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Critical and distinct roles for key RET tyrosine docking sites in renal development
Molecular mechanisms that lead to congenital anomalies of kidneys and the lower urinary tract (CAKUT) are poorly understood. To elucidate the molecular basis for signaling specificity of GDNF-mediated RET signaling in kidney development, we characterized mice that exclusively express either the huma...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Cold Spring Harbor Laboratory Press
2006
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1361703/ https://ncbi.nlm.nih.gov/pubmed/16452504 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.1387206 |
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