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1 hemical profiles are similar with respect to neurofilament protein.
2 m and heavy molecular weight subunits of the neurofilament protein.
3 e flank of tadpoles expressing the truncated neurofilament protein.
4 histochemistry using antibodies specific for neurofilament protein.
5  hybrid cells were shown to synthesize human neurofilament protein.
6 muscle myosin heavy chains, connexin-42, and neurofilament protein.
7 arkers including neuron-specific enolase and neurofilament protein.
8 o histamine or an antibody to phosphorylated neurofilament protein.
9 g immunohistochemistry for nonphosphorylated neurofilament protein.
10 P, neuropeptide-Y, tyrosine hydroxylase, and neurofilament protein.
11 for immunohistochemistry with an antibody to neurofilament protein.
12 mmunoreactive to a neuron-specific probe for neurofilament protein.
13 ellular Ca signaling as well as two forms of neurofilament protein.
14  31) and nonphosphorylated (SMI 32) forms of neurofilament protein.
15 de Y (NPY), tyrosine hydroxylase (TH), and a neurofilament protein.
16 ontained the middle and low molecular weight neurofilament proteins.
17 enous Nes-S co-assembles with peripherin and neurofilament proteins.
18 ding glutamate receptors, cell adhesion, and neurofilament proteins.
19 d precursor protein, and hyperphosphorylated neurofilament proteins.
20 al caliber through phosphorylation of axonal neurofilament proteins.
21 l perikaryal accumulations of phosphorylated neurofilament proteins.
22 haracterized pathologically by deposition of neurofilament proteins.
23                                              Neurofilament protein accumulation was dependent on the
24                There was a selective loss of neurofilament proteins after exposure to 5 or 10 mM asco
25 lores the formation of intraneuronal tau and neurofilament protein aggregates using intracisternal ad
26 he major component of these lesions although neurofilament proteins also are present.
27 the two sets of projection neurons contained neurofilament protein, although the density and distribu
28                     Degradation of the 68-kD neurofilament protein and internucleosomal DNA fragmenta
29 ers of neurons, as assessed by expression of neurofilament protein and of total cells, are present in
30 F-L 3'UTR, colocalizes with endogenous heavy neurofilament protein and, at high-level expression, lea
31 ow transport rates overlapping with those of neurofilament proteins and actin, both of which coimmuno
32 rofibrillary tangles such as tau, ubiquitin, neurofilament proteins and apolipoprotein E.
33         Colocalization of 3-NT staining with neurofilament proteins and evidence of decreased tyrosin
34 tes neuronal cytoskeletal proteins including neurofilament proteins and microtubule-associated protei
35 obleaching studies to reveal the movement of neurofilament proteins and other cytoskeletal proteins i
36 , serum levels of glial fibrillar acidic and neurofilament proteins and S100B.
37 arge myelinated (by using antibodies against neurofilament protein) and small unmyelinated (by using
38                        In the present study, neurofilament protein, and the calcium-binding proteins
39 ed by significant reduction in the levels of neurofilament proteins, and alterations in axonal fiber
40 mistry to detect APPs, beta-amyloid (Abeta), neurofilament proteins, and glial fibrillary acidic prot
41 ecific nuclear binding protein, intermediate neurofilament proteins, and parvalbumin.
42 xide synthase, nNOS) and a nonphosphorylated neurofilament protein (antibody SMI-32).
43      These data show that peripherin and the neurofilament proteins are functionally interdependent.
44  Our data show that alpha-internexin and the neurofilament proteins are functionally interdependent.
45                                              Neurofilament proteins are known to be transported along
46              Increases in non-phosphorylated neurofilament proteins are observed first, with phosphor
47 zed (NF-M) and heavy (NF-H) molecular weight neurofilament proteins, are highly phosphorylated in axo
48                                              Neurofilament proteins begin to aggregate by day 1 follo
49  analysis revealed significant inhibition of neurofilament protein breakdown by MP and other corticos
50 B(1) receptor and choline acetyltransferase, neurofilament proteins, calbindin, calretinin, synapsin
51                            The expression of neurofilament protein, calretinin, and calbindin follows
52 tereologic estimates of the total numbers of neurofilament protein-containing layer IVB cells and Mey
53 V3 exhibited a more consistent proportion of neurofilament protein-containing neurons (70-80%), regar
54 ate cortex were marked by a lower density of neurofilament protein-containing neurons, which were vir
55                                         Long neurofilament protein-containing processes extended from
56 erved between somatodendritic morphology and neurofilament protein content.
57 loss of long cross-bridges with no change in neurofilament protein content.
58      Here we will review the neurobiology of neurofilament proteins, describing current understanding
59                                              Neurofilament protein distribution was a reliable tool f
60  and distribution of the total population of neurofilament protein-enriched neurons was very differen
61 ical features, including the distribution of neurofilament protein-enriched pyramidal neurons.
62 he monoclonal antibody SMI32, which labels a neurofilament protein found in pyramidal cells, is reduc
63 ry acidic protein (GFAP), keratocan, nestin, neurofilaments, protein gene product 9.5, tyrosine hydro
64 ) is involved in neurite outgrowth and human neurofilament protein H (hNF-H) Lys-Ser-Pro (KSP) tail d
65 calretinin, calbindin, and parvalbumin), and neurofilament proteins have been explored in the develop
66                                              Neurofilament proteins have been validated as specific b
67 HF tau, and high and medium molecular weight neurofilament proteins have significantly greater cross-
68                   These results suggest that neurofilament protein identifies particular subpopulatio
69 eas V1, V2, V3, and V3A to area MT that were neurofilament protein-immunoreactive (57-100%), than to
70 performed an analysis of the distribution of neurofilament protein in corticocortical projection neur
71 We have investigated the axonal transport of neurofilament protein in cultured neurons by constrictin
72 rst demonstration of the axonal transport of neurofilament protein in cultured neurons.
73 hat expresses a photoactivatable fluorescent neurofilament protein in neurons.
74 l subtypes of plaques in Alzheimer brain and neurofilament protein in swollen neurites, like tau prot
75 rated the presence of phosphorylated tau and neurofilament proteins in neurofibrillary degeneration (
76 eight (NF-H) and low molecular weight (NF-L) neurofilament proteins in the 2 M urea extracts of spina
77 ssive degradation of both 68 kDa and 200 kDa neurofilament proteins in the cord lesion at intervals a
78                 The extent of degradation of neurofilament proteins in the lesion following trauma wa
79 a-internexin also coassembles with all three neurofilament proteins into a single network of filament
80  the primate cerebral cortex have shown that neurofilament protein is present in pyramidal neuron sub
81            In young embryos (4-5 weeks old), neurofilament protein-labeled fibers run through the sub
82 ed the effects of both NGF and acrylamide on neurofilament protein levels and synthesis indicated tha
83          In PC12 cells, acrylamide increased neurofilament protein levels and synthesis.
84 luid (CSF) levels of AB and tau species, and neurofilament protein light protein (NFL) were used as A
85 d (CSF) levels of Abeta and tau species, and neurofilament protein light protein (NFL) were used as A
86  ubiquitin C-terminal hydrolase L1 [UCH-L1], neurofilament protein-light, and total tau) were measure
87 ation, whereas 3-NT modification of striatal neurofilament proteins likely points to the ensuing dopa
88 g the low, middle, and high molecular weight neurofilament proteins, microtubule-associated protein 2
89  found that green fluorescent protein-tagged neurofilament proteins move predominantly in the form of
90                     These data indicate that neurofilament protein moves anterogradely in these axons
91 the L5 DRG, identified by their staining for neurofilament protein (N52), did not change after ligati
92 teins such as cytokeratins 8, 13, and 18 and neurofilament proteins NF-L and NF-M.
93 h cytochrome oxidase (CO) histochemistry and neurofilament protein (NF) immunoreactivity and architec
94  Co-localization of the P2X3-ir neurons with neurofilament protein (NF) showed that the majority of t
95 immunocytochemistry using antibodies against neurofilament protein (NF), 5-HT to reveal descending se
96 d with antisera against substance P (SP) and neurofilament protein (NF).
97    Hyperphosphorylated high molecular weight neurofilament protein (NF-H) exhibits extensive phosphor
98                    The high molecular weight neurofilament protein (NF-H) is highly phosphorylated in
99 y phosphorylated human high molecular weight neurofilament protein (NF-H) resulted in the identificat
100 f the Xenopus laevis middle-molecular-weight neurofilament protein (NF-M) into embryonic frog blastom
101            The distribution of middle-weight neurofilament protein (NF-M), an intermediate filament o
102 reased expression of middle molecular weight neurofilament protein (NF-M), and decreased expression o
103 compared effects on expression of the medium neurofilament protein (NF-M), the RNA for which binds hn
104 amined this issue with respect to the medium neurofilament protein (NF-M).
105                                              Neurofilament proteins (NF-Ps), particularly, NF-H, are
106             With the SMI-32 antibody against neurofilament protein (NFP) as a marker of the motion-se
107 ern analysis indicated degradation of 68 kDa neurofilament protein (NFP), a calpain substrate.
108     Qualitatively, there were phosphorylated neurofilament protein (NFP)-immunoreactive inclusions an
109                                              Neurofilament proteins (NFP) are intermediate filaments
110 uclear binding protein and nonphosphorylated neurofilament proteins (NFP-ir).
111 hanisms that might affect the degradation of neurofilament proteins (NFPs) were examined in the dista
112                                              Neurofilament proteins (NFPs), the cytoskeletal proteins
113 ic protein, GFAP), neuronal differentiation (neurofilament proteins, NFPs), and/or photoreceptor diff
114 describe the expression of nonphosphorylated neurofilament protein (NPNFP) in the human vestibular br
115 e pattern of expression of nonphosphorylated neurofilament protein (NPNFP) might define additional su
116  next examined the effects of this truncated neurofilament protein on development of the nervous syst
117                                    Mammalian neurofilament proteins, particularly midsized (NF-M) and
118  fibrillary acidic protein and a decrease in neurofilament protein, proteolipid protein, and several
119 trictions and a more gradual accumulation of neurofilament protein proximal to the constrictions.
120 d), and approximately 90% of the accumulated neurofilament protein remained in the axon after deterge
121                      Axons immunolabeled for neurofilament protein show neuritic beading following Pb
122 oreactive to nNOS, and immunoreactivity to a neurofilament protein shows many labeled cells and fiber
123                           We also noted that neurofilament protein SMI31 immunoreactivity was increas
124 een fluorescent protein (GFP) with the heavy neurofilament protein subunit (NFH).
125 uction, but completely inhibited NGF-induced neurofilament protein synthesis.
126 stinctive cell types, two of which express a neurofilament protein that labels long-range projection
127                                These include neurofilament proteins that constitute the stress-respon
128 se in the phosphorylation of NF-M subunit of neurofilament proteins that correlated with an up-regula
129 , a monoclonal antibody to nonphosphorylated neurofilament proteins that labels pyramidal neurons in
130 e are associated with abnormal aggregates of neurofilament protein, the disorganization of the axonal
131  we have measured the level of two mammalian neurofilament proteins, the 68-kDa NF-L and the 66-kDa N
132  Our results strongly suggest that efficient neurofilament protein transport in vivo minimally requir
133 mmunocytochemical staining for S100 protein, neurofilament protein, tyrosine hydroxylase, and protein
134 eflected by reduced expression of myelin and neurofilament proteins, was common to the CC and cortex;
135 eflected by reduced expression of myelin and neurofilament proteins, was common to the CC and cortex;
136  SMI-32, which recognizes non-phosphorylated neurofilament protein, we distinguished separate caudal,
137 ns of cultured neurons expressing GFP-tagged neurofilament protein were bleached by excitation with t
138 bule-associated protein 5 and phosphorylated neurofilament protein were used.
139                  These data suggest that the neurofilament proteins were transported either as assemb
140 entin(+) SW13 cells, and with peripherin and neurofilament proteins when transfected into N2a cells.
141 ter injury there was 20% degradation of both neurofilament proteins while the breakdown of 68 kDa and
142 ar calcium signaling, and down-regulation of neurofilament proteins, with DLG4 and MAPT as major hub
143 0 days of darkness also enhanced the loss of neurofilament protein within deprived dLGN layers.
144 ssible that the preferential distribution of neurofilament protein within feedforward connections to
145 e, and also reversed the significant loss of neurofilament protein within originally deprived dLGN la
146 increased neurofilament number and levels of neurofilament proteins without altering axon caliber.

 
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