Datasets (31,150)

KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of Cerebral Cavernous Malformation

Research on the effect of PRMT5 on the genomic binding sites of ?Np63a and its impact on the global transcriptomic regulation in the human tongue squamous cell carcinoma cell line UM1.

Recurrent de novo variants in the spliceosomal factor CRNKL1 cause severe microcephaly and pontocerebellar hypoplasia with seizures [HeLa]

A novel Ribociclib derivative, YW-LF, exerts anti-breast cancer effects by activating the p53 pathway.

Next Generation Sequencing of Retinal Pigment Epithelial (RPE) cells differentiated from induced pluripotent stem cells (iPSCs).

RNAseq data from myotubes after treatment with iAM373 in vitro

Sequencing_of_SW837_cells_following_CDS2_gRNA_transduction_and_selection__Transcriptome_sequencing_of_mouse_tumors

Galectin3: a novel biomarker of glycogen storage disease type III

Molecular characterisation of ameloblastoma with RNA-sequencing

Molecular signatures define BAP1-altered meningioma as a distinct CNS tumor with deregulation of Polycomb repressive complex target genes

NUDT21 in Colon Cancer

Human giant GTPase GVIN1 forms an antimicrobial coatomer around the intracellular bacterial pathogen Burkholderia thailandensis

The TET2 methylcytosine dioxygenase regulates early and late transitions in exhausted CD8+ T-cell differentiation

Bulk transcriptomic analysis on human Tregs

Ovarian tissue sequencing