Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Stuart Tinch"'
Autor:
Anindya, Dasgupta, Stuart, Tinch, Kathleen, Szczur, Rebecca, Ernst, Nathaniel, Shryock, Courtney, Kaylor, Kendall, Lewis, Eric, Day, Timmy, Truong, William, Swaney
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2086
In clinical gene transfer applications, lentiviral vectors (LV) have rapidly become the primary means to achieve permanent and stable expression of a gene of interest or alteration of gene expression in target cells. This status can be attributed pri
Autor:
Kendall Lewis, William Swaney, Nathaniel Shryock, Stuart Tinch, Anindya Dasgupta, Rebecca Ernst, Timmy Truong, Courtney Kaylor, Kathleen Szczur, Eric Day
Publikováno v:
Methods in Molecular Biology ISBN: 9781071601457
In clinical gene transfer applications, lentiviral vectors (LV) have rapidly become the primary means to achieve permanent and stable expression of a gene of interest or alteration of gene expression in target cells. This status can be attributed pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8fdf03f034e2aa5114d04a71718a218
https://doi.org/10.1007/978-1-0716-0146-4_3
https://doi.org/10.1007/978-1-0716-0146-4_3
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1937
Lentiviral vectors have rapidly become a favorite tool for research and clinical gene transfer applications which seek to permanently introduce alterations in the genome. This status can be attributed primarily to their ability to transduce dividing
Publikováno v:
Methods in Molecular Biology ISBN: 9781493990641
Lentiviral vectors have rapidly become a favorite tool for research and clinical gene transfer applications which seek to permanently introduce alterations in the genome. This status can be attributed primarily to their ability to transduce dividing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af0eb9098c01765fc75e7fdd0eb21aa8
https://doi.org/10.1007/978-1-4939-9065-8_8
https://doi.org/10.1007/978-1-4939-9065-8_8
Autor:
Venette Inskeep, Benjamin Liou, Gregory A. Grabowski, Kenneth D.R. Setchell, Yanyan Peng, You-Hai Xu, Manoj K. Pandey, Wujuan Zhang, Nupur Dasgupta, Ying Sun, Mehdi Keddache, Stuart Tinch, Rong-hua Li
Defective lysosomal acid β-glucosidase (GCase) in Gaucher disease causes accumulation of glucosylceramide (GC) and glucosylsphingosine (GS) that distress cellular functions. To study novel pathological mechanisms in neuronopathic Gaucher disease (nG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66434a5d16e319699abb88606d646031
https://europepmc.org/articles/PMC4654057/
https://europepmc.org/articles/PMC4654057/
Autor:
Charles V. Vorhees, Madison Caballero, Thomas A. Burrow, Stuart Tinch, Lindsay M. Schroeder, Manoj K. Pandey, Christina Gross, Gregory A. Grabowski
Publikováno v:
Molecular Genetics and Metabolism. 117:S90
Autor:
Manoj Pandey, Stuart Tinch, Venette Inskeep, Wujuan Zhang, Kenneth Setchell, Jörg Köhl, Gregory Grabowski
Publikováno v:
The Journal of Immunology. 194:186.14-186.14
Gaucher disease (GD) happens due to mutations in GBA1, which causes a deficiency of acid β-glucosidase critical for degradation of glucosylceramide (GC) into glucose and ceramide. Macrophages (Mɸs) were mainly having this defect and associated with
Publikováno v:
Molecular Genetics and Metabolism. 111:S84
Publikováno v:
Molecular Genetics and Metabolism. 108:S72