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Status |
Public on Mar 24, 2014 |
Title |
Sall1CreER E13.5 110228 |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
|
Summary |
We have employed whole genome microarray expression profiling to identify genes regulated by Sall1 in the kidney.
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Overall design |
Kidneys at E13.5 were obtained from inducible Sall1 deletion 24 hrs after tamoxifen treatment (2 set).
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Contributor(s) |
Nishinakamura R |
Citation(s) |
24744442 |
Submission date |
Apr 08, 2013 |
Last update date |
Feb 02, 2018 |
Contact name |
Ryuichi Nishinakamura |
E-mail(s) |
ryuichi@gpo.kumamoto-u.ac.jp
|
Phone |
+81-96-373-6615
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Fax |
+81-96-373-6618
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Organization name |
Kumamoto Univ.
|
Department |
IMEG
|
Lab |
kidney development
|
Street address |
Honjo 2-2-1
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City |
Kumamoto |
ZIP/Postal code |
860-0811 |
Country |
Japan |
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Platforms (1) |
GPL10787 |
Agilent-028005 SurePrint G3 Mouse GE 8x60K Microarray (Probe Name version) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE45845 |
Sall1 co-operated with Six2 to actively maintain nephron progenitors in the embryonic kidney |
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Relations |
BioProject |
PRJNA196587 |