scholarly article | Q13442814 |
P50 | author | Ashok Shetty | Q42600521 |
Bharathi Hattiangady | Q48164192 | ||
P2860 | cites work | Exercise enhances learning and hippocampal neurogenesis in aged mice. | Q24537320 |
Neurogenesis may relate to some but not all types of hippocampal-dependent learning | Q24629342 | ||
Hippocampal neurogenesis and neural stem cells in temporal lobe epilepsy | Q24641845 | ||
"Dormant basket cell" hypothesis revisited: relative vulnerabilities of dentate gyrus mossy cells and inhibitory interneurons after hippocampal status epilepticus in the rat | Q28182344 | ||
Axon sprouting in a model of temporal lobe epilepsy creates a predominantly excitatory feedback circuit | Q28216593 | ||
Reelin deficiency and displacement of mature neurons, but not neurogenesis, underlie the formation of granule cell dispersion in the epileptic hippocampus | Q28236724 | ||
Decreased hippocampal inhibition and a selective loss of interneurons in experimental epilepsy | Q28282728 | ||
Kainic acid-induced recurrent mossy fiber innervation of dentate gyrus inhibitory interneurons: possible anatomical substrate of granule cell hyper-inhibition in chronically epileptic rats | Q28289328 | ||
Evidence of functional mossy fiber sprouting in hippocampal formation of kainic acid-treated rats | Q28307917 | ||
Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo | Q28577046 | ||
Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants | Q29547516 | ||
Functional neurogenesis in the adult hippocampus | Q29618708 | ||
Wnt signalling regulates adult hippocampal neurogenesis | Q29619688 | ||
Neurogenesis in the adult is involved in the formation of trace memories | Q29622890 | ||
Beneficial effects of enriched environment following status epilepticus in immature rats. | Q30332214 | ||
Spatial relational memory requires hippocampal adult neurogenesis | Q33338471 | ||
Spatial memory performances of aged rats in the water maze predict levels of hippocampal neurogenesis | Q33717296 | ||
Entorhinal axons exhibit sprouting in CA1 subfield of the adult hippocampus in a rat model of temporal lobe epilepsy | Q34146609 | ||
The process of epileptogenesis: a pathophysiological approach. | Q34191970 | ||
Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus | Q34424431 | ||
Aberrant seizure-induced neurogenesis in experimental temporal lobe epilepsy | Q34464254 | ||
Potential role for adult neurogenesis in the encoding of time in new memories. | Q34531656 | ||
Reelin regulates neuronal progenitor migration in intact and epileptic hippocampus. | Q34576049 | ||
Memory impairment in temporal lobe epilepsy: the role of entorhinal lesions | Q34768837 | ||
Long term effects of refractory temporal lobe epilepsy on cognitive abilities: a cross sectional study | Q35451995 | ||
Therapy for neurobehavioral disorders in epilepsy | Q35798249 | ||
Depressive behavior and selective down-regulation of serotonin receptor expression after early-life seizures: reversal by environmental enrichment | Q35809356 | ||
Aging does not alter the number or phenotype of putative stem/progenitor cells in the neurogenic region of the hippocampus. | Q36729208 | ||
Strategies for promoting anti-seizure effects of hippocampal fetal cells grafted into the hippocampus of rats exhibiting chronic temporal lobe epilepsy. | Q36729217 | ||
Implications of decreased hippocampal neurogenesis in chronic temporal lobe epilepsy. | Q36729229 | ||
The pilocarpine model of temporal lobe epilepsy | Q36841686 | ||
Relevance of seizure-induced neurogenesis in animal models of epilepsy to the etiology of temporal lobe epilepsy. | Q36850236 | ||
Adult hippocampal neurogenesis in depression | Q36921967 | ||
Exercise builds brain health: key roles of growth factor cascades and inflammation | Q36926512 | ||
Epileptogenesis in the dentate gyrus: a critical perspective | Q36926926 | ||
Doublecortin-positive newly born granule cells of hippocampus have abnormal apical dendritic morphology in the pilocarpine model of temporal lobe epilepsy. | Q39806372 | ||
Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination | Q40709408 | ||
Kainic acid increases the proliferation of granule cell progenitors in the dentate gyrus of the adult rat. | Q42455434 | ||
Up-regulation of neuropeptide Y levels and modulation of glutamate release through neuropeptide Y receptors in the hippocampus of kainate-induced epileptic rats | Q42475710 | ||
Status epilepticus-induced hilar basal dendrites on rodent granule cells contribute to recurrent excitatory circuitry | Q42495522 | ||
Pilocarpine-induced seizures cause selective time-dependent changes to adult-generated hippocampal dentate granule cells. | Q42515771 | ||
Glutamic acid decarboxylase-67-positive hippocampal interneurons undergo a permanent reduction in number following kainic acid-induced degeneration of ca3 pyramidal neurons | Q43611984 | ||
Intracerebroventricular infusion of insulin-like growth factor-I ameliorates the age-related decline in hippocampal neurogenesis | Q43807507 | ||
Spontaneous limbic seizures after intrahippocampal infusion of brain-derived neurotrophic factor. | Q43939477 | ||
Recurrent spontaneous motor seizures after repeated low-dose systemic treatment with kainate: assessment of a rat model of temporal lobe epilepsy | Q44056599 | ||
Reassessment of the effects of cycloheximide on mossy fiber sprouting and epileptogenesis in the pilocarpine model of temporal lobe epilepsy | Q44168267 | ||
Early determination and long-term persistence of adult-generated new neurons in the hippocampus of mice | Q44238509 | ||
Neurogenesis and aging: FGF-2 and HB-EGF restore neurogenesis in hippocampus and subventricular zone of aged mice | Q44526579 | ||
Hippocampal neurotrophin levels in a kainate model of temporal lobe epilepsy: a lack of correlation between brain-derived neurotrophic factor content and progression of aberrant dentate mossy fiber sprouting | Q44581779 | ||
Perforant path activation of ectopic granule cells that are born after pilocarpine-induced seizures | Q44633580 | ||
Efficacy of doublecortin as a marker to analyse the absolute number and dendritic growth of newly generated neurons in the adult dentate gyrus | Q44729784 | ||
Seizure-associated, aberrant neurogenesis in adult rats characterized with retrovirus-mediated cell labeling. | Q44972977 | ||
Human neural stem cell transplantation reduces spontaneous recurrent seizures following pilocarpine-induced status epilepticus in adult rats | Q45063826 | ||
Physical training reverts hippocampal electrophysiological changes in rats submitted to the pilocarpine model of epilepsy. | Q45121641 | ||
Chronic temporal lobe epilepsy is associated with severely declined dentate neurogenesis in the adult hippocampus. | Q45168388 | ||
Epilepsy induced by extended amygdala-kindling in rats: lack of clear association between development of spontaneous seizures and neuronal damage | Q45173236 | ||
Advances in understanding the process of epileptogenesis based on patient material: what can the patient tell us? | Q46169515 | ||
Roles of continuous neurogenesis in the structural and functional integrity of the adult forebrain. | Q46402795 | ||
Might astrocytes play a role in maintaining the seizure-prone state? | Q46483085 | ||
Dynamics of neurogenesis in the dentate gyrus of adult rats | Q46557470 | ||
Entorhinal cortex entrains epileptiform activity in CA1 in pilocarpine-treated rats. | Q46603768 | ||
Repair of the injured adult hippocampus through graft-mediated modulation of the plasticity of the dentate gyrus in a rat model of temporal lobe epilepsy. | Q46703426 | ||
Disruption of the neurogenic potential of the dentate gyrus in a mouse model of temporal lobe epilepsy with focal seizures | Q46785506 | ||
Vascular endothelial growth factor-B (VEGFB) stimulates neurogenesis: evidence from knockout mice and growth factor administration | Q46842547 | ||
CA3 axonal sprouting in kainate-induced chronic epilepsy | Q46855098 | ||
Hippocampal neurodegeneration, spontaneous seizures, and mossy fiber sprouting in the F344 rat model of temporal lobe epilepsy. | Q46956867 | ||
Enhanced production and dendritic growth of new dentate granule cells in the middle-aged hippocampus following intracerebroventricular FGF-2 infusions. | Q46990503 | ||
Angiogenesis is associated with blood-brain barrier permeability in temporal lobe epilepsy | Q48154139 | ||
Increased dentate neurogenesis after grafting of glial restricted progenitors or neural stem cells in the aging hippocampus | Q48164120 | ||
Induction of the Wnt inhibitor, Dickkopf-1, is associated with neurodegeneration related to temporal lobe epilepsy | Q48201269 | ||
Preferential incorporation of adult-generated granule cells into spatial memory networks in the dentate gyrus. | Q48285420 | ||
Environment matters: synaptic properties of neurons born in the epileptic adult brain develop to reduce excitability | Q48333832 | ||
Balance between neurogenesis and gliogenesis in the adult hippocampus: role for reelin | Q48346671 | ||
The window and mechanisms of major age-related decline in the production of new neurons within the dentate gyrus of the hippocampus | Q48356919 | ||
Supragranular mossy fiber sprouting is not necessary for spontaneous seizures in the intrahippocampal kainate model of epilepsy in the rat. | Q48381408 | ||
Interneurones are not so dormant in temporal lobe epilepsy: a critical reappraisal of the dormant basket cell hypothesis | Q48381438 | ||
Granule cell dispersion is not accompanied by enhanced neurogenesis in temporal lobe epilepsy patients | Q48393655 | ||
Neuropeptide Y stimulates neuronal precursor proliferation in the post-natal and adult dentate gyrus | Q48925056 | ||
Seizures accelerate functional integration of adult-generated granule cells. | Q50733781 | ||
Depressed mood and memory impairment in temporal lobe epilepsy as a function of focus lateralization and localization. | Q50992124 | ||
Differences in memory performance and other clinical characteristics in patients with mesial temporal lobe epilepsy with and without hippocampal atrophy. | Q52002944 | ||
Differential impairments of spatial memory and social behavior in two models of limbic epilepsy. | Q52051528 | ||
Granule-like neurons at the hilar/CA3 border after status epilepticus and their synchrony with area CA3 pyramidal cells: functional implications of seizure-induced neurogenesis. | Q52166176 | ||
Increased number of neural progenitors in human temporal lobe epilepsy. | Q53666144 | ||
Glial reaction after seizure induced hippocampal lesion: immunohistochemical characterization of proliferating glial cells | Q63433214 | ||
Mossy fiber synaptic reorganization in the epileptic human temporal lobe | Q69240649 | ||
Long-term loss of paired pulse inhibition in the kainic acid-lesioned hippocampus of the rat | Q69591953 | ||
Inhibition in kainate-lesioned hyperexcitable hippocampi: physiologic, autoradiographic, and immunocytochemical observations | Q69830690 | ||
Fetal hippocampal grafts containing CA3 cells restore host hippocampal glutamate decarboxylase-positive interneuron numbers in a rat model of temporal lobe epilepsy | Q73258578 | ||
P433 | issue | 1 | |
P921 | main subject | temporal lobe epilepsy | Q616667 |
neurogenesis | Q1456827 | ||
P304 | page(s) | 97-112 | |
P577 | publication date | 2010-01-01 | |
P1433 | published in | Hippocampus | Q5768411 |
P1476 | title | Decreased neuronal differentiation of newly generated cells underlies reduced hippocampal neurogenesis in chronic temporal lobe epilepsy | |
P478 | volume | 20 |
Q90599497 | A Model of Chronic Temporal Lobe Epilepsy Presenting Constantly Rhythmic and Robust Spontaneous Seizures, Co-morbidities and Hippocampal Neuropathology |
Q47661055 | A Modified Chinese Herbal Decoction (Kai-Xin-San) Promotes NGF-Induced Neuronal Differentiation in PC12 Cells via Up-Regulating Trk A Signaling |
Q27335505 | A systems level, functional genomics analysis of chronic epilepsy |
Q57785581 | AMPA receptors and seizures mediate hippocampal radial glia-like stem cell proliferation |
Q47117710 | Ablation of peri-insult generated granule cells after epilepsy onset halts disease progression |
Q35691856 | Activation of Type 4 Metabotropic Glutamate Receptor Attenuates Oxidative Stress-Induced Death of Neural Stem Cells with Inhibition of JNK and p38 MAPK Signaling |
Q28728890 | Adult human brain neural progenitor cells (NPCs) and fibroblast-like cells have similar properties in vitro but only NPCs differentiate into neurons |
Q36709214 | Antidepressant therapy in epilepsy: can treating the comorbidities affect the underlying disorder? |
Q42472467 | CXCR4 Antagonist AMD3100 Suppresses the Long-Term Abnormal Structural Changes of Newborn Neurons in the Intraventricular Kainic Acid Model of Epilepsy |
Q37716754 | Calpastatin Overexpression Preserves Cognitive Function Following Seizures, While Maintaining Post-Injury Neurogenesis. |
Q59335768 | Cell-Biological Requirements for the Generation of Dentate Gyrus Granule Neurons |
Q36446158 | Clonal Analysis of Newborn Hippocampal Dentate Granule Cell Proliferation and Development in Temporal Lobe Epilepsy |
Q48134423 | Combined atorvastatin and ramipril mitigate radiation-induced impairment of dentate gyrus neurogenesis |
Q48502661 | Degeneration and regeneration of GABAergic interneurons in the dentate gyrus of adult mice in experimental models of epilepsy |
Q24634793 | Depression, stress, epilepsy and adult neurogenesis |
Q48190906 | Enriched Environment Altered Aberrant Hippocampal Neurogenesis and Improved Long-Term Consequences After Temporal Lobe Epilepsy in Adult Rats |
Q41889784 | Epilepsy and the plastic mind. |
Q38691162 | GABA-ergic cell therapy for epilepsy: Advances, limitations and challenges. |
Q30803236 | Grafted Subventricular Zone Neural Stem Cells Display Robust Engraftment and Similar Differentiation Properties and Form New Neurogenic Niches in the Young and Aged Hippocampus |
Q36547098 | Hippocampal injury-induced cognitive and mood dysfunction, altered neurogenesis, and epilepsy: can early neural stem cell grafting intervention provide protection? |
Q60952476 | Human induced pluripotent stem cell-derived MGE cell grafting after status epilepticus attenuates chronic epilepsy and comorbidities via synaptic integration |
Q30250270 | Hypothalamic-pituitary-adrenocortical axis dysfunction in epilepsy |
Q50087056 | Imaging pathological activities of human brain tissue in organotypic culture. |
Q37168681 | Implication of fibroblast growth factors in epileptogenesis-associated circuit rearrangements |
Q33620044 | Intranasal MSC-derived A1-exosomes ease inflammation, and prevent abnormal neurogenesis and memory dysfunction after status epilepticus. |
Q37636466 | Mechanisms regulating neuronal excitability and seizure development following mTOR pathway hyperactivation. |
Q34105734 | Medial ganglionic eminence-derived neural stem cell grafts ease spontaneous seizures and restore GDNF expression in a rat model of chronic temporal lobe epilepsy |
Q37992630 | Microglial activation - tuning and pruning adult neurogenesis |
Q28389854 | Mood and memory deficits in a model of Gulf War illness are linked with reduced neurogenesis, partial neuron loss, and mild inflammation in the hippocampus |
Q47094952 | Nestin-expressing cell types in the temporal lobe and hippocampus: Morphology, differentiation, and proliferative capacity. |
Q38751444 | Neural Stem Cell or Human Induced Pluripotent Stem Cell-Derived GABA-ergic Progenitor Cell Grafting in an Animal Model of Chronic Temporal Lobe Epilepsy. |
Q36729212 | Neural stem cell grafting counteracts hippocampal injury-mediated impairments in mood, memory, and neurogenesis |
Q36908246 | Neural stem cell grafting in an animal model of chronic temporal lobe epilepsy |
Q41720318 | Neurogenesis in Epilepsy: Better to Burn Out or Fade Away? |
Q38697204 | Neurogenesis in the Hippocampus of Patients with Temporal Lobe Epilepsy |
Q38164039 | Pathophysiogenesis of mesial temporal lobe epilepsy: is prevention of damage antiepileptogenic? |
Q37672412 | Physical Exercise Restores the Generation of Newborn Neurons in an Animal Model of Chronic Epilepsy. |
Q35648123 | Progress in cell grafting therapy for temporal lobe epilepsy |
Q35097960 | Promise of resveratrol for easing status epilepticus and epilepsy |
Q47645331 | Prospects of Cannabidiol for Easing Status Epilepticus-Induced Epileptogenesis and Related Comorbidities |
Q34098055 | Recent advancements in stem cell and gene therapies for neurological disorders and intractable epilepsy |
Q43073351 | Reduced hippocampal dentate cell proliferation and impaired spatial memory performance in aged-epileptic rats |
Q64062815 | Restrained Dendritic Growth of Adult-Born Granule Cells Innervated by Transplanted Fetal GABAergic Interneurons in Mice with Temporal Lobe Epilepsy |
Q36350389 | Resveratrol Treatment after Status Epilepticus Restrains Neurodegeneration and Abnormal Neurogenesis with Suppression of Oxidative Stress and Inflammation |
Q46550304 | Resveratrol for Easing Status Epilepticus Induced Brain Injury, Inflammation, Epileptogenesis, and Cognitive and Memory Dysfunction-Are We There Yet? |
Q28082885 | Role of NG2 expressing cells in addiction: a new approach for an old problem |
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Q38295325 | S-Nitrosylation in neurogenesis and neuronal development |
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Q34274308 | Water maze experience and prenatal choline supplementation differentially promote long-term hippocampal recovery from seizures in adulthood |
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