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  • 1
    Online Resource
    Online Resource
    Society for Neuroscience ; 2004
    In:  The Journal of Neuroscience Vol. 24, No. 5 ( 2004-02-04), p. 1255-1264
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 24, No. 5 ( 2004-02-04), p. 1255-1264
    Abstract: Many of the interneuron cell types present in the adult spinal cord contribute to the circuits that control locomotion and posture. Little is known, however, about the embryonic origin of these cell types or the molecular mechanisms that control their differentiation. Here we provide evidence that V1 interneurons (INs), an embryonic class of interneurons that transiently express the En1 transcription factor, differentiate as local circuit inhibitory interneurons and form synapses with motor neurons. Furthermore, we show that a subset of V1 INs differentiates as Renshaw cells, the interneuronal cell type that mediates recurrent inhibition of motor neurons. We analyze the role that two V1 IN-related transcription factor genes play in Renshaw cell development. Pax6 ( paired box gene 6 ) is necessary for an early step in Renshaw cell development, whereas Engrailed 1 ( En1 ) , which is genetically downstream of Pax6 , regulates the formation of inhibitory synapses between Renshaw cells and motor neurons. Together, these results show that Pax6 and En1 have essential roles in establishing the recurrent inhibitory circuit between motor neurons and Renshaw cells.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2004
    detail.hit.zdb_id: 1475274-8
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2001
    In:  Proceedings of the National Academy of Sciences Vol. 98, No. 17 ( 2001-08-14), p. 9617-9623
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 98, No. 17 ( 2001-08-14), p. 9617-9623
    Abstract: Upon depolarization positive charges contained in the transmembrane segment S4 of voltage-dependent channels are displaced from the cytoplasmic to the external milieu. This charge movement leads to channel opening. In Shaker K + channels four positively charged arginines in the S4 domain are transferred from the internal to the external side of the channel during activation. The distance traveled by the S4 segment during activation is unknown, but large movements should be constrained by the S3–S4 linker. Constructing deletion mutants, we show that the activation time constant and the midpoint of the voltage activation curve of the Shaker K + channel macroscopic currents becomes a periodic function of the S3–S4 linker length for linkers shorter than 7 aa residues. The periodicity is that typical of α-helices. Moreover, a linker containing only 3 aa is enough to recover the wild-type phenotype. The deletion method revealed the importance of the S3–S4 linker in determining the channel gating kinetics and indicated that the α-helical nature of S4 extends toward its N terminus. These results support the notion that a small displacement of the S4 segment suffices to displace the four gating charges involved in channel opening.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2001
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    John Benjamins Publishing Company ; 2004
    In:  Pragmatics and Cognition Vol. 12, No. 1 ( 2004-6-10), p. 200-203
    In: Pragmatics and Cognition, John Benjamins Publishing Company, Vol. 12, No. 1 ( 2004-6-10), p. 200-203
    Type of Medium: Online Resource
    ISSN: 0929-0907 , 1569-9943
    URL: Issue
    Language: English
    Publisher: John Benjamins Publishing Company
    Publication Date: 2004
    detail.hit.zdb_id: 914180-7
    detail.hit.zdb_id: 2036353-9
    SSG: 5,2
    SSG: 7,11
    Location Call Number Limitation Availability
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