Erythroid urea transporter deficiency due to novel JKnull alleles.

about

Expression of blood group genes by mesenchymal stem cells.The emerging physiological roles of the SLC14A family of urea transporters.Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors.Rare gems: null phenotypes of blood groups.Transfusion Medicine and Molecular Genetic Methods.

P2860

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P2860

Erythroid urea transporter deficiency due to novel JKnull alleles.

Item

http://www.wikidata.org/entity/Q46170803

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2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年学术文章

@wuu

2007年学术文章

@zh

2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh-hant

name

Erythroid urea transporter deficiency due to novel JKnull alleles.

@en

Erythroid urea transporter deficiency due to novel JKnull alleles.

@nl

type

Item

label

Erythroid urea transporter deficiency due to novel JKnull alleles.

@en

Erythroid urea transporter deficiency due to novel JKnull alleles.

@nl

prefLabel

Erythroid urea transporter deficiency due to novel JKnull alleles.

@en

Erythroid urea transporter deficiency due to novel JKnull alleles.

@nl

P1476

Erythroid urea transporter deficiency due to novel JKnull alleles

@en

P2093

Edmond Lee

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Elisabet S Wester

http://www.w3.org/2001/XMLSchema#string

Jill R Storry

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Ranjan Malde

http://www.w3.org/2001/XMLSchema#string

Susan T Johnson

http://www.w3.org/2001/XMLSchema#string

Tama Copeland

http://www.w3.org/2001/XMLSchema#string

P2860

A simple salting out procedure for extracting DNA from human nucleated cells

Kidd blood group and urea transport function of human erythrocytes are carried by the same protein

Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns.

Molecular biology and genetics of the Rh blood group system.

Partial deletion in the JK locus causing a Jk(null) phenotype.

Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.

Antigenic and functional properties of the human red blood cell urea transporter hUT-B1.

The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility.

Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals.

UT-B1 proteins in rat: tissue distribution and regulation by antidiuretic hormone in kidney.

P304

365-372

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P31

scholarly article

P356

10.1111/J.1537-2995.2007.01532.X

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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M L Olsson

P577

2007-11-19T00:00:00Z

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P698

18028269

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Erythroid urea transporter deficiency due to novel JKnull alleles.

about

P2860

P2860

Erythroid urea transporter deficiency due to novel JKnull alleles.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698