Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Jaundice, Chronic Idiopathic

Known as: Dubin-Johnson Syndrome, HBLRDJ, Hyperbilirubinemia 2 
A benign, autosomally recessive inherited hyperbilirubinemia characterized by the presence of a dark pigment in the centrilobular region of the liver… Expand
National Institutes of Health

Related topics

Related topics

13 relations
ABCC2 geneAutosomal recessive inheritanceCholestasisConjugated hyperbilirubinemia
Expand

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2002
Highly Cited
2002
Battery thermal models for hybrid vehicle simulations
Abstract This paper summarizes battery thermal modeling capabilities for: (1) an advanced vehicle simulator (ADVISOR); and (2… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 6
Is this relevant?
Highly Cited
1999
Highly Cited
1999
The Women's Ischemia Syndrome Evaluation (WISE) study: protocol design, methodology and feasibility report.
OBJECTIVES The Women's Ischemia Syndrome Evaluation (WISE) is a National Heart, Lung and Blood Institute-sponsored, four-center… Expand
  • table 1
  • table 2
  • figure 1
  • figure 2
  • table 3
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Mutations in the Canalicular Multispecific Organic Anion Transporter (cMOAT) Gene, a Novel ABC Transporter, in Patients with Hyperbilirubinemia II/Dubin-Johnson Syndrome
Members of the ATP-binding cassette (ABC) transporter superfamily are mutated to cause diseases that include cystic fibrosis… Expand
  • figure 1
  • figure 3
  • figure 2
  • figure 4
Is this relevant?
Highly Cited
1997
Highly Cited
1997
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin‐Johnson syndrome
The human Dubin‐Johnson syndrome (DJS) is a rare autosomal recessive liver disorder characterized by chronic conjugated… Expand
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Absence of the canalicular isoform of the MRP gene–encoded conjugate export pump from the hepatocytes in Dubin‐Johnson syndrome
The Dubin‐Johnson syndrome is characterized by an inherited defect in the secretion of amphiphilic anionic conjugates from… Expand
Is this relevant?
Highly Cited
1995
Highly Cited
1995
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
BACKGROUND People with Gilbert's syndrome have mild, chronic unconjugated hyperbilirubinemia in the absence of liver disease or… Expand
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Restenosis after Arterial Injury Caused by Coronary Stenting in Patients with Diabetes Mellitus
Diabetes mellitus is a well-known risk factor for the development of atherosclerotic coronary artery disease [1, 2]. Findings in… Expand
Is this relevant?
Highly Cited
1988
Highly Cited
1988
Toward a functional categorization of slow waves.
This study is concerned with slowly varying, long-duration brain event-related potential (ERP) components, referred to as Slow… Expand
  • figure 1
  • figure 3
  • figure 3
  • table 2
  • figure 4
Is this relevant?
Review
1986
Review
1986
Understanding and preventing relapse.
This chapter examines relapse by integrating knowledge from the disorders of alcoholism, smoking, and obesity in an attempt to… Expand
  • figure 1
  • figure 2
  • table 1
Is this relevant?
Highly Cited
1985
Highly Cited
1985
Hereditary chronic conjugated hyperbilirubinemia in mutant rats caused by defective hepatic anion transport
A mutant rat strain is described with autosomal recessive conjugated hyperbilirubinemia. Transport of conjugated bilirubin and… Expand
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE