Partial deletion in the JK locus causing a JKnull phenotype

Blood

Volumn 99, Issue 3, 2002, Pages 1079-1081

  Lucien, Nicole ^a,b   Chiaroni, Jacques ^a,b   Cartron, Jean Pierre ^a,b   Bailly, Pascal ^a,b  

^a INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

^b ETABLISSEMENT FRANÇAIS DU SANG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLOOD GROUP KIDD SYSTEM; CASE REPORT; CODON; FEMALE; GENE; GENE DELETION; GENE LOCUS; GENE MAPPING; HUMAN; JK GENE; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SOUTHERN BLOTTING; TRANSLATION INITIATION;

EID: 0036464690     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V99.3.1079     Document Type: Article

References (15)

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2. null individuals
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5. Urinary concentrating ability in patients with Jk(a-b-) blood type who lack carrier-mediated urea transport
6. Endothelial cells of the kidney vasa recta express the urea transporter HUT11
7. Evidence for distinct vascular and tubular urea transporters in the rat kidney
8. null phenotype: Expression analysis of the Jk(S291 P) mutation found in Finns
9. Genomic characterization of the Kidd blood group gene: Different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns
10. Screening of six racial groups for the intron 5 G→A 3′ splice acceptor mutation responsible for the Polynesian Kidd(a-b-) phenotype: The null mutation is not always associated with the JKB allele
11. A novel molecular basis of the Jk(a-b-) phenotype in a Swiss family
12. Isolation of RNA from whole blood for reliable use in RT-PCR amplification
13. null phenotype in non-Finnish Europeans
14. Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA