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2. Epigenetic modulators link mitochondrial redox homeostasis to cardiac function in a sex-dependent manner

4. An aptamer-mediated base editing platform for simultaneous knockin and multiple gene knockout for allogeneic CAR-T cells generation

5. A Type II-B Cas9 nuclease with minimized off-targets and reduced chromosomal translocations in vivo

6. Simultaneous inhibition of DNA-PK and Polϴ improves integration efficiency and precision of genome editing

8. Correction of a urea cycle defect after ex vivo gene editing of human hepatocytes

11. Improved nuclease-based prime editing by DNA repair modulation and pegRNA engineering

13. Universal toxin-based selection for precise genome engineering in human cells

14. Author Correction: Universal toxin-based selection for precise genome engineering in human cells

18. In vivo CRISPR editing with no detectable genome-wide off-target mutations

19. Simultaneous inhibition of DNA-PK and Polϴ improves integration efficiency and precision of genome editing

21. 11th German Conference on Chemoinformatics (GCC 2015): Fulda, Germany. 8–10 November 2015

22. Engineered Cas9 extracellular vesicles as a novel gene editing tool

23. Epigenetic modulators link mitochondrial redox homeostasis to cardiac function

25. Harnessing DSB repair to promote efficient homology-dependent and -independent prime editing

26. Universal toxin-based selection for precise genome engineering in human cells

27. Supplemental_Material_GuerrieroEtAl_Computational_Analysis_of_Arrayed_CRISPR_Screens - Delivering Robust Candidates to the Drug Pipeline through Computational Analysis of Arrayed CRISPR Screens

28. R2_Supplemental_Material_for_Arrayed_CRISPRCas_Screen_by_OShea_et_al – Supplemental material for A Novel Screening Approach for the Dissection of Cellular Regulatory Networks of NF-κB Using Arrayed CRISPR gRNA Libraries

30. Additional file 1: of BE-FLARE: a fluorescent reporter of base editing activity reveals editing characteristics of APOBEC3A and APOBEC3B

31. In vivo CRISPR-Cas gene editing with no detectable genome-wide off-target mutations

32. Understanding Cytotoxicity and Cytostaticity in a High-Throughput Screening Collection

33. Feedback

35. Pre-clinical pharmacology of AZD3965, a selective inhibitor of MCT1: DLBCL, NHL and Burkitt’s lymphoma anti-tumor activity

38. Orthologue chemical space and its influence on target prediction.

40. Letters

46. MOLMAKER:  De Novo Generation of 3D Databases for Use in Drug Design

47. Correction of a urea cycle defect after ex vivogene editing of human hepatocytes

48. 11th German Conference on Chemoinformatics (GCC 2015)

49. Inbox.

50. COME OUT WRITING.

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