Grupo de Investigación de Endocrinología, Diabetes, Nutrición, alteraciones Renales y Salud Infantil - GIC 21/144
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Centro de Investigación Cooperativa en Biotecnología
Zamudio, EspañaPublicaciones en colaboración con investigadoras/es de Centro de Investigación Cooperativa en Biotecnología (14)
2024
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A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of bona fide prions
Nature Communications, Vol. 15, Núm. 1
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Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variants
Scientific Reports, Vol. 14, Núm. 1
2022
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Description of the first Spanish case of Gerstmann–Sträussler–Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization
Journal of Neurology, Vol. 269, Núm. 8, pp. 4253-4263
2021
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E2F1 and E2F2-mediated repression of CPT2 establishes a lipid-rich tumor-promoting environment
Cancer Research, Vol. 81, Núm. 11, pp. 2874-2887
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Sporadic Creutzfeldt–Jakob disease with extremely long 14-year survival period
European Journal of Neurology, Vol. 28, Núm. 9, pp. 2901-2906
2020
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Liver osteopontin is required to prevent the progression of age-related nonalcoholic fatty liver disease
Aging Cell, Vol. 19, Núm. 8
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Variability in Cerebrospinal Fluid MicroRNAs Through Life
Molecular Neurobiology, Vol. 57, Núm. 10, pp. 4134-4142
2019
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A comprehensive study of vesicular and non-vesicular miRNAs from a volume of cerebrospinal fluid compatible with clinical practice
Theranostics, Vol. 9, Núm. 16, pp. 4567-4579
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Impaired proteostasis in rare neurological diseases
Seminars in Cell and Developmental Biology, Vol. 93, pp. 164-177
2009
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Exploring the diabetogenicity of the HLA-B18-DR3 CEH: Independent association with T1D genetic risk close to HLA-DOA
Genes and Immunity, Vol. 10, Núm. 6, pp. 596-600
2008
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Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease
Gastroenterology, Vol. 134, Núm. 3, pp. 738-746
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Reply
Gastroenterology
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The functional R620W variant of the PTPN22 gene is associated with celiac disease
Tissue Antigens, Vol. 71, Núm. 3, pp. 247-249
2006
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Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease
Genes and Immunity, Vol. 7, Núm. 7, pp. 550-554