The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair

Cancer Letters

Volumn 249, Issue 2, 2007, Pages 148-156

  Deschênes, Suzanne M ^a   Tomer, Guy ^b   Nguyen, Megan ^c   Erdeniz, Naz ^c   Juba, Nicole C ^a   Sepúlveda, Natalia ^a   Pisani, Jenna E ^a   Michael Liskay, R ^c  

^a SACRED HEART UNIVERSITY   (United States)

^b SHEBA MEDICAL CENTER   (Israel)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Mismatch repair; PMS2; Turcot syndrome

Indexed keywords

ALLELE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC ASSOCIATION; HPMS2 GENE; MAMMAL CELL; MISMATCH REPAIR; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; TURCOT SYNDROME; WILD TYPE; YEAST CELL;

ADENOSINE TRIPHOSPHATASES; ALLELES; ANIMALS; CELL LINE; DNA MISMATCH REPAIR; DNA REPAIR ENZYMES; DNA-BINDING PROTEINS; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; MICE; MUTATION; NEOPLASTIC SYNDROMES, HEREDITARY; SACCHAROMYCES CEREVISIAE;

MAMMALIA;

EID: 33947409117     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2006.08.008     Document Type: Article

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