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TranscriptomicsGene expression profiling of human monocytes and monocyte-derived-macrophages
In this study we analyzed the gene expression profiles of human monocytes and monocyte-dervied-macrophages. Keywords: Gene expression profiling Blood samples were obtained from 86 patients with symptoms of acute coronary syndrome who had undergone coronary angiography at the department of cardiolog...
ORGANISM(S): Homo sapiens 
2008-08-31 | E-GEOD-10220 | biostudies-arrayexpress
TranscriptomicsTranscriptome analysis by Illumina microarrays of the effect of overexpressing H2A.J mutants, or WT H2A.J or canonical H2A, on the transcriptome of WI-38hTERT fibroblasts
The intent of the experiment was to test the effect of overexpressing H2A.J-V11A, H2AJ-S123E, H2A.J-S123A, and H2A.J-CterH2A mutants, as well as WT-H2A.J and canonical H2A-type1, on the transcriptome of WI-38hTERT fibroblasts. pTRIPz based lentiviral constructs placing these coding sequences under t...
ORGANISM(S): Homo sapiens 
2020-11-01 | E-MTAB-9706 | biostudies-arrayexpress
TranscriptomicsImmunity and Defense Genes in Peripheral Blood Mononuclear Cells of Rheumatoid Arthritis patients
Large-scale gene expression profiling of peripheral blood mononuclear cells from Rheumatoid Arthritis (RA) patients could provide a molecular description that reflects the contribution of diverse cellular responses associated with this disease. The aim of our study is to identify peripheral blood ge...
ORGANISM(S): Homo sapiens 
2010-05-08 | E-GEOD-15573 | biostudies-arrayexpress
UnknownDisease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis.
Not available
S-EPMC6018712 | biostudies-literature
UnknownAccelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network.
Not available
S-EPMC9091203 | biostudies-literature
UnknownClinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.
Not available
S-EPMC8354853 | biostudies-literature
UnknownEpisignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.
Not available
S-EPMC10853222 | biostudies-literature
UnknownIntegrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids.
Not available
S-EPMC6702229 | biostudies-literature
UnknownABCA7 rare variants and Alzheimer disease risk.
Not available
S-EPMC4898320 | biostudies-literature
UnknownGenome sequencing for the diagnosis of intellectual disability as a paradigm for rare diseases in the French healthcare setting: the prospective DEFIDIAG study.
Not available
S-EPMC12495801 | biostudies-literature
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