Rothmund–Thomson Syndrome Responsible Gene, RECQL4: Genomic Structure and Products
- 1 November 1999
- journal article
- Published by Elsevier BV in Genomics
- Vol. 61 (3), 268-276
- https://doi.org/10.1006/geno.1999.5959
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Werner Helicase Is Localized to Transcriptionally Active Nucleoli of Cycling CellsExperimental Cell Research, 1998
- Deoxyribonucleic Acid-Protein Interactions and Expression of the Human Testis-Specific Lactate Dehydrogenase Promoter: Transcription Factor Sp1 Plays a Major Role1Biology of Reproduction, 1998
- Cloning of a Mouse Homologue of the Human Werner Syndrome Gene and Assignment to 8A4 by Fluorescencein SituHybridizationGenomics, 1997
- RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coliProceedings of the National Academy of Sciences of the United States of America, 1997
- The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase.Molecular and Cellular Biology, 1994
- Bloom SyndromeMedicine, 1993
- Molecular basis for developmental changes in interleukin-2 gene inducibility.Molecular and Cellular Biology, 1993
- Clonal lines of aneuploid cells in Rothmund‐Thomson syndromeAmerican Journal of Medical Genetics, 1990
- Mutator phenotype of Werner syndrome is characterized by extensive deletions.Proceedings of the National Academy of Sciences of the United States of America, 1989
- [14] Characterization of cap structuresMethods in enzymology, 1989