HLA-A*2416: a new allele of the HLA-A19 lineage.

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HLA-A*2416: a new allele of the HLA-A19 lineage. / Binder, Thomas; Heym, J; Horn, B; Blasczyk, R.

In: TISSUE ANTIGENS, Vol. 55, No. 2, 2, 2000, p. 178-181.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Binder, T, Heym, J, Horn, B & Blasczyk, R 2000, 'HLA-A*2416: a new allele of the HLA-A19 lineage.', TISSUE ANTIGENS, vol. 55, no. 2, 2, pp. 178-181. <http://www.ncbi.nlm.nih.gov/pubmed/10746793?dopt=Citation>

APA

Vancouver

Binder T, Heym J, Horn B, Blasczyk R. HLA-A*2416: a new allele of the HLA-A19 lineage. TISSUE ANTIGENS. 2000;55(2):178-181. 2.

Bibtex

@article{77911ea80d36462a9afa1341967e6ad0,
title = "HLA-A*2416: a new allele of the HLA-A19 lineage.",
abstract = "We here report on a new HLA-A19 allele (A*2416) found in a German kidney recipient. Serological class I typing revealed HLA-A11,19 without clear definition of the A19 split antigen. As with serology, polymerase chain reaction (PCR)-based typing also revealed inconclusive results. We therefore sequenced the gene from the 5' flanking region through the 3'-end of exon 4 of this allele after haplotype-specific PCR amplification. The sequence analysis revealed a new HLA-A allele which is identical to A*3101 with the exception of the 3' half of exon 2 which is identical to the common A9 alleles. The phylogenetic analysis constructed with the nearest-neighbor algorithm and based on exons 1-4 or introns 1-3 clearly indicated, that A*2416 belongs unequivocally to the A19 lineage.",
author = "Thomas Binder and J Heym and B Horn and R Blasczyk",
year = "2000",
language = "Deutsch",
volume = "55",
pages = "178--181",
journal = "TISSUE ANTIGENS",
issn = "0001-2815",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - HLA-A*2416: a new allele of the HLA-A19 lineage.

AU - Binder, Thomas

AU - Heym, J

AU - Horn, B

AU - Blasczyk, R

PY - 2000

Y1 - 2000

N2 - We here report on a new HLA-A19 allele (A*2416) found in a German kidney recipient. Serological class I typing revealed HLA-A11,19 without clear definition of the A19 split antigen. As with serology, polymerase chain reaction (PCR)-based typing also revealed inconclusive results. We therefore sequenced the gene from the 5' flanking region through the 3'-end of exon 4 of this allele after haplotype-specific PCR amplification. The sequence analysis revealed a new HLA-A allele which is identical to A*3101 with the exception of the 3' half of exon 2 which is identical to the common A9 alleles. The phylogenetic analysis constructed with the nearest-neighbor algorithm and based on exons 1-4 or introns 1-3 clearly indicated, that A*2416 belongs unequivocally to the A19 lineage.

AB - We here report on a new HLA-A19 allele (A*2416) found in a German kidney recipient. Serological class I typing revealed HLA-A11,19 without clear definition of the A19 split antigen. As with serology, polymerase chain reaction (PCR)-based typing also revealed inconclusive results. We therefore sequenced the gene from the 5' flanking region through the 3'-end of exon 4 of this allele after haplotype-specific PCR amplification. The sequence analysis revealed a new HLA-A allele which is identical to A*3101 with the exception of the 3' half of exon 2 which is identical to the common A9 alleles. The phylogenetic analysis constructed with the nearest-neighbor algorithm and based on exons 1-4 or introns 1-3 clearly indicated, that A*2416 belongs unequivocally to the A19 lineage.

M3 - SCORING: Zeitschriftenaufsatz

VL - 55

SP - 178

EP - 181

JO - TISSUE ANTIGENS

JF - TISSUE ANTIGENS

SN - 0001-2815

IS - 2

M1 - 2

ER -