MANUEL
PORTERO OTIN
CU
![Foto de MANUEL](/img/nophoto.png)
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Universitat de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Universitat de Barcelona (46)
2024
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Glycogen accumulation modulates life span in a mouse model of amyotrophic lateral sclerosis
Journal of Neurochemistry, Vol. 168, Núm. 5, pp. 744-759
2023
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Ether Lipid-Mediated Antioxidant Defense in Alzheimer’s Disease
Antioxidants, Vol. 12, Núm. 2
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Lipid Adaptations against Oxidative Challenge in the Healthy Adult Human Brain
Antioxidants, Vol. 12, Núm. 1
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Lipidomic Alterations in the Cerebral Cortex and White Matter in Sporadic Alzheimer’s Disease
Aging and Disease, Vol. 14, Núm. 5, pp. 1887-1916
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Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity
The Journal of clinical investigation, Vol. 133, Núm. 10
2022
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A motor neuron disease mouse model reveals a non-canonical profile of senescence biomarkers
Disease models & mechanisms, Vol. 15, Núm. 8
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Activating cannabinoid receptor 2 preserves axonal health through GSK-3β/NRF2 axis in adrenoleukodystrophy
Acta Neuropathologica, Vol. 144, Núm. 2, pp. 241-258
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Cardiac fibroblasts display endurance to ischemia, high ROS control and elevated respiration regulated by the JAK2/STAT pathway
FEBS Journal, Vol. 289, Núm. 9, pp. 2540-2561
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Modulation of mitochondrial and inflammatory homeostasis through RIP140 is neuroprotective in an adrenoleukodystrophy mouse model
Neuropathology and Applied Neurobiology, Vol. 48, Núm. 1
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Selective brain regional changes in lipid profile with human aging
GeroScience, Vol. 44, Núm. 2, pp. 763-783
2021
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Age-related changes in lipidome of rat frontal cortex and cerebellum are partially reversed by methionine restriction applied in old age
International Journal of Molecular Sciences, Vol. 22, Núm. 22
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Cell stress induces mislocalization of transcription factors with mitochondrial enrichment
International Journal of Molecular Sciences, Vol. 22, Núm. 16
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Lipid alterations in human frontal cortex in ALS-FTLD-TDP43 proteinopathy spectrum are partly related to peroxisome impairment
Neuropathology and Applied Neurobiology, Vol. 47, Núm. 4, pp. 544-563
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Lipidomic traits of plasma and cerebrospinal fluid in amyotrophic lateral sclerosis correlate with disease progression
Brain Communications, Vol. 3, Núm. 3
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New insights into human prefrontal cortex aging with a lipidomics approach
Expert Review of Proteomics, Vol. 18, Núm. 5, pp. 333-344
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The causal role of lipoxidative damage in mitochondrial bioenergetic dysfunction linked to alzheimer’s disease pathology
Life, Vol. 11, Núm. 5
2020
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Gender-Specific Beneficial Effects of Docosahexaenoic Acid Dietary Supplementation in G93A-SOD1 Amyotrophic Lateral Sclerosis Mice
Neurotherapeutics, Vol. 17, Núm. 1, pp. 269-281
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Selected cryptic exons accumulate in hippocampal cell nuclei in Alzheimer's disease with and without associated TDP-43 proteinopathy
Brain
2019
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Altered dynein axonemal assembly factor 1 expression in C-boutons in bulbar and spinal cord motor-neurons in sporadic amyotrophic lateral sclerosis
Journal of Neuropathology and Experimental Neurology, Vol. 78, Núm. 5, pp. 416-425
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Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot Study
Neurotherapeutics, Vol. 16, Núm. 4, pp. 1167-1182