Publicacións en colaboración con investigadores/as de University of Massachusetts Medical School (13)

2025

  1. Absence of MCJ/DnaJC15 promotes brown adipose tissue thermogenesis

    Nature communications, Vol. 16, Núm. 1, pp. 229

2024

  1. AI is a viable alternative to high throughput screening: a 318-target study

    Scientific Reports, Vol. 14, Núm. 1

  2. Correction to: AI is a viable alternative to high throughput screening: a 318-target study (Scientific Reports, (2024), 14, 1, (7526), 10.1038/s41598-024-54655-z)

    Scientific Reports

  3. Effect of sodium–glucose co-transporter-2 inhibitors on survival free of organ support in patients hospitalised for COVID-19 (ACTIV-4a): a pragmatic, multicentre, open-label, randomised, controlled, platform trial

    The Lancet Diabetes and Endocrinology, Vol. 12, Núm. 10, pp. 725-734

2023

  1. Hypothalamic JNK1-hepatic fatty acid synthase axis mediates a metabolic rewiring that prevents hepatic steatosis in male mice treated with olanzapine via intraperitoneal: Additional effects of PTP1B inhibition

    Redox Biology, Vol. 63

2020

  1. Neutrophil infiltration regulates clock-gene expression to organize daily hepatic metabolism

    eLife, Vol. 9

2017

  1. Hypothalamic AMPK-ER Stress-JNK1 Axis Mediates the Central Actions of Thyroid Hormones on Energy Balance

    Cell Metabolism, Vol. 26, Núm. 1, pp. 212-229.e12

2016

  1. Genomic insights into the Ixodes scapularis tick vector of Lyme disease

    Nature Communications, Vol. 7

  2. Hydrophobic CDR3 residues promote the development of self-reactive T cells

    Nature Immunology, Vol. 17, Núm. 8, pp. 946-955

2014

  1. A unified nomenclature and amino acid numbering for human PTEN

    Science Signaling, Vol. 7, Núm. 332

2013

  1. Central melanin-concentrating hormone influences liver and adipose metabolism via specific hypothalamic nuclei and efferent autonomic/JNK1 pathways

    Gastroenterology, Vol. 144, Núm. 3

2010

  1. PKCζ-regulated inflammation in the nonhematopoietic compartment is critical for obesity-induced glucose intolerance

    Cell Metabolism, Vol. 12, Núm. 1, pp. 65-77

2007

  1. Cooperation between p27 and p107 during endochondral ossification suggests a genetic pathway controlled by p27 and p130

    Molecular and Cellular Biology, Vol. 27, Núm. 14, pp. 5161-5171