Search Results - "Obis, Èlia"

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    Oxidative stress and altered lipid metabolism in Friedreich ataxia by Tamarit, Jordi, Obis, Èlia, Ros, Joaquim

    Published in Free radical biology & medicine (01-11-2016)
    “…Friedreich ataxia is a genetic disease caused by the deficiency of frataxin, a mitochondrial protein. Frataxin deficiency impacts in the cell physiology at…”
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    Frataxin deficiency in neonatal rat ventricular myocytes targets mitochondria and lipid metabolism by Obis, Èlia, Irazusta, Verónica, Sanchís, Daniel, Ros, Joaquim, Tamarit, Jordi

    Published in Free radical biology & medicine (01-08-2014)
    “…Friedreich ataxia (FRDA) is a hereditary disease caused by deficient frataxin expression. This mitochondrial protein has been related to iron homeostasis,…”
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    Metabolomics uncovers the role of adipose tissue PDXK in adipogenesis and systemic insulin sensitivity by Moreno-Navarrete, José María, Jove, Mariona, Ortega, Francisco, Xifra, Gemma, Ricart, Wifredo, Obis, Èlia, Pamplona, Reinald, Portero-Otin, Manuel, Fernández-Real, José Manuel

    Published in Diabetologia (01-04-2016)
    “…Aims/hypothesis We aimed to investigate the potential mechanisms involved in the compromised adipogenesis of visceral (VAT) vs subcutaneous adipose tissue…”
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    Frataxin Depletion in Yeast Triggers Up-regulation of Iron Transport Systems before Affecting Iron-Sulfur Enzyme Activities by Moreno-Cermeño, Armando, Obis, Èlia, Bellí, Gemma, Cabiscol, Elisa, Ros, Joaquim, Tamarit, Jordi

    Published in The Journal of biological chemistry (31-12-2010)
    “…The primary function of frataxin, a mitochondrial protein involved in iron homeostasis, remains controversial. Using a yeast model of conditional expression of…”
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    Methionine transsulfuration pathway is upregulated in long-lived humans by Mota-Martorell, Natàlia, Jové, Mariona, Borrás, Consuelo, Berdún, Rebeca, Obis, Èlia, Sol, Joaquim, Cabré, Rosanna, Pradas, Irene, Galo-Licona, José Daniel, Puig, Josep, Viña, José, Pamplona, Reinald

    Published in Free radical biology & medicine (01-01-2021)
    “…Available evidences point to methionine metabolism as a key target to study the molecular adaptive mechanisms underlying differences in longevity. The plasma…”
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    The Lipidome Fingerprint of Longevity by Jové, Mariona, Mota-Martorell, Natàlia, Pradas, Irene, Galo-Licona, José Daniel, Martín-Gari, Meritxell, Obis, Èlia, Sol, Joaquim, Pamplona, Reinald

    Published in Molecules (Basel, Switzerland) (22-09-2020)
    “…Lipids were determinants in the appearance and evolution of life. Recent studies disclose the existence of a link between lipids and animal longevity. Findings…”
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    Methionine Metabolism Is Down-Regulated in Heart of Long-Lived Mammals by Mota-Martorell, Natalia, Jové, Mariona, Berdún, Rebeca, Òbis, Èlia, Barja, Gustavo, Pamplona, Reinald

    Published in Biology (Basel, Switzerland) (14-12-2022)
    “…Methionine constitutes a central hub of intracellular metabolic adaptations leading to an extended longevity (maximum lifespan). The present study follows a…”
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    Ether Lipid-Mediated Antioxidant Defense in Alzheimer's Disease by Jové, Mariona, Mota-Martorell, Natàlia, Obis, Èlia, Sol, Joaquim, Martín-Garí, Meritxell, Ferrer, Isidre, Portero-Otin, Manuel, Pamplona, Reinald

    Published in Antioxidants (28-01-2023)
    “…One of the richest tissues in lipid content and diversity of the human body is the brain. The human brain is constitutively highly vulnerable to oxidative…”
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    Lipid alterations in human frontal cortex in ALS‐FTLD‐TDP43 proteinopathy spectrum are partly related to peroxisome impairment by Andrés‐Benito, Pol, Gelpi, Ellen, Jové, Mariona, Mota‐Martorell, Natalia, Obis, Èlia, Portero‐Otin, Manuel, Povedano, Mònica, Pujol, Aurora, Pamplona, Reinald, Ferrer, Isidro

    Published in Neuropathology and applied neurobiology (01-06-2021)
    “…Aim Peroxisomes play a key role in lipid metabolism, and peroxisome defects have been associated with neurodegenerative diseases such as X‐adrenoleukodystrophy…”
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    Lipid Adaptations against Oxidative Challenge in the Healthy Adult Human Brain by Jové, Mariona, Mota-Martorell, Natàlia, Obis, Èlia, Sol, Joaquim, Martín-Garí, Meritxell, Ferrer, Isidre, Portero-Otín, Manuel, Pamplona, Reinald

    Published in Antioxidants (12-01-2023)
    “…It is assumed that the human brain is especially susceptible to oxidative stress, based on specific traits such as a higher rate of mitochondrial free radical…”
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    Metabolomic Profiling in Children with Celiac Disease: Beyond the Gluten-Free Diet by Martín-Masot, Rafael, Jiménez-Muñoz, María, Herrador-López, Marta, Navas-López, Víctor Manuel, Obis, Elia, Jové, Mariona, Pamplona, Reinald, Nestares, Teresa

    Published in Nutrients (25-06-2023)
    “…Celiac disease (CD) is included in the group of complex or multifactorial diseases, i.e., those caused by the interaction of genetic and environmental factors…”
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    Analysis of oxidative stress-induced protein carbonylation using fluorescent hydrazides by Tamarit, Jordi, de Hoogh, Anouk, Obis, Elia, Alsina, David, Cabiscol, Elisa, Ros, Joaquim

    Published in Journal of proteomics (27-06-2012)
    “…Protein carbonyl detection has been commonly used to analyze the degree of damage to proteins under oxidative stress conditions. Most laboratories rely on…”
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    Apoptotic cell death and altered calcium homeostasis caused by frataxin depletion in dorsal root ganglia neurons can be prevented by BH4 domain of Bcl-xL protein by Mincheva-Tasheva, Stefka, Obis, Elia, Tamarit, Jordi, Ros, Joaquim

    Published in Human molecular genetics (01-04-2014)
    “…Friedreich ataxia (FRDA) is a neurodegenerative disease characterized by a decreased expression of the mitochondrial protein frataxin. Major neurological…”
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    Apoptotic cell death and altered calcium homeostasis caused by frataxin depletion in dorsal root ganglia neurons can be prevented by BH4 domain of Bcl-x sub(L) protein by Mincheva-Tasheva, Stefka, Obis, Elia, Tamarit, Jordi, Ros, Joaquim

    Published in Human molecular genetics (01-04-2014)
    “…Friedreich ataxia (FRDA) is a neurodegenerative disease characterized by a decreased expression of the mitochondrial protein frataxin. Major neurological…”
    Get full text
    Journal Article