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1 es before and after muscle injury induced by cardiotoxin.
2 d dramatically from 1 to 3 d after injury by cardiotoxin.
3 generation, we injured wild-type muscle with cardiotoxin and found that Akt induced a faster regenera
4 protected muscle from both acute injury with cardiotoxin and from chronic muscle disease in the mdx o
5 ted in PDGFRbeta(+) cells are protected from cardiotoxin and laceration-induced skeletal muscle fibro
11 bustly in regenerating skeletal muscle after cardiotoxin (CTX)-induced muscle injury in vivo and diff
12 ythroid-derived-2)-like 2 (Nrf2), aggravates cardiotoxin (CTX)-induced tibialis anterior (TA) muscle
17 the discovery of a new insulinotropic agent, cardiotoxin-I (CTX-I), from the Naja kaouthia snake veno
19 MyoR and miR-378 were anticorrelated during cardiotoxin-induced adult muscle regeneration in mice.
21 ed cells and macrophages were assessed after cardiotoxin-induced injury of chimeric mice produced by
26 dels, we studied regeneration consecutive to cardiotoxin-induced muscle injury and observed a signifi
27 ers (MyoD, myogenin, and active-Notch) after cardiotoxin-induced muscle injury in vivo and in SCs cul
31 licited by immunization with pVCL/MSP1a into cardiotoxin-induced regenerating muscle were evaluated i
32 ntiation and prolonged Pax7 expression after cardiotoxin-induced skeletal muscle injury, while single
33 ments revealed that Staufen1 increases after cardiotoxin injection before returning to the low levels
37 ersion of marrow cells to skeletal muscle in cardiotoxin-injured anterior tibialis muscle in a green
38 c gene expression and muscle regeneration in cardiotoxin-injured beta3-integrin-null mice are impaire
39 neration and that gene transfer of GEFT into cardiotoxin-injured mouse tibialis anterior muscle exert
40 ed that SP cells isolated from dystrophic or cardiotoxin-injured muscle fail to undergo myogenesis.
43 ransplantation of these committed cells into cardiotoxin-injured skeletal muscles of NOD/SCID mice re
44 d damage, exhibit delayed regeneration after cardiotoxin injury and suffer from defective myoblast fu
48 njury and improved muscle regeneration after cardiotoxin injury, as well as increased satellite cell
49 vivo model of muscle regeneration following cardiotoxin injury, ectopic miR-431 injection greatly im
56 und delay in satellite cell activation after cardiotoxin treatment in alpha7 integrin-null animals wh
57 beta1 integrin plays in muscle regeneration, cardiotoxin was used to induce damage in the tibialis an
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