Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10907201 | Experimental Hematology | 2015 | 17 Pages |
Abstract
Every 2Â years since 1978, an international group of scientists, physicians, and other researchers meet to discuss the latest developments in the underlying etiology, mechanisms of action, and developmental acquisition of cellular and systemic defects exhibited and elicited by the most common inherited human disorders, the hemoglobinopathies. The 19th Hemoglobin Switching Conference, held in September 2014 at St. John's College in Oxford, once again exceeded all expectations by describing cutting edge research in cellular, molecular, developmental, and genomic advances focused on these diseases. The conference comprised about 60 short talks over 3Â days by leading investigators in the field. This meeting report describes the highlights of the conference.
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Authors
Gerd A. Blobel, David Bodine, Marjorie Brand, John Crispino, Marella F.T.R. de Bruijn, David Nathan, Thalia Papayannopoulou, Catherine Porcher, John Strouboulis, Len Zon, Douglas R. Higgs, George Stamatoyannopoulos, James Douglas Engel,