☰

Hojun Li, Ph.D. - Publications

Affiliations: 
2011 University of Pennsylvania, Philadelphia, PA, United States 
Area:
Molecular Biology
Tree Info Grants Similar researchers PubMed Report error

23 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Solomon IH, Li H, Benson LA, Henderson LA, Degar BA, Gorman MP, Duncan CN, Lidov HG, Alexandrescu S. Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System. Journal of Neuropathology and Experimental Neurology. PMID 30295794 DOI: 10.1093/Jnen/Nly094  0.308
2018 Li H, Natarajan A, Ezike J, Barrasa MI, Yang H, Ma C, Markoulaki S, Lodish H. Single Cell Resolution of Glucocorticoid Effects on Erythroid Progenitor Cells Blood. 132: 751-751. DOI: 10.1182/Blood-2018-99-112445  0.306
2017 Pishesha N, Bilate AM, Wibowo MC, Huang NJ, Li Z, Dhesycka R, Bousbaine D, Li H, Patterson HC, Dougan SK, Maruyama T, Lodish HF, Ploegh HL. Engineered erythrocytes covalently linked to antigenic peptides can protect against autoimmune disease. Proceedings of the National Academy of Sciences of the United States of America. PMID 28270614 DOI: 10.1073/Pnas.1701746114  0.357
2016 Li H, Shi J, Huang NJ, Pishesha N, Natarajan A, Eng JC, Lodish HF. Efficient CRISPR-Cas9 mediated gene disruption in primary erythroid progenitor cells. Haematologica. PMID 26969085 DOI: 10.3324/Haematol.2015.135723  0.345
2014 Wu TL, Li H, Faust SM, Chi E, Zhou S, Wright F, High KA, Ertl HC. CD8+ T cell recognition of epitopes within the capsid of adeno-associated virus 8-based gene transfer vectors depends on vectors' genome. Molecular Therapy : the Journal of the American Society of Gene Therapy. 22: 42-51. PMID 24077034 DOI: 10.1038/Mt.2013.218  0.557
2014 Li H, Shi J, Lodish HF. Genome Editing in Erythroid Progenitor Cells Mediated By Crispr/Cas9 Blood. 124: 1345-1345. DOI: 10.1182/Blood.V124.21.1345.1345  0.458
2013 Anguela XM, Sharma R, Doyon Y, Miller JC, Li H, Haurigot V, Rohde ME, Wong SY, Davidson RJ, Zhou S, Gregory PD, Holmes MC, High KA. Robust ZFN-mediated genome editing in adult hemophilic mice. Blood. 122: 3283-7. PMID 24085764 DOI: 10.1182/Blood-2013-04-497354  0.578
2013 Parzych EM, Li H, Yin X, Liu Q, Wu TL, Podsakoff GM, High KA, Levine MH, Ertl HC. Effects of immunosuppression on circulating adeno-associated virus capsid-specific T cells in humans. Human Gene Therapy. 24: 431-42. PMID 23461589 DOI: 10.1089/Hum.2012.246  0.515
2012 Wu T, Töpfer K, Lin SW, Li H, Bian A, Zhou XY, High KA, Ertl HC. Self-complementary AAVs induce more potent transgene product-specific immune responses compared to a single-stranded genome. Molecular Therapy : the Journal of the American Society of Gene Therapy. 20: 572-9. PMID 22186792 DOI: 10.1038/Mt.2011.280  0.525
2012 Anguela XM, Sharma R, Doyon Y, Wong SY, Paschon DE, Li H, Haurigot V, Davidson RJ, Zhou S, Gregory PD, Holmes MC, Rebar E, High KA. In Vivo Genome Editing of Liver Albumin for Therapeutic Gene Expression: Rescue of Hemophilic Mice Via Integration of Factor 9 Blood. 120: 751-751. DOI: 10.1182/Blood.V120.21.751.751  0.589
2011 Li H, Haurigot V, Doyon Y, Li T, Wong SY, Bhagwat AS, Malani N, Anguela XM, Sharma R, Ivanciu L, Murphy SL, Finn JD, Khazi FR, Zhou S, Paschon DE, et al. In vivo genome editing restores haemostasis in a mouse model of haemophilia. Nature. 475: 217-21. PMID 21706032 DOI: 10.1038/Nature10177  0.563
2011 Li H, Lasaro MO, Jia B, Lin SW, Haut LH, High KA, Ertl HC. Capsid-specific T-cell responses to natural infections with adeno-associated viruses in humans differ from those of nonhuman primates. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 2021-30. PMID 21587208 DOI: 10.1038/Mt.2011.81  0.53
2011 Li H, Tuyishime S, Wu TL, Giles-Davis W, Zhou D, Xiao W, High KA, Ertl HC. Adeno-associated virus vectors serotype 2 induce prolonged proliferation of capsid-specific CD8+ T cells in mice. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 536-46. PMID 21157435 DOI: 10.1038/Mt.2010.267  0.506
2011 Li H, Malani N, Hamilton SR, Schlachterman A, Bussadori G, Edmonson SE, Shah R, Arruda VR, Mingozzi F, Wright JF, Bushman FD, High KA. Assessing the potential for AAV vector genotoxicity in a murine model. Blood. 117: 3311-9. PMID 21106988 DOI: 10.1182/Blood-2010-08-302729  0.576
2011 Anguela XM, Sharma R, Li H, Haurigot V, Bhagwat A, Davidson RJ, Zhou S, Doyon Y, Gregory PD, Holmes MC, High KA. Robust Factor IX Expression Following ZFN-Mediated Genome Editing in An Adult Mouse Model of Hemophilia B Blood. 118: 668-668. DOI: 10.1182/Blood.V118.21.668.668  0.571
2010 Li H, Haurigot V, Doyon Y, Li J, Bhagwat A, Wong S, Anguela X, Sharma R, Ivanciu L, Murphy S, Zhou S, Paschon D, Rebar E, Gregory PD, Holmes MC, et al. Phenotypic Correction of a Mouse Model of Hemophilia B by In Vivo Genetic Correction of the F9 Gene Blood. 116: LBA-5-LBA-5. DOI: 10.1182/Blood.V116.21.Lba-5.Lba-5  0.59
2009 Li H, Lin SW, Giles-Davis W, Li Y, Zhou D, Xiang ZQ, High KA, Ertl HC. A preclinical animal model to assess the effect of pre-existing immunity on AAV-mediated gene transfer. Molecular Therapy : the Journal of the American Society of Gene Therapy. 17: 1215-24. PMID 19367258 DOI: 10.1038/Mt.2009.79  0.55
2009 Murphy SL, Li H, Mingozzi F, Sabatino DE, Hui DJ, Edmonson SA, High KA. Diverse IgG subclass responses to adeno-associated virus infection and vector administration. Journal of Medical Virology. 81: 65-74. PMID 19031458 DOI: 10.1002/Jmv.21360  0.499
2009 Li H, Malani N, Hamilton SR, Schlachterman A, Zhang JZ, Bussadori G, Edmonson SA, Mingozzi F, Wright JF, Arruda VR, Bushman FD, High KA. Assessment of Insertional Mutagenesis Risk Following AAV Vector-Mediated Factor IX Gene Transfer in Mice. Blood. 114: 2465-2465. DOI: 10.1182/Blood.V114.22.2465.2465  0.551
2008 Murphy SL, Li H, Zhou S, Schlachterman A, High K. Prolonged Susceptibility to Antibody-mediated Neutralization for Adeno-associated Vectors Targeted to the Liver. Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 138-145. PMID 28192706 DOI: 10.1038/sj.mt.6300334  0.366
2008 Murphy SL, Li H, Zhou S, Schlachterman A, High KA. Corrigendum to "Prolonged Susceptibility to Antibody-mediated Neutralization for Adeno-associated Vectors Targeted to the Liver". Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 633. PMID 28178504 DOI: 10.1038/Sj.Mt.6300386  0.521
2008 Murphy SL, Li H, Zhou S, Schlachterman A, High KA, High K. Prolonged susceptibility to antibody-mediated neutralization for adeno-associated vectors targeted to the liver. Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 138-45. PMID 17955024 DOI: 10.1038/Sj.Mt.6300334  0.582
2007 Li H, Murphy SL, Giles-Davis W, Edmonson S, Xiang Z, Li Y, Lasaro MO, High KA, Ertl HC. Pre-existing AAV capsid-specific CD8+ T cells are unable to eliminate AAV-transduced hepatocytes. Molecular Therapy : the Journal of the American Society of Gene Therapy. 15: 792-800. PMID 17245353 DOI: 10.1038/Sj.Mt.6300090  0.554
Show low-probability matches.