Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
about
Immunoinformatics comes of ageThe human Major Histocompatibility Complex as a paradigm in genomics researchNomenclature for factors of the HLA system, 2010Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype ProjectThe impact of next-generation sequencing technologies on HLA researchInterrogating the major histocompatibility complex with high-throughput genomicsAlthough divergent in residues of the peptide binding site, conserved chimpanzee Patr-AL and polymorphic human HLA-A*02 have overlapping peptide-binding repertoiresImputing amino acid polymorphisms in human leukocyte antigens.Prioritizing genes of potential relevance to diseases affected by sex hormones: an example of myasthenia gravisT1DBase: integration and presentation of complex data for type 1 diabetes research.Balancing selection and its effects on sequences in nearby genome regions.MHC haplotype matching for unrelated hematopoietic cell transplantation.Sequences, annotation and single nucleotide polymorphism of the major histocompatibility complex in the domestic catMechanisms of copy number variation and hybrid gene formation in the KIR immune gene complex.The HLA class II Allele DRB1*1501 is over-represented in patients with idiopathic pulmonary fibrosis.Differential recombination dynamics within the MHC of macaque speciesMajor histocompatibility complex genomics and human disease.Evolutionary analysis of classical HLA class I and II genes suggests that recent positive selection acted on DPB1*04:01 in Japanese population.HLA and celiac disease susceptibility: new genetic factors bring open questions about the HLA influence and gene-dosage effects.Soma-to-germline feedback is implied by the extreme polymorphism at IGHV relative to MHC: The manifest polymorphism of the MHC appears greatly exceeded at Immunoglobulin loci, suggesting antigen-selected somatic V mutants penetrate Weismann's BarriePrimary sclerosing cholangitis is associated with extended HLA-DR3 and HLA-DR6 haplotypes.The vertebrate genome annotation (Vega) databasePhase-defined complete sequencing of the HLA genes by next-generation sequencingSeveral regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locusNatural polymorphisms in Tap2 influence negative selection and CD4∶CD8 lineage commitment in the ratNew advances in hematopoietic cell transplantationDominant sequences of human major histocompatibility complex conserved extended haplotypes from HLA-DQA2 to DAXXSignatures of strong population differentiation shape extended haplotypes across the human CD28, CTLA4, and ICOS costimulatory genes.HLA Typing for the Next GenerationGene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European AA highly divergent microsatellite facilitating fast and accurate DRB haplotyping in humans and rhesus macaques.Complete haplotype phasing of the MHC and KIR loci with targeted HaploSeq.The next generation of target capture technologies - large DNA fragment enrichment and sequencing determines regional genomic variation of high complexityGenome-wide variation in recombination rate in Eucalyptus.Intrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes.Assessment of complement C4 gene copy number using the paralog ratio test.Extensive haplotype diversity in African American mothers and their cord blood units.Sequencing and comparative analysis of the gorilla MHC genomic sequenceHuman MHC architecture and evolution: implications for disease association studies.A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
P2860
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P2860
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
description
2006 nî lūn-bûn
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2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2006 թվականի հունվարին հրատարակված գիտական հոդված
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2006年の論文
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2006年論文
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2006年論文
@zh-hant
2006年論文
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2006年論文
@zh-mo
2006年論文
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2006年论文
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name
Genetic analysis of completely ...... gments in recent human history
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Genetic analysis of completely ...... ments in recent human history.
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Genetic analysis of completely ...... ments in recent human history.
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Genetic analysis of completely ...... ments in recent human history.
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type
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Genetic analysis of completely ...... gments in recent human history
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Genetic analysis of completely ...... ments in recent human history.
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Genetic analysis of completely ...... ments in recent human history.
@en
Genetic analysis of completely ...... ments in recent human history.
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Genetic Analysis of Completely ...... gments in Recent Human History
@en
prefLabel
Genetic analysis of completely ...... gments in recent human history
@nl
Genetic analysis of completely ...... ments in recent human history.
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Genetic analysis of completely ...... ments in recent human history.
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Genetic analysis of completely ...... ments in recent human history.
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P2093
P2860
P4510
P50
P3181
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P1476
Genetic analysis of completely ...... ments in recent human history.
@en
P2093
Alexey M Atrazhev
Anne N Roberts
C Andrew Stewart
James A Traherne
Jane Rogers
Jeff Almeida
Jennifer L Ashurst
John F Elliott
John Trowsdale
Marcos M Miretti
P2860
P3181
P356
10.1371/JOURNAL.PGEN.0020009
P407
P577
2006-01-27T00:00:00Z