Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy
Gene knockout of the KCNJ8-encoded Kir6.1 KATP channel imparts fatal susceptibility to endotoxemia
Opposing roles for p16Ink4a and p19Arf in senescence and ageing caused by BubR1 insufficiency
A Lift of the Schur and Hall-Littlewood Bases to Non-commutative Symmetric Functions
