Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Christine L. Halbert"'
Publikováno v:
Journal of Lipid Research, Vol 40, Iss 10, Pp 1769-1781 (1999)
High density lipoprotein (HDL) phospholipids and apolipoproteins remove cellular lipids by two distinct mechanisms, but their relative contribution to reverse cholesterol transport is unknown. Whereas phospholipid-mediated cholesterol efflux from cul
Externí odkaz:
https://doaj.org/article/6c86e6b0ee154698be35a6e0047d47bb
JSRV, a simple beta-retrovirus, is the etiologic agent of ovine pulmonary adenocarcinoma, a form of non–small cell lung cancer in sheep and goats. It has been shown that the envelope protein alone is sufficient to induce tumorigenesis in the lungs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bdc2ab9ef0b5883fdf18fdb81765af8
https://doi.org/10.1158/1541-7786.c.6541450
https://doi.org/10.1158/1541-7786.c.6541450
Autor:
Niclas E. Bengtsson, Julie M. Crudele, Jordan M. Klaiman, Christine L. Halbert, Stephen D. Hauschka, Jeffrey S. Chamberlain
Publikováno v:
Mol Ther
Gene editing has shown promise for correcting or bypassing dystrophin mutations in Duchenne muscular dystrophy (DMD). However, preclinical studies have focused on young animals with limited muscle fibrosis and wasting, thereby favoring muscle transdu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f33fd42d19d0dd0ec239a07eb87d1d4
https://europepmc.org/articles/PMC9171147/
https://europepmc.org/articles/PMC9171147/
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1687
Vectors derived from adeno-associated viruses (AAV) have been generated using numerous naturally occurring and synthetic serotypes of the virus. Such vectors have proven to be extremely useful for a variety of gene transfer studies, both in vitro and
Publikováno v:
Methods in Molecular Biology ISBN: 9781493973736
Vectors derived from adeno-associated viruses (AAV) have been generated using numerous naturally occurring and synthetic serotypes of the virus. Such vectors have proven to be extremely useful for a variety of gene transfer studies, both in vitro and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01d27e824b6908a89d8f76276bb11c2a
https://doi.org/10.1007/978-1-4939-7374-3_18
https://doi.org/10.1007/978-1-4939-7374-3_18
Autor:
Zejing Wang, Tiffany Butts, Rainer Storb, Stephen J. Tapscott, Dong-Hoon Lee, Christine L. Halbert, A D Miller
Publikováno v:
Gene therapy
Animal and human gene therapy studies utilizing AAV vectors have shown that immune responses to AAV capsid proteins can severely limit transgene expression. The main source of capsid antigen is that associated with the AAV vectors, which can be reduc
Autor:
Eric E. Finn, Rainer Storb, Stephen J. Tapscott, James M. Allen, Glen B. Banks, A. Dusty Miller, Jeffrey S. Chamberlain, Tiffany Butts, Christine L. Halbert, Zejing Wang
Publikováno v:
Molecular Therapy. 20:1501-1507
Duchenne muscular dystrophy (DMD) is a fatal, X-linked muscle disease caused by mutations in the dystrophin gene. Adeno-associated viral (AAV) vector-mediated gene replacement strategies hold promise as a treatment. Studies in animal models and human
Publikováno v:
Molecular Cancer Research. 10:86-95
JSRV, a simple beta-retrovirus, is the etiologic agent of ovine pulmonary adenocarcinoma, a form of non–small cell lung cancer in sheep and goats. It has been shown that the envelope protein alone is sufficient to induce tumorigenesis in the lungs