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Andres D Klein
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RIPK3 as a potential therapeutic target for Gaucher's disease
EB Vitner, R Salomon, T Farfel-Becker, A Meshcheriakova, M Ali, ...
Nature medicine 20 (2), 204-208, 2014
1962014
Imatinib therapy blocks cerebellar apoptosis and improves neurological symptoms in a mouse model of Niemann‐Pick type C disease
AR Alvarez, A Klein, J Castro, GI Cancino, J Amigo, M Mosqueira, ...
The FASEB Journal 22 (10), 3617-3627, 2008
1622008
Is Parkinson’s disease a lysosomal disorder?
AD Klein, JR Mazzulli
Brain 141 (8), 2255-2262, 2018
1592018
Brain disorders due to lysosomal dysfunction
A Fraldi, AD Klein, DL Medina, C Settembre
Annual review of neuroscience 39, 277-295, 2016
1542016
Anatomically defined neuron-based rescue of neurodegenerative Niemann–Pick type C disorder
ME Lopez, AD Klein, UJ Dimbil, MP Scott
Journal of Neuroscience 31 (12), 4367-4378, 2011
1092011
Oxidative stress activates the c-Abl/p73 proapoptotic pathway in Niemann-Pick type C neurons
A Klein, C Maldonado, LM Vargas, M Gonzalez, F Robledo, KP de Arce, ...
Neurobiology of disease 41 (1), 209-218, 2011
772011
NPC2 is expressed in human and murine liver and secreted into bile: potential implications for body cholesterol homeostasis
A Klein, L Amigo, MJ Retamal, MG Morales, JF Miquel, A Rigotti, ...
Hepatology 43 (1), 126-133, 2006
752006
Delineating pathological pathways in a chemically induced mouse model of Gaucher disease
A Vardi, H Zigdon, A Meshcheriakova, AD Klein, C Yaacobi, R Eilam, ...
The Journal of pathology 239 (4), 496-509, 2016
672016
Identification of modifier genes in a mouse model of Gaucher disease
AD Klein, NS Ferreira, S Ben-Dor, J Duan, J Hardy, TM Cox, AH Merrill, ...
Cell reports 16 (10), 2546-2553, 2016
662016
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy
MB Mosbech, ASB Olsen, D Neess, O Ben‐David, LL Klitten, J Larsen, ...
Annals of clinical and translational neurology 1 (2), 88-98, 2014
542014
Lysosomal vitamin E accumulation in Niemann–Pick type C disease
LF Yévenes, A Klein, JF Castro, T Marín, N Leal, F Leighton, AR Alvarez, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (2), 150-160, 2012
532012
Npc1 deficiency in the C57BL/6J genetic background enhances Niemann–Pick disease type C spleen pathology
J Parra, AD Klein, J Castro, MG Morales, M Mosqueira, I Valencia, ...
Biochemical and biophysical research communications 413 (3), 400-406, 2011
522011
Neuronal and epithelial cell rescue resolves chronic systemic inflammation in the lipid storage disorder Niemann-Pick C
ME Lopez, AD Klein, J Hong, UJ Dimbil, MP Scott
Human molecular genetics 21 (13), 2946-2960, 2012
492012
Complement is dispensable for neurodegeneration in Niemann-Pick disease type C
ME Lopez, AD Klein, MP Scott
Journal of neuroinflammation 9, 1-8, 2012
462012
Lysosomal storage disorders: old diseases, present and future challenges
AD Klein, AH Futerman
Pediatr Endocrinol Rev 11 (Suppl 1), 59-63, 2013
422013
Disruption in Connexin-Based Communication Is Associated with Intracellular Ca2+ Signal Alterations in Astrocytes from Niemann-Pick Type C Mice
PJ Sáez, JA Orellana, N Vega-Riveros, VA Figueroa, DE Hernández, ...
PLoS One 8 (8), e71361, 2013
402013
Rare diseases in Chile: challenges and recommendations in universal health coverage context
G Encina, C Castillo-Laborde, JA Lecaros, K Dubois-Camacho, ...
Orphanet Journal of Rare Diseases 14, 1-8, 2019
322019
Cholinergic abnormalities, endosomal alterations and up-regulation of nerve growth factor signaling in Niemann-Pick type C disease
C Cabeza, A Figueroa, OM Lazo, C Galleguillos, C Pissani, A Klein, ...
Molecular neurodegeneration 7, 1-18, 2012
322012
c-Abl inhibition activates TFEB and promotes cellular clearance in a lysosomal disorder
PS Contreras, PJ Tapia, L González-Hódar, I Peluso, C Soldati, ...
Iscience 23 (11), 2020
302020
The unique case of the Niemann-Pick type C cholesterol storage disorder
AD Klein, A Alvarez, S Zanlungo
Pediatr. Endocrinol. Rev 12, 166-175, 2014
262014
O sistema não pode executar a operação agora. Tente novamente mais tarde.
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