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UnknownSrc family kinase inhibitor bosutinib enhances retinoic acid-induced differentiation of HL-60 leukemia cells.
Not available
S-EPMC6151292 | biostudies-literature
UnknownUse of In Vitro and Predictive In Silico Models to Study the Inhibition of Cytochrome P4503A by Stilbenes.
Not available
S-EPMC4618141 | biostudies-literature
UnknownPotential for subsets of wt-NPM1 primary AML blasts to respond to retinoic acid treatment.
Not available
S-EPMC5790527 | biostudies-literature
UnknownA hyperdynamic H3.3 nucleosome marks promoter regions in pluripotent embryonic stem cells.
Not available
S-EPMC5716099 | biostudies-literature
UnknownCognitive function after surgery with regional or general anesthesia: A population-based study.
Not available
S-EPMC6943821 | biostudies-literature
UnknownIrf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate.
Not available
S-EPMC4743694 | biostudies-literature
UnknownPAF1, a Molecular Regulator of Promoter-Proximal Pausing by RNA Polymerase II.
Not available
S-EPMC4679144 | biostudies-literature
GenomicsA Genomic History of Aboriginal Australia
The population history of Aboriginal Australians remains largely uncharacterised. We generated high-coverage genomes for 83 Aboriginal Australians (speakers of Pama-Nyungan languages) and 25 Papuans from the New Guinea Highlands. We find that Papuan and Aboriginal Australian ancestors diversified 25...
EGAS00001001766 | EGA
GenomicsThe maize methylome modulates mRNA splicing and reveals widespread paramutation guided by small RNA.
Methylation of chromosomal DNA in animals and plants is a fundamental mechanism of epigenetic regulation, and the maize genome, with its diverse complement of transposons and repeats, is a paradigm for transgenerational mechanisms such as paramutation and imprinting. We have determined the genome-wi...
ORGANISM(S): Zea mays 
2013-06-03 | E-GEOD-39232 | biostudies-arrayexpress
UnknownSignificance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.
Not available
S-EPMC5290091 | biostudies-literature
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