☰

Brendan T. Harmon, Ph.D. - Publications

Affiliations: 
Pharmaceutical Science Northeastern University, Boston, MA, United States 
Area:
Parkinson\\\'s disease, gene therapy, intranasal delivery
Tree Info Grants Similar researchers PubMed Report error

3/19 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 Aly AE, Harmon B, Padegimas L, Sesenoglu-Laird O, Cooper MJ, Yurek DM, Waszczak BL. Intranasal delivery of hGDNF plasmid DNA nanoparticles results in long-term and widespread transfection of perivascular cells in rat brain. Nanomedicine : Nanotechnology, Biology, and Medicine. PMID 30472323 DOI: 10.1016/J.Nano.2018.11.006  0.604
2018 Aly AE, Harmon BT, Padegimas L, Sesenoglu-Laird O, Cooper MJ, Waszczak BL. Intranasal Delivery of pGDNF DNA Nanoparticles Provides Neuroprotection in the Rat 6-Hydroxydopamine Model of Parkinson's Disease. Molecular Neurobiology. PMID 29779176 DOI: 10.1007/S12035-018-1109-6  0.57
2014 Harmon BT, Aly AE, Padegimas L, Sesenoglu-Laird O, Cooper MJ, Waszczak BL. Intranasal administration of plasmid DNA nanoparticles yields successful transfection and expression of a reporter protein in rat brain. Gene Therapy. 21: 514-21. PMID 24670994 DOI: 10.1038/Gt.2014.28  0.597
Low-probability matches (unlikely to be authored by this person)
2014 Saratsis AM, Kambhampati M, Snyder K, Yadavilli S, Devaney JM, Harmon B, Hall J, Raabe EH, An P, Weingart M, Rood BR, Magge SN, MacDonald TJ, Packer RJ, Nazarian J. Comparative multidimensional molecular analyses of pediatric diffuse intrinsic pontine glioma reveals distinct molecular subtypes. Acta Neuropathologica. 127: 881-95. PMID 24297113 DOI: 10.1007/S00401-013-1218-2  0.289
2014 Wing MR, Devaney JM, Joffe MM, Xie D, Feldman HI, Dominic EA, Guzman NJ, Ramezani A, Susztak K, Herman JG, Cope L, Harmon B, Kwabi-Addo B, Gordish-Dressman H, Go AS, et al. DNA methylation profile associated with rapid decline in kidney function: findings from the CRIC study. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 29: 864-72. PMID 24516231 DOI: 10.1093/Ndt/Gft537  0.165
2009 Kesari A, Neel R, Wagoner L, Harmon B, Spurney C, Hoffman EP. Somatic mosaicism for Duchenne dystrophy: evidence for genetic normalization mitigating muscle symptoms. American Journal of Medical Genetics. Part A. 149: 1499-503. PMID 19530190 DOI: 10.1002/ajmg.a.32891  0.164
2010 Harmon BT, Devaney SA, Gordish-Dressman H, Reeves EK, Zhao P, Devaney JM, Hoffman EP. Functional characterization of a haplotype in the AKT1 gene associated with glucose homeostasis and metabolic syndrome. Human Genetics. 128: 635-45. PMID 20872231 DOI: 10.1007/S00439-010-0891-7  0.129
2009 Prokunina-Olsson L, Welch C, Hansson O, Adhikari N, Scott LJ, Usher N, Tong M, Sprau A, Swift A, Bonnycastle LL, Erdos MR, He Z, Saxena R, Harmon B, Kotova O, et al. Tissue-specific alternative splicing of TCF7L2. Human Molecular Genetics. 18: 3795-804. PMID 19602480 DOI: 10.1093/Hmg/Ddp321  0.118
2009 Devaney JM, Tosi LL, Fritz DT, Gordish-Dressman HA, Jiang S, Orkunoglu-Suer FE, Gordon AH, Harmon BT, Thompson PD, Clarkson PM, Angelopoulos TJ, Gordon PM, Moyna NM, Pescatello LS, Visich PS, et al. Differences in fat and muscle mass associated with a functional human polymorphism in a post-transcriptional BMP2 gene regulatory element. Journal of Cellular Biochemistry. 107: 1073-82. PMID 19492344 DOI: 10.1002/Jcb.22209  0.105
2015 Dillingham BC, Knoblach SM, Many GM, Harmon BT, Mullen AM, Heier CR, Bello L, McCall JM, Hoffman EP, Connor EM, Nagaraju K, Reeves EK, Damsker JM. VBP15, a novel anti-inflammatory, is effective at reducing the severity of murine experimental autoimmune encephalomyelitis. Cellular and Molecular Neurobiology. 35: 377-87. PMID 25392236 DOI: 10.1007/S10571-014-0133-Y  0.102
2015 Benton MC, Johnstone A, Eccles D, Harmon B, Hayes MT, Lea RA, Griffiths L, Hoffman EP, Stubbs RS, Macartney-Coxson D. An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss. Genome Biology. 16: 8. PMID 25651499 DOI: 10.1186/s13059-014-0569-x  0.064
2010 Harmon BT, Orkunoglu-Suer EF, Adham K, Larkin JS, Gordish-Dressman H, Clarkson PM, Thompson PD, Angelopoulos TJ, Gordon PM, Moyna NM, Pescatello LS, Visich PS, Zoeller RF, Hubal MJ, Tosi LL, et al. CCL2 and CCR2 variants are associated with skeletal muscle strength and change in strength with resistance training. Journal of Applied Physiology (Bethesda, Md. : 1985). 109: 1779-85. PMID 20947712 DOI: 10.1152/Japplphysiol.00633.2010  0.063
2005 Clarkson PM, Hoffman EP, Zambraski E, Gordish-Dressman H, Kearns A, Hubal M, Harmon B, Devaney JM. ACTN3 and MLCK genotype associations with exertional muscle damage Journal of Applied Physiology. 99: 564-569. PMID 15817725 DOI: 10.1152/Japplphysiol.00130.2005  0.056
2008 Orkunoglu-Suer FE, Gordish-Dressman H, Clarkson PM, Thompson PD, Angelopoulos TJ, Gordon PM, Moyna NM, Pescatello LS, Visich PS, Zoeller RF, Harmon B, Seip RL, Hoffman EP, Devaney JM. INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men Bmc Medical Genetics. 9. PMID 19105843 DOI: 10.1186/1471-2350-9-117  0.044
2015 Bigot A, Duddy WJ, Ouandaogo ZG, Negroni E, Mariot V, Ghimbovschi S, Harmon B, Wielgosik A, Loiseau C, Devaney J, Dumonceaux J, Butler-Browne G, Mouly V, Duguez S. Age-Associated Methylation Suppresses SPRY1, Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle Cell Reports. 13: 1172-1182. DOI: 10.1016/j.celrep.2015.09.067  0.043
2007 Uthurralt J, Gordish-Dressman H, Bradbury M, Tesi-Rocha C, Devaney J, Harmon B, Reeves EK, Brandoli C, Hansen BC, Seip RL, Thompson PD, Price TB, Angelopoulos TJ, Clarkson PM, Moyna NM, et al. PPARalpha L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males. Bmc Medical Genetics. 8: 55. PMID 17705849 DOI: 10.1186/1471-2350-8-55  0.036
2011 Devaney JM, Gordish-Dressman H, Harmon BT, Bradbury MK, Devaney SA, Harris TB, Thompson PD, Clarkson PM, Price TB, Angelopoulos TJ, Gordon PM, Moyna NM, Pesca LS, VIsich PS, Zoeller RF, et al. AKT1 polymorphisms are associated with risk for metabolic syndrome. Human Genetics. 129: 129-39. PMID 21061022 DOI: 10.1007/S00439-010-0910-8  0.026
2011 Devaney JM, Thompson PD, Visich PS, Saltarelli WA, Gordon PM, Orkunoglu-Suer EF, Gordish-Dressman H, Harmon BT, Bradbury MK, Panchapakesan K, Khianey R, Hubal MJ, Clarkson PM, Pescatello LS, Zoeller RF, et al. The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations. Pediatric Research. 69: 538-43. PMID 21297524 DOI: 10.1203/Pdr.0B013E3182139227  0.02
2011 Orkunoglu-Suer FE, Harmon BT, Gordish-Dressman H, Clarkson PM, Thompson PD, Angelopoulos TJ, Gordon PM, Hubal MJ, Moyna NM, Pescatello LS, Visich PS, Zoeller RF, Hoffman EP, Devaney JM. MC4R variant is associated with BMI but not response to resistance training in young females. Obesity (Silver Spring, Md.). 19: 662-6. PMID 20725061 DOI: 10.1038/Oby.2010.180  0.01
Hide low-probability matches.