Hasil Pencarian - Birgit H. Funke

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  1. 1
    Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant

    Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant oleh Quinn S. Wells, Natalie L. Ausborn, Birgit H. Funke, Jean P. Pfotenhauer, Joseph L. Fredi, Samantha Baxter, Thomas G. DiSalvo, Charles C. Hong

    Diterbitkan 2011-08-01
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  2. 2
    The CHC22 clathrin-GLUT4 transport pathway contributes to skeletal muscle regeneration.

    The CHC22 clathrin-GLUT4 transport pathway contributes to skeletal muscle regeneration. oleh Sachiko Hoshino, Kazuho Sakamoto, Stéphane Vassilopoulos, Stéphane M Camus, Christine A Griffin, Christopher Esk, Jorge A Torres, Norio Ohkoshi, Akiko Ishii, Akira Tamaoka, Birgit H Funke, Raju Kucherlapati, Marta Margeta, Thomas A Rando, Frances M Brodsky

    Diterbitkan 2013-01-01
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  3. 3
    The Case for Laboratory Developed Procedures

    The Case for Laboratory Developed Procedures oleh Karen L. Kaul MD, PhD, Linda M. Sabatini PhD, Gregory J. Tsongalis PhD, Angela M. Caliendo MD, PhD, Randall J. Olsen MD, PhD, Edward R. Ashwood MD, Sherri Bale PhD, Robert Benirschke PhD, Dean Carlow MD, PhD, Birgit H. Funke PhD, Wayne W. Grody MD, PhD, Randall T. Hayden MD, Madhuri Hegde PhD, Elaine Lyon PhD, Kazunori Murata PhD, Melissa Pessin MD, Richard D. Press MD, PhD, Richard B. Thomson PhD

    Diterbitkan 2017-07-01
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