1. Neuroinflammation and ER-stress are key mechanisms of acute bilirubin toxicity and hearing loss in a mouse model
   Emanuele Schiavon et al, 2018, PLOS ONE CrossRef
2. ABCC2p.R393W variant contributes to Dubin-Johnson syndrome by targeting MRP2 to proteasome degradation
   Rong-Yue Sun et al, 2024, eGastroenterology CrossRef
3. High-Throughput Screening to Evaluate Inhibition of Bile Acid Transporters Using Human Hepatocytes Isolated From Chimeric Mice
   Hiroshi Kohara et al, 2020, Toxicological Sciences CrossRef
4. Mutation analysis of the ABCC2 gene in Chinese patients with Dubin‑Johnson syndrome
   Lina Wu et al, 2018, Experimental and Therapeutic Medicine CrossRef
5. Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin–Johnson syndrome
   Chenyu Zhao et al, 2022, Frontiers in Genetics CrossRef
6. A novel homozygous frameshift variant in the ABCC2-gene in Dubin-Johnson syndrome may predispose to chronic liver disease
   Cyriac Abby Philips et al, 2021, Indian Journal of Gastroenterology CrossRef