medulla | P-stage, with Scer\GAL4bsh.M.PT
medulla | P-stage, with Scer\GAL4GMR69B02
medulla | P-stage, with Scer\GAL4sens.F2
medulla | P-stage, with Scer\GAL4sev.PM181
Expressing dshΔDEP+.UAS under the control of Scer\GAL4HCH.Hand fails to induce defects in heart morphology or ostia formation in embryos.
Expression of dshΔDEP+.Scer\UAS under the control of Scer\GAL4fkh.PZ has no effect on salivary gland guidance in the embryo.
Expression of the dominant-negative dshΔDEP+.Scer\UAS in the retina behind the furrow using Scer\GAL4GMR.PF results in a strong ventral-to-dorsal R axon misrouting phenotype.
Expression of dshΔDEP+.Scer\UAS under the control of Scer\GAL4ptc-559.1 results in a polarity defect.
Expression of dshΔDEP+.Scer\UAS at 24 hours after pupariation under the control of Scer\GAL4hs.PB results in a tissue polarity phenotype in the wing.
Scer\GAL4da.G32/dshΔDEP+.UAS is a suppressor of denticle | ectopic phenotype of wgl-17
Scer\GAL4da.G32/dshΔDEP+.UAS is a suppressor of embryonic leading edge cell primordium phenotype of wgl-17
Scer\GAL4da.G32/dshΔDEP+.UAS is a suppressor of embryonic/first instar larval cuticle phenotype of wgl-17
dshΔDEP+.UAS/Scer\GAL469B is a suppressor of amnioserosa phenotype of hep1
dshΔDEP+.UAS/Scer\GAL469B is a suppressor of embryonic dorsal epidermis phenotype of hep1
dshΔDEP+.UAS/Scer\GAL469B is a suppressor of embryonic leading edge cell & actin filament phenotype of hep1
dshΔDEP+.UAS/Scer\GAL469B is a suppressor of embryonic/first instar larval cuticle | dorsal phenotype of hep1
dshΔDEP+.Scer\UAS; Scer\GAL4da.G32 partially suppresses the transformation of naked ventral cuticle into denticles and reduction in cuticle length seen in cuticles from wgl-17 homozygous embryos, and an completely suppress the dorsal hole in these cuticles. dshΔDEP+.Scer\UAS; Scer\GAL4da.G32 suppresses, the loss of dorsal ventral polarity in the leading edge cells of stage 13 wgl-17 homozygous embryos but fails to rescue elongation of these cells. However, initiation of the anterior zipper during dorsal closure is rescued.
The dorsal hole phenotype, loss of leading edge actin cable, and loss of adhesion between the amnioserosa and dorsal epidermis of hep1 mutant embryos are all partially suppressed by Scer\GAL469B with dshΔDEP+.Scer\UAS.
dshΔDEP+.UAS/Scer\GAL4hs.PB fails to rescue dsh1