BIO Investigación vasca en salud
Centro
University of Göttingen
Gotinga, AlemaniaPublikationen in Zusammenarbeit mit Forschern von University of Göttingen (17)
2023
2022
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2018
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Exploring the role of genome and structural ions in preventing viral capsid collapse during dehydration
Journal of Physics Condensed Matter, Vol. 30, Núm. 10
2016
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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Impact of chronic hepatitis C on mortality in cirrhotic patients admitted to intensive-care unit
BMC Infectious Diseases, Vol. 16, Núm. 1
2015
2014
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A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma
Blood, Vol. 123, Núm. 8, pp. 1187-1198
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Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes
Neurobiology of Aging, Vol. 35, Núm. 11, pp. 2657.e13-2657.e19
2013
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Comparison of movement related cortical potential in healthy people and amyotrophic lateral sclerosis patients
Frontiers in Neuroscience
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Health-related quality of life 12 months after severe traumatic brain injury: A prospective nationwide cohort study
Journal of Rehabilitation Medicine, Vol. 45, Núm. 8, pp. 785-791
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High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas
Genes Chromosomes and Cancer, Vol. 52, Núm. 2, pp. 150-155
2012
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GABA release by hippocampal astrocytes
Frontiers in Computational Neuroscience
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Progression of Alzheimer disease in Europe: Data from the European ICTUS study
Current Alzheimer Research, Vol. 9, Núm. 8, pp. 902-912
2009
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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Nature Genetics, Vol. 41, Núm. 7, pp. 829-832
2008
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Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation
Neurogenetics, Vol. 9, Núm. 2, pp. 109-118