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Damtew Elias van Mierlo Barbara Lie Rico Struik Paul Leeuwis Cees Lemaga Berga Smart Christine 《Systemic Practice and Action Research》2020,33(1):111-134
Systemic Practice and Action Research - There has been strong research interest in designing and testing learning approaches for enhancing and sustaining the capacity of communities to manage... 相似文献
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Norman PJ Abi-Rached L Gendzekhadze K Korbel D Gleimer M Rowley D Bruno D Carrington CV Chandanayingyong D Chang YH Crespí C Saruhan-Direskeneli G Fraser PA Hameed K Kamkamidze G Koram KA Layrisse Z Matamoros N Milà J Park MH Pitchappan RM Ramdath DD Shiau MY Stephens HA Struik S Verity DH Vaughan RW Tyan D Davis RW Riley EM Ronaghi M Parham P 《Nature genetics》2007,39(9):1092-1099
Interactions of killer cell immunoglobulin-like receptors (KIRs) with major histocompatibility complex (MHC) class I ligands diversify natural killer cell responses to infection. By analyzing sequence variation in diverse human populations, we show that the KIR3DL1/S1 locus encodes two lineages of polymorphic inhibitory KIR3DL1 allotypes that recognize Bw4 epitopes of protein">HLA-A and HLA-B and one lineage of conserved activating KIR3DS1 allotypes, also implicated in Bw4 recognition. Balancing selection has maintained these three lineages for over 3 million years. Variation was selected at D1 and D2 domain residues that contact HLA class I and at two sites on D0, the domain that enhances the binding of KIR3D to HLA class I. HLA-B variants that gained Bw4 through interallelic microconversion are also products of selection. A worldwide comparison uncovers unusual KIR3DL1/S1 evolution in modern sub-Saharan Africans. Balancing selection is weak and confined to D0, KIR3DS1 is rare and KIR3DL1 allotypes with similar binding sites predominate. Natural killer cells express the dominant KIR3DL1 at a high frequency and with high surface density, providing strong responses to cells perturbed in Bw4 expression. 相似文献
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