Graef T, Moesta A K, Norman P J, Abi-Rached L, Vago L, Older Aguilar A M, Gleimer M, Hammond J A, Guethlein L A, Bushnell D A, Robinson P J, Parham P (2009)
KIR2DS4 is a product of gene conversion with KIR3DL2 that introduced specificity for HLA-A*11 while diminishing avidity for HLA-C
Journal of Experimental Medicine 206 (11) , 2557-2572
Publisher’s version: http://dx.doi.org/10.1084/jem.20091010
Hammond J A, Guethlein L A, Abi-Rached L, Moesta A K, Parham P (2009)
Evolution and survival of marine carnivores did not require a diversity of killer Cell Ig-Like receptors or Ly49 NK cell receptors
Journal of Immunology 182 (6) , 3618-3627
Publisher’s version: http://dx.doi.org/10.4049/jimmunol.0803026
Gleimer M, Wahl A R, Hickman H D, Abi-Rached L, Norman P J, Guethlein L A, Hammond J A, Draghi M, Adams E J, Juo S, Jalili R, Gharizadeh B, Ronaghi M, Garcia K C, Hildebrand W H, Parham P (2011)
Although divergent in residues of the peptide binding site, conserved chimpanzee Patr-AL and polymorphic human HLA-A*02 have overlapping peptide-binding repertoires
Journal of Immunology 186 (3) , 1575-1588
Publisher’s version: http://dx.doi.org/10.4049/jimmunol.1002990
Hammond J A, Marsh S G E, Robinson J, Davies C J, Stear M J, Ellis S A (2012)
Cattle MHC nomenclature: is it possible to assign sequences to discrete class I genes?
Immunogenetics 64 (6) , 475-480
Publisher’s version: http://dx.doi.org/10.1007/s00251-012-0611-7
Hammond J A, Guethlein L A, Norman P J, Parham P (2012)
Natural selection on marine carnivores elaborated a diverse family of classical MHC class I genes exhibiting haplotypic gene content variation and allelic polymorphism
Immunogenetics 64 (12) , 915-933
Publisher’s version: http://dx.doi.org/10.1007/s00251-012-0651-z
Hammond J A, Hauton C, Bennett K A, Hall A J (2012)
Phocid seal leptin: Tertiary structure and hydrophobic receptor binding site preservation during distinct leptin gene evolution
PLoS ONE 7 (4) , e35395
Publisher’s version: http://dx.doi.org/10.1371/journal.pone.0035395