Direct association of Bloom’s syndrome gene product with the human mismatch repair protein MLH1

Bloom’s syndrome (BS) is a rare genetic disorder characterised by genomic instability and cancer susceptibility. BLM, the gene mutated in BS, encodes a member of the RecQ family of DNA helicases. Here, we identify hMLH1, which is involved in mismatch repair (MMR) and recombination, as a protein that...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Pedrazzi, Graziella, Perrera, Claudia, Blaser, Heiko, Kuster, Patrick, Marra, Giancarlo, Davies, Sally L., Ryu, Gi-Hyuck, Freire, Raimundo, Hickson, Ian D., Jiricny, Josef, Stagljar, Igor
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2001
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC60193/
https://ncbi.nlm.nih.gov/pubmed/11691925
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars