The role of myelin damage in Alzheimer’s disease pathology
Open accessAbstract
Although Alois Alzheimer described myelin disruption in Alzheimer's disease (AD) as early as in 1911, his observation has escaped the attention of researchers since that time. Alzheimer's disease has been mainly considered as a grey matter disorder; nevertheless, recent evidence suggests that myelin impairment may play an important role in AD pathology. Classical neuropathological changes in AD, e.g. the accumulation of aggregated Aβ 42 and the presence of neurofibrillary tangles, are responsible for neuronal loss, but they may also induce death of oligodendrocytes and myelin damage. There is also evidence that myelin pathology may even precede Aβ and tau pathologies in AD. The state of the art does not allow us to determine whether myelin damage is a primary or a secondary injury in AD subjects. The article presents an overview of current knowledge on the role of myelin in AD pathology and its interactions with Aβ and tau pathologies.
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Myelin damage likely precedes and contributes to amyloid plaque buildup in early AD.
“This is notable because myelin damage likely precedes and contributes to amyloid plaque buildup in early AD.55–57”
From TET2-mutant myeloid cells mitigate Alzheimer’s disease progression via CNS infiltration and enhanced phagocytosis in mice (2025) · cites this paper as [56]
The 'Myelin damage in AD' section says some studies suggest myelin damage precedes Aβ pathology. It also proposes that myelin loss could accelerate plaque deposition, but presents that contribution as possible; the animal-model section says it remains unclear whether myelin damage triggers AD pathology. Thus the claim is stronger than the source on contribution to plaque buildup. (LLM, conf=0.82)
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Cites
The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics
Hardy, J., & Selkoe, D. J. (2002) · Science · doi:10.1126/science.1072994 · Cited by 13,864 · see citing works
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359 · see citing works
Shankar, G. M., Li, S., Mehta, T. H., Garcia-Munoz, A., Shepardson, N. E., Smith, I., Brett, F. M., Farrell, M. A., Rowan, M. J., Lemere, C. A., et al. (2008) · Nature Medicine · doi:10.1038/nm1782 · Cited by 3,685 · see citing works
Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity
DeKosky, S. T., & Scheff, S. W. (1990) · Annals of Neurology · doi:10.1002/ana.410270502 · Cited by 2,376 · see citing works
Cognitive impairment in multiple sclerosis
Chiaravalloti, N. D., & DeLuca, J. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70259-x · Cited by 2,088 · see citing works
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
Baumann, N., & Pham-Dinh, D. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.871 · Cited by 1,828 · see citing works
Axonopathy and Transport Deficits Early in the Pathogenesis of Alzheimer’s Disease
Stokin, G. B., Lillo, C., Falzone, T. L., Brusch, R. G., Rockenstein, E., Mount, S. L., Raman, R., Davies, P., Masliah, E., Williams, D. S., et al. (2005) · Science · doi:10.1126/science.1105681 · Cited by 1,214 · see citing works
Motor skill learning requires active central myelination
McKenzie, I. A., Ohayon, D., Li, H., Paes de Faria, J., Emery, B., Tohyama, K., & Richardson, W. D. (2014) · Science · doi:10.1126/science.1254960 · Cited by 1,177 · see citing works
Age-related myelin breakdown: a developmental model of cognitive decline and Alzheimer’s disease
Bartzokis, G. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.03.001 · Cited by 968 · see citing works
A new mechanism of nervous system plasticity: activity-dependent myelination
Fields, R. D. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn4023 · Cited by 794 · see citing works
Molecular pathways to neurodegeneration
Bossy-Wetzel, E., Schwarzenbacher, R., & Lipton, S. A. (2004) · Nature Medicine · doi:10.1038/nm1067 · Cited by 740 · see citing works
Han, X., M. Holtzman, D., W. McKeel, D., Kelley, J., & Morris, J. C. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.00997.x · Cited by 626 · see citing works
Fibrillar amyloid deposition leads to local synaptic abnormalities and breakage of neuronal branches
Tsai, J., Grutzendler, J., Duff, K., & Gan, W.-B. (2004) · Nature Neuroscience · doi:10.1038/nn1335 · Cited by 561 · see citing works
Alzheimer's disease as homeostatic responses to age-related myelin breakdown
Bartzokis, G. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.08.007 · Cited by 546 · see citing works
Dynamics of Oligodendrocyte Generation and Myelination in the Human Brain
Yeung, M. S. Y., Zdunek, S., Bergmann, O., Bernard, S., Salehpour, M., Alkass, K., Perl, S., Tisdale, J., Possnert, G., Brundin, L., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.011 · Cited by 541 · see citing works
The preclinical phase of the pathological process underlying sporadic Alzheimer’s disease
Braak, H., & Del Tredici, K. (2015) · Brain · doi:10.1093/brain/awv236 · Cited by 540 · see citing works
Motor skill learning induces changes in white matter microstructure and myelination
Sampaio-Baptista, C., Khrapitchev, A. A., Foxley, S., Schlagheck, T., Scholz, J., Jbabdi, S., DeLuca, G. C., Miller, K. L., Taylor, A., Thomas, N., et al. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3048-13.2013 · Cited by 417 · see citing works
Braak, H., & Braak, E. (1996) · Acta Neuropathologica · doi:10.1007/s004010050508 · Cited by 406 · see citing works
Bartzokis, G., Sultzer, D., Lu, P. H., Nuechterlein, K. H., Mintz, J., & Cummings, J. L. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.09.005 · Cited by 363 · see citing works
Wilkins, A., Majed, H., Layfield, R., Compston, A., & Chandran, S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-12-04967.2003 · Cited by 337 · see citing works
Demyelination Causes Synaptic Alterations in Hippocampi from Multiple Sclerosis Patients
Dutta, R., Chang, A., Doud, M., Kidd, G., Ribaudo, M. V., Young, E. A., Fox, R. J., Staugaitis, S., & Trapp, B. D. (2011) · Annals of Neurology · doi:10.1002/ana.22337 · Cited by 313 · see citing works
Stricker, N. H., Schweinsburg, B. C., Delano‐Wood, L., Wierenga, C. E., Bangen, K. J., Haaland, K. Y., Frank, L. R., Salmon, D. P., & Bondi, M. W. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.11.027 · Cited by 308 · see citing works
Extensive Hippocampal Demyelination in Multiple Sclerosis
Geurts, J., Bö, L., Roosendaal, S., Hazes, T., Daniëls, R., Barkhof, F., Witter, M., Huitinga, I., & van der Valk, P. (2007) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/nen.0b013e3181461f54 · Cited by 304 · see citing works
Lee, J.-T., Xu, J., Lee, J.-M., Ku, G., Han, X., Yang, D.-I., Chen, S., & Hsu, C. Y. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200307017 · Cited by 280 · see citing works
Desai, M. K., Sudol, K. L., Janelsins, M. C., Mastrangelo, M. A., Frazer, M. E., & Bowers, W. J. (2009) · Glia · doi:10.1002/glia.20734 · Cited by 266 · see citing works
Association of Amyloid Pathology With Myelin Alteration in Preclinical Alzheimer Disease
Dean, D. C., Hurley, S. A., Kecskemeti, S. R., O’Grady, J. P., Canda, C., Davenport-Sis, N. J., Carlsson, C. M., Zetterberg, H., Blennow, K., Asthana, S., et al. (2017) · JAMA Neurology · doi:10.1001/jamaneurol.2016.3232 · Cited by 252 · cited 9× · see citing works
“Although there exists evidence for myelin damage in the normal aging brain [9, 13, 31], recent data suggest that AD pathology is influenced by myelin damage [9].”
BackgroundInfluentialEngvig, A., Fjell, A. M., Westlye, L. T., Moberget, T., Sundseth, Ø., Larsen, V. A., & Walhovd, K. B. (2012) · Human Brain Mapping · doi:10.1002/hbm.21370 · Cited by 250 · see citing works
WHITE MATTER CHANGES IN DEMENTIA OF ALZHEIMER'S TYPE: BIOCHEMICAL AND NEUROPATHOLOGICAL CORRELATES
ENGLUND, E., BRUN, A., & ALLING, C. (1988) · Brain · doi:10.1093/brain/111.6.1425 · Cited by 228 · see citing works
β‐amyloid burden is not associated with rates of brain atrophy
Josephs, K. A., Whitwell, J. L., Ahmed, Z., Shiung, M. M., Weigand, S. D., Knopman, D. S., Boeve, B. F., Parisi, J. E., Petersen, R. C., Dickson, D. W., et al. (2007) · Annals of Neurology · doi:10.1002/ana.21223 · Cited by 224 · see citing works
The case described by Alois Alzheimer in 1911
Møller, H. J., & Graeber, M. B. (1998) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s004060050027 · Cited by 223 · see citing works
Behrendt, G., Baer, K., Buffo, A., Curtis, M. A., Faull, R. L., Rees, M. I., Götz, M., & Dimou, L. (2013) · Glia · doi:10.1002/glia.22432 · Cited by 219 · see citing works
Cognitive impairment in multiple sclerosis – a review of current knowledge and recent research
Grzegorski, T., & Losy, J. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2017-0011 · Cited by 195 · see citing works
Hippocampal CA1 atrophy and synaptic loss during experimental autoimmune encephalomyelitis, EAE
Ziehn, M. O., Avedisian, A., Tiwari-Woodruff, S., & Voskuhl, R. (2010) · Laboratory Investigation · doi:10.1038/labinvest.2010.6 · Cited by 190 · see citing works
Focal demyelination in Alzheimer’s disease and transgenic mouse models
Mitew, S., Kirkcaldie, M. T. K., Halliday, G. M., Shepherd, C. E., Vickers, J. C., & Dickson, T. C. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0657-2 · Cited by 186 · see citing works
A role for oligodendrocyte‐derived IGF‐1 in trophic support of cortical neurons
Wilkins, A., Chandran, S., & Compston, A. (2001) · Glia · doi:10.1002/glia.1094 · Cited by 185 · see citing works
The node of Ranvier in CNS pathology
Arancibia-Carcamo, I. L., & Attwell, D. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1305-z · Cited by 177 · see citing works
Multiple Brain Markers are Linked to Age-Related Variation in Cognition
Hedden, T., Schultz, A. P., Rieckmann, A., Mormino, E. C., Johnson, K. A., Sperling, R. A., & Buckner, R. L. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu238 · Cited by 164 · see citing works
Apolipoprotein E and cholesterol metabolism in the pathogenesis and treatment of Alzheimer's disease
Poirier, J. (2003) · Trends in Molecular Medicine · doi:10.1016/s1471-4914(03)00007-8 · Cited by 162 · see citing works
Human brain myelination and amyloid beta deposition in Alzheimer's disease
Bartzokis, G., Lu, P. H., & Mintz, J. (2007) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2007.01.019 · Cited by 162 · see citing works
Amyloid‐ß‐directed immunotherapy for Alzheimer's disease
Lannfelt, L., Relkin, N. R., & Siemers, E. (2014) · Journal of Internal Medicine · doi:10.1111/joim.12168 · Cited by 157 · see citing works
Anderson, J. M., Hampton, D. W., Patani, R., Pryce, G., Crowther, R. A., Reynolds, R., Franklin, R. J. M., Giovannoni, G., Compston, D. A. S., Baker, D., et al. (2008) · Brain · doi:10.1093/brain/awn119 · Cited by 141 · see citing works
Kohama, S. G., Rosene, D. L., & Sherman, L. S. (2011) · AGE · doi:10.1007/s11357-011-9357-7 · Cited by 139 · see citing works
Benitez, A. M., Fieremans, E., Jensen, J. H., Falangola, M. F., Tabesh, A., Ferris, S. H., & Helpern, J. A. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.11.001 · Cited by 131 · see citing works
Diffusion tensor MRI tractography and cognitive impairment in multiple sclerosis
Mesaroš, Š., Rocca, M. A., Kac̆ar, K., Kostić, J., Copetti, M., Stošić-Opinćal, T., Preziosa, P., Sala, S., Riccitelli, G. C., Horsfield, M. A., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e31824d5859 · Cited by 121 · see citing works
Ihara, M., Tomimoto, H., Kinoshita, M., Oh, J., Noda, M., Wakita, H., Akiguchi, I., & Shibasaki, H. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200107000-00008 · Cited by 115 · see citing works
Agosta, F., Dalla Libera, D., Spinelli, E. G., Finardi, A., Canu, E., Bergami, A., Bocchio Chiavetto, L., Baronio, M., Comi, G., Martino, G., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24235 · Cited by 113 · see citing works
Zhan, X., Jickling, G. C., Ander, B. P., Stamova, B. S., Liu, D., Kao, P. F., Zelin, M. A., Jin, L., DeCarli, C. S., & Sharp, F. R. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-142013 · Cited by 102 · see citing works
On certain peculiar diseases of old age
Alzheimer, A., Förstl, H., & Levy, R. (1991) · History of Psychiatry · doi:10.1177/0957154x9100200505 · Cited by 100 · see citing works
Ziehn, M. O., Avedisian, A., Dervin, S., Umeda, E., O'Dell, T., & Voskuhl, R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2796-12.2012 · Cited by 98 · see citing works
Couttas, T. A., Kain, N., Suchowerska, A. K., Quek, L., Turner, N. A., Fath, T., Garner, B., & Don, A. S. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.03.027 · Cited by 96 · see citing works
Cognitive impairment in multiple sclerosis
Hoffmann, S., Tittgemeyer, M., & von Cramon, D. Y. (2007) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32810c8e87 · Cited by 93 · see citing works
Myelin breakdown mediates age-related slowing in cognitive processing speed in healthy elderly men
Lu, P. H., Lee, G. J., Tishler, T. A., Meghpara, M., Thompson, P. M., & Bartzokis, G. (2012) · Brain and Cognition · doi:10.1016/j.bandc.2012.09.006 · Cited by 92 · see citing works
Bendlin, B. B., Carlsson, C. M., Johnson, S. C., Zetterberg, H., Blennow, K., Willette, A. A., Okonkwo, O. C., Sodhi, A., Ries, M. L., Birdsill, A. C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037720 · Cited by 91 · see citing works
Fornari, E., Maeder, P. P., Meuli, R. A., Ghika, J. A., & Knyazeva, M. G. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.11.014 · Cited by 86 · see citing works
Contribution of changes in ubiquitin and myelin basic protein to age-related cognitive decline
Wang, D.-S., Bennett, D. A., Mufson, E. J., Mattila, P. M., Cochran, E. J., & Dickson, D. W. (2003) · Neuroscience Research · doi:10.1016/j.neures.2003.10.002 · Cited by 72 · see citing works
Llorens, F., Gil, V., & del Rı́o, J. A. (2010) · The FASEB Journal · doi:10.1096/fj.10-162792 · Cited by 70 · see citing works
Association of apolipoprotein (Apo)E genotype with plasma apo E levels
Larson, I. A., Ordovás, J. M., DeLuca, C., Barnard, J. R., Feussner, G., & Schaefer, E. J. (2000) · Atherosclerosis · doi:10.1016/s0021-9150(99)00280-4 · Cited by 64 · see citing works
Autophagy is involved in oligodendroglial precursor-mediated clearance of amyloid peptide
Li, W., Tang, Y., Fan, Z., Meng, Y. J., Yang, G., Luo, J., & Ke, Z. (2013) · Molecular Neurodegeneration · doi:10.1186/1750-1326-8-27 · Cited by 64 · see citing works
Shindo, A., Liang, A. C., Maki, T., Miyamoto, N., Tomimoto, H., Lo, E. H., & Arai, K. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.80 · Cited by 58 · see citing works
Degradation of Amyloid β Protein by Purified Myelin Basic Protein*
Liao, M.-C., Ahmed, M., Smith, S. O., & Nostrand, W. V. V. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.050856 · Cited by 54 · see citing works
Hippocampal function is compromised in an animal model of multiple sclerosis
Novkovic, T., Shchyglo, O., Gold, R., & Manahan‐Vaughan, D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.03.008 · Cited by 54 · see citing works
Alzheimer disease immunotherapeutics: Then and now
Jindal, H., Bhatt, B., Shashikantha, S. K., & Malik, J. S. (2014) · Human Vaccines & Immunotherapeutics · doi:10.4161/21645515.2014.970959 · Cited by 52 · see citing works
Maat–Schieman, M. L. C., Yamaguchi, H., Hegeman-Kleinn, I. M., Welling‐Graafland, C., Natté, R., Roos, R. A. C., & van Duinen, S. G. (2004) · Acta Neuropathologica · doi:10.1007/s00401-004-0824-4 · Cited by 42 · see citing works
Mortamais, M., Reynès, C., Brickman, A. M., Provenzano, F. A., Muraskin, J., Portet, F., Berr, C., Touchon, J., Bonafé, A., Bars, E. L., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056972 · Cited by 41 · see citing works
Myelin Basic Protein Binds to and Inhibits the Fibrillar Assembly of Aβ42 in Vitro
Hoos, M. D., Ahmed, M., Smith, S. O., & Nostrand, W. E. V. (2009) · Biochemistry · doi:10.1021/bi900037s · Cited by 35 · see citing works
C. Schmued, L., Raymick, J., G. Paule, M., Dumas, M., & Sarkar, S. (2013) · Current Alzheimer Research · doi:10.2174/1567205011310010005 · Cited by 35 · see citing works
Papuć, E., Kurys-Denis, E., Krupski, W., Tatara, M. R., & Rejdak, K. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150309 · Cited by 33 · see citing works
Self-citationDiffusion Tensor Imaging Abnormalities in Cognitively Impaired Multiple Sclerosis Patients
Akbar, N., Lobaugh, N. J., O'Connor, P. W., Moradzadeh, L., Scott, C. J. M., & Feinstein, A. (2010) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100010775 · Cited by 28 · see citing works
Long, P. T., & Corfas, G. (2014) · Science · doi:10.1126/science.1261127 · Cited by 23 · see citing works
Age-Related Changes in Frontal and Temporal Lobe Volumes in Men: A Magnetic Resonance Imaging Study
Bartzokis, G., Beckson, M., Lu, P. H., Nuechterlein, K. H., Edwards, N., & Mintz, J. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.5.461 · Cited by 14 · see citing works
An Emerging Role for Imaging White Matter in the Preclinical Risk for Alzheimer Disease
Alexander, G. E. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.4123 · Cited by 10 · see citing works
Alzheimer disease immunotherapeutics: Then and now
Jindal, H., Bhatt, B., Shashikantha, S. K., & Malik, J. S. (2014) · Human Vaccines & Immunotherapeutics · doi:10.4161/hv.29437 · Cited by 4 · see citing works
Flagged first, then by citations
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- [70]Ziehn MO Avedisian AA Tiwari-Woodruff S Voskuhl RR Hippocampal CA1 atrophy and synaptic loss during experimental autoimmune encephalomyelitis, EAE Lab Invest 2010 90 774 86 20157291 PMC3033772
- [71]Kohama SG Rosene DL Sherman LS Age-related changes in human and non-human primate white matter: from myelination disturbances to cognitive decline Age (Dordr) 2012 34 1093 110 22203458 PMC3448998
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Sorted by citations
Lau, V. Z., Ramer, L. M., & Tremblay, M. (2023) · Nature Communications · doi:10.1038/s41467-023-37304-3 · Cited by 168 · see citing works
Fast-spiking parvalbumin-positive interneurons in brain physiology and Alzheimer’s disease
Hijazi, S., Smit, A. B., & van Kesteren, R. E. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02168-y · Cited by 144 · see citing works
Transgenic Mouse Models of Alzheimer’s Disease: An Integrative Analysis
Sanchez-Varo, R. M., Mejias‐Ortega, M., Fernandez-Valenzuela, J. J., Nuñez‐Diaz, C., Cáceres-Palomo, L., Vegas‐Gomez, L., Sánchez‐Mejías, E., Trujillo‐Estrada, L., García‐León, J. A., Moreno‐González, I., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105404 · Cited by 130 · see citing works
Qiu, S., Palavicini, J. P., Wang, J., Gonzalez, N. S., He, S., Dustin, E., Zou, C., Ding, L., Bhattacharjee, A., Skike, C. E. V., et al. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00488-7 · Cited by 126 · see citing works
COVID-19 and Alzheimer’s Disease
Ciaccio, M., Sasso, B. L., Scazzone, C., Gambino, C. M., Ciaccio, A. M., Bivona, G., Piccoli, T., Giglio, R. V., & Agnello, L. (2021) · Brain Sciences · doi:10.3390/brainsci11030305 · Cited by 111 · see citing works
Oligodendrocytes in the aging brain
Sams, E. C. (2021) · Neuronal Signaling · doi:10.1042/ns20210008 · Cited by 107 · see citing works
Mechanistic Link between Vitamin B12 and Alzheimer’s Disease
Lauer, A. A., Grimm, H. S., Apel, B., Golobrodska, N., Kruse, L., Ratanski, E., Schulten, N., Schwarze, L., Slawik, T., Sperlich, S., et al. (2022) · Biomolecules · doi:10.3390/biom12010129 · Cited by 109 · see citing works
Microglia and Astrocytes in Alzheimer’s Disease: Significance and Summary of Recent Advances
Deng, Q., Wu, C., Parker, E., Liu, T. C.-Y., Duan, R., & Yang, L. (2023) · Aging and disease · doi:10.14336/ad.2023.0907 · Cited by 102 · see citing works
Oligodendrocyte progenitor cells in Alzheimer's disease: from physiology to pathology
Zou, P., Wu, C., Liu, T. C.-Y., Duan, R., & Yang, L. (2023) · Translational Neurodegeneration · doi:10.1186/s40035-023-00385-7 · Cited by 97 · see citing works
Mechanistic Link between Vitamin B12 and Alzheimer’s Disease
Lauer, A. A., Grimm, H. S., Apel, B., Golobrodska, N., Kruse, L., Ratanski, E., Schulten, N., Schwarze, L., Slawik, T., Sperlich, S., et al. (2022) · Publications of the UdS (Saarland University) · doi:10.22028/d291-35299 · Cited by 90 · see citing works
Wang, N., Wang, M., Jeevaratnam, S., Rosenberg, C., Ikezu, T. C., Shue, F., Doss, S. V., Alnobani, A., Martens, Y. A., Wren, M., et al. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00577-1 · Cited by 82 · see citing works
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Jadhav, V., Lin, P. B., Pennington, T., Prisco, G. V. D., Jannu, A. J., Xu, G., Moutinho, M., Zhang, J., Atwood, B. K., Puntambekar, S. S., et al. (2020) · Molecular Neurodegeneration · doi:10.1186/s13024-020-00409-0 · Cited by 69 · see citing works
Myelin in Alzheimer’s disease: culprit or bystander?
Maitre, M., Jeltsch-David, H., Okechukwu, N. G., Klein, C., Patte-Mensah, C., & Mensah-Nyagan, A.-G. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01554-5 · Cited by 66 · see citing works
Xie, Y., Pan, T., Xu, D.-E., Huang, X., Tang, Y., Huang, W., Chen, R., Li, L., Chi, H., & Ma, Q. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.733945 · Cited by 62 · see citing works
Oligodendroglia are emerging players in several forms of learning and memory
Munyeshyaka, M., & Fields, R. D. (2022) · Communications Biology · doi:10.1038/s42003-022-04116-y · Cited by 64 · see citing works
Role of Neuron and Glia in Alzheimer’s Disease and Associated Vascular Dysfunction
Bandyopadhyay, S. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.653334 · Cited by 62 · see citing works
A New Hypothesis for Alzheimer’s Disease: The Lipid Invasion Model
Rudge, J. D. (2022) · Journal of Alzheimer's Disease Reports · doi:10.3233/adr-210299 · Cited by 58 · see citing works
The role of glial autophagy in Alzheimer’s disease
Litwiniuk, A., Juszczak, G. R., Stankiewicz, A. M., & Urbańska, K. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02242-5 · Cited by 54 · see citing works
Maitra, S., & Vincent, B. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120986 · Cited by 54 · see citing works
Potential neurobiological links between social isolation and Alzheimer's disease risk
Drinkwater, E., Davies, C., & Spires‐Jones, T. L. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15373 · Cited by 50 · see citing works
<i>Tlr7</i> drives sex differences in age- and Alzheimer’s disease–related demyelination
Lopez-Lee, C., Kodama, L., Fan, L., Zhu, D., Zhu, J., Wong, M. Y., Ye, P., Norman, K., Foxe, N. R., Ijaz, L., et al. (2024) · Science · doi:10.1126/science.adk7844 · Cited by 49 · see citing works
Noninvasive Gamma Sensory Stimulation May Reduce White Matter and Myelin Loss in Alzheimer’s Disease
Da, X., Hempel, E., Ou, Y., Rowe, O., Malchano, Z., Hajós, M., Kern, R. Z., Megerian, J. T., & Cimenser, A. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230506 · Cited by 47 · see citing works
The role of polyunsaturated fatty acids in neuronal signaling in depression and cognitive processes
Stachowicz, K. (2023) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2023.109555 · Cited by 40 · see citing works
Myelin repair in Alzheimer’s disease: a review of biological pathways and potential therapeutics
Hirschfeld, L. R., Risacher, S. L., Nho, K. T., & Saykin, A. J. (2022) · Translational Neurodegeneration · doi:10.1186/s40035-022-00321-1 · Cited by 39 · see citing works
Gao, Y., Liu, J., Wang, J., Liu, Y., Zeng, L., Ge, W., & Ma, C. (2022) · Brain Pathology · doi:10.1111/bpa.13047 · Cited by 35 · see citing works
Association of autoimmune diseases with Alzheimer's disease: A mendelian randomization study
Yeung, C. H. C., Yeung, S. L. A., & Schooling, C. M. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.09.052 · Cited by 36 · see citing works
Zhu, J., Freitas, H. R., Maezawa, I., Jin, L., & Srinivasan, V. J. (2021) · Light Science & Applications · doi:10.1038/s41377-021-00586-7 · Cited by 35 · see citing works
A multi-scale model explains oscillatory slowing and neuronal hyperactivity in Alzheimer’s disease
Alexandersen, C. G., de Haan, W., Bick, C., & Goriely, A. (2023) · Journal of The Royal Society Interface · doi:10.1098/rsif.2022.0607 · Cited by 35 · see citing works
Zhang, J., Wu, N., Wang, S., Yao, Z., Xiao, F., Lu, J., & Chen, B. (2021) · Aging Cell · doi:10.1111/acel.13380 · Cited by 33 · see citing works
Mild Traumatic Brain Injury Results in Significant and Lasting Cortical Demyelination
Mahoney, S., Chowdhury, N. F., Ngo, V., Imms, P. E., & Andrei Irimia, A. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.854396 · Cited by 33 · see citing works
Mielcarska, M. B., Skowrońska, K., Wyżewski, Z., & Toka, F. N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010242 · Cited by 32 · see citing works
Role of Demyelination in the Persistence of Neurological and Mental Impairments after COVID-19
Khodanovich, M. Y., Kamaeva, D. A., & Naumova, A. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911291 · Cited by 31 · see citing works
Revealing the Molecular Mechanisms of Alzheimer’s Disease Based on Network Analysis
Bayraktar, A., Lam, S. C. C., Altay, Ö., Li, X., Yuan, M., Zhang, C., Arif, M., Türkez, H., Uhlén, M., Shoaie, S., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111556 · Cited by 30 · see citing works
Geng, L., Liu, W., & Chen, Y. (2019) · Journal of Biological Research - Thessaloniki · doi:10.1186/s40709-019-0102-1 · Cited by 29 · see citing works
Sharp, F. R., DeCarli, C. S., Jin, L., & Zhan, X. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1096206 · Cited by 30 · see citing works
Cortical myelin profile variations in healthy aging brain: A T1w/T2w ratio study
Sui, Y. V., Masurkar, A. V., Rusinek, H., Reisberg, ., & Lazar, M. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119743 · Cited by 28 · see citing works
Moody, J. F., Dean, D., Kecskemeti, S. R., Blennow, K., Zetterberg, H., Kollmorgen, G., Suridjan, I., Wild, N., Carlsson, C. M., Johnson, S. C., et al. (2022) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1002/dad2.12381 · Cited by 26 · see citing works
Vitamin B12 Attenuates Changes in Phospholipid Levels Related to Oxidative Stress in SH-SY5Y Cells
Theiss, E. L., Griebsch, L. V., Lauer, A. A., Janitschke, D., Erhardt, V. K. J., Haas, E. C., Kuppler, K. N., Radermacher, J., Walzer, O., Portius, D., et al. (2022) · Cells · doi:10.3390/cells11162574 · Cited by 24 · see citing works
Alternative Targets to Fight Alzheimer’s Disease: Focus on Astrocytes
Valenza, M., Facchinetti, R., Menegoni, G., Steardo, L., & Scuderi, C. (2021) · Biomolecules · doi:10.3390/biom11040600 · Cited by 25 · see citing works
Disease-Associated Oligodendrocyte: New Player in Alzheimer's Disease and CNS Pathologies
Chen, P., Guo, Z., & Zhou, B. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2204090 · Cited by 24 · see citing works
Matatall, K. A., Wathan, T. K., Nguyen, M., Chen, H., McDonald, A., Qi, G., Belk, J. A., Florez, M. A., Le, D. T., Olarinde, T., et al. (2025) · Cell Stem Cell · doi:10.1016/j.stem.2025.06.006 · Cited by 23 · see citing works
Qu, W., Canoll, P., & Hargus, G. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.05.006 · Cited by 22 · see citing works
The Current Challenges for Drug Discovery in CNS Remyelination
Balestri, S., Giovane, A. D., Sposato, C., Ferrarelli, M., & Ragnini‐Wilson, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22062891 · Cited by 23 · see citing works
Facchinetti, R., Valenza, M., Gomiero, C., Mancini, G. F., Steardo, L., Campolongo, P., & Scuderi, C. (2022) · Biomedicines · doi:10.3390/biomedicines10061236 · Cited by 22 · see citing works
Pansieri, J., Hadley, G., Lockhart, A., Pisa, M., & DeLuca, G. C. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1199491 · Cited by 20 · see citing works
Athanasiou, E., Gargalionis, A. N., Anastassopoulou, C. G., Tsakris, A., & Boufidou, F. (2022) · Brain Sciences · doi:10.3390/brainsci12081010 · Cited by 20 · see citing works
Paul, S. C., Bhardwaj, J., & Binukumar, B. K. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166986 · Cited by 21 · see citing works
Mishra, E., & Thakur, M. K. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03397-6 · Cited by 19 · see citing works
Scalable mapping of myelin and neuron density in the human brain with micrometer resolution
Chang, S., Varadarajan, D., Yang, J., Chen, A., Kura, S., Magnain, C. V., Augustinack, J. C., Fischl, B. R., Greve, D. N., Boas, D. A., et al. (2022) · Scientific Reports · doi:10.1038/s41598-021-04093-y · Cited by 17 · see citing works
The contribution of DNA methylation to the (dys)function of oligodendroglia in neurodegeneration
Fodder, K., de Silva, R., Warner, T. T., & Bettencourt, C. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01607-9 · Cited by 17 · see citing works
Radiation Therapy in Alzheimer's Disease: A Systematic Review
Kaul, D., Ehret, F., Roohani, S., Jendrach, M., Buthut, M., Acker, G., Anwar, M., Zips, D., Heppner, F. L., & Prüß, H. (2023) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2023.11.044 · Cited by 18 · see citing works
Ghassemkhani, K., Saroka, K. S., & Dotta, B. T. (2025) · npj Aging · doi:10.1038/s41514-025-00243-y · Cited by 17 · see citing works
Targeted delivery of BACE1 siRNA for synergistic treatment of Alzheimer's disease
Li, Z., Yang, J., Li, J., Zhao, S., Jiang, S., Liu, W., Li, X., Zhang, S.-M., Du, H., Ni, J., et al. (2025) · Translational Neurodegeneration · doi:10.1186/s40035-025-00503-7 · Cited by 16 · see citing works
Key brain cell interactions and contributions to the pathogenesis of Alzheimer’s disease
Saavedra, J., Nascimento, M., Liz, M. A., & Cardoso, I. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1036123 · Cited by 16 · see citing works
Haridevamuthu, B., Nayak, S. P. R. R., Murugan, R., Pachaiappan, R., Ayub, R., Aljawdah, H. M. A., Arokiyaraj, S., Guru, A., & Arockiaraj, J. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176680 · Cited by 16 · see citing works
Fernandez-Alvarez, M., Atienza, M., & Cantero, J. L. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02420-7 · Cited by 15 · see citing works
Mitochondrial Connexins and Mitochondrial Contact Sites with Gap Junction Structure
Cetin-Ferra, S., Francis, S., Cooper, A. T., Neikirk, K., Marshall, A. G., Hinton, A. O., Jr., & Murray, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24109036 · Cited by 15 · see citing works
Palanivelu, L., Chen, Y., Chang, C., Liang, Y., Tseng, H.-Y., Li, S., Chang, C., & Lo, Y. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120899 · Cited by 15 · see citing works
WWOX and metabolic regulation in normal and pathological conditions
Baryła, I., Kośla, K., & Bednarek, A. K. (2022) · Journal of Molecular Medicine · doi:10.1007/s00109-022-02265-5 · Cited by 14 · see citing works
Stamenković, S., Li, Y., Waters, J., & Shih, A. Y. (2023) · Stroke · doi:10.1161/strokeaha.122.037156 · Cited by 14 · see citing works
Sakibuzzaman, M., Hassan, A., Hayee, S., Haque, F. A., Bushra, S. S., Maliha, M., Tania, M. K., Sadat, A., Akter, F., Mazumder, T., et al. (2022) · Cureus · doi:10.7759/cureus.29297 · Cited by 13 · see citing works
Helgudóttir, S. S., Mørkholt, A. S., Lichota, J., Bruun-Nyzell, P., Andersen, M. C., Kristensen, N. M. J., Johansen, A. K., Zinn, M. R., Jensdóttir, H. M., & Nieland, J. D. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.387965 · Cited by 14 · see citing works
Murray, C. J., Vecchiarelli, H. A., & Tremblay, M. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1119552 · Cited by 12 · see citing works
Boukhvalova, M. S., Kastrukoff, L. F., & Blanco, J. C. G. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1204852 · Cited by 12 · see citing works
He, S., Qiu, S., Pan, M., Palavicini, J. P., Wang, H., Li, X., Bhattacharjee, A., Barannikov, S., Bieniek, K. F., Dupree, J. L., et al. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1332 · Cited by 12 · see citing works
Uspalenko, N. I., Mosentsov, A. A., Khmil, N. V., Pavlik, L. L., Belosludtseva, N. V., Khunderyakova, N. V., Shigaeva, M. I., Medvedeva, V. P., Malkov, A., Kitchigina, V. F., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814304 · Cited by 11 · see citing works
El-Baz, F. K., Jaleel, G. A. A., Hussein, R. A., & Saleh, D. O. (2021) · Toxicology Reports · doi:10.1016/j.toxrep.2021.11.021 · Cited by 11 · see citing works
Gomes-Copeland, K. K. P., Meireles, C. G., Gomes, J. V. D., Torres, A. G., Sinoti, S. B. P., Fonseca-Bazzo, Y. M., Magalhães, P. O., Fagg, C. W., Simeoni, L. A., & Silveira, D. (2022) · Plants · doi:10.3390/plants11223179 · Cited by 11 · see citing works
Shen, Y., Shen, Y., Wang, M., Jin, K., Yang, P., Cao, Z., Zhu, Q., Zhao, Z., Li, H., Han, L., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116073 · Cited by 10 · see citing works
Ageing, proteostasis, and the gut: Insights into neurological health and disease
Akbar, M., Toppo, P., & Nazir, A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102504 · Cited by 10 · see citing works
Role of Oxygen Radicals in Alzheimer’s Disease: Focus on Tau Protein
Atlante, A., Valenti, D., Latina, V., & Amadoro, G. (2021) · Oxygen · doi:10.3390/oxygen1020010 · Cited by 11 · see citing works
Kachouei, A. A., Singar, S., Wood, A., Flatt, J. D., Rosenkranz, S. K., Rosenkranz, R. R., & Akhavan, N. S. (2025) · Nutrients · doi:10.3390/nu17142328 · Cited by 9 · see citing works
Braissant, O., McLin, V. A., Sessa, D., & Pierzchała, K. (2025) · Scientific Reports · doi:10.1038/s41598-025-21054-x · Cited by 9 · see citing works
Nelson, R. S., Dammer, E. B., Santiago, J. V., Seyfried, N. T., & Rangaraju, S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.902146 · Cited by 9 · see citing works
Biomarkers of endothelial dysfunction and cognition: A two‐step IPD meta‐analysis
Beran, M., Jansen, W. J., Oomens, J. E., Moonen, J. E. F., Slagboom, P. E., Huisman, M. A., Kok, A. A. L., Nooyens, A. C. J., VERSCHUREN, W., Stehouwer, C. D. A., et al. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.14272 · Cited by 8 · see citing works
Wearn, A. R., Tardif, C. L., Leppert, I. R., Baracchini, G., Hughes, C. S., Tremblay‐Mercier, J., Breitner, J. C. S., Poirier, J., Villeneuve, S., Bernhardt, B. C., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2502674122 · Cited by 9 · see citing works
Taewan, K. I. M., Cho, J., & Hyunsik, K. A. N. G. (2025) · Scientific Reports · doi:10.1038/s41598-025-33262-6 · Cited by 8 · see citing works
Chauhan, P., Begum, M., Narapureddy, B., Gupta, S., Wadhwa, K., Singh, G., Kumawat, R., Sharma, N., Ballal, S., Jha, S., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04535-4 · Cited by 8 · see citing works
Methylated Ccfdna from Plasma Biomarkers of Alzheimer’s Disease Using Targeted Bisulfite Sequencing
Guemri, J., Pierre‐Jean, M., Brohard, S., Oussada, N., Horgues, C., Bonnet, É., Mauger, F., & Deleuze, J. (2022) · Epigenomics · doi:10.2217/epi-2021-0491 · Cited by 7 · see citing works
Ma, W., Frigon, É., Maranzano, J., Zeighami, Y., & Dadar, M. (2024) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2024.1477973 · Cited by 7 · see citing works
Xu, M., Yi, X., Huang, S., Wang, Q.-H., Lai, Y., Wang, Z., Fan, D., Zeng, G., Bai, Y., Shen, Y., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03369-5 · Cited by 7 · see citing works
Zhu, Q., Song, Y., Qian, Y., Zhang, R., Xue, J., & Hou, Y. (2025) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2025.25 · Cited by 6 · see citing works
Identification of Molecular Correlations of GSDMD with Pyroptosis in Alzheimer's Disease
Song, T., Chen, Y., Li, C., Yao, Y., Ma, S., Yazhen, S., & Cheng, J. (2024) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/0113862073285497240226061936 · Cited by 7 · see citing works
Bánáti, D., Hellmann‐Regen, J., Mack, I., Young, H. A., Benton, D., Eggersdorfer, M. L., Rohn, S., Dulińska-Litewka, J., Krężel, W., & Rühl, R. (2024) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831/a000808 · Cited by 7 · see citing works
Exploring non-canonical targets in Alzheimer’s disease: a departure from the norm
Jain, S., & Chauhan, N. (2024) · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · doi:10.1186/s41983-024-00908-7 · Cited by 7 · see citing works
Ohnishi, H., Matsuoka, K., Takahashi, M., Yoshikawa, H., Minami, A., Ueda, K., Fujimoto, Y., Kiuchi, K., Ochi, T., Miyasaka, T., et al. (2024) · Psychogeriatrics · doi:10.1111/psyg.13223 · Cited by 7 · see citing works
Huang, H.-T., & Tzeng, S. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105645 · Cited by 7 · see citing works
Hodgson, L. M., Li, Y., Iturria‐Medina, Y., Stratton, J. A., Wolf, G., Krishnaswamy, S., Bennett, D. A., & Bzdok, D. (2024) · Communications Biology · doi:10.1038/s42003-024-06273-8 · Cited by 6 · see citing works
Long Noncoding RNAs in CNS Myelination and Disease
Zhang, J., Guan, M.-L., Zhou, X., Berry, K., He, X.-L., & Lu, Q. R. (2022) · The Neuroscientist · doi:10.1177/10738584221083919 · Cited by 6 · see citing works
Chen, Y., Chang, C., Liang, Y., Tseng, H.-Y., Li, S., Chang, C., Wu, Y.-T., Shao, H.-H., Chen, P., Lai, M.-L., et al. (2024) · Journal of Neural Engineering · doi:10.1088/1741-2552/ad7322 · Cited by 7 · see citing works
Mitchener, V. F. T., Thackray, M. J., & Arancibia-Cárcamo, I. (2025) · Journal of Physiology · doi:10.1113/jp287015 · Cited by 6 · see citing works
Chandio, B. Q., Olivetti, E., Romero-Bascones, D., Thomopoulos, S. I., Villalón‐Reina, J. E., Nir, T. M., Harezlak, J., Thompson, P. M., & Garyfallidis, E. (2026) · Medical Image Analysis · doi:10.1016/j.media.2026.104114 · Cited by 6 · see citing works
Innate and adaptive immune mechanisms regulating central nervous system remyelination
Creswell, R., & Dombrowski, Y. (2022) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.12.002 · Cited by 6 · see citing works
Probabilistic mapping and automated segmentation of human brainstem white matter bundles
Olchanyi, M., Schreier, D. R., Li, J., Maffei, C., Sorby‐Adams, A., Kinney, H. C., Healy, B. C., Freeman, H. J., Shless, J. S., Destrieux, C., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2509321123 · Cited by 6 · see citing works
Kawaguchi, S., Kan, H., Uchida, Y., Kasai, H., Hiwatashi, A., & Ueki, Y. (2024) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2024.02.010 · Cited by 5 · see citing works
Oxenkrug, G. F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413269 · Cited by 5 · see citing works
Analysis of advanced diffusion models assessing white matter microstructure in Alzheimer’s disease
Lv, M., Zhan, K., Yang, J., Li, Y., Li, Y., Xu, X., Han, L., Feng, H., & Zhong, J. (2025) · Scientific Reports · doi:10.1038/s41598-025-09412-1 · Cited by 5 · see citing works
Shim, J.-M., Cho, S., Kang, S., & Kang, C. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.950650 · Cited by 5 · see citing works
Ali, H., Tofrizal, T., Tjong, D. H., Yanis, A., & Yarni, S. D. (2023) · Archives of Medical Science · doi:10.5114/aoms/163353 · Cited by 5 · see citing works
- Authors
- Papuć, E., & Rejdak, K.
- Affiliations
- Medical University of Lublin (PL)
- Corresponding author
- Papuć, Ewa
- Venue
- Archives of Medical Science
- Publisher
- Termedia Sp. z.o.o.
- Published
- 2020
- Volume
- 16
- Issue
- 2
- Pages
- 345-341
- ISSN
- 1734-1922 (ISSN-L)
- PMC
- PMC7069444
- OpenAlex
- W2898142024
- Cited by
- 188
- References
- 73
- Citations by year
- 2026: 22 · 2025: 33 · 2024: 31 · 2023: 33 · 2022: 40 · 2021: 20 · 2020: 8 · 2019: 1
- FWCI
- 5.67
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc-sa
- Locations
- Archives of Medical Science (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, myelin damage, oligodendrocyte death, amyloid-beta, tau pathology, neurofibrillary tangles, myelin pathology, grey matter
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