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Showing items 1 to 100 of ±143 with 100 items per page.

NCIT_C21479 IAO_0000115 "Mismatch repair endonuclease PMS2 (862 aa, ~96 kDa) is encoded by the human PMS2 gene. This protein plays a role in DNA mismatch repair." @default.
NCIT_C21479 NCIT_NHC0 "C21479" @default.
NCIT_C21479 NCIT_P100 "600259" @default.
NCIT_C21479 NCIT_P106 "Amino Acid, Peptide, or Protein" @default.
NCIT_C21479 NCIT_P106 "Enzyme" @default.
NCIT_C21479 NCIT_P107 "Mismatch Repair Endonuclease PMS2" @default.
NCIT_C21479 NCIT_P108 "Mismatch Repair Endonuclease PMS2" @default.
NCIT_C21479 NCIT_P207 "C1333235" @default.
NCIT_C21479 NCIT_P322 "CPTAC" @default.
NCIT_C21479 NCIT_P322 "CTRP" @default.
NCIT_C21479 NCIT_P366 "DNA_Mismatch_Repair_Protein-PMS2" @default.
NCIT_C21479 NCIT_P93 "P54278" @default.
NCIT_C21479 NCIT_P98 "PMS2 is part of the BASC genome surveillance complex. MSH2 and MLH1 interact with PMS1, PMS2, and MSH6. Essential for repair of replication slippage errors, PMS2 is a cloned gene for Turcot syndrome and Hereditary Non-Polyposis Colon Cancer. Transcribed from the opposite strand, JTV1 overlaps PMS2." @default.
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