Role of microRNAs in the Regulation of α-Synuclein Expression: A Systematic Review

by Recasens, Ariadna, Perier, Celine, Sue, Carolyn M.
Published 2016

A comparison of current serum biomarkers as diagnostic indicators of mitochondrial diseases

by Davis, Ryan L., Liang, Christina, Sue, Carolyn M.
Published 2016

Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction

by Park, Jin-Sung, Koentjoro, Brianada, Veivers, David, Mackay-Sim, Alan, Sue, Carolyn M.
Published 2014

Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia

by Fan, Yongjun, Wali, Gautam, Sutharsan, Ratneswary, Bellette, Bernadette, Crane, Denis I., Sue, Carolyn M., Mackay-Sim, Alan
Published 2014

Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia

by Wali, Gautam, Sutharsan, Ratneswary, Fan, Yongjun, Stewart, Romal, Tello Velasquez, Johana, Sue, Carolyn M, Crane, Denis I., Mackay-Sim, Alan
Published 2016

Variance of Gene Expression Identifies Altered Network Constraints in Neurological Disease

by Mar, Jessica C., Matigian, Nicholas A., Mackay-Sim, Alan, Mellick, George D., Sue, Carolyn M., Silburn, Peter A., McGrath, John J., Quackenbush, John, Wells, Christine A.
Published 2011

A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations

by Abrahamsen, Greger, Fan, Yongjun, Matigian, Nicholas, Wali, Gautam, Bellette, Bernadette, Sutharsan, Ratneswary, Raju, Jyothy, Wood, Stephen A., Veivers, David, Sue, Carolyn M., Mackay-Sim, Alan
Published 2013

A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations

by Abrahamsen, Greger, Fan, Yongjun, Matigian, Nicholas, Wali, Gautam, Bellette, Bernadette, Sutharsan, Ratneswary, Raju, Jyothy, Wood, Stephen A., Veivers, David, Sue, Carolyn M., Mackay-Sim, Alan
Published 2015

Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing

by Kumar, Kishore R, Wali, G.M., Kamate, Mahesh, Wali, Gautam, Minoche, André E, Puttick, Clare, Pinese, Mark, Gayevskiy, Velimir, Dinger, Marcel E, Roscioli, Tony, Sue, Carolyn M., Cowley, Mark J
Published 2016

Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1

by Tomlinson, Susan Elizabeth, Rajakulendran, Sanjeev, Tan, Stella Veronica, Graves, Tracey Dawn, Bamiou, Doris-Eva, Labrum, Robyn W, Burke, David, Sue, Carolyn M, Giunti, Paola, Schorge, Stephanie, Kullmann, Dimitri M, Hanna, Michael G
Published 2013

Thioredoxin interacting protein (TXNIP) regulates tubular autophagy and mitophagy in diabetic nephropathy through the mTOR signaling pathway

by Huang, Chunling, Zhang, Yuan, Kelly, Darren J., Tan, Christina Y. R., Gill, Anthony, Cheng, Delfine, Braet, Filip, Park, Jin-Sung, Sue, Carolyn M., Pollock, Carol A., Chen, Xin-Ming
Published 2016

C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients

by Dobson-Stone, Carol, Hallupp, Marianne, Loy, Clement T., Thompson, Elizabeth M., Haan, Eric, Sue, Carolyn M., Panegyres, Peter K., Razquin, Cristina, Seijo-Martínez, Manuel, Rene, Ramon, Gascon, Jordi, Campdelacreu, Jaume, Schmoll, Birgit, Volk, Alexander E., Brooks, William S., Schofield, Peter R., Pastor, Pau, Kwok, John B. J.
Published 2013