Lanfranco Leo
Affiliations: | 2016-2021 | Ophthalmology | University of Pennsylvania, Philadelphia, PA, United States |
Google:
"Lanfranco Leo"
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Uyhazi KE, Aravand P, Bell BA, et al. (2020) Treatment Potential for LCA5-Associated Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 61: 30 |
| Duong TT, Lim J, Vasireddy V, et al. (2019) Comparative AAV-eGFP Transgene Expression Using Vector Serotypes 1-9, 7m8, and 8b in Human Pluripotent Stem Cells, RPEs, and Human and Rat Cortical Neurons. Stem Cells International. 2019: 7281912 |
| Qiang L, Piermarini E, Muralidharan H, et al. (2018) Hereditary Spastic Paraplegia: gain-of-function mechanisms revealed by new transgenic mouse. Human Molecular Genetics |
| Song JY, Aravand P, Nikonov S, et al. (2018) Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Duong TT, Vasireddy V, Ramachandran P, et al. (2018) Use of induced pluripotent stem cell models to probe the pathogenesis of Choroideremia and to develop a potential treatment. Stem Cell Research. 27: 140-150 |
| Mills JA, Herrera PS, Kaur M, et al. (2018) NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states. Scientific Reports. 8: 1056 |
| Leo L, Weissmann C, Burns M, et al. (2017) Mutant spastin proteins promote deficits in axonal transport through an isoform-specific mechanism involving casein kinase 2 activation. Human Molecular Genetics |