Publikationen in Zusammenarbeit mit Forschern von Universitat de Barcelona (38)

2023

  1. MITF Downregulation Induces Death in Human Mast Cell Leukemia Cells and Impairs IgE-Dependent Degranulation

    International Journal of Molecular Sciences, Vol. 24, Núm. 4

  2. MRGPRX2 signaling involves the Lysyl-tRNA synthetase and MITF pathway

    Frontiers in Immunology, Vol. 14

  3. Pharmacological activation of insulin-degrading enzyme improves insulin secretion and glucose tolerance in diet-induced obese mice

    Diabetes, Obesity and Metabolism, Vol. 25, Núm. 11, pp. 3268-3278

2022

  1. Cannabinoid signaling modulation through JZL184 restores key phenotypes of a mouse model for Williams-Beuren syndrome

    eLife, Vol. 11

2021

  1. Mitochondrial cristae-remodeling protein OPA1 in POMC neurons couples Ca2+ homeostasis with adipose tissue lipolysis

    Cell Metabolism, Vol. 33, Núm. 9, pp. 1820-1835.e9

2020

  1. Kv1.3 blockade inhibits proliferation of vascular smooth muscle cells in vitro and intimal hyperplasia in vivo

    Translational Research, Vol. 224, pp. 40-54

  2. Machine Learning Representation of Loss of Eye Regularity in a Drosophila Neurodegenerative Model

    Frontiers in Neuroscience, Vol. 14

2019

  1. Corrigendum to Supplemental Material: ‘D242N, a K V 7.1 LQTS mutation uncovers a key residue for I Ks voltage dependence’ [Journal of Molecular and Cellular Cardiology, Volume 110, September 2017, Pages 61–69](S0022282817301633)(10.1016/j.yjmcc.2017.07.009)

    Journal of Molecular and Cellular Cardiology

  2. Autologous bone marrow expanded mesenchymal stem cells in patellar tendinopathy: Protocol for a phase I/II, single-centre, randomized with active control PRP, double-blinded clinical trial

    Journal of Orthopaedic Surgery and Research, Vol. 14, Núm. 1

  3. Cortistatin regulates glucose-induced electrical activity and insulin secretion in mouse pancreatic beta-cells

    Molecular and Cellular Endocrinology, Vol. 479, pp. 123-132

2018

  1. Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

    Gastroenterology, Vol. 154, Núm. 1, pp. 181-194.e20

2017

  1. A Population-Based Study on Congenital Disorders of Protein N- and Combined with O-Glycosylation Experience in Clinical and Genetic Diagnosis

    Journal of Pediatrics, Vol. 183, pp. 170-177.e1

  2. Chronic intermittent hypoxia mimicking sleep apnoea increases spontaneous tumorigenesis in mice

    European Respiratory Journal, Vol. 49, Núm. 2

  3. D242N, a KV7.1 LQTS mutation uncovers a key residue for IKs voltage dependence

    Journal of Molecular and Cellular Cardiology, Vol. 110, pp. 61-69

  4. Frequency and magnitude of intermittent hypoxia modulate endothelial wound healing in a cell culture model of sleep apnea

    Journal of Applied Physiology, Vol. 123, Núm. 5, pp. 1047-1054

  5. IKs computational modeling to enforce the investigation of D242N, a KV7.1 LQTS mutation

    Computing in Cardiology

  6. Obstructive Sleep Apnea and Cancer: Insights from Intermittent Hypoxia Experimental Models

    Current Sleep Medicine Reports, Vol. 3, Núm. 1, pp. 22-29

2015

  1. Epigenetic inactivation of the extracellular matrix metallopeptidase ADAMTS19 gene and the metastatic spread in colorectal cancer

    Clinical Epigenetics, Vol. 7, Núm. 1

  2. Erratum to: K+ Channels Expression in Hypertension After Arterial Injury, and Effect of Selective Kv1.3 Blockade with PAP-1 on Intimal Hyperplasia Formation [Cardiovascular Drugs and Therapy, 28, (2014), 501-511, DOI:10.1007/s10557-014-6554-5]

    Cardiovascular Drugs and Therapy

  3. Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

    Gastroenterology, Vol. 149, Núm. 3, pp. 563-566