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1 , thoracic, and abdominal segments along the anterior posterior axis.
2 arget genes at different positions along the anterior-posterior axis.
3 lts in abnormal gastrulation and a shortened anterior-posterior axis.
4 ted for six PP that span along the embryonic anterior-posterior axis.
5  Strikingly, phenotypes are graded along the anterior-posterior axis.
6 defined dorsal-ventral axis imposed on their anterior-posterior axis.
7 sed within the pharyngeal endoderm along the anterior-posterior axis.
8 resents a crucial event in patterning of the anterior-posterior axis.
9 dline of the developing CNS along its entire anterior-posterior axis.
10 emphasizing tonotopic organization along the anterior-posterior axis.
11 intricate scaffold of cables parallel to the anterior-posterior axis.
12 ole in establishing distinct fates along the anterior-posterior axis.
13 sor function in restricting induction of the anterior-posterior axis.
14 maintenance is crucial for completion of the anterior-posterior axis.
15 pecification of body segment identity in the anterior-posterior axis.
16 the dorso-ventral axis and in patterning the anterior-posterior axis.
17 is known to be required for formation of the anterior-posterior axis.
18 m induction and results in truncation of the anterior-posterior axis.
19 sts play in the patterning of the vertebrate anterior-posterior axis.
20 tions) followed by junction extension in the anterior-posterior axis.
21 e of signals from adjacent repeats along the anterior-posterior axis.
22 ween neighboring blast cell clones along the anterior-posterior axis.
23 skar mRNA are key events in establishing the anterior-posterior axis.
24 pecify aspects of segment identity along the anterior-posterior axis.
25 s, particularly in those patterned along the anterior-posterior axis.
26 izer development, and the positioning of the anterior-posterior axis.
27 growth and patterning of the limbs along the anterior-posterior axis.
28 ns that are ubiquitously expressed along the anterior-posterior axis.
29 ctive properties of callosal axons along the anterior-posterior axis.
30 alternative developmental pathways along the anterior-posterior axis.
31 is the first overt morphological sign of the anterior-posterior axis.
32 mation of segment specific structures in the anterior-posterior axis.
33 n do mammals, despite less complexity in the anterior-posterior axis.
34 on that result in dramatic shortening of the anterior-posterior axis.
35 proximal-distal asymmetry into an orthogonal anterior-posterior axis.
36 polarised microtubule array that defines the anterior-posterior axis.
37  for DPP, show shifts in cell fate along the anterior-posterior axis.
38 iption factors, control cell fates along the anterior-posterior axis.
39 n Drosophila embryonic development along the anterior-posterior axis.
40  which define different identities along the anterior-posterior axis.
41 pecialization for these properties along its anterior-posterior axis.
42 gut looping defects and shortening along the anterior-posterior axis.
43 e pathology was generalized along the entire anterior-posterior axis.
44  causes the egg chamber to rotate around its anterior-posterior axis.
45  striking regional differentiation along its anterior-posterior axis.
46 is responsible for correctly orientating the anterior-posterior axis.
47 d for coordinated neural signaling along the anterior-posterior axis.
48 l body organisation along all or part of the anterior-posterior axis.
49 s in an inhibition of neurogenesis along the anterior-posterior axis.
50         This Dicer mutant exhibits a reduced anterior-posterior axis.
51 A)] in the brainstem project axons along the anterior-posterior axis.
52 d by shifts in Hox gene expression along the anterior-posterior axis.
53 nt of neuronal polarity along the C. elegans anterior-posterior axis.
54 es appropriate organ specification along its anterior-posterior axis.
55  the longitudinal fibres, oriented along the anterior-posterior axis.
56 le dislocations of notochord cells along the anterior-posterior axis.
57 d asymmetric cell divisions along the entire anterior-posterior axis.
58 aces in mirror image symmetry, with a common anterior-posterior axis.
59 in opposite orientations with respect to the anterior/posterior axis.
60 ors associated with their position along the anterior/posterior axis.
61 lly to specify positional identity along the anterior/posterior axis.
62  characteristic of their positions along the anterior/posterior axis.
63 oss of other domains of expression along the anterior/posterior axis.
64 ted in an embryo dorsalized along the entire anterior/posterior axis.
65 aterians: elongation of the embryo along the anterior-posterior axis [1].
66 ne-cell embryo of C. elegans establishes the anterior--posterior axis (A-P), and is necessary for the
67                      The polarization of the anterior-posterior axis (A-P) of the Caenorhabditis eleg
68  is the polarization of the oocyte along the anterior-posterior axis, a process induced by an unknown
69  embryonic structures is polarized along the anterior/posterior axis, a subdivision first distinguish
70 genes are essential to the patterning of the anterior-posterior axis along the developing Drosophila
71 lls in the ventral midline arrayed along the anterior-posterior axis and 6 of these cells become the
72  in overlapping transverse stripes along the anterior-posterior axis and act in combination to direct
73 the alignment of cell division planes to the anterior-posterior axis and acts in parallel to known po
74 ress Smad2(Deltaexon3) correctly specify the anterior-posterior axis and definitive endoderm, and are
75 ase activity and disrupted elongation of the anterior-posterior axis and differentiation of skeletal
76 he extent to which hb is expressed along the anterior-posterior axis and displayed a reduced ability
77 set of embryos also show a shortening of the anterior-posterior axis and frequent duplication of axia
78  Pax9 plays a crucial role in patterning the anterior-posterior axis and outgrowth of the developing
79 wnstream signaling pathways differ along the anterior-posterior axis and suggests a functional role f
80            Although the specification of the anterior-posterior axis and the initial response to meso
81 nal gradients, one of Wnt activity along the anterior-posterior axis and the other of BMP signals alo
82 bditis elegans is necessary to establish the anterior-posterior axis and to ensure the proper identit
83 (TCF/LEF) transcriptional activity along the anterior-posterior axis, and 3) coelomocyte competence f
84 is, where the embryo derives from the entire anterior-posterior axis, and all segments are patterned
85   Wnt signaling controls regeneration of the anterior-posterior axis, and Bmp-Admp signaling controls
86 spects of neural crest maintenance along the anterior-posterior axis, and establish an unprecedented
87 hord development during the formation of the anterior-posterior axis, and its role in this process is
88 rgan-like structure that lengthens along its anterior-posterior axis as it grows.
89 leotides results in embryos with a truncated anterior-posterior axis, as well as elongated somites an
90  observed in large cells scattered along the anterior-posterior axis at stage 13.
91  lumbosacral neural tube are reversed in the anterior-posterior axis at stage 15 (embryonic day 2.5),
92 ment cranial or caudal) were reversed in the anterior-posterior axis at stages 13 and 14 (embryonic d
93 ve rise to descendants that stream along the anterior-posterior axis at the ventral midline and contr
94  results suggest that interactions along the anterior-posterior axis between neighboring primary blas
95 proteins regulate axonal outgrowth along the anterior-posterior axis, but the intracellular mechanism
96 , the spindle is aligned and centered on the anterior-posterior axis by a microtubule-dependent machi
97 tion and strength of Wnt signaling along the anterior-posterior axis by employing a Ror family Wnt re
98  isthmic organizer are partitioned along the anterior-posterior axis by lineage restriction boundarie
99 actors specify numerous cell fates along the anterior-posterior axis by regulating the expression of
100 nduction also directs a midbrain fate in the anterior-posterior axis by suppressing caudalization as
101 t subpopulations of follicle cells along the anterior/posterior axis can respond to Top/Egfr activati
102 apical ectodermal ridge and shortened in the anterior-posterior axis, consistent with the observed lo
103 th Wnts are expressed in gradients along the anterior-posterior axis, consistent with their role as d
104          In contrast, large errors along the anterior-posterior axis corresponding to nasal-temporal
105 l proliferation and tissue patterning during anterior-posterior axis, craniofacial and limb developme
106 y become polarized during stage 6 around the anterior-posterior axis defined by the polar cells, but
107 arization of the C. elegans zygote along the anterior-posterior axis depends on cortically enriched (
108 ulatory mechanisms during distinct stages of anterior/posterior axis development, and uncover previou
109 tino/kreisler, a hox gene regulator, produce anterior-posterior axis disruptions of pharyngeal cartil
110 pression in the palatal epithelium along the anterior-posterior axis during early palate development.
111 nd patterning of the neuroectoderm along the anterior-posterior axis during gastrulation.
112 pr177 is essential for the patterning of the anterior-posterior axis during mammalian development.
113  the ancestral deuterostome embryo along its anterior-posterior axis during the late blastula and sub
114 ges as the body extends to form the complete anterior-posterior axis during the somite-forming stages
115  signaling is essential for establishing the anterior/posterior axis during regeneration by modulatin
116            Consistent with this, the rate of anterior-posterior axis elongation is reduced relative t
117  PCP proteins, polarize node cells along the anterior-posterior axis for breaking of left-right symme
118 alized at the posterior of young oocytes for anterior-posterior axis formation and later in the dorsa
119                   Although the mechanisms of anterior-posterior axis formation are well understood in
120 we present evidence that Star is involved in anterior-posterior axis formation both in the female ger
121 ing a possible explanation for the defect in anterior-posterior axis formation caused by Notch and De
122             The Par-1 kinase is required for anterior-posterior axis formation in Drosophila.
123                                              Anterior-posterior axis formation in the Drosophila oocy
124                         BPTF is required for anterior-posterior axis formation of the mouse embryo an
125 ut the precise role of the follicle cells in anterior-posterior axis formation remains enigmatic.
126 ng early in oogenesis and are independent of anterior-posterior axis formation.
127  we observed putative HSN homologs along the anterior-posterior axis from the head to the tail, but t
128 pI cell in the epithelium oriented along the anterior-posterior axis, giving rise to pIIa and pIIb, w
129 a segmental form of cardiac defect along the anterior-posterior axis in all homozygous mice identifie
130 id (Bcd) is key for the establishment of the anterior-posterior axis in Drosophila embryos.
131       Bicoid is a morphogen that sets up the anterior-posterior axis in early Drosophila embryos.
132  exposure and extended posteriorly along the anterior-posterior axis in hemizygous mice.
133 the paraxial mesoderm is patterned along the anterior-posterior axis in metameric units, or somites,
134  gap and pair-rule gene expression along the anterior-posterior axis in relation to embryo length.
135 ed a subtle morphological gradient along the anterior-posterior axis in stem members of amniote clade
136 tive in distinct spatial registers along the anterior-posterior axis in the CNS.
137 secreted factor regulating patterning of the anterior-posterior axis in the developing limb.
138         Initiation of the development of the anterior-posterior axis in the mouse embryo has been tho
139 serves an essential role in formation of the anterior-posterior axis in Xenopus laevis embryos, and t
140  regulation of the component genes along the anterior/posterior axis in a manner that correlates with
141  HOM-C/Hox genes pattern cell fate along the anterior/posterior axis in many animals.
142 function during gastrulation to generate the anterior/posterior axis in Xenopus.
143 ng regulates fine scale cell fates along the anterior-posterior axis, in part by creating an adhesion
144 he Mullerian duct actively migrate along the anterior-posterior axis independent of the proliferative
145 vertebrate hindbrain is subdivided along the anterior-posterior axis into a series of seven segments,
146 cortex of the cerebellum is folded along the anterior-posterior axis into lobules separated by fissur
147 e hindbrain is transiently divided along the anterior-posterior axis into seven morphologically and m
148  a common mechanism for patterning along the anterior/posterior axis involving a posterior signaling
149                                          The anterior-posterior axis is a key feature of the bilateri
150  results suggest that the orientation of the anterior-posterior axis is already anticipated before AV
151 The medial-to-lateral Dpp gradient along the anterior-posterior axis is complemented by a lateral-to-
152 n Drosophila, embryonic patterning along the anterior-posterior axis is controlled by the morphogen g
153  Patterning of the vertebrate limb along the anterior-posterior axis is controlled by the zone of pol
154 in all deuterostomes, but, in chordates, the anterior-posterior axis is established at right angles t
155                  The Drosophila melanogaster anterior-posterior axis is established during oogenesis
156 ential RA responsiveness along the hindbrain anterior-posterior axis is shaped primarily by the dynam
157                               The Drosophila anterior-posterior axis is specified when the posterior
158                                          The anterior-posterior axis is therefore established by a re
159 mbryos the spindle failed to align along the anterior/posterior axis, leading to abnormal cleavage co
160 rm and ectoderm contribute to the autonomous anterior-posterior axis lengthening of ventral explants
161 differences in integrin regulation along the anterior-posterior axis may contribute to differences in
162 d endoderm formation, the positioning of the anterior-posterior axis, neural patterning and left-righ
163           HOX genes specify cell fate in the anterior-posterior axis of animal embryos.
164 le (or Pbx1) to affect development along the anterior-posterior axis of animals.
165            The Hox gene cluster patterns the anterior-posterior axis of bilaterians.
166                                          The anterior-posterior axis of Drosophila becomes polarized
167                                          The anterior-posterior axis of Drosophila originates from tw
168 ntial to reorient mitotic spindles along the anterior-posterior axis of elongation, and orthogonal to
169  started to use distinct landmarks along the anterior-posterior axis of HF to allow segmentation into
170         We show that cell position along the anterior-posterior axis of hindbrain rhombomere 8 determ
171 l patterns of Hox gene expression across the anterior-posterior axis of metazoan embryos.
172 egulate the identity of structures along the anterior-posterior axis of most animals.
173         Polarization of node cells along the anterior-posterior axis of mouse embryos is responsible
174                                          The anterior-posterior axis of RIalpha mutants is well devel
175 roteins distribute asymmetrically across the anterior-posterior axis of the 1-cell-stage C. elegans e
176 determination of pattern formation along the anterior-posterior axis of the animal embryo.
177 are regionally specified with respect to the anterior-posterior axis of the avian embryo.
178 Furthermore, slow wave propagation along the anterior-posterior axis of the brain is largely mediated
179  entry of the sperm centrosome polarizes the anterior-posterior axis of the C. elegans zygote by indu
180                                          The anterior-posterior axis of the Caenorhabditis elegans em
181                                          The anterior-posterior axis of the Caenorhabditis elegans zy
182 ng a stable concentration gradient along the anterior-posterior axis of the cell.
183 ly, we show a gradient of s-ShhNp across the anterior-posterior axis of the chick limb, demonstrating
184 d in the guidance of retinal axons along the anterior-posterior axis of the chick optic tectum.
185  the polarizing signal for patterning of the anterior-posterior axis of the developing limb bud.
186 a morphogen to regulate patterning along the anterior-posterior axis of the developing wing.
187  FGF activity occurs as a gradient along the anterior-posterior axis of the dorsal midbrain and direc
188  protein in establishing a pattern along the anterior-posterior axis of the early Drosophila embryo.
189 ity of the cytoplasm does not vary along the anterior-posterior axis of the embryo during the first c
190                                          The anterior-posterior axis of the embryo is positioned late
191  mimic cytokine gradient polarization in the anterior-posterior axis of the embryo led to differentia
192 here morphogen gradients spanning the entire anterior-posterior axis of the embryo provide positional
193 he Bicoid protein gradient that patterns the anterior-posterior axis of the embryo.
194  which form in a metameric pattern along the anterior-posterior axis of the embryo.
195 ribution of HOX protein expression along the anterior-posterior axis of the embryo.
196 in turn are required to establish the future anterior-posterior axis of the embryo.
197 rphogen gradient, a signal that patterns the anterior-posterior axis of the embryo.
198 rupt the transitions between zones along the anterior-posterior axis of the eye disc that express dif
199 mulated by the Unpaired ligand, patterns the anterior-posterior axis of the follicular epithelium.
200 nduce posterior fate, thereby polarising the anterior-posterior axis of the future embryo and then to
201 shows that Odz4 is required to establish the anterior-posterior axis of the gastrulating mouse embryo
202 rained in tissue fate and position along the anterior-posterior axis of the gut, the medial gut endod
203 ce for dissociable memory networks along the anterior-posterior axis of the hippocampus suggests that
204 fferentially interact with regions along the anterior-posterior axis of the hippocampus.
205  of the trochal lineages with respect to the anterior-posterior axis of the larva.
206 terior prestalk compartments lying along the anterior-posterior axis of the migrating slug.
207                                          The anterior-posterior axis of the mouse embryo is establish
208 fragments derived from several levels of the anterior-posterior axis of the neural tube at E14.5 and
209        Embryonic cellular position along the anterior-posterior axis of the neural tube was shown to
210 wn to specify cerebellar territory along the anterior-posterior axis of the neural tube, the mechanis
211 hus, Slmb may induce the polarisation of the anterior-posterior axis of the oocyte by targeting the P
212 monolayer organization and disruption of the anterior-posterior axis of the oocyte.
213 lls at later stages leads to a defect in the anterior-posterior axis of the oocyte.
214 aphic positioning of retinal axons along the anterior-posterior axis of the optic tectum in both Xeno
215 orting during apical tip formation, when the anterior-posterior axis of the organism is formed, by co
216  that exhibit a defined patterning along the anterior-posterior axis of the organism.
217 cked in that fewer sensory axons crossed the anterior-posterior axis of the plexus.
218 as recently been shown to correlate with the anterior-posterior axis of the postimplantation embryo.
219 signaling guides commissural axons along the anterior-posterior axis of the spinal cord.
220 out mice, MSN axons fail to extend along the anterior-posterior axis of the striatum, and many do not
221 c acid (RA) is a morphogen that patterns the anterior-posterior axis of the vertebrate hindbrain.
222 establishing different digit fates along the anterior-posterior axis of the vertebrate limb bud.
223  to organize growth and patterning along the anterior-posterior axis of the wing primordium.
224 s orthogonal to a 'backbone' that models the anterior-posterior axis of the worm.
225 rminants are partitioned unequally along the anterior-posterior axis of the zygote, ensuring the daug
226 nt of regional commitments along most of the anterior/posterior axis of the developing embryo depends
227  a concentration gradient that organizes the anterior/posterior axis of the Drosophila embryo.
228  was induced in follicle cells all along the anterior/posterior axis of the egg chamber.
229 s location with an error bar of ~1 along the anterior/posterior axis of the embryo.
230 ionally, little data is available on how the anterior/posterior axis of the heart tube is determined
231 tablishes the cerebellar territory along the anterior/posterior axis of the neural tube.
232 hancer display variably penetrant defects in anterior-posterior axis orientation and DE formation.
233 nes lead to defects in germ-layer formation, anterior-posterior axis orientation and left-right axis
234 e demonstrate that Rumpelstiltskin regulates anterior-posterior axis patterning by functioning as a d
235 Drosophila hnRNP F/H homolog, contributes to anterior-posterior axis patterning by regulating transla
236 lso suggest that homeobox gene regulation of anterior-posterior axis patterning may have evolved prio
237                                              Anterior-posterior axis patterning of the Drosophila emb
238                                        Mouse anterior-posterior axis polarization is preceded by form
239 es of cells and tissues along the developing anterior-posterior axis, probably in all bilaterian meta
240 eletal differentiation is reversed along the anterior-posterior axis relative to that of other tetrap
241 the formation of these projections along the anterior-posterior axis remain unknown.
242                         Establishment of the anterior-posterior axis requires posterior localization
243                                    Along the anterior-posterior axis, several segment polarity genes
244  As stimulation sites were sampled along the anterior-posterior axis, small amplitude, nasally direct
245                                       During anterior-posterior axis specification in the Drosophila
246 lopmental processes, including gastrulation, anterior-posterior axis specification, organ and tissue
247 d that Oncopeltus hunchback has two roles in anterior-posterior axis specification.
248 ells are asymmetrically positioned along the anterior-posterior axis such that more cilia are placed
249 rk in the Drosophila oocyte that defines the anterior-posterior axis, suggesting that microtubule org
250 split along the midline and fused across the anterior-posterior axis, suggesting that these defects m
251                                    Along the anterior-posterior axis, the posteriorly expressed prote
252 fferentiation of neuronal subtypes along the anterior-posterior axis, their mode of action is not ent
253                               The Drosophila anterior-posterior axis therefore becomes polarised by a
254 influences on cortical surface area along an anterior-posterior axis using neuroimaging data of adult
255 a-aminobutyric acid (GABAA) system along its anterior-posterior axis, using localized microinfusions
256                 Dictyostelium establishes an anterior/posterior axis utilizing seven-transmembrane cA
257 entation genes patterns the embryo along its anterior-posterior axis via subdivision of the blastoder
258  RXR caused striking malformations along the anterior-posterior axis, whereas in zebrafish only ligan
259 t signaling participates in establishing the anterior/posterior axis, whereas HOM-C genes confer regi
260 y embryo into reiterative segments along the anterior-posterior axis, while Hox genes assign segments
261 gions organized along the dorsal-ventral and anterior-posterior axis with distinct functional network
262  Loss of circular fibres led to a bifurcated anterior-posterior axis with fused heads forming in sing
263 ing activity appears as a gradient along the anterior-posterior axis with two- to threefold higher le
264 ng discs are expanded specifically along the anterior-posterior axis, with increased proliferation in

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