SNPs talk to genes using landlines: long-range chromatin interactions link genetic risk with epigenetic patterns in Takayasu arteritis
نویسندگان
چکیده
منابع مشابه
Takayasu arteritis in a young female
Background: Takayasu arteritis is a granulomatous vasculitis which mainly involves the large arterial vessels. The disease is rare and it is more common in females aged between 15-30 years old. In this paper, we report a case of takayasu arteritis in Babol, north of Iran. Case Presentation: A 22 - year old female was admitted to the Department of Infectious Diseases of Rouhani Teaching Hospital...
متن کاملMyocarditis associated with Takayasu arteritis.
This work was supported by the Stiftung Mainzer Herz and the Robert Müller Stiftung. Further support was provided by the Center for Translational Vascular Biology (CTVB), the German Center vor Cardiovascular Research (DZHK), and the Center for Thrombosis and Hemostasis (CTH). T.M. is PI oft he DZHK. C.M. is supported by the Deutsche Forschungsgemeinschaft (DFG; Heisenberg Programm and SFB 894),...
متن کاملTakayasu arteritis in pregnancy.
Takayasu arteritis is a chronic, granulomatous arteritis affecting large and medium-sized arteries. During pregnancy, maternal and foetal complications are largely as a consequence of maternal arterial hypertension. We present a case of a 35-year-old para one gravida two patient with Takayasu arteritis (group III disease) complicated by chronic hypertension and a severely dilated ascending aort...
متن کاملTakayasu arteritis in children
Takayasu arteritis (TA) is a large vessel vasculitis that usually affects young female patients during the second and third decades of life, but has been reported in children as young as 24 months of age. Aim of this report was to describe four children (two girls) with TA, as well as summarizing main published studies. The mean age at presentation of our cases was 11 years (range 8-15). Three ...
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ژورنال
عنوان ژورنال: Annals of the Rheumatic Diseases
سال: 2019
ISSN: 0003-4967,1468-2060
DOI: 10.1136/annrheumdis-2019-215957