Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Felicia Migone"'
Autor:
Cameron K. Tebbi, Aruna Badiga, Eva Sahakian, John J. Powers, Alex N. Achille, Saumil Patel, Felicia Migone
Publikováno v:
Cancer Treatment and Research Communications, Vol 26, Iss , Pp 100279- (2021)
The etiology of acute lymphoblastic leukemia (ALL) remains unknown. A recent “two-hit” model for the occurrence of precursor B cell acute lymphoblastic leukemia propose that this disease arises through a two-step process, including predisposing g
Externí odkaz:
https://doaj.org/article/adf5aca5c1084e31971177c5e17d8e94
Autor:
Felicia Migone, Eva Sahakian, John Powers, Aruna Badiga, Saumil Patel, Alex Achille, Cameron K. Tebbi, Anshul I Arora, Michael V Jaglal, Sajitha Nair
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:350-358
Acute lymphoblastic leukemia (ALL) is the most common cancer in children and is also seen in adults. Currently, no plasma-based test for the detection of ALL is available. We have cultured the home of a patient with ALL and isolated a mycovirus conta
Autor:
Saumil Patel, Eva Sahakian, Felicia Migone, Cameron K. Tebbi, Aruna Badiga, Alex Achille, John Powers
Publikováno v:
Cancer Treatment and Research Communications, Vol 26, Iss, Pp 100279-(2021)
The etiology of acute lymphoblastic leukemia (ALL) remains unknown. A recent "two-hit" model for the occurrence of precursor B cell acute lymphoblastic leukemia propose that this disease arises through a two-step process, including predisposing genet
Autor:
Felicia Migone, Andrea Amalfitano, Delila Serra, E. Y. Ding, Fang Xu, Yuan-Tsong Chen, Ayn Schneider
Publikováno v:
The Journal of Gene Medicine. 7:171-178
Background Glycogen storage disease II (GSD-II) is an autosomal recessive lysosomal storage disease, due to acid-alpha-glucosidase (GAA) deficiency. The disease is characterized by massive glycogen accumulation in the cardiac and skeletal muscles. Th
Autor:
Felicia Migone, Yuan-Tsong Chen, Delila Serra, E. Y. Ding, Andrea Amalfitano, D. Pressley, M. Mizutani, T. Kikuchi, T. Lawson, Alison McVie-Wylie
Publikováno v:
The Journal of Gene Medicine. 5:399-406
Background Previously, in murine models of acid maltase deficiency (AMD), we demonstrated that intravenous administration of an improved adenovirus (Ad) vector encoding human acid alpha glucosidase (hGAA) resulted in liver transduction, followed by h
Autor:
Delila Serra, E. Y. Ding, Felicia Migone, Fang Xu, Huimin Hu, Bradley L. Hodges, Yuan-Tsong Chen, Andrea Amalfitano
Publikováno v:
Molecular Therapy. 5:436-446
Lysosomal storage diseases are an intriguing target for gene therapy approaches, as transduction of a "depot" organ with a transgene encoding a lysosomal enzyme can be followed by secretion, systemic distribution, downstream uptake, and lysosomal tar
Autor:
E. Y. Ding, Shaoxi Liao, J Dai, Felicia Migone, Andrea Amalfitano, Yuan-Tsong Chen, Delila Serra, Fang Xu, Ayn Schneider
Publikováno v:
Gene therapy. 11(21)
Glycogen storage disease type II (GSD-II) is a lysosomal storage disorder in which the lack of human acid-alpha glucosidase (hGAA) activity results in massive accumulations of glycogen in cardiac and skeletal muscle fibers. Affected individuals die o
Publikováno v:
Journal of Cellular Biochemistry; Jun2006, Vol. 98 Issue 3, p504-518, 15p