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Abraham Acevedo Arozena
Abraham Acevedo Arozena
Hospital Universitario de Canarias, ITB, CIBERNED
Verified email at ull.edu.es
Title
Cited by
Cited by
Year
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
13146*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
5542005
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
2252008
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
1512018
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
1272011
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
1182017
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
842019
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
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
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
652015
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
502019
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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