBYfYdFOfbbQZHMPh8zGjjXH3IspYo130_provenance.
- NP322475.RAXL0b-1MpNp1ajd7jBif-efpZ6XHqRfvI36SyReRhoKg130_assertion description "[Fluorescence in situ hybridization (FISH) studies, using a specific MDR1 probe revealed no loss of an MDR1 allele in any of the deleted q- arms of the seven patients with 7q-, whereas all monosomy 7 patients lacked one MDR1 gene homologue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322475.RAXL0b-1MpNp1ajd7jBif-efpZ6XHqRfvI36SyReRhoKg130_provenance.
- NP322478.RAYk10Y1DgbBUExKQS0ZJHbomJoWeCR_Tv54eyp8ml9aA130_assertion description "[We conclude that the high expression of histone H1x in NETs is probably due to the abundance of this protein in the cells from which these tumours originate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322478.RAYk10Y1DgbBUExKQS0ZJHbomJoWeCR_Tv54eyp8ml9aA130_provenance.
- NP322479.RAcLc4rYQFDq-ymbRL_QhROXbVHoFrHK5Pby5-eQOb1YE130_assertion description "[DR4 chromosomes can be divided into diabetes prone or resistant by restriction fragment length polymorphism analyses with cDNA probes for DQ beta-gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322479.RAcLc4rYQFDq-ymbRL_QhROXbVHoFrHK5Pby5-eQOb1YE130_provenance.
- NP322483.RAXPZqaJZqkJPLXciTlfBpTFLX9BYSflIEqyRLwDVefTg130_assertion description "[Also, the expression of NOX4 was studied in PAFB isolated from the lungs of patients with idiopathic pulmonary arterial hypertension (IPAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322483.RAXPZqaJZqkJPLXciTlfBpTFLX9BYSflIEqyRLwDVefTg130_provenance.
- NP322484.RAb3_9UXbskBZvptiBQL3mwjyYDoFA8kHZkRSfVMBy2_w130_assertion description "[In the present study, employing over 100 DNA samples obtained from Lin-xian patients who underwent surgery for esophageal cancer, we have found a significant frequency of amplification of either the human epidermal growth factor receptor (HER-I) gene or the c-myc oncogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322484.RAb3_9UXbskBZvptiBQL3mwjyYDoFA8kHZkRSfVMBy2_w130_provenance.
- NP322488.RAdlrfe1nUo450eWCmaeKsKQB_3D82UPx52hWOiSNROUk130_assertion description "[In T-cell acute lymphoblastic leukemia (T-ALL), p53 gene mutations were found in 12 of 51 patients in first relapse (24%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322488.RAdlrfe1nUo450eWCmaeKsKQB_3D82UPx52hWOiSNROUk130_provenance.
- NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_assertion description "[Warts, hypogammaglobulinaemia, infections, myelokathexis (WHIM) syndrome is an inherited immune disorder associated with CXCR4 gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322492.RAUvnbDn2Q2BHtaK4yHoVx9mvw_DUQr5S4nyPsm64i0_I130_provenance.
- NP322493.RAbL7PhHsz4xxad4aD8JUIFCBP3QLmWe6RCRDT8jI8Ijg130_assertion description "[The RP3 (retinitis pigmentosa type 3) locus at Xp21.1 is believed to account for the disease in the majority of XLRP families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322493.RAbL7PhHsz4xxad4aD8JUIFCBP3QLmWe6RCRDT8jI8Ijg130_provenance.
- NP322498.RAc2qBYPJgUdwk4d9u3nL1UYXTOKz8-6DhZfRurDLF3II130_assertion description "[Characterisation of the spatial distribution of the FGFR multigene family in both normal and atherosclerotic arteries is a prerequisite to further define the functional role of FGF-1 and FGF-2 in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322498.RAc2qBYPJgUdwk4d9u3nL1UYXTOKz8-6DhZfRurDLF3II130_provenance.
- NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_assertion description "[Specifically, introduction of a subset of the mutations identified in human GBM, in the nSH2 and iSH2 domains, increases signaling through the PI3K pathway and promotes tumorigenesis of primary normal human astrocytes in an orthotopic xenograft model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322500.RAXqy-cA3WnvICuOESrYpiuDTiQJRmjM3mLXxmKlpLlZc130_provenance.
- NP322501.RATQ_7kRUHwSnpMd5nk0kSo34QgcWikUb0D74VNF8crUk130_assertion description "[To investigate the mechanisms involved in PCa (prostate cancer) metastasis and CXCR4 (CXC chemokine receptor-4)-mediated VEGF (vascular endothelial growth factor) and MMP-9 (matrix metalloproteinase-9) expression, we used lentivirus-mediated RNAi (RNA interference) to reduce the expression of CXCR4 in a PCa cell line.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322501.RATQ_7kRUHwSnpMd5nk0kSo34QgcWikUb0D74VNF8crUk130_provenance.
- NP322506.RAWt0bPrDKL3dJhLcHbkRK-rxqRV-tYlEideiiifIqLsE130_assertion description "[Clinical significance of SOD2 and GSTP1 gene polymorphisms in Chinese patients with gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322506.RAWt0bPrDKL3dJhLcHbkRK-rxqRV-tYlEideiiifIqLsE130_provenance.
- NP322508.RAbPFortOuyxziD8XVyaftEGZlDZpask6sSNu4HWGQ_7I130_assertion description "[RTS,S/AS02 is a recombinant protein malaria vaccine that contains a large portion of the C-terminal of the circumsporozoite protein (CSP) sequence of the NF54 isolate of Plasmodium falciparum fused to the hepatitis B virus surface antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322508.RAbPFortOuyxziD8XVyaftEGZlDZpask6sSNu4HWGQ_7I130_provenance.
- NP322510.RAbs-117Z26DJq0DW9Jf2vET-LCCR2zgNsIy4jyceX-Uw130_assertion description "[In 99 patients receiving IV fentanyl, midazolam, or both, we evaluated drug doses, covariates likely to influence drug effects (age, body mass index, and renal and hepatic dysfunction); delirium risk factors; concomitant administration of CYP3A and P-glycoprotein substrates/inhibitors; ABCB1, ABCG2, and CYP3A5 genetic polymorphisms; and fentanyl and midazolam plasma levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322510.RAbs-117Z26DJq0DW9Jf2vET-LCCR2zgNsIy4jyceX-Uw130_provenance.
- NP322516.RAXZYmEqEzURnN4rsiios-izVoS7md_SyWmGRixxoKX1U130_assertion description "[Patients with xeroderma pigmentosum (XP) have a 1,000-fold increase in ultraviolet (UV)-induced skin cancers while trichothiodystrophy (TTD) patients, despite mutations in the same genes, ERCC2 (XPD) or ERCC3 (XPB), are cancer-free.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322516.RAXZYmEqEzURnN4rsiios-izVoS7md_SyWmGRixxoKX1U130_provenance.
- NP322517.RAduCH7NElkql4qkkEwrKyhLIk18GMMCLqnhjt4Ax0PEY130_assertion description "[Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322517.RAduCH7NElkql4qkkEwrKyhLIk18GMMCLqnhjt4Ax0PEY130_provenance.
- NP322526.RAejcyWZEg5DRfH3XuCwXv-8Xb2kkoUDvjn6tf9dsjglY130_assertion description "[The FIP1L1-PDGFRA fusion gene is the most frequent genetic aberration in myeloid neoplasms associated with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322526.RAejcyWZEg5DRfH3XuCwXv-8Xb2kkoUDvjn6tf9dsjglY130_provenance.
- NP322541.RAf_LtbRwKleiY3EBds17PkFuyqPaigmgf-OpimoFxI2s130_assertion description "[To determine the frequency of the deletions of p15/p16 genes in adult T-cell leukemia (ATL) cells and to evaluate their value in the diagnosis of clinical subtypes of ATL patients and the prediction of their clinical outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322541.RAf_LtbRwKleiY3EBds17PkFuyqPaigmgf-OpimoFxI2s130_provenance.
- NP322542.RAYaWBP3w9bhz6ZGijZhYDsMAowy0G43D2E4f5Zm-fCow130_assertion description "[These findings establish cathepsin B as a contributor to the apoptotic phenotype of cystatin B-deficient mice and humans with EPM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322542.RAYaWBP3w9bhz6ZGijZhYDsMAowy0G43D2E4f5Zm-fCow130_provenance.
- NP322554.RAQe04QK-USFotnjA8VXuSjR6R3DJ-OwpRmqHMTR2rWd8130_assertion description "[With the exception of some lymphoblastic lymphomas, high-grade B-cell lymphomas normally expressed the pan B-cell antigens CD19 and CD22 but only immunoblastic lymphomas consistently expressed the pan B marker CD20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322554.RAQe04QK-USFotnjA8VXuSjR6R3DJ-OwpRmqHMTR2rWd8130_provenance.
- NP322558.RAZoPOvR7tCM2E9BHsMINKY4fEQSVtjcu7TQIZNYJ3wvw130_assertion description "[This family, the third reported with homozygous PARK9 mutations and the first with mutations in two genes for atypical juvenile parkinsonism, illustrates that PARK9-linked disease might display wide intra-familial clinical variability and milder phenotypes, suggesting the existence of strong, still unknown, modifiers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322558.RAZoPOvR7tCM2E9BHsMINKY4fEQSVtjcu7TQIZNYJ3wvw130_provenance.
- NP322560.RAV4KsKizrVHX34yVs188_CWWxMA1hX1VJrKzU0JPAAnk130_assertion description "[Because the surface marker CD66c (also known as carcinoembryonic antigen-related cell adhesion molecule 6) has demonstrated promise as a therapeutic target in pancreatic malignancy, the authors evaluated its potential as a target for stem cell-directed treatment of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322560.RAV4KsKizrVHX34yVs188_CWWxMA1hX1VJrKzU0JPAAnk130_provenance.
- NP322562.RAbqZtvjP_jqMJeiABnaExOgvWGUQYvBmyshtXhvws9yw130_assertion description "[Taken together, AP-1 activation by both the ERK pathway and the p38 MAPK pathway as well as their binding to TRE at position -69 to -63 in proximal promoter and TRE at position -2276 to -2270 in enhancer region is altogether essential in induction of MCP-1 mRNA in HUVEC infected with O. tsutsugamushi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322562.RAbqZtvjP_jqMJeiABnaExOgvWGUQYvBmyshtXhvws9yw130_provenance.
- NP322563.RAUh-hPVMzHkVHGoQqbNG1XSMwOyc90_6eqZ_1frwLfi8130_assertion description "[In the ADHD patients, ANCOVA revealed that there were no significant differences in the subscales and total score between the ADHD probands with the CC genotype and those with the CG and GG genotypes in ARS and the Continuous Performance Test (CPT) when adjusting for age and gender.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322563.RAUh-hPVMzHkVHGoQqbNG1XSMwOyc90_6eqZ_1frwLfi8130_provenance.
- NP322565.RAWsMBDwxdWtp1HexrfwO2kroBMmntxPL-5xvDo9AdmCM130_assertion description "[ADP-ribosyltransferases (ARTs) transfer ADP-ribose from NAD to arginine, asparagine, or cysteine residues in target proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322565.RAWsMBDwxdWtp1HexrfwO2kroBMmntxPL-5xvDo9AdmCM130_provenance.
- NP322568.RASGm57bvjNkaqIi0_mD_04KxlKhUKtN2r3n8B7pXFgvg130_assertion description "[A genetic polymorphism (C161T) at exon 6 of PPAR gamma gene (PPARG) was reported to be associated with the onset of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322568.RASGm57bvjNkaqIi0_mD_04KxlKhUKtN2r3n8B7pXFgvg130_provenance.
- NP322572.RAT3J4idhIRIalYqX0wwtbwj7srhW_DRT_3XfrtlZHlYQ130_assertion description "[Stage-specific expression of androgen receptor, follicle-stimulating hormone receptor, and anti-Müllerian hormone type II receptor in single, isolated, human preantral follicles: relevance to polycystic ovaries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322572.RAT3J4idhIRIalYqX0wwtbwj7srhW_DRT_3XfrtlZHlYQ130_provenance.
- NP322574.RAbZn9G7lWXNv2ECgbjd_SsO35kRRJSJFVP-fTvcFAA9w130_assertion description "[The aim of this study was to evaluate the predictive utility of Insulin-like growth factor-1 receptor (IGF1R), IGF1, IGF2, Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and of hemoglobin levels for tumor response to exclusive radiotherapy, in patients with locally advanced Human papillomavirus (HPV) 16-positive cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322574.RAbZn9G7lWXNv2ECgbjd_SsO35kRRJSJFVP-fTvcFAA9w130_provenance.
- NP322580.RAZolZywtswXyYRe3UBXCTjy-UM6319rll86K8ast7Tdg130_assertion description "[We identified CD23, CD58, and IL6, as molecules expressed at early times after EBV-infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322580.RAZolZywtswXyYRe3UBXCTjy-UM6319rll86K8ast7Tdg130_provenance.
- NP322581.RAYFYysOB3VrWxBT55byuFm9314cEYtBY8nfkrhaC9gJ0130_assertion description "[Differential expression of S100 gene family in human esophageal squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322581.RAYFYysOB3VrWxBT55byuFm9314cEYtBY8nfkrhaC9gJ0130_provenance.
- NP322583.RAWXDdW_Hxbsd2qOi9A8OTSE_H0ZY_AibqsKyFCDMUHS0130_assertion description "[The HLA-DRB1*0301-DQB1*0201 haplotype and IL-10 participate in the histopathological progression of SS, autoantibody production, and clinical manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322583.RAWXDdW_Hxbsd2qOi9A8OTSE_H0ZY_AibqsKyFCDMUHS0130_provenance.
- NP322589.RAUoIWmbD2vsI-5UE-flMWxaJezkkr8cLJUtnxl5momJk130_assertion description "[Both TAM infiltration alone and concomitant infiltration of TAM&T(M) are associated with improved DFS/OS, suggesting that TAM could protect HCC patients from recurrence/metastasis and prolong survival by distinct mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322589.RAUoIWmbD2vsI-5UE-flMWxaJezkkr8cLJUtnxl5momJk130_provenance.
- NP322593.RAToarxNpsVsfRvg1ER88tkeGWfQn5M8yYeFWwZ__bg74130_assertion description "[DNA hypermethylation on multiple CpG islands associated with increased DNA methyltransferase DNMT1 protein expression during multistage urothelial carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322593.RAToarxNpsVsfRvg1ER88tkeGWfQn5M8yYeFWwZ__bg74130_provenance.
- NP322601.RATeQsj8JgH1q-Zh9yX5Hh47pcKx1-IvJ0wG5QG90Qd9k130_assertion description "[A meta-review of the literature on familial PTC (FPTC) was undertaken, and characteristics of families with frequent occurrence of PTC or MNG (or both) were summarized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322601.RATeQsj8JgH1q-Zh9yX5Hh47pcKx1-IvJ0wG5QG90Qd9k130_provenance.
- NP322602.RARgRANluiuF9TXWDGHUHndplrdMxCIjvPOnViXyjFCks130_assertion description "[Patients consisted of 1953 participants enrolled in the Sequenced Treatment Alternatives to Relieve Depression study (STAR*D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322602.RARgRANluiuF9TXWDGHUHndplrdMxCIjvPOnViXyjFCks130_provenance.
- NP322604.RAeQuTlRTXkeahBXfzH0D0tEMLfRxxmmYA2IRf_0ITfyQ130_assertion description "[The aim of this study was to assess whether the C(-260)T polymorphism in the promoter of the CD14 receptor gene is associated with a higher prevalence of acute coronary syndromes (ACS) and severity of coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322604.RAeQuTlRTXkeahBXfzH0D0tEMLfRxxmmYA2IRf_0ITfyQ130_provenance.