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1 ved neurotrophic factor, neurotrophin-3, and neurotrophin-4.
3 ng for brain-derived neurotrophic factor and neurotrophin 4/5 was absent from the nerve head and supe
4 rotrophic factor, BDNF; neurotrophin 3, NT3; neurotrophin 4/5, NT4/5; or glial-derived neurotrophic f
8 ic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4/5 (NT-4/5) upon ventral mesencephalic dop
9 brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT-4/5) via TrkB, and neurotrophin-3 (
10 ic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4/5 (NT-4/5), contribute to survival and di
11 brain-derived neurotrophic factor (BDNF) or neurotrophin-4/5 (NT-4/5), or blockade of their endogeno
14 brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT4) act via the TrkB receptor and sup
15 Brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT4/5) exert their action through a co
16 rophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4/5 (NT4/5), ciliary neurotrophic factor, b
19 ved neurotrophic factor, neurotrophin-3, and neurotrophin-4/5 were detected in 22, 9, and 19% of thes
20 eptor (brain-derived neurotrophic factor and neurotrophin-4/5) acutely sensitize nociceptive afferent
22 ved neurotrophic factor, neurotrophin-3, and neurotrophin-4/5, showed that immunoreactive brain-deriv
23 nd truncated TrkB receptor, constitutive and neurotrophin-4/5-induced tyrosine phosphorylation was si
26 d express decreased levels of mRNAs encoding neurotrophin-4 and glial cell line-derived neurotrophic
27 e receptor for neurotrophic factors BDNF and neurotrophin 4, and mediates their influence on neuronal
31 neurotrophic factor (BDNF), neurotrophin-3, neurotrophin-4, ciliary neurotrophic factor (CNTF), Axok
32 or for brain-derived neurotrophic factor and neurotrophin-4, has been implicated in regulating synaps
33 lia and overexpression of neurotrophin-3 and neurotrophin-4 in muscle did not cause hyperinnervation.
34 r synapses formed on myocytes overexpressing neurotrophin-4 (M+ synapses) exhibited a higher level of
35 ic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4 (NT-4) activated the FL receptor, as dete
36 able to innervate taste buds is regulated by neurotrophin-4 (NT-4) and brain-derived neurotrophic fac
37 ated with the TrkB receptor ligands BDNF and neurotrophin-4 (NT-4) developed a full complement of Pur
38 brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT-4) inhibit agrin-induced AChR cluster
39 el system of nerve-muscle coculture in which neurotrophin-4 (NT-4) is overexpressed in a subpopulatio
40 ration of the endogenous TrkB agonist ligand neurotrophin-4 (NT-4) profoundly decreases food intake a
41 ed that the levels of trkB mRNA and BDNF and neurotrophin-4 (NT-4) proteins are normal in the thalamu
42 hic factor (BDNF), neurotrophin-3 (NT-3), or neurotrophin-4 (NT-4) results in a 30-50% reduction in n
44 , [125I]nerve growth factor (NGF), and [125I]neurotrophin-4 (NT-4) to perikarya in the ipsilateral no
46 rophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4), and glial cell line-derived neuro
47 rophic factor (GDNF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4), and their receptors because of th
48 rophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4), ciliary neuronotrophic factor (CN
49 hic factor (BDNF), neurotrophin-3 (NT-3), or neurotrophin-4 (NT-4), each at 100 ng/ml] showed a two-
50 e of BDNF and a related neurotrophin ligand, neurotrophin-4 (NT-4), in the regulation of revasculariz
51 rophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4), tyrosine kinase (trk) A, trkB, tr
52 single neurons, we determined that BDNF and neurotrophin-4 (NT-4), which both bind to the TrkB high-
56 that mRNA encoding TrkB and its two ligands, neurotrophin 4 (NT4) and brain-derived neurotrophic fact
58 ry axons in these animals was facilitated by neurotrophin 4 (NT4), because branching was virtually el
59 brain-derived neurotrophic factor (BDNF) or neurotrophin 4 (NT4), individually or together, are with
60 hic factor (BDNF), neurotrophin 3 (NT3), and neurotrophin 4 (NT4), is implicated in the physiology of
61 factor [(BDNF) alone or in combination with neurotrophin 4 (NT4)] increases the peak rate of develop
62 nd trkB mRNA expression were reduced whereas neurotrophin-4 (NT4) and trkC mRNA expression were incre
63 Brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT4) are essential for the survival of g
64 brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT4) have different developmental roles
66 urotrophin (BDNF), neurotrophin-3 (NT3), and neurotrophin-4 (NT4)-and their receptors (NTrs) TrkA, Tr
67 roblast growth factor-4, CX3CL1/fractalkine, neurotrophin 4 oncostatin-M, pulmonary and activation-re
68 factor, but not ciliary neurotrophic factor, neurotrophin-4, or glial cell line-derived neurotrophic
69 derived neurotrophic factor, neurotrophin-3, neurotrophin-4, or glial-cell-line-derived neurotrophic
70 ion of brain-derived neurotrophic factor and neurotrophin-4, which, through the receptor p75, can kil
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