Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1994 Oct 11;22(20):4352–4353. doi: 10.1093/nar/22.20.4352

Single base substitutions are detected by double strand conformation analysis.

F A Saad 1, B Halliger 1, C R Müller 1, R G Roberts 1, G A Danieli 1
PMCID: PMC331969  PMID: 7937168

Abstract

Full text

PDF
4352

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Beggs A. H., Koenig M., Boyce F. M., Kunkel L. M. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet. 1990 Nov;86(1):45–48. doi: 10.1007/BF00205170. [DOI] [PubMed] [Google Scholar]
  2. Bolshoy A., McNamara P., Harrington R. E., Trifonov E. N. Curved DNA without A-A: experimental estimation of all 16 DNA wedge angles. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2312–2316. doi: 10.1073/pnas.88.6.2312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chamberlain J. S., Gibbs R. A., Ranier J. E., Nguyen P. N., Caskey C. T. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res. 1988 Dec 9;16(23):11141–11156. doi: 10.1093/nar/16.23.11141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ganguly A., Rock M. J., Prockop D. J. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes. Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10325–10329. doi: 10.1073/pnas.90.21.10325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Roberts R. G., Bobrow M., Bentley D. R. Point mutations in the dystrophin gene. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2331–2335. doi: 10.1073/pnas.89.6.2331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Saad F. A., Vita G., Mora M., Morandi L., Vitiello L., Oliviero S., Danieli G. A. A novel nonsense mutation in the human dystrophin gene. Hum Mutat. 1993;2(4):314–316. doi: 10.1002/humu.1380020413. [DOI] [PubMed] [Google Scholar]
  7. Saad F. A., Vitiello L., Merlini L., Mostacciuolo M. L., Oliviero S., Danieli G. A. A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions. Hum Mol Genet. 1992 Aug;1(5):345–346. doi: 10.1093/hmg/1.5.345. [DOI] [PubMed] [Google Scholar]
  8. Shpigelman E. S., Trifonov E. N., Bolshoy A. CURVATURE: software for the analysis of curved DNA. Comput Appl Biosci. 1993 Aug;9(4):435–440. doi: 10.1093/bioinformatics/9.4.435. [DOI] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES