Gene interactions and pathways from curated databases and text-mining

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EGFR — ERBB4

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Bei et al., J Pathol 2001 (Carcinoma, Squamous Cell...) : Among invasive and in situ carcinoma, EGFR expression was the most prevalent ( in 29/32 and 8/11 cases, respectively ) followed by ErbB2 ( 17/32 and 2/11 ) and ErbB4 ( 9/32 and 1/10 ), while ErbB3 was only detected in invasive tumours ( 12/32 )
Shi et al., Dev Biol 2003 (MAP Kinase Signaling System) : At the molecular level, reduced expression of epidermal growth factor receptor , attenuated protein cleavage of ErbB4 , and changes in MAPK activation were also detected in TACE ( DeltaZn/DeltaZn ) knockout heart tissues
Muraoka-Cook et al., Mol Endocrinol 2008 : We found that full prolactin mediated STAT5A activation and binding to the endogenous beta-casein promoter required ErbB4/HER4 but did not require ErbB1/epidermal growth factor receptor
Frey et al., Lab Invest 2010 (Colonic Neoplasms) : Furthermore, ErbB4 expression promoted EGFR phosphorylation in the presence of heregulin, implicating ErbB4-EGFR heterodimerization in these responses