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Journal of Neurochemistry, ISSN 0022-3042, 02/2013, Volume 124, Issue 3, pp. 418 - 430
Huntingtin (Htt) protein interacts with many transcriptional regulators, with widespread disruption to the transcriptome in Huntington's disease (HD) brought... 
microRNA | REST | synaptic transmission | transcriptional dysregulation | Huntingtin | Huntington's disease | CELLS | PROTEIN | NEUROTROPHIC FACTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUTANT HUNTINGTIN | TRANSCRIPTION | NEURODEGENERATION | NEUROSCIENCES | TARGET GENES | GENE-EXPRESSION | COMPLEXIN-II | BRAIN | Neurons - pathology | RNA, Small Interfering - genetics | Humans | Huntington Disease - pathology | Cells, Cultured | Gene Expression Regulation - physiology | Repressor Proteins - genetics | Neurons - cytology | Nuclear Proteins - metabolism | Corpus Striatum - cytology | Huntington Disease - metabolism | Nerve Tissue Proteins - genetics | Repressor Proteins - antagonists & inhibitors | Gene Knock-In Techniques | Gene Knockdown Techniques | Nerve Tissue Proteins - metabolism | Repressor Proteins - physiology | Huntingtin Protein | Animals | Huntington Disease - genetics | Mice | Nuclear Proteins - genetics | Proteins | Disease transmission | MicroRNA | Huntington's chorea | Analysis | Genes | Genetic transcription | Neurochemistry | Genetic disorders | Cellular biology | Ribonucleic acid--RNA | Gene expression | Animal models | Transcription factors | Cell survival | non-coding RNA | Data processing | Nervous system | Gene silencing | Brain-derived neurotrophic factor | Repressors | Coding | Synaptic transmission | miRNA | Cytoplasm
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2010, Volume 41, Issue 1, pp. 43 - 50
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2/2010, Volume 19, Issue 4, pp. 609 - 622
Selective degeneration of striatal neurons is a pathologic hallmark of Huntington disease (HD). The exact mechanism(s) behind this specific neurodegeneration... 
BIOCHEMISTRY & MOLECULAR BIOLOGY | YAC128 MOUSE MODEL | MUTANT HUNTINGTIN | INDOLEAMINE 2,3-DIOXYGENASE | LENGTH | GENETICS & HEREDITY | DYSFUNCTION | IDENTIFICATION | METABOLITE | BRAIN | ONSET | TRANSGENIC MICE | Animals | Humans | Huntington Disease - genetics | Female | Gene Expression Profiling | Mice | Corpus Striatum - metabolism | Huntington Disease - metabolism | Disease Models, Animal
Journal Article
Journal of Neurology, ISSN 0340-5354, 06/2018, Volume 266, Issue 3, pp. 1 - 14
Huntington’s disease (HD) is a fatal neurodegenerative disease caused by mutant HTT gene expansions of CAG triplet repeat numbers that are inherited in an... 
Huntington’s disease | Polyglutamine | Cognition disorders | Neurodegeneration | Motor disorders | Huntingtons disease | Brain | Molecular modelling | Cognitive ability | Trinucleotide repeats | Gene expression | Huntington's disease | Trinucleotide repeat diseases
Journal Article
FRONTIERS IN PHARMACOLOGY, ISSN 1663-9812, 07/2019, Volume 10, p. 724
Journal Article