G. R. Wilson

发表

Expression and localization of the Parkin Co-Regulated Gene in mouse CNS suggests a role in ependymal cilia function

P. Lockhart, M. Delatycki, Juliet M. Taylor, 2009, Neuroscience Letters.

Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse.

P. Lockhart, G. Egan, M. Delatycki, 2010, Human molecular genetics.

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

P. Lockhart, S. Haas, K. Hogan, 2014, American journal of human genetics.

Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue

P. Lockhart, M. Oulad-Abdelghani, D. Finkelstein, 2019, Molecular Brain.

ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible

P. Lockhart, L. Gurrin, M. Aitken, 2012, European Journal of Human Genetics.

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

P. Lockhart, M. Bahlo, D. Amor, 2018, bioRxiv.

Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease.

P. Lockhart, E. Stanley, A. Elefanty, 2018, Stem cell research.

Generation of RAB 39 B knockout isogenic human embryonic stem cell lines to model RAB 39 B-mediated Parkinson ' s disease

P. Lockhart, E. Stanley, A. Elefanty, 2018 .

Molecular analysis of the PArkin co-regulated gene and association with male infertility.

P. Lockhart, M. Delatycki, M. O’Bryan, 2010, Fertility and sterility.