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   6 ext, the developmental increase of isotropic junctional actomyosin reduces the rate of neighbor excha
  
  
  
    10  of one such transcript, F11R (also known as junctional adhesion molecule 1, JAM1), in hypoxia is dep
    11    Mammalian orthoreoviruses use glycans and junctional adhesion molecule A (JAM-A) as attachment rec
  
    13 trocyte TJs of claudin 1 (CLDN1), CLDN4, and junctional adhesion molecule A (JAM-A) subunits is induc
  
  
  
  
    18 the main proteins associated with it such as junctional adhesion molecule-1 and vascular endothelial 
    19  protein sigma1 engages glycan receptors and junctional adhesion molecule-A (JAM-A) and is thought to
  
  
  
  
    24 g integrin alpha3beta1, VE-cadherin, ICAM-2, junctional adhesion molecule-B (JAM-B), laminin, and cel
    25 ns and/or transmembrane adhesions, including junctional adhesion molecule-C (JAM-C) and myelin-associ
  
    27  and Adenovirus Receptor (CAR) that binds to Junctional Adhesion Molecule-like (JAM-L) expressed on l
    28 ross the ventral face of the somite and that junctional adhesion molecules (JAMs) mediate this requir
  
    30 alternative Crumbs isoform recapitulates the junctional aggregation and centrosome positioning defect
    31 nt role of the V(D)J recombination-generated junctional and allele-specific residues for achieving hi
    32 unctional disassembly are periodic pulses of junctional and medial myosin II that result in progressi
    33 These observations argue that the balance of junctional and nuclear beta-catenin activity has a profo
  
  
  
  
    38 results demonstrate that LPA induces loss of junctional beta-catenin, stimulates clustering of beta1 
  
    40 ists of scaffold proteins that interact with junctional cadherins, polarity proteins and the cytoskel
    41 RQOL) domains in patients with esophageal or junctional cancer who received neoadjuvant chemoradiothe
  
  
    44 ecognized molecular mechanism for inhibiting junctional CDC-42 to control actin organization and AJ p
    45 onitor Ca(2+) transients in neurons and post-junctional cells of the murine colon evoked by exogenous
  
  
    48 f integration between hard-wired synaptic or junctional circuits and extrasynaptic signals wirelessly
    49 atter was restricted by accessibility of non-junctional claudin molecules such as claudin-4 at apical
    50 icromolar [Ca(2+) ]i , in the submembrane or junctional cleft space, is not required to maximize [Ca(
    51 uenced by the number of functional RyRs in a junctional cluster (which is reduced by tetracaine or ru
  
  
    54 etaV was invariably detected near the apical junctional complex and above the cuticular plate, a dens
    55 lls but also generates changes in the apical junctional complex and loss of epithelial barrier functi
    56 eoglycan with HS chains that is critical for junctional complex assembly and regulating the flow resp
  
    58 revealed that Notch signaling induces apical junctional complex genes that regulate cell adhesion and
    59 fficking, which were present near the apical junctional complex in the hair cells of mammalian ancest
    60 thelial flow mechanotransduction through the junctional complex is mediated by a specific pool of VE-
    61 nents of the cardiac area composita, a mixed junctional complex responsible for electromechanical cou
  
  
    64  when NPCs normally acquire organized apical junctional complexes (AJCs) in the zebrafish hindbrain. 
    65 formation revealed that disruption of apical junctional complexes (AJCs) was responsible for PH in Ne
    66  such as E-cadherin enrichment in epithelial junctional complexes and CD45 exclusion from the signali
  
    68 geometric graph, with nodes corresponding to junctional complexes and with edges corresponding to spe
  
  
    71  transient or stable breakdown of epithelial junctional complexes to permit programmed migration, inv
    72 er, enter the next cell by traveling through junctional complexes without being intercepted by a neut
    73 g imaginal discs are organized into distinct junctional complexes, including separate distributions f
    74 vary glands due to disruptions of epithelial junctional complexes, likely secondary to elevated activ
    75  at a number of levels, including epithelial junctional complexes, mucus production, and mucosa-deriv
    76  secreted bacterial protease disrupts apical-junctional complexes, paving the way for H. pylori to ac
  
    78 luding cell differentiation, the presence of junctional complexes/desmosomes and microvilli, and the 
  
  
  
    82 reases cortical tension and locally enriches junctional components to facilitate apical constriction.
  
    84  simulation and eliminate noise in simulated junctional conductance (gj) records, we transformed an S
    85 ated that such asymmetry strongly depends on junctional conductance and can lead to the unidirectiona
  
    87  model can account for dynamic modulation of junctional conductance during the spread of electrical s
    88 ice that under circadian conditions, the rod junctional conductance has a median value of 98 pS durin
    89 Adaptation to bright light decreases the rod junctional conductance to approximately 0 pS, regardless
    90 odel allowed us to replicate the kinetics of junctional conductance under different levels of intrace
    91 tion potentials, can induce a rapid decay of junctional conductance, thus demonstrating spiking activ
  
    93 la adherens (ZA) in these cells, its role in junctional contractility and its mode of regulation are 
    94 nolayer, coronin 1B is also recruited to the junctional cortex at the apoptotic/neighbor cell interfa
    95 sts by approximately 20 mV and increased gap junctional coupling between myofibroblasts and cardiomyo
    96 a factor of 4 by physiological levels of gap junctional coupling between sister MCs at the same glome
    97 m gap junction plaques and produce levels of junctional coupling similar to those for wild-type Cx32.
    98 urons was not related to the strength of gap junctional coupling, and was still prevalent in connexin
  
   100 tentials and cardiomyocyte-cardiomyocyte gap junctional coupling, TGF-beta1 depolarized cardiomyocyte
  
  
   103 here is a reduction in the early peak of the junctional current during the upstroke of the action pot
   104 ined that although GJ channel gating reduces junctional current, it does not significantly alter cond
   105 more stable and contains a high level of gap-junctional Cx43 whereas that formed with hypoxic cells i
   106 oxic melanoma cells selectively degrades gap-junctional Cx43, leading to the destabilization of the i
  
  
   109 ngiocytes to lipopolysaccharide, rescued the junctional defect in vitro, and significantly attenuated
  
   111 ngthen junctions to override Snail-dependent junctional disassembly and postpone EMT during Drosophil
   112    A major driver of apical constriction and junctional disassembly are periodic pulses of junctional
  
  
   115 analiculi in LKB1(-/-) mice, confirming that junctional disruption resulted in paracellular exchange 
  
   117 oblastic morphology, increased intercellular junctional distance, and induced paracellular permeabili
  
   119 key antigen-binding region, which arise from junctional diversity rather than differential VH gene us
   120 r of N-nucleotides has a great effect on the junctional diversity, and thereby on the total diversity
  
   122 olarity (PCP) is the formation of restricted junctional domains containing Frizzled/Dishevelled/Diego
   123 es, larger unitary channel conductances, low junctional dye permeability/permselectivity, and an over
   124  pathway might be involved to alter cellular junctional dynamics for breast cancer invasive progressi
  
  
  
   128 dred five children were recruited, 8.6% with junctional EB, 34.3% with simplex EB, 34.3% with autosom
  
   130 ively in 76 patients with severe generalized junctional epidermolysis bullosa born in the years 2000-
  
   132 ncidence of 1 of 150,000, severe generalized junctional epidermolysis bullosa occurred more often tha
   133 port on two patients with severe generalized junctional epidermolysis bullosa treated with allogeneic
  
   135 s (AP) crest, as well as between the CEJ and junctional epithelium (JE) level, were measured; the num
   136 -lymphocytic cells and T-helper cells in the junctional epithelium of SPF mice compared with GF mice 
   137 ngival inflammation, apical migration of the junctional epithelium, periodontal pocket formation, alv
  
  
  
   141 ical techniques have been used to prove the "junctional epitope" nature of VHH6, a camelid single dom
   142 c-1 embryos exhibit dynamic accumulations of junctional F-actin and an increase in AJ protein levels.
   143  broad cohort of epithelial genes, including junctional factor dlg-1 Accumulation of DLG-1 protein is
  
   145 grin stimulus, but not on the development of junctional folds, another hallmark of mature postsynapti
  
   147 kocytes actively contract the VECs to open a junctional gap and then push themselves across the gap b
   148 leukocytes preferentially extravasate across junctional gaps in the endothelial monolayer (paracellul
   149 ears to be the dominant kinase essential for junctional integrity and contractile tension at epitheli
   150 ge in this area is that barrier function and junctional integrity are difficult to study in the intac
   151 ctionally, CdGAP-Ajuba interaction maintains junctional integrity in homeostasis and diseases: (i) ga
   152 ponses to laminar shear stress and regulates junctional integrity through modulation of calcium signa
   153 We further showed that retention of adherens junctional integrity was caused by the up-regulation of 
  
   155 ess, and is necessary for the maintenance of junctional integrity, cell elongation, and suppression o
  
  
  
  
   160 ocytes, despite a lack of heterocellular gap junctional intercellular communication between the two c
   161 s used to quantitatively investigate the gap junctional intercellular communication in several homoty
   162 rences in gap junction plaque formation, gap junctional intercellular communication, Cx43 phosphoryla
   163  number of neighboring cells coupled via gap junctional intercellular communication, providing a mech
  
  
   166 rapid intra-SR Ca diffusion, such that local junctional intra-SR [Ca] can be maintained by intra-SR d
   167 +) store into the peripheral subsarcolemmnal junctional (j-SR) and the much more abundant central non
   168 rtance, Fmnl3 expression is up-regulated and junctional localization increases during collective cell
   169 s in a PLEKHA7-dependent manner, because its junctional localization is abolished by knock-out of PLE
   170 re protein Frizzled, we show that its stable junctional localization is promoted by the core proteins
   171 NL1 in epithelial cells results in decreased junctional localization of MgcRacGAP but not of ECT2, a 
   172 ld protein zonula occludens 1, and disrupted junctional localization of the structural transmembrane 
  
  
  
  
   177 ts, we identify time-dependent properties of junctional mechanics consistent with a simple viscoelast
  
  
   180 , reduced tension on VE-cadherin and loss of junctional mechanotransducers such as vinculin and PAK2,
  
  
  
   184 e of this interplay specifies the pattern of junctional network remodeling that changes wing shape.  
  
  
  
   188   CRISPR/Cas9 knockout of podocalyxin causes junctional organization defects in podocyte-like cells. 
  
   190 tions of these models revealed that this gap junctional/paracrine mechanism accounts for up to 23% of
  
  
   193 ecessary for trans-endocytosis, and adhesive junctional PCP complexes appear to be destined for degra
   194 be of high medical relevance because loss of junctional Pg is a hallmark of arrhythmogenic cardiomyop
   195 the total number of GJ channels clustered in junctional plaques, and it has the potential to describe
  
  
  
   199 but the resting rate of miniature excitatory junctional potentials (mEJPs) is significantly lower in 
  
  
   202 Mg(2+) ions relative to a reported three-way junctional pre-catalytic structure of the twister-sister
  
   204 amentous actin and the redistribution of the junctional protein beta-catenin at the wound margin duri
   205 s both structural changes in the actin-bound junctional protein complex and physical forces spanning 
  
  
   208  mutant ADF reduces actin polymerization and junctional protein disassembly, attenuates both early- a
  
   210  circuit, by increasing targeting of the gap junctional protein innexin shaking-B to gap junctions (G
  
   212 Deltalens), show that loss of this cell-cell junctional protein leads to lens degeneration, necrosis 
   213 -cadherin, a major endothelial cell-specific junctional protein that controls vascular integrity.    
  
  
  
   217 into the post-translational modifications of junctional proteins and signaling pathways regulating pl
   218 yers with similar levels and distribution of junctional proteins and transendothelial electrical resi
  
   220 veal polarized dynamics, and organization of junctional proteins between the front of FAJs and their 
  
  
  
  
   225  actin polymerization and the disassembly of junctional proteins within microvascular endothelial cel
   226 d mucosal inflammation, a loss of epithelial junctional proteins, and an increase in mucosal inflamma
   227 tin, and a reduction in endothelial cell and junctional proteins, including von Willebrand factor, CD
   228 ithelial cells by lowering the expression of junctional proteins, such as zonula occludens-1, occludi
  
  
  
  
  
  
  
  
  
   238 re thought to typically present as permanent junctional reciprocating tachycardia (permanent junction
   239 ctional reciprocating tachycardia (permanent junctional reciprocating tachycardia), they may also be 
   240 ) DAP patients manifested clinical permanent junctional reciprocating tachycardia, and these patients
  
  
  
  
   245 nsion on the E-cadherin complex promoted the junctional recruitment of the protein LGN, a core compon
   246 90)BCR-ABL peptides derived from the BCR-ABL junctional region and alternative splicing, and of adopt
   247 ently, App also recruits Dachs to the apical junctional region through protein-protein association, t
   248 ification and recruiting Dachs to the apical junctional region, thereby promoting tissue growth.     
   249 n of the atypical myosin Dachs at the apical junctional region, which in turn promotes growth by inhi
   250 der of atrophy; Zone 2 as the center of this junctional region; Zone 3 at the border between the junc
  
   252  levels, vasopermeability, and alteration in junctional-related proteins were observed in the retinas
  
   254 results indicate that the role of LET-502 in junctional remodeling is likely to be independent of its
   255 ases, E-cadherin endocytosis, and epithelial junctional remodeling, as bona fide IRF6 partner protein
  
  
  
   259  to enhanced Ca(2+) release from central non-junctional sarcoplasmic reticulum (SR) and centripetal p
   260 3) reverted ultrastructural abnormalities of junctional sarcoplasmic reticulum and transverse tubules
  
   262 spryn, minispryn and RyR2 co-localise at the junctional sarcoplasmic reticulum of isolated cardiomyoc
  
  
   265 relative NHEJ efficiency and analyze ligated junctional sequences for various types of DNA ends, incl
  
   267 ptic effects can be quite significant in the junctional spaces between cells, and that the cell activ
  
  
   270 s is too large, the depletion of Ca from the junctional SR terminates the release; and 3) very long r
   271  and calsequestrin (CSQ) localization to the junctional SR, and increases endoplasmic reticulum (ER) 
   272 he SR network, diffusion between network and junctional SR, cytosolic Ca diffusion, SERCA uptake acti
   273 rs as major transcriptional regulators of EC junctional stability, guaranteeing physiological functio
  
   275 ilize GTP-RhoA at the ZA, thereby sustaining junctional tension and inhibiting intraepithelial cell m
  
   277  adhesion plays an active role in generating junctional tension by promoting actin assembly and corti
  
   279 aling to drive the polarized organization of junctional tension necessary to build an in vivo epithel
   280 dherin localizes and tunes EGFR activity and junctional tension to inhibit premature TJ complex forma
   281 toinhibitory conformation, in the absence of junctional tension, and biophysical studies have shown t
   282 ytes and the VECs can separately perturb the junctional tensions of VECs to result in the opening of 
   283 hototype 1 skin types; RCM features, such as junctional thickening, dense dermal nests, and nucleated
  
  
   286 itment of patients with lower oesophageal or junctional tumours planned for an oesophagogastric resec
   287 nced oesophageal cancer or type I/II Siewert junctional tumours, histologically confirmed squamous-ce
  
  
   290  drive VE-cadherin expression and stabilized junctional VE-cadherin complexes through associated phos
  
   292  differentiate and expressed markers of both junctional zone and labyrinth trophoblast subtypes in a 
   293 a-HPV field cancerization arises from the HF junctional zone and predispose to squamous cell carcinom
   294   The retinal sensitivity in the bulk of the junctional zone is similar to apparently uninvolved dist
   295 ntal labyrinth (L) had a higher sO2 than the junctional zone plus decidua region (JZ+D) in C57Bl/6 mi
  
   297 P1 led to FGR, increased karyorrhexis in the junctional zone, and decreased proliferation of labyrint
   298 oise, sharpness, and ability to evaluate the junctional zone, myometrium, and musculoskeletal structu
   299 owed disturbed placental morphology, reduced junctional zone, smaller placentas, and impaired spiral 
  
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