References
- Albert MS. Changes in cognition. Neurobiol Aging 2011; 32:58-63.
- Hardy J. A hundred years of Alzheimer’s disease research. Neuron 2006; 52:3-13.
- Jucker M, Walker LC. Pathogenic protein seeding in Alzheimer disease and other neurodegenerative disorders. Ann Neurol. 2011; 70:532–540.
- Mattson MP. Pathways towards and away from Alzheimer's disease. Nature 2004; 430:631-9.
- Hardy JA, Higgins GA. Alzheimer's disease: the amyloid cascade hypothesis. Science 1992; 256:184-5.
- Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991; 82:239-59.
- Terry RD, Masliah E, Salmon DP, Butters N, DeTeresa R, Hill R et al. Physical basis of cognitive alterations in Alzheimer's disease: synapse loss is the major correlate of cognitive impairment. Ann Neurol. 1991; 30:572-80.
- Radde R, Bolmont T, Kaeser SA, Coomaraswamy J, Lindau D, Stolze L et al. Aβ42-driven cerebral amyloidosis in transgenic mice reveals early and robust pathology. EMBO reports 2006; 7:940-6.
- Lehman EJ, Kulnane LS, Gao Y, Petriello MC, Pimpis KM, Younkin L et al. Genetic background regulates beta-amyloid precursor protein processing and beta-amyloid deposition in the mouse. Hum Mol Genet. 2003; 12(22):2949-56. doi: 10.1093/hmg/ddg322.
- Djogo, N., Jakovcevski, I., Müller, C., Lee, H. J., Xu, J. C., Jakovcevski, M. et al. Adhesion molecule L1 binds to amyloid beta and reduces Alzheimer's disease pathology in mice. Neurobiology of disease 2013; 56:104–15. https://doi.org/10.1016/j.nbd.2013.04.014
- Morellini F, Sivukhina E, Stoenica L, Oulianova E, Bukalo O, Jakovcevski I et al. Improved reversal learning and working memory and enhanced reactivity to novelty in mice with enhanced GABAergic innervation in the dentate gyrus. Cereb Cortex 2010; 20:2712-27.
- Vulovic M, Divac N, Jakovcevski I. Confocal Synaptology: Synaptic Rearrangements in Neurodegenerative Disorders and upon Nervous System Injury. Front Neuroanat. 2018; 12:11. doi: 10.3389/fnana.2018.00011.
- Schmalbach B, Lepsveridze E, Djogo N, Papashvili G, Kuang F, Leshchyns'ka I et al. Age-dependent loss of parvalbumin-expressing hippocampal interneurons in mice deficient in CHL1, a mental retardation and schizophrenia susceptibility gene. J Neurochem. 2015; 135(4):830-44. doi: 10.1111/jnc.13284.
- Nikonenko AG, Sun M, Lepsveridze E, Apostolova I, Petrova I, Irintchev A et al. Enhanced perisomatic inhibition and impaired long-term potentiation in the CA1 region of juvenile CHL1-deficient mice. Eur J Neurosci. 2006; 23:1839-52.
- Gengler S, Hamilton A, Hölscher C. Synaptic plasticity in the hippocampus of a APP/PS1 mouse model of Alzheimer’s disease is impaired in old but not young mice. PLoS ONE 2010; 5:e9764.
- Saiz-Sanchez D, Ubeda-Bañon I, De la Rosa-Prieto C, Martinez-Marcos A. Differential expression of interneuron populations and correlation with amyloid-β deposition in the olfactory cortex of an AβPP/PS1 transgenic mouse model of Alzheimer's disease. J Alzheimers Dis. 2012; 31:113-29.
- Verret L, Mann EO, Hang GB, Barth AM, Cobos I, Ho K et al. Inhibitory interneuron deficit links altered network activity and cognitive dysfunction in Alzheimer model. Cell 2012; 149:708-21.
- Schwaller B, Tetko IV, Tandon P, Silveira DC, Vreugdenhil M, Henzi T et al. Parvalbumin deficiency affects network properties resulting in increased susceptibility to epileptic seizures. Mol Cell Neurosci 2004; 25:650-63.
- Meade CA, Figueredo-Cardenas G, Fusco F, Nowak TS, Pulsinelli WA, Reiner A. Transient global ischemia in rats yields striatal projection neuron and interneuron loss resembling that in Huntington's disease. Exp Neurol 2000; 166:307-23.
- Samland H, Huitron-Resendiz S, Masliah E, Criado J, Henriksen SJ, Campbell IL. Profound increase in sensitivity to glutamatergic- but not cholinergic agonist-induced seizures in transgenic mice with astrocyte production of IL-6. J Neurosci Res 2003; 73:176-87.
- Aksic M, Poleksic J, Aleksic D, Petronijevic N, Radonjic NV, Jakovcevski M et al. Maternal Deprivation in Rats Decreases the Expression of Interneuron Markers in the Neocortex and Hippocampus. Front Neuroanat. 2021; 15:670766. doi: 10.3389/fnana.2021.670766.
- Jakovljevic A, Agatonovic G, Aleksic D, Aksic M, Reiss G, Förster E et al. The impact of early life maternal deprivation on the perineuronal nets in the prefrontal cortex and hippocampus of young adult rats. Front Cell Dev Biol. 2022; 10:982663. doi: 10.3389/fcell.2022.982663.
- Wei W, Nguyen LN, Kessels H, Hagiwara H, Sisodia S, Malinow R. Amyloid beta from axons and dendrites reduces local spine number and plasticity. Nat Neurosci 2010; 13:190-6.