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1 , mechanical role that aids uncurling of the germ band.
2 tiated disk of cells at the posterior of the germ band.
3 form early in the posterior-most part of the germ band.
4 ioserosa epithelium over the tail end of the germ band.
5 ybird homeobox genes within this area of the germ band.
6 tor (INR) functions downstream of hnt in the germ band.
7 gion where the mutant fails to adhere to the germ band.
8 emarcates the procephalon from the segmented germ band.
9          However, they fail to retract their germ bands.
10  PO boundary, incurring discontinuous spider germ bands.
11                             In addition, the germ band and amnioserosa move as one coherent sheet, an
12 mid retraction, segments in the curve of the germ band are under anisotropic tension.
13 nt to drive retraction, but can support some germ band cell elongation and is thus not a full phenoco
14 ian, Pseudooides, indicates a unique mode of germ-band development.
15 erm band extension, cells within the lateral germ band do not intercalate.
16  model in which the amnioserosa "pushes" the germ band during retraction.
17 ceded major morphogenetic movements, such as germ band elongation and dorsal closure.
18 e salient tissue- and cell-scale features of germ band elongation during Drosophila gastrulation, in
19 d in the ~32h between gastrulation and early germ band elongation, and is likely to require zygotic r
20                                       During germ band elongation, widespread decapentaplegic (dpp) e
21 anogaster embryos (prior to the beginning of germ-band elongation); similarities and differences in g
22 rly blastoderm stage and subsequently during germ-band elongation.
23 es of ftz expression during gastrulation and germ-band elongation.
24 s of JH on hemimetabolous insects with short germ band embryos indicate that JH's embryonic role prec
25 ing the proportions of segments in elongated germ-band embryos.
26                                    Later, in germ band-extended embryos, Snail is also expressed in m
27  posterior ectoderm expression begins during germ band extension and continues throughout development
28          Our analysis provides evidence that germ band extension is driven by active T1 processes tha
29 g deformed by active midgut invagination and germ band extension on an ellipsoidal surface, which rob
30 sion of Drosophila SPP was first apparent at germ band extension, and in late embryos it was robust i
31 derm stripes, minor stripe expression during germ band extension, and later expression in the lateral
32 g time-lapse recordings that, in contrast to germ band extension, cells within the lateral germ band
33                                   At maximum germ band extension, dpp dorsal ectoderm expression beco
34 ve cell-cell intercalation during Drosophila germ band extension, has no effect on streak formation,
35                                        After germ band extension, the cells of the Drosophila ventral
36                                   Drosophila germ-band extension (GBE) is one example, which requires
37 traembryonic membrane (amnioserosa) prior to germ-band extension and continues in these tissues beyon
38 lus expression begins around stage 9 at full germ-band extension in a subset of mesodermal cells orga
39                                       During germ-band extension, Decapentaplegic (Dpp) signals from
40                           However, following germ-band extension, there is a premature loss of the am
41 omes anisotropic as cells intercalate during germ-band extension.
42 he dorsal mesoderm of host embryos following germ-band extension.
43 n have a normal body plan and undergo normal germ-band extension.
44 BS, shortly before the dramatic movements of germ band flexure, when the left and right halves of the
45              The structure of the developing germ band in another bilaterian, Pseudooides, indicates
46 the patterning of the dorsolateral embryonic germ band in response to Dpp signals.
47 terior patterning gene functions in two long germ band insects, Nasonia and Drosophila.
48         In Tribolium and other intermediated germ band insects, the anterior segments of the embryo a
49 to derive the AP patterning, as seen in long germ-band insects that express their Hox genes simultane
50 ich is appropriate for vertebrates and short germ-band insects, the algorithm creates gene expression
51 ed cells of the amnioserosa contract and the germ band moves so it is only on one side of the embryo.
52 rized the cellular processes associated with germ band retraction (GBR) in the Drosophila embryo.
53           Ecdysone signaling is required for germ band retraction and head involution, morphogenetic
54  (betaPS) null embryos, including failure in germ band retraction and muscle detachment.
55 tion and regression are contemporaneous with germ band retraction and shortening, respectively, sugge
56                                           As germ band retraction commences, one tissue, the germ ban
57 equired for maintaining dpp expression after germ band retraction in the dorsal ectoderm.
58                                              Germ band retraction involves a dramatic rearrangement o
59                                       During germ band retraction, CC progenitors increase in number
60 r than in wild type embryos by completion of germ band retraction.
61 the combinatorial enhancer and begins during germ band retraction.
62  dorsal ectoderm expression initiates during germ band retraction.
63 e adjacent to the epidermis-is necessary for germ band retraction.
64 hnt must function in a pathway that controls germ band retraction.
65 nd the endodermal midgut prior to and during germ band retraction.
66 smic and does not accumulate in nuclei until germ band retraction.
67 scuss a possible role for the amnioserosa in germ-band retraction in light of these mutants' unretrac
68                           Here, we show that germ-band retraction in the Drosophila embryo, during wh
69 defects, suggesting that hindsight's role in germ-band retraction is permissive rather than instructi
70               First, hindsight's function in germ-band retraction may be limited to maintenance of th
71 ion of hindsight in the early embryo rescues germ-band retraction without producing dominant gain-of-
72 of the amnioserosa results in the failure of germ-band retraction, implicating amnioserosal expressio
73  a role for this spreading in the process of germ-band retraction.
74 c midgut can be eliminated without affecting germ-band retraction.
75  cell shape changes and movements that drive germ-band retraction.
76  the cell shape changes and movements during germ-band retraction.
77 es in these tissues beyond the completion of germ-band retraction.
78                                       As the germ band shortens in Drosophila melanogaster embryos, c
79 ey also suggest that, in both short and long germ-band species, oenocytes are induced from a Spalt ma
80                          During the extended germ band stage the protein remains predominantly cytopl
81                          During the extended germ band stage, CC progenitor cells form a paired clust
82 lusters in opisthosomal segments 2-6 at late germ band stages.
83 nes simultaneously, from the ancestral short germ-band system.
84 s to and migrates over the caudal end of the germ band via lamellipodia.
85 eum, which become stripes at the base of the germ band where segments are emerging.
86  convergence and extension of the Drosophila germ-band, where polarity within the plane of the embryo
87 m band retraction commences, one tissue, the germ band, wraps around another, the amnioserosa.