Brian C. Beard, Ph.D.

Affiliations: 
2003 Washington State University, Pullman, WA, United States 
Area:
Biochemistry, Molecular Biology
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"Brian Beard"
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Parents

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Michael J. Smerdon grad student 2003 WSU
 (Base excision repair of dynamic chromatin substrates.)
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Publications

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Navarro S, Quintana-Bustamante O, Sanchez-Dominguez R, et al. (2021) Preclinical studies of efficacy thresholds and tolerability of a clinically ready lentiviral vector for pyruvate kinase deficiency treatment. Molecular Therapy. Methods & Clinical Development. 22: 350-359
Czechowicz A, Rio P, Bueren JE, et al. (2020) Changing the Natural History of Fanconi Anemia Complementation Group-À with Gene Therapy: Early Results of U.S. Phase I Study of Lentiviral-Mediated Ex-Vivo FANCA Gene Insertion in Human Stem and Progenitor Cells Biology of Blood and Marrow Transplantation. 26
Czechowicz A, Roncarolo MG, Beard BC, et al. (2019) Changing the Natural History of Fanconi Anemia Complementation Group-A with Gene Therapy: Early Results of U.S. Phase I Study of Lentiviral-Mediated Ex-VivoFANCA Gene Insertion in Human Stem and Progenitor Cells Blood. 134: 3350-3350
Almarza E, Mesa-Núñez C, Damián C, et al. (2019) Gene Therapy for Lad-I Immunodeficiency: Preclinical Evaluation of HSC Transduction Under Optimized GMP-Conditions Blood. 134: 5751-5751
Haworth KG, Ironside C, Ramirez MA, et al. (2018) Minimal conditioning in Fanconi anemia promotes multi-lineage marrow engraftment at ten-fold lower cell doses. The Journal of Gene Medicine. e3050
Ruan H, Qiu S, Beard BC, et al. (2016) Creation of zebularine-resistant human cytidine deaminase mutants to enhance the chemoprotection of hematopoietic stem cells. Protein Engineering, Design & Selection : Peds
Burtner CR, Chandrasekaran D, Santos EB, et al. (2015) (211)Astatine-Conjugated Monoclonal CD45 Antibody-Based Nonmyeloablative Conditioning for Stem Cell Gene Therapy. Human Gene Therapy. 26: 399-406
Kiem HP, Arumugam PI, Burtner CR, et al. (2014) Pigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies. Molecular Therapy. Methods & Clinical Development. 1: 14055
Adair JE, Johnston SK, Mrugala MM, et al. (2014) Gene therapy enhances chemotherapy tolerance and efficacy in glioblastoma patients. The Journal of Clinical Investigation. 124: 4082-92
Beard BC, Adair JE, Trobridge GD, et al. (2014) High-throughput genomic mapping of vector integration sites in gene therapy studies. Methods in Molecular Biology (Clifton, N.J.). 1185: 321-44
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