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1.
The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations.
Hum Mol Genet
; 25(14): 2972-2984, 2016 07 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-27206984
2.
COUP-TFI controls activity-dependent tyrosine hydroxylase expression in adult dopaminergic olfactory bulb interneurons.
Development
; 140(24): 4850-9, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24227652
3.
New AAV9 engineered variants with enhanced neurotropism and reduced liver off-targeting in mice and marmosets.
iScience
; 27(5): 109777, 2024 May 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-38711458
4.
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A.
Stem Cell Res
; 77: 103406, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38552355
5.
Synthesis and Preliminary Characterization of Putative Anle138b-Centered PROTACs against α-Synuclein Aggregation.
Pharmaceutics
; 15(5)2023 May 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37242709
6.
MCT1-dependent energetic failure and neuroinflammation underlie optic nerve degeneration in Wolfram syndrome mice.
Elife
; 122023 01 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-36645345
7.
Enhanced production of mesencephalic dopaminergic neurons from lineage-restricted human undifferentiated stem cells.
Nat Commun
; 14(1): 7871, 2023 Dec 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-38052784
8.
Modeling native and seeded Synuclein aggregation and related cellular dysfunctions in dopaminergic neurons derived by a new set of isogenic iPSC lines with SNCA multiplications.
Cell Death Dis
; 13(10): 881, 2022 10 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-36261424
9.
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.
Cell Rep
; 40(3): 111124, 2022 07 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-35858578
10.
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome.
Stem Cell Res
; 50: 102151, 2021 Jan 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33434818
11.
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives.
Front Neurol
; 12: 648916, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34168607
12.
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs.
Stem Cell Reports
; 16(8): 1953-1967, 2021 08 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34329598
13.
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON).
Stem Cell Res
; 48: 101939, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32771908
14.
Whole brain delivery of an instability-prone Mecp2 transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome.
Elife
; 92020 03 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-32207685
15.
Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons.
Nat Commun
; 11(1): 4178, 2020 08 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-32826895
16.
Reconstitution of the Human Nigro-striatal Pathway on-a-Chip Reveals OPA1-Dependent Mitochondrial Defects and Loss of Dopaminergic Synapses.
Cell Rep
; 29(13): 4646-4656.e4, 2019 12 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-31875567
17.
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models.
Cell Rep
; 22(8): 2066-2079, 2018 02 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-29466734
18.
Two factor-based reprogramming of rodent and human fibroblasts into Schwann cells.
Nat Commun
; 8: 14088, 2017 02 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28169300
19.
Rapid and efficient CRISPR/Cas9 gene inactivation in human neurons during human pluripotent stem cell differentiation and direct reprogramming.
Sci Rep
; 6: 37540, 2016 11 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-27857203
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