Sentence examples for clone mark from inspiring English sources

In the embryo, cells of the clone mark pre-denticles of row 1.

In the pre-L1 embryo, cells in the clone mark pre-denticles of row 2. In the pre-L3 larva (B' ), the same cells are the tendon cells.

In the embryo, cells in the clone mark pre-denticles of row 3 while in the larva the same two cells mark pre-denticles of row 2. (D – D' ) Four marked cells in the denticle belt.

In this way, we obtained a small fraction of brains that had an aDT-e (DA1 PN) clone and an LHN clone marked in different colors.

Note also that, in the dorsal disc (the Apterous territory), chip e55 mutant clones barely survive (indicated by asterisks in the merge in G ), compared to ssdp L7 mutant clones that appear to grow normally, like pygo S123 mutant clones; however, in the absence of Apterous, i.e. in the ventral compartment, chip e55 mutant clones grow normally (see clone marked by arrow in E ).

(B D) Ey expressing Flp-out clones (marked with GFP in green) in the three distinct regions (white arrows).

Mutant clones (marked by lack of GFP, green) also had no defects (Figs. 4C and D).

Although these clones, marked by GFP expression, exhibited smooth borders with neighboring wild-type cells (Figure 6C,C″), they did not exhibit altered accumulation of Talin (Figure 6C',C″).

We next analyzed MGM flp-out clones marked by GFP in the wing disc or by yellow (y) bristles in the adult [17].

A second phenotype associated with the capsDel1 trn28.4 double null clones (marked by lack of GFP, green) was a perturbation in ommatidial spacing in third instar eye discs (Fig. 5B, circled).

Wild-type clones (marked by the absence of GFP) induced in all regions of the wing disc formed wiggly borders with their neighboring non-clonal cells (Figure 4C',C″, see arrow and arrowheads for examples).