about
Proliferation dynamics of germinative zone cells in the intact and excitotoxically lesioned postnatal rat brainAre Microglial Cells the Regulators of Lymphocyte Responses in the CNS?Histochemical demonstration of purine nucleoside phosphorylase (PNPase) in microglial and astroglial cells of adult rat brainNeuroprotection from NMDA excitotoxic lesion by Cu/Zn superoxide dismutase gene delivery to the postnatal rat brain by a modular protein vector.Increase in Th17 and T-reg lymphocytes and decrease of IL22 correlate with the recovery phase of acute EAE in rat.Neurobehavioral and immunological consequences of prenatal immune activation in rats. Influence of antipsychotics.Antigen presentation in EAE: role of microglia, macrophages and dendritic cells.Astrocyte-targeted production of interleukin-6 reduces astroglial and microglial activation in the cuprizone demyelination model: Implications for myelin clearance and oligodendrocyte maturation.Neonatal handling and environmental enrichment effects on emotionality, novelty/reward seeking, and age-related cognitive and hippocampal impairments: focus on the Roman rat lines.Increased levels of proinflammatory cytokines in the aged rat brain attenuate injury-induced cytokine response after excitotoxic damage.Alterations in microglial phenotype and hippocampal neuronal function in transgenic mice with astrocyte-targeted production of interleukin-10.Astrocyte-targeted production of IL-10 induces changes in microglial reactivity and reduces motor neuron death after facial nerve axotomy.Glial expression of small heat shock proteins following an excitotoxic lesion in the immature rat brain.Expression of inducible nitric oxide synthase and cyclooxygenase-2 after excitotoxic damage to the immature rat brain.Activated microglial cells acquire an immature dendritic cell phenotype and may terminate the immune response in an acute model of EAE.Nonviral gene delivery to the central nervous system based on a novel integrin-targeting multifunctional protein.Leukocyte infiltration and glial reactions in xenografts of mouse brain tissue undergoing rejection in the adult rat brain. A light and electron microscopical immunocytochemical study.Triflusal posttreatment inhibits glial nuclear factor-kappaB, downregulates the glial response, and is neuroprotective in an excitotoxic injury model in postnatal brain.A double staining technique for simultaneous demonstration of astrocytes and microglia in brain sections and astroglial cell cultures.Decrease of proinflammatory molecules correlates with neuroprotective effect of the fluorinated salicylate triflusal after postnatal excitotoxic damage.Ontogeny of sensorimotor gating and immune impairment induced by prenatal immune challenge in rats: implications for the etiopathology of schizophrenia.Astroglial nitration after postnatal excitotoxic damage: correlation with nitric oxide sources, cytoskeletal, apoptotic and antioxidant proteins.RGD domains neuroprotect the immature brain by a glial-dependent mechanism.Interleukin-10 overexpression does not synergize with the neuroprotective action of RGD-containing vectors after postnatal brain excitotoxicity but modulates the main inflammatory cell responses.Interleukin-10 and interleukin-10 receptor-I are upregulated in glial cells after an excitotoxic injury to the postnatal rat brain.Distinct pattern of microglial response, cyclooxygenase-2, and inducible nitric oxide synthase expression in the aged rat brain after excitotoxic damage.Substantial migration of SVZ cells to the cortex results in the generation of new neurons in the excitotoxically damaged immature rat brain.Survivin and heat shock protein 25/27 colocalize with cleaved caspase-3 in surviving reactive astrocytes following excitotoxicity to the immature brain.Neonatal treatment with monosodium glutamate lastingly facilitates spreading depression in the rat cortex.Distinct spatial and temporal activation of caspase pathways in neurons and glial cells after excitotoxic damage to the immature rat brain.Primary cortical glial reaction versus secondary thalamic glial response in the excitotoxically injured young brain: astroglial response and metallothionein expression.Caspase-3 activation in astrocytes following postnatal excitotoxic damage correlates with cytoskeletal remodeling but not with cell death or proliferation.Microglial and astroglial reactions to anterograde axonal degeneration: a histochemical and immunocytochemical study of the adult rat fascia dentata after entorhinal perforant path lesions.Expression of growth inhibitory factor (metallothionein-III) mRNA and protein following excitotoxic immature brain injury.Primary cortical glial reaction versus secondary thalamic glial response in the excitotoxically injured young brain: microglial/macrophage response and major histocompatibility complex class I and II expression.Brain effects of the lectin from Canavalia ensiformis in adult rats previously suckled in favorable and unfavorable conditions: A spreading depression and microglia immunolabeling study.Microglial and astroglial reactions to ischemic and kainic acid-induced lesions of the adult rat hippocampus.Development of microglia in the postnatal rat hippocampus.Delayed neurodegeneration and early astrogliosis after excitotoxicity to the aged brain.Spreading depression features and Iba1 immunoreactivity in the cerebral cortex of developing rats submitted to treadmill exercise after treatment with monosodium glutamate.
P50
Q21262944-AF9BBF11-946E-48DC-BBB0-FBCCA10D4BCFQ26774826-F1E54E6F-2B63-4D7D-8EC1-0B9D3350D122Q28572093-67EEDC29-D84F-4F1D-8362-E6DC2B4C0E53Q33241058-57789F2F-6CFB-4779-8C80-A8114276E9C9Q34081554-AF0F3DE7-54E1-49C5-AFA2-03D216F34EC4Q34593081-46295646-CAB6-4CD1-B0BC-C7E5C53CEB0FQ37825198-8967D637-1540-4CD7-85F7-0DA1549568B6Q38809608-7E36AF34-E36B-4DC8-BA7D-E9E5C8D5EC9BQ41708182-3682373D-8EBF-49B8-AF4F-15D2AA860201Q42451495-9DB4DAC5-5EEC-4CC4-BBFE-F08C94C40674Q42469344-1C25A045-2E05-471B-8173-DC4B0CFF7C70Q42473088-E288B142-3544-4EA2-ACA3-1080EAC78AE5Q42519471-8D88728E-CA94-49C2-A2F8-F92E11456C1CQ42523538-EA992973-8F52-43D7-823A-4850C9C543F9Q43069753-00D63EDD-93B5-4FAB-A173-8860A541DB77Q43422053-DC024E83-714F-4FF8-BE88-B662020B047DQ43641321-381448FD-415C-4254-8BEF-0C40273BBBE9Q43757548-2A413BCE-B179-4387-A850-8E6E440B1BD9Q43857607-FDDE1893-C17A-452A-8754-920671866026Q44168411-EE94BB6A-9171-441B-A856-303B104A6206Q44647738-990A639F-6DED-4F83-A900-05213297D08EQ45234874-12ED3EC9-37D9-4228-860B-8A5168F65063Q45870463-31627C32-C330-48B4-9A17-BB959646967DQ45873376-70DA5A5A-0400-47A3-99CB-54AD3E3CB87FQ46087826-28CE1E85-3D7E-40CC-89F9-59C83F5E738BQ46548580-46CE37A3-B683-4B4B-9BCA-90E3A49EC7EBQ46628778-8FEAA037-B846-4E87-BA26-3738793A7D6AQ46688824-828EC5E6-5C96-448B-8083-92CD54641917Q47971646-4889A3C5-071A-4FE5-A945-FF50A75CDEC4Q48088476-96D7AC4E-C6C9-4EB7-B2BD-CEFF2C33757DQ48149949-A1A9F633-387E-4856-8F50-C3F0CCC47768Q48174949-1C1ECAB8-0A27-4A66-BDAD-106DA5F782DEQ48213479-70EA1320-4BD1-403B-80A8-FB0A8C359945Q48226784-78A5E72A-C984-4F0F-A390-D8812399B603Q48264262-60186292-A81C-452F-98E3-0CF8143000FDQ48296405-F107E296-5231-4AA4-8EA1-1A97042A19E4Q48329229-D911608D-F279-4D31-8F40-8D8B6D2787E5Q48344574-9E3E8122-C9B9-40AF-9477-B6E7E9492FCCQ48358196-3567FA61-0BE3-484D-890A-41C40FC93198Q48378826-A41D796C-1047-4380-9918-387E244F94B1
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Bernardo Castellano
@ast
Bernardo Castellano
@en
Bernardo Castellano
@es
Bernardo Castellano
@nl
Bernardo Castellano
@sl
type
label
Bernardo Castellano
@ast
Bernardo Castellano
@en
Bernardo Castellano
@es
Bernardo Castellano
@nl
Bernardo Castellano
@sl
prefLabel
Bernardo Castellano
@ast
Bernardo Castellano
@en
Bernardo Castellano
@es
Bernardo Castellano
@nl
Bernardo Castellano
@sl
P1006
P214
P244
P1006
P1053
G-1428-2010
P106
P1153
7003547186
P1960
EsMh4VoAAAAJ
P21
P213
0000 0004 4458 3877
P214
P244
P31
P3829
P496
0000-0003-1976-971X
P734
P735
P7859
lccn-n98012419