Search Results - "Klump, W M"

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  1. 1

    A sensitive, real-time, RNA-specific PCR method for the detection of recombinant AAV-CFTR vector expression by GERARD, C. J, DELL'ARINGA, J, HALE, K. A, KLUMP, W. M

    Published in Gene therapy (01-09-2003)
    “…Following adeno-associated virus (AAV)-mediated transduction, cellular RNA preparations can be contaminated with AAV single-stranded DNA. The single-stranded…”
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  2. 2

    Complete nucleotide sequence of infectious Coxsackievirus B3 cDNA: two initial 5' uridine residues are regained during plus-strand RNA synthesis by KLUMP, W. M, BERGMANN, I, MUÊLLER, B. C, AMEIS, D, KANDOLF, R

    Published in Journal of Virology (01-04-1990)
    “…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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  3. 3

    Promoter elements and transcriptional regulation of the acetylcholinesterase gene by Ekström, T J, Klump, W M, Getman, D, Karin, M, Taylor, P

    Published in DNA and cell biology (01-01-1993)
    “…The 5' region of the acetylcholinesterase gene from the electric ray Torpedo californica has been cloned and its cap site identified. The 5' untranslated…”
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  4. 4

    Evaluation of PCR and ELISA assays for screening clinical trial subjects for replication-competent retrovirus by Martineau, D, Klump, W M, McCormack, J E, DePolo, N J, Kamantigue, E, Petrowski, M, Hanlon, J, Jolly, D J, Mento, S J, Sajjadi, N

    Published in Human gene therapy (01-07-1997)
    “…Gene delivery via murine-based recombinant retroviral vectors is currently widely used in gene therapy clinical trials. The vectors are engineered to be…”
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  5. 5

    Expression of coxsackievirus B3 capsid proteins in Escherichia coli and generation of virus-specific antisera by Werner, S, Klump, W M, Schönke, H, Hofschneider, P H, Kandolf, R

    Published in DNA (New York, N.Y.) (01-06-1988)
    “…Subgenomic fragments of cloned infectious coxsackievirus B3 (CVB3) cDNA up to the size of the complete coding sequence of the viral polyprotein were inserted…”
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