Selective 'stencil'-aided pre-PCR cleavage of wild-type sequences as a novel approach to detection of mutant K-RAS

Nucleic Acids Research

Volumn 29, Issue 17, 2020, Pages

  Lichtenstein, Anatoly V ^a   Serdjuk, Ol'Ga I ^a   Sukhova, Tatjana I ^a   Melkonyan, Hovsep S ^b   Umansky, Samuil R ^b  

^a Cancer Research Center   (Russian Federation)

^b Xenomics Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL PRACTICE; CONTROLLED STUDY; DENSITOMETRY; DNA CLEAVAGE; DNA DENATURATION; DNA HYBRIDIZATION; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN CELL; MUTATIONAL ANALYSIS; ONCOGENE K RAS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DENATURATION; RESTRICTION SITE; STENCIL AIDED MUTATION ANALYSIS; THERMOSTABILITY; BINDING SITE; CELL CULTURE; GENETICS; GENOTYPE; METABOLISM; METHODOLOGY; MUTATION; NUCLEOTIDE SEQUENCE; ONCOGENE RAS;

DNA; ENDODEOXYRIBONUCLEASE ALUI; OLIGONUCLEOTIDE; PRIMER DNA; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

BASE SEQUENCE; BINDING SITES; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA PRIMERS; DNA, NEOPLASM; GENES, RAS; GENOTYPE; HUMANS; MUTATION; OLIGONUCLEOTIDES; POLYMERASE CHAIN REACTION; TUMOR CELLS, CULTURED;

EID: 0035461860     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/29.17.e90     Document Type: Article

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