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UnknownRNA Sequencing Identifies New RNase III Cleavage Sites in Escherichia coli and Reveals Increased Regulation of mRNA.
Not available
S-EPMC5371410 | biostudies-literature
UnknownChildhood trauma and brain structure in children and adolescents.
Not available
S-EPMC9800267 | biostudies-literature
UnknownA scoping review of geriatric emergency medicine research transparency in diversity, equity, and inclusion reporting.
Not available
S-EPMC11560720 | biostudies-literature
UnknownEvidence for sequenced molecular evolution of IDH1 mutant glioblastoma from a distinct cell of origin.
Not available
S-EPMC3236649 | biostudies-literature
UnknownAltered development of hippocampus-dependent associative learning following early-life adversity.
Not available
S-EPMC6684815 | biostudies-literature
UnknownIdentification of a Class of Protein ADP-Ribosylating Sirtuins in Microbial Pathogens.
Not available
S-EPMC4518038 | biostudies-literature
UnknownApplication of Zone Model Predictive Control Artificial Pancreas During Extended Use of Infusion Set and Sensor: A Randomized Crossover-Controlled Home-Use Trial.
Not available
S-EPMC5521973 | biostudies-literature
UnknownImpact of centre volume, surgeon volume, surgeon experience and geographic location on reoperation after intramedullary nailing of tibial shaft fractures
Not available
S-EPMC8410470 | biostudies-literature
TranscriptomicsTranscription profiling by array of human glioblastoma frozen tumors and cell lines
We have developed a nonheuristic genome topography scan (GTS) algorithm to characterize the patterns of genomic alterations in human glioblastoma (GBM), identifying frequent p18INK4C and p16INK4A codeletion. Functional reconstitution of p18INK4C in GBM cells null for both p16INK4A and p18INK4C resul...
ORGANISM(S): Homo sapiens 
2008-06-16 | E-GEOD-9171 | biostudies-arrayexpress
GenomicsAssociation studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Genomewide association studies (GWAS) have proven a powerful hypothesis-free method to identify common disease-associated variants. Even quite large GWAS, however, have only at best identified moderate proportions of the genetic variants contributing to disease heritability. To provide cost-effectiv...
EGAS00000000115 | EGA
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