MeSH Browser

MeSH Supplementary: WRN protein, human
Unique ID: C098785
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C098785
Entry Term(s): RECQ3 protein, human; RECQL2 protein, human; Werner syndrome helicase, human
Registry Numbers: EC 3.6.4.12
Previous Indexing: *DNA HELICASES (1996-2006); *ENDODEOXYRIBONUCLEASES (1996-2016); *RECQ HELICASES (2006-2016)
Heading Mapped to: *Werner Syndrome Helicase
Frequency: 618
Note: RefSeq NM_000553
Source: Science 1996 Apr 12;272(5259):258-62
Indexing Information: Werner Syndrome
Date of Entry: 1996/04/30
Revision Date: 2016/04/18

Concept UI: M0259453
Registry Numbers: EC 3.6.4.12
Terms: WRN protein, human Preferred Term
Term UI T289458
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1996); Werner syndrome helicase, human
Term UI T522964
Date10/17/2002
LexicalTag NON
ThesaurusID NLM (2002); RECQL2 protein, human
Term UI T522965
Date10/17/2002
LexicalTag NON
ThesaurusID NLM (2002); RECQ3 protein, human
Term UI T522966
Date10/17/2002
LexicalTag NON
ThesaurusID NLM (2002)

WRN protein, human MeSH Supplementary Concept Data 2025