Peter Heimann

Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2.

Acute pathophysiological effects of muscle-expressed Dp71 transgene on normal and dystrophic mouse muscle.

Elimination by necrosis, not apoptosis, of embryonic extraocular muscles in the muscular dysgenesis mutant of the mouse.

The structural examination of myocardial samples from patients with end-stage heart failure supported by ventricular assist devices using electron microscopy and amino acid analysis reveals low degree of reverse remodeling.

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse.

Panel 2.9: repair and recovery of health systems.

EHTP: improving health quality through health technology.

Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: implications for human motor neuron disease.

Schwann cells can be reprogrammed to multipotency by culture.

Isolation of novel multipotent neural crest-derived stem cells from adult human inferior turbinate.

Regrowing the adult brain: NF-κB controls functional circuit formation and tissue homeostasis in the dentate gyrus.

Generation of Schwann cell-derived multipotent neurospheres isolated from intact sciatic nerve.

Loss of vps54 function leads to vesicle traffic impairment, protein mis-sorting and embryonic lethality.

Pathoproteomics of testicular tissue deficient in the GARP component VPS54: The wobbler mouse model of globozoospermia.