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1. Activation of human RNA lariat debranching enzyme Dbr1 by binding protein TTDN1 occurs though an intrinsically disordered C-terminal domain

2. DNA binding and RAD51 engagement by the BRCA2 C-terminus orchestrate DNA repair and replication fork preservation

11. An iterative process produces oxamniquine derivatives that kill the major species of schistosomes infecting humans

13. Copper chaperones

15. Oxamniquine resistance alleles are widespread in Old World Schistosoma mansoni and predate drug deployment

16. Oxamniquine resistance alleles are widespread in Old WorldSchistosoma mansoniand predate drug deployment

17. Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection

18. Structural and enzymatic insights into species-specific resistance to schistosome parasite drug therapy

19. Metal dependence and branched RNA cocrystal structures of the RNA lariat debranching enzyme Dbr1

20. Independent origins of loss-of-function mutations conferring oxamniquine resistance in a Brazilian schistosome population

22. Engineering a Putative Zinc Binding Site in SOD5

23. Structural and Functional Characterization of the Enantiomers of the Antischistosomal Drug Oxamniquine

27. Insights into the Role of the Unusual Disulfide Bond in Copper-Zinc Superoxide Dismutase

28. Foreword

31. Candida albicans SOD5 represents the prototype of an unprecedented class of Cu-only superoxide dismutases required for pathogen defense

42. Structures of the G85R Variant of SOD1 in Familial Amyotrophic Lateral Sclerosis

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