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Series GSE195922 Query DataSets for GSE195922
Status Public on Feb 04, 2022
Title MyoD-Cre driven alterations in K-Ras and p53 lead to a mouse model with histological and molecular characteristics of human rhabdomyosarcoma [RMS_GEMM_tumors]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary We have developed a new conditional genetically engineered mouse model of rhabdomyosarcoma (RMS) with homologous molecular signature to human RMS that provides valuable pre-clinical models for evaluating novel therapies
 
Overall design Mice expressing MyoD promoter-regulated Cre-recombinase were crossed with germline p53Flox or Lox-Stop-Lox (LSL) knock-in alleles expressing oncogenic p53R172H and/or K-RasG12D mutants.
 
Contributor(s) Yustein JT, Nakahata K, Patel TD
Citation(s) 35174853
Submission date Feb 01, 2022
Last update date Feb 23, 2022
Contact name Jason T Yustein
E-mail(s) yustein@bcm.edu
Organization name Texas Children's Hospital
Department Pediatrics-Oncology
Lab Suite 1025.07
Street address 1102 Bates Ave
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (10)
GSM5856421 K-Ras wild type [MR42]
GSM5856422 K-Ras wild type [MR17]
GSM5856423 K-Ras wild type [MF21]
This SubSeries is part of SuperSeries:
GSE195923 MyoD-Cre driven alterations in K-Ras and p53 lead to a mouse model with histological and molecular characteristics of human rhabdomyosarcoma
Relations
BioProject PRJNA802674

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE195922_RMS_GEMM_tumors.rnaseq.featureCounts-genes.csv.gz 874.6 Kb (ftp)(http) CSV
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Raw data are available in SRA
Processed data are available on Series record

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