Zobrazeno 1 - 10
of 54
pro vyhledávání: '"J A Barranger"'
Autor:
P G Pentchev, J A Barranger
Publikováno v:
Journal of Lipid Research, Vol 19, Iss 4, Pp 401-409 (1978)
Externí odkaz:
https://doaj.org/article/d9acb335febb416a90f01c8d6bbae594
Publikováno v:
Methods in molecular medicine. 7
Hematopoietic stem cells (HSC) provide for contmuous replenishment of the entire immune and hematopoietic systems, and also replenish themselves in a process termed self-renewal (1).The HSCs can be enriched from hematopoietic tissues using MAbs that
Publikováno v:
Genome Research. 4:1-5
A new test for the diagnosis of Gaucher disease is described. The test is designed to screen large numbers of clinical specimens from high-risk populations. It consists of duplex PCR amplification of genomic DNA followed by hybridization to alkaline
Autor:
S A, Rosenberg, R M, Blaese, M K, Brenner, A B, Deisseroth, F D, Ledley, M T, Lotze, J M, Wilson, G J, Nabel, K, Cornetta, J S, Economou, S M, Freeman, S R, Riddell, M, Brenner, E, Oldfield, B, Gansbacher, C, Dunbar, R E, Walker, F G, Schuening, J A, Roth, R G, Crystal, M J, Welsh, K, Culver, H E, Heslop, J, Simons, R W, Wilmott, R C, Boucher, H F, Siegler, J A, Barranger, S, Karlsson, D, Kohn, J E, Galpin, C, Raffel, C, Hesdorffer, J, Ilan, P, Cassileth, J, O'Shaughnessy, L E, Kun, T K, Das, F, Wong-Staal, R E, Sobol, R, Haubrich, M, Sznol, J, Rubin, E J, Sorcher, J, Rosenblatt, R, Walker, K, Brigham, N, Vogelzang, E, Hersh, S L, Eck
Publikováno v:
Human gene therapy. 11(6)
Publikováno v:
Neurochemical research. 24(4)
The work summarized in this paper used animal and cell culture models systems to develop gene therapy approaches for the lysosomal storage disorders. The results have provided the scientific basis for a clinical trial of gene transfer to hematopoieti
Autor:
J A, Barranger, E O, Rice, J, Dunigan, C, Sansieri, N, Takiyama, M, Beeler, J, Lancia, S, Lucot, S, Scheirer-Fochler, T, Mohney, W, Swaney, A, Bahnson, E, Ball
Publikováno v:
Bailliere's clinical haematology. 10(4)
Transfer of the gene coding for glucocerebrosidase (GC) via a retroviral vector (MFG-GC) to haematopoietic progenitors results in engraftment and life-long expression of the human protein at high levels in transplanted mice. Studies of human CD34 cel
Autor:
Robert A. Fisher, J. A. Barranger, Liubomir A. Pisarov, Kenneth Dorko, Martin Charron, Jorge Reyes, Stephen C. Strom, Richard B. Towbin, Wendy S. Rubinstein, Melissa T. Thompson, L. Mieles
Publikováno v:
Transplantation proceedings. 29(4)
Autor:
C H, Evans, P D, Robbins, S C, Ghivizzani, J H, Herndon, R, Kang, A B, Bahnson, J A, Barranger, E M, Elders, S, Gay, M M, Tomaino, M C, Wasko, S C, Watkins, T L, Whiteside, J C, Glorioso, M T, Lotze, T M, Wright
Publikováno v:
Human gene therapy. 7(10)
Autor:
J A, Barranger
Publikováno v:
Gene therapy. 3(5)
Autor:
R, Learish, T, Ohashi, P A, Robbins, A, Bahnson, S S, Boggs, K, Patrene, B E, Schwartz, V, Gieselmann, J A, Barranger
Publikováno v:
Gene therapy. 3(4)
Transduction of mouse hematopoietic stem cells and their progeny was studied using a recombinant retroviral vector (MFG-ASA) which incorporates the human arylsulfatase A gene (ASA; EC 3.1.6.8). Successful transduction was demonstrated in spleen colon