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1 ral irregularity of neuronal activity in the central nervous system.
2 s and can result in damage to the developing central nervous system.
3 of encephalitogenic effector T cells in the central nervous system.
4 tinic acetylcholine receptors present in the central nervous system.
5 most severe congenital malformations of the central nervous system.
6 degenerative and autoimmune diseases of the central nervous system.
7 elements following early development of the central nervous system.
8 ng the effects of metabolic disorders on the central nervous system.
9 imination of virally transduced cells in the central nervous system.
10 d did not require microglial function in the central nervous system.
11 excitatory neurotransmission throughout the central nervous system.
12 coupled receptor abundantly expressed in the central nervous system.
13 al role for this inflammatory protein in the central nervous system.
14 ith other neurodegenerative disorders of the central nervous system.
15 ct neighbouring cell types of the Drosophila central nervous system.
16 and relay signals from the periphery to the central nervous system.
17 environment that surrounds every cell of the central nervous system.
18 tanding issue in patterning of the embryonic central nervous system.
19 table diseases such as those that affect the central nervous system.
20 tebrates and a predominant expression in the central nervous system.
21 subunit with the greatest importance in the central nervous system.
22 for studies of neurological pathways in the central nervous system.
23 ent bleeding in joints, soft tissue, and the central nervous system.
24 ce induces inflammatory demyelination in the central nervous system.
25 rmation is delivered to and perceived by the central nervous system.
26 d interleukin-8 in the respiratory tract and central nervous system.
27 an often-fatal demyelinating disease of the central nervous system.
28 of sensorimotor function after injury to the central nervous system.
29 ressed by many developing neurons within the central nervous system.
30 lus timecourse is first reconstituted in the central nervous system.
31 ged in maintaining neuron-neuron adhesion in central nervous system.
32 cious sensations from visceral organs to the central nervous system.
33 us system infection and severe spread to the central nervous system.
34 and along neuroanatomical tracts within the central nervous system.
35 associated with obesity are expressed in the central nervous system.
36 s are fundamental synaptic organizers in the central nervous system.
37 o initiation of an autoimmune process in the central nervous system.
38 eptor (IGF-1R) controls this response in the central nervous system.
39 has multiple roles in the development of the central nervous system.
40 -related oligodendroglial protein in the rat central nervous system.
41 ia are the intrinsic immune sentinels of the central nervous system.
42 l that exhibits high viral burden within the central nervous system.
43 1 and serotonin interact at the level of the central nervous system.
44 uronal damage and BACE1 up-regulation in the central nervous system.
45 ly disseminating to colonize the purine-poor central nervous system.
46 er propensity for metastasis to bone and the central nervous system.
47 lerosis (MS) is an autoimmune disease of the central nervous system.
48 o define the role of O-GlcNAc cycling in the central nervous system.
49 k of capacity of this agent to penetrate the central nervous system.
50 rain, leading to suboptimal treatment in the central nervous system.
51 restrict the genetic ablation of Lpd to the central nervous system.
53 cells, leading to a more severe spectrum of central nervous system abnormalities than is typically s
54 findings, presence of microcephaly or other central nervous system abnormalities, and timing of infe
56 mediate excitatory neurotransmission in the central nervous system and are critically involved in br
57 Motor neurons are the output neurons of the central nervous system and are responsible for controlli
58 ttention due to its pleiotropic roles in the central nervous system and implications in various brain
59 preventing inflammatory tissue damage in the central nervous system and none directly promotes repair
60 he 2016 WHO classification of tumours of the central nervous system and on scientific developments si
61 t in primary DLBCL that occurred outside the central nervous system and ophthalmic regions (46.0 mont
63 icroglia are the resident macrophages of the central nervous system and play complex roles in the mil
64 al physiology of lymphatic drainage from the central nervous system and potential aberrations in neur
65 on quantitative trait loci in tissues of the central nervous system and relevant to transcriptional r
67 ng blood from the extracellular fluid in the central nervous system and thus presents an essential ob
68 ommon vascular anomalies that develop in the central nervous system and, more rarely, the retina.
69 MeHg as a neurotoxin impacts on the human central nervous systems and especially on the developing
70 in the mouse, reducing dissemination to the central nervous system, and decreasing reactivation of c
71 catecholamine neurotransmitters of the human central nervous system, and is involved in many behavior
74 ce expressing biologically active C3a in the central nervous system, and their respective wild-type c
75 lora to modulate ongoing inflammation in the central nervous system, and we also discuss the potentia
77 ne, typically classified as a disease of the central nervous system, appeared to be most genetically
78 he neurotoxic effects of cannabis use on the central nervous system as a result of how it affects ret
80 tal abnormalities during gestation, with the central nervous system being one of the most affected or
81 s on adipocytes and through signaling in the central nervous system by dampening sympathetic outflow
84 acute myeloid leukemia (1.9 [1.5-2.4]); and central nervous system cancer (1.8 [1.2-2.8]) experience
86 ced liver injury (DILI): antimicrobials; and central nervous system, cardiovascular and oncology ther
87 the high incidence of severe defects in the central nervous system caused by human cytomegalovirus (
89 and revealed involvement of a wide range of central nervous system cell types (eg, neurons, endothel
90 LRP2 is expressed on the surface of many central nervous system cells including neurons and oligo
93 ability of Salmonella to disseminate to the central nervous system (CNS) after oral infection in C57
94 flammatory environment is induced within the central nervous system (CNS) after WNV infection, leadin
97 rectional communication pathways between the central nervous system (CNS) and peripheral immune syste
98 on evidence of parallel degeneration of both central nervous system (CNS) and peripheral nervous syst
99 that may be associated with infection of the central nervous system (CNS) and severe neurological dis
100 Herpes simplex virus (HSV) infections of the central nervous system (CNS) are associated with signifi
103 tem, the limited capacity of regeneration of central nervous system (CNS) axons is a major obstacle f
106 by KSHV, we sought to determine whether the central nervous system (CNS) can be infected by KSHV in
109 B-preferring inhibitors for the treatment of central nervous system (CNS) disorders, we sought to ide
110 ges in gene expression that occur across the central nervous system (CNS) during neurological disease
111 Unlike nonchordates, amphioxus develops its central nervous system (CNS) from a neural plate that is
114 homogeneous, static magnetic field (SMF) on Central Nervous System (CNS) glial cells are less invest
116 other tissue-resident macrophages within the central nervous system (CNS) have essential roles in neu
117 understanding of immune surveillance of the central nervous system (CNS) have repeatedly provoked di
119 of phagocytic cells, play important roles in central nervous system (CNS) homeostasis and neural plas
121 status due to inflammation are a hallmark of central nervous system (CNS) infections with neurotropic
122 is a prevalent health issue that can lead to central nervous system (CNS) inflammation with long-term
123 cells (ASC) accumulate in various models of central nervous system (CNS) inflammation, including vir
125 nant unselected cohort with mainly relapsing central nervous system (CNS) inflammatory diseases.
126 Reactive astrocytes are strongly induced by central nervous system (CNS) injury and disease, but the
128 rkers for neuroinflammatory responses during central nervous system (CNS) invasion by trypanosomes an
129 lymerase chain reaction (PCR) is a marker of central nervous system (CNS) involvement in congenital h
132 elaborated by oligodendrocytes (OLs) in the central nervous system (CNS) is required for saltatory c
133 disorder where T cells attack neurons in the central nervous system (CNS) leading to demyelination an
134 was significantly associated with ocular and central nervous system (CNS) lesions and showed the stro
137 (MS) is an autoimmune disease targeting the central nervous system (CNS) mainly in young adults, and
139 ial fraction of the lipids incorporated into central nervous system (CNS) myelin are contributed by a
141 ination gene, Sex-lethal (Sxl), functions in central nervous system (CNS) neurons as part of a relay
144 injury-induced characteristics of the adult central nervous system (CNS) pose barriers to axonal reg
145 neuronal chemokine expression and decreased central nervous system (CNS) recruitment of T lymphocyte
147 ssociated with the development of a manifest central nervous system (CNS) synucleinopathy (odds ratio
149 an inflammatory demyelinating disease of the central nervous system (CNS) that is caused by autoreact
150 NS) must signal to the motor circuits of the central nervous system (CNS) through a series of pathway
151 that nanoparticles are able to enter to the central nervous system (CNS) through regions of altered
152 lity of myelin-reactive TH17 cells to invade central nervous system (CNS) tissue and protected the mi
154 ue to noninvasively visualize B cells in the central nervous system (CNS) to monitor MS disease progr
156 ied age as the only significant predictor of central nervous system (CNS) versus PNS involvement (>50
157 ated hemangioblastomas (VHL-HB) arise in the central nervous system (CNS), and are a leading cause of
159 n two unrelated consanguineous kindreds with central nervous system (CNS), cardiac, renal, and digit
160 D1) selectively affects motor neurons in the central nervous system (CNS), causing the adult-onset de
161 cosylceramide and glucosylsphingosine in the central nervous system (CNS), demonstrating target engag
162 obutyric acid (GABA) immunoreactivity in the central nervous system (CNS), eyes, optic ganglia and st
163 of white-matter tracts throughout the human central nervous system (CNS), including loss of all comm
164 ple sclerosis (MS) that directly damages the central nervous system (CNS), promotes immune cell infil
165 communication is the vascularization of the central nervous system (CNS), which is driven by neurona
166 s depends on the input and plasticity of the central nervous system (CNS), which may explain the abse
188 her tissues, immune cell presence within the central nervous system (CNS; microglia), as well as arou
190 e targets for a number of cardiovascular and central nervous system conditions, but the current drugs
191 tion pathways between gut microbiota and the central nervous system could include autonomic, neuroend
192 e role of the inflammasome in peripheral and central nervous system cytokine/chemokine inflammatory r
194 hway that regulates synaptic activity during central nervous system development and demonstrates a ro
195 mplicated in neuron-glia interactions during central nervous system development and in hair follicle
196 ntiated from hPSCs that may be used to model central nervous system development and serve as a potent
197 nc finger protein, ZIC2, a key regulator for central nervous system development, is a substrate of K-
200 ress and future perspectives for modeling of central nervous system disease and brain development in
203 criminators between those three inflammatory central nervous system diseases in adults and children t
204 protein (MOG) are associated with autoimmune central nervous system diseases like acute disseminated
207 licated in depression, addictions, and other central nervous system disorders and, thus, is an import
208 disease in childhood resulting in widespread central nervous system dysfunction and premature death.
209 neous condition characterized by progressive central nervous system dysfunction in association with a
210 cated that cellular processes related to the central nervous system (e.g., neurogenesis, synaptic pla
211 zapine readily enters the brain and occupies central nervous system-expressed DREADDs, whereas system
212 lamic neuropeptide hormone oxytocin is a key central nervous system factor in the regulation of food
216 ys critical roles in successive steps of the central nervous system formation during embryonic and fe
219 a role of GPR17 per se as an orchestrator of central nervous system functions, they challenge the uti
222 the role of insulin-responsive GLUT4 in the central nervous system has not been well characterized.
223 In addition, while multiple cells within the central nervous system have been involved in the develop
224 nizing physiological effects of drugs in the central nervous system have led to exploring protein-bas
225 s that underlie recovery after injury of the central nervous system have rarely been definitively est
226 study demonstrate that HE is associated with central nervous system hemichannel dysfunction, with amm
227 ing HIV-1 envelope glycoprotein 120 in their central nervous system (HIVgp120tg) mount a transient IF
229 lated RNA and dipeptide repeats in the mouse central nervous system increases double strand breaks an
231 RTANCE Astroviruses are an emerging cause of central nervous system infections in mammals, and astrov
232 ement responsive to steroids (CLIPPERS) is a central nervous system inflammatory syndrome predominant
234 ed (LIP) ultrasound on memory impairment and central nervous system injury in a rat model of vascular
236 erstanding of the processes occurring in the central nervous system is crucial to the development of
237 tural and functional motif of the vertebrate central nervous system is discrete clusters of neurons o
238 Axonal regeneration in the adult mammalian central nervous system is limited in part by the non-per
239 thesis that TMEM18 itself, acting within the central nervous system, is a plausible mediator of the i
240 istinguishes several cell types from the rat central nervous system, largely based on the relative pr
242 ry tract and in phrenic motor neurons of the central nervous system led us to address the individual
243 e of the small size of most terminals in the central nervous system, little is known about the regula
245 issue of JEM, Antila et al. demonstrate that central nervous system lymphatics develop in the mouse m
246 frequent responses in patients with primary central nervous system lymphoma but was associated with
248 uman tissues tested, and particularly in the central nervous system, many pathways are regulated at t
249 onal modifications (PTMs) reportedly tied to central nervous system maturation, myelin stability, and
250 5 and SLC4A10 expression and function in the central nervous system may affect the regulation of syst
251 ligible if they had symptomatic or untreated central nervous system metastases, had received anticanc
252 The control of the human body sway by the central nervous system, muscles, and conscious brain is
256 inductive interactions direct cells to form central nervous system (neural plate) or sensory placode
260 ytosine modification that is abundant in the central nervous system of mammals and which results from
261 -deficient activated T cells to the inflamed central nervous system of mice with experimental autoimm
263 of acute severe VZV infection affecting the central nervous system or the lungs in unrelated, otherw
264 ligoanuric renal failure, involvement of the central nervous system, or death), and interventions (ie
265 ood counteracts age-related changes in these central nervous system parameters, although the identiti
266 xamined multiple sclerosis lesions and other central nervous system pathologies with prominent myelin
268 etylcholine receptor (nAChR) is important in central nervous system physiology and in mediating sever
270 oposide (950 to 450 mg/m(2)) and intrathecal central nervous system prophylaxis while omitting mainte
272 control over gastrointestinal functions, the central nervous system provides extrinsic neural inputs
273 icroglia coordinate various functions in the central nervous system ranging from removing synaptic co
274 erapy thus has potential in the treatment of central nervous system-related pathologies, such as Alzh
276 Here we show that primary cells from the rat central nervous system respond differently to photo-toxi
277 othesized that ARV-mediated ER stress in the central nervous system resulted in chronic dysregulation
278 ly in extravascular compartments such as the central nervous system, resulting in either cerebrospina
280 n is actually elevated in the late embryonic central nervous system, suggesting that CFI might play a
282 (antidepressants, antipsychotics, and other central nervous system-targeted medications) are increas
283 lial cell population in the mature mammalian central nervous system that is distinct from astrocytes,
284 herapeutic intervention into diseases of the central nervous system that require the expression of la
287 ies have targeted different sites within the central nervous system to restore motor function followi
288 put, originated from different levels of the central nervous system, to the different compartments.
289 S) is a chronic demyelinating disease of the central nervous system traditionally characterized by an
291 maternal age increased risk of leukemia and central nervous system tumors, older paternal age was no
293 es of two neuronal classes in the C. elegans central nervous system, using VGLUT-pHluorin to monitor
295 ylase 11 (HDAC11) is highly expressed in the central nervous system where it has been reported to hav
296 R1) is abundantly expressed in the mammalian central nervous system, where it regulates intracellular
297 uids where DA is at low levels, e.g., in the central nervous system, which is the usual clinical prof
298 ce an acquired demyelinating syndrome of the central nervous system will have a monophasic disease co
299 t GEBR-32a is rapidly distributed within the central nervous system with a very favourable brain/bloo
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