Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pär Remgård"'
Publikováno v:
Journal of Neurochemistry. 62:1302-1309
The release of radiolabeled material from regenerating frog sciatic nerves was studied using a multicompartment chamber, in which the ganglia and the outgrowth region, respectively, were separated from the rest of the nerve. The nerves were incubated
Publikováno v:
European Journal of Neuroscience. 7:1386-1392
Although calmodulin (CaM) is commonly considered to be an intracellular protein, it has been suggested lately that it is released and exerts functions extracellularly. In the present investigation this was studied in in vitro regenerating adult frog
Publikováno v:
Brain Research. 613:295-299
Here we present a model system which for the first time permits studies of slow axonal transport in vitro. Axonally transported proteins of rat vagus nerves were radiolabelled with [35S]methionine in the nodose ganglion in vitro and were incubated fo
Publikováno v:
Restorative Neurology and Neuroscience. 1:261-266
The adult frog sciatic nerve offers several advantages as an in vitro model to study nerve regeneration. The nerve with the attached dorsal root ganglia can easily be isolated and incubated in a culture medium for several days. If the nerve is subjec
Autor:
Pär Remgård, Martin Kanje
Publikováno v:
Brain research. 663(2)
The cultured rat vagus nerve was used to investigate the release of [35S]methionine-labelled slow axonally transported proteins during regeneration. After metabolic labelling the released proteins were collected from an isolated compartment at the di
Publikováno v:
Brain research. 572(1-2)
Labelled, rapidly transported axonal proteins were shown to be released from adult frog sciatic sensory neurons, regenerating in vitro after a crush injury. The spatial distribution of the transported, released proteins could accurately be resolved b
Publikováno v:
Journal of neurochemistry. 57(6)
The adult frog sciatic sensory neurons have been shown to regenerate in vitro. If a crush injury is made at the beginning of culture, regeneration starts after 3.4 days and proceeds at a rate of approximately 0.8 mm/day for several days. Two-dimensio