Digenic inheritance of mutations in epha2 and slc26a4 in pendred syndrome

HIGHLIGHTS

• who: Mengnan Li from the Max Planck Institute Shinshu University of Medicine, Matsumoto, Japan have published the Article: Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome, in the Journal: NATURE COMMUNICATIONS NATURE COMMUNICATIONS
• what: Given the important role of Eph/ephrin system as a regulator of co-receptors18,19,24,25, the authors focused on transmembrane_proteins for further analysis.
• how: To gain further insight into the role of EphA2 in epithelial_cells the authors carried out an interactome analysis of EphA2.

SUMMARY

Stimulation of EphA2 with ephrin . . .

 



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