Functional analysis of the putative peroxidase domain of FANCA, the Fanconi anemia complementation group A protein.

被引：0
|
作者：
Ren, J [1 ]
Youssoufian, H [1 ]
机构：
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2221
引用
收藏
页码：395 / 395
页数：1
相关论文
共 50 条
  • [41] X-linked inheritance of Fanconi anemia complementation group B
    Amom Ruhikanta Meetei
    Marieke Levitus
    Yutong Xue
    Annette L Medhurst
    Michel Zwaan
    Chen Ling
    Martin A Rooimans
    Patrick Bier
    Maureen Hoatlin
    Gerard Pals
    Johan P de Winter
    Weidong Wang
    Hans Joenje
    Nature Genetics, 2004, 36 : 1219 - 1224
  • [42] Fanconi Anemia Complementary Group A (FANCA) Facilitates the Occurrence and Progression of Liver Hepatocellular Carcinoma
    Feng-die Huang
    Yan-ping Zhong
    Guang-yu Sun
    Qi-jiang Xu
    Zhi-yong Xing
    Ke-heng Chen
    Lu-sheng Liao
    Ming-you Dong
    Digestive Diseases and Sciences, 2024, 69 : 1035 - 1054
  • [43] Pan-cancer analysis of the prognostic and immunological role of Fanconi anemia complementation group E
    Zhou, Zhixian
    Yin, Huan
    Suye, Suye
    He, Jiarong
    Fu, Chun
    FRONTIERS IN GENETICS, 2023, 13
  • [44] A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
    Meetei, AR
    Medhurst, AL
    Ling, C
    Xue, YT
    Singh, TR
    Bier, P
    Steltenpool, J
    Stone, S
    Dokal, I
    Mathew, CG
    Hoatlin, M
    Joenje, H
    de Winter, JP
    Wang, WD
    NATURE GENETICS, 2005, 37 (09) : 958 - 963
  • [45] A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
    Amom Ruhikanta Meetei
    Annette L Medhurst
    Chen Ling
    Yutong Xue
    Thiyam Ramsing Singh
    Patrick Bier
    Jurgen Steltenpool
    Stacie Stone
    Inderjeet Dokal
    Christopher G Mathew
    Maureen Hoatlin
    Hans Joenje
    Johan P de Winter
    Weidong Wang
    Nature Genetics, 2005, 37 : 958 - 963
  • [46] Fanconi anemia protein, FANCG, is a phosphoprotein and is upregulated with FANCA after TNF-α treatment
    Futaki, M
    Watanabe, S
    Kajigaya, S
    Liu, JM
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 281 (02) : 347 - 351
  • [47] Fanconi Anemia Complementation Group FANCD2 Protein Serine 331 Phosphorylation Is Important for Fanconi Anemia Pathway Function and BRCA2 Interaction
    Zhi, Gang
    Wilson, James B.
    Chen, Xiaoyong
    Krause, Diane S.
    Xiao, Yuxuan
    Jones, Nigel J.
    Kupfer, Gary M.
    CANCER RESEARCH, 2009, 69 (22) : 8775 - 8783
  • [48] Fanconi anemia group A and C double-mutant mice: Functional evidence for a multi-protein Fanconi anemia complex
    Noll, M
    Battaile, KP
    Bateman, R
    Lax, TP
    Rathbun, K
    Reifsteck, C
    Bagby, G
    Finegold, M
    Olson, S
    Grompe, M
    EXPERIMENTAL HEMATOLOGY, 2002, 30 (07) : 679 - 688
  • [49] Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A
    Ravera, Silvia
    Vaccaro, Daniele
    Cuccarolo, Paola
    Columbaro, Marta
    Capanni, Cristina
    Bartolucci, Martina
    Panfoli, Isabella
    Morelli, Alessandro
    Dufour, Carlo
    Cappelli, Enrico
    Degan, Paolo
    BIOCHIMIE, 2013, 95 (10) : 1828 - 1837
  • [50] Positional cloning of the Fanconi Anemia complementation group D (FANCD) gene.
    Timmers, CD
    Hejna, JA
    Reifsteck, C
    Olson, SB
    Moses, RE
    Thayer, MJ
    Grompe, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A20 - A20
12345