Zobrazeno 1 - 10
of 15
pro vyhledávání: '"R C Eisensmith"'
Autor:
J D Roberts, C D Montgomery, I Nasonkin, A Hughes, B Fang, R C Eisensmith, J Li, X H Li, Y C Lin-Lee, Martha P. Mims
Publikováno v:
Journal of Clinical Investigation. 95:768-773
Elevations of plasma total or LDL cholesterol are major risk factors for cardiovascular disease. Efforts directed at preventing and treating cardiovascular disease have often focused on reducing the levels of these substances in the blood. The Watana
Autor:
E. R. Naughton, R. C. Eisensmith, Li Jin, Alexei A. Goltsov, Savio L. C. Woo, Ranajit Chakraborty
Publikováno v:
Human Molecular Genetics. 2:577-581
Phenylketonuria (PKU) is an autosomal recessive genetic disorder caused by phenylalanine hydroxylase (PAH) deficiency. Individuals afflicted with PKU develop irreversible mental retardation that can be largely prevented by the administration of a low
Publikováno v:
The journal of gene medicine. 3(1)
A major limitation of adenovirus-mediated gene therapy for metabolic and inherited diseases is the instability of transgene expression in vivo. This instability results, at least in part, from the inability of the vector genome to maintain the transg
Autor:
R C, Eisensmith, S L, Woo
Publikováno v:
Thrombosis and haemostasis. 78(1)
Over the past five years, significant advances have been made in the development of novel viral vector systems for the treatment of hemophilia B by somatic gene therapy. At present, both a sustained but partial or a complete but transient correction
Publikováno v:
Gene therapy. 3(9)
Transgene expression in studies of both gene function and gene therapy may be assisted considerably through the use of transcriptional regulatory elements which permit high-level, and/or tissue-specific gene expression. We have therefore evaluated th
Autor:
R C, Eisensmith, D R, Martinez, A I, Kuzmin, A A, Goltsov, A, Brown, R, Singh, I I, Elsas LJ, S L, Woo
Publikováno v:
Pediatrics. 97(4)
To determine the molecular basis of phenylketonuria (PKU) and related hyperphenylalaninemia (HPA) and to establish correlations between phenylalanine hydroxylase (PAH) genotypes and biochemical and clinical phenotypes in an ethnically diverse US popu
Autor:
B, Fang, H, Wang, G, Gordon, D A, Bellinger, M S, Read, K M, Brinkhous, S L, Woo, R C, Eisensmith
Publikováno v:
Gene therapy. 3(3)
Two recombinant adenoviruses expressing either human alpha 1-antitrypsin (hAAT) or canine factor IX (cFIX) were modified so that they also contained a temperature-sensitive mutation (ts125) in the DNA binding protein encoded within the viral E2A regi
Autor:
M F, Wilkemeyer, K L, Smith, M M, Zarei, T A, Benke, J W, Swann, K J, Angelides, R C, Eisensmith
Publikováno v:
Journal of neuroscience research. 43(2)
Genetic manipulation offers great potential for studying the molecular and cellular processes which control or regulate the complex developmental properties of neurons. Gene transfer into neurons, however, is notoriously difficult. In this study we h
Publikováno v:
Advances in experimental medicine and biology. 369
As the technology for gene therapy develops in vitro and in vivo in animal models, it is becoming clear that the three principal approaches--recombinant retroviruses, recombinant adenovirus, and direct DNA delivery--will ultimately have applications
Autor:
R C, Eisensmith, S L, Woo
Publikováno v:
Advances in genetics. 32