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A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter (Q28219109)

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scientific article (publication date: 8 November 2002)

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English	A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter	scientific article (publication date: 8 November 2002)

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12 November 2019

A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter (English)

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12 November 2019

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12 November 2019

Ulrich M. Zanger

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Ulrich M Zanger

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12 November 2019

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Christoph Michalski

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12 November 2019

Andreas K Nuessler

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Kathrin Klein

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12 November 2019

Michel Eichelbaum

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12 November 2019

Dietrich Keppler

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12 November 2019

Jorg Konig

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12 November 2019

Peter Neuhaus

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12 November 2019

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23 August 2002

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12 November 2019

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12 November 2019

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12 November 2019

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12 November 2019

43058-43063

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12 November 2019

Transport of drugs across the hepatic sinusoidal membrane: sinusoidal drug influx and efflux in the liver

1 reference

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A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters

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Localization and genomic organization of a new hepatocellular organic anion transporting polypeptide

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21 January 2018

Hepatic uptake of bilirubin and its conjugates by the human organic anion transporter SLC21A6

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Identification of functionally variant MDR1 alleles among European Americans and African Americans

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Polymorphisms in OATP-C: identification of multiple allelic variants associated with altered transport activity among European- and African-Americans

1 reference

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21 January 2018

Genetic polymorphisms of human organic anion transporters OATP-C (SLC21A6) and OATP-B (SLC21A9): allele frequencies in the Japanese population and functional analysis

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21 January 2018

cDNA cloning of the hepatocyte canalicular isoform of the multidrug resistance protein, cMrp, reveals a novel conjugate export pump deficient in hyperbilirubinemic mutant rats

1 reference

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Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing

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Expression of the multidrug resistance proteins MRP2 and MRP3 in human hepatocellular carcinoma

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A comprehensive set of sequence analysis programs for the VAX

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Expression of the MRP gene-encoded conjugate export pump in liver and its selective absence from the canalicular membrane in transport-deficient mutant hepatocytes

1 reference

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Suggestions for the nomenclature of human alleles: relevance to ecogenetics, pharmacogenetics and molecular epidemiology

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Polymorphism of the ABC transporter genes, MDR1, MRP1 and MRP2/cMOAT, in healthy Japanese subjects

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Polymorphisms in the ABCC2 (cMOAT/MRP2) gene found in 72 established cell lines derived from Japanese individuals: an association between single nucleotide polymorphisms in the 5'-untranslated region and exon 28.

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10.1074/JBC.M207735200

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12 November 2019

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2 references

Consolidated OpenCitations Corpus – April 2017

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12196548%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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