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2002, Advances in experimental medicine and biology, ISBN 9780306474170, Volume 516., x, 121
Book
Journal Article
11/2012
Gene-specific trinucleotide repeat expansions are the cause of an ever-growing number of disorders, including myotonic dystrophy type 1 (DM1) and... 
0369 | human genetics | trinucleotide repeats
Dissertation
Conference Proceeding
11/2009
The expansion of repetitive sequences leads to more than 40 neurological, neurodegenerative and neuromuscular diseases. These diseases are frequently... 
myotonic dystrophy | 0369 | trinucleotide | Spinocerebellar ataxia | cis-element | CTCF
Dissertation
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 1 - 12
Antagonist pleiotropy, where a gene exerts a beneficial effect at early stages and a deleterious effect later on in an animal’s life, may explain the... 
Huntingtons disease | Polyglutamine | Neurodegenerative diseases | Disease | Transgenic mice | Trinucleotide repeats | Huntington's disease | Pleiotropy | Rodents | Neostriatum | Mutation | Fecundity | Trinucleotide repeat diseases
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
NATURE REVIEWS GENETICS, ISSN 1471-0056, 08/2017, Volume 18, Issue 8, pp. 454 - 454
Some common inherited diseases are caused by nucleotide repeat expansions, whereby disease occurs only when the number of repeats exceeds a critical threshold.... 
GENETICS & HEREDITY | Trinucleotide repeats | Genetic disorders | Research | Gene mutations | RNA | Ribonucleic acid--RNA | Genetics
Journal Article