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TranscriptomicsTranscripts differentially expressed in healthy blood mDCs compared to healthy monocytes
To directly compare the SLE monocyte transcriptional program with that of blood mDC precursors, we purified lineage HLA-DRhighCD11chigh mDCs and CD14+ monocytes from the blood of five healthy donors. Their gene expression profiles were then compared to those of blood SLE monocytes. An unsupervised c...
ORGANISM(S): Homo sapiens 
2014-06-03 | E-GEOD-46913 | biostudies-arrayexpress
TranscriptomicsTranscription profiling by array of adenylylation of mycobacterial Glnk (PII) protein induced by nitrogen limitation
PII proteins are pivotal regulators of nitrogen metabolism in most prokaryotes, controlling the activities of many targets, including nitrogen assimilation enzymes, two component regulatory systems and ammonium transport proteins. Escherichia coli contains two PII-like proteins, PII (product of glnB...
ORGANISM(S): Mycobacterium tuberculosis 
2013-05-10 | E-BUGS-135 | biostudies-arrayexpress
UnknownAn informatics search for the low-molecular weight chromium-binding peptide.
Not available
S-EPMC539358 | biostudies-literature
TranscriptomicsMalaria Cell Atlas: Single cell transcriptomics of malaria parasites
Single-cell RNA-sequencing is revolutionising our understanding of seemingly homogeneous cell populations but has not yet been widely applied to single-celled organisms. Transcriptional variation in unicellular malaria parasites from the Plasmodium genus is associated with critical phenotypes includ...
ORGANISM(S): Plasmodium falciparum 3D7 
2017-02-08 | E-ERAD-611 | biostudies-arrayexpress
UnknownThe Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children.
Not available
S-EPMC7736066 | biostudies-literature
TranscriptomicsLarge Granular Lymphocyte Leukemia Mesenchymal Stem Cells
The bone marrow microenvironment in Large Granular Lymphocyte Leukemia (LGLL) patients has been unexplored for it’s role in the development of cytopenias, which lead to complications resulting in the most prominent causes of morbidity and mortality. We used microarrays on primary mesenchymal stem ce...
ORGANISM(S): Homo sapiens 
2013-04-20 | E-GEOD-37470 | biostudies-arrayexpress
UnknownSPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia.
Not available
S-EPMC10319774 | biostudies-literature
UnknownShape of (101955) Bennu indicative of a rubble pile with internal stiffness.
Not available
S-EPMC6505705 | biostudies-literature
UnknownTargeted long-read sequencing identifies missing disease-causing variation.
Not available
S-EPMC8387463 | biostudies-literature
UnknownA dyadic approach to the delineation of diagnostic entities in clinical genomics.
Not available
S-EPMC7820621 | biostudies-literature
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