TY  - JOUR
AU  - Gallardo-Orihuela, Andrea
AU  - Hervás-Corpión, Irati
AU  - Hierro-Bujalance, Carmen
AU  - Sanchez-Sotano, Daniel
AU  - Jiménez-Gómez, Gema
AU  - Mora-López, Francisco
AU  - Campos-Caro, Antonio
AU  - Garcia-Alloza, Monica
AU  - Valor, Luis M
PY  - 2019
DO  - 10.1038/s41598-019-55177-9
UR  - http://hdl.handle.net/10668/14808
T2  - Scientific reports
AB  - Huntington disease (HD) is a fatal neurodegenerative disorder without a cure that is caused by an aberrant expansion of CAG repeats in exon 1 of the huntingtin (HTT) gene. Although a negative correlation between the number of CAG repeats and the age...
LA  - en
KW  - Animals
KW  - Brain
KW  - Corpus Striatum
KW  - Disease Models, Animal
KW  - Gene Expression Regulation
KW  - Humans
KW  - Huntingtin Protein
KW  - Huntington Disease
KW  - Male
KW  - Mice
KW  - Mice, Inbred C57BL
KW  - Mice, Transgenic
KW  - Neostriatum
KW  - Nerve Tissue Proteins
KW  - Neurons
KW  - Nuclear Proteins
KW  - Phenotype
KW  - Transcription, Genetic
KW  - Transcriptome
KW  - Trinucleotide Repeat Expansion
TI  - Transcriptional correlates of the pathological phenotype in a Huntington's disease mouse model.
TY  - research article
VL  - 9
ER  -