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TranscriptomicsER in Liver - 2
Liver transcriptome was analyzed at proestrus (P) and metestrus (M) in liver IGF-1-/- or LID mice. In order to elucidate the mechanism underlying ER control of liver metabolic function, we investigated the genetic programs controlled by the hepatic receptor during the physiological fluctuation of ci...
ORGANISM(S): Mus musculus 
2012-07-04 | E-MEXP-3505 | biostudies-arrayexpress
TranscriptomicsER in liver
In order to elucidate the mechanism underlying ER control of liver metabolic function, we investigated the genetic programs controlled by the hepatic receptor during the physiological fluctuation of circulating E2 in adult female mice. To this aim, we used Affymetrix GeneChip Arrays and compared the...
ORGANISM(S): Mus musculus 
2012-07-04 | E-MEXP-3504 | biostudies-arrayexpress
UnknownChronic myelogenous leukaemia exosomes modulate bone marrow microenvironment through activation of epidermal growth factor receptor.
Not available
S-EPMC4876029 | biostudies-literature
UnknownMiR-675-5p supports hypoxia induced epithelial to mesenchymal transition in colon cancer cells.
Not available
S-EPMC5421847 | biostudies-literature
UnknownEvidence that autophagy, but not the unfolded protein response, regulates the expression of IL-23 in the gut of patients with ankylosing spondylitis and subclinical gut inflammation.
Not available
S-EPMC3883901 | biostudies-literature
UnknownMiR675-5p Acts on HIF-1α to Sustain Hypoxic Responses: A New Therapeutic Strategy for Glioma.
Not available
S-EPMC4893639 | biostudies-literature
UnknownLombardy diagnostic and therapeutic network of thrombotic microangiopathy.
Not available
S-EPMC9229100 | biostudies-literature
ProteomicsGTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders
Copy number variations at 7q11.23 cause neurodevelopmental disorders with shared and opposite manifestations. Deletion leads to Williams-Beuren syndrome (WBS), while duplication causes 7q11.23 microduplication syndrome (7Dup). Converging evidence indicates GTF2I, from the 7q11.23 locus, is a key me...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD036770 | Pride
Sociability Organoids Neurodevelopment Autism Gtf2i Transcriptomics 
UnknownDysbiosis and zonulin upregulation alter gut epithelial and vascular barriers in patients with ankylosing spondylitis.
Not available
S-EPMC6599509 | biostudies-literature
UnknownMaintenance treatment of renal anaemia in haemodialysis patients with methoxy polyethylene glycol-epoetin beta versus darbepoetin alfa administered monthly: a randomized comparative trial.
Not available
S-EPMC2989790 | biostudies-literature
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