Paxillin: a crossroad in pathological cell migration

Por López-Colomé, Ana María, Lee-Rivera, Irene, Benavides-Hidalgo, Regina, López, Edith
Publicado no J Hematol Oncol (2017)

Glutamate transporter-dependent mTOR phosphorylation in Müller glia cells

Por María López-Colomé, Ana, Martínez-Lozada, Zila, Guillem, Alain M, López, Edith, Ortega, Arturo
Publicado em 2012

Thrombin-Induced Calpain Activation Promotes Protease-Activated Receptor 1 Internalization

Por Alvarez-Arce, Alejandro, Lee-Rivera, Irene, López, Edith, Hernández-Cruz, Arturo, López-Colomé, Ana María
Publicado no Int J Cell Biol (2017)

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

Por Dragileva, Ella, Hendricks, Audrey, Teed, Allison, Gillis, Tammy, Lopez, Edith T, Friedberg, Errol C, Kucherlapati, Raju, Edelmann, Winfried, Lunetta, Kathryn L, MacDonald, Marcy E, Wheeler, Vanessa C
Publicado em 2008

Muscle expression of mutant androgen receptor protein accounts for systemic and motor neuron disease phenotypes in Spinal & Bulbar Muscular Atrophy

Por Cortes, Constanza J., Ling, Shuo-Chien, Guo, Ling T., Hung, Gene, Tsunemi, Taiji, Ly, Linda, Tokunaga, Seiya, Lopez, Edith, Sopher, Bryce L., Bennett, C. Frank, Shelton, G. Diane, Cleveland, Don W., La Spada, Albert R.
Publicado em 2014

A novel approach to investigate tissue-specific trinucleotide repeat instability

Por Lee, Jong-Min, Zhang, Jie, Su, Andrew I, Walker, John R, Wiltshire, Tim, Kang, Kihwa, Dragileva, Ella, Gillis, Tammy, Lopez, Edith T, Boily, Marie-Josee, Cyr, Michel, Kohane, Isaac, Gusella, James F, MacDonald, Marcy E, Wheeler, Vanessa C
Publicado em 2010

Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches

Por Pinto, Ricardo Mouro, Dragileva, Ella, Kirby, Andrew, Lloret, Alejandro, Lopez, Edith, St. Claire, Jason, Panigrahi, Gagan B., Hou, Caixia, Holloway, Kim, Gillis, Tammy, Guide, Jolene R., Cohen, Paula E., Li, Guo-Min, Pearson, Christopher E., Daly, Mark J., Wheeler, Vanessa C.
Publicado em 2013

A Broad Phenotypic Screen Identifies Novel Phenotypes Driven by a Single Mutant Allele in Huntington’s Disease CAG Knock-In Mice

Por Hölter, Sabine M., Stromberg, Mary, Kovalenko, Marina, Garrett, Lillian, Glasl, Lisa, Lopez, Edith, Guide, Jolene, Götz, Alexander, Hans, Wolfgang, Becker, Lore, Rathkolb, Birgit, Rozman, Jan, Schrewed, Anja, Klingenspor, Martin, Klopstock, Thomas, Schulz, Holger, Wolf, Eckhard, Wursta, Wolfgang, Gillis, Tammy, Wakimoto, Hiroko, Seidman, Jonathan, MacDonald, Marcy E., Cotman, Susan, Gailus-Durner, Valérie, Fuchs, Helmut, de Angelis, Martin Hrabě, Lee, Jong-Min, Wheeler, Vanessa C.
Publicado em 2013

Large-Scale Phenotyping of an Accurate Genetic Mouse Model of JNCL Identifies Novel Early Pathology Outside the Central Nervous System

Por Staropoli, John F., Haliw, Larissa, Biswas, Sunita, Garrett, Lillian, Hölter, Sabine M., Becker, Lore, Skosyrski, Sergej, Da Silva-Buttkus, Patricia, Calzada-Wack, Julia, Neff, Frauke, Rathkolb, Birgit, Rozman, Jan, Schrewe, Anja, Adler, Thure, Puk, Oliver, Sun, Minxuan, Favor, Jack, Racz, Ildikó, Bekeredjian, Raffi, Busch, Dirk H., Graw, Jochen, Klingenspor, Martin, Klopstock, Thomas, Wolf, Eckhard, Wurst, Wolfgang, Zimmer, Andreas, Lopez, Edith, Harati, Hayat, Hill, Eric, Krause, Daniela S., Guide, Jolene, Dragileva, Ella, Gale, Evan, Wheeler, Vanessa C., Boustany, Rose-Mary, Brown, Diane E., Breton, Sylvie, Ruether, Klaus, Gailus-Durner, Valérie, Fuchs, Helmut, de Angelis, Martin Hrabě, Cotman, Susan L.
Publicado em 2012