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Annual Review of Neuroscience, ISSN 0147-006X, 2007, Volume 30, Issue 1, pp. 575 - 621
The discovery that expansion of unstable repeats can cause a variety of neurological disorders has changed the landscape of disease-oriented research for... 
Unstable repeats | Polyglutamine | Ataxin | Frataxin | Myotonic dystrophy | Huntington disease | Ataxia | Fragile X syndrome | Mental retardation | Spinal bulbar muscular atrophy | SPINOCEREBELLAR ATAXIA TYPE-1 | UBIQUITIN-PROTEASOME SYSTEM | unstable repeats | fragile X syndrome | polyglutamine | NEUROSCIENCES | X MENTAL-RETARDATION | frataxin | myotonic dystrophy | mental retardation | HUNTINGTONS-DISEASE GENE | ataxia | spinal bulbar muscular atrophy | MACHADO-JOSEPH-DISEASE | ataxin | TRANSGENIC MOUSE MODEL | DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY | DOMINANT CEREBELLAR-ATAXIA | BULBAR MUSCULAR-ATROPHY | FMR1 KNOCKOUT MICE | Fragile X Syndrome - genetics | Heredodegenerative Disorders, Nervous System - genetics | Genetic Predisposition to Disease - genetics | Cerebellar Ataxia - metabolism | Brain - physiopathology | Fragile X Syndrome - physiopathology | Humans | Peptides - genetics | Fragile X Syndrome - metabolism | Heredodegenerative Disorders, Nervous System - physiopathology | Mutation - genetics | Huntington Disease - metabolism | Brain - metabolism | Cerebellar Ataxia - physiopathology | Animals | Cerebellar Ataxia - genetics | Peptides - metabolism | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Heredodegenerative Disorders, Nervous System - metabolism | Huntington Disease - physiopathology | Trinucleotide repeats | Care and treatment | Genetic aspects | Diagnosis
Journal Article
2006, 2nd ed., ISBN 0123694620, 551
This book describes everything about DNA repeat instability and neurological disorders, covering molecular mechanisms of repeat expansion, pathogenic... 
Nervous system | Biology, life sciences | Neurogenetics
eBook
2006, Nucleic acids and molecular biology, ISBN 3540333355, Volume 19., xvii, 293
Human neurological and neuromuscular disorders caused by nucleotide expansion, first discovered in 1991, are the focus of growing interest of practicing... 
Nucleotide sequence | Medical genetics | Life Sciences | Human Genetics | Biochemistry, general | Neurosciences | Neurobiology | Cell Biology
Book
2004, Methods in molecular biology, ISBN 1588292436, Volume 277, xii, 342
The discovery that trinucleotide repeats significantly influence the age of onset and severity of a variety of hereditary neurological disorders has opened the... 
Trinucleotide repeats | Laboratory manuals | Cytology | Cell Biology | Life Sciences
Book
2009, ISBN 0199236127, xvi, 205
Book
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
Neurobiology of Disease, ISSN 0969-9961, 10/2019, Volume 130, pp. 104515 - 104515
Tandem microsatellite repeats are common throughout the human genome and intrinsically unstable, exhibiting expansions and contractions both somatically and... 
MESSENGER-RNA TRANSLATION | MYOTONIC-DYSTROPHY TYPE-1 | NON-AUG TRANSLATION | RAN TRANSLATION | STRESS GRANULE FORMATION | NUCLEOCYTOPLASMIC TRANSPORT DEFECTS | LENGTH POLYGLUTAMINE EXPANSIONS | TRANSGENIC MOUSE MODEL | MENTAL-RETARDATION PROTEIN | NEUROSCIENCES | TRINUCLEOTIDE REPEAT | Index Medicus
Journal Article