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Results: 1-7 |
Results: 7

Authors: RENDAHL KG LEFF SE OTTEN GR SPRATT SK BOHL D VANROEY M DONAHUE BA COHEN LK MANDEL RJ DANOS O SNYDER RO
Citation: Kg. Rendahl et al., REGULATION OF GENE-EXPRESSION IN-VIVO FOLLOWING TRANSDUCTION BY 2 SEPARATE RAAV VECTORS, Nature biotechnology, 16(8), 1998, pp. 757-761

Authors: MANDEL RJ RENDAHL KG SPRATT SK SNYDER RO COHEN LK LEFF SE
Citation: Rj. Mandel et al., CHARACTERIZATION OF INTRASTRIATAL RECOMBINANT ADENOASSOCIATED VIRUS-MEDIATED GENE-TRANSFER OF HUMAN TYROSINE-HYDROXYLASE AND HUMAN GTP-CYCLOHYDROLASE-I IN A RAT MODEL OF PARKINSONS-DISEASE, The Journal of neuroscience, 18(11), 1998, pp. 4271-4284

Authors: LEFF SE RENDAHL KG SPRATT SK KANG UJ MANDEL RJ
Citation: Se. Leff et al., IN-VIVO L-DOPA PRODUCTION BY GENETICALLY-MODIFIED PRIMARY RAT FIBROBLAST OR 9L GLIOSARCOMA CELL GRAFTS VIA COEXPRESSION OF GTPCYCLOHYDROLASE-I WITH TYROSINE-HYDROXYLASE, Experimental neurology, 151(2), 1998, pp. 249-264

Authors: RENDAHL KG GAUKHSHTEYN N WHEELER DA FRY TA HALL JC
Citation: Kg. Rendahl et al., DEFECTS IN COURTSHIP AND VISION CAUSED BY AMINO-ACID SUBSTITUTIONS INA PUTATIVE RNA-BINDING PROTEIN ENCODED BY THE NO-ON-TRANSIENT-A (NONA) GENE OF DROSOPHILA, The Journal of neuroscience, 16(4), 1996, pp. 1511-1522

Authors: RENDAHL KG HALL JC
Citation: Kg. Rendahl et Jc. Hall, TEMPORALLY MANIPULATED RESCUE OF VISUAL AND COURTSHIP ABNORMALITIES CAUSED BY A NONA MUTATION IN DROSOPHILA, Journal of neurogenetics, 10(4), 1996, pp. 247-256

Authors: RENDAHL KG CLEVENGER DG JARET TM NAGY D CONWAY J MANDEL RJ LEFF S
Citation: Kg. Rendahl et al., INCREASED VIABILITY OF GENETICALLY-ENGINEERED PRIMARY RAT FIBROBLASTSPREPARED FOR IMPLANTATION IN THE BRAIN, Experimental neurology, 135(2), 1995, pp. 169-169

Authors: STANEWSKY R RENDAHL KG DILL M SAUMWEBER H
Citation: R. Stanewsky et al., GENETIC AND MOLECULAR ANALYSIS OF THE X-CHROMOSOMAL REGION 14B17-14C4IN DROSOPHILA-MELANOGASTER - LOSS OF FUNCTION IN NONA, A NUCLEAR-PROTEIN COMMON TO MANY CELL-TYPES, RESULTS IN SPECIFIC PHYSIOLOGICAL AND BEHAVIORAL DEFECTS, Genetics, 135(2), 1993, pp. 419-442
Risultati: 1-7 |