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1 ler's murine encephalomyelitis virus-induced demyelinating disease.
2 icrocystic macular edema is not specific for demyelinating disease.
3 gression in a secondary progressive model of demyelinating disease.
4 ts the potential for cell-based treatment of demyelinating disease.
5 ovement disorders, psychiatric features, and demyelinating disease.
6 cephalitis, followed by a nonlethal, chronic demyelinating disease.
7 y chronic hemolysis and relapsing peripheral demyelinating disease.
8 lammatory and proliferative genes to promote demyelinating disease.
9 lding a comprehensive model for TMEV-induced demyelinating disease.
10 l role in the pathogenicity of virus-induced demyelinating disease.
11 ion against the development of virus-induced demyelinating disease.
12 t into the mechanisms promoting inflammatory demyelinating disease.
13 al infection, leading to the pathogenesis of demyelinating disease.
14 undermine vitamin D3-mediated inhibition of demyelinating disease.
15 nonuclear cells (PBMCs) of 228 subjects with demyelinating disease.
16 ler's murine encephalomyelitis virus-induced demyelinating disease.
17 T cell response offers protection from this demyelinating disease.
18 ENT Multiple sclerosis is a severe, chronic, demyelinating disease.
19 n of viral proteins during the late stage of demyelinating disease.
20 t to both viral persistence and TMEV-induced demyelinating disease.
21 model for studies of viral encephalitis and demyelinating disease.
22 ctive in experimental models of inflammatory demyelinating disease.
23 cells play in development and progression of demyelinating disease.
24 ult pathway in the CNS in nonimmune-mediated demyelinating disease.
25 specific CD4(+) T cell responses and reduced demyelinating disease.
26 tiate oligodendrocyte survival in autoimmune demyelinating disease.
27 the CNS which contributes to development of demyelinating disease.
28 he first confirmed antigenic target in human demyelinating disease.
29 al therapeutical avenue for lesion repair in demyelinating disease.
30 n HLA class II molecules in inflammatory and demyelinating disease.
31 ction and induce the pathogenesis of chronic demyelinating disease.
32 istance or susceptibility to virally induced demyelinating disease.
33 ple sclerosis (MS) is a human CNS autoimmune demyelinating disease.
34 d progression of the autoimmune response and demyelinating disease.
35 ation in OPCs, contributing to Th17-mediated demyelinating disease.
36 sponses and contribute to the development of demyelinating disease.
37 associated with an inflammatory white matter demyelinating disease.
38 f antiserum to IFN-beta led to a more severe demyelinating disease.
39 an affect the development and progression of demyelinating disease.
40 ogically distinct subsets of subjects with a demyelinating disease.
41 loped significantly less severe TMEV-induced demyelinating disease.
42 e of tissue injury in experimental and human demyelinating disease.
43 specific marker for a central nervous system demyelinating disease.
44 subsets of patients with different forms of demyelinating disease.
45 nent role in the development of TMEV-induced demyelinating disease.
46 t leukodystrophy (ADLD), a fatal adult onset demyelinating disease.
47 accelerating myelin clearance and improving demyelinating disease.
48 susceptibility of mice to the development of demyelinating disease.
49 a key target for enhancing myelin repair in demyelinating diseases.
50 A class II genes in chronic inflammatory and demyelinating diseases.
51 e for oligodendrogenesis and remyelinaton in demyelinating diseases.
52 PCs) offer a promising approach for treating demyelinating diseases.
53 and adhesion and has direct implications for demyelinating diseases.
54 may provide new avenues in the treatment of demyelinating diseases.
55 ual function and may be a general feature of demyelinating diseases.
56 humans, may find further therapeutic use in demyelinating diseases.
57 ole of the innate immune system in mediating demyelinating diseases.
58 esoxime could be useful for the treatment of demyelinating diseases.
59 his pool of progenitors to replace myelin in demyelinating diseases.
60 nesis of central nervous system inflammatory demyelinating diseases.
61 rovide an effective therapeutic approach for demyelinating diseases.
62 JME may shed new light on MS and other human demyelinating diseases.
63 yelination, which has broad implications for demyelinating diseases.
64 ernodal axon in paraneoplastic syndromes and demyelinating diseases.
65 c proteins in myelin with relevance to human demyelinating diseases.
66 mportant role in the pathogenesis underlying demyelinating diseases.
67 xonal degeneration that occurs in peripheral demyelinating diseases.
68 ying pathogenesis in autoimmune inflammatory demyelinating diseases.
69 e development of multiple sclerosis or other demyelinating diseases.
70 sclerosis and a composite end point of other demyelinating diseases.
71 ral nervous system inflammatory and acquired demyelinating diseases.
72 nt diagnoses of multiple sclerosis and other demyelinating diseases.
73 al relationship between qHPV vaccination and demyelinating diseases.
74 ferentiation in multiple sclerosis and other demyelinating diseases.
75 development of multiple sclerosis and other demyelinating diseases.
76 aluate their roles and clinical relevance in demyelinating diseases.
77 ent neuron-supportive programme in inherited demyelinating disease?
78 ecific CD8(+) T cells in the pathogenesis of demyelinating disease, a single amino acid substitution
79 6 transgene (IL-6 Tg) develop a TMEV-induced demyelinating disease accompanied by an increase in vira
81 Multiple sclerosis (MS) is an autoimmune demyelinating disease and a common cause of neurological
82 ive lesions are an uncommon manifestation of demyelinating disease and can pose a diagnostic challeng
83 In multiple sclerosis (MS), an autoimmune demyelinating disease and common cause of neurodegenerat
84 r vitamin D in the regenerative component of demyelinating disease and identify a new target for remy
85 l as other leukocytes for the development of demyelinating disease and may represent a novel therapeu
86 ation abnormalities seen in association with demyelinating disease and optic neuritis, although evide
87 and other cell types for the development of demyelinating disease and suggest that expression of VCA
88 neficial both for enhancing remyelination in demyelinating diseases and for increasing neural plastic
89 the potential for enhanced remyelination in demyelinating diseases and increased neural plasticity i
90 target, as well as an imaging biomarker, for demyelinating diseases and potentially for other disease
91 hat implicate glial gap junction proteins in demyelinating diseases and the therapeutic potential of
93 red in patients with neuromyelitis optica, a demyelinating disease, and are now being used to diagnos
95 design of neuroprotective strategies for CNS demyelinating disease, and our model identifies the spik
96 hich the olfactory system is affected in CNS demyelinating diseases, and raises intriguing questions
101 irmed that NFM was not a critical Ag driving demyelinating disease because NFM18-30-specific T cells
102 d cell leukodystrophy (GLD), a genetic fatal demyelinating disease, because its rapidly progressive d
104 immune response on development of autoimmune demyelinating disease by altering the innate immune resp
105 unogenic in C57BL/6 mice but fails to induce demyelinating disease by polyclonal T cells despite havi
106 dy definitively demonstrates that autoimmune demyelinating disease can be driven by distinct Th-polar
107 ultifocal leukoencephalopathy (PML), a fatal demyelinating disease caused by JC virus (JCV) infection
108 id-cell leukodystrophy (GLD) is an inherited demyelinating disease caused by the deficiency of the ly
109 al leukoencephalopathy (PML) is a lethal CNS demyelinating disease caused by the human neurotropic po
112 te ratio, 0.90 [95% CI, 0.70-1.15]) or other demyelinating diseases (crude incidence rates, 7.54 even
114 ng SHP-1 (me/me) display severe inflammatory demyelinating disease following inoculation with the The
115 ) from SJL/J mice, susceptible to autoimmune demyelinating disease following Theiler's virus (TMEV) i
116 nterleukin-6 (IL-6) levels contribute to the demyelinating disease found in chronically infected SJL/
118 MHV CNS infection and developed progressive demyelinating disease, germline IgM produced in activati
120 hocytes in the pathophysiology of autoimmune demyelinating disease has led to a renewed interest in B
121 ed that myelitis occurring in the idiopathic demyelinating diseases (i.e., multiple sclerosis versus
123 spectrum disorders (NMOSD) are inflammatory demyelinating diseases (IDD) with a specific biomarker,
124 D8 T cells results in an attenuated clinical demyelinating disease in C57BL/6 mice with immunization-
126 that has been linked to JME, an inflammatory demyelinating disease in Japanese macaques that mimics m
129 yelitis virus (TMEV)-induced immune-mediated demyelinating disease in susceptible mouse strains has b
130 itis virus (TMEV) induces an immune-mediated demyelinating disease in susceptible mouse strains such
131 yelitis virus (TMEV) induces immune-mediated demyelinating disease in susceptible SJL/J mice but not
132 yelin can be replaced after injury or during demyelinating diseases in a regenerative process called
134 cells against VP3(159-166), did not develop demyelinating disease, in contrast to wild-type virus or
135 dence ratio, 1.05 [95% CI, 0.79-1.38]; other demyelinating diseases: incidence ratio, 1.14 [95% CI, 0
136 risk factor for central nervous system (CNS) demyelinating diseases including multiple sclerosis (MS)
137 ar endothelium is a key step in inflammatory demyelinating diseases including multiple sclerosis (MS)
138 in the development of central nervous system demyelinating diseases, including multiple sclerosis, re
139 cations of resveratrol in human inflammatory demyelinating diseases, including multiple sclerosis.
140 on with these epitopes on the development of demyelinating disease indicated that capsid-specific CD4
141 urine encephalomyelitis virus (TMEV)-induced demyelinating disease is a relevant mouse model for the
142 ibronectin and vitronectin deposition during demyelinating disease is an important influence on micro
144 genesis of multiple sclerosis (MS) and other demyelinating diseases is controversial, in part because
145 Multiple sclerosis (MS), an inflammatory demyelinating disease, is a major cause of neurological
146 patient who died from a rapidly progressing demyelinating disease known as progressive multifocal le
149 SIRT1 reduces neuronal loss in this chronic demyelinating disease model and that this is associated
150 urine encephalomyelitis virus (TMEV)-induced demyelinating disease model of multiple sclerosis that C
152 in the pathogenesis of the human autoimmune demyelinating disease multiple sclerosis (MS) and in its
159 act role(s) of the cytokine IFN-gamma in the demyelinating disease multiple sclerosis remain controve
160 of permanent disability in the inflammatory demyelinating disease multiple sclerosis, but no therapi
166 spinal cord injury, peripheral nerve injury, demyelinating disease, neuromuscular disorders, and seiz
169 euromyelitis optica (NMO) is an inflammatory demyelinating disease of spinal cord and optic nerve cau
170 ifocal leukoencephalopathy (PML) is a severe demyelinating disease of the brain caused by JC virus (J
171 sive multifocal leukoencephalopathy (PML), a demyelinating disease of the brain caused by the polyoma
172 Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the central nervous system (CNS
173 ple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS
174 Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system (CNS
178 ple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS
179 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system asso
180 Neuromyelitis optica is an inflammatory demyelinating disease of the central nervous system asso
181 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system caus
182 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system caus
183 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system in w
185 omyelitis optica, an idiopathic inflammatory demyelinating disease of the central nervous system pred
186 tifocal leukoencephalopathy (PML) is a fatal demyelinating disease of the central nervous system resu
188 ve multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system that
189 s Devic's disease) is an idiopathic, severe, demyelinating disease of the central nervous system that
192 h multiple sclerosis, a chronic inflammatory demyelinating disease of the central nervous system with
194 onsidered the prototype for an inflammatory, demyelinating disease of the central nervous system, mod
195 autoimmune, inflammatory, neurodegenerative, demyelinating disease of the central nervous system, pre
196 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system.
197 leukoencephalopathy (PML) is an often-fatal demyelinating disease of the central nervous system.
198 Multiple sclerosis is a chronic inflammatory demyelinating disease of the central nervous system.
199 ple sclerosis (MS) is the major inflammatory demyelinating disease of the central nervous system.
200 expression of viral proteins, and induces a demyelinating disease of the central nervous system.
201 sclerosis (MS) (n=43,879), an inflammatory, demyelinating disease of the central nervous system.
203 euromyelitis optica (NMO) is an inflammatory demyelinating disease of the CNS and affects women of ch
204 Multiple sclerosis (MS) is an inflammatory demyelinating disease of the CNS and remyelination in MS
206 lls, and its role in autoimmune inflammatory demyelinating disease of the CNS has not been studied.
207 Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the CNS mediated by self-reacti
209 tiple sclerosis (MS), a chronic inflammatory demyelinating disease of the CNS of presumed autoimmune
210 Multiple sclerosis (MS) is an autoimmune demyelinating disease of the CNS resulting from a progre
211 sclerosis (MS) is an autoimmune inflammatory demyelinating disease of the CNS that causes disability
212 ultiple sclerosis (MS) is an immune-mediated demyelinating disease of the CNS that has been linked wi
213 AE) is a CD4(+) T cell-mediated inflammatory demyelinating disease of the CNS that serves as a model
214 mmune encephalomyelitis is a T cell-mediated demyelinating disease of the CNS that serves as a model
215 ultiple sclerosis (MS) is an immune-mediated demyelinating disease of the CNS, and CD8 T cells are th
216 Multiple sclerosis is a sexually dimorphic, demyelinating disease of the CNS, and experimental aller
223 ultiple Sclerosis (MS) is an immune-mediated demyelinating disease of the human central nervous syste
224 Multiple Sclerosis (MS) is an inflammatory demyelinating disease of the human central nervous syste
225 e sclerosis (MS) is an inflammatory-mediated demyelinating disease of the human central nervous syste
227 tifocal leukoencephalopathy (PML) is a fatal demyelinating disease of the white matter affecting immu
228 ve multifocal leukoencephalopathy (PML) is a demyelinating disease of the white matter of the human b
229 m the traditional view of a T cell-mediated, demyelinating disease of the white matter to include a b
230 terogeneous group of idiopathic inflammatory demyelinating diseases of the central nervous system is
231 ise for more precise diagnosis of idiopathic demyelinating diseases of the central nervous system.
232 w diagnostic markers in these two autoimmune demyelinating diseases of the central nervous system.
233 ne encephalomyelitis (EAE), are inflammatory demyelinating diseases of the CNS that are suppressed by
235 therapeutic modulation of ERK1/2 activity in demyelinating disease or peripheral neuropathies must be
236 trated to be important in the development of demyelinating disease presumably by attracting inflammat
238 virus (JCPyV) causes the rapidly progressing demyelinating disease progressive multifocal leukoenceph
239 mavirus and the causative agent of the fatal demyelinating disease progressive multifocal leukoenceph
240 tion and is the causative agent of the fatal demyelinating disease progressive multifocal leukoenceph
241 ty of the population and can cause the fatal demyelinating disease progressive multifocal leukoenceph
242 compromised individuals results in the fatal demyelinating disease progressive multifocal leukoenceph
243 ression, JCV can infect the brain, causing a demyelinating disease, progressive multifocal leukoencep
244 tral nervous system and chronic inflammatory demyelinating disease, providing an experimental animal
245 finding may have important implications for demyelinating diseases, psychiatric disorders, and cogni
247 urine encephalomyelitis virus (TMEV)-induced demyelinating disease serves as a relevant mouse model f
248 composition and low MBP concentration, as in demyelinating disease, show structural instabilities and
249 ising strategies to advance the treatment of demyelinating diseases.SIGNIFICANCE STATEMENT The benefi
250 ystem (CNS) causes an immune system-mediated demyelinating disease similar to human multiple sclerosi
251 reported in patients that recover from acute demyelinating diseases such as Guillain-Barre syndrome.
252 ss of visual function frequently accompanies demyelinating diseases such as multiple sclerosis (MS) a
253 tions including central nervous system (CNS) demyelinating diseases such as multiple sclerosis (MS) a
254 erapy in the CNS, particularly for long-term demyelinating diseases such as multiple sclerosis (MS).
255 elin regeneration can occur spontaneously in demyelinating diseases such as multiple sclerosis (MS).
256 therapeutic approaches for the treatment of demyelinating diseases such as multiple sclerosis (MS).S
257 ul in many neurological disorders, including demyelinating diseases such as multiple sclerosis and th
259 nstitute clinically debilitating sequelae in demyelinating diseases such as multiple sclerosis, but t
260 axons, associated with traumatic injury and demyelinating diseases such as multiple sclerosis, cause
271 hat Shp2 is a relevant therapeutic target in demyelinating diseases such as multiple sclerosis.SIGNIF
272 target of axonal protection in inflammatory demyelinating diseases, such as multiple sclerosis and p
275 BP is an abundant myelin protein involved in demyelinating diseases, such as multiple sclerosis.
276 gene expression and induces an inflammatory demyelinating disease that is thought to be immune media
277 ssive multifocal leukoencephalopathy, a rare demyelinating disease that occurs in the setting of prol
278 autoimmune encephalomyelitis, an autoimmune demyelinating disease that resembles multiple sclerosis.
279 are, typically fatal, central nervous system demyelinating disease that results from reactivation of
281 ically useful as immunomodulatory agents for demyelinating diseases through a novel mechanism involvi
283 ler's murine encephalomyelitis virus-induced demyelinating disease (TMEV-IDD), a well-established ani
286 nying immune responses in the development of demyelinating disease, transgenic mice expressing the P1
287 ve multifocal leukoencephalopathy (PML) is a demyelinating disease triggered by infection with the hu
288 iple sclerosis cases and 3300 cases of other demyelinating diseases were identified, of which 73 and
289 peutic enhancement of remyelination in those demyelinating diseases where GPR17 is highly expressed,
290 sceptible mice results in an immune-mediated demyelinating disease which is considered a relevant vir
291 e innate immune response developed a reduced demyelinating disease which was associated with a decrea
292 with TMEV induces the development of chronic demyelinating disease, which is considered a relevant in
293 specific CD4(+) T cell responses and reduced demyelinating disease, which was associated with decreas
294 onfirmed central nervous system inflammatory demyelinating disease who had undergone either diagnosti
295 s virus (JHMV) results in an immune-mediated demyelinating disease with clinical and histologic simil
297 Multiple sclerosis (MS) is a multifocal demyelinating disease with progressive neurodegeneration
298 e sclerosis (MS) are considered inflammatory demyelinating diseases with distinguishing pathological
299 titis virus (JHMV) develop acute and chronic demyelinating diseases with histopathological similariti
300 mmune cell infiltration in neuroinflammatory demyelinating diseases; yet, the causal link between inf
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