Sabra G. Andersen

Severe anemia in the<i>Nan</i>mutant mouse caused by sequence-selective disruption of erythroid Krüppel-like factor

Mirosława Siatecka, Kenneth E. Sahr, Sabra G. Andersen et al. · Proceedings of the National Academy of Sciences · 2010 · 76 citations · Full text

Genetics, Blood Cell, Molecular Genetics +18

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism

Babette Gwynn, Steven L. Ciciotte, Susan J. Hunter et al. · Blood · 2000 · 42 citations

Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency

Luanne L. Peters, Rebecca A. Swearingen, Sabra G. Andersen et al. · Blood · 2004 · 27 citations · Full text

Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency

Luanne L. Peters, PRISCILLA W. LANE, Sabra G. Andersen et al. · Blood Cells Molecules and Diseases · 2001 · 26 citations

Anemia, Downeast Anemia, Autoimmune Disease +10