This report describes a rapid convenient screening system with improved sensitivity to detect mutations in the cystic fibrosis transmembrane regulator (CFTR) gene based on nonisotopic SSCP analysis. Because conventional SSCP analysis is often hampered by poor yield of single-stranded DNA, we applied
β¦ LIBER β¦
Detection of single nucleotide mutations in wheat using single strand conformation polymorphism gels
β Scribed by P. Martins-Lopes; H. Zhang; R. Koebner
- Book ID
- 110678784
- Publisher
- Springer
- Year
- 2001
- Tongue
- English
- Weight
- 279 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0735-9640
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Nonisotopic detection of mutations using
Nonisotopic detection of mutations using a modified single-strand conformation polymorphism analysis
β
J. Weidner; A. Eigel; J. Horst; W. KΓΆhnlein
π
Article
π
1994
π
John Wiley and Sons
π
English
β 192 KB
Single-strand conformation polymorphism
β
Arun J. Nataraj; Isabelle Olivos-Glander; Noriko Kusukawa; W. Edward Highsmith J
π
Article
π
1999
π
John Wiley and Sons
π
English
β 122 KB
π 2 views
Enhanced detection of mutations inBRCA1e
β
Astanand Jugessur; Petter Frost; Tone Ikdahl Andersen; Solrun Steine; Annika Lin
π
Article
π
2000
π
Springer
π
English
β 172 KB
Detection of single nucleotide polymorph
β
Zhu, Weifeng; Deng, Yan; Jie, Kemin; Luo, Daya; Liu, Zhuoqi; Yu, Lehan; Zeng, Er
π
Article
π
2012
π
Springer Netherlands
π
English
β 474 KB
Rapid detection of phenylketonuria mutat
β
YEQI YAO; YOICHI MATSUBARA; KUNIAKI NARISAWA
π
Article
π
1994
π
John Wiley and Sons
π
English
β 430 KB
Detection of single nucleotide polymorph
β
Alexandra Bezak; RadosΕaw Kaczanowski; Astrid Dossenbach-Glaninger; Krzysztof Ku
π
Article
π
2005
π
John Wiley and Sons
π
English
β 242 KB
Factor XI (FXI) deficiency is a rare inherited disorder which can cause bleeding complications especially in case of hemostatic challenge and/or in tissues with high fibrinolytic activity. A number of causative mutations have been described in FXI deficient individuals which have been detected by va