ABCC13, an unusual truncated ABC transporter, is highly expressed in fetal human liver (Q34160303)

31 July 2017

ABCC13, an unusual truncated ABC transporter, is highly expressed in fetal human liver (English)

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31 July 2017

6

Toshihisa Ishikawa

1 reference

31 July 2017

5

Hiroyuki Aburatani

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31 July 2017

Hikaru Yabuuchi

1

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31 July 2017

Shin ichiro Takayanagi

series ordinal

2

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31 July 2017

Keigo Yoshinaga

series ordinal

3

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31 July 2017

Naoyuki Taniguchi

series ordinal

4

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31 July 2017

language of work or name

English

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publication date

1 December 2002

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Biochemical and Biophysical Research Communications

31 July 2017

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31 July 2017

299

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31 July 2017

3

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31 July 2017

410-417

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ABC Transporters: From Microorganisms to Man

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

An inventory of the human ABC proteins

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

The human ATP-binding cassette (ABC) transporter superfamily

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

The multidrug resistance protein family.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

7 January 2021

1 reference

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The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

7 January 2021

1 reference

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

7 January 2021

1 reference

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Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

7 January 2021

1 reference

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Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

7 January 2021

1 reference

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Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters

7 January 2021

1 reference

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The ABCs of ATP-sensitive potassium channels: more pieces of the puzzle

7 January 2021

1 reference

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Leukotriene C4 inhibits ATP-dependent transport of glutathione S-conjugate across rat heart sarcolemma. Implication for leukotriene C4 translocation mediated by glutathione S-conjugate carrier

7 January 2021

1 reference

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Evidence for leukotriene C4 transport mediated by an ATP-dependent glutathione S-conjugate carrier in rat heart and liver plasma membranes

7 January 2021

1 reference

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The ATP-dependent glutathione S-conjugate export pump

7 January 2021

1 reference

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Overexpression of the gene encoding the multidrug resistance-associated protein results in increased ATP-dependent glutathione S-conjugate transport.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene

7 January 2021

1 reference

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Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

7 January 2021

1 reference

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Multiple splicing variants of two new human ATP-binding cassette transporters, ABCC11 and ABCC12.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

MRP8, a new member of ABC transporter superfamily, identified by EST database mining and gene prediction program, is highly expressed in breast cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

MRP9, an unusual truncated member of the ABC transporter superfamily, is highly expressed in breast cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family

7 January 2021

1 reference

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Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

7 January 2021

1 reference

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A simple method for displaying the hydropathic character of a protein

7 January 2021

1 reference

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An analysis of vertebrate mRNA sequences: intimations of translational control

7 January 2021

1 reference

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The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902658-X

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

7 January 2021

1 reference

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Cloning of cDNA for the major DNA-binding protein of the erythroid lineage through expression in mammalian cells

7 January 2021

1 reference

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Arrest in primitive erythroid cell development caused by promoter-specific disruption of the GATA-1 gene

7 January 2021

1 reference

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A GATA box in the GATA-1 gene hematopoietic enhancer is a critical element in the network of GATA factors and sites that regulate this gene

7 January 2021

1 reference

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An early haematopoietic defect in mice lacking the transcription factor GATA-2

7 January 2021

1 reference

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10.1016/S0006-291X(02)02658-X

7 January 2021

Identifiers

DOI

1 reference

31 July 2017

1 reference