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Gonzalo Perez Siles
Gonzalo Perez Siles
Postdoctoral Researcher /Senior Hospital Scientist. ANZAC Research Institute
Verified email at sydney.edu.au
Title
Cited by
Cited by
Year
A novel dominant hyperekplexia mutation Y705C alters trafficking and biochemical properties of the presynaptic glycine transporter GlyT2
C Giménez, G Pérez-Siles, J Martínez-Villarreal, E Arribas-González, ...
Journal of Biological Chemistry 287 (34), 28986-29002, 2012
452012
Subcellular localization of the neuronal glycine transporter GLYT2 in brainstem
E Núñez, G Pérez‐Siles, L Rodenstein, P Alonso‐Torres, F Zafra, ...
Traffic 10 (7), 829-843, 2009
342009
Molecular basis of the differential interaction with lithium of glycine transporters GLYT1 and GLYT2
G Pérez‐Siles, A Morreale, A Leo‐Macías, G Pita, ÁR Ortíz, C Aragón, ...
Journal of neurochemistry 118 (2), 195-204, 2011
262011
Energy metabolism and mitochondrial defects in X-linked Charcot-Marie-Tooth (CMTX6) iPSC-derived motor neurons with the p. R158H PDK3 mutation
G Perez-Siles, A Cutrupi, M Ellis, R Screnci, D Mao, M Uesugi, EM Yiu, ...
Scientific Reports 10 (1), 1-13, 2020
222020
An aspartate residue in the external vestibule of GLYT2 (glycine transporter 2) controls cation access and transport coupling
G Pérez-Siles, E Núñez, A Morreale, E Jiménez, A Leo-Macías, G Pita, ...
Biochemical Journal 442 (2), 323-334, 2012
202012
Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation.
KML Perez-Siles G, Ly C, Grant A, Drew AP, Yiu EM, Ryan MM, Chuang DT, Tso ...
Neurobiology of Disease 94, 237-44, 2016
142016
Characterizing the molecular phenotype of an Atp7aT985I conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)
KML Perez-Siles G, Grant A, Ellis M, Ly C, Kidambi A, Khalil M, Llanos RM ...
Metallomics, 2016
112016
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCs
G Perez-Siles, A Cutrupi, M Ellis, J Kuriakose, S La Fontaine, D Mao, ...
Disease models & mechanisms 13 (2), 2020
92020
A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy
ML Kennerson, AC Corbett, M Ellis, G Perez-Siles, GA Nicholson
Brain, 2018
92018
Estudio estructura-función de los transportadores de glicina GLYT1 y GLYT2: identificación de una nueva mutacuón en GLYT2 en pacientes de hiperplexia hereditaria
G Pérez Siles
2011
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Articles 1–10