Načítá se...
A Meier-Gorlin Syndrome Mutation Impairs the ORC1-Nucleosome Association
Recent studies have identified several genetic mutations within the BAH domain of human Origin Recognition Complex subunit 1 (hORC1(BAH)), including the R105Q mutation, implicated in Meier-Gorlin Syndrome (MGS). However, the pathological role of the hORC1 R105Q mutation remains unclear. In this stud...
Uloženo v:
| Vydáno v: | ACS Chem Biol |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4654454/ https://ncbi.nlm.nih.gov/pubmed/25689043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/cb5009684 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|