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Items: 4

1.

FANCD2 Activates Transcription of TAp63 and Suppresses Tumorigenesis

(Submitter supplied) Fanconi Anemia (FA) is a rare genetic disorder characterized by an increased susceptibility to squamous cell cancers. Fifteen FA genes are known, and the encoded proteins cooperate in a common DNA repair pathway. A critical step is the monoubiquitination of the FANCD2 protein, and cells from most FA patients are deficient in this step. How monoubiquitinated FANCD2 suppresses squamous cell cancers is unknown. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: TXT
Series
Accession:
GSE46902
ID:
200046902

PubMed Full text in PMC Similar studies SRA Run Selector

2.

Illumina HiSeq 2000 (Homo sapiens)

Organism:
Homo sapiens
10400 Series
180082 Samples
Download data
Platform
Accession:
GPL11154
ID:
100011154

3.

FANCD2_IP_UV treated

Organism:
Homo sapiens
Source name:
FANCD2_IP_UV treated
Platform:
GPL11154
Series:
GSE46902
Download data: TXT
Sample
Accession:
GSM1140398
ID:
301140398

SRA Run Selector

4.

FANCD2_IP_UV untreated

Organism:
Homo sapiens
Source name:
FANCD2_IP_UV untreated
Platform:
GPL11154
Series:
GSE46902
Download data: TXT
Sample
Accession:
GSM1140397
ID:
301140397

SRA Run Selector

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db=gds|term=GSE46902[Accession]|query=1|qty=2|blobid=MCID_6643586d5f31ac4911891aab|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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