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Volumn 13, Issue 4, 2005, Pages 703-707
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Infrequent mutation of the human envoplakin gene is closely linked to the tylosis oesophageal cancer locus in sporadic oesophageal squamous cell carcinomas.
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
ENVOPLAKIN;
MEMBRANE PROTEIN;
MICROSATELLITE DNA;
PRIMER DNA;
PROTEIN PRECURSOR;
ALLELE;
ARTICLE;
BIOLOGICAL MODEL;
CHEMISTRY;
CODON;
DNA SEQUENCE;
ESOPHAGUS TUMOR;
EXON;
GENETIC LINKAGE;
GENETIC POLYMORPHISM;
GENETICS;
HETEROZYGOSITY LOSS;
HUMAN;
KERATOSIS PALMOPLANTARIS;
METABOLISM;
MUTATION;
PHYSIOLOGY;
PROTEIN CONFORMATION;
PROTEIN TERTIARY STRUCTURE;
REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;
RNA INTERFERENCE;
SINGLE NUCLEOTIDE POLYMORPHISM;
SINGLE STRAND CONFORMATION POLYMORPHISM;
SQUAMOUS CELL CARCINOMA;
TIME;
TUMOR CELL LINE;
ALLELES;
CARCINOMA, SQUAMOUS CELL;
CELL LINE, TUMOR;
CODON;
DNA PRIMERS;
DNA, COMPLEMENTARY;
ESOPHAGEAL NEOPLASMS;
EXONS;
HUMANS;
KERATODERMA, PALMOPLANTAR, DIFFUSE;
LINKAGE (GENETICS);
LOSS OF HETEROZYGOSITY;
MEMBRANE PROTEINS;
MICROSATELLITE REPEATS;
MODELS, GENETIC;
MUTATION;
POLYMORPHISM, GENETIC;
POLYMORPHISM, SINGLE NUCLEOTIDE;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
PROTEIN CONFORMATION;
PROTEIN PRECURSORS;
PROTEIN STRUCTURE, TERTIARY;
REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;
RNA INTERFERENCE;
SEQUENCE ANALYSIS, DNA;
TIME FACTORS;
MLCS;
MLOWN;
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EID: 23844494537
PISSN: 1021335X
EISSN: None
Source Type: Journal
DOI: 10.3892/or.13.4.703 Document Type: Article |
Times cited : (14)
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References (0)
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