Works matching DE "AMYLOID genetics"
Results: 43
BetaSerpentine: a bioinformatics tool for reconstruction of amyloid structures.
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- Bioinformatics, 2018, v. 34, n. 4, p. 599, doi. 10.1093/bioinformatics/btx629
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Transcriptome-guided amyloid imaging genetic analysis via a novel structured sparse learning algorithm.
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- Bioinformatics, 2014, v. 30, n. 17, p. i564
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Tafamidis: A Review in Transthyretin Amyloidosis with Polyneuropathy.
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- Drugs, 2019, v. 79, n. 8, p. 863, doi. 10.1007/s40265-019-01129-6
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Clinical trial design of serious gaming in mild cognitive impairment.
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- Frontiers in Aging Neuroscience, 2015, v. 7, p. 1, doi. 10.3389/fnagi.2015.00026
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Our "energy-Ca<sup>2+ </sup>signaling deficits" hypothesis and its explanatory potential for key features of Alzheimer's disease.
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- Frontiers in Aging Neuroscience, 2014, v. 6, p. 1, doi. 10.3389/fnagi.2014.00329
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Y<sub>682</sub>G mutation of amyloid precursor protein promotes endo-lysosomal dysfunction by disrupting APP-SorLA interaction.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00109
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Ex vivo <sup>18</sup>O-labeling mass spectrometry identifies a peripheral amyloid β clearance pathway.
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- Molecular Neurodegeneration, 2017, v. 12, p. 1, doi. 10.1186/s13024-017-0152-5
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Effects of CD2-associated protein deficiency on amyloid-β in neuroblastoma cells and in an APP transgenic mouse model.
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- Molecular Neurodegeneration, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13024-015-0006-y
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Reference region selection and the association between the rate of amyloid accumulation over time and the baseline amyloid burden.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2017, v. 44, n. 8, p. 1364, doi. 10.1007/s00259-017-3666-8
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Acquired, non-amyloid related factor X deficiency: review of the literature.
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- Haemophilia, 2012, v. 18, n. 5, p. 655, doi. 10.1111/j.1365-2516.2012.02773.x
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SAA1 polymorphisms are associated with variation in antiangiogenic and tumor-suppressive activities in nasopharyngeal carcinoma.
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- Oncogene, 2015, v. 34, n. 7, p. 878, doi. 10.1038/onc.2014.12
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Amyloid Associated Intermittent Network Disruptions in Cognitively Intact Older Subjects: Structural Connectivity Matters.
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- Frontiers in Aging Neuroscience, 2017, p. 1, doi. 10.3389/fnagi.2017.00418
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- Article
Preimplantation genetic testing for familial amyloid polyneuropathy.
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- Reproductive Health, 2022, v. 19, n. 1, p. 1, doi. 10.1186/s12978-022-01491-x
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Cardiac amyloidosis: state-of-the-art review.
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- Journal of Geriatric Cardiology, 2023, v. 20, n. 5, p. 361, doi. 10.26599/1671-5411.2023.05.006
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The neurotoxicity of amyloid β-protein oligomers is reversible in a primary neuron model.
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- Molecular Brain, 2017, v. 10, p. 1, doi. 10.1186/s13041-016-0284-5
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Affinity of nat/<sup>68</sup>Ga-Labelled Curcumin and Curcuminoid Complexes for β-Amyloid Plaques: Towards the Development of New Metal-Curcumin Based Radiotracers.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 9, p. 1480, doi. 10.3390/ijms17091480
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A New Folding Kinetic Mechanism for Human Transthyretin and the Influence of the Amyloidogenic V30M Mutation.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 9, p. 1428, doi. 10.3390/ijms17091428
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APOE and BDNF polymorphisms moderate amyloid β-related cognitive decline in preclinical Alzheimer's disease.
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- Molecular Psychiatry, 2015, v. 20, n. 11, p. 1322, doi. 10.1038/mp.2014.123
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Multiple Insulin Degrading Enzyme Variants Alter In Vitro Reporter Gene Expression.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021429
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Membrane-Anchored Aß Accelerates Amyloid Formation and Exacerbates Amyloid-Associated Toxicity in Mice.
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- Journal of Neuroscience, 2013, v. 33, n. 49, p. 19281, doi. 10.1523/JNEUR0SCI.2542-13.2013
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Neuronal Clearance of Amyloid-ß by Endocytic Receptor LRP1.
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- Journal of Neuroscience, 2013, v. 33, n. 49, p. 19276, doi. 10.1523/JNEUROSCI.3487-13.2013
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Functional Amyloids in the Mouse Sperm Acrosome.
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- Molecular & Cellular Biology, 2014, v. 34, n. 14, p. 2624, doi. 10.1128/MCB.00073-14
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Cutaneous biomarkers of therapeutic efficacy in early treatment of hereditary ATTR amyloid polyneuropathy with tafamidis.
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- Journal of the Peripheral Nervous System, 2024, v. 29, n. 2, p. 221, doi. 10.1111/jns.12624
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Ophthalmological involvement in wild‐type transthyretin amyloidosis: A multimodal imaging study.
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- Journal of the Peripheral Nervous System, 2023, v. 28, n. 4, p. 586, doi. 10.1111/jns.12589
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Hereditary neuropathies: A pathological perspective.
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- Journal of the Peripheral Nervous System, 2021, v. 26, p. S42, doi. 10.1111/jns.12467
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Boundaries of chronic inflammatory demyelinating polyradiculoneuropathy.
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- Journal of the Peripheral Nervous System, 2020, v. 25, n. 1, p. 4, doi. 10.1111/jns.12364
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A novel ATTR L32V mutation causes familial amyloid polyneuropathy in a Bolivian family.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 3, p. 208, doi. 10.1111/jns.12227
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Transthyretin Asp38Tyr: a new mutation associated to a late onset neuropathy.
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- Journal of the Peripheral Nervous System, 2015, v. 20, n. 1, p. 60, doi. 10.1111/jns.12112
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Protective role of human insulin against the cytotoxicity associated with human mutant S20 G islet amyloid polypeptide.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 5, p. 436, doi. 10.1111/jdi.12069
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An Enzyme from Aristolochia indica Destabilizes Fibrin-β Amyloid Co-Aggregate: Implication in Cerebrovascular Diseases.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141986
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Cognitive and cerebrovascular improvements following kinin B<sub>1</sub> receptor blockade in Alzheimer's disease mice.
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- Journal of Neuroinflammation, 2013, v. 10, n. 1, p. 1, doi. 10.1186/1742-2094-10-57
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Nodular localized primary cutaneous amyloidosis: a bullous variant.
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- Clinical & Experimental Dermatology, 2014, v. 39, n. 3, p. 344, doi. 10.1111/ced.12305
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Amyloid-ß-directed immunotherapy for Alzheimer's disease.
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- Journal of Internal Medicine, 2014, v. 275, n. 3, p. 284, doi. 10.1111/joim.12168
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Pathways to Alzheimer's disease.
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- Journal of Internal Medicine, 2014, v. 275, n. 3, p. 296, doi. 10.1111/joim.12192
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A coiled conformation of amyloid-β recognized by antibody C706.
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- Alzheimer's Research & Therapy, 2017, v. 9, p. 1, doi. 10.1186/s13195-017-0296-0
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Transcriptional regulation and its misregulation in Alzheimer's disease.
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- Molecular Brain, 2013, v. 6, n. 1, p. 1
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Utility of C‐reactive protein and serum amyloid A in the diagnosis of equine protozoal myeloencephalitis.
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- Journal of Veterinary Internal Medicine, 2018, v. 32, n. 5, p. 1726, doi. 10.1111/jvim.15254
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Acute-Phase Proteins, Oxidative Stress and Enzyme Activities of Blood Serum and Peritoneal Fluid in Cattle with Abomasal Displacement.
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- Journal of Veterinary Internal Medicine, 2012, v. 26, n. 6, p. 1470, doi. 10.1111/j.1939-1676.2012.01018.x
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Glial Draper Rescues Aβ Toxicity in a Drosophila Model of Alzheimer's Disease.
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- Journal of Neuroscience, 2017, v. 37, n. 49, p. 11881, doi. 10.1523/JNEUROSCI.0862-17.2017
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Drosophila Neprilysin 1 Rescues Memory Deficits Caused by Amyloid-β Peptide.
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- Journal of Neuroscience, 2017, v. 37, n. 43, p. 10334, doi. 10.1523/JNEUROSCI.1634-17.2017
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BACE1 Cleavage Site Selection Critical for Amyloidogenesis and Alzheimer's Pathogenesis.
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- Journal of Neuroscience, 2017, v. 37, n. 29, p. 6915, doi. 10.1523/JNEUROSCI.0340-17.2017
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Gene expression and functional annotation of human choroid plexus epithelium failure in Alzheimer's disease.
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- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/s12864-015-2159-z
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Soluble Toll-Like Receptor 4 Impairs the Interaction of Shiga Toxin 2a with Human Serum Amyloid P Component.
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- Toxins, 2018, v. 10, n. 9, p. 379, doi. 10.3390/toxins10090379
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- Article