Claudia H. Huichalaf

发表

Direct interplay between two candidate genes in FSHD muscular dystrophy

Giulia Ferri, Roberta Caccia, Davide Gabellini, 2014, Human molecular genetics.

Reduction of the Rate of Protein Translation in Patients with Myotonic Dystrophy 2

B. Schoser, L. Timchenko, C. Schneider-Gold, 2009, The Journal of Neuroscience.

Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients.

B. Schoser, R. Krahe, L. Timchenko, 2009, American Journal of Pathology.

Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1.

J. Albrecht, B. Schoser, L. Timchenko, 2008, Experimental cell research.

Regulation of the promoter of CUG triplet repeat binding protein, Cugbp1, during myogenesis.

L. Timchenko, N. Timchenko, K. Sakai, 2007, Gene.

DNA Methylation Analysis of the Macrosatellite Repeat Associated with FSHD Muscular Dystrophy at Single Nucleotide Level

Claudia H. Huichalaf, D. Gabellini, Giulia Ferri, 2014, PloS one.

Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells

O. Pereira-smith, B. Schoser, L. Timchenko, 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Amino acid starvation induces reactivation of silenced transgenes and latent HIV-1 provirus via down-regulation of histone deacetylase 4 (HDAC4)

A. Mai, R. Piccirillo, G. Casari, 2012, Proceedings of the National Academy of Sciences.

Correction: DNA Methylation Analysis of the Macrosatellite Repeat Associated with FSHD Muscular Dystrophy at Single Nucleotide Level

Claudia H. Huichalaf, D. Gabellini, Giulia Ferri, 2015, PloS one.

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.

G. Meola, A. Shyu, B. Schoser, 2011, The American journal of pathology.

Cross-species genetic screens to identify kinase targets for APP reduction in Alzheimer's disease.

Stacy D. Grunke, H. Zoghbi, J. Botas, 2019, Human molecular genetics.

cdk5 modulates β‐ and δ‐catenin/Pin1 interactions in neuronal cells

R. Maccioni, Daniel I. Orellana, Claudia H. Huichalaf, 2007 .

In vivo overexpression of frataxin causes toxicity mediated by iron-sulfur cluster deficiency

C. Bulawa, Chunyan Su, I. Pardo, 2022, Molecular therapy. Methods & clinical development.

cdk5 modulates beta- and delta-catenin/Pin1 interactions in neuronal cells.

R. Maccioni, Daniel I. Orellana, Claudia H. Huichalaf, 2007, Journal of cellular biochemistry.