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Status |
Public on Mar 24, 2014 |
Title |
Six2CrefSall1 E14.5 WTvsKO, Sall1CreERfSall1 E14.5 WTvsKO 100120 |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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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 E14.5 were obtained from nephron progenitor-specific Sall1 deletion ( 2 sets) and inducible Sall1 deletion 48 hrs after tamoxifen treatment (1 set).
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Contributor(s) |
Nishinakamura R |
Citation(s) |
24744442 |
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Submission date |
Apr 08, 2013 |
Last update date |
Jan 12, 2017 |
Contact name |
Ryuichi Nishinakamura |
E-mail(s) |
ryuichi@gpo.kumamoto-u.ac.jp
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Phone |
+81-96-373-6615
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Fax |
+81-96-373-6618
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Organization name |
Kumamoto Univ.
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Department |
IMEG
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Lab |
kidney development
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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) |
GPL7202 |
Agilent-014868 Whole Mouse Genome Microarray 4x44K G4122F (Probe Name version) |
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Samples (6)
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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 |
PRJNA196586 |