ARTICLE;
DNA DETERMINATION;
DNA SEQUENCE;
DNA TEMPLATE;
GENE DELETION;
GENE INSERTION;
GENOMICS;
NONHUMAN;
POLYMERASE CHAIN REACTION;
SITE DIRECTED MUTAGENESIS;
AGAR GEL ELECTROPHORESIS;
ANIMAL;
GENETICS;
MOUSE;
NUCLEOTIDE SEQUENCE;
ANIMALS;
BASE SEQUENCE;
DNA;
DNA PRIMERS;
ELECTROPHORESIS, AGAR GEL;
GENOMICS;
MICE;
MUTAGENESIS, SITE-DIRECTED;
POLYMERASE CHAIN REACTION;
TEMPLATES, GENETIC;
A rapid and efficient method for multiple-site mutagenesis with a modified overlap extension PCR
An Y, Ji J, Wu W, Lv A, Huang R and Wei Y 2005 A rapid and efficient method for multiple-site mutagenesis with a modified overlap extension PCR. Appl. Microbiol. Biotechnol. 68 774-778
A general method of in vitro preparation and specific mutagenesis of DNA fragments: Study of protein and DNA interactions
Higuchi R, Krummel B and Saiki R 1988 A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions. Nucleic Acids Res. 16 7351-7367
Creating randomized amino acid libraries with the QuikChange® multi site-directed mutagenesis kit
Hogrefe HH, Cline J, Youngblood GL and Allen RM 2002 Creating randomized amino acid libraries with the QuikChange® multi site-directed mutagenesis kit. Biotechniques 33 1158-1165
Determination of the secondary structure of and cellular protein binding to the 3'-untranslated region of the hepatitis C virus RNA genome
Ito T and Lai M 1997 Determination of the secondary structure of and cellular protein binding to the 3'-untranslated region of the hepatitis C virus RNA genome. J. Virol. 71 8698-8706
A direct and efficient PAGE-mediated overlap extension PCR method for gene multiple-site mutagenesis
Peng RH, Xiong AS and Yao QH 2006 A direct and efficient PAGE-mediated overlap extension PCR method for gene multiple-site mutagenesis. Appl. Microbiol. Biotechnol. 73 234-240
A new approach to 'megaprimer' polymerase chain reaction mutagenesis without an intermediate gel purification step
Tyagi R, Lai R and Duggleby R 2004 A new approach to 'megaprimer' polymerase chain reaction mutagenesis without an intermediate gel purification step. BMC Biotechnol. 4 2-7
Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange site-directed mutagenesis
Wang W and Malcolm B 1999 Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange Site-Directed Mutagenesis. Biotechniques 26 680
Asymmetric overlap extension PCR method bypassing intermediate purification and the amplification of wild-type template in site-directed mutagenesis
Xiao YH, Yin MH, Hou L, Luo M and Pei Y 2007 Asymmetric overlap extension PCR method bypassing intermediate purification and the amplification of wild-type template in site-directed mutagenesis. Biotechnol. Lett. 29 925-930
