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1 systemic impact that extends beyond the oral compartment.
2 mers that can be loaded with peptide in this compartment.
3 henotypic changes of the conventional T cell compartment.
4 d during the fascial opening of the extensor compartment.
5 tribute to inhibit viral replication in this compartment.
6 harvested from mice lacking HO-1 in myeloid compartment.
7 and the deep seafloor is their ultimate sink compartment.
8 by constructing a proteinaceous nucleus-like compartment.
9 a conspecific from the safety of an adjacent compartment.
10 re potentially protective within the humoral compartment.
11 mal compartment and a DCV biogenesis-related compartment.
12 et is completely separated from the exocrine compartment.
13 subset-specific basis in the effector/memory compartment.
14 purated Pi originates from the intracellular compartment.
15 by protein complexes within this subcellular compartment.
16 TRM precursor cells in the circulatory TEFF compartment.
17 tment model linked to a fetal and breastmilk compartment.
18 +) T cells differed according to the mucosal compartment.
19 -bias within the human pluripotent stem cell compartment.
20 as well as in the number of newly discovered compartments.
21 synthesize hyaluronan (HA) in intracellular compartments.
22 eed to target the reservoirs in all anatomic compartments.
23 omposition in the formation of hematopoietic compartments.
24 h proteins and nucleic acids coassemble into compartments.
25 s conformation matured into conventional A/B compartments.
26 g trajectories, particularly in the adaptive compartments.
27 in determining cellular characteristics and compartments.
28 ng promiscuous enzymes across multiple Golgi compartments.
29 than the nutrient concentration in host cell compartments.
30 nd metabolic enzymes from non-membrane bound compartments.
31 ted, normo-, hypo- and non-aerated pulmonary compartments.
32 cells and their kinship to other CD8+ T cell compartments.
33 data or that are currently assigned to other compartments.
34 ins were significantly decreased in both AMR compartments.
35 DCs, Dectin-1 is redistributed to endosomal compartments.
36 lular compartments and their transport among compartments.
37 s emerge from activity patterns across these compartments.
38 required for acidification of intracellular compartments.
39 CD4(+) T cell and regulatory T cell (T(reg)) compartments.
40 rier that restricts viral access to neuronal compartments.
41 nication between mucosal and systemic immune compartments.
42 ierarchical control and the notion of muscle compartments.
43 ogically associated domains, and large-scale compartments.
44 within the PM, Golgi complex, and endosomal compartments.
45 ity had different CMV genotypes in different compartments.
46 n within ventral, dorsal and pontine network compartments.
47 39a converts phagosomes into peptide-loading compartments.
48 n the late endosomal (LE) and lysosomal (Ly) compartments.
49 iated interactions between distinct cellular compartments.
50 ence from receptors present in intracellular compartments.
51 egradation occurring in acidic endolysosomal compartments.
52 ve compartments compared with differentiated compartments.
53 ved in local protein translation in synaptic compartments.
54 efficient transport of a virus between these compartments.
55 ellular membrane, cytosolic, and microtubule compartments.
56 vesicles between somatodendritic and axonal compartments.
57 n allantoin distribution between subcellular compartments.
58 ampicin concentrations were low in all three compartments.
59 s of which varied among biomes and ecosystem compartments.
60 l terminals in both the striosome and matrix compartments.
61 tain protein homeostasis in various cellular compartments.
62 es were detected in both placental and fetal compartments.
63 ids to the lumen or acidifying intracellular compartments.
64 reinforcement circuits between and within MB compartments.
65 d from the cytosol to intracellular membrane compartments.
66 autophagic flux and neutralization of acidic compartments.
67 te to the regeneration of the distal luminal compartments.
68 ral differences in the ratios of DRMs in the compartments.
69 antigens and microbes from underlying tissue compartments.
70 of chromosomes at multiple levels, including compartments(1) and topologically associated domains (TA
71 activity curves were analyzed using 1-tissue-compartment (1TC) and 2-tissue-compartment (2TC) models
73 sing 1-tissue-compartment (1TC) and 2-tissue-compartment (2TC) models and multilinear analysis 1 to c
74 ng full tracer kinetics (reversible 2-tissue-compartment [2TC] model and Logan graphical analysis [LG
78 id transcriptional changes were seen in each compartment after VEGF inhibition, including genes invol
80 ation, the lack of IRF4 expression in the DC compartment alleviates inflammation and goblet cell meta
81 tments related to its function: an endosomal compartment and a DCV biogenesis-related compartment.
82 (1) within the core of the occluded vascular compartment and controlled by (2) carotid and (3) femora
84 gate the impact of PARK2 KO on the lysosomal compartment and found a clear link between parkin defici
85 e a more detailed structure for the inversin compartment and introduce a new example of a membraneles
89 asizes the importance of the nucleocytosolic compartment and the fine-tuning of dNTP levels for chlor
90 ry cytokine levels in the maternal and fetal compartments and causes behavioral changes in offspring.
92 SEIR epidemic model to the specific dynamic compartments and epidemic parameters of COVID 19, as it
93 tion of mitochondria presented with enlarged compartments and filamentous cytoskeletal elements in th
94 exist about viral load in the different body compartments and fluids during the different disease pha
95 inct genetic architecture of human NP and AF compartments and identified 2,196 differentially express
96 mbination, on eosinophils in blood and other compartments and on the development of asthma symptoms.
97 hibit lesser TMFs, had nine values among our compartments and organisms >1.0 (range of 0.57 to 2.33);
98 in an accumulation of virus in intracellular compartments and significantly reduced viral trans-infec
99 of renin cells within the kidney and immune compartments and the consequences of distorting the reni
101 embly of many molecules in multiple cellular compartments and their transport among compartments.
102 of genomes at the large scale of epigenomic compartments and topologically associating domains (TADs
103 tent and MYC protein level in the neoplastic compartment, and identify CAFs as the specific source of
104 e typically located within the intracellular compartment, and more specifically, within the nucleus.
106 d a protein present in these two subcellular compartments, and here we report that it not only locali
107 ematopoietic stem and progenitor cell (HSPC) compartment aneuploid cells have reduced fitness and are
108 cDC1s) rarely found within the tumor myeloid compartment are crucial for effector T cell recruitment
109 hat gene-expression patterns within the mTEC compartment are heterogenous and include multiple differ
110 M reveals that DNAs transported into E-S/E-K compartments are 'clamped' in a sub-compartment created
111 for coacervation, and resulting membraneless compartments are analyzed for salt resistance, ability t
112 VI-SO-MC interfaces demonstrated that these compartments are connected by membrane-fusion points, th
115 y RNases, associated with different cellular compartments, are essential to maintain cellular homeost
116 ng cell-regulating factors into the tegument compartment as 'cargoes', and should inform future anti-
117 cellular composition of the bronchioalveolar compartment as defined by single-cell RNA sequencing and
118 -protein binding relationships that organize compartment assembly to develop a new structural model.
121 ng RNA Xist establishes an intra-chromosomal compartment by localizing at a high concentration in a t
122 gether, our data show that Xist forms the Xi compartment by seeding a heteromeric condensate that con
123 ineurin is targeted to diverse intracellular compartments by association with scaffold proteins, incl
124 he autophagosome regulators ATG16L1 and ATG9 compartments by nutrient depletion and reduced the forma
125 ibited electrolysis of water in the acceptor compartment, by accepting the charge transfer across the
126 d OCT4, specifically in the cancer stem cell compartment, by reducing the transcriptionally activatin
127 cytes engulf pathogens into a membrane bound compartment called a phagosome, but what happens when en
129 enotype and discuss how cells and biomimetic compartments can be applied to serve this function.
130 The vasculature represents a highly plastic compartment, capable of switching from a quiescent to an
131 5622 indeed affects the myeloid and lymphoid compartments, causes long-term changes in bone marrow-de
134 serve many of the properties associated with compartments - collocalization, division, and merging -
135 of mtDNA were observed in stem/proliferative compartments compared with differentiated compartments.
136 INVS is the core structural determinant of a compartment composed of novel fibril-like substructures,
137 Both young and mature neurons migrate into compartments containing astrocytes; in contrast, astrocy
138 E-S/E-K compartments are 'clamped' in a sub-compartment created by Scc2's association with engaged h
139 uted cholesterol throughout the various cell compartments, de novo cholesterol synthesis enriched thi
140 es the 3D organization of the active genomic compartments during ZGA, and causes downregulation of po
142 ering the relocalization of EcoRI inside the compartment enables targeting of the phage and protectio
143 the endoplasmic reticulum-Golgi intermediate compartment (ERGIC) membrane, ETM forms a five-helix bun
145 c analysis of the etiology of HS in the HFSC compartment establishes a formal link between genetic pr
146 sulfur metabolism elucidates frequent cross-compartment exchange of a standing pool of amino acids w
147 origin that derive either from the endosomal compartment (exosomes) or as a result of shedding from t
148 eins and as an intracellular calcium storage compartment, facilitating calcium-release-dependent cell
150 on biomass accumulation, and features a new compartment for tree branches and branch fall dynamics.
151 ed that the niche is organized into multiple compartments for orchestrating stepwise adult stem cell
152 complex coacervates, which are membraneless compartments formed by phase separation of polyelectroly
153 thogen, tends to direct its resources to the compartment from which that pathogen is most likely orig
158 are distributed across neuronal subcellular compartments, how local machinery regulates autophagy, a
159 large numbers of patients influence the Treg compartment; however, how such effects affect their dise
160 ts moderate accumulation in several cellular compartments (i.e., nucleus, lysosomes, mitochondria, an
161 le is known on the composition of the T cell compartment in early life in this vulnerable population.
162 nclusion, notable immaturities of the T cell compartment in ELGAN/ELBW neonates may at least partiall
164 pected heterogeneity within the naive T cell compartment in mice, where loss of VISTA disrupted the m
165 ection failed to stimulate the memory B cell compartment in preimmunized mice, although they were pro
169 ement and forms multiple, dispersed assembly compartments in epithelial cells, which complicates the
174 P70 inhibitor (HSP70i) that targets multiple compartments in the cancer cell, including mitochondria.
176 ht to be a disorder of the peripheral B-cell compartment, in 25% of patients, early B-cell developmen
177 ysiological signaling, and the mitochondrial compartment, in addition to oxidative stress, inflammati
178 M. tuberculosis resides in early-phagosomal compartments, in MSCs the majority of bacilli were found
179 In our model, a basal-dendrites/somatic compartment included fast-inactivating Na(+) and delayed
180 onductances, while an apical-dendrites/trunk compartment included persistent Na(+), hyperpolarization
181 racteristic response patterns for each fluid compartment individually: Intraretinal fluid showed the
186 he evolution of unique apicomplexan cellular compartments is concomitant with vast proteomic novelty.
188 ERK susbtrates across different subcellular compartments, it is important to understand how ERK acti
190 inside coral cells in a specialized membrane compartment known as the symbiosome, which shares the ph
191 onsive cap, in addition to the gelatin-based compartment, leading to concurrent delivery and sequenti
192 Similar mechanisms may occur in other small compartments like primary cilia or dendritic spines.
194 research should evaluate whether the genital compartment might contribute to viral rebound in some PW
195 Maternal dolutegravir was described by a two-compartment model linked to a fetal and breastmilk compa
202 vent of novel techniques such as multitissue compartment models and connectomics can help characteris
206 sed HIV-infected cells from various anatomic compartments obtained through a rapid autopsy program of
207 riptional modifications in the hematopoietic compartment occurred as early as preinvasive disease sta
208 amic flow of molecules into and out of these compartments occurs on faster timescales than for membra
209 By recirculating the urine over the cathodic compartment of an electrochemical cell, the pH was incre
211 alysis of the peripheral conventional T cell compartment of human extremely low gestational age neona
212 s were more highly represented in the T cell compartment of newborn nonhuman primates for all sites e
213 cGAS was initially located in the cytosolic compartment of pDCs and time-dependently colocalized wit
214 actility of the lateral more than the medial compartment of the inferior rectus (IR) in both eyes (P
215 heir significant restoration in the alveolar compartment of the lung as well as in the periphery.
216 s in concentration gradients in the anterior compartment of the wing disc, ASP and myoblasts, and act
219 ne receptors detect microbial DNA in various compartments of the cell, such as endosomes, the cytosol
220 TH(+) cell loss or altered phenotype in key compartments of the central nervous system responsible f
221 rtitioned among striosome (patch) and matrix compartments of the dorsal striatum, allowing compartmen
222 tomy to decompress the anterior and peroneal compartments of the lower leg appears to be safe with re
225 The yeast PM is segregated into the Micro-Compartment-of-Can1 (MCC) and Pma1 (MCP), which have dif
226 are performed in topologically extracellular compartments or on the cell surface; hence, diverse secr
227 nd introduce a new example of a membraneless compartment organized by protein-protein interactions.
230 ur neural network predicts more accurate sub-compartment predictions when SCI-determined sub-compartm
231 hat age-related increases in the memory Th17 compartment predispose aged mice toward the development
232 ctivation of acetate in distinct subcellular compartments provides plants with the metabolic flexibil
234 kinase domain or death domain in the T cell compartment reduced the T cell activation and maintained
237 retina, IMPG1 and IMPG2 occupy distinct IPM compartments, represent the main source of chondroitin s
238 on and the polarization of MT1-MMP recycling compartments, required for invadopodia activity and inva
239 onstrated a critical role for the host Golgi compartment-resident ATP-powered calcium pump (secretory
241 Single-cell RNA sequencing of the immune compartment showed that IL8 is primarily expressed in ci
242 The IR lateral compartment and SR medial compartment significantly co-relaxed when binocular fusi
244 setting specific (in vitro vs. in vivo) and compartment specific (BAL vs. blood) and localized to th
247 matically different dimensions, and to their compartment-specific requirements in the axon initial se
248 ogical manipulation of L-type VGCCs reversed compartment-specific responses to D1 receptor activation
250 haploids in hybrids maintain their parental compartment status at B6/Cast divergent compartments owi
251 s and nascent polypeptides into two distinct compartments, stress granules, and Q-bodies, is triggere
252 ee transcription-translation into cell-sized compartments, such as liposomes, is one of the major bot
255 ransference via the extracellular space, the compartment that is cleared by the glymphatic pathway, a
256 The primary cilium constitutes a subcellular compartment that orchestrates signal transduction indepe
257 ns across the oligodendrocyte and astroglial compartments that are at least partially mechanistically
258 y pattern were realized by printing separate compartments that could be filled with different activit
259 vesicles (EVs) are small, membrane-enclosed compartments that mediate the intercellular transport of
261 rial membranes that operate through a common compartment, the cytosol for transport at the plasma mem
262 d formation of the PD-associated replication compartments, therefore facilitating the virus intercell
263 ort of proteins and lipids from one membrane compartment to another is via intracellular vesicles.
264 its membranes from the ER Golgi intermediate compartment to create an exit route for their export.
265 us, IRF3 acts principally within the stromal compartment to exacerbate sepsis pathogenesis via differ
269 tethers, inter-connecting two intracellular compartments to enable efficient transport of a virus be
271 y and disappearance of OSBP at the cis-Golgi compartment, together with a complete loss of GOLPH3 fro
274 t to fasciotomy of the anterior and peroneal compartment using a dual-incision minimally invasive fas
275 present a deep neural network to predict sub-compartments using epigenome, replication timing, and se
277 n and quantification of fluid in all retinal compartments was applied for automated segmentation of f
278 that (i) the fate of Zn in water-soil-plant compartments was similar, regardless of the type of soil
280 ng potential relative to the nondisplaceable compartment, was derived using the simplified reference
281 ) oxidation in cytoplasmic and mitochondrial compartments, we estimated that fluxes through glucose d
282 nt beyond the known dark zone and light zone compartments, we performed single-cell (sc) transcriptom
285 CSI signal components and microscopic tissue compartments were assessed using two-sided t tests.
291 altered volume, shape, and dry mass of those compartments, whereas the relative distribution of mass
292 stand the diversity of the peripheral T cell compartment, which arises from the specialization of dif
293 compartments, which likely correspond to A/B compartments, which are detected with ensemble Hi-C.
294 microscopically defined, active and inactive compartments, which likely correspond to A/B compartment
295 data, this is reflected by the formation of compartments, whose interactions form a characteristic c
298 action potential frequency and number in all compartments, with action potential number being prefere
300 mpling of both the vascular and interstitial compartments without compromising fluidic coupling.