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| Status |
Public on Apr 27, 2020 |
| Title |
DYRK2 knockout mice exhibit fetal growth retardation |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by array
|
| Summary |
We generated DYRK2-deficient mice using the CRISPR/Cas9 genome editing method and demonstrated that loss of DYRK2 gene causes fetal growth retardation and neonatal lethality at birth. Total RNA from DYRK2-/- whole embryo was compared with those of WT mice by microarray.
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| Overall design |
mRNA expression of whole embryo from DYRK2 knockout mice was compared with those of WT mice.
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| Contributor(s) |
Yoshida K, Yogosawa S |
| Citation(s) |
34671097 |
| Submission date |
Mar 09, 2020 |
| Last update date |
Oct 27, 2021 |
| Contact name |
Satomi Yogosawa |
| Organization name |
Jikei University School of Medicine
|
| Department |
Department of Biochemistry
|
| Street address |
3-25-8, Nishi-shinbasi
|
| City |
Minato-ku |
| State/province |
Tokyo |
| ZIP/Postal code |
105-8461 |
| Country |
Japan |
| |
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| Platforms (1) |
| GPL21163 |
Agilent-074809 SurePrint G3 Mouse GE v2 8x60K Microarray [Probe Name version] |
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| Samples (4)
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| Relations |
| BioProject |
PRJNA611501 |
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