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1 n child and parent in co-construction of the human brain.
2 evaluate synaptic 5-HT changes in the living human brain.
3 ntribute to the diverse molecular network of human brain.
4  cytoarchitectures resembling the developing human brain.
5 oundation for understanding circuitry in the human brain.
6 holesterol metabolism and homeostasis in the human brain.
7 lity to study neurophysiology in situ in the human brain.
8 e of the complex biological functions of the human brain.
9 stems and is asymmetrically organized in the human brain.
10 lticellular network observed in HIV-infected human brain.
11 bstantially enhanced flatmaps of the rat and human brain.
12 ilamentous alpha-synuclein inclusions in the human brain.
13 e cell, multiunit, and LFP activity from the human brain.
14 ry mechanisms of conscious processing in the human brain.
15  native A(2A)R-D(2)R heteromers in mouse and human brain.
16 leavage products, are soluble and present in human brain.
17 combined, and enable novel inferences in the human brain.
18 e neuromodulation of discrete regions in the human brain.
19 ally, we provide proof of application to the human brain.
20 ionship to the functional segregation of the human brain.
21 ajectory of cortical Abeta deposition in the human brain.
22 ies have provided important insight into the human brain.
23 full-length coding transcripts of CACNA1C in human brain.
24  is sustained by large-scale networks in the human brain.
25 ate propagation and neurodegeneration in the human brain.
26 s as one of the most remarkable feats of the human brain.
27 ising ligand to quantify M1 receptors in the human brain.
28 erence framework of the developing and adult human brain.
29 fect window to study these principles in the human brain.
30 s to explore acute effects of alcohol on the human brain.
31 ms of fear acquisition and extinction in the human brain.
32 it is a specific characteristic of the aging human brain.
33 functional and architectonic landmark in the human brain.
34 [Formula: see text] components images of the human brain.
35 l patterns of neural activity throughout the human brain.
36 quantitative methods of (18)F-PI-2620 in the human brain.
37  at revolutionizing our understanding of the human brain.
38 tool to investigate dopamine function in the human brain.
39 ncy content of local field potentials in the human brain.
40 s under different conditions directly in the human brain.
41  consistent histology reconstructions of the human brain.
42 dered to be a critical specialization of the human brain.
43 tions of facial attractiveness emerge in the human brain.
44  since some of them are primary expressed in human brain.
45 development, evolution, and pathology of the human brain.
46 tion is very fragmentary, especially for the human brain.
47 bodies and microglial processes in mouse and human brain.
48 ying the location of face-selectivity in the human brain.
49 structures could be identified in 10 healthy human brains.
50 barely detectable in rodents but abundant in human brains.
51  expression changes were mostly conserved in human brains.
52 roplets in microglia with aging in mouse and human brains.
53 ies in rodents and imaging-based analyses of human brains.
54  of SCGN staining differ between rodents and human brains.
55 GO1 coimmunoprecipitated with BK channels in human brain, 2) coexpression of LINGO1 and BK channels r
56 re present in the inferior temporal gyrus of human brains; (2) Deltatau314 proteins are generated fro
57 present functional neuroimaging study of the human brain, a multidomain protocol was utilized to inve
58 om multivoxel and multielectrode patterns of human brain activity while human participants (both sexe
59 ephalography (MEG/EEG) non-invasively record human brain activity with millisecond resolution providi
60 ounding variety of domains, and even predict human brain activity-raising the exciting possibility th
61 tion than lower processing levels, as in the human brain, activity in low-level visual areas should e
62 resent in ~10% of neurons, SVs in developing human brain affect a comparable number of bases in the g
63                           The regions of the human brain affected on neuroimaging are similar to the
64                           Methods: Fifty-one human brain and 29 human heart tissue samples were scree
65 stem that produces sex/gender differences in human brain and behavior.
66 tified novel MDD-methylation associations in human brain and blood samples at a cell type-specific le
67  spectrum and regional variation of sQTLs in human brain and demonstrates that such regional variatio
68 al processes is a fundamental feature of the human brain and drives symptom lateralization in Parkins
69 NLK levels are significantly decreased in HD human brain and HD models.
70 ptible to the rs6971 genetic polymorphism in human brain and heart samples.
71 using in vitro competition binding assays in human brain and heart; assess whether the in vivo charac
72 ide an overview of epigenomic mapping in the human brain and highlight findings of particular relevan
73        The basic role of this network in the human brain and how it may have evolved to enable comple
74 ral to this formulation is the fact that the human brain and immune system are principally designed t
75 e visuomotor integration (VMI) system in the human brain and investigated the topology approximation
76 layer in modulating neuronal function in the human brain and propose that its localization in both gl
77  to the shared loci, 65 are expressed in the human brain and show cell type-specific expression profi
78  ITIH3 may have a role in the development of human brain and suggested a cis-eQTL effect for rs253562
79 ontrol complex networks originating from the human brain and we discover that certain brain cortex re
80  of methodological difficulties in analyzing human brains and the confounds due to a lifetime of illn
81 e cellular and structural development of the human brain, and allow the investigation of the intricat
82  compared and contrasted with the endogenous human brain, and highlight experimental strategies to us
83                           The biology of the human brain, and in particular the dynamic interactions
84 n heterogeneity is a characteristic of aging human brain, and may influence aging-related changes in
85 5, hEAAT5v at the mRNA, and protein level in human brain, and show that populations of human cortical
86 ecific epigenome in complex tissues like the human brain, and the potential of such approaches to bet
87 nsitive to synaptic serotonin release in the human brain, and when combined with a d-amphetamine chal
88 A has been detected in AD amyloid plaques in human brains, and treatment with the antiviral acyclovir
89                                       In the human brain, APOE and NFAT are selectively dysregulated
90            White matter abnormalities of the human brain are implicated in typical aging and neurodeg
91 s and consequences of sex differences in the human brain are poorly characterized and hotly debated.
92 rences found in comparative studies with the human brain are simply due to technical factors or speci
93 ctures of alpha-synuclein filaments from the human brain are unknown.
94  of AMPAR subunit gene expression in healthy human brains as well as the transcriptional E/I (tE/I) r
95                 (18)F-CFA accumulates in the human brain at 15% of blood levels (0.08 +/- 0.01 and 0.
96  derived from a 3D histological atlas of the human brain at 20-micrometer isotropic resolution (BigBr
97      Ex vivo imaging enables analysis of the human brain at a level of detail that is not possible in
98 the 1960s, the first tools for measuring the human brain at work were becoming available.
99 nal gene expression as measured by the Allen Human Brain Atlas (AHBA).
100 Integrated analysis of single-cell and Allen Human Brain Atlas expression data reveal somatostatin in
101                                 Leveraging a human brain atlas of post-mortem gene expression, we fou
102 levant for cannabinoid signaling (from Allen Human Brain Atlas postmortem tissue) were associated wit
103 pproximation of the VMI network to the Allen Human Brain Atlas, a whole-brain transcriptome-wide atla
104 ition of 3702 human brain samples from Allen Human Brain Atlas.
105 es, before evaluating the connections in the human brain based on diffusion magnetic resonance imagin
106 cted during emotional episodes-measuring the human brain, body, and subjective experience-and compare
107 n assess neural activity in all areas of the human brain but the olfactory bulb (OB).
108              Glioblastoma is the most common human brain cancer entity and is maintained by a gliobla
109 dentifies an unanticipated role of Norrin in human brain cancer progression.
110                   The chromatin landscape of human brain cells encompasses key information to underst
111                                 By culturing human brain cells with physiological microenvironmental
112 hanges in the DNA, is a common phenomenon in human brain cells, with potential functional consequence
113 ise for their model of resource-rationality: human brains co-process information with their environme
114                                       In the human brain, common fMRI methods such as cluster correct
115 ll-characterized networks of interest in the human brain connectome.
116 Recent progress in deciphering mechanisms of human brain cortical folding leave unexplained whether s
117 tion of size-fractionated, native, mouse and human brain-derived Abeta assemblies.
118  offer an unprecedented opportunity to study human brain development and dysfunction.
119 ically relevant model system to study normal human brain development and neurological diseases.
120 euron subtypes is essential for the study of human brain development and the search for potential cel
121                                        Since human brain development appear very sensitive to low T4
122 nding gene expression (dys)regulation across human brain development as a major contributor to psychi
123                                      Because human brain development cannot be studied in vivo, scien
124 terest in studying individual differences in human brain development in order to predict mental healt
125                                              Human brain development involves a finely tuned cascade
126                                              Human brain development is influenced by early-life expe
127                                              Human brain development is optimized to learn from envir
128 n deterministic, and prolonged plasticity in human brain development may also allow for subsequent am
129 om adult mouse models and in vitro models of human brain development suggest that altered lipid metab
130 rganoids has opened a window into aspects of human brain development that were not accessible before,
131  Prenatal cannabis exposure (PCE) influences human brain development, but it is challenging to model
132 be applied to address questions pertinent to human brain development, disease, and evolution.
133                    YIPF5 is expressed during human brain development, in adult brain and pancreatic i
134  and central role of the CCR4-NOT complex in human brain development.
135 lar matrix components that are essential for human brain development.
136 ic needs and to support RGC proliferation in human brain development.
137 different cell types is key to understanding human brain development.
138 s can be used to understand heterogeneity in human brain development.
139 C) to investigate the effect of PCE on early human brain development.
140 tion to inhibition (E/I ratio) imbalances in human brain diseases, is a highly relevant functional me
141 ta now support a surprising role in prenatal human brain disorders as well.
142  CD4 T cell population in both the mouse and human brain, distinct from circulating CD4 T cells.
143 cellular and molecular events that build the human brain during embryogenesis and of how abnormalitie
144 reo-EEG/polysomnography possible only in the human brain during presurgical epilepsy evaluation, we e
145 uild a more comprehensive picture of how the human brain encodes and processes outcome value.
146 ings in 27 male volunteers, we show that the human brain encodes the summary value of an extended seq
147 In inflammatory conditions, costimulation of human brain endothelial cells by NMDA agonists (NMDA or
148 nhibition of P-gp efflux in cells, including human brain endothelial cells, was observed with the lin
149 osin light chain and subsequent shrinkage of human brain endothelial cells.
150                          Larval cysts in the human brain eventually resolve and either disappear or l
151 ovides a resource for further exploration of human brain evolution and function.
152 ng the emergence of novel genes important in human brain evolution.
153 nd its plasticity.SIGNIFICANCE STATEMENT The human brain exhibits a remarkable ability to support a v
154             An efficient network such as the human brain features a combination of global integration
155                          The mouse, rat, and human brain flatmap vector graphics files (Adobe Reader/
156       Scientists have been fascinated by the human brain for centuries, yet knowledge of the cellular
157 entions.SIGNIFICANCE STATEMENT Understanding human brain function and developing new treatments requi
158                        Adolescent changes in human brain function are not entirely understood.
159 ies, the effects of kappa-opioid agonists on human brain function are not well-understood.
160  understanding the remarkable flexibility of human brain function despite having to rely on fixed ana
161 ain activity and pushes our understanding of human brain function further along the spectrum from str
162                This pattern of SA effects on human brain function is strikingly similar to that of ot
163 in the functional repertoire associated with human brain function, which is impossible to explain thr
164 ional preclinical nonhuman primate model for human brain function.
165 come popular as a nonhuman primate model for human brain function.
166 es to better understand the genetic basis of human brain function.
167 ated transcriptomic data from the developing human brain, genome-wide association findings for SCZ an
168                                          The human brain has inherent methodology to efficiently inte
169 acranial electrical stimulation (iES) of the human brain has long been known to elicit a remarkable v
170 , in the language dominant hemisphere of the human brain, has been adapted to serve higher speech fun
171 ental impact of recreational drug use on the human brain have bolstered support for draconian drug po
172          Studies that have imaged the living human brain have found only a small number of sex differ
173 honates endowed with relevant affinities for human brain I(2)-IR.
174 haracterization of circRNA expression in the human brain, in nearly 200 human brain samples, from bot
175 stress and inflammatory cytokines affect the human brain, increasing the risk for mood and cognitive
176 a from putamen and substantia nigra from 117 human brains, interrogating regulation at different RNA
177                                          The human brain is a complex organ that consists of several
178  indicates that recent adaptive evolution of human brain is causally involved in basic principles of
179 st of our knowledge about activations in the human brain is derived from studies of responses to exte
180 es, stores, and processes information in the human brain is one of the outstanding scientific challen
181                                          The human brain is organized into large-scale networks ident
182                                          The human brain is specialized for face processing, yet we s
183 of the genetic control of gene expression in human brain is vital considering this is the likely modu
184 he Broca's language production region in the human brain) is involved in the cognitive selection of o
185 he existence of mosaic SVs in the developing human brain, likely arising from cell proliferation duri
186                         The Organization for Human Brain Mapping (OHBM) has been active in advocating
187                             In recent years, human brain mapping has strongly benefited from enhanced
188                         The Organization for Human Brain Mapping undertook a group effort to gather h
189 elial interactions in both animal models and human brain metastasis samples.
190 on Economo, are invaluable for understanding human brain microstructure and its relationship with fun
191 the miR-15a/16-1 cluster in primary mouse or human brain microvascular endothelial cell cultures enha
192 es of virus egress in infected, nonpolarized human brain microvascular endothelial cells (HBMECs) and
193 irulent flavivirus that persistently infects human brain microvascular endothelial cells (hBMECs), th
194 lium was confirmed by protection of cultured human brain microvascular endothelial cells from hydroge
195 ar 3D neurovascular unit organoid containing human brain microvascular endothelial cells, pericytes,
196 , similar observations were made in cultured human brain microvessel endothelial cells, where ADMA in
197 and evaluate it in a sample of 401 realistic human brain models from healthy subjects aged 16-83.
198 ased extended frontal connectivity, allowing human brains more efficient cross talk between frontal a
199 epresentation of temporal information in the human brain needed to form episodic memories.
200 ion from node to connected node in a natural human brain network and support the idea that neurons th
201    However, methods to measure E/I ratios in human brain networks are lacking.
202 onnected neuron, similar propagation through human brain networks has not been fully documented.
203 y in detail the synaptic organization of the human brain obtained from autopsies, yielding excellent
204 hat shape the distinctive development of the human brain occur in the embryonic and fetal stages-stag
205 riguing parallels to diminished MT levels in human brains of AD.
206 with increasing functional sophistication of human brain organisation.
207                             We conclude that human brain organization is disrupted during adolescence
208 s gap, we developed a three-dimensional (3D) human brain organoid (hBORG) model containing major cell
209 culture method that can be used not only for human brain organoids but also for many other human orga
210 ure alpha-synuclein in the culture medium of human brain organoids generated from normal and idiopath
211                                              Human brain organoids provide unique platforms for model
212 e impairment in MeCP2 mutant region-specific human brain organoids that were rescued by JQ1.
213             These findings were confirmed in human brain organoids.
214 -resolution histological reconstruction of a human brain, our study showed that the dominant axis of
215 1 expression in the cerebellum of postmortem human brains (p = 4.7e-5).
216 se organoids to pioneer new understanding of human brain pathology.
217                               Interestingly, human brains possess the same mechanistic ingredients th
218 l University, Advanced Innovation Center for Human Brain Protection, National Key Research and Develo
219 then apply the method to profile the complex human brain proteome of Alzheimer's disease (AD).
220 CANCE STATEMENT Single-neuron studies of the human brain provide a unique window into the computation
221 inking multivariate response patterns of the human brain recorded with functional magnetic resonance
222        While associations between individual human brain regions and environmental or genetic factors
223 uld demonstrate spatial correspondences with human brain regions showing central/peripheral biases.
224 n co-expression networks constructed from 10 human brain regions.
225  three independent studies, covering diverse human brain regions.
226 that support this adaptive processing in the human brain remain largely unknown.
227 Yet evidence on how training molds the adult human brain remains controversial, as fMRI at standard r
228           We found that the structure of the human brain remains self-similar when the resolution of
229  DLPFC RNA-Seq data from the LIBD Postmortem Human Brain Repository (90 controls, 74 schizophrenia ca
230 he results provide new insights into how the human brain represents errors in a task-dependent manner
231       However, it is largely unknown how the human brain represents the location of others, and how a
232 hese first-of-their-kind observations in the human brain reveal a role for sub-second dopamine and se
233 fer the spatial cellular composition of 3702 human brain samples from Allen Human Brain Atlas.
234                       In RNA-Seq analyses of human brain samples from the NYGC ALS cohort, truncated
235 expression in the human brain, in nearly 200 human brain samples, from both healthy controls and auti
236 ding AD and CTE with AD (CTE/AD) post-mortem human brain samples.
237 s 2 megabase genomic region using postmortem human brain samples.
238                                     However, human brain sampling complexities limit the explanatory
239  and autoradiography in baboon, macaque, and human brain sections, that LCN2 crosses the blood-brain
240  level using in situ sequencing on mouse and human brain sections.
241 s of object knowledge representations in the human brain: sensory-derived and language- and cognition
242 amphetamine challenge, the evaluation of the human brain serotonin system in neuropsychiatric disorde
243 tion of gene expression traits unique to the human brain sheds light on the molecular mechanisms unde
244           RNA-sequencing from post-mortem AD human brains shows downregulation in the expression of m
245 A decade after speech was first decoded from human brain signals, accuracy and speed remain far below
246 erial have found some sex differences in the human brain similar to those seen in other species, and
247 nd the sex-specific impact of ELS within the human brain, specific contributions of chromosomal versu
248 rebral organoids not only recapitulate early human brain structure, biology, and electrophysiology bu
249 at the emergence of abstract concepts in the human brain, such as a "table", requires complex, perfec
250 ential implications for similar cases in the human brain, such as Alzheimer's disease (AD).
251 iants (CNVs) were detectable in normal fetal human brains, suggesting that previously reported megaba
252 appeared in aged wild-type mice and in aging human brains, suggesting their linkage to genetic and ag
253                 Here we investigated how the human brain supports private-public mappings, using an i
254        In this study, we demonstrate how the human brain tailors the implementation of effort to the
255 ate within disease-vulnerable regions of the human brain that a neuron-specific inflammatory response
256 combination (SGR) has been identified in the human brain that affects the Alzheimer's disease gene, a
257 e-binding repeats are expressed in the adult human brain, the pathological tau from different tauopat
258 oordinated patterns of expression across the human brain, their protein products had more interaction
259                                       In the human brain these consist of perineuronal nets, intersti
260 tations across the cortical hierarchy of the human brain through a gradient of mechanisms.
261  by recording the electrical activity of the human brain through electrodes implanted surgically insi
262 t a multi-omic epigenetic atlas of the adult human brain through profiling of single-cell chromatin a
263 porating chromatin interaction profiles from human brain tissue across two developmental epochs and t
264 of neuromelanin and associated metal ions in human brain tissue can be achieved using synchrotron sca
265  genomic scale of transcriptomic analyses of human brain tissue can provide an unbiased approach for
266     Immunoperoxidase analysis of macaque and human brain tissue demonstrate a conserved pattern for P
267 discovery of magnetic nanoparticles (NPs) in human brain tissue has raised concerns regarding their s
268  has both quantified and imaged aluminium in human brain tissue in neurodegenerative and neurodevelop
269  current protocol is demonstrated to work on human brain tissue samples, a source that has proven to
270 gions and axon tract orientation in prenatal human brain tissue sections that are not visible using b
271 turity of iPSC-derived neuronal cultures and human brain tissue.
272 er of studies are demonstrating aluminium in human brain tissue.
273 laments from corticobasal degeneration (CBD) human brain tissue.
274 in autoradiographic studies using postmortem human brain tissues from healthy individuals and ALS pat
275 omplexity of patterns is key information for human brain to differ objects of about the same size and
276                 The potential ability of the human brain to represent an artificial limb as a body pa
277 asticity is a valuable trait that allows the human brain to rewire and recover from injury and sensor
278    Investigating the spatial dynamics of the human brain transcriptome for genes and exploring the ex
279                           Based on available human brain transcriptomic data, we show that NCKAP1 is
280 TATEMENT A recent clinical study showed that human brain trauma patients had enhanced expression of t
281 deficient SCID mice, we focused on targeting human brain tumors with these VSV-EBOVs.
282 lied in the plasma and tumor of mice bearing human brain (U251) and breast (MDA-MB-468) tumor xenogra
283 nvestigate the formation and function of the human brain, under physiological and pathological condit
284                         We conclude that the human brain uses distributed networks to encode not only
285 ological state, and neural activity from the human brain using chronically implanted electrodes.
286  that has recently become available from the human brain using MRI-based tractography, thus providing
287 mporal expression of ITIH3 in the developing human brain using the expression data from the Allen Ins
288 e spatial representation of taste within the human brain using ultra-high resolution functional magne
289  especially between BV-2 microglia and HBVP (human brain vascular pericytes).
290 ue to the difficulties involved studying the human brain via electron microscope techniques.
291 th these particles small enough to enter the human brain via the respiratory tract and olfactory bulb
292 ategorization with neural representations in human brain visual regions.
293 ent cell types and regions of the developing human brain, we generated an atlas of open chromatin fro
294  subtypes underlying seizure activity in the human brain, we have performed single-nucleus transcript
295 n of gene co-expression modules in the aging human brain; we discover and replicate such variants in
296                         The formation of the human brain, which contains nearly 100 billion neurons m
297 de variants and 60-80% of indels detected in human brain whole-genome sequencing data.
298  datasets charting the development of normal human brain with a particular focus on recent single-cel
299 ,513 proteins and 34,173 phosphosites in the human brain with mass spectrometry, highlighting 173 pro
300           Which elements of the genome endow human brains with the capacity for heightened cognitive

 
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