Conditional deletion of Scrib gene in the developing myocardium leads to congenital heart defects

被引：0
|
作者：
Henderson, D. J. [1 ]
Boczonadi, V. [1 ]
Humbert, P. [2 ]
Chaudhry, B. [1 ]
机构：
[1] Newcastle Univ, Inst Med Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Peter Macallum Canc Ctr, Melbourne, Vic, Australia
来源：
CARDIOVASCULAR RESEARCH | 2012年 / 93卷
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：
引用
收藏
页码：S9 / S9
页数：1
相关论文
共 50 条
  • [31] Conditional Deletion of Fgfr3 in Chondrocytes leads to Osteoarthritis-like Defects in Temporomandibular Joint of Adult Mice
    Zhou, Siru
    Xie, Yangli
    Li, Wei
    Huang, Junlan
    Wang, Zuqiang
    Tang, Junzhou
    Xu, Wei
    Sun, Xianding
    Tan, Qiaoyan
    Huang, Shuo
    Luo, Fengtao
    Xu, Meng
    Wang, Jun
    Wu, Tingting
    Chen, Liang
    Chen, Hangang
    Su, Nan
    Du, Xiaolan
    Shen, Yue
    Chen, Lin
    SCIENTIFIC REPORTS, 2016, 6
  • [32] Conditional Deletion of Fgfr3 in Chondrocytes leads to Osteoarthritis-like Defects in Temporomandibular Joint of Adult Mice
    Siru Zhou
    Yangli Xie
    Wei Li
    Junlan Huang
    Zuqiang Wang
    Junzhou Tang
    Wei Xu
    Xianding Sun
    Qiaoyan Tan
    Shuo Huang
    Fengtao Luo
    Meng Xu
    Jun Wang
    Tingting Wu
    Liang chen
    Hangang Chen
    Nan Su
    Xiaolan Du
    Yue Shen
    Lin Chen
    Scientific Reports, 6
  • [33] Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects
    Volcik, KA
    Zhu, HP
    Finnell, RH
    Shaw, GM
    Canfield, M
    Lammer, EJ
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 126A (02) : 215 - 217
  • [34] Conditional Double Deletion of Dnmt3a and Dnmt3b in the Second Heart Field Progenitors Ameliorates Maternal Diabetes-Induced Congenital Heart Defects.
    Yang, Penghua
    Yang, Peixin
    REPRODUCTIVE SCIENCES, 2019, 26 : 106A - 106A
  • [35] Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
    Devriendt, K
    Matthijs, G
    Van Dael, R
    Gewillig, M
    Eyskens, B
    Hjalgrim, H
    Dolmer, B
    McGaughran, J
    Bröndum-Nielsen, K
    Marynen, P
    Fryns, JP
    Vermeesch, JR
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (04) : 1119 - 1126
  • [36] Loss of MicroRNAs in Neural Crest Leads to Cardiovascular Syndromes Resembling Human Congenital Heart Defects
    Huang, Zhan-Peng
    Chen, Jian-Fu
    Regan, Jenna N.
    Maguire, Colin T.
    Tang, Ru-Hang
    Dong, Xiu Rong
    Majesky, Mark W.
    Wang, Da-Zhi
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2010, 30 (12) : 2575 - U485
  • [37] Screening for 22q11 deletion syndrome among patients with congenital heart defects
    Machado Rosa, Rafael Fabiano
    Manique Rosa, Rosana Cardoso
    Trevisan, Patricia
    Graziadio, Carla
    Varella-Garcia, Marileila
    Paskulin, Giorgio Adriano
    Gazzola Zen, Paulo Ricardo
    SAO PAULO MEDICAL JOURNAL, 2014, 132 (02): : 125 - 126
  • [38] Conditional Deletion of the Itgb4 Integrin Gene in Schwann Cells Leads to Delayed Peripheral Nerve Regeneration
    Van der Zee, Catharina E. E. M.
    Kreft, Maaike
    Beckers, Gaby
    Kuipers, Arthur
    Sonnenberg, Arnoud
    JOURNAL OF NEUROSCIENCE, 2008, 28 (44): : 11292 - 11303
  • [39] Conditional deletion of NMNAT1 in the murine cone photoreceptor leads to severe cone degeneration with distinct neural circuitry defects
    Ramasamy, Saminathabn
    Kolandaivelu, Saravanan
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2023, 64 (08)
  • [40] Hospital Mortality and Adverse Events Following Repair of Congenital Heart Defects in Developing Countries
    Bateson, Brian P. P.
    Deng, Luqin
    Ange, Brittany
    Austin, Erle
    Dabal, Robert
    Broser, Taylor
    Pennington, John
    Sivakumar, Sivalingam
    Lee, Cheul
    Truong, Nguyen Ly Thinh
    Jacobs, Jeffery
    Cervantes, Jorge
    Kirklin, James K. K.
    St Louis, James
    WORLD JOURNAL FOR PEDIATRIC AND CONGENITAL HEART SURGERY, 2023, 14 (06) : 701 - 707
12345