Onset of hippocampus-dependent memory impairments in 5XFAD transgenic mouse model of Alzheimer’s disease

The mouse brain in stereotaxic coordinates

Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796 · see citing works

Image processing with ImageJ

Abràmoff, M. D., Magalhães, P. J., & Ram, S. J. (2004) · Utrecht University Repository (Utrecht University) · Cited by 11,816 · see citing works

Intraneuronal β-Amyloid Aggregates, Neurodegeneration, and Neuron Loss in Transgenic Mice with Five Familial Alzheimer's Disease Mutations: Potential Factors in Amyloid Plaque Formation

Oakley, H., Cole, S. L., Logan, S., Maus, E., Shao, P., Craft, J., Guillozet-Bongaarts, A., Ohno, M., Disterhoft, J., Van Eldik, L., et al. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1202-06.2006 · Cited by 3,530 · cited 5× · 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

Animal models of Alzheimer's disease and frontotemporal dementia

Götz, J., & Ittner, L. M. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2420 · Cited by 676 · see citing works

Motor deficits, neuron loss, and reduced anxiety coinciding with axonal degeneration and intraneuronal Aβ aggregation in the 5XFAD mouse model of Alzheimer's disease.

Jawhar, S., Trawicka, A., Jenneckens, C., Bayer, T. A., & Wirths, O. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.05.027 · Cited by 623 · cited 2× · see citing works

BACE1 Deficiency Rescues Memory Deficits and Cholinergic Dysfunction in a Mouse Model of Alzheimer's Disease

Ohno, M., Sametsky, E. A., Younkin, L. H., Oakley, H., Younkin, S. G., Citron, M., Vassar, R., & Disterhoft, J. F. (2004) · Neuron · doi:10.1016/s0896-6273(03)00810-9 · Cited by 549 · see citing works

Exercise, experience and the aging brain1

Churchill, J. D., Galvez, R., Colcombe, S. J., Swain, R. A., Kramer, A. F., & Greenough, W. T. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00028-3 · Cited by 533 · see citing works

Brain plasticity and functional losses in the aged: scientific bases for a novel intervention.

Mahncke, H., Bronstone, A., & Merzenich, M. (2006) · Progress in Brain Research · doi:10.1016/s0079-6123(06)57006-2 · Cited by 517 · see citing works

Brain reserve hypothesis in dementia

Fratiglioni, L., & Wang, H.-X. (2007) · Journal of Alzheimer's Disease · doi:10.3233/jad-2007-12103 · Cited by 499 · see citing works

Memory and Brain Systems: 1969–2009

Squire, L. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3575-09.2009 · Cited by 477 · see citing works

Alzheimer's disease: Aβ, tau and synaptic dysfunction

LaFerla, F. M., & Oddo, S. (2005) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2005.02.009 · Cited by 461 · see citing works

Alzheimer disease models and human neuropathology: similarities and differences

Duyckaerts, C. J., Potier, M., & Delatour, B. (2007) · Acta Neuropathologica · doi:10.1007/s00401-007-0312-8 · Cited by 441 · see citing works

Hippocampal system dysfunction and odor discrimination learning in rats: Impairment of facilitation depending on representational demands.

Eichenbaum, H., Fagan, A. M., Mathews, P., & Cohen, N. J. (1988) · Behavioral Neuroscience · doi:10.1037/0735-7044.102.3.331 · Cited by 305 · see citing works

Temporal memory deficits in Alzheimer’s mouse models: Rescue by genetic deletion of BACE1

Ohno, M., Chang, L., Tseng, W., Oakley, H., Citron, M., Klein, W. L., Vassar, R., & Disterhoft, J. F. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04551.x · Cited by 298 · see citing works

BACE1 gene deletion prevents neuron loss and memory deficits in 5XFAD APP/PS1 transgenic mice

Ohno, M., Cole, S. L., Yasvoina, M., Zhao, J., Citron, M., Berry, R., Disterhoft, J. F., & Vassar, R. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.12.008 · Cited by 290 · see citing works

A decade of modeling Alzheimer's disease in transgenic mice

MCGOWAN, E., ERIKSEN, J., & HUTTON, M. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.03.007 · Cited by 287 · see citing works

The future of Alzheimer's disease: The next 10 years

Hampel, H. J., Prvulovic, D., Teipel, S. J., Jessen, F., Luckhaus, C., Frölich, L., Riepe, M. W., Dodel, R. C., Leyhe, T., Bertram, L., et al. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.11.008 · Cited by 233 · see citing works

Learning and Memory in Transgenic Mice Modeling Alzheimer's Disease

Ashe, K. H. (2001) · Learning & Memory · doi:10.1101/lm.43701 · Cited by 224 · see citing works

Environmental influences on brain neurotrophins in rats

Pham, T. M., Winblad, B. G., Granholm, A., & Mohammed, A. H. S. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(02)00783-9 · Cited by 184 · see citing works

Behavioral phenotypes of amyloid‐based genetically modified mouse models of Alzheimer's disease

Kobayashi, D. T., & Chen, K. S. (2005) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2005.00124.x · Cited by 175 · see citing works

Plaques, Tangles, and Memory Loss in Mouse Models of Neurodegeneration

Eriksen, J. L., & Janus, C. G. (2007) · Behavior Genetics · doi:10.1007/s10519-006-9118-z · Cited by 146 · see citing works

Engraftment of human nasal olfactory stem cells restores neuroplasticity in mice with hippocampal lesions

Nivet, E., Vignes, M., Girard, S. D., Pierrisnard, C., Baril, N., Devèze, A., Magnan, J., Lanté, F., Khrestchatisky, M., Feron, F. P., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44489 · Cited by 141 · see citing works

The noradrenaline precursor L-DOPS reduces pathology in a mouse model of Alzheimer’s disease

Kalinin, S., Polak, P. E., Lin, S. X., Sakharkar, A. J., Pandey, S. C., & Feinstein, D. L. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.04.012 · Cited by 116 · see citing works

Icariin improves memory impairment in Alzheimer's disease model mice (5xFAD) and attenuates amyloid β‐induced neurite atrophy

Urano, T., & Tohda, C. (2010) · Phytotherapy Research · doi:10.1002/ptr.3183 · Cited by 101 · see citing works

Deficits in working memory and motor performance in the APP/PS1ki mouse model for Alzheimer's disease

Wirths, O., Breyhan, H., Schäfer, S., Roth, C., & Bayer, T. A. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.12.004 · Cited by 97 · see citing works

Failures to reconsolidate memory in a mouse model of Alzheimer’s disease

Ohno, M. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.05.001 · Cited by 95 · see citing works

Tissue inhibitor of metalloproteinases‐1 (TIMP‐1) modulates neuronal death, axonal plasticity, and learning and memory

Jourquin, J., Tremblay, E. C., Bernard, A., Charton, G., Chaillan, F. A., Marchetti, E., Roman, F. S., Soloway, P. D., Dive, V., Yiotakis, A., et al. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04426.x · Cited by 93 · see citing works

Accelerated tau pathology with synaptic and neuronal loss in a novel triple transgenic mouse model of Alzheimer’s disease

Saul, A., Sprenger, F., Bayer, T. A., & Wirths, O. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.05.003 · Cited by 85 · see citing works

Developmental vitamin D deficiency alters learning in C57Bl/6J mice

de Abreu, D. A. F., Nivet, E., Baril, N., Khrestchatisky, M., Roman, F. S., & Feron, F. P. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.01.005 · Cited by 67 · see citing works

Genetic reductions of BACE1 and amyloid-β ameliorate impairment of conditioned taste aversion memory in 5XFAD Alzheimer model mice

Devi, L., & Ohno, M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07031.x · Cited by 67 · see citing works

The Promnesic Effect of G-protein-Coupled 5-HT4 Receptors Activation Is Mediated by a Potentiation of Learning-Induced Spine Growth in the Mouse Hippocampus

Restivo, L., Roman, F. S., Dumuis, A., Bockaert, J., Marchetti, E., & Ammassari‐Teule, M. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301644 · Cited by 62 · see citing works

Working memory impairment in a transgenic amyloid precursor protein TgCRND8 mouse model of Alzheimer's disease

Lovasic, L., Bauschke, H. H., & Janus, C. (2004) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2004.00104.x · Cited by 51 · see citing works

Involvement of tissue inhibition of metalloproteinases-1 in learning and memory in mice

Chaillan, F. A., Rivera, S., Marchetti, E., Jourquin, J., Werb, Z., Soloway, P. D., Khrestchatisky, M., & Roman, F. S. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.06.020 · Cited by 47 · see citing works

Simultaneous olfactory discrimination elicits a strain-specific increase in dendritic spines in the hippocampus of inbred mice

Restivo, L., Roman, F. S., Ammassari‐Teule, M., & Marchetti, E. (2006) · Hippocampus · doi:10.1002/hipo.20174 · Cited by 43 · see citing works

Faster forgetting contributes to impaired spatial memory in the PDAPP mouse: Deficit in memory retrieval associated with increased sensitivity to interference?Preprint

Daumas, S., Sandin, J., Chen, K. S., Kobayashi, D. T., Tulloch, J., Martin, S. J., Games, D., & Morris, R. (2008) · Learning & Memory · doi:10.1101/lm.990208 · Cited by 41 · see citing works

Genetic and Pharmacological Basis for Therapeutic Inhibition of Band γ-Secretases in Mouse Models of Alzheimer's Memory Deficits

Ohno, M. (2006) · Reviews in the Neurosciences · doi:10.1515/revneuro.2006.17.4.429 · Cited by 32 · see citing works

The olfactory tubing maze: a new apparatus for studying learning and memory processes in mice

Roman, F. S., Marchetti, E., Bouquerel, A., & Soumireu-Mourat, B. (2002) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(02)00094-8 · Cited by 27 · see citing works

Learning discloses abnormal structural and functional plasticity at hippocampal synapses in the APP23 mouse model of Alzheimer's diseasePreprint

Middei, S., Roberto, A., Berretta, N., Panico, M. B., Lista, S., Bernardi, G., Mercuri, N. B., Ammassari‐Teule, M., & Nisticò, R. (2010) · Learning & Memory · doi:10.1101/lm.1748310 · Cited by 26 · see citing works

Impairment of spatial memory consolidation in APP751SL mice results in cue-guided response

Blanchard, J., Martel, G., Guillou, J., Noguès, X., & Micheau, J. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.02.010 · Cited by 19 · see citing works

Strain Differences in Rewarded Discrimination Learning Using the Olfactory Tubing Maze

Restivo, L., Chaillan, F. A., Ammassari‐Teule, M., Roman, F. S., & Marchetti, E. (2006) · Behavior Genetics · doi:10.1007/s10519-006-9088-1 · Cited by 18 · see citing works

Selective impairment of subcategories of long-term memory in mice with hippocampal lesions accessed by the olfactory tubing maze

Chaillan, F. A., Marchetti, E., Soumireu-Mourat, B., & Roman, F. S. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.09.008 · Cited by 9 · see citing works

LC3-Associated Endocytosis Facilitates β-Amyloid Clearance and Mitigates Neurodegeneration in Murine Alzheimer’s Disease

Heckmann, B. L., Teubner, B. J. W., Tummers, B., Boada-Romero, E., Harris, L., Yang, M., Guy, C. S., Zakharenko, S. S., & Green, D. R. (2019) · Cell · doi:10.1016/j.cell.2019.05.056 · Cited by 503 · see citing works

Temporal gene profiling of the 5XFAD transgenic mouse model highlights the importance of microglial activation in Alzheimer’s disease

Landel, V., Baranger, K., Virard, I., Loriod, B., Khrestchatisky, M., Rivera, S., Benech, P., & Féron, F. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-33 · Cited by 176 · see citing works

MT5-MMP is a new pro-amyloidogenic proteinase that promotes amyloid pathology and cognitive decline in a transgenic mouse model of Alzheimer’s disease

Baranger, K., Marchalant, Y., Bonnet, A., Crouzin, N., Carreté, A., Paumier, J.-M., Py, N., Bernard, A., Bauer, C., Charrat, E., et al. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1992-1 · Cited by 110 · see citing works

Sex Differences in Behavior and Molecular Pathology in the 5XFAD Model

Sil, A., Erfani, A., Lamb, N., Copland, R., Riedel, G., & Platt, B. (2022) · Journal of Alzheimer's Disease · doi:10.3233/jad-210523 · Cited by 109 · see citing works

Metalloproteinases and their tissue inhibitors in Alzheimer’s disease and other neurodegenerative disorders

Rivera, S., García‐González, L., Khrestchatisky, M., & Baranger, K. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03178-2 · Cited by 112 · see citing works

Modulation of neuroinflammation and pathology in the 5XFAD mouse model of Alzheimer's disease using a biased and selective beta-1 adrenergic receptor partial agonist

Ardestani, P. M., Evans, A. K., Yi, B., Nguyen, T., Coutellier, L. D., & Shamloo, M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.01.010 · Cited by 88 · see citing works

Differential spatio-temporal regulation of MMPs in the 5xFAD mouse model of Alzheimer’s disease: evidence for a pro-amyloidogenic role of MT1-MMP

Py, N., Bonnet, A., Bernard, A., Marchalant, Y., Charrat, E., Checler, F., Khrestchatisky, M., Baranger, K., & Rivera, S. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00247 · Cited by 71 · see citing works

Emerging Alternative Proteinases in APP Metabolism and Alzheimer’s Disease Pathogenesis: A Focus on MT1-MMP and MT5-MMP

García-González, L., Pilat, D., Baranger, K., & Rivera, S. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00244 · Cited by 65 · see citing works

Enhanced defense against ferroptosis ameliorates cognitive impairment and reduces neurodegeneration in 5xFAD mice

Chen, L., Dar, N. J., Na, R., McLane, K. D., Yoo, K., Han, X., & Ran, Q. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.01.002 · Cited by 80 · see citing works

Riluzole reduces amyloid beta pathology, improves memory, and restores gene expression changes in a transgenic mouse model of early-onset Alzheimer’s disease

Okamoto, M., Gray, J. D., Larson, C. S., Kazim, S. F., Soya, H., McEwen, B. S., & Pereira, A. C. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0201-z · Cited by 70 · see citing works

Metabolic changes and inflammation in cultured astrocytes from the 5xFAD mouse model of Alzheimer’s disease: Alleviation by pantethine

van Gijsel-Bonnello, M., Baranger, K., Benech, P., Rivera, S., Khrestchatisky, M., de Reggi, M. D., & Gharib, B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175369 · Cited by 59 · see citing works

Chronic treatments with a 5-HT 4 receptor agonist decrease amyloid pathology in the entorhinal cortex and learning and memory deficits in the 5xFAD mouse model of Alzheimer's disease

Baranger, K., Giannoni, P., Girard, S. D., Girot, S., Gaven, F., Stephan, D., Migliorati, M., Khrestchatisky, M., Bockaert, J., Marchetti, E., et al. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.08.031 · Cited by 68 · see citing works

Olfactory dysfunction: its early temporal relationship and neural correlates in the pathogenesis of Alzheimer’s disease

Daulatzai, M. A. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1404-6 · Cited by 63 · see citing works

Dissociable cognitive impairments in two strains of transgenic Alzheimer’s disease mice revealed by a battery of object-based tests

Creighton, S. D., Mendell, A. L., Palmer, D. D., Kalisch, B. E., MacLusky, N. J., Prado, V. F., Prado, M. A. M., & Winters, B. D. (2019) · Scientific Reports · doi:10.1038/s41598-018-37312-0 · Cited by 63 · see citing works

Visuo‐spatial learning and memory impairments in the 5xFAD mouse model of Alzheimer's disease: Effects of age, sex, albinism, and motor impairments

O’Leary, T. P., & Brown, R. E. (2022) · Genes Brain & Behavior · doi:10.1111/gbb.12794 · Cited by 61 · see citing works

Midlife physical activity is associated with lower incidence of vascular dementia but not Alzheimer’s disease

Hansson, O., Svensson, M., Gustavsson, A., Andersson, E., Yang, Y., Nägga, K., Hållmarker, U., James, S. K., & Deierborg, T. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0538-4 · Cited by 57 · see citing works

MK-0677, a Ghrelin Agonist, Alleviates Amyloid Beta-Related Pathology in 5XFAD Mice, an Animal Model of Alzheimer’s Disease

Jeong, Y.-O., Shin, S. J., Park, J., Ku, B., Song, J.-S., Kim, J.-J., Jeon, S., Lee, S. M., & Moon, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061800 · Cited by 48 · see citing works

Harnessing human iPSC-microglia for CNS-wide delivery of disease-modifying proteins

Chadarevian, J. P., Davtyan, H., Chadarevian, A. L., Nguyen, J., Capocchi, J. K., Le, L., Escobar, A., Chadarevian, T., Mansour, K., Deynega, E., et al. (2025) · Cell stem cell · doi:10.1016/j.stem.2025.03.009 · Cited by 53 · see citing works

Sex and Genotype Differences in Odor Detection in the 3×Tg-AD and 5XFAD Mouse Models of Alzheimer’s Disease at 6 Months of Age

Roddick, K. M., Roberts, A. D., Schellinck, H. M., & Brown, R. E. (2016) · Chemical Senses · doi:10.1093/chemse/bjw018 · Cited by 51 · see citing works

Distribution and inter-regional relationship of amyloid-beta plaque deposition in a 5xFAD mouse model of Alzheimer’s disease

Tsui, K. C., Roy, J., Chau, S. C., Wong, K.-H., Shi, L., Poon, C. H., Wang, Y., Strekalova, T. V., Aquili, L., Chang, R. C., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.964336 · Cited by 44 · see citing works

Donecopride, a Swiss army knife with potential against Alzheimer's disease

Rochais, C., Lecoutey, C., Hamidouche, K., Giannoni, P., Gaven, F., Cem, E., Mignani, S. M., Baranger, K., Fréret, T., Bockaert, J., et al. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14964 · Cited by 44 · see citing works

CERTL reduces C16 ceramide, amyloid-β levels, and inflammation in a model of Alzheimer’s disease

Crivelli, S. M., Luo, Q., Stevens, J., Giovagnoni, C., van Kruining, D., Bode, G. H., den Hoedt, S., Hobo, B., Scheithauer, A.-L., Walter, J., et al. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00780-0 · Cited by 41 · see citing works

Translational Assays for Assessment of Cognition in Rodent Models of Alzheimer’s Disease and Dementia

Shepherd, A. L., Tyebji, S., Hannan, A. J., & Burrows, E. L. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0837-1 · Cited by 42 · see citing works

Inhibition of acid sphingomyelinase reduces reactive astrocyte secretion of mitotoxic extracellular vesicles and improves Alzheimer’s disease pathology in the 5xFAD mouse

Crivelli, S. M., Quadri, Z., Vekaria, H. J., Zhu, Z., Tripathi, P., Elsherbini, A. M., Zhang, L., Sullivan, P. G., & Bieberich, E. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01633-7 · Cited by 39 · see citing works

The Protective Effects of PSM-04 Against Beta Amyloid-Induced Neurotoxicity in Primary Cortical Neurons and an Animal Model of Alzheimer’s Disease

Park, H., Kang, S., Nam, E., Suh, Y., & Chang, K. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00002 · Cited by 38 · see citing works

NMDA receptor antagonists reduce amyloid-β deposition by modulating calpain-1 signaling and autophagy, rescuing cognitive impairment in 5XFAD mice

Companys‐Alemany, J., Turcu, A. L., Schneider, M., Müller, C. E., Vázquez, S., Griñán‐Ferré, C., & Pallàs, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04438-4 · Cited by 38 · see citing works

Correction: Metabolic changes and inflammation in cultured astrocytes from the 5xFAD mouse model of Alzheimer's disease: Alleviation by pantethine

van Gijsel‐Bonnello, M., Baranger, K., Benech, P. D., Rivera, S., Khrestchatisky, M., Reggi, M. L. D., & Gharib, B. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194586 · Cited by 35 · see citing works

APOE expression and secretion are modulated by mitochondrial dysfunction

Wynne, M. E., Ogunbona, O., Lane, A. R., Gokhale, A., Zlatic, S. A., Xu, C., Wen, Z., Duong, D. M., Rayaprolu, S., Ivanova, A., et al. (2023) · eLife · doi:10.7554/elife.85779 · Cited by 35 · see citing works

Probing neural circuit mechanisms in Alzheimer’s disease using novel technologies

Grieco, S. F., Holmes, T. C., & Xu, X. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02018-x · Cited by 34 · see citing works

Search Strategy Analysis of 5xFAD Alzheimer Mice in the Morris Water Maze Reveals Sex- and Age-Specific Spatial Navigation Deficits

Quintanilla‐Sánchez, C., Schmitt, F. W., Curdt, N., Westhoff, A. C., Bänfer, I. W. H., Bayer, T. A., & Bouter, Y. (2023) · Biomedicines · doi:10.3390/biomedicines11020599 · Cited by 32 · see citing works

Intact olfactory memory in the 5xFAD mouse model of Alzheimer’s disease from 3 to 15 months of age

O’Leary, T. P., Stover, K. R., Mantolino, H. M., Darvesh, S., & Brown, R. E. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112731 · Cited by 30 · see citing works

Neuroimaging of mouse models of Alzheimer’s disease

Jullienne, A., Trinh, M. V., & Obenaus, A. (2022) · Biomedicines · doi:10.3390/biomedicines10020305 · Cited by 32 · see citing works

Age related weight loss in female 5xFAD mice from 3 to 12 months of age

Gendron, W. A. C., Fertan, E., Pelletier, S., Roddick, K. M., O’Leary, T. P., Anini, Y., & Brown, R. E. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113214 · Cited by 31 · see citing works

Recognition memory impairments and amyloid-beta deposition of the retrosplenial cortex at the early stage of 5XFAD mice

Kim, D.-H., Kim, H.-A., Han, Y. S., Jeon, W. K., & Han, J. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112891 · Cited by 30 · see citing works

Cortical cerebrovascular and metabolic perturbations in the 5xFAD mouse model of Alzheimer’s disease

Jullienne, A., Szu, J. I., Quan, R., Trinh, M. V., Norouzi, T., Noarbe, B. P., Bedwell, A. A., Eldridge, K., Persohn, S. A., Territo, P. R., et al. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1220036 · Cited by 30 · see citing works

The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease

Viola, K. L., Bicca, M. A., Bebenek, A. M., Kranz, D. L., Nandwana, V., Waters, E. A., Haney, C. R., Lee, M. Y., Gupta, A., Brahmbhatt, Z., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.768646 · Cited by 29 · see citing works

Glial cell reactivity and oxidative stress prevention in Alzheimer’s disease mice model by an optimized NMDA receptor antagonist

Companys‐Alemany, J., Turcu, A. L., Vázquez, S., Pallàs, M., & Griñán‐Ferré, C. (2022) · Scientific Reports · doi:10.1038/s41598-022-22963-x · Cited by 29 · see citing works

The ethanol extract of Zizyphus jujuba var. spinosa seeds ameliorates the memory deficits in Alzheimer's disease model mice

Park, H. J., Jung, I. H., Kwon, H., Yu, J., Jo, E., Kim, H., Park, S. J., Lee, Y. C., Kim, D. H., & Ryu, J. H. (2018) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2018.12.043 · Cited by 29 · see citing works

Design, synthesis, and in vitro and in vivo characterization of new memantine analogs for Alzheimer’s disease

Turcu, A. L., Companys-Alemany, J., Phillips, M. B., Patel, D. S., Griñán-Ferré, C., Loza, M. I., Brea, J. M., Pérez, B., Soto, D., Sureda, F. X., et al. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114354 · Cited by 27 · see citing works

Therapeutic Potential of Niche-Specific Mesenchymal Stromal Cells for Spinal Cord Injury Repair

Lindsay, S. L., & Barnett, S. C. (2021) · Cells · doi:10.3390/cells10040901 · Cited by 27 · see citing works

Mitochondrial PKA Is Neuroprotective in a Cell Culture Model of Alzheimer’s Disease

Banerjee, T. D., Reihl, K. D., Swain, M., Torres, M., & Dagda, R. K. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02333-w · Cited by 24 · see citing works

Microglial Hyperreactivity Evolved to Immunosuppression in the Hippocampus of a Mouse Model of Accelerated Aging and Alzheimer’s Disease Traits

Molina‐Martínez, P., Corpas, R., García-Lara, E., Cosín‐Tomás, M., Cristòfol, R. M., Kaliman, P., Solà, C., Molinuevo, J. L., Sánchez‐Valle, R., Antonell, A., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.622360 · Cited by 23 · see citing works

Pharmacological sequestration of mitochondrial calcium uptake protects against dementia and β-amyloid neurotoxicity

Shevtsova, E. F., Angelova, P. R., Stelmashchuk, O. A., Esteras, N., Васильева, Н. А., Maltsev, A. V., Shevtsov, P. N., Shaposhnikov, A. V., Фисенко, В. П., Бачурин, С. О., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-16817-9 · Cited by 24 · see citing works

Degenerate mapping of environmental location presages deficits in object-location encoding and memory in the 5xFAD mouse model for Alzheimer's disease

Zhang, H., Chen, L., Johnston, K. G., Crapser, J. D., Green, K. N., Ha, N. M.-L., Tenner, A. J., Holmes, T. C., Nitz, D. A., & Xu, X. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105939 · Cited by 23 · see citing works

Interval timing is disrupted in female 5xFAD mice: An indication of altered memory processes

Gür, E., Fertan, E., Alkins, K., Wong, A. A., Brown, R. E., & Balcı, F. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24418 · Cited by 21 · see citing works

Olfactory Evaluation in Alzheimer’s Disease Model Mice

Zhang, J., Zhao, Z., Sun, S., Li, J., Wang, Y., Dong, J., Yang, S. C., Lou, Y., Yang, J., Li, W., et al. (2022) · Brain Sciences · doi:10.3390/brainsci12050607 · Cited by 20 · see citing works

Amyloid‐β plaques affect astrocyte Kir4.1 protein expression but not function in the dentate gyrus of APP / PS1 mice

Huffels, C. F. M., Osborn, L. M., Hulshof, L. A., Kooijman, L., Henning, L., Steinhäuser, C., & Hol, E. M. (2022) · Glia · doi:10.1002/glia.24137 · Cited by 20 · see citing works

5XFAD mice show early-onset gap encoding deficits in the auditory cortex

Weible, A. P., Stebritz, A. J., & Wehr, M. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.05.013 · Cited by 17 · see citing works

Elevation of phospholipase C-β1 expression by amyloid-β facilitates calcium overload in neuronal cells

Park, J., Kim, S. H., Kim, Y. J., Kim, I. H., Oh, Y., Choi, K. Y., Kim, B. C., Lee, K. H., & Song, W. K. (2022) · Brain Research · doi:10.1016/j.brainres.2022.147924 · Cited by 17 · see citing works

Transcending the amyloid-beta dominance paradigm in Alzheimer's disease: An exploration of behavioural, metabolic, and gut microbiota phenotypes in 5xFAD mice

Vera, D. M., Zambrana-Infantes, E. N., López-Gambero, A. J., Verheul-Campos, J., Santín, L. J., Baixerás, E., Suárez, J., Pavón, F. J., Rosell‐Valle, C., & de Fonseca, F. R. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106295 · Cited by 17 · see citing works

Transcorneal electrical stimulation enhances cognitive functions in aged and 5XFAD mouse models

Yu, W. S., Aquili, L., Wong, K. H., Lo, A., Chan, L. L. H., Chan, Y., & Lim, L. W. (2022) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14850 · Cited by 17 · see citing works

Effects of Striatal Amyloidosis on the Dopaminergic System and Behavior: A Comparative Study in Male and Female 5XFAD Mice

Lansdell, T. A., Xu, H., Galligan, J., & Dorrance, A. (2023) · Journal of Alzheimer's Disease · doi:10.3233/jad-220905 · Cited by 10 · see citing works

Amyloid pathology reduces ELP3 expression and tRNA modifications leading to impaired proteostasis

Pereira, M., Ribeiro, D. R., Berg, M., Tsai, A. P., Dong, C., Nho, K. T., Kaiser, S., Moutinho, M., & Soares, A. R. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166857 · Cited by 16 · see citing works

Mouse models of neurodegenerative disease: preclinical imaging and neurovascular component

Albanese, S., Greco, A., Auletta, L., & Mancini, M. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9770-3 · Cited by 16 · see citing works

The Correlation Between Olfactory Test and Hippocampal Volume in Alzheimer's Disease and Mild Cognitive Impairment Patients: A Meta-Analysis

Su, M.-W., Ni, J., Cao, T., Wang, S., Shi, J., & Tian, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.755160 · Cited by 14 · see citing works

Age-related deficits in working memory in 5xFAD mice in the Hebb-Williams maze

Fertan, E., & Brown, R. E. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113806 · Cited by 14 · see citing works

The FVB/N mice: A well suited strain to study learning and memory processes using olfactory cues

Girard, S. D., Escoffier, G., Khrestchatisky, M., & Roman, F. S. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.09.004 · Cited by 14 · see citing works

ID1201, the ethanolic extract of the fruit of Melia toosendan ameliorates impairments in spatial learning and reduces levels of amyloid beta in 5XFAD mice

Cho, W.-H., Park, J.-C., Kim, D.-H., Kim, M.-S., Lee, S.-Y., Park, H., Kang, J.-H., Yeon, S.-W., & Han, J.-S. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.09.036 · Cited by 13 · see citing works

Neurodegenerative changes in the brains of the 5xFAD Alzheimer's disease model mice investigated by high‐field and high‐resolution magnetic resonance imaging and multi‐nuclei magnetic resonance spectroscopy

Yoo, C.-H., Kim, J., Baek, H.-M., Chang, K.-A., & Choe, B.-Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065073 · Cited by 13 · see citing works

Bridging the Gap between Gut Microbiota and Alzheimer’s Disease: A Metaproteomic Approach for Biomarker Discovery in Transgenic Mice

Ayan, E. B., DeMi̇rci̇, H., Serdar, M. A., Palermo, F., & Baykal, A. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612819 · Cited by 13 · see citing works

Effects of Red ginseng on neuroinflammation in neurodegenerative diseases

Lee, M. Y., & Kim, M. (2023) · Journal of Ginseng Research · doi:10.1016/j.jgr.2023.08.003 · Cited by 13 · see citing works

Specific exercise patterns generate an epigenetic molecular memory window that drives long-term memory formation and identifies ACVR1C as a bidirectional regulator of memory in mice

Keiser, A. A., Dong, T. N., Kramár, E. A., Butler, C., Chen, S., Matheos, D. P., Rounds, J. S., Rodriguez, A., Beardwood, J. H., Augustynski, A. S., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47996-w · Cited by 13 · see citing works

diAcCA, a Pro-Drug for Carnosic Acid That Activates the Nrf2 Transcriptional Pathway, Shows Efficacy in the 5xFAD Transgenic Mouse Model of Alzheimer’s Disease

Banerjee, P., Wang, Y., Carnevale, L. N., Patel, P. R., Raspur, C. K., Tran, N., Zhang, X., Natarajan, R., Roberts, A. J., Baran, P. S., et al. (2025) · Antioxidants · doi:10.3390/antiox14030293 · Cited by 13 · see citing works

Neonatal Neurodegeneration in Alzheimer’s Disease Transgenic Mouse Model

Mazi, A. R., Arzuman, A. S., Gürel, B., Şahin, B., Tüzüner, M. B., Ozansoy, M., & Baykal, A. T. (2018) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-170049 · Cited by 13 · see citing works

Long-Term Pantethine Treatment Counteracts Pathologic Gene Dysregulation and Decreases Alzheimer's Disease Pathogenesis in a Transgenic Mouse Model

Baranger, K., van Gijsel‐Bonnello, M., Stephan, D., Carpentier, W., Rivera, S., Khrestchatisky, M., Gharib, B., Reggi, M. L. D., & Benech, P. (2019) · Neurotherapeutics · doi:10.1007/s13311-019-00754-z · Cited by 12 · see citing works

Traumatic brain injury alters the effects of class II invariant peptide (CLIP) antagonism on chronic meningeal CLIP + B cells, neuropathology, and neurobehavioral impairment in 5xFAD mice

Iannucci, J., Dominy, R., Bandopadhyay, S., Arthur, E. M., Noarbe, B. P., Jullienne, A., Krkasharyan, M., Tobin, R. P., Pereverzev, A., Beevers, S., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03146-z · Cited by 12 · see citing works

Microglia TFEB activation attenuates Alzheimer’s disease pathology by enhancing autophagy-lysosomal function

Kim, Y., Ha, T.-Y., Kondaurova, O., Lee, M.-S., & Chang, K. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03728-z · Cited by 10 · see citing works

Characterization of cerebrovascular changes in Alzheimer’s disease mice by photoacoustic imaging

Li, X., Zhang, Z., Shi, H., & Zhou, F. (2024) · Journal of Innovative Optical Health Sciences · doi:10.1142/s179354582450007x · Cited by 9 · see citing works

Identifying the bioimaging features of Alzheimer’s disease based on pupillary light response-driven brain-wide fMRI in awake mice

Liu, X., Hike, D., Choi, S., Man, W., Ran, C., Zhou, X. A., Jiang, Y., & Yu, X. (2024) · Nature Communications · doi:10.1038/s41467-024-53878-y · Cited by 9 · see citing works

LRP/LR specific antibody IgG1-iS18 impedes neurodegeneration in Alzheimer's disease mice

Ferreira, E., Bignoux, M. J., Otgaar, T. C., Tagliatti, N., Jovanovic, K., Letsolo, B. T., & Weiss, S. F. T. (2018) · Oncotarget · doi:10.18632/oncotarget.25473 · Cited by 9 · see citing works

A peptide-neurotensin conjugate that crosses the blood-brain barrier induces pharmacological hypothermia associated with anticonvulsant, neuroprotective, and anti-inflammatory properties following status epilepticus in micePreprint

Ferhat, L., Soussi, R., Masse, M., Kyriatzis, G., Girard, S. D., Gassiot, F., Gaudin, N., Laurencin, M., Bernard, A., Bôle, A., et al. (2024) · eLife · doi:10.7554/elife.100527 · Cited by 14 · see citing works

Enhanced Anxiety and Olfactory Microglial Activation in Early-Stage Familial Alzheimer’s Disease Mouse Model

Chithanathan, K., Xuan, F.-L., Hickey, M. A., & Tian, L. (2022) · Biology · doi:10.3390/biology11060938 · Cited by 8 · see citing works

The effect of electroconvulsive therapy on neuroinflammation, behavior and amyloid plaques in the 5xFAD mouse model of Alzheimer’s disease

Svensson, M., Olsson, G., Yang, Y., Bachiller, S., Ekemohn, M., Ekstrand, J., & Deierborg, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-83998-0 · Cited by 8 · see citing works

Progressive impairments in executive function in the APP/PS1 model of Alzheimer's disease as measured by translatable touchscreen testing

Shepherd, A. L., Lim, J. K. H., Wong, V. H. Y., Zeleznikow-Johnston, A., Churilov, L. P., Nguyen, C. T. O., Bui, B. V., Hannan, A. J., & Burrows, E. L. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.08.004 · Cited by 8 · see citing works

Intranasal insulin treatment ameliorates spatial memory, muscular strength, and frailty deficits in 5xFAD mice

Gendron, W. A. C., Fertan, E., Roddick, K. M., Wong, A. A., Maliougina, M., Hiani, Y. E., Anini, Y., & Brown, R. E. (2024) · Physiology & Behavior · doi:10.1016/j.physbeh.2024.114583 · Cited by 7 · see citing works

A novel paradigm for assessing olfactory working memory capacity in mice

Huang, G.-D., Jiang, L.-X., Feng, S., Wang, H., Zhang, C., & Yu, X. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01120-w · Cited by 7 · see citing works

The protocol for assessing olfactory working memory capacity in mice

Jiang, L., Huang, G., Wang, H., Zhang, C., & Yu, X. (2022) · Brain and Behavior · doi:10.1002/brb3.2703 · Cited by 6 · see citing works

Chronic basal forebrain activation improves spatial memory, boosts neurotrophin receptor expression, and lowers BACE1 and Aβ42 levels in the cerebral cortex in mice.

Kumro, J., Tripathi, A., Lei, Y., Sword, J., Callahan, P., Terry, A., Lu, X.-Y., Kirov, S., Pillai, A., & Blake, D. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad066 · Cited by 8 · see citing works

Vulnerability of Spatial Pattern Separation in 5xFAD Alzheimer’s Disease Mouse Model

Gephine, L., Roux, C. M., Fréret, T., Boulouard, M., & Léger, M. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231112 · Cited by 5 · see citing works

A Signal Detection Analysis of Olfactory Learning in 12-Month-Old 5xFAD Mice

Roddick, K. M., Fertan, E., Schellinck, H. M., & Brown, R. E. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220049 · Cited by 5 · see citing works

Age dependent path integration deficit in 5xFAD mice

Mar, K. D., So, C., Hou, Y., & Kim, J. C. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.114919 · Cited by 5 · see citing works

Can MRI T1 be used to detect early changes in 5xFAD Alzheimer’s mouse brain?

Spencer, N. G., Lovell, D. P., Elderfield, K., Austen, B., & Howe, F. A. (2016) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-016-0593-9 · Cited by 5 · see citing works

Gene Expression Signatures of Immaturity, Decreased pH , and Neural Hyperexcitation in the Hippocampus of Alzheimer's Disease Model Mice

Naganishi, S., Hagihara, H., & Miyakawa, T. (2025) · Neuropsychopharmacology Reports · doi:10.1002/npr2.70001 · Cited by 4 · see citing works

Analysis of Expression of the Amyloid-Degrading Enzyme Neprilysin in Brain Structures of 5xFAD Transgenic Mice

Vasilev, D. S., Dubrovskaya, N. M., Tumanova, N. L., & Nalivaeva, N. N. (2022) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093022010173 · Cited by 4 · see citing works

Fermented Soybean Pulp Alleviates Disease Progression of 5×FAD Model Mice

Yang, C.-Y., Liu, Y., Lin, T.-C., Chang, K., & Hsieh‐Li, H. M. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05191-y · Cited by 3 · see citing works

A peptide-neurotensin conjugate that crosses the blood-brain barrier induces pharmacological hypothermia associated with anticonvulsant, neuroprotective and anti-inflammatory properties following status epilepticus in micePreprint

Ferhat, L., Soussi, R., Masse, M., Kyriatzis, G., Girard, S. D., Gassiot, F., Gaudin, N., Laurencin, M., Bernard, A., Bôle, A., et al. (2024) · eLife · doi:10.7554/elife.100527.3 · Cited by 3 · see citing works

Regulation of Hippocamposeptal Synaptic Transmission by GABABRs Is Altered in 5XFAD Mice in a Sex- and Age-Dependent Manner

Damborsky, J. C., & Yakel, J. L. (2024) · Journal of Molecular Neuroscience · doi:10.1007/s12031-024-02260-0 · Cited by 2 · see citing works

Early Spatial and Contextual Coding Deficits in Hippocampal CA1 Precede Performance Decline in an Alzheimer's Disease Model

Li, Y., Go, M. A., Zhang, H., Aleksynas, R., Kim, J., Gao, M., Prado, S., Sastre, M., & Schultz, S. R. (2026) · Advanced Science · doi:10.1002/advs.77419 · Cited by 3 · see citing works

Sex-dependent effects of ultra-low-dose-THC preventive treatment on neuroinflammation and cognitive decline in 5xFAD mice

Nitzan, K., Bentulila, Z., Bregman-Yemini, N., Ayalon, N., David, D., Break, E. P., Sarne, Y., & Doron, R. (2026) · Biology of Sex Differences · doi:10.1186/s13293-025-00815-3 · Cited by 2 · see citing works

Glucagon-Like Peptide-1 Signaling in Learning and Memory: Evidence, Mechanisms, and Therapeutic Implications

Bashaw, A. G., Roman-Ortiz, C., Gao, S. X., Schier, L. A., Borner, T., & Kanoski, S. E. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.06.006 · Cited by 2 · see citing works

The Helico Maze Detects Early Impairment of Reference Memory at Three Months of Age in the 5XFAD Mouse Model of Alzheimer’s Disease

Migliorati, M., Manrique, C., Rahrah, M., Escoffier, G., Ahmadi, A. E., Girard, S. D., Khrestchatisky, M., Rivera, S., Baranger, K., & Roman, F. S. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220281 · Cited by 2 · see citing works

A peptide-neurotensin conjugate that crosses the blood-brain barrier induces pharmacological hypothermia associated with anticonvulsant, neuroprotective, and anti-inflammatory properties following status epilepticus in mice

Ferhat, L., Soussi, R., Masse, M., Kyriatzis, G., Girard, S. D., Gassiot, F., Gaudin, N., Laurencin, M., Bernard, A., Bôle, A., et al. (2025) · eLife · doi:10.7554/elife.100527.4 · Cited by 2 · see citing works

The Helico Maze allows testing of early learning and subcategories of long-term memory in mice

Escoffier, G., Migliorati, M., Rahrah, M., Roman, C. S. M., Khrestchatisky, M., & Roman, F. S. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113242 · Cited by 2 · see citing works

Bis(styryl)benzene Probes for Targeting Early-Stage Amyloid-β Aggregates in Alzheimer’s Disease

GUTIERREZ, C. G., Mina, M., An, J., Bhowmik, S., Xu, K., Salaiza, J. A., Chen, K., Sayed, T. E., & Mirica, L. M. (2026) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6c00429 · Cited by 1 · see citing works

Electro-Calcium uncoupling precedes neurodegeneration in Alzheimer’s diseasePreprint

Kwon, H. C., Eiden, A. M., Li, J., MacKinnon, M., Garfinkel, J. B., Hooper, S., Liu, Y., Nelson, M. T., Koretsky, A. P., & Mughal, A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.26.701803 · Cited by 1 · see citing works

Increased astrocyte representation in the hippocampus of 5xFAD mice

Jovanović, V., Despotović, J., Balo, M., Zaletel, I. V., Despotović, S. Z., & Puškaš, N. (2021) · Medicinski podmladak · doi:10.5937/mp72-32451

Exploring sphingolipid function in the pathogenesis of Alzheimer’s disease

Luo, Q. (2022) · doi:10.26481/dis.20220215ql

Gene dosage determines the behavioural phenotype in the 5xFAD mouse model of Alzheimer’s disease: analysis of the contribution of brain insulin signalling and gut microbiotaPreprint

Vera, D. M., Zambrana-Infantes, E. N., López-Gambero, A. J., Gonzalez-Jimenez, A., Navarro, J. A., Pavón, F. J., Baixerás, E., Santín, L. J., Suárez, J., Rosell‐Valle, C., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2087511/v1

Amyloid pathology reduces ELP3 expression and tRNA modifications leading to impaired proteostasis in Alzheimer’s disease modelsPreprint

Pereira, M., Ribeiro, D. R., Berg, M., Tsai, A. P., Nho, K. T., Kaiser, S., Moutinho, M., & Soares, A. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.02.538928

The Helico Maze Detects Early Impairment of Reference Memory at Three Months of Age in the 5XFAD Mouse Model of Alzheimer’s Disease

Migliorati, M., Manrique, C., Rahrah, M., Escoffier, G., Ahmadi, A. E., Girard, S. D., Khrestchatisky, M., Rivera, S., Baranger, K., & Roman, F. S. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220281 · Cited by 2 · see citing works

Evidence for early cognitive impairment related to frontal cortex in the 5xFAD mouse model of Alzheimer’s disease.

Girard, S. D., Baranger, K., Gauthier, C., Jacquet, M., Bernard, A., Escoffier, G., Marchetti, E., Khrestchatisky, M., Rivera, S., & Roman, F. S. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-120982 · Cited by 107 · see citing works

P1‐043: Behavioral and magnetic resonance microscopic studies of a transgenic mouse model of Alzheimer's disease

Banks, B., Pych, J. C., Venkatasubramanian, P. N., & Wyrwicz, A. M. (2008) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2008.05.628

IC‐P1‐065: Behavioral and magnetic resonance microscopic studies of a transgenic mouse model of AD

Venkatasubramanian, P. N., Banks, B., Pych, J. C., & Wyrwicz, A. M. (2008) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2008.05.2507

Olfactory performance and neuropathology in the Tg6799 strain of Alzheimer’s disease model mice

Österman, H. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology)