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Injectable hydrogel scaffold incorporating microspheres containing cobalt‐doped bioactive glass for bone healing.
- Published in:
- Journal of Biomedical Materials Research, Part A, 2024, v. 112, n. 12, p. 2225, doi. 10.1002/jbm.a.37773
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- Publication type:
- Article
Genotypic analysis of gene expression in the dissection of the aetiology of complex neurological and psychiatric diseases.
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- Briefings in Functional Genomics & Proteomics, 2009, v. 8, n. 3, p. 194, doi. 10.1093/bfgp/elp028
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- Publication type:
- Article
Electrospun Antibacterial Composites for Cartilage Tissue Engineering.
- Published in:
- Macromolecular Bioscience, 2022, v. 22, n. 9, p. 1, doi. 10.1002/mabi.202200219
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- Publication type:
- Article
Facile Photochemical Modification of Silk Protein–Based Biomaterials.
- Published in:
- Macromolecular Bioscience, 2018, v. 18, n. 11, p. N.PAG, doi. 10.1002/mabi.201800216
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- Publication type:
- Article
Instructive Conductive 3D Silk Foam-Based Bone Tissue Scaffolds Enable Electrical Stimulation of Stem Cells for Enhanced Osteogenic Differentiation.
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- Macromolecular Bioscience, 2015, v. 15, n. 11, p. 1490, doi. 10.1002/mabi.201500171
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- Publication type:
- Article
CKM unitarity normalization tests, present and future.
- Published in:
- Annalen der Physik, 2013, v. 525, n. 7, p. 443, doi. 10.1002/andp.201300004
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- Publication type:
- Article
Interfacial analysis of (La<sub>0.6</sub>Sr<sub>0.4</sub>)(Co<sub>0.2</sub>Fe<sub>0.8</sub>)O<sub>3- d</sub> substrates wetted by Ag-CuO.
- Published in:
- Journal of Materials Science, 2005, v. 40, n. 9/10, p. 2341, doi. 10.1007/s10853-005-1956-1
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- Publication type:
- Article
Human myeloid progenitor glucocorticoid receptor activation causes genomic instability, type 1 IFN-response pathway activation and senescence in differentiated microglia; an early life stress model.
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- Glia, 2023, v. 71, n. 4, p. 1036, doi. 10.1002/glia.24325
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- Publication type:
- Article
Putting presenilins centre stage. Introduction to the Talking Point on the role of presenilin mutations in Alzheimer disease.
- Published in:
- EMBO Reports, 2007, v. 8, n. 2, p. 134, doi. 10.1038/sj.embor.7400899
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- Publication type:
- Article
Short-term effects of polynuclear aromatic hydrocarbons on sea-surface microlayer phytoneuston.
- Published in:
- Bulletin of Environmental Contamination & Toxicology, 1987, v. 38, n. 6, p. 1037, doi. 10.1007/BF01609092
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- Publication type:
- Article
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 258, doi. 10.1007/s00439-003-0960-2
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- Publication type:
- Article
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2001, v. 109, n. 6, p. 646, doi. 10.1007/s00439-001-0614-1
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- Publication type:
- Article
Large-scale proteomics analysis of five brain regions from Parkinson's disease patients with a GBA1 mutation.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00645-x
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- Publication type:
- Article
Large-scale proteomics analysis of five brain regions from Parkinson's disease patients with a GBA1 mutation.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00645-x
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- Publication type:
- Article
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00573-2
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- Publication type:
- Article
Author Correction: Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases.
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- 2023
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- Publication type:
- Correction Notice
Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00504-1
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- Publication type:
- Article
Elevation of gangliosides in four brain regions from Parkinson's disease patients with a GBA mutation.
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- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00363-2
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- Publication type:
- Article
Melanins as Sustainable Resources for Advanced Biotechnological Applications.
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- Global Challenges, 2021, v. 5, n. 2, p. 1, doi. 10.1002/gch2.202000102
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- Publication type:
- Article
Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology.
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- Advanced Science, 2022, v. 9, n. 23, p. 1, doi. 10.1002/advs.202201212
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- Publication type:
- Article
An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids.
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- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0843-y
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- Publication type:
- Article
An Aged Canid with Behavioral Deficits Exhibits Blood and Cerebrospinal Fluid Amyloid Beta Oligomers.
- Published in:
- Frontiers in Aging Neuroscience, 2018, p. 1, doi. 10.3389/fnagi.2018.00007
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- Publication type:
- Article
iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184104
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- Publication type:
- Article
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162592
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- Publication type:
- Article
Photochemically Controlled Drug Dosing from a Polymeric Scaffold.
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- Pharmaceutical Research, 2017, v. 34, n. 7, p. 1469, doi. 10.1007/s11095-017-2164-9
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- Publication type:
- Article
Endocan, a Soluble Marker of Endothelial Cell Activation Is a Molecular Marker of Disease Severity in Women with Preeclampsia.
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- Reproductive Sciences, 2022, v. 29, n. 8, p. 2310, doi. 10.1007/s43032-022-00858-6
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- Publication type:
- Article
Apolipoprotein E and Intellectual Achievement.
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- Journal of the American Geriatrics Society, 2002, v. 50, n. 1, p. 49, doi. 10.1046/j.1532-5415.2002.50007.x
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- Publication type:
- Article
Green Tea Epigallocatechin-3-Gallate (EGCG) Modulates Amyloid Precursor Protein Cleavage and Reduces Cerebral Amyloidosis in Alzheimer Transgenic Mice.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 38, p. 8807, doi. 10.1523/JNEUROSCI.1521-05.2005
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- Publication type:
- Article
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains.
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- Annals of Neurology, 2012, v. 72, n. 3, p. 455, doi. 10.1002/ana.23614
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- Publication type:
- Article
CR1 is associated with amyloid plaque burden and age-related cognitive decline.
- Published in:
- Annals of Neurology, 2011, v. 69, n. 3, p. 560, doi. 10.1002/ana.22277
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- Publication type:
- Article
Dissecting the familial risk of multiple sclerosis.
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- Annals of Neurology, 2011, v. 69, n. 1, p. 11, doi. 10.1002/ana.22353
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- Publication type:
- Article
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).
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- Annals of Neurology, 2010, v. 68, n. 5, p. 611, doi. 10.1002/ana.22122
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- Publication type:
- Article
Characterization of PLA2G6 as a locus for dystonia-parkinsonism.
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- Annals of Neurology, 2009, v. 65, n. 1, p. 19, doi. 10.1002/ana.21415
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- Publication type:
- Article
Neurofibrillary tau pathology modulated by genetic variation of α -synuclein.
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- Annals of Neurology, 2008, v. 64, n. 3, p. 348, doi. 10.1002/ana.21446
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- Publication type:
- Article
Genetics of Parkinson's disease and parkinsonism.
- Published in:
- Annals of Neurology, 2006, v. 60, n. 4, p. 389
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- Publication type:
- Article
Characteristics of frontotemporal dementia patients with a Progranulin mutation.
- Published in:
- Annals of Neurology, 2006, v. 60, n. 3, p. 374
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- Publication type:
- Article
Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease.
- Published in:
- Annals of Neurology, 2006, v. 59, n. 1, p. 21, doi. 10.1002/ana.20673
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- Publication type:
- Article
Phosphodiesterase 4D and 5‐lipoxygenase activating protein in ischemic stroke.
- Published in:
- Annals of Neurology, 2005, v. 58, n. 3, p. 351
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- Publication type:
- Article
Torsin A haplotype predisposes to idiopathic dystonia.
- Published in:
- Annals of Neurology, 2005, v. 57, n. 5, p. 765
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- Publication type:
- Article
How many pathways are there to nigral death?
- Published in:
- Annals of Neurology, 2004, v. 56, n. 3, p. 316
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- Publication type:
- Article
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
- Published in:
- Annals of Neurology, 2003, v. 54, n. 2, p. 271
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- Publication type:
- Article
Alzheimer's disease: Genetic evidence points to a single pathogenesis (This article is a US Government work and, as such, is in the public domain in the United States of America.).
- Published in:
- Annals of Neurology, 2003, v. 54, n. 2, p. 143
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- Publication type:
- Article
Case-Control study of the extended tau gene haplotype in Parkinson's disease.
- Published in:
- 2001
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- Publication type:
- journal article
Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy.
- Published in:
- 2001
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- Publication type:
- journal article
Lewy bodies and parkinsonism in families with parkin mutations.
- Published in:
- 2001
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- Publication type:
- journal article
Pick's disease is associated with mutations in the tau gene.
- Published in:
- Annals of Neurology, 2000, v. 48, n. 6, p. 859, doi. 10.1002/1531-8249(200012)48:6<859::AID-ANA6>3.0.CO;2-1
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- Publication type:
- Article
Genetic association of α<sub>2</sub>-macroglobulin with Alzheimer's disease in a Finnish elderly population.
- Published in:
- Annals of Neurology, 1999, v. 46, n. 3, p. 382, doi. 10.1002/1531-8249(199909)46:3<382::AID-ANA14>3.0.CO;2-5
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- Publication type:
- Article
Low frequency of α-synuclein mutations in familial Parkinson's disease.
- Published in:
- Annals of Neurology, 1998, v. 43, n. 3, p. 394, doi. 10.1002/ana.410430320
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- Publication type:
- Article
Increased Aβ42(43) from cell lines expressing presenilin 1 mutations.
- Published in:
- Annals of Neurology, 1998, v. 43, n. 2, p. 256, doi. 10.1002/ana.410430217
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- Publication type:
- Article
Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.
- Published in:
- Annals of Neurology, 1997, v. 42, n. 5, p. 794, doi. 10.1002/ana.410420516
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- Publication type:
- Article