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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
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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
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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.
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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
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Organization name |
Texas Children's Hospital
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Department |
Pediatrics-Oncology
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Lab |
Suite 1025.07
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Street address |
1102 Bates Ave
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City |
Houston |
State/province |
TX |
ZIP/Postal code |
77030 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (10)
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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 |
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Relations |
BioProject |
PRJNA802674 |