Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP205524.RAUNSD4o3jsjaIhJPg2MXroM6Pc1qCjB6uyx4volHBbrg130_assertion description "[Levels of prothrombin fragment F1+2 in patients with hyperhomocysteinemia and a history of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205524.RAUNSD4o3jsjaIhJPg2MXroM6Pc1qCjB6uyx4volHBbrg130_provenance.
- NP205526.RAVL8_Uo0hTOQAQPIquO5-Ah26Decu8LOSUE23Oa03O0g130_assertion description "[The prognostic relevance of PLD2 expression level in patients with colorectal carcinoma was also analyzed by the survival analysis of mortality follow-up data covering the period 2000-2004.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205526.RAVL8_Uo0hTOQAQPIquO5-Ah26Decu8LOSUE23Oa03O0g130_provenance.
- NP205530.RAezEJbC8MyeZy2thr7ZP1Yeer7Pz8xoS1kUQCHG4x7FE130_assertion description "[The NLRP3 E311K mutation is associated with a heterogeneous clinical spectrum, which may expand the view on MWS presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205530.RAezEJbC8MyeZy2thr7ZP1Yeer7Pz8xoS1kUQCHG4x7FE130_provenance.
- NP205542.RAaI5us9ry9mV-6kIVuxzmWbp4I1R6rHR_XDLgmRgMuSg130_assertion description "[A peptide derived from the human papillomavirus L2 protein is recognized by a myelin basic protein (MBP)-specific T cell clone from a multiple sclerosis patient and by MBP-specific autoantibodies purified from multiple sclerosis brain tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205542.RAaI5us9ry9mV-6kIVuxzmWbp4I1R6rHR_XDLgmRgMuSg130_provenance.
- NP205554.RAbd_6gA2TWH5FKkc0qV-4lsRgWD7pH5FbnU2mRFUrVnc130_assertion description "[Severe combined immune deficiency due to adenosine deaminase (ADA) deficiency is a rare, potentially fatal pediatric disease, which results from mutations within the ADA gene, leading to metabolic abnormalities and ultimately profound immunologic and nonimmunologic defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205554.RAbd_6gA2TWH5FKkc0qV-4lsRgWD7pH5FbnU2mRFUrVnc130_provenance.
- NP205569.RAdSd0y_8kAZX923FYwn7oUt2infFKee9nn5EV3NGibrM130_assertion description "[Using a pan-BRAF antibody, total BRAF protein expression was observed in the tumor cell cytoplasm in 74 of 75 colon carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205569.RAdSd0y_8kAZX923FYwn7oUt2infFKee9nn5EV3NGibrM130_provenance.
- NP205580.RAd6NIABJkj70SvXOSu92UgJrouPKJffqyt2Sme_r-wWk130_assertion description "[We further focused on the role of 1,25D- and infection-induced interleukin 1β (IL-1β) expression in response to infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205580.RAd6NIABJkj70SvXOSu92UgJrouPKJffqyt2Sme_r-wWk130_provenance.
- NP205582.RAWcSypsg4kQyN3Cb1B1sE1VP-QBrMzNMVh3vzgbRikkM130_assertion description "[SOX10 mutations in patients with Waardenburg-Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205582.RAWcSypsg4kQyN3Cb1B1sE1VP-QBrMzNMVh3vzgbRikkM130_provenance.
- NP205583.RAaskUNaz9QDcicRuKw-udyV974_YidaPOYv8rtcteK4k130_assertion description "[We sought to evaluate the importance of SULT1A1 copy number and CYP2C19*17 on disease-free survival (DFS) in postmenopausal women randomized to tamoxifen monotherapy in North Central Cancer Treatment Group 89-30-52 from January 1991 to April 1995.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205583.RAaskUNaz9QDcicRuKw-udyV974_YidaPOYv8rtcteK4k130_provenance.
- NP205589.RAYO5vpBRnKVhd14QBUfXvfx4PDSKCqG3Zc0PtvDaH_zs130_assertion description "[In 2007, an association of single nucleotide polymorphisms (SNPs) in the fat mass and obesity-associated (FTO) gene region with body mass index (BMI) and risk of obesity was identified in multiple populations, making FTO the first locus unequivocally associated with adiposity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205589.RAYO5vpBRnKVhd14QBUfXvfx4PDSKCqG3Zc0PtvDaH_zs130_provenance.
- NP205593.RATEWmAb4hLjzVB3rimiGWZv1zIh_SZr-83yz9vlqO7nY130_assertion description "[FAS and FAS ligand polymorphisms in the promoter regions and risk of gastric cancer in Southern China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205593.RATEWmAb4hLjzVB3rimiGWZv1zIh_SZr-83yz9vlqO7nY130_provenance.
- NP205599.RAS_7C9_uh1l3RCSqXL0EZfx5anerUGSlnNRITuRImDSc130_assertion description "[Taken together, these results demonstrate that suppression of PC-1 expression improves insulin sensitivity in vitro and in an animal model of diabetes, supporting the proposition that PC-1 inhibition is a potential therapeutic approach for the treatment of type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205599.RAS_7C9_uh1l3RCSqXL0EZfx5anerUGSlnNRITuRImDSc130_provenance.
- NP205601.RAYsskyakkh9bxAOtePEY9XxfBTavvxcKDHOWYELQu_IM130_assertion description "[We have demonstrated, however, that while diabetes is reduced, other autoimmune phenotypes and diseases arise in NOD congenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205601.RAYsskyakkh9bxAOtePEY9XxfBTavvxcKDHOWYELQu_IM130_provenance.
- NP205604.RAXmMgz_jj8iYtbGwsBIKwWIzYUiAtGAAldIguOp1Z1rM130_assertion description "[Using SARF, we successfully identified three different membrane proteins: fibronectin leucine-rich transmembrane protein 2 (FLRT2) from patients with systemic lupus erythematosus (SLE), intercellular adhesion molecule 1 (ICAM-1) from a patient with rheumatoid arthritis, and Pk (Gb3/CD77) from an SLE patient with hemolytic anemia, as targets for AECAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205604.RAXmMgz_jj8iYtbGwsBIKwWIzYUiAtGAAldIguOp1Z1rM130_provenance.
- NP205615.RAQrnmdbrzSl8PS0zYGWVUwWItS9_b2WKcv8uYPhOs5Qg130_assertion description "[We investigated the underlying genetic defect in an immunodeficient patient who presented with recurrent bacterial infections in his late twenties and demonstrated a transcriptional defect in major histocompatibility complex (MHC) class II regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205615.RAQrnmdbrzSl8PS0zYGWVUwWItS9_b2WKcv8uYPhOs5Qg130_provenance.
- NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_assertion description "[In addition, the seven different loci so far reported to be associated with autosomal dominant pure forms of spastic paraplegia have been tested and excluded by linkage analysis and haplotype reconstruction, including SPG4 on chromosome 2p22-p21, where a familial form of spastic paraplegia associated with dementia and epilepsy has been mapped.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_provenance.
- NP205619.RAQPigY3c6C_Nb378RgN_Vs5sZ_wiojEMDNfP-B3-qYCQ130_assertion description "[Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205619.RAQPigY3c6C_Nb378RgN_Vs5sZ_wiojEMDNfP-B3-qYCQ130_provenance.
- NP205620.RAZUX7rCrVHv9cVZfmMk5Yg1xPWM29y_lq3OCpip0RMLQ130_assertion description "[In conclusion, our findings demonstrate a significant effect of paternal HLA DQ alleles as well as antibody status on susceptibility to thyroid autoimmune disease in juvenile patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205620.RAZUX7rCrVHv9cVZfmMk5Yg1xPWM29y_lq3OCpip0RMLQ130_provenance.
- NP205625.RARKAPXIhip0L7CDFFspkqf0JTxicocZi8dTHFhYEviAI130_assertion description "[These findings provide new insights into the molecular mechanisms of the synergistic effect of caffeine related to p53 gene status in osteosarcoma, providing candidates for an assay of responsiveness to caffeine-potentiated chemotherapy for osteosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205625.RARKAPXIhip0L7CDFFspkqf0JTxicocZi8dTHFhYEviAI130_provenance.
- NP205626.RAdiv2dA43sfOBAP-b1j-_XIbWYA4PihZgdIsSaJR2bGc130_assertion description "[Our data show that molecular deletions of 13q14 are detected in a relatively large fraction of BCR/ABL- CMPD (38%), that they appear to be more frequent in MMM than in other BCR/ABL- CMPD, and that they may be present at diagnosis or occur during blastic evolution of the neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205626.RAdiv2dA43sfOBAP-b1j-_XIbWYA4PihZgdIsSaJR2bGc130_provenance.
- NP205630.RAXk1Dcot7BPNafnfVXuAZWxr6qZ2nZh1WP6wTr4KXJMo130_assertion description "[The different CD14 -260 C>T genotypes were assessed by PCR-based RFLP analysis in three cohorts: 1) A cohort (n = 576) of women attending a STD clinic, 2) a cohort (n = 253) of women with subfertility, and 3) an ethnically matched control cohort (n = 170).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205630.RAXk1Dcot7BPNafnfVXuAZWxr6qZ2nZh1WP6wTr4KXJMo130_provenance.
- NP205635.RARyX-s3K2P_mOJZo2xOH29ezmA57IhDg8MyMKnokParY130_assertion description "[Aberrant DNA methylation of P16, MGMT, and hMLH1 genes in combination with MTHFR C677T genetic polymorphism in esophageal squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205635.RARyX-s3K2P_mOJZo2xOH29ezmA57IhDg8MyMKnokParY130_provenance.
- NP205639.RAWs4z5tDdpmeo1b9EvETakmZGc9rZfbIiJDM2BLeeryI130_assertion description "[Joint binding of OTX2 and MYC in promotor regions is associated with high gene expression in medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205639.RAWs4z5tDdpmeo1b9EvETakmZGc9rZfbIiJDM2BLeeryI130_provenance.
- NP205641.RAWq8mx4ysYYFVFmOCtAr-JmcHq1yjZmueL872tU4SZos130_assertion description "[The cigarettes smoked per day (CPD) and smoking behaviors were evaluated by clinician-administered questionnaires and the Fagerstrom Test for Nicotine Dependence (FTND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205641.RAWq8mx4ysYYFVFmOCtAr-JmcHq1yjZmueL872tU4SZos130_provenance.
- NP205642.RAUw3EL9AjjXoo1DNzVN2vZ9NvTznbGCPjpHAILrr4O44130_assertion description "[DRD4 has been implicated in several psychiatric disease phenotypes and our results shed light upon the possible mode of action of SNP associations in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205642.RAUw3EL9AjjXoo1DNzVN2vZ9NvTznbGCPjpHAILrr4O44130_provenance.
- NP205644.RAZwYYnLVJs__g5q7qXx7qQOSBLvDDogqPyNNgx_MR738130_assertion description "[Glioblastoma resistance to anti-VEGF therapy: has the challenge been MET?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205644.RAZwYYnLVJs__g5q7qXx7qQOSBLvDDogqPyNNgx_MR738130_provenance.
- NP205646.RAWLL09liC8SRf8MtVuwqgBLb564FEHhzEBKZ1S5droFw130_assertion description "[In conclusion, this study provides evidence that MHC rs9257809 and FOXF1 rs9936833 variants, associated with Barrett's esophagus, also increase ESCC and EAC susceptibility in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205646.RAWLL09liC8SRf8MtVuwqgBLb564FEHhzEBKZ1S5droFw130_provenance.
- NP205651.RAXaCh5G-sosLrLLZtm3mvBhIyBYrtTf-FYKFUZqAsxg8130_assertion description "[High-mobility group A1 (Hmga1) protein is an architectural chromatin factor, and aberrant Hmga1 expression in mice causes hematopoietic malignancies with defects in cellular differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205651.RAXaCh5G-sosLrLLZtm3mvBhIyBYrtTf-FYKFUZqAsxg8130_provenance.
- NP205662.RATyy2vpiBa4-WQ1AijwDrrTq_zSmLnOfnB1pSBjkKSX4130_assertion description "[Because basal cell carcinomas have been observed to develop in association with benign trichoepitheliomas (TEs) in the same lesions, patients, and families and may share the same cell of origin, we have analyzed PTCH for mutations and expression in TEs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205662.RATyy2vpiBa4-WQ1AijwDrrTq_zSmLnOfnB1pSBjkKSX4130_provenance.
- NP205663.RAXi_KnGK1WJVvD_u3qpA6zVSvzadji0R1i4zSoiILJkg130_assertion description "[Trinucleotide repeat-containing 9 (TNRC9), a high mobility group chromatin-associated protein, has been implicated in breast cancer metastasis to the bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205663.RAXi_KnGK1WJVvD_u3qpA6zVSvzadji0R1i4zSoiILJkg130_provenance.
- NP205664.RAaWmZbIqkNIXm6vT47gf5xmMBxZtwnLsO-liIM3W9658130_assertion description "[We investigated the effect of Se supplementation on activities of glutathione peroxidase (GPX), glutathione reductase (GR) and glutathione S-transferase (GST) in different blood compartments, and expression of selected phase 1 and phase 2 genes in leucocytes (GPX1, gamma-glutamylcysteine ligase catalytic subunit (GCLC), AP-1 transcription factor Fos-related antigen 1 (Fra1), NAD(P)H:quinone oxidoreductase (NQO1), and aryl hydrocarbon receptor repressor (AhRR)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205664.RAaWmZbIqkNIXm6vT47gf5xmMBxZtwnLsO-liIM3W9658130_provenance.
- NP205665.RAZud8Z19_nkDxpKgHjtPI9xbQZapb6s249L4mHdpOHeA130_assertion description "[We report a patient with a de novo constitutional t(1;22)(p22;q11.2) who developed a malignant ependymoma at age 5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205665.RAZud8Z19_nkDxpKgHjtPI9xbQZapb6s249L4mHdpOHeA130_provenance.
- NP205668.RASCs2IXuwpd8qJ1JEw9WYSTaK9rCCMl6yGM1s1qKW5C0130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205668.RASCs2IXuwpd8qJ1JEw9WYSTaK9rCCMl6yGM1s1qKW5C0130_provenance.
- NP205669.RAX1VuD7M2dwncgmybAbxOk5x2VyX8rOOA8eAe_QRqo6Q130_assertion description "[Whereas the development of hemangioblastomas and renal cell carcinomas has been attributed to impaired HIF-1/2alpha down-regulation by pVHL mutant proteins, the molecular defects underlying the development of pheochromocytomas are still unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205669.RAX1VuD7M2dwncgmybAbxOk5x2VyX8rOOA8eAe_QRqo6Q130_provenance.
- NP205670.RATKcw-j-ujJ-c831hlkVl-eIb-9CU88IKx3wLXfvvQ8c130_assertion description "[Homozygous loss-of-function mutations in forkhead box E1/thyroid transcription factor 2 (FOXE1/TTF-2) cause syndromic congenital hypothyroidism, with thyroid dysgenesis, cleft palate, spiky hair, and variable choanal atresia and bifid epiglottis in three cases reported hitherto.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205670.RATKcw-j-ujJ-c831hlkVl-eIb-9CU88IKx3wLXfvvQ8c130_provenance.
- NP205671.RAYs7hJTEZTo-OUPFH2kZ0RI-M8nIpz50dF49AfsED9RY130_assertion description "[Serum and cerebrospinal fluid (CSF) were tested for IgM antibodies against Chandipura virus (CHPV) and Japanese encephalitis virus (JEV) and for CHPV RNA by RT-PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205671.RAYs7hJTEZTo-OUPFH2kZ0RI-M8nIpz50dF49AfsED9RY130_provenance.
- NP205675.RAfKilwagFkFU1-K_LTxVvoAWzsAQgzQjdXs2Yr1D9rHY130_assertion description "[Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205675.RAfKilwagFkFU1-K_LTxVvoAWzsAQgzQjdXs2Yr1D9rHY130_provenance.
- NP205680.RAUglUW9OFqcrDK7bn_buYc3kknPvn6W3xNesHVZN2EsI130_assertion description "[To address this prediction, we transduced skin fibroblasts from PiZZ individuals with liver disease or without liver disease with amphotropic recombinant retroviral particles designed for constitutive expression of the mutant alpha 1-AT Z gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205680.RAUglUW9OFqcrDK7bn_buYc3kknPvn6W3xNesHVZN2EsI130_provenance.
- NP205683.RAWtQU3-LHB0hqVlwkQCOHQAljkFC-97drEkCzQkr62Mg130_assertion description "[Transgenic hypergastrinemic INS-GAS mice developed a spontaneous gastric cancer, which was associated with an impaired acid secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205683.RAWtQU3-LHB0hqVlwkQCOHQAljkFC-97drEkCzQkr62Mg130_provenance.
- NP205688.RAfyeP72KiM04Uob_lR6hJrpoWd7I-VZJxrNc8GMyIbNQ130_assertion description "[The TT and CC/CG genotypes of 2 single-nucleotide polymorphisms, rs4810485 (CD40) and rs42041 (CDK6), respectively, were associated with a higher rate of joint destruction in ACPA-positive RA patients (P=0.003 and P=0.012, respectively), with rs4810485 being significant after Bonferroni correction for multiple testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205688.RAfyeP72KiM04Uob_lR6hJrpoWd7I-VZJxrNc8GMyIbNQ130_provenance.
- NP205693.RAV4ggNKWPqqfYiaCfZf6TaY72gsPb8_cI3n3fsCHhlCw130_assertion description "[These results further point out the important role of the AR in prostate tumors and support further testing of AR downregulation for treatment of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205693.RAV4ggNKWPqqfYiaCfZf6TaY72gsPb8_cI3n3fsCHhlCw130_provenance.
- NP205695.RAYLToePex1IDgMH_xXY1awrI1AdIY4XGuAIeL2uWOTPI130_assertion description "[Fusion of ETV6 to neurotrophin-3 receptor TRKC in acute myeloid leukemia with t(12;15)(p13;q25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205695.RAYLToePex1IDgMH_xXY1awrI1AdIY4XGuAIeL2uWOTPI130_provenance.
- NP205697.RAds8pvYTHPisT4E2JcNp2101l9xYZDhBArFb6e8aq8_w130_assertion description "[Enhanced cytotoxicity of RIPTK gene therapy of pancreatic cancer via PDX-1 co-delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205697.RAds8pvYTHPisT4E2JcNp2101l9xYZDhBArFb6e8aq8_w130_provenance.
- NP205699.RATjAu2gSHrAO4sWHvQJ7uIOuCUgWwsX6gyv03PPRDy5o130_assertion description "[A review of reported cases of late-onset Friedreich ataxia (25-39 years) and very late-onset Friedreich ataxia (> or =40 years) demonstrated that this is the first instance of a patient presenting with very late-onset FRDA despite carrying more than 800 GAA repeats in both expanded X25 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205699.RATjAu2gSHrAO4sWHvQJ7uIOuCUgWwsX6gyv03PPRDy5o130_provenance.
- NP205709.RAeDVXjfGnyQhQkWPPIhn27tE9XkO-Zc679HgjYzAGh4Y130_assertion description "[Furthermore, both CYR61 and CTGF were downregulated in cervical cancer tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205709.RAeDVXjfGnyQhQkWPPIhn27tE9XkO-Zc679HgjYzAGh4Y130_provenance.
- NP205711.RAaZy_cjNj5R2auo5R633eI011cAHElHxQ583iBjki1sE130_assertion description "[Five percent of the MRSA isolates harbored Panton-Valentine leukocidin and were classified as community-associated MRSA associated with ST1, 8, 30, 80, and 89.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205711.RAaZy_cjNj5R2auo5R633eI011cAHElHxQ583iBjki1sE130_provenance.
- NP205713.RARDUkRBtdeg3K4LmJ4SpvW0g51OtdlPS9PmrGvrCu3ys130_assertion description "[The polymorphism *2236T>C in the 3' untranslated region of the DRP-2 gene, which has been shown to be a negative genetic risk factor for paranoid-type schizophrenia, was analyzed in 198 patients with METH psychosis and 221 corresponding healthy controls in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205713.RARDUkRBtdeg3K4LmJ4SpvW0g51OtdlPS9PmrGvrCu3ys130_provenance.
- NP205716.RAe8CDxAnZ5RziOekxX6Vu-lhe9zYnmiI1LDJmsVJLtJI130_assertion description "[Our findings suggest a role of FGF2 in regulating PDGFRA expression in the subset of gliomas with younger age at disease onset and longer patient survival regardless of their morphological diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205716.RAe8CDxAnZ5RziOekxX6Vu-lhe9zYnmiI1LDJmsVJLtJI130_provenance.
- NP205717.RARsjg-el-FdajQsZNFQP4UTfH20LvmllSMZJesZhQzTg130_assertion description "[Comparing patients with ESRD (IgAN-ESRD) and those without ESRD (IgAN-non ESRD), there was a significant increase only in the ACE DD genotype (P < 0.05) among the four gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205717.RARsjg-el-FdajQsZNFQP4UTfH20LvmllSMZJesZhQzTg130_provenance.
- NP205722.RAcYxcSOE7aW6lU5mBqtAMmbotuqqsRaVcWUn01d22IjU130_assertion description "[Twenty-seven patients with myeloproliferative diseases were treated, six with the juvenile type of chronic myelogenous leukemia (CML), 10 with the adult type of CML, three with familial MPD, one with unclassifiable MPD, and seven with acute leukemia in whom myelofibrosis was either a prodromal or terminal event.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205722.RAcYxcSOE7aW6lU5mBqtAMmbotuqqsRaVcWUn01d22IjU130_provenance.
- NP205723.RAeaRZjNKA9wK96DnKcxj0G-O9istAOS9uFtGrHU76Vms130_assertion description "[20-Aminosteroids as a novel class of selective and complete androgen receptor antagonists and inhibitors of prostate cancer cell growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205723.RAeaRZjNKA9wK96DnKcxj0G-O9istAOS9uFtGrHU76Vms130_provenance.
- NP205727.RAfdhI1Jb35Xz7hQ4PfUhXAgwRjAjNdJJOz2zjzF0W38o130_assertion description "[We have previously studied intrathecal production of antibody to lymphotropic herpesviruses in MS patients and the presence of human herpesvirus 1 to 7 DNAs in cerebrospinal fluid (CSF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205727.RAfdhI1Jb35Xz7hQ4PfUhXAgwRjAjNdJJOz2zjzF0W38o130_provenance.
- NP205728.RAaHp8rHQbGE0LuQutzRWxJW9yh7VMX84oC_oCQBQRj2s130_assertion description "[All patients had antibodies against HBV e antigen (anti-HBe) except 1 with chronic hepatitis B and C. No precore stop mutation at codon 28 (TGG to TAG mutation) was found in 21 cloned sequences from the 7 patients with HBV and HCV infection, nor in 11 cloned sequences from 2 patients with HBV, HCV, and HDV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205728.RAaHp8rHQbGE0LuQutzRWxJW9yh7VMX84oC_oCQBQRj2s130_provenance.
- NP205732.RAUJnpJnPlZv7N41Tk-FzeHyupnEGEHzQqjBs2sDHVJmQ130_assertion description "[DBL-EBP, which are products of the erythrocyte-binding-like (ebl) gene family, act as critical determinants of erythrocyte specificity and are the best-defined ligands from invasive stages of malaria parasites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205732.RAUJnpJnPlZv7N41Tk-FzeHyupnEGEHzQqjBs2sDHVJmQ130_provenance.
- NP205733.RAQOmBSQFYYmoO1duo7h8ZorPpYLTxV0RmXisD-gB4PP4130_assertion description "[X linked hyper-IgM (XHIM) is a primary immunodeficiency caused by mutations in the tumour necrosis factor superfamily 5 gene, TNFSF5, also known as the CD40 ligand (CD40L) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205733.RAQOmBSQFYYmoO1duo7h8ZorPpYLTxV0RmXisD-gB4PP4130_provenance.
- NP205736.RAdbDbqublL6SwM0-7m5h5XNlXrlw04YDq_iQ_ue_wcvs130_assertion description "[Our study addresses the involvement of T cell downstream signalling intermediates, cytokines (IL-10 and IFN-γ) and their transcription factors (T-bet and GATA-3) in COX-2-mediated regulation of lymphocyte functions in NSCLC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205736.RAdbDbqublL6SwM0-7m5h5XNlXrlw04YDq_iQ_ue_wcvs130_provenance.
- NP205743.RAUYq8AXlfYYNjdfYgKZw139rnGxbsfCPwSBFKTdYESKs130_assertion description "[Ki67 was associated with AHGD (P = 0.02) and ADC (P = 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205743.RAUYq8AXlfYYNjdfYgKZw139rnGxbsfCPwSBFKTdYESKs130_provenance.
- NP205750.RAalKhWkreZPETSbQB31iH7k-zQU9PRjHJxudacd8a8vk130_assertion description "[The role of common polymorphisms influencing the FVII plasma levels in thromboembolic disorders has been evaluated but there is no published data related to the effect of FVII gene polymorphisms on the venous thrombosis risk in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205750.RAalKhWkreZPETSbQB31iH7k-zQU9PRjHJxudacd8a8vk130_provenance.
- NP205758.RAeqfITRNz05ux6uRVDZeDatWgfSUg0F6Tp0I3vwSCgu8130_assertion description "[JM1 and JM2 are recognized by sera from 67% of patients with IA-2 Abs, and relatives of patients with type 1 diabetes having Abs to either JM epitope had a >50% risk for developing type 1 diabetes within 6 years, even in the absence of diabetes-associated HLA genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205758.RAeqfITRNz05ux6uRVDZeDatWgfSUg0F6Tp0I3vwSCgu8130_provenance.
- NP205761.RAcBC65WRnddkQgZQjEbeLrfS15ob1FIxgPN_Q4NT6UUA130_assertion description "[These results suggested that specific p63 isoforms were associated with human oral squamous cell carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205761.RAcBC65WRnddkQgZQjEbeLrfS15ob1FIxgPN_Q4NT6UUA130_provenance.
- NP205764.RAe8m55fmHgztTFv46vnr_lGtuo82-oliy1YPorUKPK0U130_assertion description "[Increased cytoplasmic HuR expression occurs in several cancer types, including colorectal cancer where it may contribute to the increased cyclooxygenase-2 (COX- 2) expression observed during tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205764.RAe8m55fmHgztTFv46vnr_lGtuo82-oliy1YPorUKPK0U130_provenance.
- NP205766.RAen0u6AhCpaRGS4eNWKe1AGhpp8QvlpZ-uvylJnk7INo130_assertion description "[These results suggest that TNFA -308 (G/A) polymorphism may influence the susceptibility of female gender gallbladder cancer in absence of gallstones while IL6 -174 G/C polymorphism does not seem to be playing significant role in the susceptibility to gallbladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205766.RAen0u6AhCpaRGS4eNWKe1AGhpp8QvlpZ-uvylJnk7INo130_provenance.
- NP205772.RAZW48BwJcSLN244OM6nzjWrOsLnctcoC4mhjkdGkrOm0130_assertion description "[That RA promotes both neutrophil and monocyte differentiation has implications for the use of RA and D3 in treatment of leukemias and provides insight into mechanisms whereby RAR, VDR and RXR facilitate monocyte differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205772.RAZW48BwJcSLN244OM6nzjWrOsLnctcoC4mhjkdGkrOm0130_provenance.
- NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_assertion description "[On the assumption that the function of the testis is to produce hormones and spermatozoa, the hypothesis of a single Y-chromosomal testis-determining gene with a dominant effect is shown to run counter to the following observed facts: a lowering in testosterone levels and an increase in the incidence of undescended testes, in addition to sterility, in males with multiple X chromosomes; abnormalities of the testes in autosomal trisomies; phenotypic abnormalities of XX males apparently increasing with decreasing amounts of Y-chromosomal material; the occurrence of patients with gonadal dysgenesis and XY males with ambiguous genitalia in the same sibship; the occurrence of identical SRY mutations in patients with gonadal dysgenesis and fertile males in the same pedigree; and the development of XY female and hermaphrodite mice having the same genetic constitution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_provenance.
- NP205777.RAYmwyRKPDrFC0h_KQ5rjvoTHraRxHzkyJEik9_6QVKkw130_assertion description "[The expression of gankyrin was increased in all 34 hepatocellular carcinomas studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205777.RAYmwyRKPDrFC0h_KQ5rjvoTHraRxHzkyJEik9_6QVKkw130_provenance.
- NP205779.RAa75G1VKmyyE6xMxaJUyojvNr38clBsDsggqhg-Ok3l8130_assertion description "[Although tamoxifen (TAM), which is widely used in the treatment of breast cancer, also has a beneficial effect on cisplatin-refractory ovarian cancer, the biological mechanism of this effect has remained obscure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205779.RAa75G1VKmyyE6xMxaJUyojvNr38clBsDsggqhg-Ok3l8130_provenance.
- NP205783.RAcgE51W1y2_dCvhdFHxmzJmAdXwXN2yvlB2CbyQhOwkA130_assertion description "[Mutations in the transforming growth factor beta receptor type I and II genes (TGFBR1 and TGFBR2) cause Loeys-Dietz syndrome (LDS), characterised by thoracic aortic aneurysms and dissections (TAAD), aneurysms and dissections of other arteries, craniosynostosis, cleft palate/bifid uvula, hypertelorism, congenital heart defects, arterial tortuosity, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205783.RAcgE51W1y2_dCvhdFHxmzJmAdXwXN2yvlB2CbyQhOwkA130_provenance.
- NP205785.RAdazu3bwr3bt6OJ9hlTnk57AVoP9BJGuWArOdtxK2p6w130_assertion description "[An over-expression of MDM2 RNA was seen in 9/66 (14%) patients tested, including 3/9 ALL, 3/24 AML, 2/4 myelomas, 1/1 PLL, but 0/2 CML, 0/2 NHL and 0/21 MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205785.RAdazu3bwr3bt6OJ9hlTnk57AVoP9BJGuWArOdtxK2p6w130_provenance.
- NP205786.RAYfprkTP3d7e5uflAKWMucHIW1lXbntVulGkeXASRW4A130_assertion description "[Molecular alterations in the APC/beta-catenin pathway were detected in 23.5% (4 of 17) of the carcinomas, including one ACC with an activating mutation of the beta-catenin oncogene and three ACCs with truncating APC mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205786.RAYfprkTP3d7e5uflAKWMucHIW1lXbntVulGkeXASRW4A130_provenance.
- NP205787.RAfWzSHfpLUc42E0Pu_m15mGQo_kF3J2x7YvdJ5A59N1U130_assertion description "[Homozygous UGT1A7*3 is a possible risk factor for lung cancer, at least in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205787.RAfWzSHfpLUc42E0Pu_m15mGQo_kF3J2x7YvdJ5A59N1U130_provenance.
- NP205788.RAbsTJNSIK2z75UINiPHMR1VauKPT0EgxKm4ZYVKq8CEg130_assertion description "[A gel mobility shift assay showed that treatment of SCCKN cells with okadaic acid suppressed Egr-1 binding to the DIG-labeled Egr-1 consensus oligonucleotide probe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205788.RAbsTJNSIK2z75UINiPHMR1VauKPT0EgxKm4ZYVKq8CEg130_provenance.
- NP205789.RAdw8IrW2F9jBoVUQDu-W4KbSjsRukRu7bI1yMZLTmYJg130_assertion description "[Collectively, these results establish that relative changes in PSMA expression levels can be quantitatively measured using a human-ready imaging reagent and could serve as a biomarker of AR signaling to noninvasively evaluate AR activity in patients with CRPC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205789.RAdw8IrW2F9jBoVUQDu-W4KbSjsRukRu7bI1yMZLTmYJg130_provenance.
- NP205798.RAZxCEnO9QBSoGd18KYUZa_Cg_vggZLI1Yx8X6etT2VMI130_assertion description "[In the leukocyte adhesion deficiency (LAD)-1 syndrome, there is diminished expression of beta2(CD18) integrins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205798.RAZxCEnO9QBSoGd18KYUZa_Cg_vggZLI1Yx8X6etT2VMI130_provenance.
- NP205800.RAWBfqzH7IzFJC1dre2L_jzXt8BFALA3qeFsfvWtkZYI8130_assertion description "[These findings suggest that the int-1 gene may be implicated in tumorigenesis of MLS with t(12;16)(q13;p11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205800.RAWBfqzH7IzFJC1dre2L_jzXt8BFALA3qeFsfvWtkZYI8130_provenance.
- NP205801.RAaTf4yMH7oClWSKno_cZpA-svQWVdZwZE4z_bROytuLE130_assertion description "[In addition to identifying new prolactin-regulated genes in breast cancer cells, we found that prolactin-JAK2-STAT5 induces expression of the HSP90A gene, which encodes the master chaperone of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205801.RAaTf4yMH7oClWSKno_cZpA-svQWVdZwZE4z_bROytuLE130_provenance.
- NP205804.RAYlTCpcBZ_mzhTosUcZA3HDlSjv7SnI7EtKAgpsj7x1w130_assertion description "[Cytotoxic effects of camptothecin and cisplatin combined with tumor necrosis factor-related apoptosis-inducing ligand (Apo2L/TRAIL) in a model of primary culture of non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205804.RAYlTCpcBZ_mzhTosUcZA3HDlSjv7SnI7EtKAgpsj7x1w130_provenance.
- NP205809.RAaD6n5GrXSaN8dig_yfl9-1f5fRP0LH4BAyV5-kF4U38130_assertion description "[We hypothesize that catechol-O-methyltransferase (COMT), the main metabolizer of dopamine in prefrontal cortex, is related to this deficit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205809.RAaD6n5GrXSaN8dig_yfl9-1f5fRP0LH4BAyV5-kF4U38130_provenance.
- NP205812.RATqmpDlYbi3nSeLPMNeidC_6vTpQp3Nyl85wFkeb3sxQ130_assertion description "[We analyzed 20 germline polymorphisms in 10 genes (TS, MTHFR, ERCC1, XPD, XRCC1, ABCC2, AGXT, GSTP1, GSTT1 and GSTM1) from prospectively enrolled 292 Korean patients treated with adjuvant oxaliplatin plus leucovorin plus 5-fluorouracil (FOLFOX) for colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205812.RATqmpDlYbi3nSeLPMNeidC_6vTpQp3Nyl85wFkeb3sxQ130_provenance.
- NP205830.RAUJiRHg_V2HiFcXlPXSz956udsMVfwKWYPfiXpDiyRIU130_assertion description "[Individuals with the CC genotype of TLR9 (T1486C) (14.9% in the chronic periodontitis group vs. 28.6% in the periodontally healthy group) and those expressing the T allele of TLR9 (T1486C) (CT and TT) (85.1% in the chronic periodontitis group vs. 71.4% in the periodontally healthy group) were also significantly differently distributed between groups without adjustment (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205830.RAUJiRHg_V2HiFcXlPXSz956udsMVfwKWYPfiXpDiyRIU130_provenance.
- NP205832.RAb_Nj_ZrOs8eN6c4ZP57L_seyouBvPNzapejPomxSkAE130_assertion description "[Analogously, there were positive correlations of RANKL mRNA expression with total Lequesne's scores, pain scores in response to pressure, and swelling scores in OA patients at Grade I. CONCLUSSIONS: Some biochemical factors, including content of NO, MMP-3, MMP-9, and transcript levels of some genes, including MMP-9 mRNA and RANKL mRNA, may be specific and sensitive enough to diagnose OA diseases at an early stage in the pathological process of OA when radiological features do not reflect degradation of articular cartilage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205832.RAb_Nj_ZrOs8eN6c4ZP57L_seyouBvPNzapejPomxSkAE130_provenance.
- NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion description "[Differentiation between benign and malignant tumors of the adrenal cortex was attempted by microdissection of nine cases of adrenal cortical hyperplasia, 10 cortical adenomas, and 18 adrenal cortical carcinomas with subsequent polymerase chain reaction (PCR) amplification for loss of heterozygosity (LOH) of five microsatellites of putative tumor suppressor gene loci: p53 gene (17p), the neuroblastoma candidate gene (1p), the p16 gene (9p), the von Hippel Lindau gene (3p), and the retinoblastoma gene (13q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance.
- NP205838.RAViOWlxStYJ4brg5aRJz7AnrQ-RhF2T0roZ9Gv9zVV-w130_assertion description "[As TAP2*Bky2 had a strong linkage disequilibrium with DRB1*08032, TAP2*Bky2 or its haplotype with DRB1*08032 may be involved in SS-A/Ro antibody production not only in SS but also SLE patients, indicating that TAP2*Bky2 may be a susceptible gene not only to the disease of SS but also to the SS-A/Ro autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205838.RAViOWlxStYJ4brg5aRJz7AnrQ-RhF2T0roZ9Gv9zVV-w130_provenance.
- NP205839.RAWOn6RkaydAt0o-w-5Sxgww5T9hpcDoBPcXR4puL0Nfw130_assertion description "[The tetraspanin CD9 molecule was expressed in 18/18 nevi, but was lost in 20/28 primary melanomas (including thin lesions), and in 24/52 metastatic lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205839.RAWOn6RkaydAt0o-w-5Sxgww5T9hpcDoBPcXR4puL0Nfw130_provenance.
- NP205847.RAadwLdhWLABOPWRtiwmtfZeFQOB341yRG1RgdO8SGB3Q130_assertion description "[Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205847.RAadwLdhWLABOPWRtiwmtfZeFQOB341yRG1RgdO8SGB3Q130_provenance.
- NP205849.RARSMpgCgP6SCyptr6gAagJPLkyUYv5sXihvEI2RTzXpg130_assertion description "[The therapeutic application of TLR9 has been explored extensively in recent years, and many studies are being conducted to assess the safety and efficacy of TLR9 agonists in various diseases, including atopic and infectious diseases, and cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205849.RARSMpgCgP6SCyptr6gAagJPLkyUYv5sXihvEI2RTzXpg130_provenance.
- NP205852.RAQj02xYn1JQDYjT4R8nA-MehzWvNye31zLqe0jCdfhrQ130_assertion description "[We found that polymorphisms of the β1-AR and β2-AR genes are associated with differential LV remodeling in patients treated with a β1 receptor antagonist following STEMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205852.RAQj02xYn1JQDYjT4R8nA-MehzWvNye31zLqe0jCdfhrQ130_provenance.
- NP205856.RAVW6OkaN2grCn6pPJTw4RXQhVrTvq91M9uGd8jOAGxsE130_assertion description "[Our data extend the evidence that allelic variation in the TPH gene is a risk factor for deliberate self-harm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205856.RAVW6OkaN2grCn6pPJTw4RXQhVrTvq91M9uGd8jOAGxsE130_provenance.
- NP205857.RAfLhyT3T8ajFDhWfw2jyUj05YxWwiPV3_HkG7R-FzFbM130_assertion description "[These observations indicate that FOXC2 plays a central role in promoting invasion and metastasis and that it may prove to be a highly specific molecular marker for human basal-like breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205857.RAfLhyT3T8ajFDhWfw2jyUj05YxWwiPV3_HkG7R-FzFbM130_provenance.
- NP205862.RAYbnLUew8Kcgy4rTzF8WKFzl4yS1MDReXqO65xHjO4Js130_assertion description "[Previous studies have shown that cysteine-rich secretory protein containing LCCL domain 2 (CRISPLD2) is a novel lipopolysaccharide (LPS)-binding protein, and the upregulation of CRISPLD2 expression protects mice against LPS-induced lethality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205862.RAYbnLUew8Kcgy4rTzF8WKFzl4yS1MDReXqO65xHjO4Js130_provenance.
- NP205869.RAeVSxcvuvjZZiSc2AQ8_uRok74zjKKVsU37a3yQkrB48130_assertion description "[Biopsies from 83 patients with acquired proteinuric diseases were analyzed (minimal change disease [MCD; n = 13], benign nephrosclerosis [n = 16], membranous glomerulopathy [n = 31], focal and segmental glomerulosclerosis [FSGS; n = 9], and controls [n = 14]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205869.RAeVSxcvuvjZZiSc2AQ8_uRok74zjKKVsU37a3yQkrB48130_provenance.
- NP205873.RAQfo5jBNRq2ukMaUFU5HWHZhszuU2dkIGMRWRqSUnhnA130_assertion description "[The loss of the fragile X RNA binding protein, FMRP, causes macroorchidism and mental retardation in man.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205873.RAQfo5jBNRq2ukMaUFU5HWHZhszuU2dkIGMRWRqSUnhnA130_provenance.
- NP205875.RAaQ3krnnfitKAV2nQqKnKksOXa_U8RhENz_WzHgho3XE130_assertion description "[Ectopic expression and depletion of miR-181b showed that miR-181b enhanced matrix metallopeptidases (MMP)2 and MMP9 activity and promoted growth, clonogenic survival, migration and invasion of hepatocellular carcinoma (HCC) cells that could be reversed by modulating TIMP3 level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205875.RAaQ3krnnfitKAV2nQqKnKksOXa_U8RhENz_WzHgho3XE130_provenance.
- NP205878.RAc0LKTLT5Jj7hP-M66a-4BcFo0kC8voJWJGYcmH3LpXM130_assertion description "[Correlation between stromelysin-3 mRNA level and outcome of human breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205878.RAc0LKTLT5Jj7hP-M66a-4BcFo0kC8voJWJGYcmH3LpXM130_provenance.
- NP205880.RASRSuPFupZOp3ODwj9DJ6r7OFXvE1QgdVqJqFqZWfxes130_assertion description "[This study was undertaken to characterize the molecular defects of DAX-1 in 3 unrelated Korean patients with AHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205880.RASRSuPFupZOp3ODwj9DJ6r7OFXvE1QgdVqJqFqZWfxes130_provenance.
- NP205881.RAQ_wK6zKmVt4dqnmE6wGILwAxOZjFSzJImdL2Pq8f9lA130_assertion description "[The four secretory mucin genes clustered on chromosome 11, MUC2, MUC5AC, MUC5B and MUC6, were screened in 37 patients with cancers in the left hemi-colon or rectum and 10 normal rectal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205881.RAQ_wK6zKmVt4dqnmE6wGILwAxOZjFSzJImdL2Pq8f9lA130_provenance.
- NP205893.RAbquDmwzwLTsDf7xIITWsWKdTkWpBzNZxBFM0RbVeAH4130_assertion description "[We conclude that tumor suppressor miRNAs are direct and influential regulators of Msi1, affecting its expression pattern during tumorigenesis of malignant nervous system tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205893.RAbquDmwzwLTsDf7xIITWsWKdTkWpBzNZxBFM0RbVeAH4130_provenance.
- NP205900.RAe3GmFQz2Dc7kw-Nkn791zK5tVHl1rU69XwkQM9c1MJ4130_assertion description "[The CD8 memory T cell repertoire to the influenza A derived M1(58-66) epitope shows a restricted V genes and CDR3 sequences usage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205900.RAe3GmFQz2Dc7kw-Nkn791zK5tVHl1rU69XwkQM9c1MJ4130_provenance.
- NP205907.RAbegs-AWXvi0FPPM-LDlGio_g8UDNbEg-VqM78ZWrYDU130_assertion description "[The objectives of the study were a detailed phenotyping for CNC manifestations in 12 kindreds bearing the same PRKAR1A mutation and a study of the consequences of the mutation and a potential founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205907.RAbegs-AWXvi0FPPM-LDlGio_g8UDNbEg-VqM78ZWrYDU130_provenance.
- NP205909.RAZP6xO32joNvLRbilR-LrIihE19miiTcesWsM8PRVb1c130_assertion description "[Thirty-two percent of the AU patients were HLA B27+, as were 42% of males (19% females) with their first attack of AU compared with 60% of males (23% females) with recurrent AU.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205909.RAZP6xO32joNvLRbilR-LrIihE19miiTcesWsM8PRVb1c130_provenance.
- NP205920.RASYe2h5EFm5qmSeGkl3mkjGtWQqJBDeGySTQzsijQL3I130_assertion description "[We show that the t(4;11)(p12;q23) translocation results in the creation of a chimeric RNA encoding a putative fusion protein containing 1,362 amino acids from the NH2-terminal part of MLL and 712 amino acids from the COOH-terminal part of AF4p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205920.RASYe2h5EFm5qmSeGkl3mkjGtWQqJBDeGySTQzsijQL3I130_provenance.