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1 igodendrocyte-myelin glycoprotein), and MAG (myelin-associated glycoprotein).
2 ant proteins but also brain proteins such as myelin associated glycoprotein.
3 eled fatty acid and immunostaining of P0 and myelin associated glycoprotein.
4  in the growth cone induced by the repellent myelin-associated glycoprotein.
5 drocyte apoptosis and a preferential loss of myelin-associated glycoprotein.
6 vation and neurite inhibition in response to myelin-associated glycoprotein.
7 wth and overcame growth inhibition caused by myelin-associated glycoprotein.
8 PP1 mediate growth cone repulsion induced by myelin-associated glycoprotein.
9                     In line with these data, myelin-associated glycoprotein addition to cerebellar gr
10 go, oligodendrocyte-myelin glycoprotein, and myelin-associated glycoprotein, all bind to an axonal No
11 glecs were known, namely sialoadhesin, CD22, myelin-associated glycoprotein and CD33.
12 ditions, but also promotes neurite growth on myelin-associated glycoprotein and chondroitin sulfate p
13                                              Myelin-associated glycoprotein and chondroitin sulfate p
14 ing of neuronal growth cones to netrin-1 and myelin-associated glycoprotein and for netrin-1/DCC-depe
15              Immunofluorescence labeling for myelin-associated glycoprotein and for the protein Caspr
16                                     However, myelin-associated glycoprotein and semaphorin 3A regulat
17 inding of the myelin inhibitors Nogo-A, MAG (myelin-associated glycoprotein), and OMgp (oligodendrocy
18            Three myelin proteins, Nogo, MAG (myelin-associated glycoprotein), and OMgp (oligodendrocy
19  (sialoadhesin), siglec-3 (CD33), siglec-4a (myelin-associated glycoprotein), and siglec-5 to alpha2-
20 ntified constituents of this activity (Nogo, myelin-associated glycoprotein, and oligodendrocyte myel
21 iated, structurally distinct proteins, Nogo, myelin-associated glycoprotein, and oligodendrocyte myel
22  nervous system (CNS) myelin proteins, Nogo, myelin-associated glycoprotein, and oligodendrocyte myel
23    The 7E11 monoclonal antibody blocks Nogo, myelin-associated glycoprotein, and oligodendrocyte myel
24 t or second Ig domains of the I-type lectins myelin-associated glycoprotein, and sialoadhesin did not
25 her known Siglec family members (CD22, CD33, myelin-associated glycoprotein, and sialoadhesin) show t
26 valuated Ig gene usage in patients with anti-myelin-associated glycoprotein (anti-MAG) neuropathy, an
27 usion body myositis and paraproteinemic anti-myelin-associated glycoprotein antibody demyelinating po
28 pain substrates [myelin basic protein (MBP); myelin-associated glycoprotein] are degraded in this dis
29  S-100 antigen as a pan-Schwann cell marker, myelin-associated glycoprotein as a marker for myelinati
30                                              Myelin-associated glycoprotein binds to LRP1 with high a
31 rin-1, brain-derived neurotrophic factor and myelin-associated glycoprotein, but not to semaphorin 3A
32 action and stabilization of oligodendrocytic myelin-associated glycoprotein by neuronal gangliosides
33 at cleaves one class of axonal receptors for myelin-associated glycoprotein, enhances spinal axon out
34 ets for autoantibodies include gangliosides, myelin associated glycoprotein, Hu antigen and extractab
35     Moreover, the GPR12-mediated rescue from myelin-associated glycoprotein inhibition was attributab
36 elin basic protein and protein zero, whereas myelin-associated glycoprotein is largely unaffected.
37   This shortened induction was also found in myelin-associated glycoprotein knock-out mice, but not i
38 ys revealed that C1q interacts directly with myelin associated glycoprotein (MAG) in myelin, resultin
39  axon growth on the nonpermissive substrates myelin-associated glycoprotein (MAG) and chondroitin sul
40 binds the myelin inhibitors NogoA, OMgp, and myelin-associated glycoprotein (MAG) and has been propos
41 racted to affect expression of genes such as myelin-associated glycoprotein (Mag) and myelin basic pr
42                               In addition to myelin-associated glycoprotein (MAG) and Nogo-A, availab
43                    The neural sialoadhesins, myelin-associated glycoprotein (MAG) and Schwann cell my
44     We have analyzed mice that lack both the myelin-associated glycoprotein (MAG) and the myelin gala
45                   We subsequently identified myelin-associated glycoprotein (MAG) as a cross-reactive
46 roteins including neurofascin155 (NF155) and myelin-associated glycoprotein (MAG) at axo-glial juncti
47                                              Myelin-associated glycoprotein (MAG) binds to the nerve
48 brain-derived neurotrophic factor (BDNF), or myelin-associated glycoprotein (MAG) but not by a gradie
49 hmidt-Lantermann (S-L) incisures contain the myelin-associated glycoprotein (MAG) but not P(0) or pro
50 ealed a 9 mum dissociation constant for PirB-myelin-associated glycoprotein (MAG) ectodomain interact
51 nel of myelin antibodies, we discovered that myelin-associated glycoprotein (MAG) expression is drama
52 trates that mice with a null mutation of the myelin-associated glycoprotein (MAG) gene have a chronic
53 Sox10 synergy, including a novel site in the Myelin-associated glycoprotein (Mag) gene, is also reduc
54                                              Myelin-associated glycoprotein (MAG) has been implicated
55 I(3,5)P2 deficiency leads to accumulation of myelin-associated glycoprotein (MAG) in LAMP1(+)perinucl
56              Immunocytochemical detection of myelin-associated glycoprotein (MAG) indicated that Schw
57                                          The myelin-associated glycoprotein (MAG) is a member of the
58                                              Myelin-associated glycoprotein (MAG) is a potent inhibit
59                                              Myelin-associated glycoprotein (MAG) is a sialic acid-bi
60                                              Myelin-associated glycoprotein (MAG) is a transmembrane
61                                              Myelin-associated glycoprotein (MAG) is an abundant myel
62                                              Myelin-associated glycoprotein (MAG) is expressed in per
63                                              Myelin-associated glycoprotein (MAG) is susceptible to p
64  myelination, myelin basic protein (MBP) and myelin-associated glycoprotein (MAG) myelin proteins wer
65 n GD1a and GT1b gangliosides on the axon and myelin-associated glycoprotein (MAG) on myelin.
66               In the injured nervous system, myelin-associated glycoprotein (MAG) on residual myelin
67 n was enhanced, and the repulsion induced by myelin-associated glycoprotein (MAG) or myelin membrane
68 dhesion molecules neurofascin155 (NF155) and myelin-associated glycoprotein (MAG) require membrane mi
69 godendrocyte myelin glycoprotein (OMgp), and myelin-associated glycoprotein (MAG) to mediate neurite
70 ic protein (MBP), proteolipid protein (PLP), myelin-associated glycoprotein (MAG), "Rip," and the neu
71 crease in calpain content and degradation of myelin-associated glycoprotein (MAG), a calpain substrat
72                                              Myelin-associated glycoprotein (MAG), a membrane-bound p
73 e reported in mice with a disrupted gene for myelin-associated glycoprotein (MAG), a myelin receptor
74                                              Myelin-associated glycoprotein (MAG), a nervous system c
75                                              Myelin-associated glycoprotein (MAG), a sialic acid bind
76                      We now demonstrate that myelin-associated glycoprotein (MAG), a well known inhib
77                                              Myelin-associated glycoprotein (MAG), an inhibitor of ax
78                            Antibodies to P0, myelin-associated glycoprotein (MAG), and neural cell ad
79 und along axons: myelin basic protein (MBP), myelin-associated glycoprotein (MAG), and neuron-glia ce
80 the myelin inhibitory proteins Nogo/Nogo-66, myelin-associated glycoprotein (MAG), and oligodendrocyt
81 '-cyclic nucleotide phosphodiesterase (CNP), myelin-associated glycoprotein (MAG), and P0.
82  mutants, is defective for the expression of myelin-associated glycoprotein (MAG), and the misregulat
83 xonal receptors, Cadm2 and Cadm3, as well as myelin-associated glycoprotein (MAG), are enriched at th
84                               One inhibitor, myelin-associated glycoprotein (MAG), binds to sialoglyc
85 growth cone turning induced by a gradient of myelin-associated glycoprotein (MAG), cAMP acts by modul
86 igodendrocyte myelin glycoprotein (OMgp) and myelin-associated glycoprotein (MAG), exert their effect
87          For example, the endogenous lectin, myelin-associated glycoprotein (MAG), is reported to bin
88                      One glial molecule, the myelin-associated glycoprotein (MAG), located in the ada
89 , internode-forming morphology co-expressing myelin-associated glycoprotein (MAG), necessary for axon
90 part to myelin-associated inhibitors such as myelin-associated glycoprotein (MAG), Nogo-A, and oligod
91 nhibitors of regeneration in myelin, such as myelin-associated glycoprotein (MAG), play an important
92 olecules associated with CNS myelin, such as myelin-associated glycoprotein (MAG), represent major ob
93 obulin-like family member lectins (siglecs), myelin-associated glycoprotein (MAG), Schwann cell myeli
94  general and by a specific myelin component, myelin-associated glycoprotein (MAG), than in the same t
95 lated expression of splice variants encoding myelin-associated glycoprotein (MAG), which generates tw
96 eurofascin and NrCAM at sites independent of myelin-associated glycoprotein (MAG)-staining Schwann ce
97 igodendrocytes and oligodendrocyte- derived, myelin-associated glycoprotein (MAG).
98 part, via the cell-surface adhesion protein, myelin-associated glycoprotein (MAG).
99 g junctional adhesion molecule-C (JAM-C) and myelin-associated glycoprotein (MAG).
100 ed by inhibitory proteins in myelin, such as myelin-associated glycoprotein (MAG).
101 n receptors during chemorepulsion induced by myelin-associated glycoprotein (MAG).
102 d responsiveness to neurotrophin 3 (NT3) and myelin-associated glycoprotein (MAG).
103 ssociated inhibitors of regeneration such as myelin-associated glycoprotein (MAG).
104 owth cone chemotaxis, including netrin-1 and myelin-associated glycoprotein (MAG).
105  limited by two proteins in myelin, Nogo and myelin-associated glycoprotein (MAG).
106                                              Myelin-associated glycoprotein (MAG, Siglec-4) is one of
107 nhibitory cytokines (TNFalpha, IL-1beta) and myelin-associated glycoproteins (MAG, Nogo).
108 pathies, such as Guillain-Barre syndrome and myelin-associated glycoprotein neuropathy (MAG), are cau
109                                    Anti-MAG (myelin-associated glycoprotein) neuropathy is a disablin
110                                 ARIs include myelin-associated glycoprotein, Nogo, oligodendrocyte-my
111                                 We show that myelin-associated glycoprotein or CNS myelin, in general
112 g molecules--such as myelin-derived Nogo and myelin-associated glycoprotein--or reactive astrocyte-pr
113 ite matter and preferentially became Olig2+, Myelin Associated Glycoprotein-positive, Myelin Basic Pr
114                Others showed that siglec-4a (myelin-associated glycoprotein) prefers Neu5Ac over Neu5
115              ELISAs were used to measure the myelin-associated glycoprotein:proteolipid protein-1 rat
116                                     Instead, myelin-associated glycoprotein recruited p75 neurotrophi
117 erized siglecs, sialoadhesin, CD22, CD33 and myelin-associated glycoprotein, several new ones, siglec
118         Most remarkable was the finding that myelin-associated glycoprotein (Siglec-4) binds with 500
119 ctions of hypoxia-inducible factors, and the myelin associated glycoprotein to proteolipid protein 1
120 amined the relationship between the ratio of myelin-associated glycoprotein to proteolipid protein 1
121            We previously showed the ratio of myelin-associated glycoprotein to proteolipid protein 1
122 th factor in the context of reduced ratio of myelin-associated glycoprotein to proteolipid protein 1
123 ignificant correlations between the ratio of myelin-associated glycoprotein to proteolipid protein 1
124  matter perfusion, indicated by the ratio of myelin-associated glycoprotein to proteolipid protein 1,
125  Collapsin-1/Semaphorin III/D (Sema III) and myelin-associated glycoprotein trigger repulsive turning
126                                Expression of myelin-associated glycoprotein was also decreased by abo
127                                          The myelin-associated glycoprotein was appropriately sorted
128 in, myelin oligodendrocyte glycoprotein, and myelin-associated glycoprotein, was delayed in the spina
129 by 206.5% while the levels of 68 kDa NFP and myelin-associated glycoprotein were decreased by 42.9 an
130 n overcame neurite outgrowth inhibition from myelin-associated glycoprotein, which was mirrored by ac
131            Indeed, there is an early loss of myelin-associated glycoprotein within the lesion, despit
132 ing of beta1-integrin adhesions triggered by myelin-associated glycoprotein, yet permitted integrin c

 
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