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Links from GEO DataSets

Items: 10

1.

RNA-Seq analysis comparing p53-null versus ΔNp63Δ/Δ;p53-null or ΔNp73Δ/Δ;p53-null thymic lymphoma tumors

(Submitter supplied) We performed an RNA-Seq analysis comparing thymic lymphoma tissues from the p53-null(n=2) and ΔNp63Δ/Δ;p53-/- (n=3) or ΔNp73Δ/Δ;p53-/-(n=3). Mice at 10 weeks of age were injected with either Ad-mCherry or Ad-CRE-mCherry to delete ΔNp63/ΔNp73 in the thymic lmyphomas. We aimed to test by deleting the DNp63/DNp73 in these p53-deficient tumors will mediate tumor regression and analyze the expression profile of the genes
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: TXT
Series
Accession:
GSE60827
ID:
200060827
2.

miRNA array after p63 knock down in human squamous cell carcinoma

(Submitter supplied) A central challenge in human cancer therapy is the identification of pathways that control tumor cell survival and chemosensitivity in the absence of functional p53. The p53-related transcription factors p63 and p73 exhibit distinct, p53-independent roles in development and cancer: p73 promotes genome stability and mediates chemosensitivity, while p63 largely lacks these p53-like functions and instead promotes proliferation and cell survival. more...
Organism:
Rattus norvegicus; JC polyomavirus; Homo sapiens; Murid gammaherpesvirus 4; Betapolyomavirus hominis; Mus musculus; Human alphaherpesvirus 1; Human betaherpesvirus 5; Murid betaherpesvirus 1; Human immunodeficiency virus 1; human gammaherpesvirus 4; Human gammaherpesvirus 8; Betapolyomavirus macacae
Type:
Non-coding RNA profiling by array
Platform:
GPL7722
2 Samples
Download data: TXT
Series
Accession:
GSE25524
ID:
200025524
3.

p73 inhibits malignant transformation

(Submitter supplied) sh RNA of p73 in Fibroblasts compared to non-silencing control Keywords: cell growth, shRNA, p73
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE7201
ID:
200007201
4.

CBFB cooperates with p53 to maintain TAp73 expression and suppress breast cancer

(Submitter supplied) The goal of this study is to use H3K4me3 signal to mark the promoter regions of the p73 gene. The p73 gene expresses TAp73 and DNp73 isoforms, which use two different promoters. H3K4me3 is generally associated with the promoter of a gene and, therefore, can be used to mark the promoters for TAp73 and DNp73.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
5 Samples
Download data: TXT
Series
Accession:
GSE169716
ID:
200169716
5.

Identifying transcripts regulated by p53 in MCF10A cells

(Submitter supplied) Total RNA was extracted from five million wild type (WT) and p53 knockout (p53_KO) MCF10A cells using Qiagen RNAeasy kit. Ribosomal RNAs were removed and the rest of RNAs were subject to RNAseq.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: XLSX
6.

Dichotomous transactivation domains contribute to growth inhibitory and promotion functions of TAp73

(Submitter supplied) The transcription factor p73, a member of the p53 tumor-suppressor family, regulates cell death and also supports tumorigenesis, though the mechanistic basis for the dichotomous functions is poorly understood. We report here the identification of an alternate transactivation domain (TAD) located at the extreme carboxyl (C)-terminus of TAp73β, a commonly expressed p73 isoform. Mutational disruption of this TAD significantly reduced TAp73β’s transactivation activity, to a level observed when the amino (N)-TAD that is similar to p53’s TAD is mutated. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
17 Samples
Download data: CEL, TXT
Series
Accession:
GSE262279
ID:
200262279
7.

Common activities and predictive gene signature identified for genetic hypomorphs of TP53

(Submitter supplied) Mutational inactivation of TP53 is a common event in cancer. Germline mutations in TP53 that inactivate this protein also occur in Li Fraumeni syndrome, which predisposes to early-onset cancer. In addition, there are dozens of other germline variants in TP53 that do not completely inactivate the function of this protein. In many cases studies have shown strong support for an impact of these lesser-functioning hypomorphs with increased cancer risk in humans and mouse models; however, the majority of these hypomorphs have yet to be categorized as pathogenic in clinical genetics databases. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
100 Samples
Download data: TXT
Series
Accession:
GSE209837
ID:
200209837
8.

Head and neck cancer neural reprogramming

(Submitter supplied) We investigated the route of neurotrophic cue delivery to the nerves
Organism:
Mus musculus; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL22858
8 Samples
Download data: TXT
Series
Accession:
GSE140324
ID:
200140324
9.

Head and neck cancer neural reprogramming [ClariomSMouse]

(Submitter supplied) We investigated the route of neurotrophic cue delivery to the nerves
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL23038
12 Samples
Download data: CEL
Series
Accession:
GSE140189
ID:
200140189
10.

neural reprogramming in head and neck cancer

(Submitter supplied) mRNA: profiling the neural identity of cancer associated neurons miRNA: investigating the p53 dependant exosomal miRNA content
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL20301 GPL21103 GPL18573
37 Samples
Download data: TXT
Series
Accession:
GSE134220
ID:
200134220
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