Učitavanje...

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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Jezik:Inglês
Izdano: Oxford University Press 2001
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC60193/
https://ncbi.nlm.nih.gov/pubmed/11691925
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!