Immunodetection of Human Double Homeobox 4

Por Geng, Linda N., Tyler, Ashlee E., Tapscott, Stephen J.
Publicado em 2011

Behçet's disease with major vascular involvement

Por Geng, Linda N, Conway, Delaney, Barnhart, Scott, Nowatzky, Johannes
Publicado em 2013

DNA methylation of developmental genes in pediatric medulloblastomas identified by denaturation analysis of methylation differences

Por Diede, Scott J., Guenthoer, Jamie, Geng, Linda N., Mahoney, Sarah E., Marotta, Michael, Olson, James M., Tanaka, Hisashi, Tapscott, Stephen J.
Publicado em 2009

DUX4 Binding to Retroelements Creates Promoters That Are Active in FSHD Muscle and Testis

Por Young, Janet M., Whiddon, Jennifer L., Yao, Zizhen, Kasinathan, Bhavatharini, Snider, Lauren, Geng, Linda N., Balog, Judit, Tawil, Rabi, van der Maarel, Silvère M., Tapscott, Stephen J.
Publicado em 2013

DUX4 activates germline genes, retroelements and immune-mediators: Implications for facioscapulohumeral dystrophy

Por Geng, Linda N., Yao, Zizhen, Snider, Lauren, Fong, Abraham P., Cech, Jennifer N., Young, Janet M, van der Maarel, Silvere M., Ruzzo, Walter L., Gentleman, Robert C., Tawil, Rabi, Tapscott, Stephen J.
Publicado em 2011

Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene

Por Snider, Lauren, Geng, Linda N., Lemmers, Richard J. L. F., Kyba, Michael, Ware, Carol B., Nelson, Angelique M., Tawil, Rabi, Filippova, Galina N., van der Maarel, Silvère M., Tapscott, Stephen J., Miller, Daniel G.
Publicado em 2010

RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

Por Snider, Lauren, Asawachaicharn, Amy, Tyler, Ashlee E., Geng, Linda N., Petek, Lisa M., Maves, Lisa, Miller, Daniel G., Lemmers, Richard J.L.F., Winokur, Sara T., Tawil, Rabi, van der Maarel, Silvère M., Filippova, Galina N., Tapscott, Stephen J.
Publicado em 2009

Generation of Isogenic D4Z4 Contracted and Noncontracted Immortal Muscle Cell Clones from a Mosaic Patient: A Cellular Model for FSHD

Por Krom, Yvonne D., Dumonceaux, Julie, Mamchaoui, Kamel, den Hamer, Bianca, Mariot, Virginie, Negroni, Elisa, Geng, Linda N., Martin, Nicolas, Tawil, Rabi, Tapscott, Stephen J., van Engelen, Baziel G.M., Mouly, Vincent, Butler-Browne, Gillian S., van der Maarel, Silvère M.
Publicado em 2012

COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the copper transporter ATP7A

Por Phillips-Krawczak, Christine A., Singla, Amika, Starokadomskyy, Petro, Deng, Zhihui, Osborne, Douglas G., Li, Haiying, Dick, Christopher J., Gomez, Timothy S., Koenecke, Megan, Zhang, Jin-San, Dai, Haiming, Sifuentes-Dominguez, Luis F., Geng, Linda N., Kaufmann, Scott H., Hein, Marco Y., Wallis, Mathew, McGaughran, Julie, Gecz, Jozef, van de Sluis, Bart, Billadeau, Daniel D., Burstein, Ezra
Publicado no Mol Biol Cell (2015)