[46] Sui T, Xu L, Lau YS, Liu D, Liu T, Gao Y, Lai L, Han R, Li Z. (2020) Correction: Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutations. Cell Death Dis doi: 10.1038/s41419-020-2659-x: . Full Text

[45] Dwivedi P, Kiran S, Han S, Dwivedi M, Khatik R, Fan R,Mangrio F, Du K, Zhu Z, Yang C, Huang F, Ejaz A, Han R, Si T, Xu R. (2020) Magnetic targeting and ultrasound activation of liposome-microbubble conjugate for enhanced delivery of anti-cancer therapies. ACS Applied Materials & Interfaces 12(21): 23737-23751. Full Text

[44] Wang P, Xu L, Gao Y and Han R*. (2020) BEON: A functional fluorescence reporter for quantification and enrichment of adenine base editing activity. Molecular Therapy 28(7): 1696-1705. Full Text

[43] Zhang C, Li H and Han R*. (2020) An open-source video tracking system for mouse locomotor activity analysis. BMC Res Notes 13(1): 48. Full Text

[42] Brown P, RELISH Consortium and Zhou Y. (2019) Large expert-curated database for benchmarking document similarity detection in biomedical literature search. Database doi: 10.1093/database/baz085. Full Text

[41] Xu L, Liu Y, Han R*. (2019) BEAT: A python program to quantify base editing from Sanger sequencing. CRISPR J 2(4): 223-229. Full Text

[40] Xu L#, Lau YS#, Gao Y#, Li H, Han R*. (2019) Life-long AAV-mediated CRISPR genome editing in dystrophic heart improves cardiomyopathy without causing serious lesions in mdx mice. Molecular Therapy 27: 1407-1414. Full Text

[39] Lau YS, Xu L, Gao Y, Han R*. (2018) Automated muscle histopathology analysis using CellProfiler. Skelet Muscle 8: 32. Full Text

[38] Sui T, Xu L, Lau YS, Liu D, Liu T, Gao Y, Lai L*, Han R*, Li Z*. (2018) Development of muscular dystrophy in a rabbit model with Ano5 mutations generated by CRISPR/Cas9. Cell Death Dis 9: 609. Full Text

[37] Xu L, Gao Y, Lau YS, Han R*. (2018) Adeno-Associated Virus-Mediated Delivery of CRISPR for Cardiac Gene Editing in Mice. J Vis Exp doi: 10.3791/57560. Full Text

[36] Sui T, Lau YS, Liu D, Liu T, Xu L, Gao Y, Lai L*, Li Z*, Han R*. (2018) A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9. Dis Model Mech 11: dmm032201. Full Text

[35] Xu J, Xu L, Lau YS, Gao Y, Moore SA, Han R*. (2018) A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide. J Pathol Clin Res 4: 135-145. Full Text

[34] El Refaey M, Xu L, Gao Y, Canan BD, Adesanya TMA, Warner SC, Akagi K, Symer DE, Mohler PJ, Ma J, Janssen PML, Han R*. (2017) In Vivo Genome Editing Restores Dystrophin Expression and Cardiac Function in Dystrophic Mice. Circulation Research 121: 923-929. Full Text

[33] Xu L, Zhao L, Gao Y, Xu J, Han R*. (2017) Empower multiplex cell and tissue-specific CRISPR-mediated gene manipulation with self-cleaving ribozymes and tRNA. Nucleic Acids Research 45: e28. Full Text

[32] Du L, Wu J, Qian P, Xin R, Ni Y, Han R, Meng Z, Xia J. (2017) Phylogeographical Analysis Reveals Distinct Sources of HIV-1 and HCV Transmitted to Former Blood Donors in China. AIDS Res Hum Retroviruses 33: 284-289. Full Text

[31] Dumbleton J, Agarwal P, Huang H, Hogrebe N, Han R, Gooch KJ, He X. (2016) The effect of RGD peptide on 2D and miniaturized 3D culture of HEPM cells, MSCs, and ADSCs with alginate hydrogel. Cell Mol Bioeng 9: 277-288. Full Text

[30] Meng Z, Du L, Hu N, Byrd D, Amet T, Desai M, Shepherd N, Lan J, Han R, Yu Q. (2016) Antiretroviral Therapy Normalizes Autoantibody Profile of HIV Patients by Decreasing CD33+CD11b+HLA-DR+ Cells: A Cross-Sectional Study. Medicine (Baltimore) 95: e3285. Full Text

[29] Zhu H, Han R, Duan DD. (2016) Novel Biomarkers and Treatments of Cardiac Diseases. Biomed Res Int 2016: 1315627. Full Text

[28] Xu J, El Refaey M, Xu L, Zhao L, Gao Y, Floyd K, Karaze T, Janssen PM, Han R*. (2015) Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy. Skelet Muscle 5: 43. Full Text

[27] Xu L, Park KH, Zhao L, Xu J, El Refaey M, Gao Y, Zhu H, Ma J, Han R*. (2015) CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice. Molecular Therapy 24: 564-569. Full Text

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