Aging alters the molecular dynamics of synapses in a sexually dimorphic pattern in zebrafish (Danio rerio)
暂无分享,去创建一个
M. Adams | Elif Tuğçe Karoğlu | O. Konu | Ayca Arslan-Ergul | Bahriye Erkaya | Dilara O Halim | Ferda Altaytaş
[1] M. Wullimann,et al. Neuroanatomy of the Zebrafish Brain: A Topological Atlas , 2019 .
[2] M. Adams,et al. Short-term dietary restriction in old zebrafish changes cell senescence mechanisms , 2016, Neuroscience.
[3] A. Bilkei-Gorzo,et al. Oxidation and Cognitive Impairment in the Aging Zebrafish , 2015, Gerontology.
[4] David G. Jones,et al. Characterizing synaptic protein development in human visual cortex enables alignment of synaptic age with rat visual cortex , 2015, Front. Neural Circuits.
[5] I. Braasch,et al. Subdivisions of the adult zebrafish pallium based on molecular marker analysis. , 2014, F1000Research.
[6] Corinna Singleman,et al. Growth and maturation in the zebrafish, Danio rerio: a staging tool for teaching and research. , 2014, Zebrafish.
[7] Emma L. Baar,et al. Depletion of Rictor, an essential protein component of mTORC2, decreases male lifespan , 2014, Aging cell.
[8] J. Meier,et al. Palmitoylation of Gephyrin Controls Receptor Clustering and Plasticity of GABAergic Synapses , 2014, PLoS biology.
[9] J. Fritschy,et al. Gephyrin: a master regulator of neuronal function? , 2014, Nature Reviews Neuroscience.
[10] M. Adams,et al. Gene expression changes in aging Zebrafish (Danio rerio) brains are sexually dimorphic , 2014, BMC Neuroscience.
[11] S. D. Santos,et al. Ghrelin triggers the synaptic incorporation of AMPA receptors in the hippocampus , 2013, Proceedings of the National Academy of Sciences.
[12] J. Ståhlberg,et al. Quantum mechanical calculations suggest that lytic polysaccharide monooxygenases use a copper-oxyl, oxygen-rebound mechanism , 2013, Proceedings of the National Academy of Sciences.
[13] N. Spitzer,et al. Development of GABA Circuitry of Fast-Spiking Basket Interneurons in the Medial Prefrontal Cortex of erbb4-Mutant Mice , 2013, The Journal of Neuroscience.
[14] M. Pavlidis,et al. Husbandry of zebrafish, Danio rerio, and the cortisol stress response. , 2013, Zebrafish.
[15] J. Ninkovic,et al. Increased radial glia quiescence, decreased reactivation upon injury and unaltered neuroblast behavior underlie decreased neurogenesis in the aging zebrafish telencephalon , 2013, The Journal of comparative neurology.
[16] M. Cayuela,et al. Premature aging in telomerase-deficient zebrafish , 2013, Disease Models & Mechanisms.
[17] R. Vierk,et al. Sexual dimorphism in estrogen-induced synaptogenesis in the adult hippocampus. , 2013, The International journal of developmental biology.
[18] C. Dermon,et al. Cell proliferation pattern in adult zebrafish forebrain is sexually dimorphic , 2012, Neuroscience.
[19] Elly Nedivi,et al. Clustered Dynamics of Inhibitory Synapses and Dendritic Spines in the Adult Neocortex , 2012, Neuron.
[20] J. Morrison,et al. The ageing cortical synapse: hallmarks and implications for cognitive decline , 2012, Nature Reviews Neuroscience.
[21] P. Reddy,et al. Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease. , 2011, Human molecular genetics.
[22] H. D. Vanguilder,et al. Hippocampal dysregulation of synaptic plasticity-associated proteins with age-related cognitive decline , 2011, Neurobiology of Disease.
[23] E. Chapman,et al. Synaptophysin Regulates the Kinetics of Synaptic Vesicle Endocytosis in Central Neurons , 2011, Neuron.
[24] H. D. Vanguilder,et al. Aging alters the expression of neurotransmission‐regulating proteins in the hippocampal synaptoproteome , 2010, Journal of neurochemistry.
[25] D. Parichy,et al. Normal table of postembryonic zebrafish development: Staging by externally visible anatomy of the living fish , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[26] B. Slack,et al. Zebrafish as a Genetic Model in Biological and Behavioral Gerontology: Where Development Meets Aging in Vertebrates – A Mini-Review , 2009, Gerontology.
[27] J. Epstein,et al. Transcriptome analysis of the zebrafish pineal gland , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[28] A. Cuello,et al. Variations in excitatory and inhibitory postsynaptic protein content in rat cerebral cortex with respect to aging and cognitive status , 2009, Neuroscience.
[29] C. Cotman,et al. Gene expression changes in the course of normal brain aging are sexually dimorphic , 2008, Proceedings of the National Academy of Sciences.
[30] D. Riddle,et al. Effects of aging and caloric restriction on dentate gyrus synapses and glutamate receptor subunits , 2008, Neurobiology of Aging.
[31] M. Adams,et al. Caloric restriction and age affect synaptic proteins in hippocampal CA3 and spatial learning ability , 2008, Experimental Neurology.
[32] P. Kille,et al. Sexually dimorphic gene expression in the brains of mature zebrafish. , 2008, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[33] M. McCarthy,et al. Impact of sex and hormones on new cells in the developing rat hippocampus: a novel source of sex dimorphism? , 2008, The European journal of neuroscience.
[34] A. Cuello,et al. Cognitive impairment and transmitter‐specific pre‐ and postsynaptic changes in the rat cerebral cortex during ageing , 2007, The European journal of neuroscience.
[35] Wendou Yu,et al. Gephyrin expression and clustering affects the size of glutamatergic synaptic contacts , 2007, Journal of neurochemistry.
[36] M. Adams,et al. Caloric restriction eliminates the aging-related decline in NMDA and AMPA receptor subunits in the rat hippocampus and induces homeostasis , 2007, Experimental Neurology.
[37] P. Currie,et al. Animal models of human disease: zebrafish swim into view , 2007, Nature Reviews Genetics.
[38] K. Ampatzis,et al. Sex differences in adult cell proliferation within the zebrafish (Danio rerio) cerebellum , 2007, The European journal of neuroscience.
[39] Valter Tucci,et al. Cognitive Aging in Zebrafish , 2006, PloS one.
[40] Yu Tian Wang,et al. A balance between excitatory and inhibitory synapses is controlled by PSD-95 and neuroligin. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[41] R. Nicoll,et al. Postsynaptic Density-95 Mimics and Occludes Hippocampal Long-Term Potentiation and Enhances Long-Term Depression , 2003, The Journal of Neuroscience.
[42] Junzo Uchiyama,et al. The zebrafish as a vertebrate model of functional aging and very gradual senescence , 2003, Experimental Gerontology.
[43] Cristina Broglio,et al. Conservation of Spatial Memory Function in the Pallial Forebrain of Reptiles and Ray-Finned Fishes , 2002, The Journal of Neuroscience.
[44] J. Bergado,et al. Aging impairs amygdala-hippocampus interactions involved in hippocampal LTP , 2002, Neurobiology of Aging.
[45] D. Riddle,et al. Effects of age and insulin-like growth factor-1 on neuron and synapse numbers in area CA3 of hippocampus , 2001, Neuroscience.
[46] J. Morrison,et al. Different modes of hippocampal plasticity in response to estrogen in young and aged female rats , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[47] M. Sheng,et al. Molecular organization of the postsynaptic specialization , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[48] Matthew C Smear,et al. Perception of Fourier and non-Fourier motion by larval zebrafish , 2000, Nature Neuroscience.
[49] J. Morrison,et al. Circuit-Specific Alterations in Hippocampal Synaptophysin Immunoreactivity Predict Spatial Learning Impairment in Aged Rats , 2000, The Journal of Neuroscience.
[50] J. Brandstätter,et al. Loss of Postsynaptic GABAA Receptor Clustering in Gephyrin-Deficient Mice , 1999, The Journal of Neuroscience.
[51] R. Morris,et al. Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein , 1998, Nature.
[52] D. Ingram,et al. Hippocampal neuron and synaptophysin-positive bouton number in aging C57BL/6 mice , 1998, Neurobiology of Aging.
[53] M. Gallagher,et al. Preserved neuron number in the hippocampus of aged rats with spatial learning deficits. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[54] R. Auer,et al. Effect of age and sex on N-methyl-D-aspartate antagonist-induced neuronal necrosis in rats. , 1996, Stroke.
[55] Jens Christian Sørensen,et al. Memory impaired aged rats: No loss of principal hippocampal and subicular neurons , 1996, Neurobiology of Aging.
[56] C. Kimmel,et al. Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.
[57] M. Igarashi,et al. Decreased synaptic density in aged brains and its prevention by rearing under enriched environment as revealed by synaptophysin contents , 1994, Journal of neuroscience research.
[58] C. Woolley,et al. Roles of estradiol and progesterone in regulation of hippocampal dendritic spine density during the estrous cycle in the rat , 1993, The Journal of comparative neurology.
[59] H. Gundersen,et al. Unbiased stereological estimation of the total number of neurons in the subdivisions of the rat hippocampus using the optical fractionator , 1991, The Anatomical record.
[60] Bertram Wiedenmann,et al. Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles , 1985, Cell.
[61] P. Greengard,et al. A 38,000-dalton membrane protein (p38) present in synaptic vesicles. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[62] Colon Ej. The elderly brain. A quantitative analysis in the cerebral cortex of two cases. , 1972 .
[63] H BRODY,et al. Organization of the cerebral cortex. III. A study of aging in the human cerebral cortex , 1955, The Journal of comparative neurology.
[64] A. Dayan. Quantitative histological studies on the aged human brain , 2004, Acta Neuropathologica.
[65] D. Nicholson,et al. Differences in the expression of AMPA and NMDA receptors between axospinous perforated and nonperforated synapses are related to the configuration and size of postsynaptic densities , 2004, The Journal of comparative neurology.
[66] Andy P. Field,et al. Discovering Statistics Using SPSS , 2000 .