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Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples"Genotype-first" approaches on a curious case of idiopathic progressive cognitive declineDevelopment of a blood-based gene expression algorithm for assessment of obstructive coronary artery disease in non-diabetic patientsLNCaP Atlas: gene expression associated with in vivo progression to castration-recurrent prostate cancerMolecular analysis of endothelial progenitor cell (EPC) subtypes reveals two distinct cell populations with different identities.Mutation screening of melatonin-related genes in patients with autism spectrum disordersHigh quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarraysTiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumorsAn in silico analysis of dynamic changes in microRNA expression profiles in stepwise development of nasopharyngeal carcinomaGenes associated with MUC5AC expression in small airway epithelium of human smokers and non-smokersMicroRNA profiling of a CD133(+) spheroid-forming subpopulation of the OVCAR3 human ovarian cancer cell line"Who owns your poop?": insights regarding the intersection of human microbiome research and the ELSI aspects of biobanking and related studiesMicroRNA-34a modulates genes involved in cellular motility and oxidative phosphorylation in neural precursors derived from human umbilical cord mesenchymal stem cellsGenome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN studySystematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic informationGeneration of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysisGenotyping of human neutrophil antigens (HNA) from whole genome sequencing dataGene expression profiling identifies activated growth factor signaling in poor prognosis (Luminal-B) estrogen receptor positive breast cancerGenomic approaches to identifying targets for treating β hemoglobinopathiesIndividualized medicine enabled by genomics in Saudi ArabiaEfficient and biologically relevant consensus strategy for Parkinson's disease gene prioritization.A comparison of genomic profiles of complex diseases under different models.Meta-analysis of prostate cancer gene expression data identifies a novel discriminatory signature enriched for glycosylating enzymesPregnant women carrying microcephaly foetuses and Zika virus contain potentially pathogenic microbes and parasites in their amniotic fluidIdentification of co-expression gene networks, regulatory genes and pathways for obesity based on adipose tissue RNA Sequencing in a porcine modelGene expression meta-analysis supports existence of molecular apocrine breast cancer with a role for androgen receptor and implies interactions with ErbB familySFRP1 is a possible candidate for epigenetic therapy in non-small cell lung cancerGenome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinomaPathways affected by asbestos exposure in normal and tumour tissue of lung cancer patientsIron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseasesDevelopment of a fingerprinting panel using medically relevant polymorphismsInteraction of a traditional Chinese Medicine (PHY906) and CPT-11 on the inflammatory process in the tumor microenvironmentAn integrated transcriptome and epigenome analysis identifies a novel candidate gene for pancreatic cancerShort and long term gene expression variation and networking in human proximal tubule cells when exposed to cadmiumInsight in modulation of inflammation in response to diclofenac intervention: a human intervention studyUsing gene expression signatures to identify novel treatment strategies in gulf war illnessExplorations to improve the completeness of exome sequencingUnsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' viewsInferring drug-disease associations based on known protein complexesDifferentially private distributed logistic regression using private and public data
P1433
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P1433
description
revista científica
@es
revue scientifique
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rivista scientifica
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scientific journal
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vědecký časopis
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wetenschappelijk tijdschrift van BioMed Central
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wissenschaftliche Fachzeitschrift
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науковий журнал
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مجلة
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name
BMC Medical Genomics
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BMC Medical Genomics
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BMC Medical Genomics
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BMC Medical Genomics
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BMC Medical Genomics
@fr
BMC Medical Genomics
@it
BMC Medical Genomics
@nl
type
label
BMC Medical Genomics
@ast
BMC Medical Genomics
@de
BMC Medical Genomics
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BMC Medical Genomics
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BMC Medical Genomics
@fr
BMC Medical Genomics
@it
BMC Medical Genomics
@nl
prefLabel
BMC Medical Genomics
@ast
BMC Medical Genomics
@de
BMC Medical Genomics
@en
BMC Medical Genomics
@es
BMC Medical Genomics
@fr
BMC Medical Genomics
@it
BMC Medical Genomics
@nl
P31
P3181
P4616
P1055
P1058
P1156
17300154707
P123
P1277
P1476
BMC Medical Genomics
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P166
P236
P407
P5115
P571
2008-01-01T00:00:00Z