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1 blocked the development of acute and chronic cephalic allodynia in the chronic nitroglycerin model, a
2                   Emphasis was placed on the cephalic and anterior pedal regions that are commonly th
3 ynergistically to disrupt differentiation of cephalic and axial mesendoderm, show a delay in otic dev
4      To explore neural mechanisms underlying cephalic and extracephalic allodynia.
5                                              Cephalic and genital involvement was frequent.
6 tors at the maternal-fetal interface, and in cephalic and non-cephalic embryonic tissues from BTBR co
7 lii revealed shared and distinct features of cephalic and non-cephalic r-opsin1-expressing cells.
8 hat gives rise to parasympathetic outflow to cephalic and ocular/nasal structures.
9 tive neuromasts located within five pairs of cephalic and one pair of trunk canals, as well as superf
10 as informed by the segmental affinity of the cephalic appendages [1, 4-6].
11 dictive of elastic recoil (P < .001), as was cephalic arch stenosis in fistulas (P = .047) and autoge
12 de a neural mechanism by which extracerebral cephalic blood flow couples to brain events; this mechan
13 tic arch arteries, cardiac outflow tract and cephalic blood vessels.
14 eadache selectively elicit relief of ongoing cephalic, but not postsurgical, noncephalic pain.
15                         Excluded larvae bear cephalic caps of immune complexes that may physically bl
16 at vessel structures, which are derived from cephalic (cardiac) neural crest.
17 ent light conditions reveals that in the non-cephalic cells light - mediated by r-Opsin1 - adjusts th
18                                          Non-cephalic cells possess a full set of phototransduction c
19 eparated by 0.50 mm, was implanted through a cephalic chamber targeting the STN.
20 nine infants with microcephaly (defined by a cephalic circumference of </=32 cm) with a presumed diag
21 embryonic development and exhibit incomplete cephalic closure similar to that observed in a subset of
22 ry neuron type K (ASK) and the male-specific cephalic companion neuron (CEM), are required for male a
23 producing a more extensive reorganisation of cephalic crest than has been previously described.
24                                          The cephalic decussation of the pyramidal tract, an enlarged
25                             There are severe cephalic defects in slp1 mutants, including the complete
26 ternal outer labial dendrite (OL1); a second cephalic dendrite in the female (CEP2/CEM); an accessory
27                                              Cephalic depolarization was sufficient for coordination.
28 ied at embryonic day (E) 10.5 with defective cephalic development.
29 were more often seen in infants with smaller cephalic diameter at birth and in infants whose mothers
30 en normal, showed lower ADC values than more cephalic disks.
31  with cortical expansion are associated with cephalic disorders.
32 n all patients but was not as predictable as cephalic displacement.
33 ose of extant panarthropods demonstrate that cephalic domains of C. catenulum predate the evolution o
34  unsegmented head and brain comprising three cephalic domains, distinct from the metameric ventral ne
35 ogous to trilobite-free cheeks, to trilobite cephalic doublure, or independently derived.
36 e generated mouse lines lacking Pbx genes in cephalic ectoderm and demonstrated that they exhibit ful
37 nal-fetal interface, and in cephalic and non-cephalic embryonic tissues from BTBR compared to C57BL/6
38  positioned cross-talk between the embryonic cephalic epithelia and mesenchyme.
39 tive and responsive interactions between the cephalic epithelia and the cranial neural crest (CNC) an
40 d its associated sensory nerves develop from cephalic epithelial thickenings called neurogenic placod
41 ed in tissues (olfactory epithelium, ventral cephalic epithelium) that are believed to derive from th
42                                              Cephalic explants isolated from Chrd;Nog double mutant e
43     Ectopic application of BMP2 to wild-type cephalic explants results in decreased FGF8 and SHH expr
44 meric opsins (r-opsins) are light sensors in cephalic eye photoreceptors, but also function in additi
45 ypostome, a slit-like mouth, and distinctive cephalic feeding appendages.
46 osition, ventral to the hypothalamus, as the cephalic flexure occurs and the jaws and mouth form.
47                                          The cephalic furrow (CF), one of the first morphological man
48 the embryo that ultimately gives rise to the cephalic furrow and may account for the effect of paired
49 lows, the model requires the presence of the cephalic furrow, a fold located anteriorly of the extend
50  concentrations in cells at positions of the cephalic furrow, an early morphological marker, differ b
51 e absence of proper connectivity between the cephalic ganglia and the ventral nerve cords, neurally d
52 rranea, hedgehog (hh) is expressed in medial cephalic ganglia neurons, suggesting a possible role in
53  mediterraneaat different time points during cephalic ganglia regeneration.
54 wn compounds to be followed as a function of cephalic ganglia regeneration.
55 ng, our results suggest that even though the cephalic ganglia structure is visible after 6 days of re
56 n CNS regeneration, including failure of the cephalic ganglia to properly pattern and a loss of expre
57 ed tissues at the midline; these include the cephalic ganglia, ventral nerve cords, photoreceptors, a
58  bilaterally paired neuron descends from the cephalic ganglion and projects uninterrupted through the
59 are dependent on signals descending from the cephalic ganglion.
60  Our study is the first demonstration that a cephalic gap gene is directly regulated by Bcd.
61 at a small regulatory region upstream of the cephalic gap gene orthodenticle (otd) is sufficient to r
62                      Here, we focused on the cephalic gap gene orthodenticle (otd), which establishes
63 otd acts in a combinatorial fashion with the cephalic gap genes empty spiracles (ems) and buttonhead
64                                          The cephalic gap genes specify anterior head development in
65 een proposed that Bcd directly activates the cephalic gap genes, which are the first zygotic genes to
66 s idea directly, although recent analyses of cephalic gene expression patterns in insects suggest a s
67  to females if cantharidin is added to their cephalic gland.
68 ngest cantharidin secrete cantharidin from a cephalic gland.
69                                  These are a cephalic horn resulting from an extreme modification of
70 roduction of ectopic, dorsal outgrowths with cephalic identity.
71 arge, medium, small), sex (male, female) and cephalic index (brachycephalic, mesocephalic, dolichocep
72 demographic estimates, regarding age, breed, cephalic index, and body size.
73                     We suggest that hell ant cephalic integration-analogous to the vertebrate skull-t
74 endage with elongate flagella, four biramous cephalic limbs, 11 trunk segments with biramous limbs an
75                    Consecutive patients with cephalic locally advanced pancreatic cancer who underwen
76 lator of both IFT dynamics and length in the cephalic male (CEM) cilia of Caenorhabditis elegans.
77                              In EV-releasing cephalic male (CEM) cilia, TTLL-11 and the deglutamylase
78 rom nine ciliary A-B doublet microtubules in cephalic male (CEM) neurons.
79                            CCE, also seen in Cephalic male (CEM) sensory neurons, is stereotyped and
80 dimorphic survival of the male-specific CEM (cephalic male) sensory neurons; the homologous cells of
81                The greatest displacement was cephalic (mean, 1.5 cm; range, 0.5-2.4 cm).
82 s effect is mediated, at least in part, by a cephalic mechanism that involves recruitment of the vagu
83  the tunicate Ciona intestinalis possesses a cephalic melanocyte lineage (a9.49) similar to neural cr
84 hages was eliminated, whereas the arrival of cephalic mesenchyme and stromal choroid plexus BAMs was
85  its expression in the primitive heart tube, cephalic mesenchyme, and yolk sac vasculature.
86 formations, and marked cell death within the cephalic mesenchyme.
87 onia simplicifolia isolectin B4 (IB4) in the cephalic mesenchyme.
88 ogenesis from preformed blood vessels in the cephalic mesenchyme.
89                      These data suggest that cephalic mesendoderm, including prechordal mesendoderm a
90         Several embryonic tissues, including cephalic mesendoderm, notochord, and hindbrain, have bee
91 ulation in the prechordal plate and paraxial cephalic mesendoderm, tissues that either pass beneath o
92                 Cranial dermis develops from cephalic mesoderm and neural crest cells, but what signa
93  experiments and mutant analysis reveal that cephalic mesoderm is the source of Fgf signals.
94 t population of macrophages that arises from cephalic mesoderm.
95 , but instead expresses molecular markers of cephalic mesoderm.
96 helia and the cranial neural crest (CNC) and cephalic mesodermal mesenchyme.
97 activates the underlying neural mechanism of cephalic migraine symptoms, central sensitization, also
98 er jaw-like structures, suggesting that some cephalic NCCs alter their "identity" in the absence of E
99 omous role in the development of cardiac and cephalic NCCs and provides a model for the study of aber
100                      An outgroup analysis of cephalic neural characters among extant metazoans also i
101  their fossil record, the variation in their cephalic neural characters, and the development of these
102 nisms mediating the genetic specification of cephalic neural circuits in arthropods correspond to tho
103       The lower jaw skeleton is derived from cephalic neural crest (CNC) cells that reside in the man
104 blasts and adipocytes originate in part from cephalic neural crest (CNC) precursors.
105 djacent mesenchyme that is derived from both cephalic neural crest and paraxial mesoderm.
106  start addressing this question, we used the cephalic neural crest as a model system and looked at th
107 ing further analysis of the role of dHAND in cephalic neural crest cell development.
108                                  Cardiac and cephalic neural crest cells (NCCs) are essential compone
109  pathway for inductive communication between cephalic neural crest cells and their environmental coun
110   Intriguingly, Otx is also expressed in the cephalic neural crest cells as well as mesenchymal and e
111 t our transgene is not globally expressed in cephalic neural crest cells within the pharyngeal arches
112 at dHAND is first expressed in postmigratory cephalic neural crest cells within the pharyngeal arches
113 e in the craniofacial region is derived from cephalic neural crest cells, which undergo three primary
114 tissue of the craniofacial region arise from cephalic neural crest cells.
115 sage of treacle is essential for survival of cephalic neural crest cells.
116 lopmental defects in structures derived from cephalic neural crest cells.
117 ular nature of the cell-cell interactions in cephalic neural crest development.
118 rom salamander embryos prior to the onset of cephalic neural crest migration, taste buds developed in
119 ilencing in the anterior head of frog or the cephalic neural crest of chick embryos show that Cubn is
120 s expressed in dorsal neural tube, eyes, and cephalic neural crest.
121 keletal defects, in tissues derived from the cephalic neural crest.
122 occur, including the developing limb and the cephalic neural crest.
123 zo1 is required for the migration of Xenopus cephalic neural crest.
124 oderm, prechordal plate, and the prospective cephalic neural plate, and at later stages of developmen
125 y activated in the overlying ectoderm of the cephalic neural plate, suggesting that inductive contact
126 ior visceral and definitive endoderm and the cephalic neural plate.
127 iffuse nerve nets and possibly, ganglionated cephalic neural systems existed in Ediacaran organisms.
128 nd (deutocerebral) and third (tritocerebral) cephalic neuromeres have been recently resolved on the b
129 e role of calcitonin gene-related peptide in cephalic pain driven by raised ICP by inhibiting calcito
130 ort the rationale that reducing ICP improves cephalic pain in conditions of raised ICP.
131                                              Cephalic pain was unmasked in rats by assessment of moti
132 ated with altered cerebral haemodynamics and cephalic pain.
133 rat dura mater to elicit a presumed state of cephalic pain.
134 ogenitors originate from hedgehog-responsive cephalic paraxial mesoderm (Mes) cells, which migrate ra
135     Since cells that originate from both the cephalic paraxial mesoderm and the neural crest populate
136                              The median (SD) cephalic perimeter at birth was 31 (3) cm, a value lower
137                                          The cephalic perimeter was inversely proportional with the d
138 th and without ocular findings regarding the cephalic perimeter: mean (SD) of 28.8 (1.7) and 30.3 (1.
139 etion and motor activity associated with the cephalic phase of feeding.
140  infusion of glucose and water to bypass the cephalic phase of food intake.
141 ood intake by interfering with anticipatory, cephalic phase, and metabolic hormone responses.
142 ) and allows new comparisons with the dorsal cephalic plate of radiodontans, large nektonic predators
143 t flow velocities were identified within the cephalic portion of the inferior vena cava.
144 93 women, who had term, singleton, liveborn, cephalic pregnancies requiring operative delivery in the
145 ticularly for term singleton pregancies with cephalic presentation and in case of obstructed labour a
146 gave birth to a singleton, term pregnancy in cephalic presentation and in spontaneous labor).
147 ays' gestation who were in active labor with cephalic presentation and who delivered vaginally or via
148 included a total of 435 281 live births with cephalic presentation in labor (median gestational age a
149 win pregnancy and with the first twin in the cephalic presentation to planned cesarean section or pla
150 ays of gestation, with the first twin in the cephalic presentation, planned cesarean delivery did not
151  gestational age in which the fetus was in a cephalic presentation.
152 rts along with a striking array of horn-like cephalic projections [4-6].
153  such as congenital candidiasis and neonatal cephalic pustulosis to potentially fatal infections with
154 ed and distinct features of cephalic and non-cephalic r-opsin1-expressing cells.
155 own disrupts nervous system structure during cephalic regeneration: the newly regenerated brain and v
156 sion and abnormal remodeling occurred in the cephalic region concomitant with marked mesenchymal cell
157  is dynamically expressed in the prospective cephalic region of the embryo during gastrulation.
158  found that the calcification process in the cephalic region was not limited to mystacial vibrissae b
159 ession in the most dorsoanterior part of the cephalic region, and (iii) vnd/NK-2 protein is required,
160 ern in the nerve cord but not in part of the cephalic region.
161  which subsequently became restricted to the cephalic region.
162 ype mice and localized the expression to the cephalic regions of the developing neural tube.
163 , with the deficits particularly apparent in cephalic regions.
164  MSF were prolonged beyond the period of the cephalic response and these may be relevant for longer-t
165               Preclinically, we examined the cephalic response properties of central trigeminocervica
166                        In male-specific CEM (cephalic sensilla, male) cilia, ccpp-1 also controls the
167 expression of GFP in the sheath cells of the cephalic sensilla.
168 a single male-specific class of neurons, the cephalic sensory neurons (CEMs).
169        In at least one case, that of the CEM cephalic sensory neurons, cilium architecture is disrupt
170 sive accumulation of EVs in the lumen of the cephalic sensory organ, and failure to release PKD-2::GF
171 r development and function of the C. elegans cephalic sheath (CEPsh) glia.
172  factor 1 (hsf-1) in the four astrocyte-like cephalic sheath cells of Caenorhabditis elegans induces
173                                              Cephalic sheath glial hsf-1 overexpression also leads to
174  anterior field formed by the oral plate and cephalic shield) of the nudibranch Phestilla sibogae aft
175 rospective cohort study of 18,880 full-term, cephalic singletons born in San Francisco, California, d
176 les of the blastoderm embryo and in a single cephalic stripe.
177 romote the differentiation of pharyngeal and cephalic structures.
178 es - moult by breaking the exoskeleton along cephalic sutures, a strategy that has contributed to the
179 a pair of lateral eyes, a putative condensed cephalic synganglion, and a metameric ventral nerve cord
180 phores (>4,000/mm2), and TSCs in the tips of cephalic tentacles (100/mm2).
181 evels in the nerve ring, the osphradium, the cephalic tentacles, the buccal tissues, and the foot, wh
182 snails when compared with the innervation of cephalic tentacles, which are involved in mechanorecepti
183                                              Cephalic tetanus was initially suspected but laboratory
184 contaminated head wound can be confused with cephalic tetanus.
185 a body plan is composed of a linear array of cephalic, thoracic, and abdominal segments along the ant
186 te Walliserops carries a remarkable anterior cephalic trident posing a challenge to functional interp
187  tested (luminal acid, prostaglandin E2, and cephalic-vagal stimulation) in patients with duodenal ul
188              The results indicate that while cephalic vascular tone is controlled by endogenous nitri
189 8.0, and by E8.5 there is a complete lack of cephalic vascularization, a reduction in the number of s
190 ogenous nitrite acts as a vasodilator in the cephalic vasculature of the intact, near term fetal shee
191    Spatial transcriptomic analysis of canine cephalic vein after initial conduit harvest and distenti
192                                              Cephalic vein grafts were interposed bilaterally in the
193   A primary open strategy by cut-down of the cephalic vein, if necessary enhanced by a modified Seldi
194 ies in which FUra was administered through a cephalic vein.
195                         Mean peak diastolic (cephalic) velocities were 3.9 and 3.4 cm/sec in the IS a
196                                     External cephalic version (ECV) is a safe procedure that reduces
197 reech presentation was detected, an external cephalic version (ECV) was routinely offered.
198 ndard antenatal referral pathway or external cephalic versions (ECVs) performed during the study peri

 
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