about
Detectable clonal mosaicism and its relationship to aging and cancerCharacterization of large structural genetic mosaicism in human autosomeAnalysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesA variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virusAllelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVKFrom noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locusFemale chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeThe systemic lupus erythematosus-associated PDCD1 polymorphism PD1.3A in lupus nephritisA genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3Genome-wide interaction study of smoking and bladder cancer riskA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociA common variant associated with dyslexia reduces expression of the KIAA0319 geneNo association between a candidate TCF7L2 variant and risk of breast or ovarian cancer.Alternative splicing of TCF7L2 gene in omental and subcutaneous adipose tissue and risk of type 2 diabetes.IFNL4-ΔG genotype is associated with slower viral clearance in hepatitis C, genotype-1 patients treated with sofosbuvir and ribavirin.Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations.Endogenous intrahepatic IFNs and association with IFN-free HCV treatment outcome.Splicing diversity of the human OCLN gene and its biological significance for hepatitis C virus entry.A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort.A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background.Fine mapping of 14q24.1 breast cancer susceptibility locusBreast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression.IL-29 is the dominant type III interferon produced by hepatocytes during acute hepatitis C virus infectionSelection on a variant associated with improved viral clearance drives local, adaptive pseudogenization of interferon lambda 4 (IFNL4)The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive diseaseIFN-λ4: the paradoxical new member of the interferon lambda family.Common genetic variants in miR-1206 (8q24.2) and miR-612 (11q13.3) affect biogenesis of mature miRNA formsIL28B rs12979860 genotype and spontaneous clearance of hepatitis C virus in a multi-ethnic cohort of injection drug users: evidence for a supra-additive associationInterferon Lambda 4 Genotype Is Not Associated with Recurrence of Oral or Genital HerpesMapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.Common genetic variants in the PSCA gene influence gene expression and bladder cancer riskFine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.Vitamin D Status and Virologic Response to HCV Therapy in the HALT-C and VIRAHEP-C Trials.Comparison of functional variants in IFNL4 and IFNL3 for association with HCV clearance.Association of IFNL3 and IFNL4 polymorphisms with liver-related mortality in a multiracial cohort of HIV/HCV-coinfected womenExpression of Interferon Lambda 4 Is Associated with Reduced Proliferation and Increased Cell Death in Human Hepatic Cells.Modification of Occupational Exposures on Bladder Cancer Risk by Common Genetic Polymorphisms.
P50
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P50
description
hulumtuese
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researcher
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հետազոտող
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name
Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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type
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Prokunina-Olsson L
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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Ludmila Prokunina-Olsson
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P1053
A-8240-2019
P106
P1153
16426739500
P21
P2798
P31
P496
0000-0002-9622-2091