1              Importantly, although TRAF4 has little or no ability to activate JNK independently, coex

2  antagonist (p-Chloro-D-Phe6, Leu17)-VIP had little or no ability to antagonize the PACAP38 effect.

3 ptake demonstrated minimal DNA synthesis and little or no ability to distinguish cell number or viahi

4 uli whereas other bacteria and cytokines had little or no ability to induce human beta-defensin-2 syn

5 ons we employed, some of the analogs showing little or no ability to induce luminescence were inhibit

6 terminal kinase domain of MEKK1 demonstrated little or no ability to interact with 14-3-3 proteins.

7 1P) are severely impaired, since it exhibits little or no ability to interact with DNA or other prote

8                   Early-passage cultures had little or no ability to maintain growth in transforming

9  purified PhzM alone demonstrate that it has little or no ability to methylate phenzine-1-carboxylic

10                      Three CCR5 mutants with little or no ability to mobilize calcium in response to

11 ys215-Asn246 and Lys215-Thr222 alone possess little or no ability to promote microtubule assembly, an

12 , like P strains, carry P elements, but have little or no ability to repress dysgenesis.

13                         The wax synthase had little or no ability to synthesize cholesteryl esters, d

14 we created mutated forms of CX3CR1 that have little or no ability to transduce intracellular signals.