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1 spatially varying tissue mechanics along the anteroposterior axis.
2  gradient and initiates patterning along the anteroposterior axis.
3 t patterns developing egg chambers along the anteroposterior axis.
4 and serves to polarize these cells along the anteroposterior axis.
5 ormation, and embryonic elongation along the anteroposterior axis.
6 notochord in the posterior, along the entire anteroposterior axis.
7 pression of genes along the dorsoventral and anteroposterior axis.
8 f the paraxial mesoderm into units along the anteroposterior axis.
9 lly differentiated cells, organized along an anteroposterior axis.
10 vulval precursor cells distributed along the anteroposterior axis.
11 anizer pattern the neural ectoderm along the anteroposterior axis.
12 sgene was consistently seen across the whole anteroposterior axis.
13 pecification of segmental identity along the anteroposterior axis.
14  of the conceptus or failure to elongate the anteroposterior axis.
15 itions the migrating Q descendants along the anteroposterior axis.
16 the caudal aspect of the embryo and thus the anteroposterior axis.
17 al is required for patterning the developing anteroposterior axis.
18 omponent of the sperm normally specifies the anteroposterior axis.
19 ical neurons or white matter cells along the anteroposterior axis.
20  new gut branches are added along the entire anteroposterior axis.
21 ange in signaling by the notochord along the anteroposterior axis.
22 ng the complete pattern of digits across the anteroposterior axis.
23 ogical and molecular heterogeneity along the anteroposterior axis.
24 rently depending on their location along the anteroposterior axis.
25 arget area because of guidance errors in the anteroposterior axis.
26  as somite pairs sequentially form along the anteroposterior axis.
27 lling polarizes neural progenitors along the anteroposterior axis.
28 f cilia, depending on the location along the anteroposterior axis.
29 t is the establishment of polarity along the anteroposterior axis.
30 that of visceral muscle precursors along the anteroposterior axis.
31 enesis is differentially regulated along the anteroposterior axis.
32 ting the existing proximodistal axis into an anteroposterior axis.
33 or a functional division primarily along the anteroposterior axis.
34 ells and Gli3 is broadly expressed along the anteroposterior axis.
35 genes cooperate to pattern the FRT along the anteroposterior axis.
36  link somitogenesis to the elongation of the anteroposterior axis.
37 ly blood and endothelial genes all along the anteroposterior axis.
38 fer positional identities to cells along the anteroposterior axis.
39 n essential step in the determination of the anteroposterior axis.
40 ween Bicoid and Hunchback, which pattern the anteroposterior axis.
41 e induction of multiple structures along the anteroposterior axis.
42 s by which the embryo is patterned along the anteroposterior axis.
43 core of the nucleus accumbens and across its anteroposterior axis.
44 dent of cell interactions conveyed along the anteroposterior axis.
45  anterior and posterior cell fates along the anteroposterior axis.
46       Rotating rhombomeres 5 and 6 along the anteroposterior axis also impacts cochlear duct morphoge
47 tly associated, such as specification of the anteroposterior axis and anterior neural development, or
48 n of individual sclerotome progeny along the anteroposterior axis and development of the axial skelet
49  Here we identify the cue that specifies the anteroposterior axis, and investigate how this cue is in
50 erning of the pharyngeal apparatus along the anteroposterior axis, and local regulation of retinoic a
51 ic defects including spina bifida, shortened anteroposterior axis, and reduced anterior structures.
52  long axis of the ellipse oriented along the anteroposterior axis, and this orientation may adversely
53 yos are characterised by a truncation of the anteroposterior axis anterior to the somites, defects in
54 ed limbs are typically very narrow along the anteroposterior axis, are occasionally truncated, and ex
55 ry in the epiblast is regionalized along the anteroposterior axis as in lower vertebrates.
56 of amphioxus, AmphiEn is expressed along the anteroposterior axis as metameric stripes, each located
57 ertebrate body is its segmentation along the anteroposterior axis, as illustrated by the repetition o
58 Hox genes has shifted dramatically along the anteroposterior axis between Onychophora and different a
59  otic vesicle is highly asymmetric about the anteroposterior axis, both morphologically and molecular
60  ablation of Aurora A properly establish the anteroposterior axis but fail to progress through gastru
61 orphogen controls cell fate along 70% of the anteroposterior axis but is translated from mRNA localiz
62 ments with respect to distribution along the anteroposterior axis but support a 'leaky' resegmentatio
63 g completely reverses the orientation of the anteroposterior axis, but gives otherwise normal develop
64 n signaling to polarize the termini of their anteroposterior axis, but little is known about how rege
65 By contrast, Bozozok can rescue the complete anteroposterior axis, but not notochord, in embryos bloc
66 ating morphogenetic activity: patterning the anteroposterior axis by diffusion of a transcription fac
67 fferences in neuronal architecture along the anteroposterior axis by the selective elimination of mat
68                      Elongation of the mouse anteroposterior axis depends on a small population of pr
69  reproductive tract differentiates along the anteroposterior axis during postnatal development.
70 esponsible for organizing and patterning the anteroposterior axis during the development of amphibian
71  Blimp1 is required for the establishment of anteroposterior axis formation and the formation of head
72 s on the early evolution of spiral cleavage, anteroposterior axis formation, body axis segmentation,
73 s establish that Eomes is a key regulator of anteroposterior axis formation, EMT and definitive endod
74 cing atRAL levels and is required for proper anteroposterior axis formation, neuroectoderm patterning
75 ntation groups on chromosome 3R that disrupt anteroposterior axis formation.
76 bryonic from extra-embryonic cells along the anteroposterior axis from the outset of development - a
77                         The formation of the anteroposterior axis in mice requires a Wnt3-dependent s
78  expression of these genes defined a precise anteroposterior axis in shield explants.
79 re expressed symmetrically across the entire anteroposterior axis in talpid3 limb buds.
80 and retinoic acid, and is uniform across the anteroposterior axis in talpid3 mutants.
81 ry, we identify new muscle domains along the anteroposterior axis in the zebrafish that are defined b
82 acZ expression to distinct regions along the anteroposterior axis including the ventral midline of th
83 genes specify appendage identities along the anteroposterior axis independently of Tc-hth/Tc-exd and
84 ific factors in response to dorsoventral and anteroposterior axis information.
85         In Xenopus, the establishment of the anteroposterior axis involves two key signalling pathway
86 , when differential Hox expression along the anteroposterior axis is being established, we found conc
87        Together, these results show that the anteroposterior axis is correctly positioned by the acti
88 ntity within dorsolateral mesoderm along the anteroposterior axis is determined by the combined actio
89                   The Caenorhabditis elegans anteroposterior axis is established in response to ferti
90                    Specification of the otic anteroposterior axis is one of the earliest patterning e
91 ssion of genes such as omb and sal along the anteroposterior axis is restricted by lateral-to-medial
92 have defined expression boundaries along the anteroposterior axis (known as the axial Hox code).
93 g is required for correct positioning of the anteroposterior axis, normal anterior and midline patter
94 different morphologies of segments along the anteroposterior axis of animals.
95                                          The anteroposterior axis of Drosophila is defined during oog
96 ans, Hox genes determine cell fate along the anteroposterior axis of embryos and are implicated in dr
97 eneity was observed between groups and along anteroposterior axis of healthy hippocampus in both grou
98 nases are asymmetrically localized along the anteroposterior axis of newly fertilized C. elegans embr
99 ir major axis of orientation parallel to the anteroposterior axis of the brain.
100 ed in specifying positional values along the anteroposterior axis of the caudal central nervous syste
101 lished in the one-cell embryo determines the anteroposterior axis of the developing animal and is ess
102                                          The anteroposterior axis of the developing embryo becomes mo
103 cated in conferring regional identity to the anteroposterior axis of the developing embryo.
104 ntial nuclear organisation of Hoxb along the anteroposterior axis of the developing neural tube is co
105 ern of expression with that of Mn1 along the anteroposterior axis of the developing palatal shelves a
106 A exhibits differential expression along the anteroposterior axis of the developing secondary palate,
107                                      For the anteroposterior axis of the Drosophila embryo, the first
108 les and cellular hairs (trichomes) along the anteroposterior axis of the Drosophila thorax (notum).
109 roduction of individual embryos the original anteroposterior axis of the egg is lost and axial patter
110 ex-expressing cells distinguishes the future anteroposterior axis of the embryo and provide landmarks
111 y in the mouse embryo and indicates that the anteroposterior axis of the embryo develops from convers
112  develop at two specific positions along the anteroposterior axis of the embryo, whereas other region
113  mirror-image pattern duplications along the anteroposterior axis of the embryo.
114 f polarising activity, which establishes the anteroposterior axis of the limb bud and maintains proli
115 he long-distance movement of ShhN across the anteroposterior axis of the limb bud.
116 nstrate that long-range diffusion across the anteroposterior axis of the limb is possible.
117 ld) locus do not form a proper ridge and the anteroposterior axis of the limb is shortened.
118 role for the ExE in the specification of the anteroposterior axis of the mouse embryo.
119 oxd13, and Fgf4 are expressed throughout the anteroposterior axis of the mutant limb bud, despite nor
120 rhythmic movements are distributed along the anteroposterior axis of the nervous system.
121 that controls spatial organization along the anteroposterior axis of the neural tube and is particula
122 f retinoic acid signalling in patterning the anteroposterior axis of the neural tube remains uncertai
123  oocyte is located adjacent to them, and the anteroposterior axis of the oocyte is re-oriented with r
124 rrounding follicle cells and establishes the anteroposterior axis of the oocyte.
125 rning process that passes wavelike along the anteroposterior axis of the presomitic mesoderm (PSM).
126  L1-minus temporal axons extended across the anteroposterior axis of the SC like wild-type axons but
127 uence of positional values ordered along the anteroposterior axis of the segmental repeat.
128           Second, 180 degree rotation in the anteroposterior axis of the target results in anterior i
129                                          The anteroposterior axis of the vertebrate embryo becomes ex
130                        Patterning across the anteroposterior axis of the vertebrate limb bud involves
131 ed pattern of neurons is specified along the anteroposterior axis of the vertebrate spinal cord by in
132 hat control developmental pathways along the anteroposterior axis of vertebrates.
133 RE strongly suggest a role for Hoxb-1 in the anteroposterior axis patterning of the gut and a critica
134 l cord at two restricted locations along the anteroposterior axis, presumably the subpopulation of mo
135 eotides resulted in a phenotype of shortened anteroposterior axis, reduced head structure, and pertur
136 sibility that the later dispersion along the anteroposterior axis results from the parasagittal patte
137 mediated activation of Vent2 and Cdx4 during anteroposterior axis specification.
138 istinct midline expression domains along the anteroposterior axis that overlap with the expression pa
139 like gene are expressed in domains along the anteroposterior axis that reset to new positions during
140 is divided into three main regions along the anteroposterior axis: the forebrain, midbrain and hindbr
141  achieves much of its power to diversify the anteroposterior axis through fine spatiotemporal differe
142 nin specifies the posterior character of the anteroposterior axis throughout the Bilateria and specif
143 al germ layer becomes regionalized along its anteroposterior axis to give rise to a variety of organs
144 he dorsal adult muscles are polarised in the anteroposterior axis: we disprove the hypothesis that mu
145 s first differentiate in intervals along the anteroposterior axis, whereas in deep neural explants, m
146  of the Bicoid (Bcd) morphogen organizes the anteroposterior axis while the ends of the embryo are pa
147 dition, disrupts the proper alignment of the anteroposterior axis with the shape of the embryo and th
148 proximodistal axis, but uniformly across the anteroposterior axis, with all proximal limb bud cells e
149 ertebrates is relatively symmetric about the anteroposterior axis, with only two semicircular canals
150  are expressed in distinct domains along the anteroposterior axis within the dorsal vessel, and, in p

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