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1 e coronavirus 2 from nasopharyngeal swab and cerebral spinal fluid.
2 mission tomography and glucose monitoring in cerebral spinal fluid.
3 aqueduct to the canalostomy due to influx of cerebral spinal fluid.
4 9 areas of normal appearing white matter and cerebral spinal fluid.
5 al canal where they block circulation of the cerebral spinal fluid.
6 infected hamsters using 2-microl aliquots of cerebral spinal fluid.
7 mixture of peptides dissolved in artificial cerebral spinal fluid.
8 ular space where they are transported to the cerebral spinal fluid.
9 leotide delivered by a single injection into cerebral spinal fluid.
11 jority of interneurons (21/25) in artificial cerebral spinal fluid (aCSF) exhibited spontaneous tonic
13 ted context, BLA was infused with artificial cerebral spinal fluid (ACSF) or ACSF containing an N-met
14 plasma, synthetic urine (SU), and artificial cerebral spinal fluid (aCSF) using ethyl acetate as the
17 is followed by microdialysis with artificial cerebral spinal fluid allowed isolation of 14C-glutamine
18 nclusion were absence of correlation between cerebral spinal fluid amyloid-beta1-42 and Boston naming
19 nal fluid t-tau, brain amyloid-beta load via cerebral spinal fluid amyloid-beta1-42 and vascular dise
20 rebral spinal fluid t-tau) and amyloid load (cerebral spinal fluid amyloid-beta1-42) all independentl
23 Notably, ALA and PBG concentrations in the cerebral spinal fluid and CNS regions were markedly elev
26 ulin forms in human neocortex, white matter, cerebral spinal fluid, and serum by immunostaining and m
29 S induces nuclear ASPP2 in vivo at the blood-cerebral spinal fluid barrier (the brain's barrier to in
31 isolated primary viruses from autopsy brain, cerebral spinal fluid, blood, spleen, and lymph node sam
32 observed to correlate with viral RNA in the cerebral spinal fluid but not with plasma viral load, co
33 ntrathecal (IT) delivery of AAV vectors into cerebral spinal fluid can avoid many issues, although di
36 ic modulator (NAM) that achieves exposure in cerebral spinal fluid (CSF) 2.5x above the in vitro IC(5
39 er analysis of neurofilament light chain and cerebral spinal fluid (CSF) alpha-synuclein oligomer loa
40 ciates investigated the status of HIV in the cerebral spinal fluid (CSF) and revealed ongoing presenc
42 one of two delivery devices showed improved cerebral spinal fluid (CSF) biomarker profiles and slowe
44 ng were reviewed to identify the presence of cerebral spinal fluid (CSF) clefts around the tumors.
46 concentrations (measured by immunoassay) in cerebral spinal fluid (CSF) from tuberculous meningitis
54 eatments for HD only alleviate symptoms, but cerebral spinal fluid (CSF) or central nervous system (C
61 v compartmentalization between the blood and cerebral spinal fluid (CSF) was apparent with all neurol
63 of the three constituent tissue types (i.e., cerebral spinal fluid (CSF), gray matter, white matter)
64 the presence of antiviral antibodies in the cerebral spinal fluid (CSF), indicating local maintenanc
65 orectal and lymph node tissues, bone marrow, cerebral spinal fluid (CSF), plasma, and very large numb
66 nvolved in the production and circulation of cerebral spinal fluid (CSF), suggesting that loss of mFu
67 ectivity between brain parenchymal fluid and cerebral spinal fluid (CSF), we reasoned enhancing drug
71 age fluid (n = 152), pleural fluid (n = 76), cerebral spinal fluid (CSF; n = 152), pericardial fluid
72 ment include the use of brain and spine MRI, cerebral spinal fluid cytology, neurological examination
74 rt of folates across the choroid plexus into cerebral spinal fluid due to inactivating mutations in t
75 0 expands functionality to urine, blood, and cerebral spinal fluid, enhancing the realism of blood sp
76 lar tonsillar crowding and restore posterior cerebral spinal fluid flow, but regional tissue biomecha
78 dividuals; and protein QTLs were measured in cerebral spinal fluid from 544 individuals and plasma fr
79 tify a proteolytic fragment of cystatin C in cerebral spinal fluids from patients diagnosed with mult
81 -67 exhibited robust in vivo activity in the cerebral spinal fluid glycine biomarker model in both ro
83 Notice of retraction: the article "Role of Cerebral Spinal Fluid in Space Flight Induced Ocular Cha
84 4 (ST4) was the predominant sequence type of cerebral spinal fluid isolates from cases of meningitis.
85 Age, temporal or hemorrhagic lesions, and cerebral spinal fluid lymphocytosis were significantly a
89 ell tolerated in humans and elevates cGMP in cerebral spinal fluid of healthy volunteers, confirming
93 95% CI, 1.13-1.56) and ACE protein levels in cerebral spinal fluid (OR per 1-SD decrease, 1.12; 95% C
95 ent and lumbar puncture for determination of cerebral spinal fluid phosphorylated tau (P-tau) and bet
97 ith neuroinflammatory symptoms, neutrophilic cerebral spinal fluid pleocytosis, and complement consum
98 ient neuroinflammation included neutrophilic cerebral spinal fluid pleocytosis, constitutive compleme
99 inflammatory secretome of AD iNs and patient cerebral spinal fluid revealed a neuronal senescence-ass
101 R analysis was used to genotype parasites in cerebral spinal fluid samples from 8 of 10 human immunod
102 dentify druggable targets in cPIIRS, patient cerebral spinal fluid samples underwent transcriptional
104 dult respiratory, pediatric stool, and adult cerebral spinal fluid specimens, and detected 64% of cli
107 olyadenylation sequences, ASO injection into cerebral spinal fluid successfully corrected Stmn2 pre-m
108 y (structural magnetic resonance imaging and cerebral spinal fluid t-tau) and amyloid load (cerebral
109 gnetic resonance images, neuronal injury via cerebral spinal fluid t-tau, brain amyloid-beta load via
111 plate brain as well as GM, white matter, and cerebral spinal fluid tissue probability maps to facilit
112 n increase in CXCL1 and CXCL10 levels in the cerebral spinal fluid, TNF-alpha expression in the epend
113 oit the interconnectivity of parenchymal and cerebral spinal fluid to enhance the amount of temozolom
114 and perfusing them with hyperoxic artificial cerebral spinal fluid to minimize peripheral chemorecept
118 e it exists in steady-state equilibrium with cerebral spinal fluid where it has the potential to serv
119 regulin activity is also detectable in human cerebral spinal fluid where its expression appears to be