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...
Հիմնական հեղինակներ: | van Bueren, K, Papangeli, I, Rochais, F, Pearce, K, Roberts, C, Calmont, A, Szumska, D, Kelly, R, Bhattacharya, S, Scambler, P |
---|---|
Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2010
|
Նմանատիպ նյութեր
-
Dissecting the embryonic requirement of the Notch pathway gene, Hes1, in the context of DiGeorge syndrome
: Papangeli, I, և այլն
Հրապարակվել է: (2009) -
HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region.
: Dykes, I, և այլն
Հրապարակվել է: (2014) -
HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region
: Dykes, IM, և այլն
Հրապարակվել է: (2014) -
Defective Vagal Innervation in Murine Tbx1 Mutant Hearts
: Amélie Calmont, և այլն
Հրապարակվել է: (2018-09-01) -
Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.
: Murim Choi, և այլն
Հրապարակվել է: (2009-02-01)