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Items: 4

1.

In vivo reprogramming drives Kras-induced cancer development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL6246
22 Samples
Download data: BW, CEL
Series
Accession:
GSE100842
ID:
200100842
2.

In vivo reprogramming drives Kras-induced cancer development [ChIP-seq]

(Submitter supplied) Accumulation of genetic mutations is thought to be a primary cause of cancer. However, a set of genetic mutations sufficient for cancer development remains unclear in most cancers, including pancreatic cancer. Here, we examined the effect of in vivo reprogramming on Kras-induced cancer development. We first demonstrate that Kras and p53 mutations are insufficient to induce activation of ERK signaling and cancer development in the pancreas. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
14 Samples
Download data: BW
Series
Accession:
GSE100841
ID:
200100841
3.

Illumina NextSeq 500 (Mus musculus)

Platform
Accession:
GPL19057
ID:
100019057
4.

I_C_OSKM_3d_2w_Input

Organism:
Mus musculus
Source name:
Pancreas
Platform:
GPL19057
Series:
GSE100841 GSE100842
Download data: BW
Sample
Accession:
GSM3028860
ID:
303028860
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Supplemental Content

db=gds|term=GSM3028860[Accession]|query=1|qty=2|blobid=MCID_67274da9d7c5c43eb677a3a6|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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