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UnknownOptimizing the Safety Profile of Everolimus by Delayed Initiation in De Novo Heart Transplant Recipients: Results of the Prospective Randomized Study EVERHEART.
Not available
S-EPMC5828375 | biostudies-literature
UnknownNext Generation Immuno-Oncology Strategies: Unleashing NK Cells Activity.
Not available
S-EPMC9562848 | biostudies-literature
TranscriptomicsTranscription profiling of p53 knock-out mouse to analyse neural stem cell (neurosphere) prolifieration
The effects of gene p53 knock-out on mouse neural stem cell (neurosphere) prolifieration.
ORGANISM(S): Mus musculus 
2005-11-15 | E-MEXP-483 | biostudies-arrayexpress
UnknownHistone deacetylase inhibition synergistically enhances pemetrexed cytotoxicity through induction of apoptosis and autophagy in non-small cell lung cancer.
Not available
S-EPMC4198757 | biostudies-literature
UnknownFortnightly or fractionated weekly docetaxel-cisplatin-5-FU as first-line treatment in advanced gastric and gastroesophageal junction adenocarcinoma: The randomized phase II DoGE study.
Not available
S-EPMC8267119 | biostudies-literature
TranscriptomicsTransformics experiment on BALB/c 3T3 cells treated with B(a)P 0.02 µg/ml to investigate BaP mechanisms of carcinogenic action
This analysis utilised the \"Transformics Assay\" and evaluated the effect of cell exposure to 0.02 μg/ml of Benzo(a)pyrene, the lowest transforming concentration, using the BALB / c 3T3 A31-1-1 cell line. The Transformic assay is an integrated approach combining the Cell Transformation Assay (CTA)...
ORGANISM(S): Mus musculus 
2021-09-01 | E-MTAB-10405 | biostudies-arrayexpress
UnknownCharacterisation of the blood RNA host response underpinning severity in COVID-19 patients.
Not available
S-EPMC9288817 | biostudies-literature
TranscriptomicsTranscription profiling of mouse primary capillary PlGF-/- endothelial cells treated with 100 ng/ml PlGF for 6 hours
PlGF expression profile in primary capillary PlGF-/- endothelial cells treated with 100 ng/ml PlGF during 6 hours.
ORGANISM(S): Mus musculus 
2003-05-28 | E-MEXP-6 | biostudies-arrayexpress
TranscriptomicsKMT2D haploinsufficiency in Kabuki Syndrome disrupts neuronal function through transcriptional and chromatin rewiring independent of H3K4-monomethylation
Kabuki Syndrome (KS) is a multisystemic rare disorder, characterized by growth delay, distinctive facial features, intellectual disability, and rarely autism spectrum disorder. This condition is mostly caused by de novo mutations of KMT2D, encoding a catalytic subunit of the COMPASS complex involved...
ORGANISM(S): Homo sapiens 
2022-12-25 | E-MTAB-10244 | biostudies-arrayexpress
UnknownA multi-tissue study of immune gene expression profiling highlights the key role of the nasal epithelium in COVID-19 severity.
Not available
S-EPMC8861187 | biostudies-literature
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