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Volumn 8, Issue 1, 1998, Pages 64-72

Axon guidance to and from choice points

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOATTRACTANT; EPHRIN; LIGAND; NETRIN; NEUROPILIN; RECEPTOR; SEMAPHORIN; UNCLASSIFIED DRUG;

EID: 0031968197     PISSN: 09594388     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-4388(98)80009-3     Document Type: Article
Times cited : (52)

References (69)
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    • (1997) Neuron , vol.19 , pp. 519-530
    • Taniguchi, M.1    Yuasa, S.2    Fujisawa, H.3    Naruse, I.4    Saga, S.5    Mishina, M.6    Yagi, T.7
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    • Neuropilin is a receptor for the axonal chemorepellent semaphorin III
    • of special interest. Together with [43], this paper reports the expression cloning and binding properties of neuropilin as a repulsion receptor for Sema III. Neuropilin is shown to be expressed on Sema III-responsive axons, and neutralizing antineuropilin antibodies block Sema III-mediated repulsive responses in vitro.
    • He Z, Tessier-Lavigne M. Neuropilin is a receptor for the axonal chemorepellent semaphorin III. of special interest Cell. 90:1997;739-751 Together with [43], this paper reports the expression cloning and binding properties of neuropilin as a repulsion receptor for Sema III. Neuropilin is shown to be expressed on Sema III-responsive axons, and neutralizing antineuropilin antibodies block Sema III-mediated repulsive responses in vitro.
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    • He, Z.1    Tessier-Lavigne, M.2
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    • of special interest. Together with [42], this paper describes the identification and characterization of neuropilin as a Sema III receptor. It also describes the cloning of neuropilin-2 (see also [45]).
    • Kolodkin AL, Levengood DV, Rowe EG, Tai Y-T, Giger RJ, Ginty DD. Neuropilin is a semaphorin III receptor. of special interest Cell. 90:1997;753-762 Together with [42], this paper describes the identification and characterization of neuropilin as a Sema III receptor. It also describes the cloning of neuropilin-2 (see also [45]).
    • (1997) Cell , vol.90 , pp. 753-762
    • Kolodkin, A.L.1    Levengood, D.V.2    Rowe, E.G.3    Tai Y-T4    Giger, R.J.5    Ginty, D.D.6
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    • of special interest. Identification of a second member of the neuropilin family. The study reveals differential affinities of individual semaphorins for neuropilin-1 and -2, as well as largely nonoverlapping expression patterns for the two neuropilins in the developing nervous system. See also [43]
    • Chen H, Chédotal A, He Z, Goodman CS, Tessier-Lavigne M. Neuropilin-2, a novel member of the neuropilin family, is a high affinity receptor for the semaphorins Sema E and Sema IV but not Sema III. of special interest Neuron. 19:1997;547-559 Identification of a second member of the neuropilin family. The study reveals differential affinities of individual semaphorins for neuropilin-1 and -2, as well as largely nonoverlapping expression patterns for the two neuropilins in the developing nervous system. See also [43].
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    • Secreted chick semaphorins bind recombinant neuropilin with similar affinities but bind different subsets of neurons in situ
    • of special interest. Reports the use of AP-tagged collapsins/semaphorins to assess the distribution of their receptors during neural development. Individual members of the family show distinct anatomical patterns of binding in tissue sections, and the semaphorin domain is shown to determine binding specificity.
    • Feiner L, Koppel AM, Kobayashi H, Raper JA. Secreted chick semaphorins bind recombinant neuropilin with similar affinities but bind different subsets of neurons in situ. of special interest Neuron. 19:1997;539-545 Reports the use of AP-tagged collapsins/semaphorins to assess the distribution of their receptors during neural development. Individual members of the family show distinct anatomical patterns of binding in tissue sections, and the semaphorin domain is shown to determine binding specificity.
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    • of special interest. Domain swapping experiments show that a small region of the semaphorin domain confers specificity of binding and biological activity on individual members of the collapsin/semaphorin family.
    • Koppel A, Feiner L, Kobayashi H, Raper JA. A 70 amino acid region within the semaphorin domain activates specific cellular response of semaphorin family members. of special interest Neuron. 19:1997;531-537 Domain swapping experiments show that a small region of the semaphorin domain confers specificity of binding and biological activity on individual members of the collapsin/semaphorin family.
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    • Neuropilin-semaphorin III/D-mediated chemorepulsive signals play a crucial role in peripheral nerve projection in mice
    • of special interest. Reports the phenotype of neuropilin knockout mice, showing substantial similarity to the sema III knockout phenotype described by Taniguchi et al. [41].
    • Kitsukawa T, Shimizu M, Sanbo M, Hirata T, Taniguchi M, Bekku Y, Yagi T, Fujisawa H. Neuropilin-semaphorin III/D-mediated chemorepulsive signals play a crucial role in peripheral nerve projection in mice. of special interest Neuron. 19:1997;995-1005 Reports the phenotype of neuropilin knockout mice, showing substantial similarity to the sema III knockout phenotype described by Taniguchi et al. [41].
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    • of outstanding interest. Ephrins are expressed in the posterior half-somite, and repel motor axons and migrating neural crest cells in a variety of in vitro assays. Together with [58], this study identifies ephrins as candidates for mediating peripheral nerve segmentation in higher vertebrates.
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    • of outstanding interest. This study describes the restriction of ephrin expression in the somites to the posterior half-sclerotomes. Cognate Eph receptors are expressed by migrating neural crest cells, and crest migration patterns are perturbed in explants of chick embryo trunks treated with soluble ephrin. Together with [57], this study identifies ephrins as candidates for mediating peripheral nerve segmentation in higher vertebrates.
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    • of special interest. This study uses explants of chick embryo DRGs and surrounding tissues in collagen gels to show that linear axon trajectories can be generated by gradients of diffusible repulsion molecules flanking axon pathways.
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    • Keynes, R.J.1    Tannahill, D.2    Morgenstern, D.A.3    Johnson, A.R.4    Cook, G.M.W.5    Pini, A.6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.