Impaired nuclear localization of defective DNA helicases in Werner's syndrome
- 1 August 1997
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 16 (4), 335-336
- https://doi.org/10.1038/ng0897-335
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese populationHuman Genetics, 1997
- Analysis of helicase gene mutations in Japanese Werner's syndrome patientsHuman Genetics, 1997
- Homozygous and compound heterozygous mutations at the Werner syndrome locusHuman Molecular Genetics, 1996
- Optimized Codon Usage and Chromophore Mutations Provide Enhanced Sensitivity with the Green Fluorescent ProteinNucleic Acids Research, 1996
- Mutation-causing mutationsNature, 1996
- Positional Cloning of the Werner's Syndrome GeneScience, 1996
- The Bloom's syndrome gene product is homologous to RecQ helicasesCell, 1995
- Nuclear protein localizationBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1991
- Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literatureClinical Genetics, 1981
- A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging ProcessMedicine, 1966