UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
W W0 W1 W4 W6 WA WB WD WE WF WH WI WN WO WR WT WU WV WY
WEA WEB WEC WED WEE WEG WEI WEL WEN WER WES WET
selected terms: 3 page 1 of 1

1. Werdnig Hoffmann paralysis
[ ] (UMLS (CSP) C0599201) =Disease or Syndrome ;
3. Werner Syndrome Protein
[The WS gene encodes WRN, a 1,432-amino acid polypeptide. WRN is a member of the RecQ family of DNA helicases that unwind duplex DNA. It can also digest DNA exonucleolytically with 3'-5' polarity. WRN may facilitate pol d-mediated DNA replication and/or DNA repair and disruption of WRN-DNA polymerase delta interaction in WS cells may contribute to the S-phase defects and/or the unusual sensitivity to a limited number of DNA damaging agents. (Proc Natl Acad Sci U S A 2000 Apr 25;97(9):4603-8) ( NCI )] (UMLS (NCI) C0388246) =Amino Acid, Peptide, or Protein; Enzyme ;
2. Werner Syndrome Gene
[This gene is involved in DNA repair and the unwinding of DNA. ( NCI )] (UMLS (NCI) C1337007) WRN;
WRN Gene;
=Gene or Genome ;

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