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1 sociated glycoprotein (MAG), and neuron-glia cell adhesion molecule (L1).
2 ders (FASD) in part by disrupting the neural cell adhesion molecule L1.
3  motoneuron axons they encounter express the cell adhesion molecule L1.
4            Many of these axons expressed the cell adhesion molecule L1.
5 ion relative to axon tracts that express the cell adhesion molecule L1.
6 cell adhesion mediated by the immunoglobulin cell adhesion molecule L1.
7  children with mutations in the gene for the cell adhesion molecule L1.
8 lar neurons as novel binding partners of the cell adhesion molecule L1.
9 h two tyrosine kinases, Fyn and Lyn, and the cell adhesion molecule, L1.
10  that the expression of the glycoprotein and cell adhesion molecule L1, a member of the immunoglobuli
11                     Two proteins, the neural cell adhesion molecule L1 and dipeptidyl peptidase 4, we
12 ntially relevant to skin homeostasis: neural cell adhesion molecule L1 and dipeptidyl peptidase 4.
13                                          The cell adhesion molecule L1 and the extracellular matrix p
14 ellular sources in lesion sites produced the cell adhesion molecules L1 and laminin, and these molecu
15       It has long been known that the neural cell adhesion molecules L1 and NCAM-180 promote neurite
16                     The structurally related cell adhesion molecules L1 and Nr-CAM have overlapping e
17 ar levels of Sema3A receptors (neuropilin-1, cell adhesion molecule L1, and plexinA4), but significan
18 ited myelination decreased expression of the cell adhesion molecule L1, and stimulation under conditi
19    We have investigated the structure of the cell adhesion molecule L1 by electron microscopy.
20                                           L1-cell adhesion molecule (L1-CAM) belongs to a functionall
21  alpha v beta 3 can interact with the neural cell adhesion molecule L1-CAM; a member of the immunoglo
22 embly of Nav1.6, betaIV spectrin, and the L1 cell adhesion molecules (L1 CAMs) neurofascin and NrCAM
23 entalization, we focused on two L1 family of cell adhesion molecules (L1-CAMs) [L1/neuron-glia cell a
24 that promotes neurite growth on the neuronal cell adhesion molecule L1, did not interact with any NCA
25  expression of polysialic acid (PSA) and the cell adhesion molecule L1 during axonal regeneration and
26                                   The neural cell adhesion molecule L1 engages the spectrin-actin cyt
27 rowth-associated protein 43 (GAP-43) and the cell adhesion molecule L1 has been correlated with CNS a
28                                          The cell adhesion molecule L1 has been implicated in a varie
29                                   The neural cell adhesion molecule L1 has been implicated in a varie
30                                   The neural cell adhesion molecule L1 has been shown to function as
31 tor, we expressed the regeneration-promoting cell adhesion molecule L1 in both neurons and glia in th
32    Previous reports on the expression of the cell adhesion molecule L1 in pancreatic ductal adenocarc
33                         The functions of the cell adhesion molecule L1 in the developing and adult ne
34                                       Neural cell adhesion molecule L1 is a cell surface glycoprotein
35                                          The cell adhesion molecule L1 is a Lewis(x)-carrying glycopr
36                                          The cell adhesion molecule L1 is highly expressed on embryon
37 congenital hydrocephalus secondary to neural cell adhesion molecule L1 (L1CAM) gene mutations include
38             Mutations in the gene for neural cell adhesion molecule L1 (L1CAM) result in a debilitati
39                                          The cell adhesion molecule L1 mediates axonal guidance durin
40                                          The cell adhesion molecule L1 mediates neurite outgrowth and
41               We investigated how the neural cell adhesion molecule L1 mediates neurite outgrowth thr
42                                   The neural cell adhesion molecule L1 mediates the axon outgrowth, a
43 munohistochemistry, the distributions of the cell adhesion molecules L1, NCAM, and TAG-1 and the extr
44 d previously that axonal accumulation of the cell adhesion molecule L1/neuron-glia cell adhesion mole
45  NEEP21 in correct trafficking of the axonal cell adhesion molecule L1/neuron-glia cell adhesion mole
46 adhesion molecules (L1-CAMs) [L1/neuron-glia cell adhesion molecule (L1/NgCAM) and neurofascin (NF)]
47 ficking of multiple receptors, including the cell adhesion molecule L1/NgCAM, the neurotransmitter re
48                 Coordinate expression of the cell adhesion molecule L1 on Schwann cells and axons cor
49 ctor-2 (FGF2), nerve growth factor (NGF), L1 cell adhesion molecule (L1), or beta-galactosidase (LacZ
50 lucose-6-phosphate dehydrogenase, the neural cell adhesion molecule L1, phenylalanine hydroxylase, pa
51                                          The cell adhesion molecule L1 regulates axonal guidance and
52 d using the cytoplasmic domain of the axonal cell adhesion molecule L1 to identify binding partners t
53 cin-C (tenascin) and an antibody (Ab) to the cell adhesion molecule L1 to specifically mimic survival
54                                   The neural cell adhesion molecule L1, which is present on axons and

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