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Centrosome amplification is a common feature of human tumors, but whether this is a cause or a consequence of human cancer remains unclear. Here, we report the creation of a mouse model in which centrosome number can be persistently increased in the absence of additional genetic defects. We show tha...
ORGANISM(S): Mus musculus 
Low coverage whole-genome sequencing of induced murine squamous cell carcinoma. 17 samples are included.
ORGANISM(S): Mus musculus 
RNA-sequencing of induced murine squamous cell carcinoma.
ORGANISM(S): Mus musculus 
Whole-exome sequencing of induced murine squamous cell carcinoma. 26 samples are included.
ORGANISM(S): Mus musculus 
Tumour buds undergo phenotype switching while detaching from the main tumour, as they acquire more migratory characteristics and tend to stop proliferating. Simultaneously, an EMT-like signature is observed in the tumour buds under the form of active WNT, TGF and receptor tyrosine kinase signalling....
ORGANISM(S): Homo sapiens 
Single cell sequencing of 5 dissected lung tumors.
ORGANISM(S): Homo sapiens 
The mammalian TET dioxygenases contribute to global waves of DNA demethylation in the zygote and in primordial germ cells, but their involvement during de novo DNA methylation at peri/post-implantation development is unknown. Here, we show novel physiological functions of Tet1 in the pre-primitive s...
ORGANISM(S): Mus musculus 
While aneuploidy is found in more than 90% of solid tumors, it is unclear whether aneuploidy is the cause or the consequence of tumorigenesis. Different mouse models deficient in centrosomal or spindle checkpoint proteins that induce aneuploidy show either a promotion or a decrease in tumorigenesis ...
ORGANISM(S): Mus musculus 
Single cell sequencing of 3 lung tumours. 3 malignant tumor parts were sequenced for each tumor
ORGANISM(S): Homo sapiens 
The experiment aimed at refining the classification of endometrial cancer by profiling somatic copy number aberrations (SCNAs). SCNAs affecting chromosome 1q32.1 significantly correlated with worse survival and functional validation of a plausible oncogene showed MDM4 as an oncogenic driver in 1q32....
ORGANISM(S): Homo sapiens 
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