Sentence examples for possibility deletion from inspiring English sources

Exact(1)

To test this possibility, deletion derivatives of p39E containing (p15-2, p7-2) or lacking the TFS (p4-1, p11-1) were treated with TFO−C141S.

Similar(59)

To rule out the possibility that deletion of the IDE binding domain of gE does not adversely affect gE myristylation, we labeled ROka or ROka68D32-71 infecellscells with 3H-myristic acid and immunoprecipitated gE.

To rule out the possibility that deletion of ATF3 caused some defect in the receptor signaling pathways, MEF cells were treated with TNF-α to evaluate both NF-κB and JNK activation.

We have not ruled out the possibility that deletion of sequences from the N-terminus, including the N-terminal extension to RRM1, increase the ability of ΔRS to bind to pre-mRNA and promote splicing merely by increasing solubility of the SR protein.

Finally, we analyzed the changes in copy number of the miR-139 locus to exclude the possibility of deletion of this chromosomal region (Fig. S1C).

To explore the possibility that deletion of Rictor later in life would prove beneficial, we aged control and UbC-RKO mice to 9 months of age, and then treated these mice with tamoxifen for 1 week.

We cannot exclude the possibility that deletion of Piezo1 alters RBC membrane properties, resulting in decreased activity of a separate mechanosensitive ion channel rather than calcium entering the cell through Piezo1 itself.

Modifications at Master subsystem have several possibilities: addition, deletion, or modification of records within tm.

Consistent with both of these possibilities, experimental deletion of three homologs (orc1, orc5 and orc10) demonstrated that they are dispensable for cell growth under normal laboratory conditions, indicative of either redundancy of function within this gene family [43].

Nevertheless, we cannot rule out the possibility that deletions are more common, as hypothesized recently [ 88].

This multitude is further widened by possibility of deletions (Dichgans et al., 2000, 2002; Opherk et al., 2004) and splice site mutations (Joutel et al., 2000 b ).

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