Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancer

Anticancer Research

Volumn 22, Issue 2 A, 2002, Pages 969-975

  Arzimanoglou, Iordanis I ^a   Hansen, Lise Lotte ^a   Chong, David ^a   Li, Zhen ^a   Psaroudi, Maria C ^a   Dimitrakakis, Constantine ^a   Jacovina, Andrew T ^a   Shevchuk, Maria ^a   Reid, Linda ^a   Hajjar, Katherine A ^a   Vassilaros, Stamatis ^a   Michalas, Stylianos ^a   Gilbert, Fred ^a   Chervenak, Frank A ^a   Barber, Hugh R K ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

Coding DNA instability; LOH; Mismatch DNA repair genes; Ovarian cancer; SNP

Indexed keywords

DNA; PROTEIN MLH1; PROTEIN MSH3;

ALLELE; ARTICLE; CONTROLLED STUDY; DNA REPAIR; DNA SEQUENCE; FEMALE; GENETIC ANALYSIS; GENETIC STABILITY; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MISMATCH REPAIR; OVARY CANCER; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

BASE SEQUENCE; CARRIER PROTEINS; DNA REPAIR; DNA, NEOPLASM; DNA-BINDING PROTEINS; FEMALE; HUMANS; LOSS OF HETEROZYGOSITY; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MULTIDRUG RESISTANCE-ASSOCIATED PROTEINS; NEOPLASM PROTEINS; NUCLEAR PROTEINS; OVARIAN NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0036244657     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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