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1 ng component of this receptor complex is the p75 neurotrophin receptor.
2 Trk receptor tyrosine kinases and the shared p75 neurotrophin receptor.
3 sociate with the intracellular domain of the p75 neurotrophin receptor.
4 he iota PKC.IRAK complex is recruited to the p75 neurotrophin receptor.
5 very similar gamma-secretase cleavage is the p75 neurotrophin receptor.
6 mechanism, supported by up-regulation of the p75 neurotrophin receptor.
7 the actions of BDNF are mediated through the p75 neurotrophin receptor.
8 so be induced by selective activation of the p75 neurotrophin receptor.
9 uce Schwann cell death via engagement of the p75 neurotrophin receptor.
10 ival or cell death decisions mediated by the p75 neurotrophin receptor.
11 ia a yet undefined mechanism mediated by the p75 neurotrophin receptor.
12 ransducer for the effects of NGF through the p75 neurotrophin receptor.
13 ergic neurons and terminals that express the p75 neurotrophin receptor.
14  the Fas receptor, the p75 TNF receptor, and p75 neurotrophin receptor.
15 f NGF or by antibodies to either trkB or the p75 neurotrophin receptor.
16 dependent signalling mechanism involving the p75 neurotrophin receptor.
17 e extracellular neurotrophin binding site of p75 neurotrophin receptor.
18 n of the kinase-active Trk receptors and the p75 neurotrophin receptor.
19 l-like receptor superfamilies, including the p75 neurotrophin receptor.
20  ARMS can physically associate with TrkA and p75 neurotrophin receptors.
21 GF binds to the TrkA tyrosine kinase and the p75 neurotrophin receptor, a member of the tumor necrosi
22                                          The p75 neurotrophin receptor, a member of the tumor necrosi
23                                          The p75 neurotrophin receptor, a member of the tumor necrosi
24             Mechanistically, blockade of the p75 neurotrophin receptor abolished BDNF-induced postsyn
25 e studies provide a new reagent for altering p75 neurotrophin receptor actions after injury and sugge
26 t regulated intramembrane proteolysis of the p75 neurotrophin receptor (also known as p75 cleavage).
27 ls via the tyrosine receptor kinase B (TrkB)/p75 neurotrophin receptor and Fyn kinase in transfected
28               First, SC-1 interacts with the p75 neurotrophin receptor and is redistributed from the
29 eurotrophin receptor types: the multifaceted p75 neurotrophin receptor and the tropomyosin receptor k
30 s were characterized using antibodies to the p75 neurotrophin receptor and trkB receptors.
31     Thirty years ago, it was discovered that p75 neurotrophin receptor and tropomyosin receptor kinas
32 an interact through its TRAF domain with the p75 neurotrophin receptor and weakly with the lymphotoxi
33 factor induced apoptosis in cells expressing p75 neurotrophin receptor, and enhances neurite outgrowt
34                                In adulthood, p75 neurotrophin receptor becomes down-regulated and pro
35 educes binding of pro-nerve growth factor to p75 neurotrophin receptor, blocks pro-nerve growth facto
36 erve growth factor (NGF) in complex with the p75 neurotrophin receptor but is distinct from that of m
37 t dependence, these neurons express trkB and p75 neurotrophin receptor but not trkA or trkC mRNAs.
38 ng to mature oligodendrocytes expressing the p75 neurotrophin receptor, but not trkA, resulted in a s
39 ta, osteoprotegerin, FOXC2 and FOXF2, BMP-2, p75 neurotrophin receptor, caspase-11, guanylate-binding
40                     Germline deletion of the p75 neurotrophin receptor causes dramatic axon guidance
41 are closely related to NRAGE, which mediates p75 neurotrophin receptor-dependent apoptosis, and necdi
42    This consolidates a potential role of the p75 neurotrophin receptor during stress and inflammatory
43 e-bolus propofol applications at the peak of p75 neurotrophin receptor expression after experimental
44  cause is the lack of NO, which up-regulated p75 neurotrophin receptor expression, a receptor require
45 ate developmental-like programs and increase p75 neurotrophin receptor expression, probably to foster
46 DNF-tyrosine-related kinase B (TrkB) p75NTR (p75 neurotrophin receptor) facilitates stabilization of
47 ed a cDNA for the LacZ reporter or the human p75 neurotrophin receptor, for which species-specific an
48  combines the 192 monoclonal antibody to the p75 neurotrophin receptor found on terminals and cell bo
49                                          The p75 neurotrophin receptor has been implicated in neurotr
50 n contrast, optical density for low-affinity p75 neurotrophin receptor immunoreactivity in the VLDB d
51 terferes with oligomerization of full-length p75 neurotrophin receptor in a dose-dependent manner.
52 1 receptor-associated kinase (IRAK) with the p75 neurotrophin receptor in PC12 cells.
53 rescence for either ChAT or the low-affinity p75 neurotrophin receptor in the nucleus basalis Meynert
54 arget-derived NGF promotes expression of the p75 neurotrophin receptor, in turn causing a reduction i
55               Schwann cell factor 1 (SC1), a p75 neurotrophin receptor-interacting protein, is a memb
56                                              p75 neurotrophin receptor is highly expressed during ear
57                                          The p75 neurotrophin receptor is important in multiple physi
58  a valine residue at position 264 in the rat p75 neurotrophin receptor is necessary for the ability o
59               Previously, we have shown that p75 neurotrophin receptor is required for glioma invasio
60                            Activation of the p75 neurotrophin receptor leads to a variety of effects
61 itory signals through the same Nogo receptor/p75 neurotrophin receptor/LINGO-1 (NgR1/p75/LINGO-1) com
62  neurotrophic factor ratio, which aggravates p75 neurotrophin receptor-mediated cell death.
63                  Pathway analyses implicated p75 neurotrophin receptor/nerve growth factor signaling
64                             BMP9 induced the p75 neurotrophin receptor (NGFR), a marker of BFCN, and
65 enesis and recent evidence suggests that the p75 neurotrophin receptor (NTR) contributes significantl
66 sal forebrain neurons immunoreactive for the P75 neurotrophin receptor (NTR) in male and female Sprag
67                             We show that the p75 neurotrophin receptor (NTR) serves this role in reti
68 tors while down-regulating the expression of p75 neurotrophin receptor (NTR), phospho-JNK, and Bcl-2-
69 -hybrid library with the death domain of the p75 neurotrophin receptor (NTR), we identified the Sall2
70 al neurons mediated to a great extent by the p75 neurotrophin receptor (NTR).
71 ) migration and promotes myelination via the p75 neurotrophin receptor (NTR).
72                       BDNF acts via TrkB and p75 neurotrophin receptors (NTR), and restoring its sign
73 ived compound, EVT901, which interferes with p75 neurotrophin receptor oligomerization through direct
74                             ProNGF activates p75 neurotrophin receptor (p75(NTR)) and sortilin recept
75 that TAp73 is a transcriptional activator of p75 neurotrophin receptor (p75(NTR)) and that p75(NTR) m
76 ctor (BDNF) activate two distinct receptors: p75 neurotrophin receptor (p75(NTR)) and TrkB.
77                                          The p75 neurotrophin receptor (p75(NTR)) belongs to the tumo
78 eurotrophic factor (BDNF)-activated TrkB and p75 neurotrophin receptor (p75(NTR)) by disrupting the e
79                                          The p75 neurotrophin receptor (p75(NTR)) functions at the mo
80 al role in Alzheimer's disease (AD), and the p75 neurotrophin receptor (p75(NTR)) has been implicated
81                                          The p75 neurotrophin receptor (p75(NTR)) has been proposed t
82                              The role of the p75 neurotrophin receptor (p75(NTR)) in adult cholinergi
83                            Expression of the p75 neurotrophin receptor (p75(NTR)) in primary melanoma
84                      Here we report that the p75 neurotrophin receptor (p75(NTR)) is a co-receptor of
85                         We show that cleaved p75 neurotrophin receptor (p75(NTR)) is a component of t
86                                          The p75 neurotrophin receptor (p75(NTR)) is a member of the
87                                          The p75 neurotrophin receptor (p75(NTR)) is a multifunctiona
88                        Here we show that the p75 neurotrophin receptor (p75(NTR)) is a regulator of g
89 f nerve growth factor (NGF) signaling by the p75 neurotrophin receptor (p75(NTR)) is critical for neu
90 e of distinct structural determinants in the p75 neurotrophin receptor (p75(NTR)) is crucial for the
91                                          The p75 neurotrophin receptor (p75(NTR)) is expressed on man
92                                          The p75 neurotrophin receptor (p75(NTR)) is highly expressed
93                      During development, the p75 neurotrophin receptor (p75(NTR)) is widely expressed
94                                          The p75 neurotrophin receptor (p75(NTR)) mediates neuronal d
95                                          The p75 neurotrophin receptor (p75(NTR)) mediates the death
96 can be initiated by activation of either the p75 neurotrophin receptor (p75(NTR)) or the more selecti
97                                          The p75 neurotrophin receptor (p75(NTR)) regulates a wide ra
98                                              p75 neurotrophin receptor (p75(NTR)) signaling pathways
99 cellular signaling networks regulated by the p75 neurotrophin receptor (p75(NTR)) substantially overl
100                           Here, we show that p75 neurotrophin receptor (p75(NTR)) undergoes hypoxia-i
101  neuron loss, distal axonal degeneration and p75 neurotrophin receptor (p75(NTR)) upregulation in the
102     Strikingly, mutant male mice lacking the p75 neurotrophin receptor (p75(NTR)) were resistant to t
103 erestingly, mutant male mice that lacked the p75 neurotrophin receptor (p75(NTR)) were seen to be res
104  structures of complexes formed by the DD of p75 neurotrophin receptor (p75(NTR)) with RhoGDI, for ac
105 s the de novo expression of the low-affinity p75 neurotrophin receptor (p75(NTR)), a gene that plays
106                                          The p75 neurotrophin receptor (p75(NTR)), a member of the tu
107                     Here, we report that the p75 neurotrophin receptor (p75(NTR)), a TNF receptor sup
108  examined the expression of the low affinity p75 neurotrophin receptor (p75(NTR)), an excellent marke
109 c efferents, identified by the low-affinity, p75 neurotrophin receptor (p75(NTR)), with interneurons
110     This produced a substantial loss of both p75 neurotrophin receptor (p75(NTR))-positive and cholin
111 proNGF, is a potent apoptotic ligand for the p75 neurotrophin receptor (p75(NTR))-sortilin complex.
112 s performance on cognitive tasks through the p75 neurotrophin receptor (p75(NTR)).
113 erated synapse elimination via activation of p75 neurotrophin receptor (p75(NTR)).
114 ent prevented by blocking antibodies against p75 neurotrophin receptor (p75(NTR)).
115  engaging in a complex with sortilin and the p75 neurotrophin receptor (p75(NTR)).
116 tropomyosin kinase receptor B (TrkB) and the p75 neurotrophin receptor (p75) are the primary regulato
117 oting signals are generated by activation of p75 neurotrophin receptors (p75(NTR)).
118 pomyosin-related kinase receptors (Trks) and p75 neurotrophin receptors (p75) compete to regulate sur
119 eled for choline acetyltransferase (ChAT) or p75-neurotrophin receptor (p75(NTR) ).
120 r (EMMPRIN), with the cognate apical marker, p75-neurotrophin receptor (p75-NTR).
121  Proneurotrophins bind with high affinity to p75 neurotrophin receptor (p75NTR) and lack the capacity
122 types and mediates its effects by binding to p75 neurotrophin receptor (p75NTR) and sortilin.
123 atory ligand B7-1 (hB7-1) interacts with the p75 neurotrophin receptor (p75NTR) and that the B7-1:p75
124 tment with antisense oligonucleotides to the p75 neurotrophin receptor (p75ntr) decreased basal survi
125 pment of the sympathetic nervous system, the p75 neurotrophin receptor (p75NTR) has a dual function:
126 tate gyrus, the distribution of low-affinity p75 neurotrophin receptor (p75NTR) immunoreactivity (IR)
127 septum, choline acetyltransferase (ChAT) and p75 neurotrophin receptor (p75NTR) immunoreactivity, and
128      Here, we investigate the involvement of p75 neurotrophin receptor (p75NTR) in Abeta-treated huma
129 , we identify an anti-migratory role for the p75 neurotrophin receptor (p75NTR) in cerebellar develop
130              We investigated the role of the p75 neurotrophin receptor (p75NTR) in mediating neurotro
131                 To determine the role of the p75 neurotrophin receptor (p75NTR) in sympathetic neuron
132    Our goal was to determine the role of the p75 neurotrophin receptor (p75NTR) in the loss of islet
133 ad, myelin-associated glycoprotein recruited p75 neurotrophin receptor (p75NTR) into a complex with L
134               Previously, we have shown that p75 neurotrophin receptor (p75NTR) is a novel mediator o
135                                          The p75 neurotrophin receptor (p75NTR) is a proximate cell m
136                                          The p75 neurotrophin receptor (p75NTR) is highly expressed i
137          Emerging evidence suggests that the p75 neurotrophin receptor (p75NTR) mediates cell death;
138                                          The p75 neurotrophin receptor (p75NTR) regulates numerous ce
139                                          The p75 neurotrophin receptor (p75NTR) regulates the time co
140         Plasticity was rescued by inhibiting p75 neurotrophin receptor (p75NTR) signaling or its down
141                        Here we show that the p75 neurotrophin receptor (p75NTR) undergoes presenilin-
142 nizes trkA, trkB, and trkC) and low-affinity p75 neurotrophin receptor (p75NTR) was examined in the h
143 ors, tropomyosin related kinase B (TrkB) and p75 neurotrophin receptor (p75NTR), are increasingly app
144                             They express the p75 neurotrophin receptor (p75NTR), which is known to si
145 ohol drinking produces a mobilization of DLS p75 neurotrophin receptor (p75NTR), whose activities opp
146 s, the TrkA tyrosine kinase receptor and the p75 neurotrophin receptor (p75NTR).
147  that was triggered by overexpression of the p75 neurotrophin receptor (p75NTR).
148 lls (SCs) and an increased expression of the p75 neurotrophin receptor (p75NTR).
149 ro-NGF increased LDLR expression through the p75 neurotrophin receptor (p75NTR).
150 mbers in G1H mice that re-express the common p75 neurotrophin receptor (p75NTR).
151  mice with and without the expression of the p75 neurotrophin receptor (p75NTR).
152 mesenchymal cells expressing both desmin and p75 neurotrophin receptor (p75NTR): HSCs in the liver pa
153   Here, we demonstrate that mice lacking the p75 neurotrophin receptor, p75NTR, decrease their feedin
154 or the pro-brain-derived neurotrophic factor-p75 neurotrophin receptor pathway.
155 the same set of transcription factors from a p75 neurotrophin receptor peptide (p75NTRp)-tagged adeno
156                                              p75 neurotrophin receptor plays an important role in the
157 NF appear to be mediated by the low-affinity p75 neurotrophin receptor, rather than a trk receptor.
158                                          The p75 neurotrophin receptor regulates neuronal survival, p
159                             Furthermore, the p75 neurotrophin receptor restricts PSD formation, sugge
160 (brain-derived neurotrophic factor, proBDNF, p75 neurotrophin receptor, S100B), neuropsychometric tes
161  that of NRAGE, a MAGE protein that mediates p75 neurotrophin receptor signaling and neuronal apoptos
162 e results revealed new functions for proBDNF-p75 neurotrophin receptor signaling pathway in the contr
163  by unbalancing neurotrophin homeostasis via p75 neurotrophin receptor signaling.
164 ermore, we demonstrate that EVT901 abrogates p75 neurotrophin receptor signalling by other ligands, s
165 rauma and other neurological disorders where p75 neurotrophin receptor signalling is affected.
166  and gp120 were blocked by inhibitors of the p75 neurotrophin receptor, suggesting that proBDNF and g
167 c inhibition of the cell death domain of the p75 neurotrophin receptor (TAT-Pep5) and in mice lacking
168 urotrophins such as BDNF can bind to p75NTR (p75 neurotrophin receptor), their precursors are the hig
169 rve growth factor (NGF) and the low-affinity p75 neurotrophin receptor, their sensory nerve fibers ex
170 ecule, nicotinic acetylcholine receptor, and p75 neurotrophin receptor), thus demonstrating that pseu
171 t Par-3 directly associates and recruits the p75 neurotrophin receptor to the axon-glial junction, fo
172 s ability to redirect the apically localized P75 neurotrophin receptor to the basolateral membrane do
173 ding assays with cysteine-rich domains-fused p75 neurotrophin receptor, we confirmed that EVT901 inte
174 opomyosin receptor kinase (Trk) A, TrkB, and p75 neurotrophin receptor were all expressed in primary
175 he p75 TNF receptor, the Fas antigen, or the p75 neurotrophin receptor, which are other members of th
176                        Here we show that the p75 neurotrophin receptor, which is abundantly expressed

 
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