Genética de Enfermedades Humanas
Publicaciones (137) Publicaciones en las que ha participado algún/a investigador/a
2024
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A cohort analysis of familial partial lipodystrophy from two Mediterranean countries
Diabetes, Obesity and Metabolism, Vol. 26, Núm. 11, pp. 4875-4886
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Bilateral Uveal Melanoma: An Insight into Genetic Predisposition in Four New Unrelated Patients and Review of Published Cases
Journal of Clinical Medicine, Vol. 13, Núm. 11
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Granulomatous rosacea: a clue to the diagnosis of STAT1 gain of function in a child with immunodeficiency
Clinical and Experimental Dermatology, Vol. 49, Núm. 5, pp. 516-518
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The activity of therapeutic molecular cluster Ag5 is dependent on oxygen level and HIF-1 mediated signalling
Redox Biology, Vol. 76
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Yao syndrome: a clinical observation of a non-paradigmatic autoinflammatory disease
JDDG - Journal of the German Society of Dermatology
2023
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Natural history and comorbidities of generalised and partial lipodystrophy syndromes in Spain
Frontiers in Endocrinology, Vol. 14
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Targets, Mechanisms and Cytotoxicity of Half-Sandwich Ir(III) Complexes Are Modulated by Structural Modifications on the Benzazole Ancillary Ligand
Cancers, Vol. 15, Núm. 1
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Two cases of familial glomuvenous malformation and description of a novel pathogenic mutation in glomulin gene (GLMN)
International Journal of Dermatology
2022
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GNAQ and GNA11 Genes: A Comprehensive Review on Oncogenesis, Prognosis and Therapeutic Opportunities in Uveal Melanoma
Cancers, Vol. 14, Núm. 13
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Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process
Endocrine Pathology, Vol. 33, Núm. 4, pp. 484-493
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Silver Clusters of Five Atoms as Highly Selective Antitumoral Agents Through Irreversible Oxidation of Thiols
Advanced Functional Materials, Vol. 32, Núm. 29
2021
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A Simple Entropic-Driving Separation Procedure of Low-Size Silver Clusters, Through Interaction with DNA
ChemistryOpen, Vol. 10, Núm. 8, pp. 760-763
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O-GlcNAcylated p53 in the liver modulates hepatic glucose production
Nature Communications, Vol. 12, Núm. 1
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Role of somatic mutations and chromosomal aberrations in the prognosis of uveal melanoma in a Spanish patient cohort
Acta Ophthalmologica, Vol. 99, Núm. 7, pp. e1077-e1089
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The risk of thrombosis in essential thrombocythemia is associated with the type of CALR mutation: A multicentre collaborative study
European Journal of Haematology, Vol. 106, Núm. 3, pp. 371-379
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Variable expressivity and allelic heterogeneity in type 2 familial partial lipodystrophy: The p.(thr528met) lmna variant
Journal of Clinical Medicine, Vol. 10, Núm. 7
2019
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Expanding the clinical and molecular spectrum of the CWC27-related spliceosomopathy
Journal of Human Genetics, Vol. 64, Núm. 11, pp. 1133-1136
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New half-sandwich ruthenium(ii) complexes as proteosynthesis inhibitors in cancer cells
Chemical Communications, Vol. 55, Núm. 8, pp. 1140-1143
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Novel TMEM127 Variant Associated to Bilateral Phaeochromocytoma with an Uncommon Clinical Presentation
Case Reports in Endocrinology, Vol. 2019
2018
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Adult Sox2+ stem cell exhaustion in mice results in cellular senescence and premature aging
Aging Cell, Vol. 17, Núm. 5