| Year |
Citation |
Score |
| 2018 |
Srikanth P, Lagomarsino VN, Muratore CR, Ryu SC, He A, Taylor WM, Zhou C, Arellano M, Young-Pearse TL. Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids. Translational Psychiatry. 8: 77. PMID 29643329 DOI: 10.1038/S41398-018-0122-X |
0.346 |
|
| 2017 |
Muratore CR, Zhou C, Liao M, Fernandez MA, Taylor WM, Lagomarsino VN, Pearse RV, Rice HC, Negri JM, He A, Srikanth P, Callahan DG, Shin T, Zhou M, Bennett DA, et al. Cell-type Dependent Alzheimer's Disease Phenotypes: Probing the Biology of Selective Neuronal Vulnerability. Stem Cell Reports. PMID 29153990 DOI: 10.1016/J.Stemcr.2017.10.015 |
0.33 |
|
| 2016 |
Liao MC, Muratore CR, Gierahn TM, Sullivan SE, Srikanth P, De Jager PL, Love JC, Young-Pearse TL. Single-Cell Detection of Secreted Aβ and sAPPα from Human IPSC-Derived Neurons and Astrocytes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 1730-46. PMID 26843653 DOI: 10.1523/Jneurosci.2735-15.2016 |
0.309 |
|
| 2015 |
Srikanth P, Han K, Callahan DG, Makovkina E, Muratore CR, Lalli MA, Zhou H, Boyd JD, Kosik KS, Selkoe DJ, Young-Pearse TL. Genomic DISC1 Disruption in hiPSCs Alters Wnt Signaling and Neural Cell Fate. Cell Reports. PMID 26299970 DOI: 10.1016/J.Celrep.2015.07.061 |
0.303 |
|
| 2014 |
Muratore CR, Rice HC, Srikanth P, Callahan DG, Shin T, Benjamin LN, Walsh DM, Selkoe DJ, Young-Pearse TL. The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons. Human Molecular Genetics. 23: 3523-36. PMID 24524897 DOI: 10.1093/Hmg/Ddu064 |
0.335 |
|
| 2013 |
Hodgson N, Trivedi M, Muratore C, Li S, Deth R. Soluble oligomers of amyloid-β cause changes in redox state, DNA methylation, and gene transcription by inhibiting EAAT3 mediated cysteine uptake. Journal of Alzheimer's Disease : Jad. 36: 197-209. PMID 23579332 DOI: 10.3233/Jad-130101 |
0.678 |
|
| 2013 |
Muratore CR, Hodgson NW, Trivedi MS, Abdolmaleky HM, Persico AM, Lintas C, De la Monte S, Deth RC. Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism. Plos One. 8: e56927. PMID 23437274 DOI: 10.1371/Journal.Pone.0056927 |
0.663 |
|
| 2013 |
Muratore C, Rice H, Srikanth P, Selkoe D, Young-Pearse T. O1-01-05: Human iPSC-derived neurons reveal novel effects of the APP London mutation and show cell fate-specific Alzheimer's disease relevant phenotypes Alzheimer's & Dementia. 9: P126-P127. DOI: 10.1016/J.Jalz.2013.04.053 |
0.312 |
|
| 2010 |
Deth R, Muratore C, Waly M. Oxidative stress in autism and its implications for dopamine-stimulated phospholipid methylation The Neurochemical Basis of Autism: From Molecules to Minicolumns. 185-199. DOI: 10.1007/978-1-4419-1272-5_12 |
0.582 |
|
| 2010 |
Deth R, Waly M, Muratore C, Hodgson N. Redox Imbalance and the Metabolic Pathology of Autism Developmental Neurotoxicology Research: Principles, Models, Techniques, Strategies, and Mechanisms. 477-499. DOI: 10.1002/9780470917060.ch22 |
0.661 |
|
| 2008 |
Deth R, Muratore C, Benzecry J, Power-Charnitsky VA, Waly M. How environmental and genetic factors combine to cause autism: A redox/methylation hypothesis. Neurotoxicology. 29: 190-201. PMID 18031821 DOI: 10.1016/J.Neuro.2007.09.010 |
0.636 |
|
| 2007 |
Deth RC, Muratore C, Waly M, Bojkovic J. Methionine Synthase as a Sensor of Cellular Redox Status: Implications for Neurological Disorders The Faseb Journal. 21. DOI: 10.1096/Fasebj.21.5.A345 |
0.528 |
|
| 2006 |
Deth RC, Muratore C, Hodgson N, Zhang Y, Trivedi MS. P4-260: AGE-DEPENDENT CHANGES IN HUMAN CORTEX ANTIOXIDANT AND METHYLATION METABOLIC PATHWAYS: IMPLICATIONS AND OPPORTUNITIES FOR ALZHEIMER'S DISEASE RISK REDUCTION Alzheimer's & Dementia. 14: P1546-P1546. DOI: 10.1016/J.Jalz.2018.07.082 |
0.681 |
|
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