Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jaminder Khinder"'
Autor:
Jey M. Jeyakumar, Azadeh Kia, Lawrence C. S. Tam, Jenny McIntosh, Justyna Spiewak, Kevin Mills, Wendy Heywood, Elisa Chisari, Noemi Castaldo, Daniël Verhoef, Paniz Hosseini, Petya Kalcheva, Clement Cocita, Carlos J. Miranda, Miriam Canavese, Jaminder Khinder, Cecilia Rosales, Derralynn Hughes, Rose Sheridan, Romuald Corbau, Amit Nathwani
Publikováno v:
Gene Therapy.
Fabry disease is an X-linked lysosomal storage disorder caused by loss of alpha-galactosidase A (α-Gal A) activity and is characterized by progressive accumulation of glycosphingolipids in multiple cells and tissues. FLT190, an investigational gene
Autor:
Venette Fannin, Natalie Northcott, Jaminder Khinder, Benjamin Liou, Elisa Chisari, Amit C. Nathwani, Miriam Canavese, Jalpa Pandya, Rachel Blackwood, Azadeh Kia, Romuald Corbau, Ying Sun, Rose Sheridan, Carlos Henrique Miranda, Allison P Dane
Publikováno v:
Molecular Genetics and Metabolism. 129:S110
Autor:
Olivier D. Christophe, Andreas Schulze, Elisa Chisari, Allison P Dane, Azadeh Kia, Jalpa Pandya, Maria Portillo, Fabrizio Comper, Renee Kober, Segen Negash, Cécile V. Denis, Jonathan H. Foley, Florian Sonntag, Hattie Ollerton, Samantha Correia, Jenny McIntosh, Jaminder Khinder, Rebecca Alade, Jey Jeyakumar, Clement Cocita, Caterina Casari, Romuald Corbau, Dodev Tihomir, Erald Shehu
Publikováno v:
Blood. 134:4638-4638
Background: Several first-generation gene therapies are currently in clinical trials for Haemophilia A. These trials have to date exhibited varying results including issues with large patient to patient variation in FVIII levels and lack of durabilit