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1 erentiation of a unique blood cell type, the lamellocyte.
2 this cascade also prevents the generation of lamellocytes.
3 te concentration, and abundant production of lamellocytes.
4 ception, the encapsulation is carried out by lamellocytes.
5 not compromised in their ability to generate lamellocytes.
6 ood cells: plasmatocytes, crystal cells, and lamellocytes.
7  with layers of specialized hemocytes called lamellocytes.
8 se bacteria as well as to differentiate into lamellocytes.
9 ired for the emergence of the injury-induced lamellocytes.
10 apsulation response and for the formation of lamellocytes.
11  AP downregulate JAK-STAT signaling and form lamellocytes.
12 ferentiation, except for a late induction of lamellocytes.
13 is response relies on the differentiation of lamellocytes, a cryptic cell type, dedicated to pathogen
14 asmatocytes, the major hemocyte subset, from lamellocytes, an activated subset present in gain-of-fun
15         In addition, many cells exhibit both lamellocyte and crystal cell markers.
16 to a dramatic increase in the number of both lamellocytes and crystal cells in the Drosophila larval
17 ction in which specialized host blood cells, lamellocytes and crystal cells, are activated and recrui
18 acterized in the lymph gland: plasmatocytes, lamellocytes, and crystal cells, which are analogous to
19 e to three mature cell types: plasmatocytes, lamellocytes, and crystal cells.
20  produced, plasmatocytes, crystal cells, and lamellocytes, and their differentiation is tightly contr
21  comprising plasmatocytes, crystal cells and lamellocytes are peripherally located in the cortical zo
22 tion to ensure the proper differentiation of lamellocytes at the expense of crystal cells.
23                          Similar capsules of lamellocytes, called melanotic capsules, are also formed
24 ell maturation and postinfection circulating lamellocyte concentration.
25 constitutive expression of dorsal can induce lamellocyte differentiation and cause the formation of m
26 at PSEDN members function with GATA to block lamellocyte differentiation and maintain the prohemocyte
27  that circulating hemocyte concentration and lamellocyte differentiation constitute two distinct phys
28  contributions of hemocyte concentration vs. lamellocyte differentiation to wasp egg encapsulation ar
29 l larval hemocyte proliferation and suppress lamellocyte differentiation, likely regulating hematopoi
30 cally reducing JAK-STAT signaling permits PP lamellocyte differentiation.
31  of hemocytes and copious differentiation of lamellocytes during larval stages.
32 cipates in a switch between plasmatocyte and lamellocyte fate in a common precursor and further sugge
33 fferent kinds of specialized cells, like the lamellocytes in D. melanogaster, for the encapsulation o
34              Constitutive differentiation of lamellocytes in larvae carrying these mutations is accom
35                                              Lamellocytes in mutants are either free in circulation o
36  development as well as the emergence of the lamellocyte lineage following active cellular immunity c
37 ndance of highly differentiated blood cells (lamellocytes), normally not found in healthy larvae.
38 tion, but Dif controls both plasmatocyte and lamellocyte production.
39 recursors of specialized immune cells called lamellocytes that were previously only produced after in
40    Plasmatocytes differentiate into adhesive lamellocytes to form multilayered capsules around foreig
41 ystal cells (involved in wound healing), and lamellocytes (which encapsulate parasites).