Zobrazeno 1 - 10 of 495 pro vyhledávání: '"Kinnon, C."'
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Akademický článek
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Akademický článek
The Wiskott–Aldrich syndrome.
Autor: Thrasher, A. J.1, Kinnon, C.1
Publikováno v: Clinical & Experimental Immunology. Apr2000, Vol. 120 Issue 1, p2-9. 8p.
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3
CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome
Autor: Notarangelo, L, Peitsch, M, Abrahamsen, T, Bachelot, C, Bordigoni, P, Cant, A, Chapel, H, Clementi, M, Deacock, S, de Saint Basile, G, Duse, M, Espanol, T, Etzioni, A, Fasth, A, Fischer, A, Giliani, S, Gomez, L, Hammarstorm, L, Jones, A, Kanariou, M, Kinnon, C, Klemola, T, Kroczek, R, Levy, J, Matamoros, N
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding the CD40 ligand (CD40L). A database (CD40Lbase) of CD40L mutations has now been established, and the resultant information, together with other mutati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1064::d11b4a4f9b3696a60f6cb5e67a3067dc
https://doi.org/10.1016/0167-5699(96)30059-5
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5
Morphological, neurochemical and electrophysiological features of parvalbumin-expressing cells: a likely source of axo-axonic inputs in the mouse spinal dorsal horn
Autor: Hughes, D I, Sikander, S, Kinnon, C M, Boyle, K A, Watanabe, M, Callister, R J, Graham, B A
Axo-axonic synapses on the central terminals of primary afferent fibres modulate sensory input and are the anatomical correlate of presynaptic inhibition. Although several classes of primary afferents are under such inhibitory control, the origin of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f31bc5865a294ddbcd68ec8219650772
https://europepmc.org/articles/PMC3476641/
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6
Codon optimisation of human factor VIII cDNAs leads to high level expression
Autor: Ward, N., Buckley, S., Waddington, S., VandenDriessche, Thierry, Nathwani, A., Mcintosch, J., Tuddenham, E., Kinnon, C., Thrasher, A., Mcvey, J., Chuah, Marinee
Gene therapy for hemophilia A would be facilitated by development of smaller expression cassettes encoding factor VIII (FVIII) which demonstrate improved biosynthesis and/or enhanced biological properties. B-domain deleted (BDD) FVIII retains full pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3848::9cdac76421a0161de1bbdd97891c1d9c
https://hdl.handle.net/20.500.14017/77097efb-6439-45c5-90c2-61ba876ef848
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8
Evidence that the Wiskott-Aldrich syndrome protein may be involved in lymphoid cell signaling pathways
Autor: Go, Cory, MacCarthy-Morrogh L, Banin S, Gout I, Pm, Brickell, Rj, Levinsky, Kinnon C, Ruth Lovering
Publikováno v: Europe PubMed Central
Wiskott-Aldrich syndrome is an X-linked combined immunodeficiency affecting cells of several different hemopoietic lineages. The Wiskott-Aldrich syndrome protein (WASP), which has no homology with any other known protein families, is rich in proline
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5b13f021fdec9fd35b7f01ced2ca8f58
https://pubmed.ncbi.nlm.nih.gov/8892607
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