Adenoviral Vectors and Gene Transfer to the Blood Vessel Wall
نویسندگان
چکیده
منابع مشابه
Neuronal birthdate-specific gene transfer with adenoviral vectors.
The multilayered structure of the cerebral cortex has been studied in detail. Early-born neurons migrate into the inner layer and late-born neurons migrate into more superficial layers, thus establishing an inside-out gradient. The progenitor cells appear to acquire layer-specific properties at the time of neuronal birth; however, the molecular mechanisms of cell-fate acquisition are still uncl...
متن کاملImpact of Blood Vessel Wall Flexibility on the Temperature and Concentration Dispersion
The analysis of solute and thermal dispersion in pulsatile flow through the stenotic tapered blood vessel is presented. The present problem is an extension of the work done by Ramana et al. who considered the time-invariant arterial wall. In the present model, the flexible nature of the arterial wall through the obstruction (called stenosis) is considered and it is achieved with the he...
متن کاملAdenoviral Vectors for Hemophilia Gene Therapy
Hemophilia is an inherited blood clotting disorder resulting from deficiency of blood coagulation factors. Current standard of care for hemophilia patients is frequent intravenous infusions of the missing coagulation factor. Gene therapy for hemophilia involves the introduction of a normal copy of the deficient coagulation factor gene thereby potentially offering a definitive cure for the bleed...
متن کاملStudies on in vivo gene transfer in pituitary tumors using herpes-derived and adenoviral vectors.
Suicide gene therapy has met limited success for the treatment of rat pituitary tumors. In order to determine the cause of primary pituitary tumor resistance to suicide gene therapy, we studied the transgene expression of an adenoviral (Ad.RSV.beta gal.nls) and a herpes simplex virus-derived (tsK/beta-gal) vector, both harboring the beta-galactosidase reporter gene in rat prolactinomas. Rats ca...
متن کاملOral tolerization to adenoviral antigens permits long-term gene expression using recombinant adenoviral vectors.
Recombinant adenoviruses (Ads) efficiently transfer foreign genes into hepatocytes in vivo, but the duration of transgene expression is limited by the host immune response which precludes gene expression upon readministration of the virus. To test if this immune response can be abrogated by oral tolerization, we instilled protein extracts of a recombinant adenovirus type-5 via gastroduodenostom...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Arteriosclerosis, Thrombosis, and Vascular Biology
سال: 2000
ISSN: 1079-5642,1524-4636
DOI: 10.1161/01.atv.20.6.1414