Auto-anti-Leb in the serum of a renal dialysis patient

Autor: Joyce Poole, Carolyn M. Giles

Publikováno v: Clinical & Laboratory Haematology. 1:239-242

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa71d7fe16c1a1e2b2b95bea049069dc
https://doi.org/10.1111/j.1365-2257.1979.tb00472.x

C4 Reference Typing Report

Autor: Gabriele Doxiadis, Beate Stradmann-Bellinghausen, Beatrice Uring-Lambert, Ch. Rittner, Martina Brenden, Carolyn M. Giles, Georges Hauptmann, Gottfried Mauff, Peter M. Schneider, Margot Braun-Stilwell

Publikováno v: Complement and Inflammation. 7:193-212

Human C4 is most polymorphic at the protein level, distinction between allotypes of the C4A and C4B proteins resting on electrophoretic migration patterns and difference in hemolytic activity. The aim of the C4 reference typing has been the definitio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f29c6ca0d3dabb4a09c4c447737384
https://doi.org/10.1159/000463148

Human leukocyte antigens (HLA) class I (Bg) on red cells studied with monoclonal antibodies

Autor: Carolyn M. Giles

Publikováno v: Immunohematology. 6:53-58

Monoclonal antibodies, capable of detecting monomorphic epitopes on HLA class I polypeptides and beta-microglobulin (β2-M), have been used by a variety of techniques to ascertain the type of structure detected on red blood cells (RBCs). Hemagglutina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::76a90d8506df2990567d832ce8a96b8e
https://doi.org/10.21307/immunohematology-2019-1041

Hereditary complement factor I deficiency

Autor: Timothy J. Vyse, P Philippe, Bernard J Morley, Mark Walport, Carolyn M. Giles, K A Davies, P. Athanassiou, Peter J. Späth

Publikováno v: Vyse, T.J.; Späth, P.J.; Davies, K.A.; Morley, B.J.; Philippe, P.; Athanassiou, P.; Giles, C.M.; Walport, M.J. (1994). Hereditary complement factor I deficiency. QJM-an international journal of medicine, 87(7), pp. 385-401. Oxford University Press 10.1093/oxfordjournals.qjmed.a068946

Summary We describe four cases (from three families) of hereditary factor I deficiency, bringing the total number of cases now reported to 23. In one family there are two affected siblings: one has suffered recurrent pyogenic infections; the other is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::082e05eb255634fbce0f948b190c1f8b
https://doi.org/10.1093/oxfordjournals.qjmed.a068946

Three decades of reference serology

Autor: Carolyn M. Giles

Publikováno v: Transfusion medicine (Oxford, England). 1(3)

Summary. I have tried to show that blood group serology developed rapidly out of necessity and demonstrated a high degree of polymorphism on red cells that was unmatched at that time in man. With new knowledge, these observations have proved to be ac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b611d79f73106e94b711369c6be6d6
https://pubmed.ncbi.nlm.nih.gov/9259840