Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1
- 30 April 2007
- journal article
- Published by Elsevier in Experimental and Molecular Pathology
- Vol. 82 (2) , 190-196
- https://doi.org/10.1016/j.yexmp.2006.10.004
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- The genetic basis of premature ovarian failureAustralian and New Zealand Journal of Obstetrics and Gynaecology, 2006
- Size bias of fragile X premutation alleles in late-onset movement disordersJournal of Medical Genetics, 2006
- A question of timing: emerging links between transcription and replicationCurrent Opinion in Genetics & Development, 2006
- Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instabilityTrends in Genetics, 2005
- An ATR- and Chk1-Dependent S Checkpoint Inhibits Replicon Initiation following UVC-Induced DNA DamageMolecular and Cellular Biology, 2002
- CTG repeats associated with human genetic disease are inherently flexibleJournal of Molecular Biology, 1998
- Anomalous Rapid Electrophoretic Mobility of DNA Containing Triplet Repeats Associated with Human Disease GenesBiochemistry, 1995
- Molecular‐neurobehavioral associations in females with the fragile X full mutationAmerican Journal of Medical Genetics, 1994
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Effect of benzo[a]pyrene-diol-epoxide-I on growth of nascent DNA in synchronized human fibroblastsCarcinogenesis: Integrative Cancer Research, 1986