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Depletion of microglia and inhibition of exosome synthesis halt tau propagation.Tau accumulation causes mitochondrial distribution deficits in neurons in a mouse model of tauopathy and in human Alzheimer's disease brainElectrophysiological changes precede morphological changes to frontal cortical pyramidal neurons in the rTg4510 mouse model of progressive tauopathyDendritic vulnerability in neurodegenerative disease: insights from analyses of cortical pyramidal neurons in transgenic mouse modelsEffects of normal aging on prefrontal area 46 in the rhesus monkey.Diversity of glutamatergic synaptic strength in lateral prefrontal versus primary visual cortices in the rhesus monkey.Functional consequences of age-related morphologic changes to pyramidal neurons of the rhesus monkey prefrontal cortex.Neural precursor lineages specify distinct neocortical pyramidal neuron types.Age-related changes to layer 3 pyramidal cells in the rhesus monkey visual cortex.Influence of highly distinctive structural properties on the excitability of pyramidal neurons in monkey visual and prefrontal cortices.Changes in the structural complexity of the aged brainA mutant prion protein sensitizes neurons to glutamate-induced excitotoxicityPyramidal Neurons Are Not Generalizable Building Blocks of Cortical Networks.The intersection of amyloid β and tau in glutamatergic synaptic dysfunction and collapse in Alzheimer's disease.Strength and Diversity of Inhibitory Signaling Differentiates Primate Anterior Cingulate from Lateral Prefrontal Cortex.Automated evolutionary optimization of ion channel conductances and kinetics in models of young and aged rhesus monkey pyramidal neurons.Homeostatic responses by surviving cortical pyramidal cells in neurodegenerative tauopathy.Increased action potential firing rates of layer 2/3 pyramidal cells in the prefrontal cortex are significantly related to cognitive performance in aged monkeys.Comparative ultrastructural features of excitatory synapses in the visual and frontal cortices of the adult mouse and monkey.Area-Specific Features of Pyramidal Neurons-a Comparative Study in Mouse and Rhesus Monkey.Reducing the RNA binding protein TIA1 protects against tau-mediated neurodegeneration in vivo.GABAA receptor-mediated neurotransmission in the dentate gyrus of the rhesus monkey: comparison with the rat.Electrophysiological properties of rat hippocampal principal cells are unaltered by prenatal protein malnutrition.Inhibitory action of muscarinic agonists on neurons in the rat laterodorsal tegmental nucleus in vitro.Distinct Neocortical Progenitor Lineages Fine-tune Neuronal Diversity in a Layer-specific Manner.Labelling and recording from dissociated target-specific rat superior cervical ganglion neurons.Differential changes to D1 and D2 medium spiny neurons in the 12-month-old Q175+/- mouse model of Huntington's DiseaseSomatostatin-, vasoactive intestinal polypeptide- and neuropeptide Y-like immunoreactivity in eye- and submandibular gland-projecting sympathetic neuronsSensory neuron N-type calcium currents are inhibited by both voltage-dependent and -independent mechanismsMultiple calcium channel types control glutamatergic synaptic transmission in the hippocampus
P50
Q27311815-5C7B0E4F-30B2-4E2F-8E70-B95ACBBB1113Q28116593-EEF5F8A6-DB30-4536-B104-7EAC5EC01DF0Q30528756-F7B8F0B7-8785-493C-BD65-22BCE727C49DQ33533576-676CC395-3E1D-480E-BF58-7F7A8A567192Q33653544-2B49A43B-60CF-4506-AE88-9C45E371E1D0Q34869537-F630E9EC-D3D6-4E4E-84C5-BD76D784DA43Q35155034-B1FC4A6A-CFFD-471A-8ACD-6A0081761B6AQ35423756-F8E1E254-E707-41C5-9E61-0C394D8F9B03Q35596239-5C5A5A4F-B558-4295-B635-71B19E417380Q36359860-5F20F91E-8091-402A-940D-DC590FF51D68Q36739538-730C7D2D-AE5F-4B92-88D2-2B618775C50FQ37013751-815C1919-760E-4124-BA68-8826D30899FAQ37683087-FC31C392-3233-41D6-A7A7-6B801440FB77Q38092945-41A60393-A42E-4163-8152-CB4C37721730Q38734418-B426DF4A-79EA-41C2-9C8B-B8B8484BBF4CQ39828912-2D011414-D73B-4D45-BFB8-253EF515D5A1Q44199130-1CE34A53-BF83-4E4F-9480-BA6EA62E5B18Q45305052-3D81B8CB-9468-403C-860B-85B5C5BC7DDAQ46409889-6E3940C5-B9CD-48F0-8AC4-E6A0C22ADE85Q46581718-D2AE2E1D-A4B4-4795-A011-E2168DB7BC08Q47256125-993E10B8-CF98-41AF-A621-018EFA27F53BQ48270006-B33A9BD1-4107-4B5C-A58A-C66BFAC10B64Q48392539-E659FFD3-0488-4D75-9C84-681E37CD09CDQ48858980-C517265E-F2D8-420A-91D9-AC3E322F356AQ50132761-E2979AAF-D635-4751-BBB9-B4C86CCB68EEQ50795617-C9CF0BF5-490A-4218-AF5E-8EB49B43D255Q58771741-CA36FF9E-B07A-40C3-A76A-70E9D67774ECQ69373620-44796FE6-2717-47BC-A6A2-1AEE306E4899Q72482048-D4B5F485-0A1E-49A4-937C-4434244DC54CQ72658211-EA100CAE-BE43-4A83-ABED-DAC0DF50652D
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jennifer Luebke
@ast
Jennifer Luebke
@en
Jennifer Luebke
@es
Jennifer Luebke
@nl
type
label
Jennifer Luebke
@ast
Jennifer Luebke
@en
Jennifer Luebke
@es
Jennifer Luebke
@nl
prefLabel
Jennifer Luebke
@ast
Jennifer Luebke
@en
Jennifer Luebke
@es
Jennifer Luebke
@nl
P106
P21
P31
P496
0000-0003-1399-6073