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Status |
Public on Dec 15, 2014 |
Title |
A human integrin-α3 mutation confers major renal developmental defects. |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Integrin-α3 plays a central role in the interplay of cells, morphogens and ECM, required for proper nephrogenesis, thus adding ITGA3 to the list of CAKUT (congenital anomalies of the kidney and urinary tract)-causing genes.
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Overall design |
we used renal tissue originally obtained from a patient with an ITGA3 mutation and assessed its gene expression profile as compared to controls
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Contributor(s) |
Shukrun R, Vivante A, Pleniceanu O, Vax E, Anikster Y, Dekel B, Lotan D |
Citation(s) |
24621570 |
Submission date |
Jan 20, 2014 |
Last update date |
Oct 25, 2022 |
Contact name |
jasmine Jacob |
E-mail(s) |
j-jacob@sheba.health.gov.il
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Phone |
0523790500
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Organization name |
Sheba Medical Center at Tel HaShomer
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Street address |
haChevel 33
|
City |
Shoham |
State/province |
-Select- |
ZIP/Postal code |
60850 |
Country |
Israel |
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Platforms (1) |
GPL15207 |
[PrimeView] Affymetrix Human Gene Expression Array |
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Samples (4)
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Relations |
BioProject |
PRJNA236572 |