Nanopublications

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

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NP320955.RAYTbrV0pvxsNp_Lr0s3QGU7tL7gBYtBYVwj18s62-UuU130_assertion description "[SIRT6-deficient mice are small and at 2-3 weeks of age develop abnormalities that include profound lymphopenia, loss of subcutaneous fat, lordokyphosis, and severe metabolic defects, eventually dying at about 4 weeks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320955.RAYTbrV0pvxsNp_Lr0s3QGU7tL7gBYtBYVwj18s62-UuU130_provenance.
NP320962.RARzWUMGpZRZgqx3PMLqbFno0QasbAuon1RsH_9d6wgyI130_assertion description "[Replication in an independent sample of 21,408 cases and 19,185 controls identified five loci newly associated with CAD (P < 5 × 10⁻⁸ in the combined discovery and replication analysis): LIPA on 10q23, PDGFD on 11q22, ADAMTS7-MORF4L1 on 15q25, a gene rich locus on 7q22 and KIAA1462 on 10p11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320962.RARzWUMGpZRZgqx3PMLqbFno0QasbAuon1RsH_9d6wgyI130_provenance.
NP320963.RASNSGskP0hSzXgAiDklVnl9UqNXOdG4UBFMFFLvbewrQ130_assertion description "[The mean peroxidase activity was however significantly increased in CSF and serum of ALS patients with the specificity of 80% and 73%, and the sensitivity of 78% and 85%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320963.RASNSGskP0hSzXgAiDklVnl9UqNXOdG4UBFMFFLvbewrQ130_provenance.
NP320964.RAeyedwIL3EKd4A7NLQSebPcUe9sKgNpO332Jj__koXp4130_assertion description "[Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320964.RAeyedwIL3EKd4A7NLQSebPcUe9sKgNpO332Jj__koXp4130_provenance.
NP320969.RAf3OYKifg1bgXfdbYeUvowBSTkBTi5auFNRgwTR_6gc8130_assertion description "[Universal HLA-B*15:02 screening represents good value for the money in terms of preventing SJS/TEN in CBZ-treated patients with neuropathic pain at the Thai ceiling ratio of 120,000 THB/QALY gained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320969.RAf3OYKifg1bgXfdbYeUvowBSTkBTi5auFNRgwTR_6gc8130_provenance.
NP320975.RAWQCU3RV_R6ToQxzH1SzWpIismZ6WrSE3pII7Z2368Bk130_assertion description "[Moreover, it is demonstrated that MYH9 mutations also result in two other FTNS-like macrothrombocytopenia syndromes: Epstein syndrome (EPS) and Alport syndrome with macrothrombocytopenia (APSM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320975.RAWQCU3RV_R6ToQxzH1SzWpIismZ6WrSE3pII7Z2368Bk130_provenance.
NP320978.RASD54odePz9uh6rwxO9r8CSHwsveqQgfBIQu99ZScJ48130_assertion description "[Both TET1 and HOXA9 suppress breast tumor growth and metastasis in mouse xenografts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320978.RASD54odePz9uh6rwxO9r8CSHwsveqQgfBIQu99ZScJ48130_provenance.
NP320983.RAd0YlNnGIMCHwz-wvLpMchBOsgR3ZhGLiY23b69G7RbM130_assertion description "[Moreover , our immunohistochemistrical results indicated that the COX-2 protein was significantly over-expressed in well-differentiated HCC, but not significantly increased in expression in poorly-differentiated HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320983.RAd0YlNnGIMCHwz-wvLpMchBOsgR3ZhGLiY23b69G7RbM130_provenance.
NP320984.RAS9BZk94rXXYgQ8vUPBlzKy-faNKR58ehjBFJ9as-2WM130_assertion description "[The combined ORs for NAT2 slow or rapid acetylator and gastric cancer risk were 1.05 (95% CI 0.810-1.35) and 0.96 (95% CI 0.74-1.23), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320984.RAS9BZk94rXXYgQ8vUPBlzKy-faNKR58ehjBFJ9as-2WM130_provenance.
NP320986.RAT3Dl1GO1YmXKzkuoZ0Fps0LDG9tqp1zvuGe6FMWBVZg130_assertion description "[The difference was, however, mainly secondary to a strong linkage disequilibrium between these TAP alleles and DR8, which is significantly increased in JRA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320986.RAT3Dl1GO1YmXKzkuoZ0Fps0LDG9tqp1zvuGe6FMWBVZg130_provenance.
NP320988.RAesB1g0AxUOwoOo1VZgaRm2yt0-O-tM8yrFacwIDd3Iw130_assertion description "[A set of 662 FFPE DNA samples not only confirmed that APOLD1 and SRPX2 are hypomethylated in CRC but also revealed hypomethylation to be significantly (p < 0.01) associated with tumors being localized in the left side, CpG island methylator phenotype negative, MSS, BRAF wt, undifferentiated and of adenocarcinoma histosubtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320988.RAesB1g0AxUOwoOo1VZgaRm2yt0-O-tM8yrFacwIDd3Iw130_provenance.
NP320991.RAZ0ydrlbseIxw0tj_aY-g8cRqxFQBReHTdPyiPYGjBdM130_assertion description "[LIM protein and homeodomain protein genes are frequently involved in translocations of hematological malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320991.RAZ0ydrlbseIxw0tj_aY-g8cRqxFQBReHTdPyiPYGjBdM130_provenance.
NP320992.RAVOeEFnnKhZ-rnhpAZ2Go7zz4Z8M5oY5z7yjevoB8etM130_assertion description "[Moreover, it is the human CYP2E1 that restores these effects of ethanol, which suggests that results for fatty liver and oxidant stress from rodent models of ethanol intake and mouse CYP2E1 can be extrapolated to human models of ethanol intake and to human CYP2E1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320992.RAVOeEFnnKhZ-rnhpAZ2Go7zz4Z8M5oY5z7yjevoB8etM130_provenance.
NP320997.RAbX0L0ZasddfNeiFPfosBosxwia3pHHKEZWqmqq1ifuQ130_assertion description "[We report that the seizure-induced decrease in GABA(A)R alpha1 subunit expression associated with epilepsy is mediated by the Janus kinase (JAK)/signal transducer and activator of transcription (STAT) pathway regulated by brain-derived neurotrophic factor (BDNF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320997.RAbX0L0ZasddfNeiFPfosBosxwia3pHHKEZWqmqq1ifuQ130_provenance.
NP320998.RAeeo_m_J9sQhyv817hdNMo5NCuGDaL0_KZcWjKM6MAxw130_assertion description "[Disruption of the murine cyp4a14 and cyp4a10 genes, homologues of human CYP4A11, was reported recently to cause hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320998.RAeeo_m_J9sQhyv817hdNMo5NCuGDaL0_KZcWjKM6MAxw130_provenance.
NP321002.RAZysKjslJdesNAWHt_ieT5QtJKtnMzr96CFRp-lfAlvw130_assertion description "[These peptides were examined for their ability to induce peptide-specific T cell responses in peripheral blood mononuclear cells (PBMCs) obtained from HLA-A*02(+) healthy donors and/or HLA-A*02(+) cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321002.RAZysKjslJdesNAWHt_ieT5QtJKtnMzr96CFRp-lfAlvw130_provenance.
NP321003.RAUNNgXMYeA43q7-oyH1UXyBQZ7MKmjY30Ec6hQsLnSOE130_assertion description "[Mammaglobin B is a uteroglobin gene family member recently found highly differentially expressed in serous papillary ovarian cancer by gene expression profiling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321003.RAUNNgXMYeA43q7-oyH1UXyBQZ7MKmjY30Ec6hQsLnSOE130_provenance.
NP321006.RAdwz1PNxkrqRIJRl5WWHV9JLY4U9O1QKQpYfl0Rn7wyY130_assertion description "[A rare genetic form of insulin resistance is Dunnigan-type familial partial lipodystrophy (FPLD; OMIM #151660), which is characterized by loss of subcutaneous fat from extremities, trunk, and gluteal region, and always by insulin resistance and hyperinsulinemia, often with hypertension, dyslipidemia, type-2 diabetes and early endpoints of atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321006.RAdwz1PNxkrqRIJRl5WWHV9JLY4U9O1QKQpYfl0Rn7wyY130_provenance.
NP321010.RAanSyrf5cajuoxeFfQdD6AyMINwlW5CZRuE8AOWx8to8130_assertion description "[Neurochemical dementia diagnostics (NDD) can significantly improve the clinically based categorization of patients with early dementia disorders, and the cerebrospinal fluid (CSF) concentrations of amyloid beta peptides ending at the amino acid position of 42 (A beta x-42 and A beta 1-42) are widely accepted biomarkers of Alzheimer's disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321010.RAanSyrf5cajuoxeFfQdD6AyMINwlW5CZRuE8AOWx8to8130_provenance.
NP321012.RAbYUrdYGKhiB7r3jCfBm1gKPcHZVj1ivKd0p90j4QJMk130_assertion description "[In clinical prostate cancer specimens, the expression of uncoupling protein 1 (UCP1), a brown fat-specific marker, was enhanced with the level of expression correlated to disease progression from primary to bone metastatic cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321012.RAbYUrdYGKhiB7r3jCfBm1gKPcHZVj1ivKd0p90j4QJMk130_provenance.
NP321013.RAQHGUl-bKVDoFD3EY-W8X49UnOtkXKs4knJ8Ptd7zVvU130_assertion description "[Moderate gynaecomastia and testicular atrophy are usually present, suggesting a defect in androgen receptor function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321013.RAQHGUl-bKVDoFD3EY-W8X49UnOtkXKs4knJ8Ptd7zVvU130_provenance.
NP321014.RAXi2cLUqbYJJQQhxyATYXjPPQn6QNbQFebEl47vLPuM0130_assertion description "[The data indicate that H11/HspB8 overload causes melanoma growth arrest and apoptosis through TAK1 activation and suggest that H11/HspB8 is a promising molecular therapy target.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321014.RAXi2cLUqbYJJQQhxyATYXjPPQn6QNbQFebEl47vLPuM0130_provenance.
NP321019.RAewbikSNU1LImZUfrGfSoapGoovwkgsZDmJ4B-UYtCLo130_assertion description "[DYX1C1 has been associated with dyslexia and neuronal migration in the developing neocortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321019.RAewbikSNU1LImZUfrGfSoapGoovwkgsZDmJ4B-UYtCLo130_provenance.
NP321022.RAZghMw10XwaGWikd6hqa0gU4XHb_rPxMLdZ_iZ1dJk5A130_assertion description "[The overall expression of the KLK8 gene and the amounts of the KLK8-T3 and KLK8-T4 mRNAs were significantly increased in lung tumor tissue (P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321022.RAZghMw10XwaGWikd6hqa0gU4XHb_rPxMLdZ_iZ1dJk5A130_provenance.
NP321025.RAdoPESR7lsxqaAi0Ep2euacnhIiAYQTK_1hQSznp4pOE130_assertion description "[Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321025.RAdoPESR7lsxqaAi0Ep2euacnhIiAYQTK_1hQSznp4pOE130_provenance.
NP321030.RAV9ugjllrRdaRYmBW3Jpg-YXLAJC7Ovwmyu_kudPVkwM130_assertion description "[Two members of the S100 gene family, S100A6 and S100A4 have been suggested to be associated with cancer invasion and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321030.RAV9ugjllrRdaRYmBW3Jpg-YXLAJC7Ovwmyu_kudPVkwM130_provenance.
NP321035.RAdfoNCBTJVze_HZFwSwrc3U7UzE3WdOyTdcdTP2K6O_A130_assertion description "[All of the five known MODY genes, HNF-4alpha, glucokinase, HNF-1alpha, HNF-1beta, and IPF1, were previously excluded as being the cause of diabetes in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321035.RAdfoNCBTJVze_HZFwSwrc3U7UzE3WdOyTdcdTP2K6O_A130_provenance.
NP321046.RAXM-4m5LeO0SCtAnHRfzMQTWjZdiJ8DDRpK2SORm7RSM130_assertion description "[In support of this hypothesis, our screen revealed significantly higher levels of two hnRNP A1 transcripts in oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321046.RAXM-4m5LeO0SCtAnHRfzMQTWjZdiJ8DDRpK2SORm7RSM130_provenance.
NP321049.RAfRUnAJgEjy0PsjmiFtbRBAwKXn8ccVECLvfWYr4BgrM130_assertion description "[Progressive familial heart block type I (PF-HBI) is a dominantly inherited cardiac bundle-branch conduction disorder that has been traced through nine generations of a large South African kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321049.RAfRUnAJgEjy0PsjmiFtbRBAwKXn8ccVECLvfWYr4BgrM130_provenance.
NP321050.RAUxiMuhsbYVbHU15X20zFMHSWHUu8BsG6qe9B44gZGbw130_assertion description "[Moreover, patients with liver diseases such as fulminant hepatitis, liver cirrhosis due to hepatitis virus infection and primary biliary cirrhosis show elevation of serum levels of IL-18, that correlates with the corresponding disease severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321050.RAUxiMuhsbYVbHU15X20zFMHSWHUu8BsG6qe9B44gZGbw130_provenance.
NP321052.RAaWaZXNEEdvries8iYeBWvmMKWBSeh2uNROL4CIj8gqI130_assertion description "[PRKAR1A mutations leading to cAMP pathway dysregulation are observed in primary pigmented nodular adrenocortical diseases (PPNADs) and some sporadic ACAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321052.RAaWaZXNEEdvries8iYeBWvmMKWBSeh2uNROL4CIj8gqI130_provenance.
NP321053.RAYUlfb7YA2h4Dy-9w3I_wHqUj-SHaWE8lKjUGEV7BAos130_assertion description "[Comparatively, expression of COX-2 protein is higher in eutopic endometria from women with endometriosis compared with women without endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321053.RAYUlfb7YA2h4Dy-9w3I_wHqUj-SHaWE8lKjUGEV7BAos130_provenance.
NP321054.RARtvGjOn7d2eb24QXj-D2vZ9VR7CFicBmKXSf9abrGjE130_assertion description "[HMGA2 protein was detectable in four out of 21 follicular carcinomas, 30 out of 45 papillary carcinomas, and 11 out of 12 undifferentiated carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321054.RARtvGjOn7d2eb24QXj-D2vZ9VR7CFicBmKXSf9abrGjE130_provenance.
NP321055.RAWpMyyqMfmwlG_ewlh76KSnv6RsrjSs-ohATPdEhm040130_assertion description "[We studied a population-based cohort of 288 sporadic ductal invasive cancers and found 9% positive for CK5/14 and 4% positive for p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321055.RAWpMyyqMfmwlG_ewlh76KSnv6RsrjSs-ohATPdEhm040130_provenance.
NP321061.RAYxRLUKmWiT4OzYLhgdlh2585_9BUlkGctFMLMmLAwz8130_assertion description "[All cases of cellular angiofibroma (1/1), spindle cell lipoma (6/6), and mammary-type myofibroblastoma (4/4), which were used as a control group, showed monoallelic or biallelic loss of RB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321061.RAYxRLUKmWiT4OzYLhgdlh2585_9BUlkGctFMLMmLAwz8130_provenance.
NP321062.RAesqM2-tNkfH6bfOzdys4RU5ULLYlcbmqSXUXCzpeyIM130_assertion description "[Translocations involving BCL10 in the mucosa-associated lymphoid tissue (MALT) lymphomas are associated with constitutive activation of NF-κB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321062.RAesqM2-tNkfH6bfOzdys4RU5ULLYlcbmqSXUXCzpeyIM130_provenance.
NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion description "[Even though mutations in LMNA have been reported in patients with typical dilated cardiomyopathy (DCM) and atrioventricular block (AVB) previously, the purpose of this study was to disclose this novel genetic abnormality in one Chinese family with the atypical phenotype of progressive AVB followed by DCM with normal QRS interval.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance.
NP321070.RAZYhVf0116M4ZDp1LYPSwrtEpj1REUrBPoopAjWxkRLs130_assertion description "[HLA-DQB1 associations with anti-topoisomerase-1 antibodies in patients with systemic sclerosis and their first degree relatives. United Kingdom Systemic Sclerosis Study Group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321070.RAZYhVf0116M4ZDp1LYPSwrtEpj1REUrBPoopAjWxkRLs130_provenance.
NP321072.RAdnaV8VchEjQEUyDH-ydxhM2DWFfNSiBKSwJgH3s4vzI130_assertion description "[We applied this test to pedigree data from the NIMH Alzheimer's Disease Genetics Initiative Database separated into AP and NAP pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321072.RAdnaV8VchEjQEUyDH-ydxhM2DWFfNSiBKSwJgH3s4vzI130_provenance.
NP321075.RAWfCIVvAjv87YqYa1muTnKQ4KcXG79I5jCZhq1RDmkIc130_assertion description "[A three generation family from northern Sweden with both trichorhinophalangeal syndrome type I (TRP I) and systemic lupus erythematosus (SLE)-like syndrome with complement C4 homozygous null alleles is described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321075.RAWfCIVvAjv87YqYa1muTnKQ4KcXG79I5jCZhq1RDmkIc130_provenance.
NP321081.RAbtOnkY9Aveq2poXLs2-82BwztLY8bElJtMYZOukt8P4130_assertion description "[ALT-type sarcomas were also sensitive to OBP-301 because of upregulation of human telomerase reverse transcriptase (hTERT) mRNA following virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321081.RAbtOnkY9Aveq2poXLs2-82BwztLY8bElJtMYZOukt8P4130_provenance.
NP321084.RAUdPsc2cRmCNkjMH01oy8q894pFZM941GsLmptmyMjDc130_assertion description "[Our aim was to evaluate the influence of CYP2D6 genotype on psychopathological symptoms and the occurrence of EPS in Slovenian outpatients with schizophrenia or schizoaffective disorder in stable remission, receiving long-term maintenance antipsychotic treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321084.RAUdPsc2cRmCNkjMH01oy8q894pFZM941GsLmptmyMjDc130_provenance.
NP321085.RAUnMOUeVdLGK0CXWxYLDgG35awIAWiHFCJY9J-X6_Oto130_assertion description "[As a consequence, the Mamu-DPB1*01 allele may represent one of the risk factors involved in determining susceptibility to EAE in an outbred population of rhesus macaques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321085.RAUnMOUeVdLGK0CXWxYLDgG35awIAWiHFCJY9J-X6_Oto130_provenance.
NP321089.RAaFrDldRPUwKVIT11Au3U8w36m1b1ynOwz8zN9YBv8NY130_assertion description "[Further analyses to examine the joint effect of MBL2 and IL-1B polymorphisms, previously shown to predispose to stomach cancer, indicated that the combination of at-risk IL-1B genotypes (CT or TT at location -511) and HYD MBL2 haplotype was associated with a 3.5-fold risk (OR = 3.5, 95% CI 1.6-7.6; p = 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321089.RAaFrDldRPUwKVIT11Au3U8w36m1b1ynOwz8zN9YBv8NY130_provenance.
NP321094.RAaRFi1HI3_ditLBW75LortJ_Yxjj-JTHYw8AjPxJf2OE130_assertion description "[Effect of apolipoprotein E alleles and angiotensin-converting enzyme insertion/deletion polymorphisms on lipid and lipoprotein markers in middle-aged men and in patients with stable angina pectoris or healed myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321094.RAaRFi1HI3_ditLBW75LortJ_Yxjj-JTHYw8AjPxJf2OE130_provenance.
NP321100.RAcuu3rZYfUP41-6oq-rQM3bHobev2UIVqRKdKNG1hUB8130_assertion description "[An important role for HDAC6 in kinesin-1 dependent transport of brain-derived neurotrophic factor (BDNF) from the cortex to the striatum has also been demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321100.RAcuu3rZYfUP41-6oq-rQM3bHobev2UIVqRKdKNG1hUB8130_provenance.
NP321102.RASkRAf1_3D5_bqpFwwuXF9GesF4Za1dFnT13saYnIlgI130_assertion description "[Recently, HDAC1 has been reported to be overexpressed in hepatocellular carcinoma (HCC), but its biological roles in hepatocarcinogenesis remain to be elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321102.RASkRAf1_3D5_bqpFwwuXF9GesF4Za1dFnT13saYnIlgI130_provenance.
NP321103.RAd9sECnWTPIfCI9QevdbqNMuQLK9QacqqX2YejS3XEMM130_assertion description "[Understanding alpha-globin gene regulation: Aiming to improve the management of thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321103.RAd9sECnWTPIfCI9QevdbqNMuQLK9QacqqX2YejS3XEMM130_provenance.
NP321111.RAeb520HxRSbYTdiIpG4-3gjOJORyQiDHy0LdZOwVcAMk130_assertion description "[Of the 50 (50%) solid-pseudopapillary neoplasms, 25 showed diffuse expression (in >50% neoplastic cells) of KIT and additional five (10%) cases showed focal staining (in 10-50% neoplastic cells).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321111.RAeb520HxRSbYTdiIpG4-3gjOJORyQiDHy0LdZOwVcAMk130_provenance.
NP321114.RAePOWRD_S78t8fgzOrI_zx93y2xagApuC1_zdN-Yhic0130_assertion description "[Fibroblasts bearing PS1 M146V and H163Y mutations showed a 30% increase in soluble PKC levels and a 40% decrease in PKC-mediated APPs secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321114.RAePOWRD_S78t8fgzOrI_zx93y2xagApuC1_zdN-Yhic0130_provenance.
NP321120.RAXQ7VRcpb5yoOJCAbOa3AFYsHxtKR_0uTmwVOaHSrCaI130_assertion description "[Moreover, ex vivo stimulation of gammadelta T cells with zoledronic acid and interleukin-2 compensated in part for this deficiency, as it stimulated the proliferation, cytokine production, and enhanced the expression of messenger RNA of granzyme B. Interestingly, when the known granzyme B gene polymorphism was screened, we found the prevalence of the mutated genotype RAH/RAH to be significantly (p<0.017) associated with breast cancer patients (14.30%) compared with normal donors (1.40%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321120.RAXQ7VRcpb5yoOJCAbOa3AFYsHxtKR_0uTmwVOaHSrCaI130_provenance.
NP321122.RAcIu4-YzXN5FdeJgUFVpICljmWdJxffJn0uHzctOaUyA130_assertion description "[To determine the function of TREM-1 in pneumococcal pneumonia, we first established TREM-1 up-regulation in infected lungs and human plasma together with augmented alveolar macrophage responsiveness toward Streptococcus pneumoniae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321122.RAcIu4-YzXN5FdeJgUFVpICljmWdJxffJn0uHzctOaUyA130_provenance.
NP321129.RASjxCaXpUzin6NZ7A3bA38HR-7X6wkXTLytGLIoXVSHI130_assertion description "[An expression of MMP-1 (interstitial collagenase), MMP-2 (72-kDa type IV collagenase) and MMP-3 (stromelysin-1) was investigated in squamous cell carcinoma (SCC) and its precancerous condition, actinic keratosis (AK), using in situ hybridization techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321129.RASjxCaXpUzin6NZ7A3bA38HR-7X6wkXTLytGLIoXVSHI130_provenance.
NP321134.RAckeJ9vADr4IEBBrfjPVBcz-BjGUD0PMaeiksrcPYSRk130_assertion description "[In conclusion, this is the first evidence that genetic polymorphisms in the MHC class III region are significantly associated with ER-positive breast cancer in the Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321134.RAckeJ9vADr4IEBBrfjPVBcz-BjGUD0PMaeiksrcPYSRk130_provenance.
NP321137.RAaOw2wfTgk1BhBS5CL-oa4Jt0XIInVEZuGhY-jhDpAjI130_assertion description "[In order to achieve a better understanding of the aetiology of iodine deficiency-based mental retardation in the Qinba mountainous area, we conducted further studies of ApoE allele frequencies obtained from the local population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321137.RAaOw2wfTgk1BhBS5CL-oa4Jt0XIInVEZuGhY-jhDpAjI130_provenance.
NP321142.RAUr9gDcE86JAwAblbTzCeHglxj_1M3jA-rGkNhfsIMAc130_assertion description "[DSS-induced colitis was ameliorated by pretreatment with a potent AhR activator, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321142.RAUr9gDcE86JAwAblbTzCeHglxj_1M3jA-rGkNhfsIMAc130_provenance.
NP321144.RAYW7uTYcMIhvZFKKYmmQFBGszkCc0AuuH03l6nC7_Ptw130_assertion description "[Familial hepatic veno-occlusive disease with immunodeficiency (VODI, OMIM: 235550), a rare form of severe combined immune deficiency, was first described in Australian Lebanese patients as being associated with homozygous mutations in SP110, a gene encoding a PML nuclear body-associated protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321144.RAYW7uTYcMIhvZFKKYmmQFBGszkCc0AuuH03l6nC7_Ptw130_provenance.
NP321145.RAcb0h0gzrgmnR_S7RQnA5LLhEHYQuNCjCdz_nPAsDdDY130_assertion description "[Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321145.RAcb0h0gzrgmnR_S7RQnA5LLhEHYQuNCjCdz_nPAsDdDY130_provenance.
NP321150.RAUzUx9oTRMt6LoLdto4b8_YiRXkaAt_KsBA7-X7uXCaE130_assertion description "[Significantly higher C-reactive protein levels occurred in CHD patients with lower NQO1 activity (P=0.001), however, due to the large variations in CRP levels seen in CHD patients; the clinical importance of this difference is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321150.RAUzUx9oTRMt6LoLdto4b8_YiRXkaAt_KsBA7-X7uXCaE130_provenance.
NP321152.RASXhBI9Ritw9nlUeppLmSAkYLLbSrrwJakHZPBM1QK_E130_assertion description "[It may be concluded that aberrant mitogenic signaling in human breast cancer in vivo involves Pak, p38 MAPK and MAPKAPK2 downstream of PI3-K, but neither of PKB or p70 S6K.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321152.RASXhBI9Ritw9nlUeppLmSAkYLLbSrrwJakHZPBM1QK_E130_provenance.
NP321156.RATLguHhgbfn2e9dBOfcILSk3jBmIbQM-9vqMPFDB04Ss130_assertion description "[No association was found between the IRS-I G972R, PPAR-gamma P12A, and KCNJ11 E23K, or TNF-alpha -308G/A polymorphic variants and the metabolic syndrome, or its components, for either definition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321156.RATLguHhgbfn2e9dBOfcILSk3jBmIbQM-9vqMPFDB04Ss130_provenance.
NP321159.RASBpdBBnv80tlPoBa2GxQrORZpYrP0dqBeTxveZXruMY130_assertion description "[Myeloid differentiation 2 (MD-2) plays a critical role in orchestrating the innate immune response and the development of sepsis and subsequent organ dysfunction after trauma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321159.RASBpdBBnv80tlPoBa2GxQrORZpYrP0dqBeTxveZXruMY130_provenance.
NP321162.RARo_vbF3u0MAUDv6SGol8EMEtOayZLSY6_KWsC9TRmyI130_assertion description "[When combined with histopathology, multiplex PCR could detect 97.5% of all the cases in the intestinal tuberculosis group, while in combination adenosine deaminase levels (ADA) in cases of peritoneal tuberculosis it increased the specificity of diagnosis of peritoneal tuberculosis to 95%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321162.RARo_vbF3u0MAUDv6SGol8EMEtOayZLSY6_KWsC9TRmyI130_provenance.
NP321163.RAczWSAazrNuj4wb9alzlvQqJCTnbLgiwWqI0QMHh2CQ4130_assertion description "[Stromal cell-derived factor 1 alpha (SDF-1alpha) and its receptor CXCR4 play important roles in the pathogenesis of human immunodeficiency virus type one (HIV-1)-associated dementia (HAD) by serving as a HIV-1 co-receptor and affecting cell migration, virus-mediated neurotoxicity, and neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321163.RAczWSAazrNuj4wb9alzlvQqJCTnbLgiwWqI0QMHh2CQ4130_provenance.
NP321168.RAULuwIiwxwiaTHEhNQxWAnHTjxl1tk68taJELVktxzlE130_assertion description "[These paradoxical effects of PTHrP on renovascular SMC proliferation appear to be reversed in the SHR model of genetic hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321168.RAULuwIiwxwiaTHEhNQxWAnHTjxl1tk68taJELVktxzlE130_provenance.
NP321174.RAWFj5LexKpsDpXkkSrtWUst-AcIjbZXnkVJotoMJnK58130_assertion description "[Patients with severe bacterial infection and ED or unexplained mycobacterial sensitivity were evaluated for NEMO mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321174.RAWFj5LexKpsDpXkkSrtWUst-AcIjbZXnkVJotoMJnK58130_provenance.
NP321177.RAaOyEyRBjg7uUAoCRBTli899qiNxFIvPoKzKPzosIR54130_assertion description "[The data indicate that constitutive activation of the Wnt signaling pathway caused by CTNNB1 mutation is involved in the development and/or progression of a subset of lung carcinoma, preferentially in adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321177.RAaOyEyRBjg7uUAoCRBTli899qiNxFIvPoKzKPzosIR54130_provenance.
NP321178.RAe55ej5ZBn4dACj89SuY2glRiVK-0BFsepbjhf2SHhL8130_assertion description "[To analyse fibronectin (FN) gene polymorphisms in type II mixed cryoglobulinemic syndrome (MCsn), an immune-complex mediated systemic vasculitis linked to hepatitis C virus (HCV) infection and characterised by rheumatoid factor (RF) positive B-cell proliferation at high risk for the progression into non-Hodgkin's lymphoma (NHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321178.RAe55ej5ZBn4dACj89SuY2glRiVK-0BFsepbjhf2SHhL8130_provenance.
NP321180.RAQFPGgjilRZhMa9H7v2fB17gaLHSHQFTcRHDWelWQGOM130_assertion description "[Four CRY2 SNPs spanning from intron 2 to downstream 3'UTR were analyzed for association to bipolar disorder type 1 (n = 497), bipolar disorder type 2 (n = 60) and bipolar disorder with the feature rapid cycling (n = 155) versus blood donors (n = 1044) in Sweden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321180.RAQFPGgjilRZhMa9H7v2fB17gaLHSHQFTcRHDWelWQGOM130_provenance.
NP321181.RAaSslDIAUeBBz1PWWIJfI2OLNrwrVPBvihWrmZHz7SFk130_assertion description "[The results of the present study indicate that targeting therapies for HER-2, such as trastuzumab, may be used for EMPD particularly in patients with invasive and/or metastatic EMPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321181.RAaSslDIAUeBBz1PWWIJfI2OLNrwrVPBvihWrmZHz7SFk130_provenance.
NP321182.RATuHAkoddL9Lapk3SB3FLRonnjcapRjgtj7genG8kZfY130_assertion description "[To explore the natural history of antibodies against tissue transglutaminase (TGA), endomysium (EMA), reticulin (ARA), and gliadin (AGA-IgG and AGA-IgA) in children carrying HLA-conferred risk for celiac disease (CD) and observed frequently from birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321182.RATuHAkoddL9Lapk3SB3FLRonnjcapRjgtj7genG8kZfY130_provenance.
NP321187.RATC38B8_XUhMroCiaThpTGcQtE4M0JX1juuEGH5xnKxQ130_assertion description "[Apolipoprotein (Apo) E and three main serum markers of glycosylation defects (transferrin, Tf, alpha1-antitrypsin, aAT and ApoCIII) in patients with Alzheimer's dementia (AD), Parkinson's disease (PD) and vascular dementia (n=62, 139 and 44, respectively) were analyzed by isoelectric focusing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321187.RATC38B8_XUhMroCiaThpTGcQtE4M0JX1juuEGH5xnKxQ130_provenance.
NP321188.RAUNzsoUp8sV_EawI39sKsoBXbxELBE9WRpVtRitfP9xY130_assertion description "[These expression profiles of MUC1 and MUC2 related to the prognoses of the patients were also observed in biliary neoplasms such as intrahepatic cholangiocarcinoma (ICC)-mass-forming type (MF), mucin-producing bile duct tumor (MPBT), and extrahepatic bile duct carcinoma (EHBDC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321188.RAUNzsoUp8sV_EawI39sKsoBXbxELBE9WRpVtRitfP9xY130_provenance.
NP321189.RAWrLOsdTcMSZ_5jU-nr1wJCAsSq6SndDoPsM60UcAz_0130_assertion description "[TSA could be a candidate of a therapeutic agent for reversing the TGF-beta1-induced ECM synthesis that leads to nasal polyp development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321189.RAWrLOsdTcMSZ_5jU-nr1wJCAsSq6SndDoPsM60UcAz_0130_provenance.
NP321192.RAaeAbB-TGwYX3LApmHurwlU760EiVoS7DqiE76c7xaWw130_assertion description "[Infection by measles virus (MV) induces type I IFN via the retinoic acid-inducible gene I/melanoma differentiation-associated gene 5/mitochondrial antiviral signaling protein (MAVS) pathway in human cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321192.RAaeAbB-TGwYX3LApmHurwlU760EiVoS7DqiE76c7xaWw130_provenance.
NP321198.RAb6Sd8nWzxTTfaL5DcP9-zHxORvgrp59_F14NeuzNLU4130_assertion description "[In multivariate, random-effects linear models adjusted for age, education, gender, and race, the risk factors diabetes and APOE epsilon4 genotype were independently associated with a decline in performance on the DSS test (both P < .005), whereas hypertension and stroke were not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321198.RAb6Sd8nWzxTTfaL5DcP9-zHxORvgrp59_F14NeuzNLU4130_provenance.
NP321199.RAfzXfh8p179MqpvjkW8sDuY66IosCE5dgaXIvaQXHXxM130_assertion description "[MET amplification identifies a small and aggressive subgroup of esophagogastric adenocarcinoma with evidence of responsiveness to crizotinib.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321199.RAfzXfh8p179MqpvjkW8sDuY66IosCE5dgaXIvaQXHXxM130_provenance.
NP321202.RAbrAzekelq8lkj-ze0E5Rqy50UQdoFY2MAvwV0zTnJjg130_assertion description "[Here, we show that this oncolytic vector (Ad5/Ad35.IR-E1A/TRAIL) efficiently infects the GBM tumor cell lines SF767, T98G, and U-87 MG. Tumor cell killing was markedly enhanced with Ad5/Ad35.IR-E1A/TRAIL compared with wild-type Ad5 and Ad35 virus or Ad5/Ad35.IR-E1A- vectors without TRAIL expression in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321202.RAbrAzekelq8lkj-ze0E5Rqy50UQdoFY2MAvwV0zTnJjg130_provenance.
NP321208.RAe0jFc0oz0e7d7Ct-ANammyJjigEBZpY6BFLrAsbb090130_assertion description "[PKD1 and PKD2 were screened for mutations or large genomic rearrangements in 3 unrelated patients with ADPKD presenting with laterality defects: dextrocardia in one and situs inversus totalis in 2 others.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321208.RAe0jFc0oz0e7d7Ct-ANammyJjigEBZpY6BFLrAsbb090130_provenance.
NP321209.RATcPm1Hb3oYqL3J9Imc0s9KrUTKeP_AYXJyTh1KExd1s130_assertion description "[We recently have characterized a new disorder (DA2B) with a phenotype intermediate between DA1 and FSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321209.RATcPm1Hb3oYqL3J9Imc0s9KrUTKeP_AYXJyTh1KExd1s130_provenance.
NP321210.RARocAeiqCy3IH7m54JIFTiE86wJ8tpiY8ziKMKSMh9SU130_assertion description "[Epigenetic dysregulation of the Jak/STAT pathway by frequent aberrant methylation of SHP1 but not SOCS1 in acute leukaemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321210.RARocAeiqCy3IH7m54JIFTiE86wJ8tpiY8ziKMKSMh9SU130_provenance.
NP321215.RAfV6HSZp1IkFnn8jYRaTj4MN6q6-VV89Kmht4Xa3-_Ck130_assertion description "[Gene copy number losses predominated over gains, and the most frequent region of loss was 9p21.3 (17/26 cases), the locus of CDKN2A and CDKN2B, both known to be commonly lost in MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321215.RAfV6HSZp1IkFnn8jYRaTj4MN6q6-VV89Kmht4Xa3-_Ck130_provenance.
NP321219.RAW6JSzRNzzUnfymIHssttBg1fx9TIacu9UtgBmJCxG_4130_assertion description "[Taken together, these results suggest that although the common BRAF mutations found in cutaneous melanoma do not play a role in tumorigenesis of uveal tract melanocytes, activation of the RAF/mitogen-activated protein kinase pathway may nevertheless play an important role in uveal melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321219.RAW6JSzRNzzUnfymIHssttBg1fx9TIacu9UtgBmJCxG_4130_provenance.
NP321224.RAap3HMQmC94_p-QuhC3BivYWTWUdCWBuA7tuK2u0hWLM130_assertion description "[HCC and HPBL have clearly different patterns of gene expression, with genes IGF2, Fibronectin, DLK1, TGFb1, MALAT1 and MIG6 being over-expressed in HPBL versus HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321224.RAap3HMQmC94_p-QuhC3BivYWTWUdCWBuA7tuK2u0hWLM130_provenance.
NP321226.RAcuMV5NQq2nuOdFiQ5bI15bW0BxtLrxfGJWzzSnQMVag130_assertion description "[In women, low expression of MAOA (MAOA-L) was related significantly to greater happiness (0.261 SD increase with one L-allele, 0.522 SD with two L-alleles, P=0.002) after adjusting for the potential effects of age, education, household income, marital status, employment status, mental disorder, physical health, relationship quality, religiosity, abuse history, recent negative life events and self-esteem use in linear regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321226.RAcuMV5NQq2nuOdFiQ5bI15bW0BxtLrxfGJWzzSnQMVag130_provenance.
NP321233.RAWj46RX1cIpdP9lALDdtnCpHvwKEFtUSwTZs53-KOoWs130_assertion description "[Oculodentodigital dysplasia (ODDD) is primarily an autosomal dominant human disease caused by any one of over 60 mutations in the GJA1 gene encoding the gap junction protein Cx43.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321233.RAWj46RX1cIpdP9lALDdtnCpHvwKEFtUSwTZs53-KOoWs130_provenance.
NP321240.RAUK-CJWNkPiBHYw_3AjBjUDvC7myE1Res8VaADtD-ZZU130_assertion description "[Mutations in both SCO1 and SCO2 are associated with distinct clinical phenotypes as well as tissue-specific COX deficiency, but the reason for such tissue specificity is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321240.RAUK-CJWNkPiBHYw_3AjBjUDvC7myE1Res8VaADtD-ZZU130_provenance.
NP321243.RAQBf1PQY0QsXa495GLR8NXV8mY0Xwjjv-AGX3DYggYNQ130_assertion description "[Five major categories are now established: HFE-related or type1 hemochromatosis, frequently found in Caucasians, and four rarer diseases which are type 2 (A and B) hemochromatosis (juvenile hemochromatosis), type 3 hemochromatosis (transferrin receptor 2 hemochromatosis), type 4 (A and B) hemochromatosis (ferroportin disease), and a(hypo)ceruloplasminemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321243.RAQBf1PQY0QsXa495GLR8NXV8mY0Xwjjv-AGX3DYggYNQ130_provenance.
NP321246.RAR2RomIFx53_r-mXpl4eWj7NQ1YG2XqTmeEfypA2pT1A130_assertion description "[Together with other in vitro data indicating connections between TR and p53, Rb, cyclin D and other cell cycle regulators and oncogenes, these results suggest that THRA and THRB may be involved in human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321246.RAR2RomIFx53_r-mXpl4eWj7NQ1YG2XqTmeEfypA2pT1A130_provenance.
NP321262.RAQZOudKsehIARbLYjG6L9XmJQq1vCBQKNRwpS5nA5EXM130_assertion description "[MALAT1, also known as nuclear-enriched transcript 2 (NEAT2), was discovered as a prognostic marker for lung cancer metastasis but also has been linked to several other human tumor entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321262.RAQZOudKsehIARbLYjG6L9XmJQq1vCBQKNRwpS5nA5EXM130_provenance.
NP321267.RARPIMKinblSwvwNIP1VBnZtA-JSc2w8WgSWO7aVBaeZ4130_assertion description "[One hundred and twenty-nine men with symptoms of urethritis seen at 2 STD clinics in Songkla Province, Thailand were enrolled.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321267.RARPIMKinblSwvwNIP1VBnZtA-JSc2w8WgSWO7aVBaeZ4130_provenance.
NP321268.RAZXyJOaN4Np07R43Webt7kHJTVOq0FriuhYD8boqcLBs130_assertion description "[We conclude that the TNF gene complex, at least in Caucasoid individuals and for the considered polymorphisms, does not seem to play a major role as genetic risk factor in COPD and bronchiectasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321268.RAZXyJOaN4Np07R43Webt7kHJTVOq0FriuhYD8boqcLBs130_provenance.
NP321269.RAdXizDFbvacJNVSN9385b15Rm45eJrJBhtw7Clq4mUHU130_assertion description "[Peroxisome proliferator-activated receptor alpha (PPARalpha) ligands are medications used to treat hyperlipidaemia and atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321269.RAdXizDFbvacJNVSN9385b15Rm45eJrJBhtw7Clq4mUHU130_provenance.
NP321272.RAT7QoWfbvsYOEshXRhbchkC_L--REKApuHtuG7LgAjzA130_assertion description "[Polymorphism of the ERalpha and CYP1B1 genes in endometrial cancer in a Polish subpopulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321272.RAT7QoWfbvsYOEshXRhbchkC_L--REKApuHtuG7LgAjzA130_provenance.
NP321275.RAeaIwUxj6_fSzMBaY7bFPffokF_YOEo_WH-XSITd1Q48130_assertion description "[We found normal colonic mucosal expression of SLC6A4 in diarrhea (IBS-D)- or constipation-predominant IBS (IBS-C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321275.RAeaIwUxj6_fSzMBaY7bFPffokF_YOEo_WH-XSITd1Q48130_provenance.
NP321278.RAbSyi_lUhq1k-1TQylw06G8UAs53QhGoEwnZkWZSdojA130_assertion description "[Heritable germline mutations of the p53 gene have been described in patients with Li-Fraumeni syndrome, occasionally in nonfamilial malignancies such as multifocal osteosarcoma, in a small subgroup of young patients with two or more primary malignancies, and in patients with sporadic breast carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321278.RAbSyi_lUhq1k-1TQylw06G8UAs53QhGoEwnZkWZSdojA130_provenance.
NP321280.RAVI0N5Kye7u3TzF3Gr45WI--9-mad7BySgtezG-uINP0130_assertion description "[RNA binding motif protein 15 (RBM15) was originally described as a 5' translocation partner of the MAL gene in t(1;22)(p13;q13)infant acute megakaryocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321280.RAVI0N5Kye7u3TzF3Gr45WI--9-mad7BySgtezG-uINP0130_provenance.
NP321283.RAY_Fx7LKX_mYUsCXKCZgls6g8n-J5D-93UdcXWFlD16o130_assertion description "[Because patients with RAPADILINO syndrome and a subset of patients with RTS have RECQL4 mutations, we reassessed two previously reported BGS families and found causal mutations in RECQL4 in both.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321283.RAY_Fx7LKX_mYUsCXKCZgls6g8n-J5D-93UdcXWFlD16o130_provenance.
NP321301.RAd3Q3moW8a_pFimFBxKauKd75fASCW_b8vdYDdikdqGk130_assertion description "[Expression of the nonstructural protein (NS)3/4A protease in cells infected with hepatitis C virus (HCV) results in cleavage of the mitochondrial antiviral-signaling protein (MAVS) and disruption of signaling pathways that lead to viral activation of interferon regulatory factor 3 (IRF-3) and synthesis of type 1 interferons (IFN-alpha/beta).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321301.RAd3Q3moW8a_pFimFBxKauKd75fASCW_b8vdYDdikdqGk130_provenance.
NP321302.RAWrms7hbX1CAmHpeh-RD3wOfPy_5SKpnJUc41V7QQ3M0130_assertion description "[An analysis of gene expression affected by PTTG1 indicated an association with invasive and metastatic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321302.RAWrms7hbX1CAmHpeh-RD3wOfPy_5SKpnJUc41V7QQ3M0130_provenance.

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