Zobrazeno 1 - 8
of 8
pro vyhledávání: '"N. L. Nadon"'
Autor:
John H. Morrison, Carol A. Barnes, Kevin M. Kelly, N. L. Nadon, Eric M. Blalock, Olivier Thibault
Publikováno v:
Epilepsy Research. 68:5-20
Basic principles of the neurobiology of aging were reviewed within selected topic areas chosen for their potential relevance to epileptogenesis in the aging brain. The availability of National Institute on Aging-supported aged mouse and rat strains a
Autor:
Kay L. Medina, N. L. Nadon, C.-J. Doersen, Michael D. Rohrer, Jeffrey M. Gimble, Linda F. Thompson, D. A. Lade
Publikováno v:
Calcified Tissue International. 67:449-454
The 6093 line of transgenic mice exhibits altered bone development as a result of an insertional mutation by the transgene. Female transgenic mice show a marked kyphosis as early as 2 weeks of age. Vertebrae from female mice have lower total bone are
Autor:
N L Nadon, S. M. Jamshedur Rahman, M Franklin, Regina Resta, Thomas B. Knudsen, Scott W. Hooker, Linda F. Thompson, Aletha B. Laurent
Publikováno v:
Journal of Clinical Investigation. 99:676-683
The adenosine producing enzyme ecto-5'-nucleotidase (5'-NT) is not normally expressed during thymocyte development until the medullary stage. To determine whether earlier expression would lead to adenosine accumulation and/or be deleterious for thymo
Autor:
N L, Nadon
Publikováno v:
The Journal of comparative neurology. 416(2)
Transgenic mice were produced that carry a construct encoding a mutant form of the DM20 isoform of myelin proteolipid protein. The transgene is under the direction of the human Plp gene promoter, which has previously been shown to direct tissue-speci
Publikováno v:
Journal of neuroscience research. 47(3)
A point mutation in exon 3 of the proteolipid protein (PLP) gene of the myelin-deficient (md) rat leads to a failure of oligodendrocyte maturation and early death of oligodendrocytes, resulting in dysmyelination. It has been suggested that an alterna
Publikováno v:
Developmental neuroscience. 19(4)
We previously showed that the jimpy-4J mouse mutation is located on the X chromosome, in or closely linked to the proteolipid protein (Plp) gene. The phenotype is characterized by the most severe hypomyelination of any of the naturally occurring myel
Autor:
Michael R. Wells, Katharine F. Lunn, Charles K. Csiza, N. L. Nadon, R. L. Hoffman, Ian D. Duncan
Publikováno v:
Journal of neurocytology. 24(10)
This study has examined cellular and molecular aspects of glial cell function in a newly described long-lived myelin deficient rat mutant. In contrast to the shorter-lived mutants which died at 25-30 days, the longer-lived mutant rats lived to 75-80
Autor:
N. L. Nadon, Ian D. Duncan
Publikováno v:
Journal of neuroscience research. 41(1)
The proteolipid proteins play a major role in the structure of the CNS myelin sheath, but they have also been implicated in the oligodendrocyte development leading to myelination. Mutations in the PLP gene result in severe dysmyelination and a paucit