Augmented Senile Plaque Load in Aged Female β-Amyloid Precursor Protein-Transgenic Mice

Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice

Hsiao, K., Chapman, P., Nilsen, S., Eckman, C., Harigaya, Y., Younkin, S., Yang, F., & Cole, G. (1996) · Science · doi:10.1126/science.274.5284.99 · Cited by 4,210

The efficiency of systematic sampling in stereology and its prediction*

Gundersen, H. J. G., & Jensen, E. B. V. (1987) · Journal of Microscopy · doi:10.1111/j.1365-2818.1987.tb02837.x · Cited by 3,519

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

The new stereological tools: Disector, fractionator, nucleator and point sampled intercepts and their use in pathological research and diagnosis

Gundersen, H. J. G., Bagger, P. V., Bendtsen, T. F., Evans, S. M., Korbo, L., Marcussen, N., Møller, A., Nielsen, K. N., Nyengaard, J. R., Pakkenberg, B., et al. (1988) · Apmis · doi:10.1111/j.1699-0463.1988.tb00954.x · Cited by 2,480

Effect of oestrogen during menopause on risk and age at onset of Alzheimer's disease

Tang, M., Jacobs, D. M., Stern, Y., Marder, K. S., Schofield, P., Gurland, B. J., Andrews, H., & Mayeux, R. P. (1996) · The Lancet · doi:10.1016/s0140-6736(96)03356-9 · Cited by 1,647

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid

Mullan, M., Crawford, F., Axelman, K., Houlden, H., Lilius, L., Winblad, B., & Lannfelt, L. (1992) · Nature Genetics · doi:10.1038/ng0892-345 · Cited by 1,513

Two amyloid precursor protein transgenic mouse models with Alzheimer disease-like pathology

Sturchler-Pierrat, C., Abramowski, D., Duke, M., Wiederhold, K.-H., Mistl, C., Rothacher, S., Ledermann, B., Bürki, K., Frey, P., Paganetti, P. A., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.24.13287 · Cited by 1,507

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

The prevalence of dementia: A quantitative integration of the literature

Jorm, A. F., Korten, A. E., & Henderson, A. S. (1987) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1987.tb02906.x · Cited by 1,301

Estrogen Replacement Therapy for Treatment of Mild to Moderate Alzheimer Disease

Mulnard, R. A., Cotman, C. W., Kawas, C. H., van Dyck, C. H., Sano, M. C., Doody, R. S., Koss, E., Pfeiffer, E., Jin, S., Gamst, A., et al. (2000) · JAMA · doi:10.1001/jama.283.8.1007 · Cited by 989

SENP1 and SENP2 regulate SUMOylation of amyloid precursor protein

Maruyama, T., Abe, Y., & Niikura, T. (2018) · Heliyon · doi:10.1016/j.heliyon.2018.e00601 · Cited by 20

Animal Models of Psychosis in Alzheimer Disease

Krivinko, J. M., Koppel, J. L., Savonenko, A. V., & Sweet, R. A. (2019) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2019.05.009 · Cited by 19

Novel aspects of accumulation dynamics and Aβ composition in transgenic models of AD

Lewis, H. D., Beher, D., Smith, D., Hewson, L., Cookson, N., Reynolds, D. S., Dawson, G. R., Jiang, M., der Ploeg, L. H. T. V., Qian, S., et al. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.12.009 · Cited by 21

Brainwide distribution and variance of amyloid-beta deposits in tg-ArcSwe mice

Lillehaug, S., Skaaraas, G. H. E. S., Nilsson, L. N. G., Bjaalie, J. G., Leergaard, T. B., & Torp, R. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.09.013 · Cited by 18

Not all depression is created equal: sex interacts with disease to precipitate depression

Nemeth, C. L., Harrell, C. S., Beck, K. D., & Neigh, G. N. (2013) · Biology of Sex Differences · doi:10.1186/2042-6410-4-8 · Cited by 19

Aging, sex, metabolic and life experience factors: Contributions to neuro-inflammaging in Alzheimer’s disease research

Singhaarachchi, P. H., Antal, P., Calon, F., Culmsee, C., Delpech, J.-C., Feldotto, M., Geertsema, J., Hoeksema, E. E., Kőrösi, A., Layé, S., et al. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105724 · Cited by 20

Pharmacological properties of a novel and potent γ-secretase modulator as a therapeutic option for the treatment of Alzheimer’s disease

Murakami, K., Watanabe, T., Koike, T., Kamata, M., Igari, T., & Kondo, S. (2015) · Brain Research · doi:10.1016/j.brainres.2015.12.016 · Cited by 18

Estrogen pendulum in schizophrenia and Alzheimer’s disease: Review of therapeutic benefits and outstanding questions

Androvičová, R., Pfaus, J. G., & Ovsepian, S. V. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136038 · Cited by 19

Assessment of Cognitive Phenotyping in Inbred, Genetically Modified Mice, and Transgenic Mouse Models of Alzheimer's Disease

Kim, D.-H., Jang, Y.-S., Jeon, W. K., & Han, J. (2019) · Experimental Neurobiology · doi:10.5607/en.2019.28.2.146 · Cited by 19

Augmented axonal defects and synaptic degenerative changes in female GRK5 deficient mice

Li, L., Rasul, I., Liu, J., Zhao, B., Tang, R., Premont, R. T., & Suo, W. Z. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.09.019 · Cited by 18

Enhancement of β-amyloid oligomer accumulation after intracerebroventricular injection of streptozotocin, which involves central insulin signaling in a transgenic mouse model

Lin, F., Jia, J., & Qin, W. (2014) · Neuroreport · doi:10.1097/wnr.0000000000000261 · Cited by 17

Longitudinal Monitoring of Sex-Related in vivo Metabolic Changes in the Brain of Alzheimer's Disease Transgenic Mouse Using Magnetic Resonance Spectroscopy

van Duijn, S., Nabuurs, R. J. A., van Duinen, S. G., Natté, R., van Buchem, M. A., & Alia, A. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-122188 · Cited by 16

Experience-dependent regulation of vesicular zinc in male and female 3xTg-AD mice

Nakashima, A. S., Oddo, S., LaFerla, F. M., & Dyck, R. H. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.05.028 · Cited by 16

The 5×FAD mouse model of Alzheimer's disease

Ismeurt, C., Giannoni, P., & Claeysen, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815854-8.00013-6 · Cited by 18

Widespread hyperphosphorylated tau in the working memory circuit early after cortical impact injury of brain (Original study)

Zhao, Z., Ning, Y., Li, P., Yang, N., Peng, Y., Xiong, R., Zhao, Y., Liu, D., Zeng, X., Chen, J., et al. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.02.002 · Cited by 15

Low‐dose total‐body carbon‐ion irradiations induce early transcriptional alteration without late Alzheimer's disease‐like pathogenesis and memory impairment in mice

Wang, B., Tanaka, K., Ji, B., Ono, M., Fang, Y., Ninomiya, Y., Maruyama, K., Nakajima, N. I., Begum, N., Higuchi, M., et al. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23363 · Cited by 14

Rodent Models for Alzheimer’s Disease in Drug Discovery

Barrett, J. E., & McGonigle, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802810-0.00012-x · Cited by 15

Chronic Mild Stress Assay Leading to Early Onset and Propagation of Alzheimer’s Disease Phenotype in Mouse Models

Cuadrado‐Tejedor, M., & García‐Osta, A. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2627-5_14 · Cited by 14

Selective Vulnerability of Neurons in Primary Cultures and in Neurodegenerative Diseases

Chen, J., & Herrup, K. (2008) · Reviews in the Neurosciences · doi:10.1515/revneuro.2008.19.4-5.317 · Cited by 15

The Role of Aβ-Peptide on Spatial Memory, EEG, Auditory Evoked Potentials And Nicotinic Cholinergic Receptors in A/P Transgenic Mice

Wang, J. (2003) · Cited by 14

The Past as Seen by Women and Men With Alzheimer Disease

Haj, M. E., Boutoleau‐Bretonnière, C., & Gallouj, K. (2020) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0000000000000363 · Cited by 15

Can Animal Models Inform on the Relationship between Depression and Alzheimer Disease?

Nyarko, J. N. K., Quartey, M. O., Baker, G. B., & Mousseau, D. D. (2018) · The Canadian Journal of Psychiatry · doi:10.1177/0706743718772514 · Cited by 12

Local perfusion of capillaries reveals disrupted beta-amyloid homeostasis at the blood-brain barrier in Tg2576 murine Alzheimer’s model

Hanafy, A. S., Lamprecht, A., & Dietrich, D. (2023) · Fluids and Barriers of the CNS · doi:10.1186/s12987-023-00492-7 · Cited by 11

Retinal Changes in Transgenic Mouse Models of Alzheimer’s Disease

Guo, L., Ravindran, N., Shamsher, E., Hill, D., & Cordeiro, M. F. (2021) · Current Alzheimer Research · doi:10.2174/1567205018666210414113634 · Cited by 13

TSPO contributes to neuropathology and cognitive deficits in Alzheimer’s disease

Ceyzériat, K., Badina, A. M., Abjean, L., Meyer, L., Bouteldja, F., Bałkota, M., Amossé, Q., Prudhomme, O., Middleton, R. J., Liu, G.-J., et al. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03583-4 · Cited by 14

Disease modifying effects of the amyloid-beta protofibril-selective antibody mAb158 in aged Tg2576 transgenic mice

Rizoska, B., Zachrisson, O., Appelkvist, P., Boström, E., Björklund, M., Rachalski, A., Gkanatsiou, E., Kylefjord, H., Söderberg, L., Nygren, P., et al. (2024) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2024.103950 · Cited by 10

Sex Differences in Hypothalamic Changes and the Metabolic Response of TgAPP Mice to a High Fat Diet

Freire‐Regatillo, A., Díaz-Pacheco, S., Frago, L. M., Arévalo, M., Argente, J., García‐Segura, L. M., CEBALLOS, M. L. D., & Chowen, J. A. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.910477 · Cited by 10

Low-Dose Radiation Therapy Impacts Microglial Inflammatory Response without Modulating Amyloid Load in Female TgF344-AD Rats

Ceyzériat, K., Jaques, E., Gloria, Y., Badina, A. M., Millet, P., Koutsouvelis, N., Dipasquale, G., Frisoni, G. B., Zilli, T., Garibotto, V., et al. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-231153 · Cited by 10

Sex-Specific Effects of Anxiety on Cognition and Activity-Dependent Neural Networks: Insights From (Female) Mice and (Wo)men

Hunsberger, H. C., Lee, S., Jin, M., Lanio, M., Whye, A., Cha, J., Scarlata, M., Matthews, L. C., Jayaseelan, K., & Denny, C. A. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.09.016 · Cited by 10

Effects of Genistein and Exercise Training on Brain Damage Induced by a High‐Fat High‐Sucrose Diet in Female C57BL/6 Mice

Li, R., Ding, X.-W., Geetha, T., Fadamiro, M., Aubin, C. R. S., Shim, M., Al‐Nakkash, L., Broderick, T. L., & Babu, J. R. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1560435 · Cited by 9

Alzheimer diseases

Savonenko, A. V., Wong, P. C., & Li, T. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85654-6.00022-8 · Cited by 8

Amyloid-β Processing in Aged S100B Transgenic Mice Is Sex Dependent

Wartchow, K. M., Rodrigues, L., Swierzy, I. J., Buchfelder, M., Souza, D. O., Gonçalves, C., & Kleindienst, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910823 · Cited by 8

Models of Alzheimer's Disease

LeVine, H., & Walker, L. C. (2006) · Elsevier eBooks · doi:10.1016/b978-012369391-4/50012-6 · Cited by 8

Y10W β(1–40) fluorescence reflects epitope exposure in conformers of Alzheimer’s β-peptide

LeVine, H. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/s0003-9861(03)00322-9 · Cited by 8

Age‐related synaptic dysfunction in Tg2576 mice starts as a failure in early long‐term potentiation which develops into a full abolishment of late long‐term potentiation

Fernández‐Fernández, D., Dorner‐Ciossek, C., Kroker, K. S., & Rosenbrock, H. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23701 · Cited by 7

Aβ∗56 is a stable oligomer that impairs memory function in mice

Liu, P., Lapcinski, I. P., Hlynialuk, C. J. W., Steuer, E. L., Loude, T. J., Shapiro, S. L., Kemper, L. J., & Ashe, K. H. (2024) · iScience · doi:10.1016/j.isci.2024.109239 · Cited by 6

Gender Differences in the Effects of Exercise Interventions on Alzheimer’s Disease

Dong, Y., Shi, L., Ma, Y., Liu, Y., Sun, Y., & Jin, Q. (2025) · Brain Sciences · doi:10.3390/brainsci15080812 · Cited by 9

Cell Type-Specific Human APP Transgene Expression by Hippocampal Interneurons in the Tg2576 Mouse Model of Alzheimer’s Disease

Höfling, C., Shehabi, E., Kuhn, P., Lichtenthaler, S. F., Hartlage‐Rübsamen, M., & Roßner, S. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00137 · Cited by 5

Biological Sex Disparities in Alzheimer’s Disease

Almutairi, J. A., & Kidd, E. J. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_545 · Cited by 4

Avenanthramide-C Mitigates High-Fat Diet-Accelerated Alzheimer’s Pathologies via NOD1-Driven Neuroinflammation in 5×FAD Mice

Wang, M., Jin, B., Xu, J., & Wang, C. (2025) · Nutrients · doi:10.3390/nu17162679 · Cited by 4

Caspase-dependent degradation of MDMx/MDM4 cell cycle regulatory protein in amyloid β-induced neuronal damage

Colacurcio, D. J., Zyskind, J. W., Jordan‐Sciutto, K. L., & Akay, C. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.10.031 · Cited by 4

Age-related cerebral amyloid angiopathy accumulation in the APPSw mouse model is associated with perivascular inflammation and brain-wide vascular and inflammatory gene and protein changes

Krick, K. E., Weekman, E. M., Johnson, S. N., Sudduth, T. L., Rogers, C. B., Nicolayson, E. J., Kleinhenz, M. T., & Wilcock, D. M. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107013 · Cited by 3

Unveiling FOXO3's metabolic contribution to menopause and Alzheimer's disease

O'Mahony, C., Hidalgo‐Lanussa, O., & Barreto, G. E. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112679 · Cited by 3

Non-invasive In Vivo Brain Astrogenesis and Astrogliosis Quantification Using a Far-red E2-Crimson Transgenic Reporter Mouse

Boitet, M., Eun, H., Lee, T., Kim, J., & Grailhe, R. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02997-y · Cited by 3

Dentate Gyrus Granule Cells Show Stability of BDNF Protein Expression in Mossy Fiber Axons with Age, and Resistance to Alzheimer’s Disease Neuropathology in a Mouse Model

Criscuolo, C., Chartampila, E., Ginsberg, S. D., & Scharfman, H. E. (2023) · eNeuro · doi:10.1523/eneuro.0192-23.2023 · Cited by 6

Spatiotemporal development of the neuronal accumulation of amyloid precursor protein and the amyloid plaque formation in the brain of 3xTg-AD mice

Ono, M., Ito, T., Yamaki, S., Hori, Y., Zhou, Q., Zhao, X., Muramoto, S., Yamamoto, R., Furuyama, T., Sakata‐Haga, H., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28821 · Cited by 3

Physiological factors could enhance amyloid-beta toxicity

Hunya, Á. G. (2013) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.1674 · Cited by 3

Cerebral Aβ amyloidosis and postmenopausal hormone deficiency: roles in the genesis of Alzheimer’s disease

Gandy, S. (2004) · Human Pathology · doi:10.1016/j.humpath.2004.01.003 · Cited by 3

Sagacious confucius’ pillow elixir ameliorates Dgalactose induced cognitive injury in mice via estrogenic effects and synaptic plasticity

Zhao, D.-P., Lei, X., Wang, Y., Ao, X., Zhao, C.-Y., Xu, Y., Zhang, Y., Liu, G., Geng, F., Xu, H., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.971385 · Cited by 2

Species, Strain, and Gender Issues in the Development and Validation of Animal Models of Dementia

Dijck, A. V., Dam, D. V., & Deyn, P. P. D. (2010) · Neuromethods · doi:10.1007/978-1-60761-898-0_4 · Cited by 2

Sex differences in microglia as a risk factor for Alzheimer’s disease

Delage, C. I., Rendina, D. N., Malacon, K. E., Tremblay, M., & Bilbo, S. D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819344-0.00008-9 · Cited by 2

Sex differences in the injured brain

Melcangi, R. C., & García‐Segura, L. M. (2011) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci.2011.112 · Cited by 1

Dietary methionine regulation of cognitive function: Evidence, mechanisms, and implementation strategies

Xu, Y., Yang, Y., Jiang, Y., Li, B., Xie, Y., Shi, Y., & Le, G. (2025) · Food Research International · doi:10.1016/j.foodres.2025.116858 · Cited by 3

The Role of Apolipoprotein E Concentration and Isoform in Amyloid-beta Metabolism In Vivo

Castellano, J. M. (2011) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7416v3s

Amyloid precursor protein with the Alzheimer´s disease 670/671 mutation : Animal and cellular models

Kloskowska, E. (2008) · Figshare

Characterising transgenic APP mutation mouse models of amyloid pathology for use in preclinical immunotherapy

Hvoslef‐Eide, M. (2012) · ORCA Online Research @Cardiff (Cardiff University)

The effect of dietary omega-3 polyunsaturated fattyacids and curcumin on cognition and pathology in amouse model of amyloid pathology

Hall, K. (2011) · ORCA Online Research @Cardiff (Cardiff University)

Animal models of Alzheimer’s disease for preclinical research

Takahashi, H. (2010) · Folia Pharmacologica Japonica · doi:10.1254/fpj.136.6

Genetic markers of neurodegeneration: a role for paraoxonase 1 in sporadic Alzheimer's disease?

Leduc, V. (2009)

An Investigation into the Role of Iron, Copper, and Gender in a Transgenic Mouse Model of Alzheimer's Disease.

Groeber, C. M. (2013) · doi:10.13021/mars/5636

Transgenic mouse models of Alzheimer's disease

Brooks, S. P., & Dunnett, S. B. (2005) · CRC Press eBooks · doi:10.1201/b13239-71

The effect of estrogen deficiency on learning and memory in two novel rat models of Alzheimer's disease

Klakotskaia, D. (2017) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/63858

A cholesterol-coupled N-acetyl-aspartyl-glutamate metabolic network facilitates the neuroprotective impact of estradiol in neuronsPreprint

Chow, H., Sun, J. K., Wu, D., Peng, A. Z., Wong, G. C., Hart, R. P., & Herrup, K. (2024) · Research Square · doi:10.21203/rs.3.rs-4489289/v1

The β-amyloid oligomer Aβ*56 is associated with Alzheimer’s dementia independently of amyloid pathologyPreprint

Lapcinski, I. P., Petersen, A. J., Ashe, K. H., & Liu, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.11.648457

Additional file 1 of Local perfusion of capillaries reveals disrupted beta-amyloid homeostasis at the blood-brain barrier in Tg2576 murine Alzheimer’s model

Hanafy, A. S., Lamprecht, A., & Dietrich, D. (2023) · Figshare · doi:10.6084/m9.figshare.24628136

Additional file 1 of Infusion of blood from mice displaying cerebral amyloidosis accelerates amyloid pathology in animal models of Alzheimer’s disease

Morales, R., Duran-Aniotz, C. A., Bravo-Alegria, J. B., Estrada, L. D., Shahnawaz, M., Hu, P.-P., Kramm, C., Morales‐Scheihing, D., Urayama, A., & Soto, C. (2020) · Figshare · doi:10.6084/m9.figshare.13346964

Additional file 1 of Aβ43 aggregates exhibit enhanced prion-like seeding activity in mice

Ruiz‐Riquelme, A., Mao, A., Barghash, M. M., Lau, H. H. C., Stuart, E., Kovacs, G. G., Nilsson, K. P. R., Fraser, P. E., Schmitt‐Ulms, G., & Watts, J. C. (2021) · Figshare · doi:10.6084/m9.figshare.14570473

Validation préclinique de l'efficacité de l'ANAVEX2-73 dans des modèles transgénique et non transgénique de la maladie d'Alzheimer

Lahmy, V. (2014) · theses.fr (ABES) · doi:10.70675/23744d67zb26bz4a32zadbfz3931ecca70f5

Mitochondria, neurosteroids and biological rhythms : implications in health and disease states

Grimm, A. (2015) · theses.fr (ABES) · doi:10.70675/8aac5aa9z77cdz49bdz9cf5z0ff0b5dd0f84

Caractérisation et modulation du microbiote intestinal dans le contexte de la maladie d’Alzheimer : vers une nouvelle piste thérapeutique

Ismeurt, C. (2021) · theses.fr (ABES) · doi:10.70675/159d4638zb5f8z4580zb26fzd0419dba4d37

De novo formation of familial Alzheimer’s disease-relevant Aβ strains occurs exclusively in the human brain

Mao, A., Ruiz‐Riquelme, A., Barghash, M. M., Silver, N. R. G., Lau, H. H. C., Stuart, E., Zampar, S., Sehlin, D., Syvänen, S., Pollanen, M. S., et al. (2026) · Acta Neuropathologica Communications · doi:10.1186/s40478-026-02390-z

Retinal manifestations of Alzheimer's Disease: Insights from animal models, clinical detection, and future translation

Zhang, X., Zhuang, D., Lai, C., Zheng, C., Soh, Z. D., Wagner, S. K., Cai, V. Y., Yang, Z., Wang, S., Geng, X., et al. (2026) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2026.101504

Impact of stroke on respiratory function and amyloid-β pathology in Tg-2576 mice

Zhang, Y., Hamamy, A. E., Iqbal, Z., Ranjan, A., Sumani, D., Souza, K. A. D., Lee, J., Marrelli, S. P., McCullough, L. D., & Li, J. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261476022

Genetic and Pharmacological Targeting of Hsp72 Overexpression/Induction in an Alzheimer's Disease Mouse Model With Combined Amyloid and Tau Pathology

Marshall, J. P. S., Harutyunyan, A., Ng, J., West, O. M., Collins, J. M., King, A. E., Morizzi, J., Wright, P., Calkin, A. C., Drew, B. G., et al. (2026) · Journal of Neuroscience Research · doi:10.1002/jnr.70161

Gender differences in the amount and deposition of amyloidβ in APPswe and PS1 double transgenic mice

Wang, J., Tanila, H., Puoliväli, J., Kadish, I., & Groen, T. V. (2003) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.08.009 · Cited by 316

Males vs females: differences in the AB accumulation

Ordóñez‐Gutiérrez, L., Fernández, I. L., Antón, M., & Wandosell, F. G. (2015) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · doi:10.13039/100008054

Increased β-amyloid deposition in female transgenic mice overexpressing human βAPP

Callahan, M. J., Lipinski, W. J., Bian, F., Pack, A., & Walker, L. C. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)83352-7

Females exhibit more extensive amyloid, but not tau, pathology in an Alzheimer transgenic model

Hirata-Fukae, C., Li, H.-F., Hoe, H.-S., Gray, A. J., Minami, S. S., Hamada, K., Niikura, T., Hua, F., Tsukagoshi-Nagai, H., Horikoshi-Sakuraba, Y., et al. (2008) · Brain Research · doi:10.1016/j.brainres.2008.03.079 · Cited by 284

Sex‐Dependent Differences in Amyloid‐β Deposition in a Mouse Model of Alzheimer's Disease

Gee, M. T., Thai, S., & Pires, P. W. (2021) · The FASEB Journal · doi:10.1096/fasebj.2021.35.s1.02207 · Cited by 1