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… (More)
National Institutes of Health

Related topics

Related topics

13 relations
ABCC2 geneAutosomal recessive inheritanceCholestasisConjugated hyperbilirubinemia
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Papers overview

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Highly Cited
2007
Highly Cited
2007
Opposing Effects of PKCθ and WASp on Symmetry Breaking and Relocation of the Immunological Synapse
The immunological synapse (IS) is a junction between the T cell and antigen-presenting cell and is composed of supramolecular… (More)
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Highly Cited
2006
Highly Cited
2006
Extinction: How Life on Earth Nearly Ended 250 Million Years Ago, Douglas H. Erwin. Princeton University Press (2006), £15.95 hbk (306 pages), ISBN: 0-691-00524-9
How do you sell a mass extinction without dinosaurs? How about giving it a catchy Kirk Johnson’s papers as I surmise?), which… (More)
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Highly Cited
2002
Highly Cited
2002
Battery thermal models for hybrid vehicle simulations
This paper summarizes battery thermal modeling capabilities for: (1) an advanced vehicle simulator (ADVISOR); and (2) battery… (More)
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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… (More)
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Highly Cited
1999
Highly Cited
1999
Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome.
Dubin-Johnson syndrome (DJS) is an autosomal recessive disease characterized by conjugated hyperbilirubinemia. Previous studies… (More)
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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… (More)
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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… (More)
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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… (More)
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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… (More)
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Review
1986
Review
1986
Understanding and preventing relapse.
" This article examines relapse by integrating knowledge from the addictive disorders of alcoholism, smoking, and obesity… (More)
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