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1              Synaptopodin depletion prevents junctional accumulation of alpha-actinin-4, vinculin, an
2                                 We show that junctional actin assembly is maintained by contractility
3 ed result reflects a more dynamic and mobile junctional actin in EEF1A-depleted cells.
4 on assembly, but rather is needed for proper junctional actin regulation during elongation.
5 ceptivity including modulation of epithelial junctional activity.
6 ext, the developmental increase of isotropic junctional actomyosin reduces the rate of neighbor excha
7 ons in junction length, regulated in part by junctional actomyosin.
8       HH is a risk factor for esophageal and junctional adenocarcinoma (EGJA).
9                                In platelets, junctional adhesion molecule (JAM)-A was previously iden
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
12                                              Junctional adhesion molecule A (JAM-A) is a broadly expr
13 trocyte TJs of claudin 1 (CLDN1), CLDN4, and junctional adhesion molecule A (JAM-A) subunits is induc
14                      Among these proteins is junctional adhesion molecule A (JAM-A), an Ig fold trans
15      Reovirus binds to cell surface glycans, junctional adhesion molecule A (JAM-A), and the Nogo-1 r
16 urface glycans or the proteinaceous receptor junctional adhesion molecule A (JAM-A).
17                                              Junctional adhesion molecule C (JAM-C) is an immunoglobu
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
20                                              Junctional adhesion molecule-A (JAM-A) is a tight juncti
21                                              Junctional adhesion molecule-A (JAM-A) is an adherens an
22                  We have recently shown that junctional adhesion molecule-A (JAM-A) renders protectio
23 aged myofibres through the modulation of the junctional adhesion molecule-A.
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
26 ed expression and/or functionality of the EC junctional adhesion molecule-C (JAM-C).
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
29 pond to elevated contractility by increasing junctional afadin.
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
34 r fluids of patients affected by dystrophic, junctional, and simplex EB.
35 hology of AJs and TJs but attenuated de novo junctional assembly.
36                                              Junctional association of YAP inhibits nuclear transloca
37 ry neuroepithelium, especially at the apical junctional belt of the sustentacular cells.
38 results demonstrate that LPA induces loss of junctional beta-catenin, stimulates clustering of beta1
39 n assembly, and loss of Rap1B led to loss of junctional border organization.
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
42 nts because of a dose-limiting toxicity (ie, junctional cardiac rhythm).
43                 To more accurately mimic the junctional CCC, we designed a constitutively monomeric c
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
46 brates whose proteins mainly function as non-junctional channels on the cell surface.
47 ppear to be involved on the cone side of the junctional channels.
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
52 d by voltage-gated calcium signaling and gap-junctional communication.
53 naling cascade leading to enhancement of gap junctional communication.
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
57 f transporters and specialized intercellular junctional complex components.
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
62 ibutes to the maturation and assembly of the junctional complex.
63 58 is essential for flow sensing through the junctional complex.
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
67 oteins essential to maintain normal cellular junctional complexes and tissue homeostasis.
68 geometric graph, with nodes corresponding to junctional complexes and with edges corresponding to spe
69 -1 and stabilin-1 and was facilitated by the junctional complexes between HSECs.
70                         Unique intercellular junctional complexes between the central nervous system
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
77  lipid bilayer by ankyrin and by actin-based junctional complexes.
78 luding cell differentiation, the presence of junctional complexes/desmosomes and microvilli, and the
79 where they interact with the essential glial junctional component neurofascin 155.
80                        We establish that the junctional components alpha-catenin, beta-catenin, and c
81                                   Imaging of junctional components and genetic analyses suggest that
82 reases cortical tension and locally enriches junctional components to facilitate apical constriction.
83  tension-induced sequential incorporation of junctional components.
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
86                  In C57BL/6 mice, the median junctional conductance between dark-adapted rods is appr
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
92  signalling and the organization of adherens junctional contacts.
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
99                            The effect of gap junctional coupling, sodium ion channel distribution, an
100 tentials and cardiomyocyte-cardiomyocyte gap junctional coupling, TGF-beta1 depolarized cardiomyocyte
101  if they do, produce little or no detectable junctional coupling.
102  labyrinthine structures adjoining the PM at junctional couplings (JCs).
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
107 nd contains a significant lower level of gap-junctional Cx43.
108 cteria were observed in the absence of tight junctional damage.
109 ngiocytes to lipopolysaccharide, rescued the junctional defect in vitro, and significantly attenuated
110 e of calcium signaling rescues the cell-cell junctional defects.
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
113                               In both cases, junctional disassembly can be blocked by simultaneous in
114 ter embryos to assess apical domain loss and junctional disassembly.
115 analiculi in LKB1(-/-) mice, confirming that junctional disruption resulted in paracellular exchange
116                                        After junctional disruption with the FBA, dilatation was simil
117 oblastic morphology, increased intercellular junctional distance, and induced paracellular permeabili
118                    Similarly, immunoglobulin junctional diversification is impaired in cells.
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
121  function might be necessary for normal CDR3 junctional 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
125  cytoskeletal network may contribute to cell junctional dynamics.
126 ctivation by Wnt4a-Cdc42 signaling increases junctional E-cadherin in maturing pouches.
127 sruption, however, increased the mobility of junctional E-cadherin.
128 dred five children were recruited, 8.6% with junctional EB, 34.3% with simplex EB, 34.3% with autosom
129 nds, particularly dominant in dystrophic and junctional EB.
130 ively in 76 patients with severe generalized junctional epidermolysis bullosa born in the years 2000-
131              Treatment of severe generalized junctional epidermolysis bullosa by SCT is a last-ditch
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
134                           Severe generalized junctional epidermolysis bullosa, a lethal hereditary bl
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
138 ils that migrate from the vasculature to the junctional epithelium.
139                                              Junctional epitope antibodies, like VHH6, not only offer
140                    Here we introduce VHH6, a junctional epitope antibody capable of specifically reco
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
144 R clusters became fragmented with diminished junctional folds and synaptic vesicles.
145 grin stimulus, but not on the development of junctional folds, another hallmark of mature postsynapti
146                                      To test junctional function, we used intravital microscopy to qu
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
154 ewed toward loss of differentiation, reduced junctional integrity, and impaired innate defense.
155 ess, and is necessary for the maintenance of junctional integrity, cell elongation, and suppression o
156            Butyrate restoration improved IEC junctional integrity, decreased apoptosis and mitigated
157 to inhibit ROCK activity, and to maintain EC junctional integrity.
158 rives expression of VE-cadherin and controls junctional integrity.
159 tial repair process that is dependent on gap junctional intercellular communication (GJIC).
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
164 nt number of MSCs was down-regulated via gap junctional intercellular communication.
165 dock between adjacent cells to allow for gap junctional intercellular communication.
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
173  binds to and requires VAV2 function for its junctional localization.
174  in TTX-insoluble fractions, consistent with junctional localization.
175  that leads to defective Tie2 clustering and junctional localization.
176 ar morphogenesis or express the foot process junctional markers nephrin and podocin.
177 ts, we identify time-dependent properties of junctional mechanics consistent with a simple viscoelast
178              VEGFR3 levels, a component of a junctional mechanosensory complex, mediate these differe
179  we now identify as another component of the junctional mechanosensory complex.
180 , reduced tension on VE-cadherin and loss of junctional mechanotransducers such as vinculin and PAK2,
181                                              Junctional membrane complexes (JMCs) in myocytes are cri
182                                   RATIONALE: Junctional membrane complexes (JMCs) in myocytes are cri
183                       At homotypic contacts, junctional N-cadherin bonds downregulate Myosin-II contr
184 e of this interplay specifies the pattern of junctional network remodeling that changes wing shape.
185          Once engaged with the astrocyte gap-junctional network, brain metastatic cancer cells use th
186  neurulation events, we term this phenomenon junctional neurulation.
187 j-SR) and the much more abundant central non-junctional (nj-SR) SR.
188   CRISPR/Cas9 knockout of podocalyxin causes junctional organization defects in podocyte-like cells.
189 in loading order, resulting in many possible junctional outcomes from one DSB.
190 tions of these models revealed that this gap junctional/paracrine mechanism accounts for up to 23% of
191                                       Ringed junctional pattern and dermal nests were associated with
192                                    Aspecific junctional pattern, basaloid cords, and ulceration were
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
196         However, the mechanisms that control junctional plasticity are not fully understood.
197 polysaccharide secretion system known as the junctional pore complex (JPC).
198 le hormogonia corresponds to the site of the junctional pore complex.
199 but the resting rate of miniature excitatory junctional potentials (mEJPs) is significantly lower in
200 tude of both evoked and miniature excitatory junctional potentials.
201                                 Our four-way junctional pre-catalytic structure differs significantly
202 Mg(2+) ions relative to a reported three-way junctional pre-catalytic structure of the twister-sister
203                         The mechanosensitive junctional protein alpha-catenin acts through vinculin a
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
206                  The contribution of the gap junctional protein connexin 36 (Cx36) to the regulation
207        Expression of the redox-sensitive gap junctional protein Cx43 (Connexin 43) was reduced in the
208  mutant ADF reduces actin polymerization and junctional protein disassembly, attenuates both early- a
209                                 PLEKHA7 is a junctional protein implicated in stabilization of the ca
210  circuit, by increasing targeting of the gap junctional protein innexin shaking-B to gap junctions (G
211 eased phosphorylation of p38 MAPK and of the junctional protein JAM-A.
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.
214 ures correlating with mislocalization of the junctional protein, cingulin.
215 ed enterocyte TNF-alpha while it upregulated junctional protein-coding mRNAs.
216 titis, a finding supported by maintenance of junctional proteins and polarity markers.
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
219 conserved redistribution of cytoskeletal and junctional proteins around the wound.
220 veal polarized dynamics, and organization of junctional proteins between the front of FAJs and their
221                                              Junctional proteins Neph1 and ZO-1 and their interaction
222                      Although transcripts of junctional proteins such as connexin43, ZO-1, occludin,
223 hesion markers and lower levels of cell-cell junctional proteins when compared to lean mice.
224 ns and reduced the expression of endothelial junctional proteins when compared to lean serum.
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
229 ed altered subcellular distribution of tight junctional proteins.
230 ore apically localized F-actin and BTB tight junctional proteins.
231 n and other plakins harbor binding sites for junctional proteins.
232  bind different sets of actin-regulating and junctional proteins.
233 barrier-associated transcription factors and junctional proteins.
234 KO mice revealed a reduced expression of BBB junctional proteins.
235 al permeability and the expression levels of junctional proteins.
236        Using a cutoff 5% allele fraction for junctional reads, 7 different rearrangements were presen
237 Actomyosin cable formation is accompanied by junctional rearrangements at the wound margin.
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
241  DAPs do not present with clinical permanent junctional reciprocating tachycardia.
242 h those with DAPs without clinical permanent junctional reciprocating tachycardia.
243                        ZO-1 was required for junctional recruitment of JACOP, which, in turn, recruit
244                                          The junctional recruitment of nectin-1 and nectin-3 and thei
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
251  occurs is found to be cablelike in that the junctional regions act like inverted cables.
252  levels, vasopermeability, and alteration in junctional-related proteins were observed in the retinas
253 Pg-mutant S665A abrogated both cAMP-mediated junctional remodeling and increase of cohesion.
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
256 pression and a corresponding increase in gap-junctional resistivity.
257 ions involved in the spatial localization of junctional RhoA signaling.
258                        Transient accelerated junctional rhythm during injections, and transient noctu
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
261 ganized in a lattice to form clusters in the junctional sarcoplasmic reticulum membrane.
262 spryn, minispryn and RyR2 co-localise at the junctional sarcoplasmic reticulum of isolated cardiomyoc
263             KCNQ1 mainly resides in the jSR (junctional sarcoplasmic reticulum), whereas KCNE1 reside
264 cking and parallel to the Scribble module of junctional scaffolding proteins.
265 relative NHEJ efficiency and analyze ligated junctional sequences for various types of DNA ends, incl
266              Lnp subsequently moves into the junctional sheets and forms oligomers.
267 ptic effects can be quite significant in the junctional spaces between cells, and that the cell activ
268  consistent with the STIM1 localizing to the junctional SR (jSR).
269 ted more often in central regions of the non-junctional SR compared to normal cells.
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
274  not due to secondary effects on polarity or junctional structures.
275 ilize GTP-RhoA at the ZA, thereby sustaining junctional tension and inhibiting intraepithelial cell m
276  actin nucleation apparatus is necessary for junctional tension and integrity.
277  adhesion plays an active role in generating junctional tension by promoting actin assembly and corti
278 IA responds to Rho-ROCK signaling to support junctional tension in MCF-7 cells.
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
284                             At steady-state, junctional transmission of lactate (a chemical base) fro
285 malemma), which can explain the advantage of junctional transmission over MCT in vivo.
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
288  structure and cleavage assays of a four-way junctional twister-sister self-cleaving ribozyme.
289 to myofibroblasts during pharmacological gap junctional uncoupling.
290  drive VE-cadherin expression and stabilized junctional VE-cadherin complexes through associated phos
291 nal region; Zone 3 at the border between the junctional zone and adjacent "normal" retina.
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
296                                          The junctional zone, a ring 500 mum in width, surrounding th
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
300  further induced overgrowth of the placental junctional zone.

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