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Status |
Public on Jun 27, 2018 |
Title |
p21 misexpression in the left growth plates |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
To study mechanisms of long bone growth regulation, p21 misexpression was induced in the left hindlimb of mouse embryos using an intersectional approach that requires both Cre and (r)tTA activity. Doxycycline was provided to the pregnant female at embryonic day (E)12.5 to activate the transgene, and embryos were collected at E17.5. Distal femur and proximal tibia growth plates were dissected out, keeping left and right separated, deprived of perichondrium and flash frozen. After RNA extraction, mRNA libraries were prepared and all samples were deep sequenced in parallel
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Overall design |
6 samples (left and right growth plates from embryos #386, #387, #388) were sequenced in parallel
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Contributor(s) |
Joyner AL, Roselló-Díez A |
Citation(s) |
29944650 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
R21 HD083860 |
A novel genetic approach to perturb and study coordination of organ growth |
Sloan Kettering Institute for Cancer Research |
ALEXANDRA L. JOYNER |
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Submission date |
Mar 30, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Alexandra L Joyner |
E-mail(s) |
joynera@mskcc.org
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Organization name |
Sloan Kettering Institute
|
Street address |
1275 York Avenue. Box 511
|
City |
New York |
State/province |
NY |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA381042 |
SRA |
SRP102791 |