基本信息
浏览量:6
职业迁徙
个人简介
Our goal is to elucidate the genetic and developmental basis of congenital malformations. The majority of our work is currently focussed upon cardiovascular development. Previous and current work indicates that analysis of human congenital malformation can uncover novel genetic mechanisms and offer insights into general mechanisms of development and even common disease. For instance, the deletion 22q11.2 causing a birth defect syndrome is the greatest known genetic risk factor for schizophrenia (previously known as DiGeorge syndrome). Three genes under investigation (Tbx1, Chd7 and Hira) have roles in control of transcription within progenitor or stem cell populations. Others, e.g. Semaphorins, Slits, and CXCL12 are involved in intercellular signalling. In particular, the CXCL12 pathway is involved in the development of the coronary arteries and this pathway is of interest in the development of new therapies designed to assist revascularization.
研究兴趣
论文共 539 篇作者统计合作学者相似作者
按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Daniyal J Jafree,Charith Perera, Mary Ball,Daniele Tolomeo,Gideon Pomeranz,Laura Wilson,Benjamin Davis,William J Mason, Eva Maria Funk,Maria Kolatsi-Joannou, Radu Polschi,Saif Malik,Benjamin J Stewart,Karen L Price,Hannah Mitchell,Reza Motallebzadeh,Yoshiharu Muto, Robert Lees, Sarah Needham,Dale Moulding, Jennie C Chandler,Claire L Walsh,Adrian S Woolf,Paul J D Winyard,Peter J Scambler,René Hägerling,Menna R Clatworthy,Benjamin D Humphreys,Mark F Lythgoe,Simon Walker-Samuel,David A Long
crossref(2024)
Journal of molecular and cellular cardiology (2023): 102-102
Cardiovascular researchno. 11 (2023): 2089-2105
Daniyal Jafree,Kevin Cao, Aleksandra Letunovska, Radu Polschi,Reem Al-Saadi,Guillaume Morcrette, Bonnie Man,Paul Winyard,Peter Scambler,Ciaran Hutchinson,Naima Smeulders,Tanzina Chowdhury,Kathy Pritchard-Jones,David Long
PEDIATRIC BLOOD & CANCER (2023)
引用0浏览0引用
0
0
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2023): 102-102
引用0浏览0引用
0
0
Journal of the American Society of Nephrologyno. 11S (2022): 15-15
Journal of the American Society of Nephrologyno. 11S (2022): 39-39
The Chromosome 22q11.2 Deletion Syndromepp.54-76, (2022)
加载更多
作者统计
#Papers: 536
#Citation: 32659
H-Index: 88
G-Index: 170
Sociability: 8
Diversity: 0
Activity: 1
合作学者
合作机构
D-Core
- 合作者
- 学生
- 导师
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn