1                                    Recently, Doyle and colleagues demonstrated that highly specific l

2  originally reported in a racemic fashion by Doyle and Molander.

3                      In this issue of Blood, Doyle et al provide evidence that knockout of the genes

4 ompared to experimental values determined by Doyle et al.

5          New structures and experiments from Doyle et al.

6             In this issue, Heiman et al. and Doyle et al. introduce a new strategy (TRAP) that enable

7                                     However, Doyle et al. reveal that MAGE proteins interact with RIN

8 ness is maintained in a dynamic equilibrium (Doyle et al., 1988).

9                              As predicted by Doyle et al., a large geometry change was observed upon

10 esolved in the crystallographic structure of Doyle et al..

11                                 Finally, via Doyle-Fuller-Newman (DFN) simulations, we investigate th

12                        Finally, we present a Doyle-Fuller-Newman model of a KIB full cell with realis

13                         In recent years, the Doyle group-along with many others-has pursued the study

14 volving allylic sulfides and diazo reagents (Doyle-Kirmse reaction) is reported.

15 F), which is capable of mediating asymmetric Doyle-Kirmse reactions with an enantiomeric excess up to

16 -substituted gem-difluoroalkenes, along with Doyle-Kirmse rearrangements and trifluoromethylcycloprop

17 ms for adventure were shaped by Arthur Conan Doyle's Sherlock Holmes, Percival Christopher Wren's Bea