Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in down syndrome
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Volume 6, issue 1, December 2013
58 articles in this issue
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Correlation of WWOX, RUNX2 and VEGFA protein expression in human osteosarcoma
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Unraveling the characteristics of microRNA regulation in the developmental and aging process of the human brain
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Systematic genomic identification of colorectal cancer genes delineating advanced from early clinical stage and metastasis
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Integrated molecular portrait of non-small cell lung cancers
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NeuroGeM, a knowledgebase of genetic modifiers in neurodegenerative diseases
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Co-expression network analysis and genetic algorithms for gene prioritization in preeclampsia
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ChIP-seq in steatohepatitis and normal liver tissue identifies candidate disease mechanisms related to progression to cancer
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Transcriptional profiling of left ventricle and peripheral blood mononuclear cells in a rat model of postinfarction heart failure
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Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2
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Vitamin D related genes in lung development and asthma pathogenesis
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DNA methylation status of NKX2-5, GATA4 and HAND1in patients with tetralogy of fallot
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Integrating multiple oestrogen receptor alpha ChIP studies: overlap with disease susceptibility regions, DNase I hypersensitivity peaks and gene expression
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Assessment of inflammatory resilience in healthy subjects using dietary lipid and glucose challenges
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Association of candidate single nucleotide polymorphisms with somatic mutation of the epidermal growth factor receptor pathway
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Gene profiling suggests a common evolution of bladder cancer subtypes
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Transcriptome signatures in Helicobacter pylori-infected mucosa identifies acidic mammalian chitinase loss as a corpus atrophy marker
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Intratumoral genetic heterogeneity in metastatic melanoma is accompanied by variation in malignant behaviors
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Treatment of mouse liver slices with cholestatic hepatotoxicants results in down-regulation of Fxr and its target genes
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Molecular differential diagnosis of follicular thyroid carcinoma and adenoma based on gene expression profiling by using formalin-fixed paraffin-embedded tissues
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Circadian transcriptome analysis in human fibroblasts from Hunter syndrome and impact of iduronate-2-sulfatase treatment
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MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm
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Genomic pathway analysis reveals that EZH2 and HDAC4 represent mutually exclusive epigenetic pathways across human cancers
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Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome
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An integrated transcriptome and epigenome analysis identifies a novel candidate gene for pancreatic cancer
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De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies
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Genotyping of human neutrophil antigens (HNA) from whole genome sequencing data
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Identification of potential synthetic lethal genes to p53 using a computational biology approach
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Polymorphisms in nitric oxide synthase and endothelin genes among children with obstructive sleep apnea
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Whole transcriptome sequencing identifies tumor-specific mutations in human oral squamous cell carcinoma
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Small nucleolar RNAs as new biomarkers in chronic lymphocytic leukemia
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Microarray characterization of gene expression changes in blood during acute ethanol exposure
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Genetic lineages of undifferentiated-type gastric carcinomas analysed by unsupervised clustering of genomic DNA microarray data
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Validation of microarray data in human lymphoblasts shows a role of the ubiquitin-proteasome system and NF-kB in the pathogenesis of Down syndrome
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Alteration of human blood cell transcriptome in uremia
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Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways
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Interplay between estrogen receptor and AKT in Estradiol-induced alternative splicing
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Saliva sampling in global clinical studies: the impact of low sampling volume on performance of DNA in downstream genotyping experiments
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Genotype-driven recruitment: a strategy whose time has come?
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Cidofovir selectivity is based on the different response of normal and cancer cells to DNA damage
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A specific immune transcriptomic profile discriminates chronic kidney disease patients in predialysis from hemodialyzed patients
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Serum microRNAs profile from genome-wide serves as a fingerprint for diagnosis of acute myocardial infarction and angina pectoris
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Genome-wide search for the genes accountable for the induced resistance to HIV-1 infection in activated CD4+ T cells: apparent transcriptional signatures, co-expression networks and possible cellular processes
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A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation
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Analysis of a gene co-expression network establishes robust association between Col5a2 and ischemic heart disease
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Genome-wide associations of signaling pathways in glioblastoma multiforme
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Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
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Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population
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