Fragile X syndrome and Friedreich’s ataxia: two different paradigms for repeat induced transcript insufficiency
- 19 November 2001
- journal article
- review article
- Published by Elsevier in Brain Research Bulletin
- Vol. 56 (3-4), 367-373
- https://doi.org/10.1016/s0361-9230(01)00572-x
Abstract
No abstract availableKeywords
This publication has 82 references indexed in Scilit:
- Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiaeHuman Molecular Genetics, 2000
- Isolation of an FMRP-Associated Messenger Ribonucleoprotein Particle and Identification of Nucleolin and the Fragile X-Related Proteins as Components of the ComplexMolecular and Cellular Biology, 1999
- DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy modelJournal of Clinical Investigation, 1999
- Purified Recombinant Fmrp Exhibits Selective RNA Binding as an Intrinsic Property of the Fragile X Mental Retardation ProteinJournal of Biological Chemistry, 1998
- In Vitro Reactivation of the FMR1 Gene Involved in Fragile X SyndromeHuman Molecular Genetics, 1998
- The GAA Triplet-Repeat Expansion in Friedreich Ataxia Interferes with Transcription and May Be Associated with an Unusual DNA StructureAmerican Journal of Human Genetics, 1998
- Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial MembranesHuman Molecular Genetics, 1997
- Regulation of Mitochondrial Iron Accumulation by Yfh1p, a Putative Homolog of FrataxinScience, 1997
- Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat ExpansionScience, 1996
- Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications.Proceedings of the National Academy of Sciences, 1995