USP48 May Be Potential Therapeutic Target in Fanconi Anemia: Inactivation of USP48 reduced chromosomal instability of Fanconi anemia defective cells and highlights a role for this enzyme in controlling DNA repair

被引：0
作者：
不详
机构：
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2018年 / 176卷 / 09期
关键词：
D O I：
10.1002/ajmg.a.40522
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：1794 / 1795
页数：2
相关论文
共 3 条
  • [1] Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2
    Alter, Blanche P.
    Rosenberg, Philip S.
    Brody, Lawrence C.
    [J]. JOURNAL OF MEDICAL GENETICS, 2007, 44 (01) : 1 - 9
  • [2] Haematopoietic cell transplantation for acute leukaemia and advanced myelodysplastic syndrome in Fanconi anaemia
    Mitchell, Richard
    Wagner, John E.
    Hirsch, Betsy
    DeFor, Todd E.
    Zierhut, Heather
    MacMillan, Margaret L.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2014, 164 (03) : 384 - 395
  • [3] Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48
    Velimezi, Georgia
    Robinson-Garcia, Lydia
    Munoz-Martinez, Francisco
    Wiegant, Wouter W.
    da Silva, Joana Ferreira
    Owusu, Michel
    Moder, Martin
    Wiedner, Marc
    Rosenthal, Sara Brin
    Fisch, Kathleen M.
    Moffat, Jason
    Menche, Joerg
    van Attikum, Haico
    Jackson, Stephen P.
    Loizou, Joanna I.
    [J]. NATURE COMMUNICATIONS, 2018, 9
1