Functional analyses of CSX/NKX2.5 mutations that cause human congenital heart disease

被引：0
|
作者：
Zhu, W [1 ]
Shiojima, I [1 ]
Oka, T [1 ]
Monzen, K [1 ]
Hiroi, Y [1 ]
Hosoda, T [1 ]
Zou, Y [1 ]
Komuro, I [1 ]
机构：
[1] Univ Tokyo, Grad Sch Med, Tokyo, Japan
来源：
CIRCULATION | 2000年 / 102卷 / 18期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
1762
引用
收藏
页码：359 / 359
页数：1
相关论文
共 50 条
  • [1] Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease
    Zhu, WD
    Shiojima, I
    Hiroi, Y
    Zou, YZ
    Akazawa, H
    Mizukami, M
    Toko, H
    Yazaki, Y
    Nagai, R
    Komuro, I
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (45) : 35291 - 35296
  • [2] Functional analysis of the mutated Csx/Nkx2.5 in patients with a congenital heart disease
    Kasahara, H
    Lee, B
    Schott, JJ
    Benson, DW
    Seidman, JG
    Seidman, CE
    Izumo, S
    [J]. CIRCULATION, 1999, 100 (18) : 354 - 354
  • [3] Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
    Kasahara, H
    Lee, B
    Schott, JJ
    Benson, DW
    Seidman, JG
    Seidman, CE
    Izumo, S
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (02): : 299 - 308
  • [4] NKX2.5 mutations in patients with congenital heart disease
    McElhinney, DB
    Geiger, E
    Blinder, J
    Benson, DW
    Goldmuntz, E
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 42 (09) : 1650 - 1655
  • [5] NKX2.5 mutations in patients with congenital heart disease (CHD)
    McElhinney, DB
    Geiger, E
    Blinder, J
    Benson, DW
    Goldmuntz, E
    [J]. CIRCULATION, 2002, 106 (19) : 166 - 167
  • [6] NKX2.5 mutations and congenital heart disease: Is it a marker of cardiac anomalies?
    Balci, Mustafa M.
    Akdemir, Ramazan
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2011, 147 (03) : E44 - E45
  • [7] NKX2.5 mutations in patients with non-syndromic congenital heart disease
    Gioli-Pereira, Luciana
    Pereira, Alexandre Costa
    Mesquita, Sonia M.
    Xavier-Neto, Jose
    Lopes, Antonio Augusto
    Krieger, Jose Eduardo
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 138 (03) : 261 - 265
  • [8] Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease
    Ikeda, Y
    Hiroi, Y
    Hosoda, T
    Utsunomiya, T
    Matsuo, S
    Ito, T
    Inoue, J
    Sumiyoshi, T
    Takano, H
    Nagai, R
    Komuro, I
    [J]. CIRCULATION JOURNAL, 2002, 66 (06) : 561 - 563
  • [9] Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
    Stallmeyer, B.
    Fenge, H.
    Nowak-Goettl, U.
    Schulze-Bahr, E.
    [J]. CLINICAL GENETICS, 2010, 78 (06) : 533 - 540
  • [10] Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease
    Tong, Yi-Fan
    [J]. GENE, 2016, 588 (01) : 86 - 94
12345