Neurociencias
Departamento
University Medical Center Hamburg-Eppendorf
Hamburgo, AlemaniaPublicaciones en colaboración con investigadoras/es de University Medical Center Hamburg-Eppendorf (21)
2024
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Generation of adult hippocampal neural stem cells occurs in the early postnatal dentate gyrus and depends on cyclin D2
EMBO Journal, Vol. 43, Núm. 3, pp. 317-338
2023
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Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))
Nature communications
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Gender differences in the management of acute psychiatric episodes in the emergency department: a cross-sectional analysis of the 2017–2019 triennium
Archives of Women's Mental Health, Vol. 26, Núm. 6, pp. 777-783
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Microglia and meningeal macrophages depletion delays the onset of experimental autoimmune encephalomyelitis
Cell death & disease, Vol. 14, Núm. 1, pp. 16
2022
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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
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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
2020
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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)
Acta Neuropathologica
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P2X7 Receptors as a Therapeutic Target in Cerebrovascular Diseases
Frontiers in Molecular Neuroscience, Vol. 13
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The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis
Cells, Vol. 9, Núm. 1
2019
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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
Acta Neuropathologica, Vol. 138, Núm. 2, pp. 237-250
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Clinical and genetic characteristics of late-onset Huntington's disease
Parkinsonism and Related Disorders, Vol. 61, pp. 101-105
2018
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P2X4 receptor controls microglia activation and favors remyelination in autoimmune encephalitis
EMBO Molecular Medicine, Vol. 10, Núm. 8
2017
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Coupled Proliferation and Apoptosis Maintain the Rapid Turnover of Microglia in the Adult Brain
Cell Reports, Vol. 18, Núm. 2, pp. 391-405
2016
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Analysis of plasminogen genetic variants in multiple sclerosis patients
G3: Genes, Genomes, Genetics, Vol. 6, Núm. 7, pp. 2073-2079
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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
2015
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Blockade of P2X7 receptors or pannexin-1 channels similarly attenuates postischemic damage
Journal of Cerebral Blood Flow and Metabolism, Vol. 35, Núm. 5, pp. 843-850
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Genome-wide significant association with seven novel multiple sclerosis risk loci
Journal of Medical Genetics, Vol. 52, Núm. 12, pp. 848-855
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Targeted screening for the detection of Pompe disease in patients with unclassified limb-girdle muscular dystrophy or asymptomatic hyperCKemia using dried blood: A Spanish cohort
Neuromuscular Disorders, Vol. 25, Núm. 7, pp. 548-553
2013
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Use of asenapine in clinical practice for the management of bipolar mania
Journal of Psychopharmacology, Vol. 27, pp. 3-13