In vivo evidence that truncated trkB.T1 participates in nociception.
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BDNF released during neuropathic pain potentiates NMDA receptors in primary afferent terminalsPain, Genes, and Function in the Post-Hip Fracture PeriodTrkB.T1 contributes to neuropathic pain after spinal cord injury through regulation of cell cycle pathways.Transection of preganglionic axons leads to CNS neuronal plasticity followed by survival and target reinnervation.Peripheral nerve injury modulates neurotrophin signaling in the peripheral and central nervous system.Truncated TrkB.T1-Mediated Astrocyte Dysfunction Contributes to Impaired Motor Function and Neuropathic Pain after Spinal Cord InjuryA role for BDNF/TrkB signaling in behavioral and physiological consequences of social defeat stress.Brain-derived neurotrophic factor modulates antiretroviral-induced mechanical allodynia in the mouse.
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P2860
In vivo evidence that truncated trkB.T1 participates in nociception.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 29 October 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
In vivo evidence that truncated trkB.T1 participates in nociception.
@en
In vivo evidence that truncated trkB.T1 participates in nociception.
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type
label
In vivo evidence that truncated trkB.T1 participates in nociception.
@en
In vivo evidence that truncated trkB.T1 participates in nociception.
@nl
prefLabel
In vivo evidence that truncated trkB.T1 participates in nociception.
@en
In vivo evidence that truncated trkB.T1 participates in nociception.
@nl
P2093
P2860
P356
P1433
P1476
In vivo evidence that truncated trkB.T1 participates in nociception.
@en
P2093
Carmen C Leitch
Cynthia L Renn
Susan G Dorsey
P2860
P2888
P356
10.1186/1744-8069-5-61
P577
2009-10-29T00:00:00Z
P5875
P6179
1043724701