Suivre
Abraham Acevedo Arozena
Abraham Acevedo Arozena
Hospital Universitario de Canarias, ITB, CIBERNED
Adresse e-mail validée de ull.edu.es
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
13208*2021
α-Synuclein impairs macroautophagy: implications for Parkinson’s disease
AR Winslow, CW Chen, S Corrochano, A Acevedo-Arozena, DE Gordon, ...
Journal of Cell Biology 190 (6), 1023-1037, 2010
9532010
Dynein mutations impair autophagic clearance of aggregate-prone proteins
B Ravikumar, A Acevedo-Arozena, S Imarisio, Z Berger, C Vacher, ...
Nature genetics 37 (7), 771-776, 2005
5552005
Rilmenidine attenuates toxicity of polyglutamine expansions in a mouse model of Huntington's disease
C Rose, FM Menzies, M Renna, A Acevedo-Arozena, S Corrochano, ...
Human molecular genetics 19 (11), 2144-2153, 2010
2322010
ENU mutagenesis, a way forward to understand gene function
A Acevedo-Arozena, S Wells, P Potter, M Kelly, RD Cox, SDM Brown
Annu. Rev. Genomics Hum. Genet. 9, 49-69, 2008
2282008
SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments
PI Joyce, P Fratta, EMC Fisher, A Acevedo-Arozena
Mammalian Genome 22, 420-448, 2011
1652011
Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis
P Fratta, P Sivakumar, J Humphrey, K Lo, T Ricketts, H Oliveira, ...
The EMBO journal 37 (11), e98684, 2018
1542018
A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis
A Acevedo-Arozena, B Kalmar, S Essa, T Ricketts, P Joyce, R Kent, ...
Disease models & mechanisms 4 (5), 686-700, 2011
1282011
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’knockin mice
A Devoy, B Kalmar, M Stewart, H Park, B Burke, SJ Noy, Y Redhead, ...
Brain 140 (11), 2797-2805, 2017
1192017
Analysis of individual mouse activity in group housed animals of different inbred strains using a novel automated home cage analysis system
RS Bains, HL Cater, RR Sillito, A Chartsias, D Sneddon, D Concas, ...
Frontiers in behavioral neuroscience 10, 106, 2016
1182016
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease
PK Potter, MR Bowl, P Jeyarajan, L Wisby, A Blease, ME Goldsworthy, ...
Nature communications 7 (1), 12444, 2016
952016
Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis
F De Giorgio, C Maduro, EMC Fisher, A Acevedo-Arozena
Disease models & mechanisms 12 (1), dmm037424, 2019
852019
IGF-1 receptor antagonism inhibits autophagy
M Renna, CF Bento, A Fleming, FM Menzies, FH Siddiqi, B Ravikumar, ...
Human molecular genetics 22 (22), 4528-4544, 2013
832013
Colocalization of tyrosine hydroxylase and GAD65 mRNA in mesostriatal neurons
T González‐Hernández, P Barroso‐Chinea, A Acevedo, E Salido, ...
European Journal of Neuroscience 13 (1), 57-67, 2001
762001
Dyneins, autophagy, aggregation and neurodegeneration
DC Rubinsztein, B Ravikumar, A Acevedo-Arozena, S Imarisio, ...
Autophagy 1 (3), 177-178, 2005
712005
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity
PI Joyce, P Mcgoldrick, RA Saccon, W Weber, P Fratta, SJ West, N Zhu, ...
Human molecular genetics 24 (7), 1883-1897, 2015
672015
Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease
H Tateossian, S Morse, A Parker, P Mburu, N Warr, A Acevedo-Arozena, ...
Human molecular genetics 22 (13), 2553-2565, 2013
672013
Haplotype sharing suggests that a genomic segment containing six genes accounts for the pulmonary adenoma susceptibility 1 (Pas1) locus activity in mice
G Manenti, F Galbiati, R Gianni-Barrera, A Pettinicchio, A Acevedo, ...
Oncogene 23 (25), 4495-4504, 2004
572004
EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
S Tan, L Kermasson, A Hoslin, P Jaako, A Faille, A Acevedo-Arozena, ...
Blood, The Journal of the American Society of Hematology 134 (3), 277-290, 2019
512019
Loss-of-function mutations in FRRS1L lead to an epileptic-dyskinetic encephalopathy
M Madeo, M Stewart, Y Sun, N Sahir, S Wiethoff, I Chandrasekar, ...
The American Journal of Human Genetics 98 (6), 1249-1255, 2016
492016
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