Mouse (55 sources):
abnormal angiogenesis,
abnormal common lymphocyte progenitor cell morphology,
abnormal definitive hematopoiesis,
abnormal double-negative T cell morphology,
abnormal embryonic erythropoiesis,
abnormal erythropoiesis,
abnormal hematopoietic stem cell morphology,
abnormal hemoglobin content,
abnormal liver development,
abnormal liver sinusoid morphology,
abnormal megakaryocyte differentiation,
abnormal megakaryocyte morphology,
abnormal myeloblast morphology/development,
abnormal seminal vesicle morphology,
abnormal single-positive T cell number,
abnormal T cell differentiation,
absent common myeloid progenitor cells,
arrested B cell differentiation,
arrested T cell differentiation,
decreased B-1 B cell number,
decreased body size,
decreased CD4-positive, alpha beta T cell number,
decreased common myeloid progenitor cell number,
decreased double-negative T cell number,
decreased double-positive T cell number,
decreased eosinophil cell number,
decreased erythrocyte cell number,
decreased gamma-delta T cell number,
decreased hematocrit,
decreased hematopoietic stem cell number,
decreased mature B cell number,
decreased pre-B cell number,
decreased prepulse inhibition,
decreased single-positive T cell number,
decreased spleen white pulp amount,
decreased T cell proliferation,
decreased thymocyte number,
hematopoietic system phenotype,
immune system phenotype,
increased bone marrow cell number,
increased CD8-positive, alpha-beta T cell number,
increased double-negative T cell number,
increased hematopoietic stem cell number,
increased nucleated erythrocyte cell number,
increased number of Howell-Jolly bodies,
increased spleen red pulp amount,
lethality throughout fetal growth and development, complete penetrance,
macrocytosis,
no abnormal phenotype detected,
polychromatophilia,
premature death,
preweaning lethality, incomplete penetrance,
small liver,
small spleen,
small thymus
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