Sentence examples for mutant clones contained from inspiring English sources

bantam mutant clones contained fewer mature INP compared with control clones or with mutant clones carrying a UAS- bantam transgene (Fig. 3G).

Because tkv 8 and mad 1 2 single mutant clones contained many ECs whereas put null or tkv 8 mad 1 2 double mutant clones contained little if any ECs at the time we did PH3 staining, we suspected that the non-cell-autonomous effect of tkv 8 and mad 1 2 single mutant clones was due to BMP signaling defects in ECs.

Although both control and bantam mutant clones contained only one large Dpn+Ase− neuroblast per clone, the Dpn+ neuroblasts were smaller on average in bantam mutant type II clones than in the control clones (Fig. 3E).

At 120 h ALH, bantam mutant clones contained fewer GFP-labeled small cells compared with the control clones or with mutant clones carrying a UAS- bantam transgene (Fig. 3F).

As previously reported, posterior midgut Apc1 −/− mutant clones contained significantly more cells and displayed increased ISC proliferation when compared with control (MARCM Lac-Z) clones (Cordero et al, 2012a; Fig 4A, B, E and F).

Control clones contained one or more Delta-positive ISCs (Fig 1A, arrows), but esg G66B mutant clones contained virtually no Delta-positive ISCs, although ISCs could often be found adjacent to the clones (Fig 1B, arrowhead, quantification in C).

In Figure 2, we showed that vps22 and vps36 mutant clones contain increased Notch protein levels.

In parallel, mock-transfected cell clones were also developed bearing empty vector only, as well as mutant clones containing a putative PTPase-dead mutant Tensin3 (Tns3 Mut) cDNA.

To further analyse the relationships between dpn and the members of the E spl) complex, we induced MARCM mutant clones containing the deficiency E spl Xp (Bardin et al., 2010) and simultaneously depleted dpn by means of a dpn RNAi.

Although trx mutant clones also contained an average of 3 INPs and 4 INP-derived GMCs, these cells were located at the extreme distal end of the clone, consistent with trx mutant type II neuroblasts adopting a type I neuroblast identity following the clone induction.

We generated an insertion mutant library, in which the clones contained a single genomic insertion.