Neuroplasticity Failure in Alzheimer's Disease

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works

Mild Cognitive Impairment: Clinical Characterization and Outcome

Petersen, R. C., Smith, G. E., Waring, S. C., Ivnik, R. J., Tangalos, E. G., & Kokmen, E. (1999) · Archives of Neurology · doi:10.1001/archneur.56.3.303 · Cited by 8,980 · see citing works

Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment

Terry, R. D., Masliah, E., Salmon, D. P., Butters, N., DeTeresa, R., Hill, R., Hansen, L. A., & Katzman, R. (1991) · Annals of Neurology · doi:10.1002/ana.410300410 · Cited by 4,397 · see citing works

Diffusible, nonfibrillar ligands derived from Aβ _1–42 are potent central nervous system neurotoxins

Lambert, M. P., Barlow, A. K., Chromy, B. A., Edwards, C., Freed, R., Liosatos, M., Morgan, T. E., Rozovsky, I., Trommer, B., Viola, K. L., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6448 · Cited by 3,506 · see citing works

Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease

Arriagada, P. V., Growdon, J. H., Hedley-Whyte, E. T., & Hyman, B. T. (1992) · Neurology · doi:10.1212/wnl.42.3.631 · Cited by 2,668 · see citing works

Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein

Games, D., Adams, D., Alessandrini, R., Barbour, R., Borthelette, P., Blackwell, C., Carr, T., Clemens, J., Donaldson, T., Gillespie, F., et al. (1995) · Nature · doi:10.1038/373523a0 · Cited by 2,516 · see citing works

Profound Loss of Layer II Entorhinal Cortex Neurons Occurs in Very Mild Alzheimer’s Disease

Gómez-Isla, T., Price, J. L., McKeel Jr., D. W., Morris, J. C., Growdon, J. H., & Hyman, B. T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-14-04491.1996 · Cited by 1,796 · see citing works

Brain Infarction and the Clinical Expression of Alzheimer Disease<subtitle>The Nun Study</subtitle>

Snowdon, D. A. (1997) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.1997.03540340047031 · Cited by 1,590 · see citing works

Editorial on Consensus Recommendations for the Postmortem Diagnosis of Alzheimer Disease from the National Institute on Aging and the Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer Disease

HYMAN, B. T., & TROJANOWSKI, J. Q. (1997) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199710000-00002 · Cited by 1,542 · see citing works

Neuronal loss correlates with but exceeds neurofibrillary tangles in Alzheimer's disease

Gómez‐Isla, T., Hollister, R., West, H., Mui, S., Growdon, J. H., Petersen, R. C., Parisi, J. E., & Hyman, B. T. (1997) · Annals of Neurology · doi:10.1002/ana.410410106 · Cited by 1,489 · see citing works

The topographical and neuroanatomical distribution of neurofibrillary tangles and neuritic plaques in the cerebral cortex of patients with Alzheimer's disease

Arnold, S. E., Hyman, B. T., Flory, J., Damasio, A. R., & Van Hoesen, G. W. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.103 · Cited by 1,380 · see citing works

Amyloid, the presenilins and Alzheimer’s disease

Hardy, J. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)01030-2 · Cited by 1,370 · 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

Cortical Map Reorganization Enabled by Nucleus Basalis Activity

Kilgard, M. P., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.279.5357.1714 · Cited by 1,197 · see citing works

Cellular actions of beta-amyloid precursor protein and its soluble and fibrillogenic derivatives

Mattson, M. P. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.4.1081 · Cited by 1,006 · see citing works

Consensus Recommendations for the Postmortem Diagnosis of Alzheimer’s Disease

(1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00057-2 · Cited by 981 · see citing works

A prospective study of estrogen replacement therapy and the risk of developing Alzheimer's disease

Kawas, C. H., Resnick, S. M., Morrison, A., Brookmeyer, R., Corrada, M. M., Zonderman, A. B., Bacal, C., Lingle, D. D., & Metter, E. J. (1997) · Neurology · doi:10.1212/wnl.48.6.1517 · Cited by 967 · see citing works

Mechanisms of Neuronal Degeneration in Alzheimer's Disease

Yankner, B. A. (1996) · Neuron · doi:10.1016/s0896-6273(00)80115-4 · Cited by 947 · see citing works

Impaired synaptic plasticity and learning in aged amyloid precursor protein transgenic mice

Chapman, P. F., White, G. L., Jones, M. W., Cooper-Blacketer, D., Marshall, V. J., Irizarry, M., Younkin, L., Good, M. A., Bliss, T. V. P., Hyman, B. T., et al. (1999) · Nature Neuroscience · doi:10.1038/6374 · Cited by 946 · see citing works

Release of Alzheimer Amyloid Precursor Derivatives Stimulated by Activation of Muscarinic Acetylcholine Receptors

Nitsch, R. M., Slack, B. E., Wurtman, R. J., & Growdon, J. H. (1992) · Science · doi:10.1126/science.1411529 · Cited by 898 · see citing works

The biochemical pathway of neurofibrillary degeneration in aging and Alzheimer's disease.

Delacourte, A., David, J. P., Sergeant, N., Buée, L., Wattez, A., Vermersch, P., Ghozali, F., Fallet-Bianco, C., Pasquier, F., Lebert, F., et al. (1999) · Neurology · doi:10.1212/wnl.52.6.1158 · Cited by 828 · see citing works

Differential Effects of Apolipoproteins E3 and E4 on Neuronal Growth in Vitro

Nathan, B. P., Bellosta, S., Sanan, D. A., Weisgraber, K. H., Mahley, R. W., & Pitas, R. E. (1994) · Science · doi:10.1126/science.8171342 · Cited by 795 · see citing works

Alzheimer's Disease: A Central Role for Amyloid

Selkoe, D. J. (1994) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199409000-00003 · Cited by 752 · see citing works

Evolution of the neuropathology of Alzheimer's disease

Braak, H., & Braak, E. (1996) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1996.tb05866.x · Cited by 710 · see citing works

Apolipoprotein E in animal models of CNS injury and in alzheimer's disease

Poirier, J. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90156-2 · Cited by 637 · see citing works

Water-soluble Aβ(N-40, N-42) oligomers in normal and Alzheimer disease brains

Kuo, Y.-M., Emmerling, M. R., Vigo-Pelfrey, C., Kasunic, T. C., Kirkpatrick, J. B., Murdoch, G. H., Ball, M. J., & Roher, A. E. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.8.4077 · Cited by 618 · see citing works

Cerebral amyloid deposition and diffuse plaques in ``normal'' aging: Evidence for presymptomatic and very mild Alzheimer's disease

Morris, J. C., Storandt, M., McKeel, D. W., Rubin, E. H., Price, J. L., Grant, E. A., & Berg, L. (1996) · Neurology · doi:10.1212/wnl.46.3.707 · Cited by 603 · see citing works

Alzheimer neuropathologic alterations in aged cognitively normal subjects

Davis, D. G., Schmitt, F. A., Wekstein, D. R., & Markesbery, W. R. (1999) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199904000-00008 · Cited by 516 · see citing works

Destabilization of β-catenin by mutations in presenilin-1 potentiates neuronal apoptosis

Zhang, Z., Hartmann, H., Do, V. M., Abramowski, D., Sturchler, C., Staufenbiel, M., Sommer, B., van de Wetering, M., Clevers, H. C., Säftig, P., et al. (1998) · Nature · doi:10.1038/27208 · Cited by 511 · see citing works

Nerve growth factor-induced neurite outgrowth in PC12 cells involves the coordinate induction of microtubule assembly and assembly-promoting factors.

Drubin, D. G., Feinstein, S. C., Shooter, E. M., & Kirschner, M. W. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.101.5.1799 · Cited by 510 · see citing works

Neuron loss in APP transgenic mice

Calhoun, M. E., Wiederhold, K.-H., Abramowski, D., Phinney, A. L., Probst, A., Sturchler-Pierrat, C., Staufenbiel, M., Sommer, B., & Jucker, M. (1998) · Nature · doi:10.1038/27351 · Cited by 502 · see citing works

Ovarian steroids and the brain

McEwen, B. S., Alves, S. E., Bulloch, K., & Weiland, N. G. (1997) · Neurology · doi:10.1212/wnl.48.5_suppl_7.8s · Cited by 482 · see citing works

Apolipoprotein E and Alzheimer's disease

Strittmatter, W. J., & Roses, A. D. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.000413 · Cited by 477 · see citing works

Dendritic Growth in the Aged Human Brain and Failure of Growth in Senile Dementia

Buell, S. J., & Coleman, P. D. (1979) · Science · doi:10.1126/science.493989 · Cited by 475 · see citing works

The 'Preclinical Phase' of Probable Alzheimer's Disease

Linn, R. T. (1995) · Archives of Neurology · doi:10.1001/archneur.1995.00540290075020 · Cited by 437 · see citing works

Large-Scale Sprouting of Cortical Connections After Peripheral Injury in Adult Macaque Monkeys

Florence, S. L., Taub, H. B., & Kaas, J. H. (1998) · Science · doi:10.1126/science.282.5391.1117 · Cited by 432 · see citing works

Environmental stimulation of 129/SvJ mice causes increased cell proliferation and neurogenesis in the adult dentate gyrus

Kempermann, G., Brandon, E. P., & Gage, F. H. (1998) · Current Biology · doi:10.1016/s0960-9822(07)00377-6 · Cited by 385 · see citing works

Effects of PS1 Deficiency on Membrane Protein Trafficking in Neurons

Naruse, S., Thinakaran, G., Luo, J.-J., Kusiak, J. W., Tomita, T., Iwatsubo, T., Qian, X., Ginty, D. D., Price, D. L., Borchelt, D. R., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80637-6 · Cited by 355 · see citing works

Assessment of normal and mutant human presenilin function in Caenorhabditis elegans

Levitan, D. J., Doyle, T. G., Brousseau, D., Lee, M. K., Thinakaran, G., Slunt, H. H., Sisodia, S. S., & Greenwald, I. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.25.14940 · Cited by 354 · see citing works

Neurochemical Studies of Early-Onset Alzheimer's Disease

Francis, P. T., Palmer, A. M., Sims, N. R., Bowen, D. M., DAVISON, A. N., Esiri, M. M., Neary, D., Snowden, J. S., & Wilcock, G. K. (1985) · New England Journal of Medicine · doi:10.1056/nejm198507043130102 · Cited by 353 · see citing works

Plastic Neuronal Remodeling Is Impaired in Patients with Alzheimer’s Disease Carrying Apolipoprotein ε4 Allele

Arendt, T., Schindler, C., Brückner, M. K., Eschrich, K., Bigl, V., Zedlick, D., & Marcova, L. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-02-00516.1997 · Cited by 319 · see citing works

β-amyloid deposition and other measures of neuropathology predict cognitive status in Alzheimer's disease

Cummings, B. J., Pike, C. J., Shankle, R., & Cotman, C. W. (1996) · Neurobiology of Aging · doi:10.1016/s0197-4580(96)00170-4 · Cited by 305 · see citing works

Comparative evaluation of synaptophysin-based methods for quantification of synapses

Calhoun, M. E., Jucker, M., Martin, L. J., Thinakaran, G., Price, D. L., & Mouton, P. R. (1996) · Journal of Neurocytology · doi:10.1007/bf02284844 · Cited by 303 · see citing works

Discussion

Lovestone, S., & Reynolds, C. H. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00577-5 · Cited by 278 · see citing works

Cell Biology of Synaptic Plasticity

Cotman, C. W., & Nieto‐Sampedro, M. (1984) · Science · doi:10.1126/science.6382610 · Cited by 273 · see citing works

Tau Is Enriched on Dynamic Microtubules in the Distal Region of Growing Axons

Black, M. M., Slaughter, T., Moshiach, S., Obrocka, M., & Fischer, I. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-11-03601.1996 · Cited by 270 · see citing works

Synaptotrophic effects of human amyloid β protein precursors in the cortex of transgenic mice

Mucke, L., Masliah, E., Johnson, W. B., Ruppe, M. D., Alford, M. F., Rockenstein, E. M., Forss‐Petter, S., Pietropaolo, M., Mallory, M. E., & Abraham, C. R. (1994) · Brain Research · doi:10.1016/0006-8993(94)90767-6 · Cited by 265 · see citing works

Presymptomatic cognitive deficits in individuals at risk of familial Alzheimer's disease. A longitudinal prospective study

Fox, N. C. (1998) · Brain · doi:10.1093/brain/121.9.1631 · Cited by 263 · see citing works

Increase of synaptic density and memory retention by a peptide representing the trophic domain of the amyloid beta/A4 protein precursor.

Roch, J., Masliah, E., Roch‐Levecq, A., Sundsmo, M. P., Otero, D. A., Veinbergs, I., & Saitoh, T. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.16.7450 · Cited by 255 · see citing works

Patterns of aberrant sprouting in alzheimer's disease

Masliah, E., Mallory, M. E., Hansen, L. A., Alford, M. F., Albright, T., DeTeresa, R. M., Terry, R. D., Baudier, J., & Saitoh, T. (1991) · Neuron · doi:10.1016/0896-6273(91)90170-5 · Cited by 245 · see citing works

Synaptic plasticity in cortical systems

Klintsova, A. Y., & Greenough, W. T. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80028-2 · Cited by 237 · see citing works

Increased Synaptic Sprouting in Response to Estrogen via an Apolipoprotein E-Dependent Mechanism: Implications for Alzheimer’s Disease

Stone, D. J., Rozovsky, I., Morgan, T. E., Anderson, C. P., & Finch, C. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03180.1998 · Cited by 237 · see citing works

Research advances in Alzheimer's disease and related disorders

Iqbal, K., & Disorders, R. (1995) · Wiley eBooks · Cited by 228 · see citing works

Target-Dependent Structural Changes Accompanying Long-Term Synaptic Facilitation in Aplysia Neurons

Glanzman, D. L., Kandel, E. R., & Schacher, S. (1990) · Science · doi:10.1126/science.2389145 · Cited by 224 · see citing works

Selective decline in memory function among healthy elderly

Small, S. A., Stern, Y., Tang, M. X., & Mayeux, R. P. (1999) · Neurology · doi:10.1212/wnl.52.7.1392 · Cited by 219 · see citing works

Growth-associated protein GAP-43 is expressed selectively in associative regions of the adult human brain.

Neve, R. L., Finch, E., Bird, E. D., & Benowitz, L. I. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.10.3638 · Cited by 219 · see citing works

The apolipoprotein E epsilon 4 allele is associated with increased neuritic plaques and cerebral amyloid angiopathy in Alzheimer's disease and Lewy body variant

Olichney, J. M., Hansen, L. A., Galasko, D., Saitoh, T., Hofstetter, C. R., Katzman, R., & Thal, L. J. (1996) · Neurology · doi:10.1212/wnl.47.1.190 · Cited by 216 · see citing works

Estrogen-enhanced neurite growth: evidence for a selective induction of Tau and stable microtubules

Ferreira, A., & Cáceres, A. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-02-00392.1991 · Cited by 203 · see citing works

Re-examination of ex-boxers' brains using immunohistochemistry with antibodies to amyloid ?-protein and tau protein

Tokuda, T., Ikeda, S., Yanagisawa, N., Ihara, Y., & Glenner, G. G. (1991) · Acta Neuropathologica · doi:10.1007/bf00308813 · Cited by 197 · see citing works

Presenilin 1 Facilitates the Constitutive Turnover of β-Catenin: Differential Activity of Alzheimer’s Disease–Linked PS1 Mutants in the β-Catenin–Signaling Pathway

Kang, D. E., Soriano, S., Frosch, M. P., Collins, T., Naruse, S., Sisodia, S. S., Leibowitz, G., Levine, F., & Koo, E. H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04229.1999 · Cited by 193 · see citing works

Decline in reactive fiber growth in the dentate gyrus of aged rats compared to young adult rats following entorhinal cortex removal

Scheff, S. W., Benardo, L. S., & Cotman, C. W. (1980) · Brain Research · doi:10.1016/0006-8993(80)90227-9 · Cited by 186 · see citing works

Sense and antisense transfection analysis of tau function: tau influences net microtubule assembly, neurite outgrowth and neuritic stability

Esmaeli‐Azad, B., McCarty, J. H., & Feinstein, S. C. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.4.869 · Cited by 184 · see citing works

Secreted form of β-amyloid precursor protein shifts the frequency dependency for induction of LTD, and enhances LTP in hippocampal slices

Ishida, A., Furukawa, K., Keller, J. N., & Mattson, M. P. (1997) · Neuroreport · doi:10.1097/00001756-199707070-00009 · Cited by 178 · see citing works

The adult rat olfactory system expresses microtubule-associated proteins found in the developing brain

Viereck, C., Tucker, R., & Matus, A. I. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-10-03547.1989 · Cited by 176 · see citing works

Dendritic sprouting in Alzheimer's presenile dementia

Scheibel, A. B., & Tomiyasu, U. (1978) · Experimental Neurology · doi:10.1016/0014-4886(78)90164-4 · Cited by 176 · see citing works

Cerebral cortex pathology in aging and Alzheimer's disease: a quantitative survey of large hospital-based geriatric and psychiatric cohorts

Giannakopoulos, P., Hof, P. R., Michel, J., Guimón, J., & Bouras, C. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00023-4 · Cited by 173 · see citing works

Stress-induced activation of nitric oxide-producing neurons in the rat brain

Krukoff, T. L., & Khalili, P. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970127)377:4 · Cited by 167 · see citing works

Assessment of CSF levels of tau protein in mildly demented patients with Alzheimer's disease

Galasko, D. R., Clark, C., Chang, L., Miller, B. L., Green, R. C., Motter, R. N., & Seubert, P. A. (1997) · Neurology · doi:10.1212/wnl.48.3.632 · Cited by 153 · see citing works

Distribution of the phosphorylated microtubule-associated protein tau in developing cortical neurons

Brion, J., Octave, J., & Couck, A. M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90533-9 · Cited by 141 · see citing works

Neuropsychological Patterns and Language Deficits in 20 Consecutive Cases of Autopsy-Confirmed Alzheimer's Disease

Price, B. H., Gurvit, H. I., Weıntraub, S., Geula, C., Leimkuhler, E., & Mesulam, M. M. (1993) · Archives of Neurology · doi:10.1001/archneur.1993.00540090038008 · Cited by 136 · see citing works

Early and rapid de novo synthesis of Alzheimer βA4‐Amyloid precursor protein (APP) in activated microglia

Banati, R. B., Gehrmann, J., Czech, C., Mönning, U., Jones, L. L., König, G., Beyreuther, K. T., & Kreutzberg, G. W. (1993) · Glia · doi:10.1002/glia.440090305 · Cited by 132 · see citing works

Dendrites, dementia and the down syndrome

Takashima, S., Ieshima, A., Nakamura, H., & Becker, L. E. (1989) · Brain and Development · doi:10.1016/s0387-7604(89)80082-8 · Cited by 128 · see citing works

Cortical distribution of neurofibrillary tangles in Alzheimer's disease matches the pattern of neurons that retain their capacity of plastic remodelling in the adult brain

Arendt, T., Brückner, M. K., Gertz, H.-J., & Marcova, L. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00509-5 · Cited by 122 · see citing works

Chapter 28 The systems-level organization of cholinergic innervation in the human cerebral cortex and its alterations in Alzheimer's disease

Mesulam, M. M. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62112-3 · Cited by 120 · see citing works

Effects of cholinergic depletion on experience-dependent plasticity in the cortex of the rat

Baskerville, K. A., Schweitzer, J. B., & Herron, P. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00064-x · Cited by 120 · see citing works

Amyloid precursor protein in the cerebral cortex is rapidly and persistently induced by loss of subcortical innervation.

Wallace, W., Ahlers, S. T., Gotlib, J. R., Bragin, V., Sugar, J., Gluck, R., SHEA, P. A., Davis, K. L., & Haroutunian, V. H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8712 · Cited by 118 · see citing works

Neurofibrillary tangles, but not Alzheimer‐type pathology, in a young boxer

Geddes, J. F., Vowles, G. H., Robinson, S. F. D., & Sutcliffe, J. C. (1996) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1996.tb00840.x · Cited by 116 · see citing works

Soluble derivatives of the β amyloid protein precursor in cerebrospinal fluid

Palmert, M. R., Usiak, M., Mayeux, R. P., Raskind, M. A., Tourtellotte, W. W., & Younkin, S. G. (1990) · Neurology · doi:10.1212/wnl.40.7.1028 · Cited by 106 · see citing works

Progressive failure of cerebral angiogenesis supporting neural plasticity in aging rats

Black, J., Polinsky, M. N., & Greenough, W. T. (1989) · Neurobiology of Aging · doi:10.1016/0197-4580(89)90048-1 · Cited by 103 · see citing works

β-Amyloid from Alzheimer disease brains inhibits sprouting and survival of sympathetic neurons

Roher, A. E., Ball, M. J., Bhave, S. V., & Wakade, A. R. (1991) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(91)91455-l · Cited by 102 · see citing works

Amygdala neurons in vitro: Neurite growth and effects of estradiol

Lorenzo, A., Díaz, H., Carrer, H. F., & Cáceres, A. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490330308 · Cited by 97 · see citing works

Selective Alteration of Long-Term Potentiation-Induced Transcriptional Response in Hippocampus of Aged, Memory-Impaired Rats

Lanahan, A. A., Lyford, G. L., Stevenson, G. S., Worley, P. F., & Barnes, C. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02876.1997 · Cited by 89 · see citing works

Neuroanatomic correlates of visual agnosia in Alzheimer’s disease

Giannakopoulos, P., Gold, G., Duc, M., Michel, J., Hof, P. R., & Bouras, C. (1999) · Neurology · doi:10.1212/wnl.52.1.71 · Cited by 84 · see citing works

Cerebrospinal Fluid Levels of -Secretase--Cleaved Soluble Amyloid Precursor Protein Mirror Cognition in a Swedish Family With Alzheimer Disease and a Gene Mutation

Almkvist, O., Basun, H., Wagner, S. L., Rowe, B. A., Wahlund, L., & Lannfelt, L. (1997) · Archives of Neurology · doi:10.1001/archneur.1997.00550170111022 · Cited by 79 · see citing works

Alzheimer's disease amyloid precursor protein on the surface of cortical neurons in primary culture co-localizes with adhesion patch components

Storey, E., Beyreuther, K. T., & Masters, C. L. (1996) · Brain Research · doi:10.1016/0006-8993(96)00608-7 · Cited by 79 · see citing works

Perforated synapses on double-headed dendritic spines: a possible structural substrate of synaptic plasticity

Geinisman, Y., Morrell, F., & de Toledo‐Morrell, L. (1989) · Brain Research · doi:10.1016/0006-8993(89)90201-1 · Cited by 77 · see citing works

Cholinergic depletion reduces plasticity of barrel field cortex

Zhu, X. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.1.63 · Cited by 77 · see citing works

Dendritic reorganisation in the basal forebrain under degenerative conditions and its defects in Alzheimer's disease. III. The basal forebrain compared with other subcortical areas

Arendt, T., Brückner, M. K., Bigl, V., & Marcova, L. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903510204 · Cited by 72 · see citing works

Role of apolipoprotein E and estrogen in mossy fiber sprouting in hippocampal slice cultures

Teter, B., Harris‐White, M. E., Frautschy, S. A., & Cole, G. M. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00630-7 · Cited by 70 · see citing works

Synthesis and transport of GAP-43 in entorhinal cortex neurons and perforant pathway during lesion-induced sprouting and reactive synaptogenesis

Lin, L., Bock, S., Carpenter, K., Rose, M., & Norden, J. J. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90024-6 · Cited by 65 · see citing works

Synaptic β-amyloid precursor proteins increase with learning capacity in rats

Huber, G., Bailly, Y. J. R., Martin, J. R., Mariani, J., & Brugg, B. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00120-6 · Cited by 59 · see citing works

Age and damage induced changes in amyloid protein precursor immunohistochemistry in the rat brain

Beeson, J. G., Shelton, E. R., Chan, H. W., & Gage, F. H. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903420108 · Cited by 49 · see citing works

Increased tau messenger RNA in Alzheimer's disease hippocampus.

BARTON, A. J. L., Harrison, P. J., Najlerahim, A., Heffernan, J. M., McDonald, B., Robinson, J. R., Davies, D. C., Harrison, W. J., Mitra, P., & Hardy, J. (1990) · Europe PMC (PubMed Central) · Cited by 43 · see citing works

Concentrations of amyloid-β protein in cerebrospinal fluid increase with age in patients free from neurodegenerative disease

van Gool, W. A., Schenk, D. B., & Bolhuis, P. A. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90677-7 · Cited by 42 · see citing works

Increased numerical density of synapses in CA3 region of hippocampus and molecular layer of motor cortex after self-stimulation rewarding experience

Rao, B. S. S., Raju, T. R., & Meti, B. L. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00083-4 · Cited by 32 · see citing works

Prospective neuropsychological assessment of nondemented patients with biopsy proven senile plaques

Mackenzie, I. R., McLachlan, R. S., Kubu, C. S., & Miller, L. A. (1996) · Neurology · doi:10.1212/wnl.46.2.425 · Cited by 32 · see citing works

Alzheimer's Disease: Maladaptive Synaptoplasticity Hypothesis

Neill, D. (1995) · Neurodegeneration · doi:10.1006/neur.1995.0027 · Cited by 32 · see citing works

The Role of the Amyloid Protein Precursor (APP) in Alzheimer's Disease: Does the Normal Function of APP Explain the Topography of Neurodegeneration?

Small, D. H. (1998) · Neurochemical Research · doi:10.1023/a:1022471729291 · Cited by 29 · see citing works

Toward Understanding of the Molecular Basis of Loss of Neuronal Plasticity in Ageing

Mori, N. (1993) · Age and Ageing · doi:10.1093/ageing/22.suppl_1.s5 · Cited by 29 · see citing works

An immunocytochemical and biochemical study of the microtubule-associated protein Tau during post-lesion afferent reorganization in the hippocampus of adult rats

Busciglio, J. A., Ferreira, A., Steward, O., & Cáceres, A. (1987) · Brain Research · doi:10.1016/0006-8993(87)90590-7 · Cited by 28 · see citing works

Abnormal synaptic regeneration in hAPP transgenic and ApoE knockout mice

San Diego, C. A. (1994) · Neurobiology of Aging · doi:10.1016/0197-4580(94)92498-8 · Cited by 26 · see citing works

Apolipoprotein E Role in Maintaining the Integrity of the Aging Central Nervous System

Masliah, E., Mallory, M. E., Alford, M. F., Veinbergs, I., & Roses, A. D. (1996) · Springer eBooks · doi:10.1007/978-3-642-80109-9_6 · Cited by 25 · see citing works

Neuronal plasticity and ageing processes in the frame of the ‘Red Queen Theory’

Agnati, L. F., Zoli, M., Biagini, G., et al. (1992) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1992.tb09370.x · Cited by 25 · see citing works

Alzheimer transgenic mouse models come of age

Duff, K. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01093-x · Cited by 25 · see citing works

Structure, development, and maintenance of the nerve net of the body column in hydra

Sakaguchi, M., Mizusina, A., & Kobayakawa, Y. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960909)373:1 · Cited by 24 · see citing works

Chapter 1 Neural plasticity in aging and Alzheimer's disease: some selected comments

Phelps, C. H. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)63162-3 · Cited by 23 · see citing works

Tangle-bearing neurons show more extensive dendritic trees than tangle-free neurons in area CA1 of the hippocampus in Alzheimer's disease

Gertz, H., Krüger, H., Patt, S., & Cervós‐Navarro, J. (1991) · Brain Research · doi:10.1016/0006-8993(91)91130-s · Cited by 20 · see citing works

Production of paired helical filament, tau‐like proteins by PC12 cells: A model of neurofibrillary degeneration

Bondareff, W., Matsuyama, S., & Dell'Albani, P. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980601)52:5 · Cited by 12 · see citing works

Apolipoprotein E and Alzheimer's Disease

Stephens, D. J. (1996) · Journal of the Royal Society of Health · doi:10.1177/146642409611600109 · Cited by 11 · see citing works

Autoradiographic and in situ hybridization localization of corticotropin-releasing factor 1 and 2 receptors in nonhuman primate brain

S�nchez, M. M., Young, L. J., Plotsky, P. M., & Insel, T. R. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990607)408:3

Untitled work

Christensen (1997) · doi:10.1002/(sici)1099-1166(199703)12:3

Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers

Jack, C. R., Knopman, D. S., Jagust, W. J., Petersen, R. C., Weiner, M. W., Aisen, P. S., Shaw, L. M., Vemuri, P., Wiste, H. J., Weigand, S. D., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70291-0 · Cited by 4,396 · see citing works

Triple-Transgenic Model of Alzheimer’s Disease with Plaques and Tangles

Oddo, S., Caccamo, A., Shepherd, J. D., Murphy, M. P., Golde, T. E., Kayed, R., Metherate, R., Mattson, M. P., Akbari, Y., & LaFerla, F. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00434-3 · Cited by 4,126 · see citing works

The Cellular Phase of Alzheimer’s Disease

De Strooper, B., & Karran, E. (2016) · Cell · doi:10.1016/j.cell.2015.12.056 · Cited by 1,990 · see citing works

Deciphering the Molecular Basis of Memory Failure in Alzheimer's Disease

Walsh, D. M., & Selkoe, D. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.010 · Cited by 1,207 · see citing works

The cellular neurobiology of depression

Manji, H. K., Drevets, W. C., & Charney, D. S. (2001) · Nature Medicine · doi:10.1038/87865 · Cited by 1,182 · see citing works

Alzheimer’s disease

Cummings, J. L. (2004) · New England Journal of Medicine · doi:10.1056/nejmra040223 · Cited by 1,152 · see citing works

Biomarker Modeling of Alzheimer’s Disease

Jack, C. R., & Holtzman, D. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.12.003 · Cited by 1,002 · see citing works

Amyloid deposition precedes tangle formation in a triple transgenic model of Alzheimer's disease

Oddo, S. (2003) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.08.012 · Cited by 980 · see citing works

Adult neurogenesis: from precursors to network and physiology

Abrous, D. N., Koehl, M., & Le Moal, M. (2005) · Physiological Reviews · doi:10.1152/physrev.00055.2003 · Cited by 971 · see citing works

Altered Histone Acetylation Is Associated with Age-Dependent Memory Impairment in Mice

Peleg, S., Sananbenesi, F., Zovoilis, A., Burkhardt, S., Bahari-Javan, S., Agis-Balboa, R. C., Cota, P., Wittnam, J. L., Gogol-Doering, A., Opitz, L., et al. (2010) · Science · doi:10.1126/science.1186088 · Cited by 951 · see citing works

Increased hippocampal activation in mild cognitive impairment compared to normal aging and AD

Dickerson, B. C., Salat, D. H., Greve, D. N., Chua, E. F., Rand-Giovannetti, E., Rentz, D. M., Bertram, L., Mullin, K., Tanzi, R. E., Blacker, D., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000171450.97464.49 · Cited by 910 · see citing works

Altered Gene Expression of Brain-Derived Neurotrophic Factor and Receptor Tyrosine Kinase B in Postmortem Brain of Suicide Subjects

Dwivedi, Y., Rizavi, H. S., Conley, R. R., Roberts, R. C., Tamminga, C. A., & Pandey, G. N. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.8.804 · Cited by 875 · see citing works

Brain-derived neurotrophic factor in the control human brain, and in Alzheimer’s disease and Parkinson’s disease

Murer, M. G., Yan, Q., & Raisman-Vozari, R. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00014-9 · Cited by 874 · see citing works

Neuronal plasticity and survival in mood disorders

Duman, R. S., Malberg, J., Nakagawa, S., & D’Sa, C. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00935-5 · Cited by 652 · see citing works

Targeting acetylcholinesterase and butyrylcholinesterase in dementia

Lane, R. M., Potkin, S. G., & Enz, A. (2005) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145705005833 · Cited by 654 · see citing works

Alzheimer's Disease: From Pathology to Therapeutic Approaches

Jakob‐Roetne, R., & Jacobsen, H. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200802808 · Cited by 626 · see citing works

Soluble oligomers of β amyloid (1-42) inhibit long-term potentiation but not long-term depression in rat dentate gyrus

Wang, H.-W., Pasternak, J. F., Kuo, H., Ristic, H., Lambert, M. P., Chromy, B., Viola, K. L., Klein, W. L., Stine, W. B., Krafft, G. A., et al. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03058-x · Cited by 527 · see citing works

Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia

Mesulam, M., Wicklund, A., Johnson, N., Rogalski, E., Léger, G. C., Rademaker, A., Weintraub, S., & Bigio, E. H. (2008) · Annals of Neurology · doi:10.1002/ana.21388 · Cited by 513 · see citing works

Functional network disruption in the degenerative dementias

Pievani, M., de Haan, W., Wu, T., Seeley, W. W., & Frisoni, G. B. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70158-2 · Cited by 481 · see citing works

The Cholinergic Lesion of Alzheimer's Disease: Pivotal Factor or Side Show?

Mesulam, M. (2004) · Learning & Memory · doi:10.1101/lm.69204 · Cited by 467 · see citing works

A Systems Level Analysis of Transcriptional Changes in Alzheimer's Disease and Normal Aging

Miller, J. A., Oldham, M. C., & Geschwind, D. H. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4098-07.2008 · Cited by 385 · see citing works

Locus coeruleus neurofibrillary degeneration in aging, mild cognitive impairment and early Alzheimer's disease

Grudzien, A., Shaw, P., Weintraub, S., Bigio, E., Mash, D. C., & Mesulam, M. M. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.02.007 · Cited by 396 · see citing works

Intraneuronal β-amyloid accumulation and synapse pathology in Alzheimer’s disease

Gouras, G. K., Tampellini, D., Takahashi, R. H., & Capetillo-Zarate, E. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0679-9 · Cited by 372 · see citing works

Hippocampal hypometabolism predicts cognitive decline from normal aging

Mosconi, L., De Santi, S., Li, J., Tsui, W. H., Li, Y., Boppana, M., Laska, E., Rusinek, H., & de Leon, M. J. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.12.008 · Cited by 360 · see citing works

Reversible paired helical filament-like phosphorylation of tau is an adaptive process associated with neuronal plasticity in hibernating animals

Arendt, T., Stieler, J., Strijkstra, A. M., Hut, R. A., Rüdiger, J., Van der Zee, E. A., Harkany, T., Holzer, M., & Härtig, W. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-18-06972.2003 · Cited by 357 · see citing works

Locus coeruleus cellular and molecular pathology during the progression of Alzheimer’s disease

Kelly, S. C., He, B., Perez, S. E., Ginsberg, S. D., Mufson, E. J., & Counts, S. E. (2017) · Acta Neuropathologica Communications · doi:10.1186/s40478-017-0411-2 · Cited by 286 · see citing works

Opposing roles of transient and prolonged expression of p25 in synaptic plasticity and hippocampus-dependent memory

Fischer, A., Sananbenesi, F., Pang, P. T., Lu, B., & Tsai, L.-H. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.033 · Cited by 277 · see citing works

Lifespan brain activity, β-amyloid, and Alzheimer's disease

Jagust, W. J., & Mormino, E. C. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.09.004 · Cited by 221 · see citing works

The cholinergic innervation of the human cerebral cortex.

Mesulam, M.-M. (2004) · Progress in Brain Research · doi:10.1016/s0079-6123(03)45004-8 · Cited by 211 · see citing works

Does Alzheimer's disease begin in the brainstem?

Simic, G., Stanic, G., Mladinov, M., Jovanov‐Milosevic, N., Kostovic, I., & Hof, P. R. (2009) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2009.01038.x · Cited by 204 · see citing works

Feeling, learning from and being aware of inner states: interoceptive dimensions in neurodegeneration and stroke

García-Cordero, I., Sedeño, L., de la Fuente, L., Slachevsky, A., Forno, G., Klein, F., Lillo, P., Ferrari, J., Rodriguez, C., Bustin, J., et al. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0006 · Cited by 199 · see citing works

Cellular correlates of cortical thinning throughout the lifespan

Vidal-Pineiro, D., Parker, N., Shin, J., French, L., Grydeland, H., Jackowski, A. P., Mowinckel, A. M., Patel, Y., Pausova, Z., Salum, G., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-78471-3 · Cited by 154 · see citing works

Neurons associated with aggrecan-based perineuronal nets are protected against tau pathology in subcortical regions in Alzheimer's disease

Morawski, M., Brückner, G., Jäger, C., Seeger, G., & Arendt, T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.05.022 · Cited by 156 · see citing works

Alzheimer's Disease Neurodegenerative Biomarkers Are Associated with Decreased Cognitive Function but Not β-Amyloid in Cognitively Normal Older Individuals

Wirth, M., Madison, C. M., Rabinovici, G. D., Oh, H., Landau, S. M., & Jagust, W. J. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.4409-12.2013 · Cited by 151 · see citing works

Mesenchymal Stromal Cell Therapies for Neurodegenerative Diseases

Staff, N. P., Jones, D. T., & Singer, W. (2019) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2019.01.001 · Cited by 150 · see citing works

A plasticity-based theory of the pathogenesis of Alzheimer's disease.

MESULAM, M. ‐. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05559.x · Cited by 130 · see citing works

Aberrant Activation of Focal Adhesion Proteins Mediates Fibrillar Amyloid β-Induced Neuronal Dystrophy

Grace, E. A., & Busciglio, J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00493.2003 · Cited by 113 · see citing works

Amyloid PET in clinical practice: Its place in the multidimensional space of Alzheimer's disease

Vandenberghe, R., Adamczuk, K., Dupont, P., Laere, K. V., & Chételat, G. (2013) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.03.014 · Cited by 99 · see citing works

Cognitive reserve, cortical plasticity and resistance to Alzheimer's disease

Esiri, M. M., & Chance, S. A. (2012) · Alzheimer's Research & Therapy · doi:10.1186/alzrt105 · Cited by 95 · see citing works

Potential benefits of mindfulness-based interventions in mild cognitive impairment and Alzheimer’s disease: an interdisciplinary perspective.

Larouche, E., Hudon, C., & Goulet, S. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.058 · Cited by 93 · see citing works

ApoE isoform-specific effects on LTP: blockade by oligomeric amyloid-β1–42

Trommer, B. L., Shah, C., Yun, S. H., Gamkrelidze, G., Pasternak, E. S., Blaine Stine, W., Manelli, A., Sullivan, P., Pasternak, J. F., & LaDu, M. J. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.08.011 · Cited by 82 · see citing works

Magnetic resonance and PET studies in the early diagnosis of Alzheimer’s disease

Mosconi, L., De Santi, S., Rusinek, H., Convit, A., & de Leon, M. J. (2004) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.4.5.831 · Cited by 46 · see citing works

Oligodendrocytes are a Novel Source of Amyloid Peptide Generation

Skaper, S. D., Evans, N. A., Soden, P. E., Rosin, C., Facci, L., & Richardson, J. C. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0022-9 · Cited by 43 · see citing works

The presence of apoE4, not the absence of apoE3, contributes to AD pathology

Teter, B., Raber, J., Nathan, B., & Crutcher, K. A. (2002) · Journal of Alzheimer's Disease · doi:10.3233/jad-2002-4305 · Cited by 37 · see citing works

ИСПОЛЬЗОВAНИЕ ПОТЕНЦИAЛA СОЦИAЛЬНЫХ ПAРТНЕРОВ В ПОДГОТОВКЕ БУДУЩИХ ПЕДAГОГОВ

Атабекова, Б. Б. (2024) · Habaršy. Pedagogika ġylymdary seriâsy · doi:10.51889/2959-5762.2023.80.4.019

Susquehanna Chorale Spring Concert "Roots and Wings"

Hawkins, D. (2017)

A NEUROPLASTICITY AND FUNCTIONAL RESTORATION AFTER STROKE

(2019) · Physical and rehabilitation medicine medical rehabilitation · doi:10.36425/2658-6843-2019-2-32-36 · Cited by 1 · see citing works

Personality correlates and utilitarian judgments in the everyday context: Psychopathic traits and differential effects of empathy, social dominance orientation, and dehumanization beliefs

Takamatsu, R. (2019) · Personality and Individual Differences · doi:10.1016/j.paid.2019.03.029 · Cited by 22 · see citing works

Amount of altruistic punishment accounts for subsequent emotional gratification in participants with primary psychopathy

Masui, K., Iriguchi, S., Nomura, M., & Ura, M. (2011) · Personality and Individual Differences · doi:10.1016/j.paid.2011.07.006 · Cited by 14 · see citing works