Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP199563.RAfkA_Iq2Skh97hzWrY-B5OLV6YE5KTk1Saf-o8n-_T4U130_assertion description "[The t(14;19)(q32;q13) is a recurring translocation found in some patients with chronic lymphocytic leukemia (CLL), and the t(14;19) juxtaposes the BCL3 gene on chromosome 19 with the immunoglobulin heavy chain gene (IGH) locus on chromosome 14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199563.RAfkA_Iq2Skh97hzWrY-B5OLV6YE5KTk1Saf-o8n-_T4U130_provenance.
- NP199564.RAaBti3uaZLZyl9SLUbZWyFHMhMkEC53PJwPdrIZrSQxQ130_assertion description "[Expression of human intestinal mucin is modulated by the beta-galactoside binding protein galectin-3 in colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199564.RAaBti3uaZLZyl9SLUbZWyFHMhMkEC53PJwPdrIZrSQxQ130_provenance.
- NP199567.RAR6DvBpSEbnR5ZIQEOkdMja-KafItPGnvwsBQOzVCSwU130_assertion description "[The aim of this study was to determine whether variants of the EPPIN gene are risk factors for idiopathic male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199567.RAR6DvBpSEbnR5ZIQEOkdMja-KafItPGnvwsBQOzVCSwU130_provenance.
- NP199569.RAa0al2PIx_UEE9EYN5MQrRXSIqkYdw31q0StsJh0-L_w130_assertion description "[Our results indicate that increased p53 expression is positively correlated with increased histologic grade and with the presence of metastatic disease in patients with prostatic adenocarcinoma, and they suggest that mutations of the p53 gene may play a role in mediating the behavior of a biologically aggressive subset of this common neoplasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199569.RAa0al2PIx_UEE9EYN5MQrRXSIqkYdw31q0StsJh0-L_w130_provenance.
- NP199571.RAZ_XXe6CnkimfpEKKw5rZF6UEu9Y0K_19T2Kot7UOK_w130_assertion description "[A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199571.RAZ_XXe6CnkimfpEKKw5rZF6UEu9Y0K_19T2Kot7UOK_w130_provenance.
- NP199579.RAXLWR9wA5-_DaFBC8iHbF2EuJjCtKAvRd4eSgFgFsNlo130_assertion description "[Inactivation of TSC2 and Rb synergistically induce oxidative stress via increased protein synthesis, inhibited de novo lipid synthesis, and decreased reactive oxygen species scavenger enzyme SOD2 induction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199579.RAXLWR9wA5-_DaFBC8iHbF2EuJjCtKAvRd4eSgFgFsNlo130_provenance.
- NP199583.RAXZ6YnFvl2YSZJ-HBBQG01CQWRDLyieFR5D1GYG59mIY130_assertion description "[We analysed the mutation status in KRAS, BRAF and PIK3CA and PTEN expression in two separate CRC cohorts, Northern Sweden Health Disease Study (NSHDS; n=197) and Colorectal Cancer in Umeå Study (CRUMS; n=414).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199583.RAXZ6YnFvl2YSZJ-HBBQG01CQWRDLyieFR5D1GYG59mIY130_provenance.
- NP199588.RAWBtU59dKxONKxGsTKoaSYhBsTaS8gkM_1ZDA4nTozPo130_assertion description "[Alterations of MLH1 and microsatellite instability in esophageal squamous cell carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199588.RAWBtU59dKxONKxGsTKoaSYhBsTaS8gkM_1ZDA4nTozPo130_provenance.
- NP199589.RAYF4mLw2fBQoEnX5GvZSObYDrxyL_3rp3Er2qff572nk130_assertion description "[The 27-bp tandem repeat polymorphism in intron 4 of the endothelial nitric oxide synthase gene is not associated with coronary artery disease in a hospital-based Taiwanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199589.RAYF4mLw2fBQoEnX5GvZSObYDrxyL_3rp3Er2qff572nk130_provenance.
- NP199595.RAd4GSoVrTydRM0l4gErgdT4rK4tg317W9M-Gcor2_RE8130_assertion description "[Furthermore, composite Mmp2(-/-);Col1a1(r/r) animals had very abnormal craniofacial features with shorter snouts, bulging skulls, incompletely developed calvarial bones and unclosed cranial sutures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199595.RAd4GSoVrTydRM0l4gErgdT4rK4tg317W9M-Gcor2_RE8130_provenance.
- NP199596.RAeOvq8Dvt0kBKTojRhwgttsGydHJ9VSvnj9VkD_wRfYM130_assertion description "[Using the 3' rapid amplification of cDNA ends (RACE) technique, we identified six different fusion transcripts of the HMGIC gene among 13 uterine leiomyomas; three of these variants had not been described before.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199596.RAeOvq8Dvt0kBKTojRhwgttsGydHJ9VSvnj9VkD_wRfYM130_provenance.
- NP199597.RAc3dlWtH6JSsgkMxPVLqy_usjWUPaL-Yu2qEhYIn_Mok130_assertion description "[In 1977, Birt, Hogg and Dube (BHD) described a genodermatosis characterised by benign tumours of the hair follicle that has been associated with renal neoplasms and spontaneous pneumothorax.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199597.RAc3dlWtH6JSsgkMxPVLqy_usjWUPaL-Yu2qEhYIn_Mok130_provenance.
- NP199599.RAYfgMjhugn9gtGTvYMkNb-t1mJk9nA7hgjBRN6bCMZR4130_assertion description "[DNA repair gene ERCC2, XPC, XRCC1, XRCC3 polymorphisms and associations with bladder cancer risk in a French cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199599.RAYfgMjhugn9gtGTvYMkNb-t1mJk9nA7hgjBRN6bCMZR4130_provenance.
- NP199600.RAWyWlH4kzWVhUwiEsSn9xFXrq_KTAiJPlQBPwVEKQ0iA130_assertion description "[Redox regulation of lipopolysaccharide (LPS)-induced interleukin-8 (IL-8) gene expression mediated by NF kappa B and AP-1 in human astrocytoma U373 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199600.RAWyWlH4kzWVhUwiEsSn9xFXrq_KTAiJPlQBPwVEKQ0iA130_provenance.
- NP199601.RAc6ya-tPxhWGxvjcb_J6ynRE6dcr4CxLh9khB6ZICJ_c130_assertion description "[Protein C replacement therapy with a monoclonal antibody purified, virus inactivated protein C concentrate was carried out in nine infants (three male, six female) with severe congenital protein C deficiency and life-threatening purpura fulminans and/or thrombosis associated with disseminated intravascular coagulation (DIC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199601.RAc6ya-tPxhWGxvjcb_J6ynRE6dcr4CxLh9khB6ZICJ_c130_provenance.
- NP199608.RAWqO1T_F5Y1gXJe4cmByFBLkBpMaWfZ40u0NMGf1iKfs130_assertion description "[This study investigated the basic expression levels and the ex vivo inducibility of hBD2 mRNA in peripheral whole blood cells from patients with severe sepsis in comparison to non-septic critically ill patients and healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199608.RAWqO1T_F5Y1gXJe4cmByFBLkBpMaWfZ40u0NMGf1iKfs130_provenance.
- NP199614.RAW_rFi-VdZOaD-lk8SK_g9f4N4BoabsDqaPZ5k33NrOc130_assertion description "[Pancreatic involvement commonly is found in patients with HHT (31% in our study), mainly in patients with ALK1 mutation; pancreatic telangiectases or AVMs are only diagnosed duringthe arterial phase at multidetector CT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199614.RAW_rFi-VdZOaD-lk8SK_g9f4N4BoabsDqaPZ5k33NrOc130_provenance.
- NP199615.RAVhp07JCA4Vt3j4NDdWXUlzo_i49uEwzu_M5GBMCPJak130_assertion description "[Here, we describe that the PI3 kinase/Akt-signaling pathway, but not that of the MAP kinases ERK and p38, protects RA FLS from TRAIL-induced apoptosis by modulating the expression of the cell survival regulators p21, XIAP, Mcl-1 and RIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199615.RAVhp07JCA4Vt3j4NDdWXUlzo_i49uEwzu_M5GBMCPJak130_provenance.
- NP199617.RAR9hXoRXCKG3aCj1oe_Ai1LERax2qaacHJUJAXkziGIM130_assertion description "[RUNX2 duplications (3 copies) are exceedingly rare but have been reported to cause craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199617.RAR9hXoRXCKG3aCj1oe_Ai1LERax2qaacHJUJAXkziGIM130_provenance.
- NP199622.RAcrbF3yQyAXGF7MSMLgUaqdT1WS2YLOw5C4i85kXvTxI130_assertion description "[Together, our findings indicate that menin suppresses lung cancer partly through increasing Polycomb gene-mediated H3K27 methylation and repressing PTN transcription, unraveling a novel, epigenetically regulated PTN-ALK signaling pathway in suppressing lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199622.RAcrbF3yQyAXGF7MSMLgUaqdT1WS2YLOw5C4i85kXvTxI130_provenance.
- NP199625.RAaqMEZqZmgCrHY6DjgzwWSxhOU9nkbPpBodIM41wbM0A130_assertion description "[Optimization of nonmuscle invasive bladder cancer recurrence detection using a urine based FGFR3 mutation assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199625.RAaqMEZqZmgCrHY6DjgzwWSxhOU9nkbPpBodIM41wbM0A130_provenance.
- NP199627.RAWmD8EAvIPYGy2v-nO79SA48qXjvUsGe4Bt5tUUpepio130_assertion description "[We report here that the genotypes of CYP1A1 and CYP2D6 are not associated with gastric carcinoma risk; GSTM1 null, but not GSTT1 null inheritably increases risk of some pathological types of gastric carcinoma in Han ethnic population of Hunan Province.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199627.RAWmD8EAvIPYGy2v-nO79SA48qXjvUsGe4Bt5tUUpepio130_provenance.
- NP199634.RAfZfeuWecJyOAhgMICdpLC8Q9i3QA1wr-4JReIamC2rY130_assertion description "[Abnormalities of tyrosine kinase proteins are well recognised in myeloid malignancies, mutation in the cytoplasmic tyrosine kinase JAK2 (V617F) is key in the pathogenesis of myeloproliferative neoplasms, and translocations involving ABL key in the development of chronic myeloid leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199634.RAfZfeuWecJyOAhgMICdpLC8Q9i3QA1wr-4JReIamC2rY130_provenance.
- NP199635.RASCGZ1uBbQHl_8XtlewgLsxD_Kx0BfUHUKQc489g4eVY130_assertion description "[The mediodorsal nucleus of the thalamus (MD) has connections with central autonomic centers involved in cardiovascular control and undergoes severe degeneration in fatal familial insomnia, a human disease characterized by progressive dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199635.RASCGZ1uBbQHl_8XtlewgLsxD_Kx0BfUHUKQc489g4eVY130_provenance.
- NP199638.RAcJuP7tiukw4kijO5aqeZYCvovp-fKSW62a7VEsWLXaU130_assertion description "[Several functional PON1 variants may act together to modify PD risk for ambient OP exposures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199638.RAcJuP7tiukw4kijO5aqeZYCvovp-fKSW62a7VEsWLXaU130_provenance.
- NP199639.RAYbdOXU8YLi5QKDDnP_f439F9zGRi6a71oyFDzV5TxwQ130_assertion description "[The most remarkable risk was seen for the small cell carcinoma among subjects with the GSTP1*B/*B genotype and concurrent lack of the GSTM1 gene (OR = 6.9, 95% CI 1.6-30.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199639.RAYbdOXU8YLi5QKDDnP_f439F9zGRi6a71oyFDzV5TxwQ130_provenance.
- NP199649.RATi6DAY5yC9AyYfBlOwFX0vlhJ2a4dFjIIs8hLdFn9Lk130_assertion description "[Distribution of HLA-G alternative mRNAs including soluble forms in normal lymphocytes and in lymphoid cell-derived leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199649.RATi6DAY5yC9AyYfBlOwFX0vlhJ2a4dFjIIs8hLdFn9Lk130_provenance.
- NP199656.RAZb1uewNWUJmIHHH-anqvwAFqJCBkkRsGm8bztwEJ8hg130_assertion description "[Our aim was to clarify whether substitution of cytosine for adenine at position 1166 (A1166C) polymorphism of the angiotensin II type 1 receptor (AT1R) gene is associated with susceptibility to essential hypertension in Han, Tibetan and Yi populations in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199656.RAZb1uewNWUJmIHHH-anqvwAFqJCBkkRsGm8bztwEJ8hg130_provenance.
- NP199660.RAZYtUHzVfv1K6VVUYgJqPscbSatVRILd5OvjMkOTrRP4130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199660.RAZYtUHzVfv1K6VVUYgJqPscbSatVRILd5OvjMkOTrRP4130_provenance.
- NP199666.RAX-PpZye2HUmBTbdBL7pOvufFXqkBVr4FtIltnWze36E130_assertion description "[The influence of PS1 mutations on the generation of endogenous intracellular amyloid beta-protein (A beta) species was assessed using a highly sensitive immunoblotting technique with inducible mouse neuroblastoma (Neuro 2a) cell lines expressing the human wild-type (wt) or mutated PS1 (M146L or delta exon 10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199666.RAX-PpZye2HUmBTbdBL7pOvufFXqkBVr4FtIltnWze36E130_provenance.
- NP199678.RAVnGIepsi2elv7SAaxzN0d2zUOCk9ns_qB85KShO4K50130_assertion description "[This study examined whether secondary medical diagnoses that affect CNS function (i.e., seizures, malformations, or genetic disorders), are more likely to occur in individuals with fragile X syndrome (FXS) and autism spectrum disorder (FXS + ASD) or FXS alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199678.RAVnGIepsi2elv7SAaxzN0d2zUOCk9ns_qB85KShO4K50130_provenance.
- NP199688.RAV_EXnXA9AkWFSVCZbjH0Xb2etSSXmVHHyO9fWcqd1dI130_assertion description "[We hypothesized that ETV5 regulates MMP2 in human chondrosarcoma with the protease acting as a downstream effector.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199688.RAV_EXnXA9AkWFSVCZbjH0Xb2etSSXmVHHyO9fWcqd1dI130_provenance.
- NP199689.RAUuon8yxA5GhxQuMmSrzbFW3OXDnWzOTQ5UDxPs0YkCU130_assertion description "[The chondrosarcoma initially stained for vimentin, S100, muscle-specific actin, proliferating cell nuclear antigen, and Ki67, but it lost actin expression in its first recurrence, accompanied by more extensive Ki67 staining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199689.RAUuon8yxA5GhxQuMmSrzbFW3OXDnWzOTQ5UDxPs0YkCU130_provenance.
- NP199692.RASIxhkGtt9EtSC-wIc0X4rqNCM1z2USA-yr29aoejrm4130_assertion description "[For instance, mutations in both BFSP1 and BFSP2 cause cataract in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199692.RASIxhkGtt9EtSC-wIc0X4rqNCM1z2USA-yr29aoejrm4130_provenance.
- NP199698.RAeHSthYJzswdzHnZNVdTkYrodY3_clTFf61t6VHX8gNE130_assertion description "[The overexpression of eukaryotic translation initiation factor 4E (eIF4E), a key regulator of protein synthesis, is involved in the malignant progression of human breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199698.RAeHSthYJzswdzHnZNVdTkYrodY3_clTFf61t6VHX8gNE130_provenance.
- NP199701.RAeo89SK6w1rvDCs4FL-fmJCSfWl7px8Kp1DuGxtD_sCE130_assertion description "[We conclude that connexin 46 mutations might account for as much as 3.3% of the hereditary congenital cataract in the Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199701.RAeo89SK6w1rvDCs4FL-fmJCSfWl7px8Kp1DuGxtD_sCE130_provenance.
- NP199704.RAbnxMu-IP393QdJsZ_N0LPabXngTts2fdAJrmEJCs7Q0130_assertion description "[Therefore, ETV6 and p16(INK4A)/p15(INK4B) do not play a significant role in the pathogenesis of infant ALL, further emphasizing the distinctive biology of this subset of leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199704.RAbnxMu-IP393QdJsZ_N0LPabXngTts2fdAJrmEJCs7Q0130_provenance.
- NP199706.RAV7A1LEmgWyNrq4Sd0JIn-d9FM3SnnodYfV0NN4nvBUM130_assertion description "[Detection of the LGA fetus should first prompt the provider to rule out incorrect dates and maternal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199706.RAV7A1LEmgWyNrq4Sd0JIn-d9FM3SnnodYfV0NN4nvBUM130_provenance.
- NP199712.RAVBgjT5WzE2oI3akwN2PbodcD-l0J2q7TiWPPuxAPPIQ130_assertion description "[A Mutations in the gene encoding the ABCA12 protein are associated with different subtypes of autosomal recessive congenital ichthyosis (ARCI), including Harlequin ichthyosis (HI), lamellar ichthyosis (LI) and non-bullous congenital ichthyosiform erythroderma (NCIE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199712.RAVBgjT5WzE2oI3akwN2PbodcD-l0J2q7TiWPPuxAPPIQ130_provenance.
- NP199714.RASY-kS--q0fLp0vxvd7vUhMfOXYvTuEj92PS_vqlRDFw130_assertion description "[Moreover, we found a positive relationship between OM AM and tumor necrosis factor alpha mRNA levels and AM-immunoreactive area in OM tissue followed the features of the metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199714.RASY-kS--q0fLp0vxvd7vUhMfOXYvTuEj92PS_vqlRDFw130_provenance.
- NP199716.RAUoWwm8r87v3CbcIHFnmdfXSow-w_a5eDjGZ9sORlTpc130_assertion description "[Twenty-two (27.2%) and 19 (23.4%) of 81 HCC patients had AFP mRNA in their pre- and postoperative PB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199716.RAUoWwm8r87v3CbcIHFnmdfXSow-w_a5eDjGZ9sORlTpc130_provenance.
- NP199718.RAUlRujzhknL1-LOz3MYqqgt5TVdBnnUE76VgmpDVGEcI130_assertion description "[We did not find mutations in Lamin A/C (LMNA) gene in four WRS patients, and in particular, we did not find the G608G mutation (GGC > GGT transition) which is associated with most cases with Hutchinson-Gilford progeria (OMIM 176670).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199718.RAUlRujzhknL1-LOz3MYqqgt5TVdBnnUE76VgmpDVGEcI130_provenance.
- NP199737.RAaAkdxnRyvoLzDxPxLXB94L9kGz-hrGO0epV5NPT7HVs130_assertion description "[Our results collectively suggest that the OGG1 Ser326Cys polymorphism might not be a potential candidate risk factor for the development of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199737.RAaAkdxnRyvoLzDxPxLXB94L9kGz-hrGO0epV5NPT7HVs130_provenance.
- NP199742.RAcW9UO9HRcUnbmbLmc6Y-ACNdbZL2lvWQarZ7yXbtGws130_assertion description "[The htSNPs were genotyped in 5,603 invasive breast cancer cases and 7,480 controls from the Cancer Prevention Study-II (CPS-II), European Prospective Investigation on Cancer and Nutrition (EPIC), Multiethnic Cohort (MEC), Nurses' Health Study (NHS), and Women's Health Study (WHS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199742.RAcW9UO9HRcUnbmbLmc6Y-ACNdbZL2lvWQarZ7yXbtGws130_provenance.
- NP199743.RAVR0yRSKKjJznwaYdcjftJ9NczFMYu2MSPnSvaHDTLPc130_assertion description "[Real-time PCR analysis showed that Shf mRNA is highly expressed in non-metastatic neuroblastomas compared to metastatic tumor samples (P < 0.030, n = 106).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199743.RAVR0yRSKKjJznwaYdcjftJ9NczFMYu2MSPnSvaHDTLPc130_provenance.
- NP199745.RAbh_y4fymWmpY34HGXtToJZgEna097AZdpPgtFKdDm8E130_assertion description "[Spinal and bulbar muscular atrophy (SBMA) is a late-onset motor neuron disease characterized by proximal muscle atrophy, weakness, contraction fasciculations, and bulbar involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199745.RAbh_y4fymWmpY34HGXtToJZgEna097AZdpPgtFKdDm8E130_provenance.
- NP199749.RASxlfe-UvbQ9xgFr7Jv7fwpfYTRLZuYEBxO5Ji13vkbo130_assertion description "[A correlation was found between loss of heterozygosity on chromosome 1p32-pter and amplification of the MYC (formerly c-myc) protooncogene (P = 0.003), suggesting that these two genetic events may collaborate during tumor progression in human breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199749.RASxlfe-UvbQ9xgFr7Jv7fwpfYTRLZuYEBxO5Ji13vkbo130_provenance.
- NP199750.RAVQPQ8RZEov-sVy6FQnUoyOMw7-WWlo_FktemekMCvUI130_assertion description "[MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199750.RAVQPQ8RZEov-sVy6FQnUoyOMw7-WWlo_FktemekMCvUI130_provenance.
- NP199753.RAfAgyLhFtnehY3KXmXnjTWu4sraiRituwrOlFrkDM8aU130_assertion description "[Overexpressed in over 30% of breast cancers, IKKε has been recently identified as a potential breast cancer oncogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199753.RAfAgyLhFtnehY3KXmXnjTWu4sraiRituwrOlFrkDM8aU130_provenance.
- NP199754.RAei-XX8rZL43fK4ZoWLLWbnj_LPZ3GsxwLA2d3pdclwI130_assertion description "[Within the group of differentially expressed genes were SPARC, DAB2, CP, EVI1, ELF3, and EHD2, known to play a role in ovarian cancer, genes implicated in other cancers, such as GREM1 and GLIPR1, as well as genes not previously reported in a cancer context such as AKAP2 and ATAD4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199754.RAei-XX8rZL43fK4ZoWLLWbnj_LPZ3GsxwLA2d3pdclwI130_provenance.
- NP199761.RARVg8bciEcDkmvILAxUXRE--qQWszXl7zIkkDCnKVUmY130_assertion description "[Recently, we reported that a missense Glu298Asp variant in exon 7 of the eNOS gene is a possible genetic factor involved in the pathogenesis of coronary spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199761.RARVg8bciEcDkmvILAxUXRE--qQWszXl7zIkkDCnKVUmY130_provenance.
- NP199766.RAZuxkVcqV195WHo4vf_c62lOnuzTnc00YxzRkHTzFQ7c130_assertion description "[Subjects carrying both the ABCA1 (-477) TT genotype and the NPC1 (exon 6) GG genotype (OR=1.89; 95% CI 1.04-3.41), NPC1 (intron 20) AA genotype (OR=2.05; 95% CI 1.26-3.33), NPC1 (intron 22) AA genotype (OR=2.05; 95% or NPC1 (intron 24) GG genotype (OR=1.89; 95% higher risk of developing AD than subjects without these risk genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199766.RAZuxkVcqV195WHo4vf_c62lOnuzTnc00YxzRkHTzFQ7c130_provenance.
- NP199769.RAUH_LiiVZue1ECx4HnXNYTJb-Ch64v1eKgZFH8pB72Vw130_assertion description "[CD10 and BCL-6 expression in paraffin sections of normal lymphoid tissue and B-cell lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199769.RAUH_LiiVZue1ECx4HnXNYTJb-Ch64v1eKgZFH8pB72Vw130_provenance.
- NP199771.RAd-YEIgxz6d8NmJwGmEuKkySfQQvufa5GCH7gU6JQccA130_assertion description "[BRCA2 functions as a tumour-suppressor gene in about 35% of large familial breast-cancer clusters; its role in the pathogenesis of sporadic breast cancer is less clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199771.RAd-YEIgxz6d8NmJwGmEuKkySfQQvufa5GCH7gU6JQccA130_provenance.
- NP199774.RAfmAzPG2Prfv421pSeryJFgTeH11Zy6NFKV5A1vU8jBk130_assertion description "[The role of FSH in gonadal tumorigenesis and, in particular, in human ovarian cancer has been debated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199774.RAfmAzPG2Prfv421pSeryJFgTeH11Zy6NFKV5A1vU8jBk130_provenance.
- NP199787.RAZPiQfTqtFu4Uj9VaFzSCNRHE3HMMGTwGw5UzyCTOr4o130_assertion description "[Our results suggested that p-p27 Thr157 protein expression may be a favorable independent poor prognostic parameter for HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199787.RAZPiQfTqtFu4Uj9VaFzSCNRHE3HMMGTwGw5UzyCTOr4o130_provenance.
- NP199791.RARuuQg2lsgtAJ0XyQX4KlmeBkLR2o2Ug19LtWGTuneBM130_assertion description "[There was no significant difference in the allelic HLA-DQB1 0309 distribution between DCM patients with and without viral genomes detected in the heart (24.2% versus 29.5%, p=0.668).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199791.RARuuQg2lsgtAJ0XyQX4KlmeBkLR2o2Ug19LtWGTuneBM130_provenance.
- NP199794.RAbusph0oj4ag9dQ3U18_4JO77ix8G4q6R1s0wuJwLLaU130_assertion description "[Untreated PC-3 cells show high DNA binding activity of nuclear factor kappaB (NF-kappaB), an antiapoptotic transcriptional factor, but this was inhibited by SVT and accompanied by a significant inhibition of p50 translocation into the nucleus, as well as phosphorylation of inhibitory kappaB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199794.RAbusph0oj4ag9dQ3U18_4JO77ix8G4q6R1s0wuJwLLaU130_provenance.
- NP199801.RAWfZDs9HIvPwxo-NH5BgcT7Kyi7oQ5OJ0ZJfSHX_DVGU130_assertion description "[XRCC1 polymorphisms at codon 399 were found to be protective in the development of lung cancer (OR--0.6, 95% CI--0.46-0.80, p-0.0008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199801.RAWfZDs9HIvPwxo-NH5BgcT7Kyi7oQ5OJ0ZJfSHX_DVGU130_provenance.
- NP199803.RAdsZs54k6IQpW09_q5PnoxrR6HgKxJxInJouwPK2HWaQ130_assertion description "[An absence of the glutathione S-transferase (GST) enzyme may genetically predispose individuals to AA or MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199803.RAdsZs54k6IQpW09_q5PnoxrR6HgKxJxInJouwPK2HWaQ130_provenance.
- NP199811.RAay3tGGCk9t4Ffcoh1z2GrhVdk7oh_3gwCaMFB6YQSyY130_assertion description "[Our array-based analyses of gene expression in patients with chronic myeloid leukemia (CML) revealed several genes (MMP8, MMP9, PCNA, JNK2, MAPK p38) with significant increased expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199811.RAay3tGGCk9t4Ffcoh1z2GrhVdk7oh_3gwCaMFB6YQSyY130_provenance.
- NP199813.RAUi_fPs7bKo0oR43k39FSXA38J-4LB36nOvV-HOKDbOg130_assertion description "[Of the 30 carriers with probable disease-causing sequence variations for LCA, 5 (16.7%) carriers had an AIPL1 variation, 4 (13.3%) CRB1, 0 (0%) CRX, 5 (16.7%) GUCY2D, 9 (30%) RPE65, and 7 (23.3%) carriers had a RPGRIP1 variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199813.RAUi_fPs7bKo0oR43k39FSXA38J-4LB36nOvV-HOKDbOg130_provenance.
- NP199814.RAazbHSWimlDhWvKoii4ud6ymoo-ypTC19-cjvNx5fo0o130_assertion description "[Even though the pig is a widely used model for obesity related metabolic symptoms, the expression of ORM has not yet been characterized in such pig models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199814.RAazbHSWimlDhWvKoii4ud6ymoo-ypTC19-cjvNx5fo0o130_provenance.
- NP199816.RASgwZ9mcWgJAE8I6dwT7HwMnUoD50DqolHpeXdUFeDQo130_assertion description "[The frequency of GSTM1 null (-) genotype was observed to be 45.2% in infertile men as against 20.09% in fertile men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199816.RASgwZ9mcWgJAE8I6dwT7HwMnUoD50DqolHpeXdUFeDQo130_provenance.
- NP199824.RAaImEkBsmV8_tXGg-98aQEH8EyCqfWQalKJbP_9pYt2c130_assertion description "[Our results show that HuR is important for the pathogenesis of liver fibrosis development in the cholestatic injury model, for HSC activation, and for the response of activated HSC to PDGF and TGF-β.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199824.RAaImEkBsmV8_tXGg-98aQEH8EyCqfWQalKJbP_9pYt2c130_provenance.
- NP199833.RARsbCH8IJdySA6tA5fuK52snSknpg8yg15hTsn_2P5k8130_assertion description "[FASL and FAS map to loci linked to type II diabetes and estimates of insulin resistance, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199833.RARsbCH8IJdySA6tA5fuK52snSknpg8yg15hTsn_2P5k8130_provenance.
- NP199835.RAYhLpiESZB9eZWawFUJLpaDFln1svUfy6c_usq7DCfjI130_assertion description "[Mutations in cartilage oligomeric matrix protein (COMP) cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199835.RAYhLpiESZB9eZWawFUJLpaDFln1svUfy6c_usq7DCfjI130_provenance.
- NP199838.RAZYhViVYkeiO7UbTvwMHx62wwCM0Y-jze_ERpEdMsbbQ130_assertion description "[To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199838.RAZYhViVYkeiO7UbTvwMHx62wwCM0Y-jze_ERpEdMsbbQ130_provenance.
- NP199839.RAbmWSjqobcMzjSzdxSXcEnitfBBeB62WsUyljHgReI84130_assertion description "[Nuclear MTA2 expression was detected in 148 cases of NSCLC (66.4%), and was correlated with advanced TNM stages (p=0.023), tumor size (p=0.036), and lymph node metastasis (p=0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199839.RAbmWSjqobcMzjSzdxSXcEnitfBBeB62WsUyljHgReI84130_provenance.
- NP199840.RAQjOq36ja016DD_TNMsRz6iM3qh5n3b0nrvsp2RI6mpk130_assertion description "[The CLN3 locus which is involved in Batten disease had been localized to chromosome 16p11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199840.RAQjOq36ja016DD_TNMsRz6iM3qh5n3b0nrvsp2RI6mpk130_provenance.
- NP199845.RAf7j9zQx_tKZE2G10sNPs4sZCKjuLBckFpNvwY8FsI6w130_assertion description "[In three isolated LCA patients, the authors identified large homozygous regions on chromosome 3 encompassing the IQCB1 gene, which has been associated with Senior-Loken syndrome (SLSN), characterized by nephronophthisis and retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199845.RAf7j9zQx_tKZE2G10sNPs4sZCKjuLBckFpNvwY8FsI6w130_provenance.
- NP199850.RAZ2e_5SLeUfdkyHJxGr2OPzR1j3cg9BOmezhHa-AvlzQ130_assertion description "[However, patients with TOP2A aberrations receiving methotrexate-based therapy exhibited a significant decrease in 5-year distant disease-free survival and breast cancer-specific overall survival, especially for patients with TOP2A deletions (disease-free survival: hazard ratio, 5.31 [P = .001], and breast cancer-specific overall survival: hazard ratio, 6.45 [P ≤ .001]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199850.RAZ2e_5SLeUfdkyHJxGr2OPzR1j3cg9BOmezhHa-AvlzQ130_provenance.
- NP199858.RAVs7CY2T7W86A2GlwbFpkPXE_uqnYFRZ207U25h2hces130_assertion description "[The aberrations are associated with the phenotype in five patients (4.6%), based on the following criteria: de novo aberration; involvement of a known or candidate X-linked nonsyndromic(syndromic) MR (MRX(S)) gene; segregation with the disease in the family; absence in control individuals; and skewed X-inactivation in carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199858.RAVs7CY2T7W86A2GlwbFpkPXE_uqnYFRZ207U25h2hces130_provenance.
- NP199868.RAWPw83kbZaFrkiX3hFslZppGkowID95Cq_84Y-KD_5vg130_assertion description "[On the basis of studies in experimental animals demonstrating that AdVEGF121, an E1(-)E3(-) serotype 5 adenovirus coding the 121 isoform of vascular endothelial growth factor (VEGF), could mediate the generation of new blood vessels and reverse coronary ischemia, a clinical study of direct myocardial administration of AdVEGF121 was initiated in patients with late-stage, diffuse coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199868.RAWPw83kbZaFrkiX3hFslZppGkowID95Cq_84Y-KD_5vg130_provenance.
- NP199870.RAZkEoeS7YDTwC1Wl4qlHi-w-S6Q1Ny6iOFA2O5begh5I130_assertion description "[These preliminary data suggest that CLL in the most suffered contingent due to Chernobyl NPP accident might have some specific features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199870.RAZkEoeS7YDTwC1Wl4qlHi-w-S6Q1Ny6iOFA2O5begh5I130_provenance.
- NP199871.RAWkdMIj97a7y9cWSwONkit4aPPfwPVXi_RBztwe7tuOg130_assertion description "[CK8/18 expression was independently associated with BRCA1-associated breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199871.RAWkdMIj97a7y9cWSwONkit4aPPfwPVXi_RBztwe7tuOg130_provenance.
- NP199873.RAZ2xA3A3IDkvaaDRpn5k50BNpwUxZqvwl1fCia3raB6c130_assertion description "[In all three Philadelphia chromosome-positive acute lymphatic leukemia models, p210(BCR/ABL)-transformed cells were more sensitive to GNF-2 than were p185BCR/ABL-positive cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199873.RAZ2xA3A3IDkvaaDRpn5k50BNpwUxZqvwl1fCia3raB6c130_provenance.
- NP199877.RAeT2odYsSCnPVazcu1C14L6nsBAaN8zsPIRIbwocdDVo130_assertion description "[In accordance with previous studies, our case showed positive findings of FUS rearrangement, reinforcing the notion of a close relationship between low grade fibromyxoid sarcoma and SEF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199877.RAeT2odYsSCnPVazcu1C14L6nsBAaN8zsPIRIbwocdDVo130_provenance.
- NP199878.RASokeFXFJXgMkTPCgF_ckow2pOJhrfzZWTKU1QmGvKFU130_assertion description "[We report a case of T-PLL with t(6;11)(q21;q23) as the sole chromosomal abnormality and suggest that the cytogenetically identified translocation also implicates the ATM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199878.RASokeFXFJXgMkTPCgF_ckow2pOJhrfzZWTKU1QmGvKFU130_provenance.
- NP199894.RAUpw1xm2kZTQA7CJOP0nN9Fo0O6VCyCXiH-IF8PvGiYI130_assertion description "[Other characteristics of patients presenting with severe PH were poor compliance to ERT (4/9 patients) or no ERT (5/9 patients), a family history of a sib with GD and PH (2/2 patients), an excess of ACE I allele (OR 2.3, 95% CI 1.1-4.9, P=0.034) and an excess of non-N370S GBA mutation (OR 6.0, 95% CI 1.1-33, P=0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199894.RAUpw1xm2kZTQA7CJOP0nN9Fo0O6VCyCXiH-IF8PvGiYI130_provenance.
- NP199895.RAYh4bykiBRHk6MqBUOe0KpOXJKLQwX6BYIZeB874H1E4130_assertion description "[Because bone homeostasis involves a precise balance between the activities of osteoblasts and osteoclasts, our studies raise the possibility that attenuated osteoblast maturation caused by TRE17 overexpression may contribute to the bone loss/destruction observed in ABC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199895.RAYh4bykiBRHk6MqBUOe0KpOXJKLQwX6BYIZeB874H1E4130_provenance.
- NP199896.RASk-7cXMbpKk3lAI1EQqUTbHAwYdSAeURgElWS70qgy0130_assertion description "[This study confirms that polymorphisms in the ITPA gene are associated with protection from RBV-induced anemia in HIV/HCV-coinfected patients but not improved clinical outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199896.RASk-7cXMbpKk3lAI1EQqUTbHAwYdSAeURgElWS70qgy0130_provenance.
- NP199901.RAVHcaaDzETDttuuN6VuxX174svAIjN__UBdZlijlXlDY130_assertion description "[Detection of t(2;5)(p23;q35) in anaplastic large-cell lymphoma by long-range nested polymerase chain reaction assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199901.RAVHcaaDzETDttuuN6VuxX174svAIjN__UBdZlijlXlDY130_provenance.
- NP199916.RASVmaPyqcgFAsrdQfSjAU3_RwGpQSMvqy-iMSJpUQJ8o130_assertion description "[Together, GRIN2A and GRIN2B genotype variations explain 7.2% additional variance in AO for HD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199916.RASVmaPyqcgFAsrdQfSjAU3_RwGpQSMvqy-iMSJpUQJ8o130_provenance.
- NP199925.RAZASdl2RJwvQu2UK8EXHODmnX_A0CVOCCqUVtZXG0SO4130_assertion description "[Let-7 microRNA and HMGA2 levels of expression are not inversely linked in adipocytic tumors: analysis of 56 lipomas and liposarcomas with molecular cytogenetic data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199925.RAZASdl2RJwvQu2UK8EXHODmnX_A0CVOCCqUVtZXG0SO4130_provenance.
- NP199926.RAdFq7X3zhChdGDw1eLyZz1aBxR273V07RcBNkRtMgopE130_assertion description "[Epigenetic silencing of TNFSF7 (CD70) by DNA methylation during progression to breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199926.RAdFq7X3zhChdGDw1eLyZz1aBxR273V07RcBNkRtMgopE130_provenance.
- NP199929.RATDqlPTcutpX9Y30bJoPfCxD1Joo4ADY4gERBeyNkguk130_assertion description "[Overexpression and localization of cyclin D1 mRNA and antigen in esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199929.RATDqlPTcutpX9Y30bJoPfCxD1Joo4ADY4gERBeyNkguk130_provenance.
- NP199934.RAbHeyxin7O3U2-EnJ_Moq2ZFaYGGh3Jjtq9g3ks_Lomw130_assertion description "[Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199934.RAbHeyxin7O3U2-EnJ_Moq2ZFaYGGh3Jjtq9g3ks_Lomw130_provenance.
- NP199935.RASXMlgKyiRzupJcokTuuLkmATUiZ1Thvii0OKkELZ704130_assertion description "[Although ATM deficient cells failed to increase IRF-1 in response to genotoxic stress, the induction of IRF-1 in response to viral mimetics remained intact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199935.RASXMlgKyiRzupJcokTuuLkmATUiZ1Thvii0OKkELZ704130_provenance.
- NP199954.RAVuC50hDjcDs5ZoUnoFKhddEwynjP1VEo5KRhC8B91iw130_assertion description "[Recently, polymorphisms in thrombospondin (THBS) genes coding for THBS-1 (N700S), THBS-2 (T>G substitution in 3'-untranslated region), and THBS-4 (A387P) genes were proposed to modulate the risk of premature coronary artery disease (CAD) or myocardial infarction (MI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199954.RAVuC50hDjcDs5ZoUnoFKhddEwynjP1VEo5KRhC8B91iw130_provenance.
- NP199955.RAUEO7YBZgTf2jnOzRyR7-lqzyTA6bpeOK7QAt2ZtjWKs130_assertion description "[It was recently reported that the reduced expression of hypoxia-inducible factor prolyl 4-hydroxylase PHD2 inhuman cancers correlates with increased angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199955.RAUEO7YBZgTf2jnOzRyR7-lqzyTA6bpeOK7QAt2ZtjWKs130_provenance.
- NP199965.RAQxeVSHjRBQbWr1o2HGVeSt4PvOrMdsgTS9rnzSclgWY130_assertion description "[ACTH therapy was introduced, resulting in a significant improvement in EEG activity and gradual reduction in seizure frequency, with cessation at age 13 weeks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199965.RAQxeVSHjRBQbWr1o2HGVeSt4PvOrMdsgTS9rnzSclgWY130_provenance.
- NP199966.RAWcOikzAQ8kvEQv6ZNxKz1yJShXbYkQk7XVKTHHNRIMM130_assertion description "[tPSA and f/t PSA are the best available tools for discriminating between localized PC and BPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199966.RAWcOikzAQ8kvEQv6ZNxKz1yJShXbYkQk7XVKTHHNRIMM130_provenance.
- NP199968.RAaGoS9tCjft65mp1md9sJVYog9-BcOZBP4SYZfDgvKCM130_assertion description "[We previously observed that tumor cells in Kaposi's sarcoma (a common AIDS-related cutaneous neoplasm) completely lack both CD80 and CD86, and these tumor cells fail to stimulate T-cell proliferation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199968.RAaGoS9tCjft65mp1md9sJVYog9-BcOZBP4SYZfDgvKCM130_provenance.
- NP199976.RAY1UvYnLlt1s-Tdi4mcC3-63qcMetEKm5AnqTeKu8uEM130_assertion description "[The aim of the study was to determine the significance of the ABCB1 gene SNPs: 1236 and 2677 for peptic ulcer risk and development of Helicobacter pylori infection in peptic ulcer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199976.RAY1UvYnLlt1s-Tdi4mcC3-63qcMetEKm5AnqTeKu8uEM130_provenance.
- NP199986.RAT2g5udopabtQkvXnRIaAJH8AGoP3uNB0FxF9_OIEdsE130_assertion description "[Neither of the GST-null genotypes increased the risk for SCCA (p>0.05); however, the combination of the GSTM-1 and GSTT1-null genotypes showed a non-significant trend for an increased risk for developing cervical cancer with an adjusted OR of 2.7 (95%CI=0.8-9.0, p=0.10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199986.RAT2g5udopabtQkvXnRIaAJH8AGoP3uNB0FxF9_OIEdsE130_provenance.
- NP199989.RAYkGshIRukk4i_5KMXv1F4W5z97Zv7nwVnQqflnDKC4M130_assertion description "[Established biomarkers (abnormal DNA content, p53, and cyclin A expression) and new biomarkers (levels of sialyl Lewis(a), Lewis(x), and Aspergillus oryzae lectin [AOL] and binding of wheat germ agglutinin) were assessed in paraffin-embedded tissue samples from patients with a first diagnosis of BE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199989.RAYkGshIRukk4i_5KMXv1F4W5z97Zv7nwVnQqflnDKC4M130_provenance.
- NP199990.RAUtAL96TJKEtwr7e_7tHbtH4kcOfvD9KJYJTGlJ31khk130_assertion description "[We wanted to study the expression of interferon regulatory factor 4 (IRF4) in various hematologic disorders, especially chronic myeloid leukemia (CML), and its association with response to interferon alfa (IFN-alpha) treatment in CML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199990.RAUtAL96TJKEtwr7e_7tHbtH4kcOfvD9KJYJTGlJ31khk130_provenance.
- NP199991.RAVDUzVpn7whk3OCKad0cgPJJQnradkgpdkRERX-UfL0U130_assertion description "[Even when subjects with HLA-DQA1*0103, -DQA1*0301, -DQB1*0302, -DQB1*0303, and -DQB1*0401 were considered separately, no significant differences was found in the distribution of TAP1 and TAP2 alleles between IDDM patients and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199991.RAVDUzVpn7whk3OCKad0cgPJJQnradkgpdkRERX-UfL0U130_provenance.
- NP199995.RAdOKcUdCHC3yJsELIdGr_vhOmbArGr1w5oh1TApR6If8130_assertion description "[Similarly, human HS showed genetic or epigenetic inactivation of PTEN, p16(INK4A), and p14(ARF), supporting the relevance of this genetically engineered mouse model of HS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199995.RAdOKcUdCHC3yJsELIdGr_vhOmbArGr1w5oh1TApR6If8130_provenance.