Universidad de Salamanca-ko ikertzaileekin lankidetzan egindako argitalpenak (57)

2023

  1. Insulin-degrading enzyme (IDE) as a modulator of microglial phenotypes in the context of Alzheimer’s disease and brain aging

    Journal of Neuroinflammation, Vol. 20, Núm. 1

  2. Predominantly Pro-Inflammatory Phenotype with Mixed M1/M2 Polarization of Peripheral Blood Classical Monocytes and Monocyte-Derived Macrophages among Patients with Excessive Ethanol Intake

    Antioxidants, Vol. 12, Núm. 9

  3. The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism

    Endocrine, Vol. 80, Núm. 1, pp. 47-53

2022

  1. Functional Alterations Involved in Increased Bleeding in Hereditary Hemorrhagic Telangiectasia Mouse Models

    Frontiers in Medicine, Vol. 9

  2. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

    Endocrine, Vol. 77, Núm. 1, pp. 86-101

  3. PSTPIP1-LYP phosphatase interaction: structural basis and implications for autoinflammatory disorders

    Cellular and Molecular Life Sciences, Vol. 79, Núm. 2

  4. Polymorphisms in autophagy genes are genetic susceptibility factors in glioblastoma development

    BMC Cancer, Vol. 22, Núm. 1

2021

  1. Hot and cold tumors: Is endoglin (cd105) a potential target for vessel normalization?

    Cancers, Vol. 13, Núm. 7

  2. Impairment of autophagic flux participates in the antitumor effects of tat-cx43266-283 in glioblastoma stem cells

    Cancers, Vol. 13, Núm. 17

2020

  1. Angiogenesis in cardiopulmonary dirofilariosis: Does the Wolbachia surface protein have a pro-or anti-angiogenic effect?

    Journal of Helminthology

  2. Dopamine D4 receptor subtype activation reduces the rat cardiac parasympathetic discharge

    Pflugers Archiv European Journal of Physiology, Vol. 472, Núm. 12, pp. 1693-1703

  3. Phosphatidylinositol-3-kinase-Akt pathway in negative-stranded RNA virus infection: a minireview

    Archives of Virology, Vol. 165, Núm. 10, pp. 2165-2176

2019

  1. Comparative genomic hybridization analysis of basal cell carcinoma

    JDDG - Journal of the German Society of Dermatology

2018

  1. Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

    Molecular and Cellular Endocrinology, Vol. 473, pp. 1-16

  2. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

    British Journal of Dermatology, Vol. 178, Núm. 1, pp. 198-206

  3. Polymorphisms in receptors involved in opsonic and nonopsonic phagocytosis, and correlation with risk of infection in oncohematology patients

    Infection and Immunity, Vol. 86, Núm. 12

2017

  1. A case of mosaicism in ectodermal dysplasia–skin fragility syndrome

    British Journal of Dermatology

  2. Circulating soluble endoglin modifies the inflammatory response in mice

    PLoS ONE, Vol. 12, Núm. 11

  3. Endoglin-based biological therapy in the treatment of angiogenesis-dependent pathologies

    Expert Opinion on Biological Therapy, Vol. 17, Núm. 9, pp. 1053-1063

  4. Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas

    British Journal of Dermatology, Vol. 177, Núm. 6, pp. 1654-1663