| Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1 E Salisbury, K Sakai, B Schoser, C Huichalaf, C Schneider-Gold, ... Experimental cell research 314 (11-12), 2266-2278, 2008 | 129 | 2008 |
| Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells C Huichalaf, K Sakai, B Jin, K Jones, GL Wang, B Schoser, ... The FASEB Journal 24 (10), 3706, 2010 | 118 | 2010 |
| Reduction of the rate of protein translation in patients with myotonic dystrophy 2 C Huichalaf, B Schoser, C Schneider-Gold, B Jin, P Sarkar, L Timchenko Journal of Neuroscience 29 (28), 9042-9049, 2009 | 108 | 2009 |
| Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients E Salisbury, B Schoser, C Schneider-Gold, GL Wang, C Huichalaf, B Jin, ... The American journal of pathology 175 (2), 748-762, 2009 | 102 | 2009 |
| Amino acid starvation induces reactivation of silenced transgenes and latent HIV-1 provirus via down-regulation of histone deacetylase 4 (HDAC4) I Palmisano, G Della Chiara, RL D’Ambrosio, C Huichalaf, P Brambilla, ... Proceedings of the National Academy of Sciences 109 (34), E2284-E2293, 2012 | 55 | 2012 |
| DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level C Huichalaf, S Micheloni, G Ferri, R Caccia, D Gabellini PloS one 9 (12), e115278, 2014 | 48 | 2014 |
| RNA Foci, CUGBP1, and ZNF9 are the primary targets of the mutant CUG and CCUG repeats expanded in myotonic dystrophies type 1 and type 2 K Jones, B Jin, P Iakova, C Huichalaf, P Sarkar, C Schneider-Gold, ... The American journal of pathology 179 (5), 2475-2489, 2011 | 46 | 2011 |
| In vivo overexpression of frataxin causes toxicity mediated by iron-sulfur cluster deficiency C Huichalaf, TL Perfitt, A Kuperman, R Gooch, RC Kovi, KA Brenneman, ... Molecular Therapy-Methods & Clinical Development 24, 367-378, 2022 | 41 | 2022 |
| Direct interplay between two candidate genes in FSHD muscular dystrophy G Ferri, CH Huichalaf, R Caccia, D Gabellini Human Molecular Genetics 24 (5), 1256-1266, 2015 | 31 | 2015 |
| cdk5 modulates β‐and δ‐catenin/Pin1 interactions in neuronal cells JP Munoz, CH Huichalaf, D Orellana, RB Maccioni Journal of cellular biochemistry 100 (3), 738-749, 2007 | 30 | 2007 |
| Regulation of the promoter of CUG triplet repeat binding protein, Cugbp1, during myogenesis CH Huichalaf, K Sakai, GL Wang, NA Timchenko, L Timchenko Gene 396 (2), 391-402, 2007 | 18 | 2007 |
| Cross-species genetic screens to identify kinase targets for APP reduction in Alzheimer's disease CH Huichalaf, I Al-Ramahi, KW Park, SD Grunke, N Lu, M de Haro, ... Human Molecular Genetics 28 (12), 2014-2029, 2019 | 7 | 2019 |
| A modified mouse model of Friedreich’s ataxia with conditional Fxn allele homozygosity delays onset of cardiomyopathy TL Perfitt, C Huichalaf, R Gooch, A Kuperman, Y Ahn, X Chen, S Ullas, ... American Journal of Physiology-Heart and Circulatory Physiology 326 (2 …, 2024 | 1 | 2024 |
| New Insights into the Toxicity of AAV-Mediated Overexpression of Frataxin C Huichalaf, TL Perfitt, A Kuperman, R Gooch, RC Kovi, K Brenneman, ... MOLECULAR THERAPY 30 (4), 365-365, 2022 | | 2022 |
| BASES CELULARES Y MOLECULARES DE LOS PROCESOS NEURODEGENERATIVOS: UNA VISION INTEGRATIVA DESDE LA PERSPECTIVA DEL CITOESQUELETO NEURONAL R Maccioni-Baraona, BKC Niven, C Huichalaf, LFO Davila, DI Orellana, ... | | 2017 |
| BASES CELULARES Y MOLECULARES DE LOS PROCESOS NEURODEGENERATIVOS: UNA VISION INTEGRATIVA DESDE LA PERSPECTIVA DEL CITOESQUELETO NEURONAL BKC Niven, C Huichalaf, LFO Davila, DI Orellana, O Ramirez | | 2002 |
