Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP181158.RAYd8sofcAc4sdSrK-rHh0jXIBuo1BBc2pKbOPttqTTZc130_assertion description "[Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181158.RAYd8sofcAc4sdSrK-rHh0jXIBuo1BBc2pKbOPttqTTZc130_provenance.
- NP181161.RAUuvXnvCeOa0HvdI45TCvI8SrNPtaY_B80URAnNTFDBI130_assertion description "[We report on a novel LMNA mutation (p.R471G) in a proband affected by a syndrome comprising partial lipodystrophy, insulin-resistant diabetes, acanthosis nigricans, liver steatosis, muscle weakness, and contractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181161.RAUuvXnvCeOa0HvdI45TCvI8SrNPtaY_B80URAnNTFDBI130_provenance.
- NP181165.RAdBfva3bViLAtRsOTSyqi8pCLU88DlR_43qeOyUJ5n8s130_assertion description "[We conclude that many of the genes within the CDR associated with the 5q- syndrome exhibit significantly decreased expression and that SPARC, as a potential tumor suppressor gene, may play a role in the pathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181165.RAdBfva3bViLAtRsOTSyqi8pCLU88DlR_43qeOyUJ5n8s130_provenance.
- NP181168.RAatcgI7I1MUCMMaonLtN9YNnM_EhxjY0OzjFOSfv-f1M130_assertion description "[To study the relationship between low birth weight and the presence of gestational diabetes mellitus (GDM) or peripheral insulin resistance during pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181168.RAatcgI7I1MUCMMaonLtN9YNnM_EhxjY0OzjFOSfv-f1M130_provenance.
- NP181178.RAcrFJEvDymlhlGcyps75RSspLF8XWFE2dsXCqR_8R_lQ130_assertion description "[We have previously shown that increases in astrocytic monoamine oxidase-B (MAO-B) expression, mimicking that which occurs with aging and in neurodegenerative disease, in a doxycycline (dox)-inducible transgenic mouse model evokes neuropathological similarities to what is observed in the human parkinsonian brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181178.RAcrFJEvDymlhlGcyps75RSspLF8XWFE2dsXCqR_8R_lQ130_provenance.
- NP181184.RASsl7A5ZALaOK95ZjolakpmsD_HPImZLlcA3ORvWduPs130_assertion description "[CKIT mutation in therapy-related acute myeloid leukemia with MLLT3/MLL chimeric transcript from t(9;11)(p22;q23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181184.RASsl7A5ZALaOK95ZjolakpmsD_HPImZLlcA3ORvWduPs130_provenance.
- NP181186.RAXJ2HhYmsYJl1el0S12Vaiqyy_NVeVZDmm-canlWpaXo130_assertion description "[Genetic study of common variants at the Apo E, Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181186.RAXJ2HhYmsYJl1el0S12Vaiqyy_NVeVZDmm-canlWpaXo130_provenance.
- NP181187.RAfxVdT8CmB61j_yW9KmKXuGKnwJOrNh3obiypnsn11gs130_assertion description "[Here we have identified TRK-fused gene (TFG) as a new ALK partner in 2 ALCL, 1 of which exhibited a t(2;3)(p23;q21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181187.RAfxVdT8CmB61j_yW9KmKXuGKnwJOrNh3obiypnsn11gs130_provenance.
- NP181190.RARYPImjSO9qTs2bgm2V3FTU1ED2sjXmwXFAyB85KblLo130_assertion description "[Patients carrying CYP2D6*10/*10 and heterozygous null allele (IM) showed higher risks of developing recurrence and metastasis (OR 13.14; 95% CI 1.57-109.94; P = 0.004) than patients with CYP2D6*1/*1 and *1/*10 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181190.RARYPImjSO9qTs2bgm2V3FTU1ED2sjXmwXFAyB85KblLo130_provenance.
- NP181193.RAaXKDTZXWc8bMCulb7sP-KQ8c7Ab-UV_KqNaUW2Sfmmc130_assertion description "[There was a 13-year difference in the age at onset of dementia in DS associated with the number of tetranucleotide repeat alleles in APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181193.RAaXKDTZXWc8bMCulb7sP-KQ8c7Ab-UV_KqNaUW2Sfmmc130_provenance.
- NP181194.RAcK0oN4z3fAH1gCMcOwZfqgjcMo1BKrkzVX98hvUlpAs130_assertion description "[These results strongly suggest that MRP and gamma-GCS genes are coordinately up-regulated during colorectal carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181194.RAcK0oN4z3fAH1gCMcOwZfqgjcMo1BKrkzVX98hvUlpAs130_provenance.
- NP181202.RAW52WU-FnuQCo6_GyITmUqidc0dBGgv9yXGl2H8Xdwtk130_assertion description "[The aim of this study was to determine the distribution of angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism, and its effects on clinical, laboratory, histological findings, treatment responses and progression to end-stage renal disease in childhood idiopathic nephrotic syndrome (NS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181202.RAW52WU-FnuQCo6_GyITmUqidc0dBGgv9yXGl2H8Xdwtk130_provenance.
- NP181203.RAQn0fgp8nrIdXSczwBkQEnWrHMtA-BBZ_AJRBFLu5FU0130_assertion description "[Downregulation of the KIP family members p27(KIP1) and p57(KIP2) by SKP2 and the role of methylation in p57(KIP2) inactivation in nonsmall cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181203.RAQn0fgp8nrIdXSczwBkQEnWrHMtA-BBZ_AJRBFLu5FU0130_provenance.
- NP181206.RAaThSTAsgEkC16havAqPbRtTqU0DLcIUkxerqd3pZG1o130_assertion description "[We present a restriction fragment length polymorphism (RFLP) analysis of 29 benign and 30 malignant prostatic tumors, using polymorphic DNA probes to the putative tumor suppressor genes DCC (Deleted in Colorectal Carcinoma; chromosome 18q21.3), nm23-H1 (17q21.3), APC (Adenomatous Polyposis Coli; 5q21) and p53 (17p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181206.RAaThSTAsgEkC16havAqPbRtTqU0DLcIUkxerqd3pZG1o130_provenance.
- NP181207.RARWsIU9GyZoi0Qfj1ej2YkM-W_RBo0P-UQ-974XlwaO8130_assertion description "[CD133 silencing inhibits stemness properties and enhances chemoradiosensitivity in CD133-positive liver cancer stem cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181207.RARWsIU9GyZoi0Qfj1ej2YkM-W_RBo0P-UQ-974XlwaO8130_provenance.
- NP181208.RAQod93SppE-P2j7yjjNbpPMxNOrGjML1zuRBiFRqCGeI130_assertion description "[The MLL-ENL fusion was not detectable in blood at the time of ALL diagnosis or after 0.7, 2, 8, 10, and 12 months of therapy but was detectable in blood at 16 months (one in 2.3 x 10(4) cells).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181208.RAQod93SppE-P2j7yjjNbpPMxNOrGjML1zuRBiFRqCGeI130_provenance.
- NP181210.RAf96Qn8Gqkf1hZlvXhBFUCG12dJE2QhS1SmzG0eFqHvw130_assertion description "[DTD was purified from rat liver cytosol and from Escherichia coli in which rat liver or human lung tumor DTD complementary DNA was expressed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181210.RAf96Qn8Gqkf1hZlvXhBFUCG12dJE2QhS1SmzG0eFqHvw130_provenance.
- NP181211.RAVa_KyYhqpITiOtkRkful7e6wgFKJwVAB1UqCugbW_gA130_assertion description "[Portuguese-type amyloidosis is an autosomal dominant condition caused by a point mutation of the prealbumin (transthyretin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181211.RAVa_KyYhqpITiOtkRkful7e6wgFKJwVAB1UqCugbW_gA130_provenance.
- NP181212.RAQumtOifBuzfDIIQfpCxHCgubz5Z_yaUypG2HC2fFTzM130_assertion description "[Upregulation of CD14 in Kupffer cells and hyperreactivity against low-dose LPS were observed in high-fat diet (HFD)-induced steatosis mice, but not chow-fed-control mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181212.RAQumtOifBuzfDIIQfpCxHCgubz5Z_yaUypG2HC2fFTzM130_provenance.
- NP181215.RAfmausqh6bQ0B7ryBeEA-nff6qMRI_4QKhYOYxOVVD8Q130_assertion description "[Here, we scanned the genome for putative miR-200 binding sites and found them in the 3'-untranslated region (3'-UTR) of 35 genes that are amplified in human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181215.RAfmausqh6bQ0B7ryBeEA-nff6qMRI_4QKhYOYxOVVD8Q130_provenance.
- NP181223.RAZwHWjTPNnirRKykbv0U1ZG7cBu74bCzE2dojKBjLB7M130_assertion description "[In the case of the arrhythmogenic disorders, the long QT syndromes and Brugada syndrome, mutations have been described in a number of ion channel proteins, including cardiac potassium (KVLQT1, HERG and minK) and sodium (SCN5A) channels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181223.RAZwHWjTPNnirRKykbv0U1ZG7cBu74bCzE2dojKBjLB7M130_provenance.
- NP181227.RAQ9ulIDTWNZu74tMLK5CnXf0e9dq43kEt6aziSavvuZs130_assertion description "[A correlation between MMP-9 and ALOX5 protein expression was established by immunohistochemical analysis of PTC and normal thyroid tissues using a tissue array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181227.RAQ9ulIDTWNZu74tMLK5CnXf0e9dq43kEt6aziSavvuZs130_provenance.
- NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_assertion description "[To evaluate the prognostic value of genetic mutations for acute myeloid leukemia (AML) patients, we examined the gene status for both fusion products such as AML1 (CBFα)-ETO, CBFβ-MYH11, PML-RARα, and MLL rearrangement as a result of chromosomal translocations and mutations in genes including FLT3, C-KIT, N-RAS, NPM1, CEBPA, WT1, ASXL1, DNMT3A, MLL, IDH1, IDH2, and TET2 in 1185 AML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_provenance.
- NP181248.RAU6n8_rxgcttfpNLCvBztrKTBOIaTucDAphboMbuUqWg130_assertion description "[DRD2/ANKK1 TaqIA genotype distribution is significantly associated to AD (O.R.=1.551, p=0.023), with A1* allele displaying an O.R.=1.403 (p=0.029).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181248.RAU6n8_rxgcttfpNLCvBztrKTBOIaTucDAphboMbuUqWg130_provenance.
- NP181252.RAbcqRi-A0XJOVs_GFLEQs3srBKOzH5gRRsfMiTCPetwM130_assertion description "[APS-1 is characterized by presence of chronic candidiasis, chronic hypoparathyroidism, Addison's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181252.RAbcqRi-A0XJOVs_GFLEQs3srBKOzH5gRRsfMiTCPetwM130_provenance.
- NP181254.RAaOIX8IA9BP_NCsqtgMCWJXEh4HOxmEONssJo5qBSjuU130_assertion description "[Here we investigated whether SFRP2 is also implicated in human breast cancer, and if so whether SFRP2 promoter methylation might serve as a potential tumor biomarker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181254.RAaOIX8IA9BP_NCsqtgMCWJXEh4HOxmEONssJo5qBSjuU130_provenance.
- NP181255.RAds5NxYkESE5rdwM4ILStkMGzMG-kt7BGMJYje7kNsTE130_assertion description "[Mutations resulting in reduced or completely abrogated serotonin-transporter (SERT) function in mice have led to the identification of more than 50 different phenotypic changes, ranging from increased anxiety and stress-related behaviours to gut dysfunction, bone weakness and late-onset obesity with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181255.RAds5NxYkESE5rdwM4ILStkMGzMG-kt7BGMJYje7kNsTE130_provenance.
- NP181258.RAYeYQp2A7DqyQuLs8DfytqqhDPrNKE9ZMmUrvxGNKp8k130_assertion description "[Cryptorchidism and semen quality: a TEM and molecular study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181258.RAYeYQp2A7DqyQuLs8DfytqqhDPrNKE9ZMmUrvxGNKp8k130_provenance.
- NP181259.RAaz0U4jVXnNMZeKP80_qsLXinfNlDZNY6SnA4WDrHZ5Y130_assertion description "[Evidence suggests that lead and selected genes known to modify the toxicokinetics of lead--namely, those for the vitamin D receptor (VDR) and delta-aminolevulinic acid dehydratase (ALAD)--may independently influence blood pressure and hypertension risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181259.RAaz0U4jVXnNMZeKP80_qsLXinfNlDZNY6SnA4WDrHZ5Y130_provenance.
- NP181260.RAXUVBh7vg2NqABaMh3V7Bba-yCb5OP7k_F17HTfZPGvQ130_assertion description "[To clarify the tissue specificity of the expression of C4A and C4B genes, human monocytoid cell line U937 and hepatoma-derived HepG2 cells were studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181260.RAXUVBh7vg2NqABaMh3V7Bba-yCb5OP7k_F17HTfZPGvQ130_provenance.
- NP181263.RAc3cQB_WSJF_UOGwJZerzaRC70s_P9dtt85n9xoTTx5w130_assertion description "[Children with HbS and hereditary persistence of fetal hemoglobin (S/HPFH) had essentially 100% F cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181263.RAc3cQB_WSJF_UOGwJZerzaRC70s_P9dtt85n9xoTTx5w130_provenance.
- NP181268.RAT2Q20a3dGo38OifLnxuX2x6iSU3GSXBbxr5ljkPsfk8130_assertion description "[The percentage of peripheral CD4(+)CD25(+)CD127(low) Tregs and the expression of FoxP3 mRNA were significantly increased in elderly patients with NSCLC comparing with the other groups and in elderly healthy individuals compared with young healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181268.RAT2Q20a3dGo38OifLnxuX2x6iSU3GSXBbxr5ljkPsfk8130_provenance.
- NP181270.RAcCHuFK_GfHvx2nofhzT9ytAVMlssLXX6YKg-t-WS934130_assertion description "[KRT19, CEACAM5, EPCAM, DSG3, SFTPA, SFTPC and SFTPB mRNA levels were initially validated by real-time reverse transcription PCR-based quantification in 16 NSCLC tumors and 22 LNs and 12 PB samples from individuals without known cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181270.RAcCHuFK_GfHvx2nofhzT9ytAVMlssLXX6YKg-t-WS934130_provenance.
- NP181271.RAclzVvUk4TLjwPPZOPHaUir41fJ45gK-Cz8S-KQ19GMw130_assertion description "[The mutation increases endoplasmic reticulum stress and induces apoptotic cell death compared with wild-type SP-C in alveolar type II cells, supporting the significance of this mutation in the pathogenesis of pulmonary fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181271.RAclzVvUk4TLjwPPZOPHaUir41fJ45gK-Cz8S-KQ19GMw130_provenance.
- NP181272.RASool5gGy5dK0vDJune2oTtsOd4tnh1Mo_T8sxjZ3d8I130_assertion description "[Adult non-insulin requiring diabetes includes latent autoimmune diabetes of adults (LADA), distinguished from type 2 diabetes by the presence of islet autoantibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181272.RASool5gGy5dK0vDJune2oTtsOd4tnh1Mo_T8sxjZ3d8I130_provenance.
- NP181276.RARR9TWFVruVSScVCDsX7Lir7OSBCuO5dgRPvJb3CrULA130_assertion description "[Mutations in KCNJ11, ABCC8, or INS are the cause of permanent neonatal diabetes mellitus in about 50% of patients diagnosed with diabetes before 6 months of age and in a small fraction of those diagnosed between 6 and 12 months.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181276.RARR9TWFVruVSScVCDsX7Lir7OSBCuO5dgRPvJb3CrULA130_provenance.
- NP181278.RAYEjONQL0mg8N78bbde-OfDdmroz9k369DlFXqj8BMTY130_assertion description "[We administered plasmid DNA encoding the gp100 melanoma-melanocyte differentiation antigen to 22 patients with metastatic melanoma and evaluated immunologic and clinical responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181278.RAYEjONQL0mg8N78bbde-OfDdmroz9k369DlFXqj8BMTY130_provenance.
- NP181281.RAQ03GuA2xodruxJv_kyM_ozVwTPu2_9PhvrdGLh4V2pM130_assertion description "[Missense mutations in the small heat shock protein HSPB8 cause distal hereditary motor neuropathy (dHMN) and axonal Charcot-Marie-Tooth disease (CMT2L).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181281.RAQ03GuA2xodruxJv_kyM_ozVwTPu2_9PhvrdGLh4V2pM130_provenance.
- NP181285.RASLjVsWR9pBbhMTaN4UdDKnDiNOCpK48HQX4-IfZAoZE130_assertion description "[Further oxidation of this substrate by the fatty alcohol:nicotinamide-adenine dinucleotide oxidoreductase (FAO) enzyme complex, in which one component, ALDH3A2, is known to be mutated in Sjögren-Larsson syndrome (characterized by ichthyosis and spastic paraplegia), would lead to 20-carboxy-(R)-trioxilin A3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181285.RASLjVsWR9pBbhMTaN4UdDKnDiNOCpK48HQX4-IfZAoZE130_provenance.
- NP181290.RAZArnuVJIpl6pK5yCLiZ2KWV_zAC0sLbEmbPHUHnqw_Q130_assertion description "[Implication of the proliferation and apoptosis associated CSE1L/CAS gene for breast cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181290.RAZArnuVJIpl6pK5yCLiZ2KWV_zAC0sLbEmbPHUHnqw_Q130_provenance.
- NP181294.RAfIFsXwD9iIH97vbO9Uty0HMOrkfu-oNYtmb08ix2AsQ130_assertion description "[The transmembrane serine protease hepsin is one of the most highly upregulated genes in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181294.RAfIFsXwD9iIH97vbO9Uty0HMOrkfu-oNYtmb08ix2AsQ130_provenance.
- NP181296.RAbIGPbxW7iVFes1esXFJ4a1q4YjkMd40dYx-SPB5qveM130_assertion description "[Tau-mediated nuclear depletion and cytoplasmic accumulation of SFPQ in Alzheimer's and Pick's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181296.RAbIGPbxW7iVFes1esXFJ4a1q4YjkMd40dYx-SPB5qveM130_provenance.
- NP181303.RASsSchwziel59a918TC1B9PlyOY_uq8HGgizSQwofDv4130_assertion description "[APEX1 Asp148Glu gene polymorphism is a risk factor for lung cancer in relation to smoking in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181303.RASsSchwziel59a918TC1B9PlyOY_uq8HGgizSQwofDv4130_provenance.
- NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_assertion description "[A functional SNP of the EP2 gene associated with risk of AIA should decrease the transcription level, resulting in reduction of the PGE(2) braking mechanism of inflammation and involvement in the molecular mechanism underlying AIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_provenance.
- NP181321.RAeXTFXTCFOBq03J8gigAAtGlZnOqL6ICtMsEAQD6IGyw130_assertion description "[Serosubtype III-2/multilocus sequence type (ST)-17 represents a virulent clone which is significantly associated with late onset GBS neonatal infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181321.RAeXTFXTCFOBq03J8gigAAtGlZnOqL6ICtMsEAQD6IGyw130_provenance.
- NP181323.RAQAKsnzxz0vYEKzDPkrvk-JKVttvI0tXpWBHjV1vCFpE130_assertion description "[Here we show that UV-induced RPA-p34 hyperphosphorylation depends on expression of ATM, the product of the gene mutated in the human genetic disorder ataxia telangiectasia (A-T).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181323.RAQAKsnzxz0vYEKzDPkrvk-JKVttvI0tXpWBHjV1vCFpE130_provenance.
- NP181327.RAVYihgYmTQliI2Tlq4J7w3XzQPuE5zdlQK4lFZgDluIo130_assertion description "[The expression of the hsp27 gene was enhanced in one-half the patients with common acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181327.RAVYihgYmTQliI2Tlq4J7w3XzQPuE5zdlQK4lFZgDluIo130_provenance.
- NP181329.RAcX0G9HiSn_hHBXRvuuDhoxKz8kjQl3q9Yzwv9wAvwoA130_assertion description "[Although none of these SNPs individually had a significant effect on risk of SCCHN, nor did their combined putative risk genotypes (i.e., MDM2 SNP309 GT + GG, 2164 AA, and p53 codon 72 CC), we found that individuals with two to three risk genotypes had significantly increased risk of non-oropharyngeal cancer (OR = 1.42; 95% CI = 1.07-1.88).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181329.RAcX0G9HiSn_hHBXRvuuDhoxKz8kjQl3q9Yzwv9wAvwoA130_provenance.
- NP181330.RAbnUAY0KPRisfolwO0vaFlzt7GtvFO-kCDwasBjGmdlQ130_assertion description "[High expression of spindle assembly checkpoint proteins CDC20 and MAD2 is associated with poor prognosis in urothelial bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181330.RAbnUAY0KPRisfolwO0vaFlzt7GtvFO-kCDwasBjGmdlQ130_provenance.
- NP181341.RAdqPGn-olvc6T10BehFiN4oQNEgQWfZVLBLq6oC7JznY130_assertion description "[EML4-ALK fusion gene and efficacy of an ALK kinase inhibitor in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181341.RAdqPGn-olvc6T10BehFiN4oQNEgQWfZVLBLq6oC7JznY130_provenance.
- NP181348.RAWZ0sXC859dMDB9TsUAEuF6aIINSQ6Q-swpOWsey5eSQ130_assertion description "[Hypothalamic leptin and INS levels and OB-R gene expression were significantly lower in obese rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181348.RAWZ0sXC859dMDB9TsUAEuF6aIINSQ6Q-swpOWsey5eSQ130_provenance.
- NP181355.RAZoKJBpKYLNtsNO07x7uf229NRl85IsEihsFs0quOaro130_assertion description "[Patients with progressive aortic disease had higher levels of Macrophage Colony Stimulating Factor (M-CSF) in blood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181355.RAZoKJBpKYLNtsNO07x7uf229NRl85IsEihsFs0quOaro130_provenance.
- NP181358.RAdunGSPvhNzoZjjLOBY6NDyq9CHzgRihLKVNA3at9XN0130_assertion description "[We therefore investigated the role of TNF-α and found that it supports survival of CML SPCs by promoting nuclear factor κB/p65 pathway activity and expression of the interleukin 3 and granulocyte/macrophage-colony stimulating factor common β-chain receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181358.RAdunGSPvhNzoZjjLOBY6NDyq9CHzgRihLKVNA3at9XN0130_provenance.
- NP181359.RAc6vmjOzwZlPNBGTzPlYENUUsWfkjuuQ6fcJPRahHn18130_assertion description "[Mammalian target of rapamycin (mTOR) regulates cellular proliferation and tumor growth in urothelial carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181359.RAc6vmjOzwZlPNBGTzPlYENUUsWfkjuuQ6fcJPRahHn18130_provenance.
- NP181364.RAaMfvll-7EKVcidx2v_--g_LfxrAkASI82FdOiIHaBww130_assertion description "[Cellular responses in gastric inflammation are mediated by lipopolysaccharide of H. pylori, which activate monocytes to express cytokine expression and growth factors via CD14 and toll-like receptor 4 (TLR4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181364.RAaMfvll-7EKVcidx2v_--g_LfxrAkASI82FdOiIHaBww130_provenance.
- NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_assertion description "[The c.-1973T >C polymorphism located in the SERPINA1 promoter region is found more frequent in A1AT deficiency patients with liver disease compared to patients with pulmonary disease, but data are lacking regarding contribution to the development of liver diseases caused by other aetiologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_provenance.
- NP181367.RAQeBOX5_hEM_TuBzaFbh4q0xqfnALhvDY0q3SAjOuD48130_assertion description "[AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181367.RAQeBOX5_hEM_TuBzaFbh4q0xqfnALhvDY0q3SAjOuD48130_provenance.
- NP181369.RAc8NZJ6nKLJduCCdVBGbWhbpLMvL-IVvvpv7M_dMYdzA130_assertion description "[Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181369.RAc8NZJ6nKLJduCCdVBGbWhbpLMvL-IVvvpv7M_dMYdzA130_provenance.
- NP181373.RAbgOQqk1FD1iE9XyUensw5y2JzH1MUOvfVCcOY74jYag130_assertion description "[No significant association with prostate cancer was observed for polymorphic variants in SOD3 or SOD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181373.RAbgOQqk1FD1iE9XyUensw5y2JzH1MUOvfVCcOY74jYag130_provenance.
- NP181374.RAVZkq_hgionKfQwZTl8JpTnGaPRm3ctsrX_gczvtzFBw130_assertion description "[The SFRP1 promoter was found to be highly methylated in 95% (19/20) of the ESCC tissues and in nine ESCC cell lines, compared with 65% (13/20) of the paired nontumor tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181374.RAVZkq_hgionKfQwZTl8JpTnGaPRm3ctsrX_gczvtzFBw130_provenance.
- NP181378.RAXY8h1ZLDkg7Yw-0DPvKRQsjrYQD_PgSbnJ4HDW3JQs4130_assertion description "[Hemoglobin Denver [alpha 2 beta 2(41) (C7) Phe-->Ser]: a low-O2-affinity variant associated with chronic cyanosis and anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181378.RAXY8h1ZLDkg7Yw-0DPvKRQsjrYQD_PgSbnJ4HDW3JQs4130_provenance.
- NP181381.RAc2Cq9djsilh0gMqKYXZ9YvVSadrI6FB0yqBdbS7gu8U130_assertion description "[We evaluated the effect of meat consumption and cigarette smoking in combination with N-acetyltransferases 1 and 2 (NAT1 and NAT2), and glutathione S-transferase M1 (GSTM1) genotypes on colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181381.RAc2Cq9djsilh0gMqKYXZ9YvVSadrI6FB0yqBdbS7gu8U130_provenance.
- NP181382.RAXs0F_GjGm__9s36a2Ph99lcdpbxSKL38bSiz96A-z0E130_assertion description "[Molecular biologists have identified two distinct pathways, microsatellite instability (MSI) and chromosomal instability (CIN), which are involved in CRC progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181382.RAXs0F_GjGm__9s36a2Ph99lcdpbxSKL38bSiz96A-z0E130_provenance.
- NP181390.RARFHnJ8mvYLErIJc3ejH9MewX4nwQCboOdzucHoEe5Qc130_assertion description "[Anti-TNC antibodies, already used successfully in clinical trials to treat malignant human gliomas, may be an appropriate new therapeutic strategy for NF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181390.RARFHnJ8mvYLErIJc3ejH9MewX4nwQCboOdzucHoEe5Qc130_provenance.
- NP181392.RATcoJ_NOm6OrmOGsvQQjgs836wy-AoiYgK-78I1iHm8U130_assertion description "[Taken together, these findings suggest attenuation of G1-arrest is related to the differentiation status of neuroblastomas and occurs downstream of p53 nuclear accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181392.RATcoJ_NOm6OrmOGsvQQjgs836wy-AoiYgK-78I1iHm8U130_provenance.
- NP181399.RAdEkO2DFoIlOIopss9FvAm3NN97lgAX81yXq2zBNFVlk130_assertion description "[Analysis of type 1 diabetes-susceptible HLA alleles revealed high frequencies of the B54 and DRB1*0405 allele, but not the B61 and DRB1*0901 alleles, in the high-titer subgroup, whereas the frequency of the protective DRB1*1502 allele was decreased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181399.RAdEkO2DFoIlOIopss9FvAm3NN97lgAX81yXq2zBNFVlk130_provenance.
- NP181403.RAdLmkh1wn5EdljGc-j91Z_asIGjf0gAfa25_futjOIrw130_assertion description "[We found three different unreported mutations 689delT, 857del17, corresponding to two macular dystrophy families and G208D in a retinitis pigmentosa (RP) family giving us a proportion of about 20% of RDS mutations in autosomal dominant Spanish macular dystrophies and 3% in ADRP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181403.RAdLmkh1wn5EdljGc-j91Z_asIGjf0gAfa25_futjOIrw130_provenance.
- NP181404.RAdGf050dvhIJbzXFmS50OrCgJNW6MYj1IupUnPE3g-JE130_assertion description "[Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181404.RAdGf050dvhIJbzXFmS50OrCgJNW6MYj1IupUnPE3g-JE130_provenance.
- NP181405.RAfZN4VRmNkIAYtWwOnZ0K17BaAkcD6Qi_ZJ1mp_e8kp8130_assertion description "[Bcr-Abl efficiently induces a myeloproliferative disease and production of excess interleukin-3 and granulocyte-macrophage colony-stimulating factor in mice: a novel model for chronic myelogenous leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181405.RAfZN4VRmNkIAYtWwOnZ0K17BaAkcD6Qi_ZJ1mp_e8kp8130_provenance.
- NP181407.RAVubE8Kv2CDv7rBxiqNVnoiIddbeNMMOlbmLydwZX0nc130_assertion description "[To investigate the potential interaction between folate intake and the paraoxonase 1 (PON1) Q192R polymorphism with the risk of incident coronary heart disease (CHD) and ischemic stroke in the Atherosclerosis Risk in Communities study, a population-based prospective cohort of cardiovascular disease in 15,792 white and African-American subject.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181407.RAVubE8Kv2CDv7rBxiqNVnoiIddbeNMMOlbmLydwZX0nc130_provenance.
- NP181410.RAYa7n-_aIyWN1hL4uR74sBbwo-MQWWE-vnNghJ347Y-E130_assertion description "[alpha-Globin gene triplications may exacerbate the alpha chain and beta chain imbalance in beta-thalassemia (beta-thal) and may compensate for the effect of alpha-globin gene deletion in alpha-thal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181410.RAYa7n-_aIyWN1hL4uR74sBbwo-MQWWE-vnNghJ347Y-E130_provenance.
- NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_assertion description "[The ESCC and EAC genomes showed some copy number abnormalities with similar frequencies (eg, CDKN2A, EGFR, KRAS, MYC, CDK6, MET) but also many copy number abnormalities with different frequencies between histologic types, most of which were amplification events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_provenance.
- NP181421.RAbkVhJLmcTrfLqTU880QyptBLD6OOWKym1nEku3rqpYM130_assertion description "[Failure of detection of the tyrosine to histidine substitution at the residue 33 of thymidylate synthase in human colorectal cancer. A preliminary study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181421.RAbkVhJLmcTrfLqTU880QyptBLD6OOWKym1nEku3rqpYM130_provenance.
- NP181423.RASsOGehGnc7vdZWVHhz_1f1e9LJ0ygmy_RLlYFMXxQm8130_assertion description "[However, tumor-specific stroma of hepatocellular carcinomas showed little or no expression of HSPG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181423.RASsOGehGnc7vdZWVHhz_1f1e9LJ0ygmy_RLlYFMXxQm8130_provenance.
- NP181424.RATpRRo03ohHWWYTlDBbI3PeXgqTtLCnH2CwFKXImVP0Y130_assertion description "[In the current study, the authors investigated the association between polymorphisms in 3 genes--glutathione-S-transferase M1 (GSTM1), glutathione-S-transferase T1 (GSTT1), and XRCC1, with roles in protection from a variety of DNA-damaging agents-and the risk of subsequent malignancy in 650 survivors of HD enrolled in the Childhood Cancer Survivor Study who had received radiotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181424.RATpRRo03ohHWWYTlDBbI3PeXgqTtLCnH2CwFKXImVP0Y130_provenance.
- NP181430.RAffm-KwlMM-_RhuE3HsRxwUTzpvokOjLlZnMEMnfTU4c130_assertion description "[Furthermore, many patients with chronic hepatitis C virus infection have reactivity to an autoantigen of unknown significance known as GOR that has protein sequence homology with both hepatitis C virus nucleocapsid protein as well as HTLV-1 gag.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181430.RAffm-KwlMM-_RhuE3HsRxwUTzpvokOjLlZnMEMnfTU4c130_provenance.
- NP181432.RAQNbzUcf-7TcNp2yXDIUrKV2b2NE3F1QnVyhjfD8lJcU130_assertion description "[Thus, although p19(ARF) is required in some cell types to transmit an oncogenic response signal to p53, it is dispensable for this function in an in vivo epithelial system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181432.RAQNbzUcf-7TcNp2yXDIUrKV2b2NE3F1QnVyhjfD8lJcU130_provenance.
- NP181433.RAYeD76-ZR2Fea_yYqbvI0LXFmj8Dgwl6dbFjT1Umawls130_assertion description "[FANCE is predominantly localized in the nucleus and acts as a molecular bridge between the FA core complex and FANCD2, through direct binding of both FANCC and FANCD2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181433.RAYeD76-ZR2Fea_yYqbvI0LXFmj8Dgwl6dbFjT1Umawls130_provenance.
- NP181437.RAa4yzEdnIsA4Sjj-_1vyZJNMSJTmmgYz5QT0PW5WeOxo130_assertion description "[In the interferon (IFN) treatment of chronic hepatitis B, there is no accepted definition of virological response as measured by highly sensitive HBV DNA assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181437.RAa4yzEdnIsA4Sjj-_1vyZJNMSJTmmgYz5QT0PW5WeOxo130_provenance.
- NP181439.RAUxeaq08uwvINMUdnyAxgNDqykcSUCp25_WiEUR7LgMw130_assertion description "[We examined the promoter methylation status and LOH of the chromosome 3p genes, von Hippel-Lindau disease (VHL), retinoic acid receptor beta (RAR-beta), RAS association domain family 1A (RASSF1A), and fragile histidine triad (FHIT), in 37 samples of cervical squamous cell carcinoma and corresponding noncancerous tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181439.RAUxeaq08uwvINMUdnyAxgNDqykcSUCp25_WiEUR7LgMw130_provenance.
- NP181453.RARDiIvrnvEqgVuopB9khi8bxoJkmRjv8kkhBAP2mGAEQ130_assertion description "[This study was designed to determine the prevalence of the MTHFR mutation in Japanese patients with migraine and tension-type headache (TH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181453.RARDiIvrnvEqgVuopB9khi8bxoJkmRjv8kkhBAP2mGAEQ130_provenance.
- NP181455.RAR-d-HOA2tTwxDFDXASOHyynhz3BofucGMo4l01NSSVk130_assertion description "[Local and distant immunity induced by intralesional vaccination with an oncolytic herpes virus encoding GM-CSF in patients with stage IIIc and IV melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181455.RAR-d-HOA2tTwxDFDXASOHyynhz3BofucGMo4l01NSSVk130_provenance.
- NP181461.RAYJOfir-N7iCreEPVAkl0Ywyjy7MeZ9jKFUZKwmjyO5s130_assertion description "[We sought to study whether EAT and subcutaneous adipose tissue (SAT) adiponectin mRNA levels are similar in patients with and without MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181461.RAYJOfir-N7iCreEPVAkl0Ywyjy7MeZ9jKFUZKwmjyO5s130_provenance.
- NP181464.RAdbJpJ_8jstPQ7YJB8M8UyG_g4NCrT2OSG5tVzOM7fyA130_assertion description "[This new paradigm places EMP centrally in the process of tumour progression and metastasis, as well as modulating drug response to current forms of chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181464.RAdbJpJ_8jstPQ7YJB8M8UyG_g4NCrT2OSG5tVzOM7fyA130_provenance.
- NP181466.RARgsaSSMRonimkVLmYqeCWxueuNUlMYwJFI0HC-yh8cI130_assertion description "[TRiDAK cells reactive with autologous tumor cells could be generated in a CEA-positive gastric cancer patient with malignant ascites, in whom effector cell generation using DCs and CEA peptides had failed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181466.RARgsaSSMRonimkVLmYqeCWxueuNUlMYwJFI0HC-yh8cI130_provenance.
- NP181467.RATXN4BDGLo53Vr3y9E1NUEKEnNI5t1TxqOgXs8Lor_uc130_assertion description "[The prognostic significance of p53 aberration in hepatocellular carcinoma (HCC) remains inconclusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181467.RATXN4BDGLo53Vr3y9E1NUEKEnNI5t1TxqOgXs8Lor_uc130_provenance.
- NP181468.RAQu5weru0AMV-ESb-F8ESbgE7jKLfxUE6r1cHLFSNNG0130_assertion description "[The status of RB1, INK4A, INK4B, INK4C, INK4D, and ARF in 13 adult and 2 juvenile ovarian GCTs was determined by reverse transcription-polymerase chain reaction of total RNA and exon-specific sequencing of genomic DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181468.RAQu5weru0AMV-ESb-F8ESbgE7jKLfxUE6r1cHLFSNNG0130_provenance.
- NP181470.RAS97o7J7T6XlERZZqUk2hSmPb4IphWRtEpMvWi79U5Z0130_assertion description "[Two new mutations in the MTATP6 gene associated with Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181470.RAS97o7J7T6XlERZZqUk2hSmPb4IphWRtEpMvWi79U5Z0130_provenance.
- NP181473.RAcRyrEj3aXx5W5TmWN_wYxjN743Td0yyu0IRo7u9T6_c130_assertion description "[We discuss how specific pregnancy, labour and delivery issues for mothers with methylmalonic acidemia, homocystinuria, propionic acidemia, glutaric acidemia type 1, ornithine transcarbamylase (OTC) deficiency and 3-hydroxy-3-methylglutaric(HMG)-CoA lyase deficiency were managed and the outcome for the mother and child in each case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181473.RAcRyrEj3aXx5W5TmWN_wYxjN743Td0yyu0IRo7u9T6_c130_provenance.
- NP181480.RASBJ3_5d4UB4ezEasBeomwEAgWynQMoRrnRyLLwiW1B4130_assertion description "[The prevalence of sacroiliitis was assessed clinically and radiologically in 261/323 1st degree relatives of 47 B27 positive probands who had ankylosing spondylitis (AS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181480.RASBJ3_5d4UB4ezEasBeomwEAgWynQMoRrnRyLLwiW1B4130_provenance.
- NP181482.RAWNEP03jYmRErz5Pgi1GGW2a-SQTCS6CJqCSFynRVxwE130_assertion description "[The goal of our research was to assess the association of ACE gene I/D polymorphism with myocardial infarction in Polish population regarding different variables related to the disease (smoking, concomitant hypertension, obesity, plasma cholesterol level and family history).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181482.RAWNEP03jYmRErz5Pgi1GGW2a-SQTCS6CJqCSFynRVxwE130_provenance.
- NP181484.RAYY3jESbhNdImajcwcJNAuJHEoih8cjkXN5uUURVUcx8130_assertion description "[Comparing patients with RA to unaffected NAN controls, the Fok1 SNP was associated with RA using both genotypic [FF vs Ff vs ff: RA 20%, 54%, 26% vs control 22%, 44%, 34% (chi-square 13.35, p=0.003)] and dominant models [FF/Ff vs ff: RA 74% vs 26% control 66% vs 34% (OR 1.5, 95% CI 1.16-1.96, p=0.003)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181484.RAYY3jESbhNdImajcwcJNAuJHEoih8cjkXN5uUURVUcx8130_provenance.
- NP181485.RAYF6fhUa8s8vKbuFMPIYe9ZrxVYbcxCAs9euohAWzqCQ130_assertion description "[Chronic adrenal stimulation by ACTH in Cushing's disease or GIP in GIP-dependent ACTH-independent macronodular adrenal hyperplasia both lead to the induction of genes implicated in adrenal proliferation and steroidogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181485.RAYF6fhUa8s8vKbuFMPIYe9ZrxVYbcxCAs9euohAWzqCQ130_provenance.
- NP181488.RAQESdi2_oUROZBlAKr_052yTjrfexyZGhlzZ3AlcO-nA130_assertion description "[Taken together, these findings reveal a novel mechanism that differentially regulates p73 isoforms and underscores the role of cell-cell interaction in p73 regulation, which may advance our understanding of p73 expression and function in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181488.RAQESdi2_oUROZBlAKr_052yTjrfexyZGhlzZ3AlcO-nA130_provenance.
- NP181495.RAbBh7qdZiuaH6uwityLObcDZDFcGFwvWZMWQPfqdnBVo130_assertion description "[Previous case-control studies suggested the single nucleotide polymorphism of cyclooxygenase-2 (COX-2) gene (G-765C) is associated with coronary artery disease (CAD) and ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181495.RAbBh7qdZiuaH6uwityLObcDZDFcGFwvWZMWQPfqdnBVo130_provenance.
- NP181496.RARfjXqO13ZUc52tpxoh0wThexzeZJITTdUmRkHKNSXA4130_assertion description "[The performance of the Digene Hybrid Capture II HBV DNA Test HC II and the Roche Cobas Amplicor Monitor Test (Cobas-HBV) was evaluated on 252 serum samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181496.RARfjXqO13ZUc52tpxoh0wThexzeZJITTdUmRkHKNSXA4130_provenance.
- NP181499.RAZ1R9ok1H3ny2Qq2mJbfLSptK_Ir_o5isXt6ukPQW4aw130_assertion description "[Resected, stage III colon carcinomas from patients (N = 2,686) randomly assigned to FOLFOX ± cetuximab (North Central Cancer Treatment Group N0147 trial) were analyzed for mismatch repair (MMR) protein expression and mutations in BRAF(V600E) (exon 15) and KRAS (codons 12 and 13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181499.RAZ1R9ok1H3ny2Qq2mJbfLSptK_Ir_o5isXt6ukPQW4aw130_provenance.
- NP181506.RAbSrEDhOWtQcvOHPIFjQK9jRS6gPYx6DlS--VJl4UR4g130_assertion description "[Mutations of the survival of motor neuron gene (SMN1) are responsible for spinal muscular atrophies (SMA), a frequent recessive autosomal motor neuron disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181506.RAbSrEDhOWtQcvOHPIFjQK9jRS6gPYx6DlS--VJl4UR4g130_provenance.
- NP181508.RAUH-KpBT0IhhZTUKOGuy2G6JlCIMU5hCAoKsqdpwIeq0130_assertion description "[The sebaceous nevus: a nevus with deletions of the PTCH gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181508.RAUH-KpBT0IhhZTUKOGuy2G6JlCIMU5hCAoKsqdpwIeq0130_provenance.
- NP181513.RAYfTSStgk8kpIJgDPmMsS_FUzY89Xaia2esAWP0i8w8M130_assertion description "[Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181513.RAYfTSStgk8kpIJgDPmMsS_FUzY89Xaia2esAWP0i8w8M130_provenance.