Sort   by:  
 Page size 
TranscriptomicsGenome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function [cultured cortical neurons]
To examine potential differences in activity-dependent gene expression, we analyzed mRNA expression in cultured neurons isolated from Wild-type vs MeCP2 S421A mice at 0 (unstimulated), 1 or 6 hours after membrane depolarization by exposure to high extracellular KCl (55mM) All mice were male litterma...
ORGANISM(S): Mus musculus 
2011-09-07 | E-GEOD-31849 | biostudies-arrayexpress
UnknownConstruct Validity of the Toronto IBD Global Endoscopic Reporting Score Compared to Inflammatory Biomarkers After 12-Month Follow-Up.
Not available
S-EPMC12638056 | biostudies-literature
UnknownBiallelic EPCAM deletions induce tissue-specific DNA repair deficiency and cancer predisposition.
Not available
S-EPMC10928233 | biostudies-literature
UnknownSerologic Response and Safety after a Third Dose of the COVID-19 BNT162b2 Vaccine in Patients with Inflammatory Bowel Diseases.
Not available
S-EPMC10386081 | biostudies-literature
UnknownAnti-TNFα Treatment Impairs Long-Term Immune Responses to COVID-19 mRNA Vaccine in Patients with Inflammatory Bowel Diseases.
Not available
S-EPMC9330864 | biostudies-literature
UnknownMutations in the RAS/MAPK Pathway Drive Replication Repair-Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition.
Not available
S-EPMC8406556 | biostudies-literature
UnknownCombined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti-PD-1 Monotherapy: A Report from the International RRD Consortium.
Not available
S-EPMC10850948 | biostudies-literature
UnknownDNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells.
Not available
S-EPMC8223607 | biostudies-literature
GenomicsGenome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function [ChIP-Seq]
Autism spectrum disorders such as Rett syndrome (RTT) have been hypothesized to arise from defects in experience-dependent synapse maturation. RTT is caused by mutations in MECP2, a nuclear protein that becomes phosphorylated at S421 in response to neuronal activation. We show here that disruption o...
ORGANISM(S): Mus musculus 
2011-09-08 | E-GEOD-31951 | biostudies-arrayexpress
UnknownCancers from Novel Pole-Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade.
Not available
S-EPMC8218238 | biostudies-literature
Sort   by:  
 Page size