Publicaciones en las que colabora con MARÍA DEL CARMEN MARTÍN SIERRA (13)

2024

  1. The absence of seroconversion after exposition to hepatitis C virus is not related to KIR-HLA genotype combinations (GEHEP-012 study)

    Antiviral Research, Vol. 222

2023

  1. SARS-CoV-2 viral RNA detection using the novel CoVradar device associated with the CoVreader smartphone app

    Biosensors and Bioelectronics, Vol. 230

2020

  1. Elevated soluble TNFα levels and upregulated TNFα mRNA expression in purified peripheral blood monocyte subsets associated with high-grade hepatocellular carcinoma

    Journal of Inflammation (United Kingdom), Vol. 17, Núm. 1

  2. Tumor Resection Induces Alterations on Serum Phospholipidome of Liver Cancer Patients

    Lipids, Vol. 55, Núm. 2, pp. 185-191

2019

  1. Functional Impairment of Circulating FcεRI+ Monocytes and Myeloid Dendritic Cells in Hepatocellular Carcinoma and Cholangiocarcinoma Patients

    Cytometry Part B - Clinical Cytometry, Vol. 96, Núm. 6, pp. 490-495

  2. Functional and Phenotypic Characterization of Tumor-Infiltrating Leukocyte Subsets and Their Contribution to the Pathogenesis of Hepatocellular Carcinoma and Cholangiocarcinoma

    Translational Oncology, Vol. 12, Núm. 11, pp. 1468-1479

  3. Lipoxidation and cancer immunity

    Redox Biology, Vol. 23

2018

  1. Modulation of the inflammatory response of immune cells in human peripheral blood by oxidized arachidonoyl aminophospholipids

    Archives of Biochemistry and Biophysics, Vol. 660, pp. 64-71

  2. Subcutaneous immunotherapy induces alterations in monocytes and dendritic cells homeostasis in allergic rhinitis patients

    Allergy, Asthma and Clinical Immunology, Vol. 14, Núm. 1

2017

  1. Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease

    European Journal of Human Genetics, Vol. 25, Núm. 2, pp. 200-207

2016

  1. A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease

    Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415

2015

  1. Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

    Human Molecular Genetics, Vol. 24, Núm. 4, pp. 1119-1126

2014

  1. Ménière’s syndrome and migraine

    Vestibular Migraine and Related Syndromes (Springer International Publishing), pp. 129-142