Works matching IS 17558794 AND DT 2014 AND VI 7
Results: 95
Meta-analysis of prostate cancer gene expression data identifies a novel discriminatory signature enriched for glycosylating enzymes.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s12920-014-0074-9
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- Article
PD_NGSAtlas: a reference database combining next-generation sequencing epigenomic and transcriptomic data for psychiatric disorders.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s12920-014-0071-z
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A 3-biomarker-panel predicts renal outcome in patients with proteinuric renal diseases.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 200, doi. 10.1186/s12920-014-0075-8
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Transcriptome profiling and pathway analysis of genes expressed differentially in participants with or without a positive response to topiramate treatment for methamphetamine addiction.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 40, doi. 10.1186/s12920-014-0065-x
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SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 150, doi. 10.1186/s12920-014-0070-0
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Heterogeneity analysis of the proteomes in clinically nonfunctional pituitary adenomas.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 118, doi. 10.1186/s12920-014-0069-6
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Overexpression of miR-21-5p as a predictive marker for complete tumor regression to neoadjuvant chemoradiotherapy in rectal cancer patients.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 89, doi. 10.1186/s12920-014-0068-7
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High throughput exome coverage of clinically relevant cardiac genes.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 69, doi. 10.1186/s12920-014-0067-8
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Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 183, doi. 10.1186/s12920-014-0073-x
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Integrated differential transcriptome maps of Acute Megakaryoblastic Leukemia (AMKL) in children with or without Down Syndrome (DS).
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s12920-014-0063-z
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"Genotype-first" approaches on a curious case of idiopathic progressive cognitive decline.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/s12920-014-0066-9
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FLAGS, frequently mutated genes in public exomes.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/s12920-014-0064-y
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Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panel
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 62, doi. 10.1186/s12920-014-0062-0
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Sleep quality, BDNF genotype and gene expression in individuals with chronic abdominal pain.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s12920-014-0061-1
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A common gene expression signature in Huntington's disease patient brain regions.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s12920-014-0060-2
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Identification of co-expression gene networks, regulatory genes and pathways for obesity based on adipose tissue RNA Sequencing in a porcine model.
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- BMC Medical Genomics, 2014, v. 7, p. 1
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Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
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- BMC Medical Genomics, 2014, v. 7, p. 1
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Genetic network identifies novel pathways contributing to atherosclerosis susceptibility in the innominate artery.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/1755-8794-7-51
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Gene signatures ESC, MYC and ERG-fusion are early markers of a potentially dangerous subtype of prostate cancer.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/1755-8794-7-50
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Global transcriptome-wide analysis of CIK cells identify distinct roles of IL-2 and IL-15 in acquisition of cytotoxic capacity against tumor.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/1755-8794-7-49
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Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.
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- BMC Medical Genomics, 2014, v. 7, p. 1, doi. 10.1186/1755-8794-7-48
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Identification of gene-based responses in human blood cells exposed to alpha particle radiation.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-43
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Novel application of multi-stimuli network inference to synovial fibroblasts of rheumatoid arthritis patients.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-40
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MutaCYP: Classification of missense mutations in human cytochromes P450.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-47
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MicroRNA and mRNA expression profiling in rat acute respiratory distress syndrome.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-46
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Functional characterization of breast cancer using pathway profiles.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-45
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Protein and microRNA biomarkers from lavage, urine, and serum in military personnel evaluated for dyspnea.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 58, doi. 10.1186/1755-8794-7-58
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Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 56, doi. 10.1186/1755-8794-7-56
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Identification of a prognostic signature for old-age mortality by integrating genome-wide transcriptomic data with the conventional predictors: the Vitality 90+ Study.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 54, doi. 10.1186/1755-8794-7-54
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Global population-specific variation in miRNA associated with cancer risk and clinical biomarkers.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 53, doi. 10.1186/1755-8794-7-53
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Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 52, doi. 10.1186/1755-8794-7-52
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Measurement of absolute copy number variation reveals association with essential hypertension.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 44, doi. 10.1186/1755-8794-7-44
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Placental gene-expression profiles of intrahepatic cholestasis of pregnancy reveal involvement of multiple molecular pathways in blood vessel formation and inflammation.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 42, doi. 10.1186/1755-8794-7-42
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Complexity of the 5′UTR region of the CLCN5 gene: eleven 5′UTR ends are differentially expressed in the human kidney.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 41, doi. 10.1186/1755-8794-7-41
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Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-39
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Selection of competent blastocysts for transfer by combining time-lapse monitoring and array CGH testing for patients undergoing preimplantation genetic screening: a prospective study with sibling oocytes.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-38
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Human rhinovirus infection causes different DNA methylation changes in nasal epithelial cells from healthy and asthmatic subjects.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-37
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Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 3, doi. 10.1186/1755-8794-7-36
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A systems biology approach to understand the pathophysiological mechanisms of cardiac pathological hypertrophy associated with rosiglitazone.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-35
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On the identification of potential regulatory variants within genome wide association candidate SNP sets.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-34
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Using logistic regression to improve the prognostic value of microarray gene expression data sets: application to early-stage squamous cell carcinoma of the lung and triple negative breast carcinoma.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8794-7-33
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Conserved recurrent gene mutations correlate with pathway deregulation and clinical outcomes of lung adenocarcinoma in never-smokers.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-32
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Overlap of expression Quantitative Trait Loci (eQTL) in human brain and blood.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-31
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Imaging genomic mapping of an invasive MRI phenotype predicts patient outcome and metabolic dysfunction: a TCGA glioma phenotype research group project.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-30
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Differential expression and role of hyperglycemia induced oxidative stress in epigenetic regulation of β1, β2 and β3-Adrenergic Receptors in retinal endothelial cells.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-29
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Integrative analysis of the transcriptome profiles observed in type 1, type 2 and gestational diabetes mellitus reveals the role of inflammation.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-28
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Cellular dissection of psoriasis for transcriptome analyses and the post-GWAS era.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-27
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Small non-coding RNA signature in multiple sclerosis patients after treatment with interferon-β.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-26
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Translating a gene expression signature for multiple Myeloma prognosis into a robust high-throughput assay for clinical use.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-25
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Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients.
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- BMC Medical Genomics, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8794-7-24
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