The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases
- 1 May 2000
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 16 (5) , 213-220
- https://doi.org/10.1016/s0168-9525(99)01970-8
Abstract
No abstract availableKeywords
This publication has 69 references indexed in Scilit:
- Functional and Physical Interaction between WRN Helicase and Human Replication Protein AJournal of Biological Chemistry, 1999
- Human Werner Syndrome DNA Helicase Unwinds Tetrahelical Structures of the Fragile X Syndrome Repeat Sequence d(CGG)Journal of Biological Chemistry, 1999
- Characterization of Werner syndrome protein DNA helicase activity: Directionality, substrate dependence and stimulation by replication protein ANucleic Acids Research, 1998
- The Werner syndrome protein is a DNA helicaseNature Genetics, 1997
- DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus systemNucleic Acids Research, 1997
- Positional Cloning of the Werner's Syndrome GeneScience, 1996
- Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell linesExperimental Cell Research, 1992
- Mutator phenotype of Werner syndrome is characterized by extensive deletions.Proceedings of the National Academy of Sciences, 1989
- Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrationsHuman Genetics, 1982
- Cytogenetics of Werner’s syndrome cultured skin fibroblasts: variegated translocation mosaicismCytogenetic and Genome Research, 1981