Elizabeth P. Blankenhorn
Affiliations: | Microbiology and Immunology | Drexel University College of Medicine, Philadelphia, PA, United States |
Area:
Molecular Biology, GeneticsGoogle:
"Elizabeth Blankenhorn"Children
Sign in to add trainee| Cheryl DeScipio | grad student | 2003 | Drexel Medical School |
| Danielle T. Loughlin | grad student | 2010 | Drexel Medical School |
| Angela Richardson | grad student | 2011 | Drexel Medical School |
| Kristen B. Long | grad student | 2012 | Drexel Medical School |
| Ryan A. Eberwine | grad student | 2013 | Drexel Medical School |
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Publications
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| Mordes JP, Cort L, Liu Z, et al. (2021) T Cell Receptor Genotype and Determine Susceptibility to Rat Autoimmune Diabetes. Genes. 12 |
| Bogdani M, Faxius L, Fex M, et al. (2021) The Vbeta13 T Cell Receptor Monoclonal Antibody Reduces Hyaluronan and CD68+, CD3+, and CD8+ Cell Infiltrations to Delay Diabetes in Congenic BB DR Rats. Frontiers in Endocrinology. 12: 629242 |
| Tyler AL, Raza A, Krementsov DN, et al. (2019) Network-Based Functional Prediction Augments Genetic Association To Predict Candidate Genes for Histamine Hypersensitivity in Mice. G3 (Bethesda, Md.) |
| Aydemir Ö, Noble JA, Bailey J, et al. (2019) Genetic Variation Within the Gene Modulates Susceptibility to Type 1 Diabetes in HLA-DR3 Homozygotes. Diabetes |
| Bearoff F, Del Rio R, Case LK, et al. (2016) Natural genetic variation profoundly regulates gene expression in immune cells and dictates susceptibility to CNS autoimmunity. Genes and Immunity |
| Sargent JL, Li Z, Aliprantis AO, et al. (2016) Interspecies comparative genomics identifies optimal mouse models of systemic sclerosis. Arthritis & Rheumatology (Hoboken, N.J.) |
| Case LK, Wall EH, Osmanski EE, et al. (2015) Copy number variation in Y chromosome multicopy genes is linked to a paternal parent-of-origin effect on CNS autoimmune disease in female offspring. Genome Biology. 16: 28 |
| Heiman-Patterson TD, Blankenhorn EP, Sher RB, et al. (2015) Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease. Plos One. 10: e0117848 |
| Bearoff F, Case LK, Krementsov DN, et al. (2015) Identification of genetic determinants of the sexual dimorphism in CNS autoimmunity. Plos One. 10: e0117993 |
| Long KB, Li Z, Burgwin CM, et al. (2015) The Tsk2/+ mouse fibrotic phenotype is due to a gain-of-function mutation in the PIIINP segment of the Col3a1 gene. The Journal of Investigative Dermatology. 135: 718-27 |