S. Hindle

发表

Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease

C. Elliott, S. Hindle, 2013, Autophagy.

Invertebrate models of lysosomal storage disease: what have we learned so far?

S. Sweeney, Sarita Hebbar, S. Hindle, 2011, Invertebrate Neuroscience.

The Drosophila surface glia transcriptome: evolutionary conserved blood-brain barrier processes

M. Eddison, Zeid M. Rusan, R. Bainton, 2014, Front. Neurosci..

Lipid metabolic perturbation is an early-onset phenotype in adult spinster mutants: a Drosophila model for lysosomal storage disorders

D. Schwudke, Avinash Khandelwal, J. Yew, 2016, bioRxiv.

Evolutionarily Conserved Roles for Blood-Brain Barrier Xenobiotic Transporters in Endogenous Steroid Partitioning and Behavior.

Michael J. Keiser, H. Ishimoto, T. Kitamoto, 2017, Cell reports.

Evolutionarily conserved roles for blood-brain barrier xenobiotic transporters in endogenous steroid partitioning and behavior

Michael J. Keiser, H. Ishimoto, T. Kitamoto, 2017, bioRxiv.

Dopaminergic expression of the Parkinsonian gene LRRK2-G2019S leads to non-autonomous visual neurodegeneration, accelerated by increased neural demands for energy

C. Elliott, S. Sweeney, M. Stark, 2013, Human molecular genetics.

Barrier mechanisms in the Drosophila blood-brain barrier

R. Bainton, S. Hindle, 2014, Front. Neurosci..

A saposin deficiency model in Drosophila: Lysosomal storage, progressive neurodegeneration and sensory physiological decline

D. Schwudke, C. Elliott, S. Sweeney, 2017, Neurobiology of Disease.

A Saposin deficiency model in Drosophila: lysosomal storage, progressive neurodegeneration, sensory physiological decline and defective calcium homeostasis

D. Schwudke, C. Elliott, S. Sweeney, 2016, bioRxiv.

Evolutionarily conserved roles for blood-brain barrier xenobiotic transporters in endogenous steroid partitioning and behavior

Michael J. Keiser, H. Ishimoto, T. Kitamoto, 2017, bioRxiv.