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2. Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates

6. Rab5 is necessary for the biogenesis of the endolysosomal system in vivo

7. Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter

8. Liver-Specific siRNA-Mediated Stat3 or C3 Knockdown Improves the Outcome of Experimental Autoimmune Myocarditis

9. Liquid-crystal organization of liver tissue

11. Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing

12. Control of liver size by RNAi-mediated multiplex knockdown and its application for discovery of regulatory mechanisms

13. Large-Scale Quantitative Proteomics Identifies the Ubiquitin Ligase Nedd4-1 as an Essential Regulator of Liver Regeneration

14. Cell-Cycle-Targeting MicroRNAs as Therapeutic Tools against Refractory Cancers

15. Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo

16. Regulation of Liver Metabolism by the Endosomal GTPase Rab5

17. Loss of α-catenin elicits a cholestatic response and impairs liver regeneration

20. Knockdown and knockout of β1-integrin in hepatocytes impairs liver regeneration through inhibition of growth factor signalling

23. MICU2, a Paralog of MICU1, Resides within the Mitochondrial Uniporter Complex to Regulate Calcium Handling

24. Systemic RNAi-mediated Gene Silencing in Nonhuman Primate and Rodent Myeloid Cells

26. Loss of α-catenin elicits a cholestatic response and impairs liver regeneration.

27. The Roles of Individual Mammalian Argonautes in RNA Interference In Vivo.

28. Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates.

29. Corrigendum: Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.

30. The Roles of Individual Mammalian Argonautes in RNA Interference In Vivo.

31. In vivo endothelial siRNA delivery using polymeric nanoparticles with low molecular weight

32. Nanoparticle-formulated siRNA targeting integrins inhibits hepatocellular carcinoma progression in mice

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