1  immature crystalloid granules in eosinophil myelocytes.

2 scriptionally repressed at the transition to myelocytes.

3 osegmented neutrophils, consisting mainly of myelocytes and metamyelocytes, was noted.

4 ll population, which includes promyelocytes, myelocytes and metamyelocytes; mean (+/- SD) cell recove

5 ranscription was restricted to promyelocyte, myelocyte, and very early metamyelocyte stages of the gr

6  gangliosides characteristic of neutrophils, myelocytes, and other blood cells.

7 zed by increased bone marrow myeloblasts and myelocytes, as well as extramedullary myelopoiesis.

8 ripheral blood eosinophils and an eosinophil myelocyte cell line (AML14.3D10).

9 actors in nuclear extracts of the eosinophil myelocyte cell line, AML14.3D10.

10                           Although roles for myelocytes have been suggested in the pathophysiology of

11 turation from myeloblasts with peak level in myelocytes (MC)/metamyelocytes (MM), when the cells stop

12 myeloid precursors such as promyelocytes and myelocytes, only mature monocytes and granulocytes were

13 crease in NOX-2S and NOX-2 expression in the myelocyte rather than promyelocyte stages of differentia

14 ll shear stress significantly enhances HL-60 myelocyte rolling on P- and E-selectin at site densities

15 ension yielded minimal maturation beyond the myelocyte stage, after 72 hours of exposure to ATRA on l

16 e granulocytic lineage expressed MEFV at the myelocyte stage, concurrently with lineage commitment.

17 ng with an increase in immature eosinophilic myelocytes that showed abnormal basophilic granulation.

18 rement for C/EBPepsilon for the promyelocyte-myelocyte transition in myeloid differentiation.