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TranscriptomicsSingle cell profiling of CRC primary tumors generated by the injection of AKTP mouse tumor organoid
The objective of this scRNAseq was to explore the heterogeneity between tumor epithelial CRC cells in our AKTP mouse models. We compared it to human datasets and found that mouse and human CRCs share similar tumor subpopulations.
ORGANISM(S): Mus musculus 
2022-09-16 | E-MTAB-11284 | biostudies-arrayexpress
ProteomicsTau Profiling of Brain Extracellular Vesicles Reveals PHF6 Peptide as Core for Pathological Tau Seeding in Alzheimer's Disease
EVs are bilipid spheres known for their role in cellular communication through transport of proteins, lipids, RNA and more. In the brain, EVs are directly released in the interstitial fluid surrounding neural cells and hence entitled brain-derived EVs (BD-EVs). Human BD-EVs of AD patients contain se...
ORGANISM(S): Homo Sapiens 
PXD067593 | panorama
UnknownIntegrative genome analyses identify key somatic driver mutations of small-cell lung cancer.
Not available
S-EPMC4915822 | biostudies-literature
Genomicsena-DATASET-ICM-19-09-2016-19:27:01:379-11 - samples
Exome sequencing of for 10 patients: 10 tumors, 10 cell lines and 7 blood samples (for 3 patients blood was not available)
EGAD00001002690 | EGA
Genomicsena-DATASET-ICM-19-09-2016-19:29:23:436-12 - samples
RNAseq data for 10 patients: 10 tumors and 10 cell lines
EGAD00001002691 | EGA
GenomicsMulti-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Glioblastoma (GBM) is the deadliest primary brain cancer in adults. Emerging innovative therapies hold promise for personalized cancer treatment. Improving therapeutic options depends on research relying on relevant preclinical models. In this line we have established in the setting of the GlioTeX p...
EGAS00001001871 | EGA
GenomicsGlioTex-ICM
Data Access Committee EGAC00001000513
EGAC00001000513 | EGA
UnknownAcetyl-CoA metabolism drives epigenome change and contributes to carcinogenesis risk in fatty liver disease.
Not available
S-EPMC9219160 | biostudies-literature
UnknownGenetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
Not available
S-EPMC5360844 | biostudies-literature
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