The effects of normal aging on myelinated nerve fibers in monkey central nervous system
Open accessAbstract
The effects of aging on myelinated nerve fibers of the central nervous system are complex. Many myelinated nerve fibers in white matter degenerate and are lost, leading to some disconnections between various parts of the central nervous system. Other myelinated nerve fibers are affected differently, because only their sheaths degenerate, leaving the axons intact. Such axons are remyelinated by a series of internodes that are much shorter than the original ones and are composed of thinner sheaths. Thus the myelin-forming cells of the central nervous system, the oligodendrocytes, remain active during aging. Indeed, not only do these neuroglial cell remyelinate axons, with age they also continue to add lamellae to the myelin sheaths of intact nerve fibers, so that sheaths become thicker. It is presumed that the degeneration of myelin sheaths is due to the degeneration of the parent oligodendrocyte, and that the production of increased numbers of internodes as a consequence of remyelination requires additional oligodendrocytes. Whether there is a turnover of oligodendrocytes during life has not been studied in primates, but it has been established that over the life span of the monkey, there is a substantial increase in the numbers of oligodendrocytes. While the loss of some myelinated nerve fibers leads to some disconnections, the degeneration of other myelin sheaths and the subsequent remyelination of axons by shorter internodes slow down the rate conduction along nerve fibers. These changes affect the integrity and timing in neuronal circuits, and there is evidence that they contribute to cognitive decline.
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A significant fraction of adult-born OLs survive long-term.
“Nevertheless, the data suggest that a significant fraction of adult-born OLs survive long-term, in keeping with previous reports that OLs continue to accumulate with age in the mouse corpus callosum (McCarthy and Leblond, 1988) and the primate optic nerve (Sandell and Peters, 2002; Peters, 2009).”
From Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling (2013) · cites this paper as Peters, 2009
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Cites
Longitudinal Magnetic Resonance Imaging Studies of Older Adults: A Shrinking Brain
Resnick, S. M., Pham, D. L., Kraut, M. A., Zonderman, A. B., & Davatzikos, C. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03295.2003 · Cited by 1,425 · see citing works
Pfefferbaum, A., Mathalon, D. H., Sullivan, E. V., Rawles, J. M., Zipursky, R. B., & Lim, K. O. (1994) · Archives of Neurology · doi:10.1001/archneur.1994.00540210046012 · Cited by 1,363 · see citing works
Life and Death of Neurons in the Aging Brain
Morrison, J. H., & Hof, P. R. (1997) · Science · doi:10.1126/science.278.5337.412 · Cited by 1,344 · see citing works
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961 · see citing works
The oligodendrocyte precursor cell in health and disease
Levine, J. M., Reynolds, R., & Fawcett, J. W. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01691-x · Cited by 673 · see citing works
Marked loss of myelinated nerve fibers in the human brain with age
Marner, L., Nyengaard, J., Tang, Y., & Pakkenberg, B. (2003) · The Journal of comparative neurology · doi:10.1002/cne.10714 · Cited by 625 · see citing works
White matter changes with normal aging.
Guttmann, C. R. G., Jolesz, F. A., Kikinis, R., Killiany, R. J., Moss, M. B., Sandor, T., & Albert, M. S. (1998) · Neurology · doi:10.1212/wnl.50.4.972 · Cited by 466 · see citing works
General Organization of Callosal Connections in the Cerebral Cortex
Innocenti, G. M. (1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1_9 · Cited by 394 · see citing works
Age-induced white matter changes in the human brain: a stereological investigation.
Tang, Y., Nyengaard, J., Pakkenberg, B., & Gundersen, H. (1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00155-3 · Cited by 345 · see citing works
Elmquist, J. K., Scammell, T. E., Jacobson, C. D., & Saper, C. B. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960715)371:1 · Cited by 335 · see citing works
(1978) · PubMed · Cited by 297 · see citing works
Aging and the myelinated fibers in prefrontal cortex and corpus callosum of the monkey
Peters, A., & Sethares, C. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.10099 · Cited by 274 · see citing works
Self-citationKeirstead, H. S., & Blakemore, W. (1997) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199711000-00003 · Cited by 272 · see citing works
Age‐Related White Matter Atrophy in the Human Brain
Meier-Ruge, W., Ulrich, J., Brühlmann, M., & Meier, E. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb27462.x · Cited by 252 · see citing works
Feature article: are neurons lost from the primate cerebral cortex during normal aging?
Peters, A. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.4.295 · Cited by 245 · see citing works
Self-citationSurvival rate and life span of rhesus monkeys at the Yerkes regional primate research center
Tigges, J., Gordon, T. P., McClure, H. M., Hall, E. C., & Peters, A. (1988) · American Journal of Primatology · doi:10.1002/ajp.1350150308 · Cited by 242 · see citing works
Self-citationSteininger, T. L., Gong, H., McGinty, D., & Szymusiak, R. S. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20010122)429:4 · Cited by 240 · see citing works
Effects of age and sex on volumes of the thalamus, pons, and cortex
Sullivan, E. V., Rosenbloom, M. J., Serventi, K. L., & Pfefferbaum, A. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00044-7 · Cited by 217 · see citing works
The effects of aging on area 46 of the frontal cortex of the rhesus monkey.
Peters, A., Leahu, D., Moss, M. B., & McNally, K. J. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.6.621 · Cited by 214 · see citing works
Self-citationFreeman, S. H., Kandel, R., Cruz, L., Rozkalne, A., Newell, K. L., Frosch, M. P., Hedley‐Whyte, E. T., Locascio, J. J., Lipsitz, L. A., & Hyman, B. T. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31818fc72f · Cited by 212 · see citing works
Conduction in Segmentally Demyelinated Mammalian Central Axons
Felts, P. A., Baker, T. A., & Smith, K. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07267.1997 · Cited by 211 · see citing works
Cerghet, M., Skoff, R. P., Bessert, D. A., Zhang, Z., Mullins, C. M., & Ghandour, M. S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2219-05.2006 · Cited by 203 · see citing works
Remyelination in multiple sclerosis
Brück, W., Kuhlmann, T., & Stadelmann, C. (2003) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(02)00191-0 · Cited by 202 · see citing works
Peters, A., Josephson, K., & Vincent, S. L. (1991) · The Anatomical Record · doi:10.1002/ar.1092290311 · Cited by 196 · see citing works
Self-citationSenile plaques in cortex of aged normal monkeys.
Struble, R., Price, D. L., & Cork, L. (1985) · Brain Research · doi:10.1016/0006-8993(85)91298-3 · Cited by 182 · see citing works
Neuropsychological and neurophysiological changes in healthy adult humans across the age range
Albert, M. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90049-h · Cited by 158 · see citing works
Fields of origin and pathways of the interhemispheric commissures in the temporal lobe of macaques
Demeter, S., Rosene, D. L., & Hoesen, G. W. V. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020104 · Cited by 154 · see citing works
Oligodendrocytes, their Progenitors and other Neuroglial Cells in the Aging Primate Cerebral Cortex
Peters, A. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh060 · Cited by 147 · see citing works
Self-citationAMNESIA FOLLOWING DAMAGE TO THE LEFT FORNIX AND TO OTHER SITES: A COMPARATIVE STUDY
Gaffan, E. A., GAFFAN, D., & Hodges, J. R. (1991) · Brain · doi:10.1093/brain/114.3.1297 · Cited by 146 · see citing works
Gross, C. G., Bender, D. B., & Mishkin, M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90517-0 · Cited by 141 · see citing works
Amnesia following traumatic bilateral fornix transection
D’Esposito, M., Verfaellie, M. H., ALEXANDER, M. P., & Katz, D. I. (1995) · Neurology · doi:10.1212/wnl.45.8.1546 · Cited by 140 · see citing works
Smith, D. E., Rapp, P., McKay, H. M., Roberts, J. A., & Tuszynski, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4289-03.2004 · Cited by 140 · see citing works
Effects of age on the thickness of myelin sheaths in monkey primary visual cortex
Peters, A., Sethares, C., & Killiany, R. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1205 · Cited by 139 · see citing works
Self-citationREDUNDANT MYELIN SHEATHS AND OTHER ULTRASTRUCTURAL FEATURES OF THE TOAD CEREBELLUM
Rosenbluth, J. (1966) · Journal of Cell Biology · doi:10.1083/jcb.28.1.73 · Cited by 138 · see citing works
No evidence for chronic demyelination in spared axons after spinal cord injury in a mouse
Lasiene, J., Shupe, L., Perlmutter, S., & Horner, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4756-07.2008 · Cited by 133 · see citing works
Duce, J. A., Podvin, S., Hollander, W., Kipling, D., Rosene, D. L., & Abraham, C. R. (2007) · Glia · doi:10.1002/glia.20593 · Cited by 131 · see citing works
Dense amnesia in the monkey after transection of fornix, amygdala and anterior temporal stem
Gaffan, D., Parker, A. J., & Easton, A. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00097-x · Cited by 122 · see citing works
Disrupted myelin and axon loss in the anterior commissure of the aged rhesus monkey
Sandell, J., & Peters, A. (2003) · The Journal of comparative neurology · doi:10.1002/cne.10859 · Cited by 121 · see citing works
Self-citationIs there remyelination during aging of the primate central nervous system?
Peters, A., & Sethares, C. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10639 · Cited by 112 · see citing works
Self-citationDegradation of Signal Timing in Cortical Areas V1 and V2 of Senescent Monkeys
Wang, Y. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh143 · Cited by 112 · see citing works
Silver, M. H., Newell, K. L., Brady, C. B., Hedley-White, E. T., & Perls, T. T. (2002) · Psychosomatic Medicine · doi:10.1097/00006842-200205000-00014 · Cited by 110 · see citing works
Cellular pathology of the central nervous system.
Graeber, M. B., Blakemore, W. F., & Kreutzberg, G. W. (2002) · Max Planck Institute for Plasma Physics · Cited by 108 · see citing works
Cortical field of origin of the anterior commissure of the rhesus monkey
Jouandet, M. L., & Gazzaniga, M. S. (1979) · Experimental Neurology · doi:10.1016/0014-4886(79)90088-8 · Cited by 105 · see citing works
Lack of correlation between plaque burden and cognition in the aged monkey
Sloane, J. A., Pietropaolo, M., Rosene, D. L., Moss, M. B., Peters, A., Kemper, T. L., & Abraham, C. R. (1997) · Acta Neuropathologica · doi:10.1007/s004010050735 · Cited by 101 · see citing works
Self-citationOWEN, M. (1981) · Behavioural Brain Research · doi:10.1016/0166-4328(81)90032-2 · Cited by 99 · see citing works
Ballooning of myelin sheaths in normally aged macaques
Feldman, M. L., & Peters, A. (1998) · Journal of Neurocytology · doi:10.1023/a:1006926428699 · Cited by 96 · see citing works
Self-citationMalamud, N. (1957) · University of California Press eBooks · doi:10.1525/9780520323261 · Cited by 94 · see citing works
Basic electrophysiological properties of spinal cord motoneurons during old age in the cat
Morales, F. R., Boxer, P. A., Fung, S. J., & Chase, M. H. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.1.180 · Cited by 94 · see citing works
Kapsimali, M., Vidal, B., González, A., Dufour, S., & Vernier, P. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000410)419:3 · Cited by 91 · see citing works
Age‐related molecular reorganization at the node of Ranvier
Hinman, J., Peters, A., Cabral, H., Rosene, D., Hollander, W., Rasband, M., & Abraham, C. R. (2006) · The Journal of comparative neurology · doi:10.1002/cne.20886 · Cited by 87 · see citing works
Self-citationEffects of age on the glial cells in the rhesus monkey optic nerve
Sandell, J. H., & Peters, A. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.10162 · Cited by 84 · see citing works
Self-citationThe neuroglial population in the primary visual cortex of the aging rhesus monkey
Peters, A., Verderosa, A., & Sethares, C. (2008) · Glia · doi:10.1002/glia.20686 · Cited by 82 · see citing works
Self-citationAn MRI study of age-related white and gray matter volume changes in the rhesus monkey
Wisco, J. J., Killiany, R., Guttmann, C. R. G., Warfield, S. K., Moss, M. B., & Rosene, D. L. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.03.022 · Cited by 79 · see citing works
Lintl, P., & Braak, H. (1983) · Acta Neuropathologica · doi:10.1007/bf00691983 · Cited by 76 · see citing works
Hof, P. R., Nimchinsky, E. A., Young, W. G., & Morrison, J. H. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000424)420:1 · Cited by 71 · see citing works
Sullivan, M. V., & Hamilton, C. R. (1973) · Physiology & Behavior · doi:10.1016/0031-9384(73)90322-3 · Cited by 69 · see citing works
Memory establishment via the anterior commissure of monkeys
Sullivan, M. V., & Hamilton, C. R. (1973) · Physiology & Behavior · doi:10.1016/0031-9384(73)90283-7 · Cited by 68 · see citing works
Changes in Neuroglia and Myelination in the White Matter of Aging Mice
Sturrock, R. R. (1976) · Journal of Gerontology · doi:10.1093/geronj/31.5.513 · Cited by 66 · see citing works
Age-associated changes in rhesus CNS composition identified by MRI
Andersen, A. H., Zhang, Z., Zhang, M., Gash, D. M., & Avison, M. J. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01343-8 · Cited by 64 · see citing works
In aging, is it gray or white?
Peters, A., & Rosene, D. L. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10715 · Cited by 62 · see citing works
Self-citationSobótka, S., & Ringo, J. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04222.1996 · Cited by 60 · see citing works
Pathophysiology of demyelinated axons
Waxman, S. G., Kocsis, J. D., & Black, J. A. (1995) · doi:10.1093/acprof:oso/9780195082937.003.0023 · Cited by 55 · see citing works
The cytoarchitectonic distribution of senile plaques in three aged monkeys
Heilbroner, P. L., & Kemper, T. L. (1990) · Acta Neuropathologica · doi:10.1007/bf00662638 · Cited by 54 · see citing works
Ultrastructural analysis of the paranodal junction of myelinated fibers in 31‐month‐old‐rats
Sugiyama, I., Tanaka, K., Akita, M., Yoshida, K., Kawase, T., & Asou, H. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10386 · Cited by 50 · see citing works
Chronic copper poisoning and changes in the central nervous system of sheep
Howell, J. M., Blakemore, W. F., Gopinath, C., Hall, G. A., & Parker, J. H. (1974) · Acta Neuropathologica · doi:10.1007/bf00684387 · Cited by 50 · see citing works
Fletcher, B. R., Calhoun, M. E., Rapp, P. R., & Shapiro, M. L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4441-05.2006 · Cited by 50 · see citing works
The effects of aging on the frequency of nerve fibers in rhesus monkey striate cortex
Nielsen, K. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00169-x · Cited by 48 · see citing works
Postmortem Indices Linking Risk Factors to Cognition
Bennett, D. A. (2006) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-200607001-00009 · Cited by 46 · see citing works
Norton, W. T. (1996) · Neurochemical Research · doi:10.1007/bf02527715 · Cited by 46 · see citing works
Severe radicular pathology in rats with longstanding diabetes
Tamura, E., & Parry, G. J. (1994) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)90131-7 · Cited by 44 · see citing works
Changes in the axonal conduction velocity of pyramidal tract neurons in the aged cat
Xi, M., Liu, R.-H., Engelhardt, J. K., Morales, F. R., & Chase, M. H. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00754-4 · Cited by 44 · see citing works
Remodelling of optic nerve myelin sheaths and axons during metamorphosis in Xenopus laevis
Cullen, M. J., & Webster, H. D. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901840209 · Cited by 36 · see citing works
Pathology of the myelin sheath
Ludwin, S. K. (1995) · doi:10.1093/acprof:oso/9780195082937.003.0022 · Cited by 33 · see citing works
Morphological features of degenerating oligodendrocytes in twitcher mice
LeVine, S. M., & Torres, M. V. (1992) · Brain Research · doi:10.1016/0006-8993(92)91018-a · Cited by 27 · see citing works
An ultrastructural characterization of the newly generated cells in the adult monkey dentate gyrus
Ngwenya, L. B., Rosene, D. L., & Peters, A. (2007) · Hippocampus · doi:10.1002/hipo.20384 · Cited by 23 · see citing works
Self-citationReview of the Morphological Aspects of Remyelination
Hirano, A. (1989) · Developmental Neuroscience · doi:10.1159/000111892 · Cited by 19 · see citing works
Fornix Transection Impairs Learning of Randomly Changing Object Discriminations
Wilson, C. R. E., Charles, D. P., Buckley, M. J., & Gaffan, D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3536-07.2007 · Cited by 18 · see citing works
Myelin breakdown in the posterior funiculus of the kitten after dorsal rhizotomy
Franson, P., & Ronnevi, L. (1989) · Anatomy and Embryology · doi:10.1007/bf00315885 · Cited by 17 · see citing works
Interhemispheric sharing of visual memory in macaques
Doty, R. W., Ringo, J. L., & Lewine, J. D. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90120-1 · Cited by 15 · see citing works
Urbano, F. J., Sierra, F., Colombo, J. A., Velasco, J. M., & Bu�o, W. (1997) · Glia · doi:10.1002/(sici)1098-1136(199702)19:2 · Cited by 9 · see citing works
Larsson, E. (1996) · Rivista di Neuroradiologia · doi:10.1177/19714009960090s108 · Cited by 5 · see citing works
Herman (2000) · doi:10.1002/1096-9861(20000703)422:3
Flagged first, then by citations
Research works printed but not linked: 3
- Garner A. Sarks S. Sraks J. P. (1994). Degenerative and related disorders of the retina and choroid. In Pathobiology of Ocular Disease; A Dynamic Approach, Garner A. Klintworth G. K., eds (New York, Marcel Decker), pp. 631– 674
- Guillery R. W. (1970). Light- and electron-microscopical studies of normal and degenerating axons. In Contemporary Research Methods in Neuroanatomy, Nauta W. J. H. Ebbesson S. O. E. eds (New York, Springer), pp. 77– 105
- Kemper T. L. (1994). Neuroanatomical and neuropathological changes during aging and dementia. In Clinical Neurology of Aging, Albert M. Knoefel J. E. eds (New York: Oxford University Press), pp. 3– 67
Cited by
Sorted by citations
Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling
Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 872 · see citing works
“Nevertheless, the data suggest that a significant fraction of adult-born OLs survive long-term, in keeping with previous reports that OLs continue to accumulate with age in the mouse corpus callosum (McCarthy and Leblond, 1988) and the primate optic nerve (Sandell and Peters, 2002; Peters, 2009).”
ResultLazari, A., & Lipp, I. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117744 · Cited by 176 · see citing works
Slowing down: age-related neurobiological predictors of processing speed
Eckert, M. A. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00025 · Cited by 162 · see citing works
Inflammatory cytokines influence measures of white matter integrity in Bipolar Disorder
Benedetti, F., Poletti, S., Hoogenboezem, T. A., Mazza, E., Ambrée, O., de Wit, H., Wijkhuijs, A. J. M., Locatelli, C., Bollettini, I., Colombo, C., et al. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.05.047 · Cited by 151 · see citing works
Bartzokis, G., Lu, P. H., Heydari, P., Couvrette, A., Lee, G. J., Kalashyan, G., Freeman, F., Grinstead, J. W., Villablanca, P., Finn, J. P., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.07.010 · Cited by 152 · see citing works
Neuroglialpharmacology: Myelination as a shared mechanism of action of psychotropic treatments
Bartzokis, G. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.01.015 · Cited by 142 · see citing works
Advanced MRI techniques to improve our understanding of experience-induced neuroplasticity
Tardif, C. L., Gauthier, C. J., Steele, C. J., Bazin, P.-L., Schäfer, A., Schaefer, A., Turner, R., & Villringer, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.047 · Cited by 127 · see citing works
A review of the structural alterations in the cerebral hemispheres of the aging rhesus monkey
Peters, A., & Kemper, T. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.11.015 · Cited by 135 · see citing works
Self-citationWhite matter lesions defined by diffusion tensor imaging in older adults
Back, S. A., Kroenke, C. D., Sherman, L. S., Lawrence, G., Gong, X., Taber, E. N., Sonnen, J. A., Larson, E. B., & Montine, T. J. (2011) · Annals of Neurology · doi:10.1002/ana.22484 · Cited by 109 · see citing works
Chang, W., Weaver, C., Medalla, M., Moore, T., & Luebke, J. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.09.012 · Cited by 20 · see citing works
- Authors
- Peters, A.
- Affiliations
- Boston University (US)
- Corresponding author
- Peters, Alan
- ORCID
- Peters, Alan
- Venue
- Frontiers in Neuroanatomy
- Publisher
- Frontiers Media SA
- Published
- 2009
- Volume
- 3
- Pages
- 11-11
- ISSN
- 1662-5129 (ISSN-L)
- PMC
- PMC2713738
- OpenAlex
- W2048501712
- Cited by
- 211
- References
- 83
- Citations by year
- 2026: 11 · 2025: 12 · 2024: 16 · 2023: 23 · 2022: 14 · 2021: 20 · 2020: 12 · 2019: 14 · 2018: 16 · 2017: 6 · 2016: 17 · 2015: 7 · 2014: 10 · 2013: 10 · 2012: 6
- FWCI
- 2.41
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Neuroanatomy (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- OpenBU (Boston University) (submittedVersion, other-oa)
- Funders
- National Institutes of Health
- National Institute on Aging (P01AG000001)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- normal aging, myelinated axons, central nervous system, oligodendrocytes, remyelination, myelin degeneration, internodes, white matter degeneration, myelin lamellae, nerve conduction slowing, cognitive decline, monkeys
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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