Search Results - Feener, Chris A.

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  1. 1
    LGMD2I in a North American population

    LGMD2I in a North American population by Kang, Peter B, Feener, Chris A, Estrella, Elicia, Thorne, Marielle, White, Alexander J, Darras, Basil T, Amato, Anthony A, Kunkel, Louis M

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  2. 2
    A Mutation in the Alpha 3 Chain of type IX Collagen Causes Autosomal Dominant Multiple Epiphyseal Dysplasia with Mild Myopathy

    A Mutation in the Alpha 3 Chain of type IX Collagen Causes Autosomal Dominant Multiple Epiphyseal Dysplasia with Mild Myopathy by Bonnemann, Carsten G., Cox, Gerald F., Shapiro, Frederic, Wu, Jiann-Jiu, Feener, Chris A., Thompson, Teryl G., Anthony, Douglas C., Eyre, David R., Darras, Basil T., Kunkel, Louis M.

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  3. 3
    Cloning of Human Basic A1, a Distinct 59-kDa Dystrophin-Associated Protein Encoded on Chromosome 8q23-24

    Cloning of Human Basic A1, a Distinct 59-kDa Dystrophin-Associated Protein Encoded on Chromosome 8q23-24 by Ahn, Andrew H., Yoshida, Mikiharu, Anderson, MaryDilys S., Feener, Chris A., Selig, Sara, Hagiwara, Yasuko, Ozawa, Eijiro, Kunkel, Louis M.

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  4. 4
    The genomic organization of human dystrobrevin

    The genomic organization of human dystrobrevin by Sadoulet-Puccio, H M, Feener, C A, Schaid, D J, Thibodeau, S N, Michels, V V, Kunkel, L M

    Published in Neurogenetics
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  5. 5
    Sebetralstat: A Rapidly Acting Oral Plasma Kallikrein Inhibitor for the On-Demand Treatment of Hereditary Angioedema

    Sebetralstat: A Rapidly Acting Oral Plasma Kallikrein Inhibitor for the On-Demand Treatment of Hereditary Angioedema by Feener, Edward P., Davie, Rebecca L., Murugesan, Nivetha, Pethen, Stephen J., Hampton, Sally L., Smith, Michael D., Audhya, Paul K., Yea, Chris M.

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  6. 6
    Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus

    Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus by Feener, Chris Anne, Koenig, Michel, Kunkel, Louis M

    Published in Nature (London)
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  7. 7
    Conservation of the Duchenne Muscular Dystrophy Gene in Mice and Humans

    Conservation of the Duchenne Muscular Dystrophy Gene in Mice and Humans by Hoffman, Eric P., Monaco, Anthony P., Feener, Chris C., Kunkel, Louis M.

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  8. 8
    Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

    Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene by Monaco, Anthony P, Neve, Rachael L, Colletti-Feener, Chris, Bertelson, Corlee J, Kurnit, David M, Kunkel, Louis M

    Published in Nature (London)
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  9. 9
    Dystrophin is Transcribed in Brain from a Distant Upstream Promoter

    Dystrophin is Transcribed in Brain from a Distant Upstream Promoter by Boyce, Frederick M., Beggs, Alan H., Feener, Chris, Kunkel, Louis M.

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  10. 10
    Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

    Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy by MONACO, A. P, BERTELSON, C. J, COLLETTI-FEENER, C, KUNKEL, L. M

    Published in Human genetics
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