Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.
22q11 deletion syndrome (22q11DS) is characterised by aberrant development of the pharyngeal apparatus and the heart with haploinsufficiency of the transcription factor TBX1 being considered the major underlying cause of the disease. Tbx1 mutations in mouse phenocopy the disorder. In order to identi...
Những tác giả chính: | van Bueren, K, Papangeli, I, Rochais, F, Pearce, K, Roberts, C, Calmont, A, Szumska, D, Kelly, R, Bhattacharya, S, Scambler, P |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
2010
|
Những quyển sách tương tự
-
Dissecting the embryonic requirement of the Notch pathway gene, Hes1, in the context of DiGeorge syndrome
Bằng: Papangeli, I, et al.
Được phát hành: (2009) -
HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region.
Bằng: Dykes, I, et al.
Được phát hành: (2014) -
HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region
Bằng: Dykes, IM, et al.
Được phát hành: (2014) -
Defective Vagal Innervation in Murine Tbx1 Mutant Hearts
Bằng: Amélie Calmont, et al.
Được phát hành: (2018-09-01) -
Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.
Bằng: Murim Choi, et al.
Được phát hành: (2009-02-01)