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TranscriptomicsTranscription profiling of human lung adenocarcinoma and a carcinogen-induced mouse model
Lung tumors
ORGANISM(S): Mus musculus 
2007-07-20 | E-GEOD-2514 | biostudies-arrayexpress
TranscriptomicsApplication of SNP microarrays to the genome-wide analysis of chromosomal instability in premalignant airway lesions
Chromosomal instability is central to the process of carcinogenesis. The detection of somatic chromosomal alterations in small premalignant lesions genome-wide remains challenging since sample heterogeneity dilutes the aberrant cell information. We introduced an analytic metric termed "delta-θ&...
ORGANISM(S): Homo sapiens 
2014-03-07 | E-GEOD-43168 | biostudies-arrayexpress
UnknownHands-on workshops as an effective means of learning advanced technologies including genomics, proteomics and bioinformatics.
Not available
S-EPMC4049090 | biostudies-literature
UnknownPredicting survival in patients with metastatic kidney cancer by gene-expression profiling in the primary tumor.
Not available
S-EPMC165812 | biostudies-literature
TranscriptomicsTranscription profiling of mutations in the yeast TRR1 gene encoding thioredoxin reductase
The Saccharomyces cerevisiae Yap1p transcription factor is required for the H2O2-dependent activation of many antioxidant genes including the TRX2 gene encoding thioredoxin 2. To identify factors that regulate Yap1p activity, we carried out a genetic screen for mutants that show elevated expression ...
ORGANISM(S): Saccharomyces cerevisiae 
2005-06-30 | E-SMDB-2716 | biostudies-arrayexpress
TranscriptomicsRole of thioredoxin reductase in the Yap1p-dependent response to oxidative stress
The Saccharomyces cerevisiae Yap1p transcription factor is required for the H2O2-dependent activation of many antioxidant genes including the TRX2 gene encoding thioredoxin 2. To identify factors that regulate Yap1p activity, we carried out a genetic screen for mutants that show elevated expression ...
ORGANISM(S): Saccharomyces cerevisiae 
2005-07-22 | E-GEOD-2977 | biostudies-arrayexpress
TranscriptomicsIdentification of Copy Number Variants in Patients with Hypoplastic Left Heart Syndrome and Other Congenital Heart Defects
Hypoplastic left heart syndrome (HLHS) is a heterogeneous, lethal combination of congenital malformations that result in a heart unable to sustain systemic circulation. The genetic determinants of this disorder are largely unknown. Evidence of copy number variants (CNVs) contributing to the genetic ...
ORGANISM(S): Homo sapiens 
2015-12-10 | E-GEOD-66032 | biostudies-arrayexpress
UnknownClassical dendritic cells contribute to hypoxia-induced pulmonary hypertension.
Not available
S-EPMC11462638 | biostudies-literature
UnknownBlood Transcriptional Biomarkers for Active Tuberculosis among Patients in the United States: a Case-Control Study with Systematic Cross-Classifier Evaluation.
Not available
S-EPMC4733166 | biostudies-literature
UnknownIntegrative Multiomics in the Lung Reveals a Protective Role of Asporin in Pulmonary Arterial Hypertension.
Not available
S-EPMC11473243 | biostudies-literature
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