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Reference
Figure
ID
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J:333283
Guan N, et al., Disruption of mitochondrial complex III in cap mesenchyme but not in ureteric progenitors results in defective nephrogenesis associated with amino acid deficiency. Kidney Int. 2022 Jul;102(1):108-120
S4
MGI:7718695
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| Caption | Abb.: CM, cap mesenchyme; CSB, comma-shaped body; gl, glomerulus; Lhx1, LIM homeobox 1; Pax2; paired box gene 2, Rel, relative; Ret; ret proto-oncogene; RV, renal vesicle; SSB; S-shaped body; Wnt9b, wingless-type MMTV integration site family, member 9b. | ||||||||||||||||||||||||||||||
| Copyright | This image is from Guan N, Kidney Int 2022 Jul;102(1):108-120, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. | ||||||||||||||||||||||||||||||
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Associated Assays |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 09/08/2026 MGI 6.24 |
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