Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2017 Mar;65(3):1065-1068.
doi: 10.1002/hep.28950. Epub 2017 Jan 6.

Loss of organic anion transporting polypeptide 1B3 function causes marked delay in indocyanine green clearance without any clinical symptoms

Affiliations
Case Reports

Loss of organic anion transporting polypeptide 1B3 function causes marked delay in indocyanine green clearance without any clinical symptoms

Tatehiro Kagawa et al. Hepatology. 2017 Mar.
No abstract available

PubMed Disclaimer

Figures

Figure 1
Figure 1
Hepatic OATP1B3 protein expression in patients P1, P2, and P4 and a control. Positive staining for OATP1B3 is observed along the basolateral membrane of hepatocytes in centrilobular areas in control liver tissue (antibody HPA004943; Sigma‐Aldrich, St. Louis, MO). In contrast, OATP1B3 expression is not detected in any of the patients. Scale bar, 200 μm. Inset, high magnification.

Comment in

Similar articles

Cited by

References

    1. Namihisa T, Nambu M, Kobayashi N, Kuroda H. Nine cases with marked retention of indocyanine green test and normal sulfobromophthalein test without abnormal liver histology: constitutional indocyanine green excretory defect. Hepatogastroenterology 1981;28:6‐12. - PubMed
    1. van de Steeg E, Stranecky V, Hartmannova H, Noskova L, Hrebicek M, Wagenaar E, et al. Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver. J Clin Invest 2012;122:519‐528. - PMC - PubMed
    1. Kagawa T, Oka A, Kobayashi Y, Hiasa Y, Kitamura T, Sakugawa H, et al. Recessive inheritance of population‐specific intronic LINE‐1 insertion causes a Rotor syndrome phenotype. Hum Mutat 2015;36:327‐332. - PubMed
    1. Vaz FM, Paulusma CC, Huidekoper H, de Ru M, Lim C, Koster J, et al. Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: conjugated hypercholanemia without a clear clinical phenotype. Hepatology 2015;61:260‐267. - PubMed
    1. de Graaf W, Hausler S, Heger M, van Ginhoven TM, van Cappellen G, Bennink RJ, et al. Transporters involved in the hepatic uptake of (99m)Tc‐mebrofenin and indocyanine green. J Hepatol 2011;54:738‐745. - PubMed

Publication types

Substances