We are seeking highly motivated postdoctoral fellow candidates to join the laboratory of Brett McCray, MD, PhD, at the University of Michigan to lead studies elucidating mechanisms of hereditary neuromuscular disease. Our primary focus is on diseases caused by mutations in the ion channel TRPV4, which result in Charcot-Marie-Tooth disease type 2C and related forms of spinal muscular atrophy. In collaboration with Dr. McCray and other members of the laboratory, the fellow will contribute to the design, management, coordination, and implementation of in vitro and in vivo studies focused on defining mechanisms of disease pathogenesis. Specific potential pathogenic mechanisms to explore include the role of TRPV4 in regulating actin cytoskeletal dynamics and the integrity of blood-brain barriers. Candidates should have a doctoral degree and strong research background with expertise in molecular and cellular biology. This is an interdisciplinary project with opportunities to learn new skills in biochemistry and molecular and cellular biology, including fluorescence microscopy, live-cell imaging, ratiometric calcium imaging, transcriptomics, proteomics, mammalian cell culture, induced pluripotent stem cell culture/differentiation, utilization of microfluidic devices, immunohistochemistry, and mouse models of disease. Opportunities to become involved in clinical research projects are also available.