Search Results - "Baughan, Travis D."

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  1. 1

    A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia by Guyenet, Stephan J, Furrer, Stephanie A, Damian, Vincent M, Baughan, Travis D, La Spada, Albert R, Garden, Gwenn A

    Published in Journal of visualized experiments (21-05-2010)
    “…We describe a protocol for the rapid and sensitive quantification of disease severity in mouse models of cerebella ataxia. It is derived from previously…”
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    Journal Article
  2. 2

    Development of a single vector system that enhances trans-splicing of SMN2 transcripts by Coady, Tristan H, Baughan, Travis D, Shababi, Monir, Passini, Marco A, Lorson, Christian L

    Published in PloS one (22-10-2008)
    “…RNA modalities are developing as a powerful means to re-direct pathogenic pre-mRNA splicing events. Improving the efficiency of these molecules in vivo is…”
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  3. 3

    Delivery of bifunctional RNAs that target an intronic repressor and increase SMN levels in an animal model of spinal muscular atrophy by Baughan, Travis D., Dickson, Alexa, Osman, Erkan Y., Lorson, Christian L.

    Published in Human molecular genetics (01-05-2009)
    “…Spinal muscular atrophy (SMA) is a motor neuron disease caused by the loss of survival motor neuron-1 (SMN1). A nearly identical copy gene, SMN2, is present in…”
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    Journal Article
  4. 4

    Functional Epitope on Human Neutrophil Flavocytochrome b558 by Burritt, James B, Foubert, Thomas R, Baniulis, Danas, Lord, Connie I, Taylor, Ross M, Mills, John S, Baughan, Travis D, Roos, Dirk, Parkos, Charles A, Jesaitis, Algirdas J

    Published in The Journal of immunology (1950) (15-06-2003)
    “…mAb NL7 was raised against purified flavocytochrome b(558), important in host defense and inflammation. NL7 recognized the gp91(phox) flavocytochrome b(558)…”
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  5. 5

    415. Stimulating Full-Length SMN2 Expression by Delivering Bi-Functional RNAs Via a Viral Vector by Baughan, Travis D., Shababi, Monir, Tullis, Gregory E., Lorson, Christian L.

    Published in Molecular therapy (01-05-2006)
    “…Spinal Muscular Atrophy is an autosomal recessive neuromuscular disorder that is the leading genetic cause of infant mortality. SMA is caused by the homozygous…”
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  6. 6
  7. 7

    Functional Epitope on Human Neutrophil Flavocytochrome b 558 by Burritt, James B., Foubert, Thomas R., Baniulis, Danas, Lord, Connie I., Taylor, Ross M., Mills, John S., Baughan, Travis D., Roos, Dirk, Parkos, Charles A., Jesaitis, Algirdas J.

    Published in The Journal of immunology (1950) (15-06-2003)
    “…mAb NL7 was raised against purified flavocytochrome b558, important in host defense and inflammation. NL7 recognized the gp91phox flavocytochrome b558 subunit…”
    Get full text
    Journal Article