Rod Chalk
Postdoctoral Scientist (Mass Spectrometry)
Recent publications
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome.
Journal article
Miller KA. et al, (2024), J Med Genet, 61, 490 - 501
Regulation of inositol 5-phosphatase activity by the C2 domain of SHIP1 and SHIP2.
Journal article
Bradshaw WJ. et al, (2024), Structure, 32, 453 - 466.e6
Structural basis of the mechanism and inhibition of a human ceramide synthase
Preprint
Pascoa TC. et al, (2023)
Regulation of inositol 5-phosphatase activity by the C2 domain of SHIP1 and SHIP2
Preprint
Bradshaw WJ. et al, (2023)
