Publications
[53] Li H, Lin P-H, Pranav G, Li X, Zhao L, Zhou X, Li Z, Wei S, Xu L, Han R, Lu J, Tan T, Yang D-H, Chen Z-S, Pawlik TM, Merritt RE, Ma J (2021) MG53 suppresses tumor progression and stress granule formation by modulating G3BP2 activity in non-small cell lung cancer. Molecular Cancer 20: 118. Full Text
[52] Zou X, Ouyang H, Pang D, Han R* and Tang X*. (2021) Pathological alterations in the gastrointestinal tract of a porcine model of DMD. Cell & Bioscience 11(1): 131. Full Text
[51] Xu L, Zhang C, Li H, Wang P, Gao Y, Mokadam NA, Ma J, Arnold WD, Han R*. (2021) Efficient precise in vivo base editing in adult dystrophic mice. Nature Communications 12(1): 3719. Full Text
[50] Yang D, Liang X, Pallas B, Hoenerhoff M, Ren Z, Han R, Zhang J, Chen YE, Jin J-P, Sun F, Xu J. (2021) Production of CFTR-deltaF508 Rabbits. Frontiers in Genetics 11: 627666. Full Text
[49] Xu J, Zhang J, Yang D, Song J, Pallas B, Zhang C, Hu J, Peng X, Christensen N, Han R* and Chen YE*. (2021) Gene editing in rabbits: unique opportunities for translational biomedical research. Frontiers in Genetics 12: 642444. Full Text
[48] Li H, Zhao L, Lau YS, Zhang C, Han R*. (2020) Genome-wide CRISPR screen identifies LGALS2 as an oxidative stress-responsive gene with an inhibitory function on colon tumor growth. Oncogene 40(1): 177-188. Full Text
[47] Lau YS, Zhao L, Zhang C, Li H, Han R*. (2020) Genetic disruption of the inflammasome adaptor ASC has minimal impact on the pathogenesis of Duchenne muscular dystrophy in mdx Mice. Life Sciences 257: 118069. Full Text
[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
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