A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric.
about
HLA class I molecular variation and peptide-binding properties suggest a model of joint divergent asymmetric selection.Understanding rare and common diseases in the context of human evolutionA limit to the divergent allele advantage model supported by variable pathogen recognition across HLA-DRB1 allele lineages.Determination of HLA-A, -B, and -DRB1 Allele and Haplotype Frequencies in the Croatian Population Based on a Family Study.HLA class I haplotype diversity is consistent with selection for frequent existing haplotypes.Nonfrequent but well-documented, rare and very rare HLA alleles observed in the Croatian population.
P2860
A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric.
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2012 nî lūn-bûn
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A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@ast
A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@en
type
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A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@ast
A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@en
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A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@ast
A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
@en
P2860
P356
P1476
A sequence-based approach demo ...... igen (HLA) loci is asymmetric.
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P2093
Henry A Erlich
Paola G Bronson
P2860
P304
P356
10.1093/HMG/DDS424
P577
2012-10-12T00:00:00Z